| A | B | C | D | E | F | G | H | I | J | K | L | M | N | O | P | Q | R | S | T | U | V | W | X | Y | Z | AA | AB | AC | AD | AE | AF | AG | AH | AI | AJ | AK | AL | AM | AN | AO | AP | AQ | AR | AS | |
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1 | extra-Amazônia | úteis/manejadas | Madeira | Guias para Coleta, herborização, Identificação e ensino de botânica | Familia | Titulo | Autor | tese/artigo | Editora (apenas para livros e teses) | Cidade | título da obra / periódico | volume | suplemento | parte | número / edição | paginação | Ano | Palavras-chave | Formato arquivo | acesso liberado | disponível em algum site | Link | OBS | Lingua | Resumo | ||||||||||||||||||||
2 | Rubiaceae | Manipulus Rubiacearum V - a revision of the genus Capirona | Joseph H. Kirkbride | artigo | Acta Amazônica | 15 | 1-2 | 47-60 | 1985 | Capirona, Rio Amazonas, Rio Tapajós, Uncaria guianensis (Aubl.) Gmel., Uncaria tomentosa (Willd.) DC., Alseis peruviana Standl., Manettia acutifolia R. & P.Fl., Manettia albert-smithii Standl., Manettia asclepiadacea Standl., Manettia coccinea (Aubl.) Willd., Manettia cordifolia Mart., Manettia cordifolia var. attenuata (Nees & Mart.) Wernham, Manettia cordifolia glabra (C. & S.) Standl., Manettia divaricata Wernham, Manettia dubia Wernham, Manettia glandulosa P.& E., Manettia hispida P. & E., Manettia leucantha Krause, Manettia modica Standl., Manettia paniculata P. & E., Manettia peruviana Standl., Manettia poliodes Standl., Manettia racemosa R. & P., Manettia schunkei Standl., Manettia tarapotensis Wernham, Manettia thysanophora Wernham, Manettia tomentulosa Standl., Manettia umbellata R. & P., Manettia vacillans Standl., Manettia veronicoides Standl., Manettia weberbaueri Krause, Stilpnophyllum lineatum Hook. f., Lecanosperma lycioides Rusby, Cinchona carabayensis Wedd., Cinchona coronulata Miq., Cinchona delessertiana Standl., Cinchona glandulifera R. & P., Cinchona govana Miq., Cinchona hirsuta R. & P., Cinchona humboldtiana Lamb., Cinchona legitima Ruiz ex Lamb., Cinchona micrantha R. & P., Cinchona officinalis L., Cinchona pubescens Vahl, Cinchona umbellulifera Pavon ex Howard, Joosia dichotoma (R. & P.) Karst., Joosia dielsiana Standl., Joosia umbellifera Karst., Macrocnemum cinchonoides Wedd., Macrocnemum pilosinervium Standl., Macrocnemum roseum (R. & P.) Wedd., Remijia megistocaula Krause, Remijia peruviana Standl., Pimentelia glomerata Wedd., Ladenbergia acutifolia (R. & P.) Klotzsch, Ladenbergia bullata (Wedd.) Standl., Ladenbergia garua (Wedd.) Standl., Ladenbergia coriacea Krause, Ladenbergia crassifolia (Pavon) Standl., Ladenbergia discolor Schum., Ladenbergia ferruginea Standl., Ladenbergia gavanensis (Schlecht.) Standl., Ladenbergia graciliflora Schum., Ladenbergia heterophylla (Wedd.) Standl., Ladenbergia magnifolia (R. & P.) Klotzsch, Ladenbergia malacophylla Standl., Ladenbergia pedunculata (Karst.) Schum., Ladenbergia Riveroana (Wedd.) Standl., Ladenbergia stenocarpa (Lamb.) Klotzsch, Capirona decorticans Spruce, Hillia illustris (Veil.) Schum., Hillia killipii Standl., Hillia macbridei Standl., Hillia parasitica Jacq., Hillia ulei Krause, Hillia weberbaueri Standl., Cosmibuena grandiflora (R. & P.) Rusby, Calycophyllum Spruceanum (Benth.) Hook. f. ex Schum., Loretoa peruviana Standl., Ferdinandusa chlorantha (Wedd.) Standl., Ferdinandusa loretensis Standl., Exostema bicolor P. & E., Exostema corymbosum (R. & P.) Spreng., Exostema maynense P. & E., Exostema peruvianum Humb. & Bonpl., Coutarea hexandra (Jacq.) Schum., Pogonopus tubulosus (DC.) Schum., Condaminea corymbosa (R. & P.) DC., Condaminea corymbosa var. pubescens Spruce ex Schum., Condaminea glabrata DC., Condaminea macrophylla P. & E., Condaminea microcarpa (R. & P.) DC., Condaminea venosa (R. & P.) DC., Chimarrhis dioica Schum. & Krause, Chimarrhis hookeri Schum., Chimarrhis williamsii Standl., Warscewiczia ambigua Standl., Warscewiczia coccinea (Vahl) Klotzsch, Warscewiczia cordata Spruce ex Schum., Warscewiczia schwackei Schum., Rondeletia loretensis Standl., Rondeletia peruviana Standl., Dolichodelphys chlorocrater Schum. & Krause, Sickingia tinctoria (HBK.) Schum., Sickingia williamsii Standl., Bathysa obovata (Ruiz) Schum. ex Standl., Bathysa peruviana Krause, Sipanea hispida Benth. ex Wernham, Macbrideina peruviana Standl., Elaeagia Mariae Wedd., Phitopis multiflora Hook. f., Phitopis sterculioides Standl., Oldenlandia corymbosa L., Oldenlandia herbacea (L.) DC., Arcytophyllum ciliolatum Standl., Arcytophyllum ericoides (Willd.) Standl., Arcytophyllum filiforme (R. & P.) Standl., Arcytophyllum macbridei Standl., Arcytophyllum riveti Dang. & Cherm., Arcytophyllum setosum (R. & P.) Standl., Arcytophyllum thymifolium (R. & P.) Standl., Arcytophyllum weberbaueri Krause, Schradera subandina Krause, Schradera umbellata Presl, Gonzalagunia bunchosioides Standl., Gonzalagunia cornifolia (HBK.) Standl., Gonzalagunia dependens R. & P., Gonzalagunia pachystachya Standl., Isertia alba Sprague, Isertia hoehnei Krause, Isertia krausei Standl., Isertia parvifolia Standl., Isertia rosea Spruce ex Schum., Isertia weberbaueri Standl., Coccocypselum condalia Pers., Coccocypselum decumbens Krause, Coccocypselum hirsutum Bartl. ex DC., Coccocypselum lanceolatum (R. & P.) Pers., Hippotis brevipes Spruce ex Schum., Hippotis triflora R. & P., Hippotis tubiflora Spruce ex Schum., Sommera sabiceoides Schum., Pentagonia gigantifolia Ducke, Pentagonia spathicalyx Schum., Pentagonia subauriculata Standl., Pentagonia velutina Standl., Pentagonia williamsii Standl., Sabicea amazonensis Wernham, Sabicea cana Hook., Sabicea klugii Standl., Sabicea paraensis (Schum.) Wernham, Sabicea pearcei Wernham, Sabicea pumila Bartl. ex DC., Sabicea subinvolucrata Wernham, Sabicea umbellata (R. & P.) Pers., Sabicea villosa R. & S., Sabicea villosa R. & S. var. adpressa (Wernham) Standl., Hoffmannia aggregata (R. & P.) Schum., Hoffmannia latifolia (Bartl.) Kuntze, Hoffmannia mathewsii Standl., Hoffmannia obovata (R. & P.) Standl., Hoffmannia verticillata (R. & P.) Standl., Hoffmannia villosula Standl., Hoffmannia williamsii Standl., .Bertiera guianensis Aubl., Bertiera parviflora Spruce ex Schum., Hamelia Klugii Standl., Hamelia lutea Rohr ex Smith, Hamelia patens Jacq., Bothriospora corymbosa (Benth.) Hook. f., Posoqueria latifolia (Rudge) R. & S., Posoqueria longiflora Aubl., Tocoyena amazonica Standl., Tocoyena foetida P. & E., Tocoyena williamsii Standl., Sphinctanthus maculatus Spruce ex Schum., Randia armata (Sw.) DC., Randia armata var. pubescens (HBK.) Standl., Randia aurantiaca Standl., Randia boliviana Rusby, Randia calycina Cham., Randia killipii Standl., Randia obovata R. & P., Randia rotundifolia R. & P., Randia ruiziana DC., Randia tessmannii Standl., Randia Williamsii Standl., Genipa americana L., Gardenia augusta (L.) Merr., Duroia hirsuta (P. & E.) Schum., Duroia longifolia (P. & E.) Schum., Duroia stenophylla Standl., Duroia trichocarpa Standl., Amaioua corymbosa HBK., Amaioua guianensis Aubl., Amaioua urophylla Standl., Alibertia claviflora Schum., Alibertia curviflora Schum., Alibertia edulis (L. Rich.), Alibertia stenantha Standl., Retiniphyllum angustiflorum Krause, Retiniphyllum fuchsioides Krause,, Machaonia peruviana Wernham, Machaonia williamsii Standl., Guettarda aromatica P. & E., Guettarda boliviana Standl., Guettarda comata Standl., Guettarda dependens (R. & P.) DC., Guettarda ferox Standl., Guettarda hirsuta (R. & P.) Pers., Guettarda ochreata Schlecht., Guettarda ulei Krause, Malanea boliviana Standl., Chomelia barbellata Standl., Chomelia unguis-cati Standl., Anisomeris klugii Standl., Anisomeris paniculata (Bartl.) Standl., Anisomeris peruviana Standl., Anisomeris sessilis (Muell. Arg.) Standl., Chiococca alba (L.) Hitchc., Coffea arabica L., Coffea longifolia R. & P., Ixora chinensis Lam., Ixora coccinea L., Ixora escalerae Standl., Ixora finlaysoniana Wall., Ixora intensa Krause, Ixora killipii Standl., Ixora peruviana (Spruce) Standl., Ixora ulei Krause, Coussarea auriculata Standl., Coussarea brevicaulis Krause, Coussarea flava P. & E., Coussarea hirticalyx Standl., Coussarea hydrangeifolia (Benth.) B. & H. ex Muell. Arg., Coussarea liliiflora Standl., Coussarea longiacuminata Standl., Coussarea macrantha Standl., Coussarea megalocarpa Standl., Coussarea obliqua Standl., Coussarea ovalis Standl., Coussarea rudgeoides Rusby, Coussarea sessilifolia Standl., Coussarea tenuiflora Standl., Coussarea tortilis Standl., Coussarea tricephala Standl., Faramea amplifolia Standl., Faramea anisocalyx P. & E., Faramea axillaris Standl., Faramea capillipes Muell. Arg., Faramea coerulescens Schum. & Krause, Faramea congesta Huber, Faramea exemplaris Standl., Faramea glandulosa P. & E., Faramea harmsiana Standl., Faramea maynensis Spruce ex B. & H., Faramea miconioides Standl., Faramea occidentalis (L.) A. Rich., Faramea phyllonomoides Standl., Faramea quinqueflora P. & E., Faramea rectinervia Standl., Faramea subsessilis (R. & P.) Standl., Pagamea guianensis Aubl., Stachyococcus adinanthus Standl., Geophila gracilis (R. & P.) DC., Geophila herbacea (Jacq.) Schum., Geophila macropoda (R. & P.) DC., Geophila trichogyne (Muell. Arg.) Standl., Cephaelis acreana Krause, Cephaelis affinis Standl., Cephaelis barcellana (Muell. Arg.) Standl., Cephaelis bella Standl., Cephaelis blepharophylla Standl., Cephaelis dolichophylla Standl., Cephaelis flaviflora (Krause) Standl., Cephaelis iodotricha (Muell. Arg.) Standl., Cephaelis killipii Standl., Cephaelis leucantha (Krause) Standl., Cephaelis oinochrophylla Standl., Cephaelis oleandrella Standl., Cephaelis pebasensis Standl., Cephaelis pubescens Hoffmannsegg ex R. & S., Cephaelis rosea Benth., Cephaelis Schraderoides (Krause) Standl., Cephaelis Schunkeana Standl., Cephaelis tomentosa (Aubl.) Vahl, Cephaelis trichocephala (P. & E.) Standl., Cephaelis umbellata (R. & P.) Standl., Cephaelis williamsii Standl., Declieuxia peruviana Wernham, Rudgea acuminata (R. & P.) Standl., Rudgea amazonica Muell. Arg., Rudgea angustissima Standl., Rudgea canephorantha (Wernham) Standl., Rudgea ceriantha Schum., Rudgea ciliata (R. & P.) Spreng., Rudgea cryptantha Standl., Rudgea foveolata (R. & P.) Zahlbr., Rudgea hispidula Standl., Rudgea insolita Standl., Rudgea justicioides Standl., Rudgea klugii Standl., Rudgea loretensis Standl., Rudgea mexiae Standl., Rudgea microcarpa (R. & P.) Standl., Rudgea nitida (R. & P.) Spreng., Rudgea obesiflora Standl., Rudgea poeppigii Schum., Rudgea psychotriaefolia Standl., Rudgea racemosa (R. & P.) Spreng., Rudgea retifolia Standl., Rudgea sessiliflora Standl., Rudgea sororia Standl., Rudgea sprucei Standl., Rudgea stenophylla (Krause) Standl., Rudgea tambillensis Zahlbr., Rudgea verticillata (R. & P.) Spreng., Rudgea Woronowii Standl., Psychotria abdita Standl., Psychotria acreana Krause, Psychotria alba R. & P., Psychotria albert-smithii Standl., Psychotria alboviridula Krause, Psychotria anceps HBK., Psychotria aschersoniana Schum. & Krause, Psychotria brachiata Sw., Psychotria buchtieni (Winkl.) Standl., Psychotria bullatifolia Standl., Psychotria calochlamys Standl., Psychotria candelabrum Standl., Psychotria capitata R. & P., Psychotria carthaginensis Jacq., Psychotria compta Standl., Psychotria costato-venosa Schlecht., Psychotria cupularis (Muell. Arg.) Standl., Psychotria cuspidata Bredem. ex R. & S., Psychotria cuspidulata (Krause) Standl., Psychotria educta Standl., Psychotria egensis Muell. Arg., Psychotria emetica L. f., Psychotria epiphytica Krause, Psychotria ernesti Krause, Psychotria falcata Rusby, Psychotria herzogii S. Moore, Psychotria hoffmannseggiana R. & S., Psychotria hospitalis Standl., Psychotria huallagae Standl., Psychotria huantensis Standl., Psychotria involucrata Sw., Psychotria iquitosensis Standl., Psychotria japurensis Muell. Arg., Psychotria juninensis Standl., Psychotria klugii Standl., Psychotria limitanea Standl., Psychotria loretensis Standl., Psychotria lupulina Benth., Psychotria luxurians Rusby, Psychotria macrophylla R. & P., Psychotria marcgraviella Standl., Psychotria marginata Sw., Psychotria mathewsii Standl., Psychotria pongoana Standl., Psychotria microbotrys Ruiz ex Standl., Psychotria moyobambana Standl., Psychotria nautensis Standl., Psychotria nigricans Standl., Psychotria nudiceps Standl., Psychotria opima Standl., Psychotria patens Sw., Psychotria pichisensis Standl., Psychotria pilosa R. & P., Psychotria pluriceps Standl., Psychotria racemifera Standl., Psychotria racemosa (Aubl.) Willd., Psychotria repanda R. & P., Psychotria reticulata R. & P., Psychotria retifera Standl., Psychotria rhodophylla Standl., Psychotria rhodothamna Standl., Psychotria ruizii Standl., Psychotria santaremica Muell. Arg., Psychotria semimetralis Krause, Psychotria stenostachya Standl., Psychotria striolata Krause, Psychotria subtomentosa R. & P., Psychotria tarapotensis Standl., Psychotria tenuicaulis Krause, Psychotria tessmannii Standl., Psychotria tinctoria R. & P., Psychotria trifida R. & P., Psychotria victoriae Standl., Psychotria villosa R. & P., Psychotria virgata R. & P., Psychotria viridis R. & P., Psychotria weberbaueri Standl., Psychotria williamsii Standl., Psychotria yapasensis Standl., Psychotria zepelaciana Standl., Palicourea amethystina (R. & P.) DC., Palicourea angustifolia HBK., Palicourea aphthosa Standl., Palicourea attenuata Rusby, Palicourea bracteosa Standl., Palicourea buchtienii Standl., Palicourea caerulea (R. & P.) R. & S., Palicourea charianthema Standl., Palicourea chlorocaerulea Krause, Palicourea chrysotricha (Zahlbr.) Standl., Palicourea condensata Standl., Palicourea consobrina Standl., Palicourea corymbifera (Muell. Arg.) Standl., Palicourea crocea (Sw.) R. & S., Palicourea cymosa (R. & P.) Standl., Palicourea haenkeana DC., Palicourea herrerae Standl., Palicourea jelskii Standl., Palicourea kanehirae Standl., Palicourea Klugii Standl., Palicourea lachnantha Standl., Palicourea lasiantha Krause, Palicourea lasiophylla Krause, Palicourea latifolia Krause, Palicourea laxa (R. & P.) R. & S., Palicourea lechleri Standl., Palicourea levis Standl., Palicourea longistipula Standl., Palicourea lucentifolia Standl., Palicourea lucidula Standl., Palicourea macbridei Standl., Palicourea macrobotrys (R. & P.) R. & S., Palicourea macrophylla (HBK.) Standl., Palicourea mitis (R. & P.) DC., Palicourea nigricans Krause, Palicourea obovata (R. & P.) DC., Palicourea paraensis (Muell. Arg.) Standl., Palicourea perquadrangularis Wernham, Palicourea polyneura Krause, Palicourea ponasae Krause, Palicourea punicea (R. & P.) DC., Palicourea punoensis Standl., Palicourea raimondii Standl., Palicourea saligna Standl., Palicourea sandiensis Krause, Palicourea stenoclada (Muell. Arg.) Standl., Palicourea subspicata Huber, Palicourea sulphurea (R. & P.) DC., Palicourea triphylla DC., Palicourea weberbaueri Krause, Paederia diffusa (Britton) Standl., Corynula pilosa (Benth.) Hook. f., Gomozia granadensis L. f., Emmeorrhiza umbellata (Spreng.) Schum., Mitracarpus frigidus (Willd.) Schum., Mitracarpus hirtus (L.) DC.Richardia humistrata (C. & S.) Steud., ichardia lomensis (Krause) Standl., Richardia rigidifolia (Krause) Standl., Richardia rosea (St. Hil.) Schult. f., Richardia scabra L., Diodia alata Nees & Mart., Diodia dichotoma (HBK.) Schum., Diodia hyssopifolia (Willd.) C. & S., Diodia teres Walt., Hemidiodia ocimifolia (Willd.) Schum., Spermacoce glabra Michx., Spermacoce confusa Rendle, Borreria alata (Aubl.) DC., Borreria capitata (R. & P.) DC., Borreria corymbosa (R. & P.) DC., Borreria laevis (Lam.) Griseb., Borreria latifolia (Aubl.) Schum., Borreria ocimoides (Burm.) DC., Borreria suaveolens G. Mey., Spermacoce erioclada DC., Spermacoce inconspicua Bartl. ex DC., Sherardia arvensis L., Relbunium ciliatum (R. & P.) Hemsl., Relbunium corymbosum (R. & P.) Schum., Relbunium croceum (R. & P.) Schum., Relbunium ericoides (Lam.) Schum., Relbunium hirsutum (R. & P.) Schum., Relbunium hypocarpium (L.) Hemsl., Relbunium ovale (R. & P.) Schum., Galium aparine L., Galium canescens HBK., Galium eriocarpum Bartl. ex DC., Galium ferrugineum Krause, Galium limense Standl., Galium pumilio Standl., Riqueuria avenia R. & P. | sim | Scielo | http://www.scielo.br/pdf/aa/v15n1-2/1809-4392-aa-15-1-2-0047.pdf | inglês | The taxonomic history of the genus Capirona is presented. Complete synonymies, description, common names, distributions and discussions are given for Capirona and its two species C. Descorticans and C. Leiophloea. The generic distribution is the Amazon valley and eastern Guianas and coincides with that of the genus Hevea. C. Descorticans is known from the western and southeastern Amazon valley; C. Leiophloea is reported from the eastern Guianas and the northeastern Amazon valley. The zone of contact between the two species is along the southern edge of the Amazon River and the lower drainage of the Rio Tapajoz in Pará, Brazil. | ||||||||||||||||||||||||||||||
3 | Rubiaceae | Re-Establishment of Carapichea (Rubiaceae, Psychotrieae) | Lennart Andersson | artigo | Kew Bulletin | 57 | 2 | 363-374 | 2002 | Carapichea | não | JSTOR (read online) | https://www.jstor.org/stable/4111112?seq=1 | inglês | Three species presently referred to Psychotria subgen. Heteropsychotria are shown by cladistic analysis of nucleotide sequence variation in the rps 16 intron (cpDNA) to form a strongly supported monophyletic group. It is suggested that this group be recognised taxonomically as a separate genus of the tribe Psychotrieae. The group includes the type species of Carapichea, C. guianensis, and Carapichea thus becomes the correct name of the genus. Morphologically, Carapichea is characterized by having stipules that are not shed by formation of an abscission layer, leaves that dry greenish or greyish, aperturate pollen, and planoconvex pyrenes with an adaxial furrow and preformed germination slits on abaxial ridges, but not along the margins. Two new combinations are made, Carapichea affinis (StandI.) L. Andersson and C. ipecacuanha (Brot.) L. Andersson. The rhizomes of C. ipecacuanha are the source of the drug ipecac. | ||||||||||||||||||||||||||||||
4 | Rubiaceae | The Genus Carapichea (Rubiaceae, Psychotrieae) | Charlotte Taylor & Roy E. Gerau | artigo | Annals of the Missouri Botanical Garden | 99 | 1 | 100-127 | 2013 | Carapichea | não | Bioone / ResearchGate (Request full-text) | https://bioone.org/journals/annals-of-the-missouri-botanical-garden/volume-99/issue-1/2011064/The-Genus-Carapichea-Rubiaceae-Psychotrieae1/10.3417/2011064.short | inglês | The Neotropical species that have been included in Psychotria L. comprise a heterogeneous group, morphologically and systematically. Carapichea Aubl. (Rubiaceae, Psychotrieae) was separated from Psychotria based on molecular analyses to include C. affinis (Standl.) L. Andersson, C. guianensis Aubl., and C. ipecacuanha (Brot.) L. Andersson; two more species were later included based on morphological characters, C. ligularis (Rudge) Delprete and C. lucida J. G. Jardim & Zappi. Here Carapichea is reviewed morphologically and circumscribed to include 23 Neotropical species found from Nicaragua to southeastern Brazil that share characters of the stipules and inflorescence arrangement. The genus is diagnosed mainly by its distinctive stipules, while pyrene characters, previously considered characteristic for the genus, actually vary widely. A revised morphological description of the genus includes more variation than previously documented, which is outlined in the key to species. Seven informal species groups are separated and characterized, and the following new nomenclatural combinations are made here: Carapichea adinantha (Standl.) C. M. Taylor, based on Retiniphyllum adinanthum Standl. and the sole species of Stachyococcus Standl., which fully synonymizes Stachyococcus with Carapichea; Carapichea altsonii (Sandwith) C. M. Taylor, based on Cephaelis altsonii Sandwith; Carapichea araguariensis (Steyerm.) C. M. Taylor, based on P. araguariensis Steyerm.; Carapichea crebrinervia (Standl.) C. M. Taylor, based on Cephaelis crebrinervia Standl.; Carapichea fimbriflora (Steyerm.) C. M. Taylor, based on P. fimbriflora Steyerm.; Carapichea franquevilleana (Müll. Arg.) C. M. Taylor, based on P. franquevilleana Müll. Arg.; Carapichea klugii (Standl.) C. M. Taylor, based on P. klugii Standl.; Carapichea maturacensis (Steyerm.) C. M. Taylor, based on P. maturacensis Steyerm.; Carapichea necopinata (Standl.) C. M. Taylor, based on P. necopinata Standl.; Carapichea nivea (Sandwith) C. M. Taylor, based on Cephaelis nivea Sandwith; Carapichea pacimonica (Müll. Arg.) C. M. Taylor, based on P. pacimonica Müll. Arg.; Carapichea panurensis (Müll. Arg.) C. M. Taylor, based on Mapouria panurensis Müll. Arg.; Carapichea sandwithiana (Steyerm.) C. M. Taylor, based on Cephaelis sandwithiana Steyerm.; Carapichea tillettii (Steyerm.) C. M. Taylor, based on P. tillettii Steyerm.; Carapichea urniformis (Steyerm.) C. M. Taylor, based on P. urniformis Steyerm.; and Carapichea vasivensis (Müll. Arg.) C. M. Taylor, based on Mapouria vasivensis Müll. Arg. Newly described here is Carapichea verrucosa C. M. Taylor of Amazonian Peru, Colombia, and Brazil, which is notable for its relatively large, abaxially (i.e., dorsally) verrucose pyrenes. | ||||||||||||||||||||||||||||||
5 | Rubiaceae | Rubiacearum Americanarum Magna Hama Pars XXXIX. New Species of Carapichea and Rudgea (Palicoureeae) from Western Amazonia | Charlotte Taylor & Carla Poleselli Bruniera | artigo | Novon | 26 | 2 | 240-251 | 2018 | Carapichea, Rudgea | não | Bioone / ResearchGate (Request full-text) | https://bioone.org/journals/Novon-A-Journal-for-Botanical-Nomenclature/volume-26/issue-2/2018026/Rubiacearum-Americanarum-Magna-Hama-Pars-XXXIX-New-Species-of-iCarapichea/10.3417/2018026.short | inglês | Several species of Rudgea Salisb. and Carapichea Aubl. from the lowlands of the western Amazon basin have been confused due to their morphological similarity, in particular their relatively large leaves of similar aspect and relatively large, fleshy, yellow or white fruits, and are reviewed here. Three belong to Carapichea, the previously described species C. adinantha (Standl.) C. M. Taylor and C. verrucosa C. M. Taylor and one newly described here, C. cardenasiana C. M. Taylor from southern Colombia and western Brazil. Four species belong to Rudgea, R. bracteata J. H. Kirkbr. and three newly described here: R. huashikatii C. M. Taylor & Bruniera of southeastern Ecuador and adjacent Peru, R. spiciformis C. M. Taylor & Bruniera of northeastern Peru, and R. yasuniana C. M. Taylor & Bruniera of eastern Ecuador and adjacent Peru. | ||||||||||||||||||||||||||||||
6 | Rubiaceae | Eumachia expanded, a pantropical genus distinct from Psychotria (Rubiaceae, Palicoureeae) | Charlotte M. Taylor, Sylvain G. Razafimandimbison, Laure Barrabé, Jomar G. Jardim & Maria Regina V. Barbosa | artigo | Candollea | 72 | 2 | 289-318 | 2017 | Eumachia, Margaritopsis, Psychotria | não | Bioone / ResearchGate (Download full-text) | https://bioone.org/journals/candollea/volume-72/issue-2/c2017v722a6/Eumachia-expanded-a-pantropical-genus-distinct-from-Psychotria-Rubiaceae-Palicoureeae/10.15553/c2017v722a6.short | https://www.researchgate.net/publication/318543990_Eumachia_expanded_a_pantropical_genus_distinct_from_Psychotria_Rubiaceae_Palicoureeae | inglês | The pantropical genus Margaritopsis C. Wright (Rubiaceae, Palicoureeae) was recently separated from Psychotria L. and transferred to a different tribe, Palicoureeae, based on both molecular and morphological data. Margaritopsis has been studied in the Neotropics, and in Africa as Chazaliella E.M.A. Petit & Verdc.; the species that belong to this group in the Pacific are enumerated for the first time here. Recently Eumachia DC. was found to be an older name for this group, and a few species of Margaritopsis have been transferred nomenclaturally to that genus. Here Eumachia is surveyed comprehensively for the first time, with a list of species and an overview of morphological characteristics. The remaining species of Margaritopsis are nomenclaturally transferred here to Eumachia, along with one species of Hodgkinsonia F. Müll., one species of Mapouria Aubl., and several species of Psychotria from Asia, Australia, New Guinea, and the Pacific region. In this new circumscription Eumachia includes 83 species, and is characterized within Palicoureeae by a yellowish green drying color ; stipules that are persistent or fall by fragmentation and are generally glandular when young and hardened when old ; green to whitened inflorescence axes ; white to cream or yellowish green, often rather small corollas ; orange to red fruits ; pyrenes with marginal pre-formed germination slits and no ethanol-soluble pigments ; and non-ruminate endosperm. Eumachia includes 20 species, 8 subspecies, and 7 varieties in Africa, 27 species in the Neotropics, and 36 species and 6 varieties in Asia, Australasia, and the Pacific region. Here we publish 81 new nomenclatural combinations in Eumachia and two new synonymies for Neotropical names, and 11 names from various regions are lectotypified. | |||||||||||||||||||||||||||||
7 | Rubiaceae | Another Taxonomic Review of the Neotropical Genus Joosia (Rubiaceae, Cinchoneae) | Charlotte Taylor | artigo | Novon | 25 | 2 | 214-237 | 2017 | Joosia | não | Bioone / Mobot Novon / ResearchGate (Request full-text) | https://bioone.org/journals/Novon-A-Journal-for-Botanical-Nomenclature/volume-25/issue-2/2015029/Another-Taxonomic-Review-of-the-Neotropical-Genus-Joosia-Rubiaceae-Cinchoneae/10.3417/2015029.short | https://novon.mobot.org/index.php/novon/article/view/260 / https://www.researchgate.net/publication/320111997_Another_Taxonomic_Review_of_the_Neotropical_Genus_Joosia_Rubiaceae_Cinchoneae | inglês | Recent botanical explorations in western tropical South America provide new documentation of Joosia H. Karst., which has clarified some species identities and discovered some new species. Eighteen species are recognized here, with J. umbellifera H. Karst. circumscribed more narrowly than in previous taxonomies and J. panamensis Dwyer and J. ulei Steyerm. separated from it. Two new nomenclatural combinations are made: J. loretensis (Standl.) C. M. Taylor is based on Rondeletia loretensis Standl., and J. sericea (Standl.) C. M. Taylor is based on Ladenbergia sericea Standl. and is an older name for J. multiflora L. Andersson. Three species are newly described here: J. capitata C. M. Taylor from northern Peru, with subcapitate inflorescences and dense hirtellous to hirsute pubescence; J. confusa C. M. Taylor from Ecuador and Peru, with dichasial axes and shallowly lobed calyx limbs; and J. frondosa C. M. Taylor from Colombia, with enlarged whitened bracts and calyx lobes. Joosia has its center of species diversity in montane Ecuador and Peru; it is now documented also from Bolivia, where J. sericea is found, and from Venezuela, but that material is inadequate for identification to species. | |||||||||||||||||||||||||||||
8 | Rubiaceae | New combinations in Kutchubaea (Gardenieae-Rubiaceae) | Claes Persson | artigo | Rev. Biol. Neotrop. | 2 | 2 | 65-74 | 2005 | Kutchubaea, Alibertia, Duroia, Ibetralia | sim | Revista de Biologia Neotropical | https://www.revistas.ufg.br/RBN/article/view/6056/0 | inglês | Based on evidence from recent phylogenetic analyses of DNA sequence data and critical morphological observations, Ibetralia surinamensis and Duroia oocarpa are transferred to the genus Kutchubaea. Both species have several characters that are often used to distinguish Kutchubaea from other neotropical genera of the tribe Gardenieae, such as persisten interpetiolar stipules, cymose male inflorescences with well-developes branches and/or distinct pedicels, porate pollen grains released in monads, and ellipsoid fruits | ||||||||||||||||||||||||||||||
9 | Rubiaceae | The neotropical Rosenbergiodendron (Rubiaceae, Gardenieae) | Claes G.R. Gustafsson | artigo | Brittonia | 50 | 4 | 452-466 | 1998 | Rosenbergiodendron, Gardenieae, Randia | não | Springer / JSTOR (read online) | https://link.springer.com/article/10.2307/2807754 | https://www.jstor.org/stable/2807754?seq=1 | inglês | Rosenbergiodendron has usually been relegated to the synonymy of Randia, but differs from Randia by being unarmed and having hermaphrodite flowers and pollen in monads. Three species are recognized. One new combination, R. formosum var. nitidum, is made. Rosenbergiodendron formosum is neotypified. Rosenbergiodendron formosum var. nitidum, R. longiflorum, R. densiflorum, and Randia speciosa are lectotypified. A key to the species, descriptions, illustrations, and distribution maps are provided. | |||||||||||||||||||||||||||||
10 | Rubiaceae | Flora da Reserva Ducke, Amazonas, Brasil: Rubiaceae | Charlotte M. Taylor, Marina T. V. A. Campos & Daniela Zappi | artigo | Rodriguesia | 58 | 3 | 549-616 | 2007 | Sabicea, Geophila, Psychotria, Sipanea, Spermacoce, Henriquezia, Capirona, Isertia, Morinda, Palicourea, Margaritopsis, Psychotria, Pagamea, Amaioua, Duroia, Rudgea, Ferdinandusa, Chimarrhis, Warszewiczia, Remijia, Ronabea, Chomelia, Malanea, Kutchubaea, Cordiera, Alibertia, Ibetralia, Schradera, Cosmibuena, Hillia, Coussarea, Faramea, Ixora, Psychotria, Ladenbergia, Botryarrhena, Posoqueria, Tocoyena, chave de identificação de gêneros, chave de identificação de espécies | sim | Scielo | https://www.scielo.br/j/rod/a/LQcBFWLHSf8GZrHPnbMwNZN/?lang=pt | português | não possui resumo | ||||||||||||||||||||||||||||||
11 | Melastomataceae | A New Species of Graffenrieda (Merianieae, Melastomataceae) with a Calyptrate Calyx | Renato Goldenberg & Julia Meirelles | artigo | Systematic Botany | 36 | 1 | 119-123 | 2011 | Graffenrieda glandulosa, Merianieae, Acre, espécie nova | não | Bioone / ResearchGate (Download full-text) / JSTOR (read online) | https://bioone.org/journals/systematic-botany/volume-36/issue-1/036364411X553199/A-New-Species-of-Graffenrieda-Merianieae-Melastomataceae-with-a-Calyptrate/10.1600/036364411X553199.short | https://www.jstor.org/stable/23028956?seq=1 / https://www.researchgate.net/publication/230661213_A_New_Species_of_Graffenrieda_Merianieae_Melastomataceae_with_a_Calyptrate_Calyx | inglês | Graffenrieda glandulosa can be distinguished from other species in the genus by the 3-nerved leaves with barbate nerve bases on the abaxial surface, the calyptrate calyx, and the short connective appendages covered with glandular trichomes. This new species has been collected only in the western tip of the state of Acre, Brazil, near the border with Peru. | |||||||||||||||||||||||||||||
12 | Melastomataceae | A new species of Miconia (Melastomataceae) from Amazonas, Brazil | Renato Goldenberg, Mayara Krasinski Caddah & Fabián Michelangeli | artigo | Brittonia | 63 | 2 | 245-249 | 2011 | Miconia manauara, Miconieae, Amazonas, Pará | não | Springer / ResearchGate (Download full-text) / Academia.edu | https://link.springer.com/article/10.1007/s12228-010-9157-x | No Academia.edu é possível ler o texto online / https://www.researchgate.net/publication/230028716_A_new_species_of_Miconia_Melastomataceae_from_Amazonas_Brazil / https://www.academia.edu/23099152/A_new_species_of_Miconia_Melastomataceae_from_Amazonas_Brazil | Miconia manauara has been collected several times in two municipalities in the state of Amazonas, Brazil, and once in nearby Pará. It can be recognized among species in Miconia sect. Miconia by the leaves with obtuse to rounded bases, entire margins, cuspidate apices and five basal to shortly suprabasal nerves. The leaves also have glabrous mature adaxial leaf surfaces and the abaxial surface with two indument layers, the first consisting of moderate to dense, ferruginous, sessile stellate trichomes, 0.1–0.2 mm diam., and the second consisting of a dense, granulose-furfuraceous layer. The inflorescences are glomerulate, the 5-merous flowers have a caducous calyx, minutely papillose petals, ten stamens that are ventrally bilobed and with a small dorsal, obtuse tooth, and the ovaries are furfuraceous and usually covered by unbranched trichomes on their apices. Resumo Miconia manauara tem sido coletada várias vezes em dois municípios no estado do Amazonas e uma vez no Pará. Esta espécie pode ser reconhecida entre as espécies de Miconia sect. Miconia pelas folhas com base obtuse a arredondada, margem inteira, ápice cuspidado e cinco nervuras basais a curtamente suprabasais, e também com a face adaxial glabra e abaxial coberta por duas camadas de indumento, a primeira com tricomas estrelados 0.1–0.2 mm diam., sésseis, ferrugíneos, moderados a densos, e a segunda densamente granuloso-furfurácea. As inflorescências são glomeruladas, enquanto que as flores pentâmeras apresentam o cálice caduco, pétalas minutamente papilosas, dez estames ventralmente bilobados e com um pequeno dente dorsal obtuso, e ovário com ápice furfuráceo e geralmente coberto por tricomas simples. | ||||||||||||||||||||||||||||||
13 | Melastomataceae | A new species of Miconia (Miconieae, Melastomataceae) from the Brazillian Amazon | Julia Meirelles & Renato Goldenberg | artigo | Phytotaxa | 173 | 4 | 278-284 | 2014 | Miconia suberosa, Seriatiflorae, Floresta de Igapó, Rio Purus, Rio Madeira, Amazonas | não | Biotaxa / ResearchGate (Download full-text) / Academia.edu | https://www.biotaxa.org/Phytotaxa/article/view/phytotaxa.173.4.2 / https://www.researchgate.net/publication/265727075_A_new_species_of_Miconia_Miconieae_Melastomataceae_from_the_Brazilian_Amazon / https://www.academia.edu/23099030/_p_strong_A_new_species_of_em_Miconia_em_Miconieae_Melastomataceae_from_the_Brazilian_Amazon_strong_p_ | No Academia.edu é possível ler o texto online | Miconia manauara has been collected several times in two municipalities in the state of Amazonas, Brazil, and once in nearby Pará. It can be recognized among species in Miconia sect. Miconia by the leaves with obtuse to rounded bases, entire margins, cuspidate apices and five basal to shortly suprabasal nerves. The leaves also have glabrous mature adaxial leaf surfaces and the abaxial surface with two indument layers, the first consisting of moderate to dense, ferruginous, sessile stellate trichomes, 0.1–0.2 mm diam., and the second consisting of a dense, granulose-furfuraceous layer. The inflorescences are glomerulate, the 5-merous flowers have a caducous calyx, minutely papillose petals, ten stamens that are ventrally bilobed and with a small dorsal, obtuse tooth, and the ovaries are furfuraceous and usually covered by unbranched trichomes on their apices. | ||||||||||||||||||||||||||||||
14 | Melastomataceae | A new species of Graffenrieda (Melastomataceae) from the northern Amazon basin | Fabián Michelangeli & Renato Goldenberg | artigo | Brittonia | 66 | 2 | 170-173 | 2014 | Graffenrieda laevicarpa, Merianeae, Serra do Aracá | não | Springer / ResearchGate (Download full-text) | https://link.springer.com/article/10.1007/s12228-013-9321-1 | https://www.researchgate.net/publication/258176818_A_new_species_of_Graffenrieda_Melastomataceae_from_the_northern_Amazon_basin | A new species of Graffenrieda (Melastomataceae: Merianieae) from northern Brazil and southern Venezuela is described. Graffenrieda laevicarpa closely resembles the morphologically variable and complex G. caryophyllea, but can be distinguished based on leaf morphology and pubescence, and by its shiny capsules. | ||||||||||||||||||||||||||||||
15 | Melastomataceae | Miconia macuxi (Miconieae, Melastomataceae): a new species from the Amazonian white sand vegetation | Julia Meirelles, Mayara Krasinski Caddah & Renato Goldenberg | artigo | Phytotaxa | 220 | 1 | 54-60 | 2015 | Miconia macuxi, Seriatiflorae, Roraima, Amazonas, campina, campinarana | não | Biotaxa / ResearchGate (Download full-text) | https://www.biotaxa.org/Phytotaxa/article/view/phytotaxa.220.1.4 | https://www.researchgate.net/publication/280556032_Miconia_macuxi_Miconieae_Melastomataceae_A_new_species_from_the_Amazonian_white_sand_vegetation | Miconia macuxi is described from the states of Roraima and Amazonas, in northern Brazil, and Atabapo and Amazonas, in southern Venezuela. It occurs in white sand vegetation, and can be recognized by the strongly discolorous leaves with dense stellate trichomes on their abaxial surfaces, secund inflorescences, petal margins with glandular-stipitate trichomes, and white stamens, the antepetalous with the connective with two ventral lobes and a dorsal tooth | ||||||||||||||||||||||||||||||
16 | Melastomataceae | Miconia papillosperma (Melastomataceae, Miconieae): a new species from Amazonas, Brazil | Fabián Michelangeli & Renato Goldenberg | artigo | Phytokeys | 63 | 31-40 | 2016 | Miconia papillosperma, Clidemia, testa papilosa, semente, inflorescência terminal, pétalas arredondadas, Tococa, Manaus, Caracaraí | sim | Phytokeys | https://phytokeys.pensoft.net/article/7368/ | inglês | Miconia papillosperma, a new species of Melastomataceae shrubs from Northern Brazil is described and illustrated. This new species is characterized by elliptic lanceolate leaves with the only pair of secondary veins running close to the margin. It is also unique in having seeds with a papillose testa, a character until now unknown in the Miconieae. The description of this new species from a relatively well collected area near a major road north of Manaus, Amazonas, Brazil, is further evidence of our lack of knowledge on plants in many Neotropical areas. | |||||||||||||||||||||||||||||||
17 | Melastomataceae | Melastomataceae in the Reserva de Desenvolvimento Sustentável do Tupé, Amazonas, Brazil | André Luis Corrêa, Veridiana Vizoni Scudeller & Renato Goldenberg | artigo | Phytotaxa | 323 | 2 | 101-127 | 2017 | Rio Negro, Miconia, Clidemia, Aciotis, Bellucia, Tococa, Henriettea, Tibouchina, Adelobotrys, Maieta | não | Phytotaxa | https://www.biotaxa.org/Phytotaxa/article/view/phytotaxa.323.2.1 | temos a tese | inglês | We present a taxonomic study of the Melastomataceae that occur in the “Reserva de Desenvolvimento Sustentável do Tupé”, lower Negro River, Amazonas. Forty-two species from nine genera: Miconia (21 spp.), Clidemia (6 spp.), Aciotis, Bellucia and Tococa (3 spp. each), Henriettea and Tibouchina (2 spp. each), Adelobotrys and Maieta (1 sp. each). We present detailed descriptions and an identification key prepared through DELTA software. We also present illustrations and data on geographical distribution for the species. This study presents the first record for 27 species in the Reserve. | |||||||||||||||||||||||||||||
18 | Melastomataceae | Melastomataceae na Reserva de Desenvolvimento Sustentável do Tupé, Amazonas, Brasil | André Luis Corrêa | Dissertação | Instituto Nacional de Pesquisas da Amazônia | 88 | 2014 | Rio Negro, Miconia, Clidemia, Aciotis, Bellucia, Tococa, Henriettea, Tibouchina, Adelobotrys, Maieta | sim | INPA | https://bdtd.inpa.gov.br/handle/tede/1611 | português | Neste trabalho são apresentados estudos taxonômicos das espécies de Melastomataceae, ocorrentes na Reserva de Desenvolvimento Sustentável do Tupé (RDS do Tupé), Manaus, Amazonas. Onde foram feitas análises de espécimes provenientes de coletas realizadas de 2012 a 2014, além de materiais desta localidade incorporados ao acervo Biotupé. Neste estudo foram registradas 42 espécies, distribuídas em nove gêneros: Miconia (21 spp.), Clidemia (6 spp.), Aciotis, Bellucia, Tococa (3 spp. cada), Henriettea e Tibouchina (2 spp. cada), Adelobotrys e Maieta (1 sp. cada). Após análise detalhada das partes vegetativas e reprodutivas foram elaboradas descrições detalhadas e padronizadas para as espécies encontradas e elaboração de chave de identificação, ambos com auxílio do software livre DELTA. Também são apresentados ilustrações e dados de distribuição geográfica das espécies. Este estudo apresenta o primeiro registro de ocorrência de 27 espécies para a área de estudo / This work, presented studies of species of Melastomataceae, occurring in Tupé Sustainable Development Reserve (RDSTupe), Manaus, Amazonas. Were made analysis of specimens from collections made of the 2012 to 2014 and of materials incorporated into the acquis Biotupé. This study were recorded 42 species were recorded, belonging to nine genera Miconia (21 spp.), Clidemia (6 spp.), Aciotis, Bellucia, Tococa (3 spp. each), Henriettea e Tibouchina (2 spp. each), Adelobotrys e Maieta (1 sp. each). After detailed analysis of parts vegetative and reproductive were prepared detailed descriptions and standardized for the species found and elaboration of identification key, both with aid of free software DELTA. Also were presented illustration and data geographical distribution of the species. This study presents the first occurrence of 27 species for the study area. | ||||||||||||||||||||||||||||||||
19 | Melastomataceae | Two new species of Miconia (Melastomataceae, Miconieae) from the Brazilian northern border and adjacent French Guiana | Renato Goldenberg & Lucas Katsumi Rocha Hinoshita | artigo | Brittonia | 69 | 4 | 535-543 | 2017 | Miconia amapaënsis, Miconia forzzae, Amapá, Amazonas, Pará, Escudo das Guianas, Maçiço da Neblina | não | Springer / ResearchGate (Download full-text) | https://link.springer.com/article/10.1007/s12228-017-9488-y | https://www.researchgate.net/publication/318185427_Two_new_species_of_Miconia_Melastomataceae_Miconieae_from_the_Brazilian_northern_border_and_adjacent_French_Guiana | Two new species of Miconia from northern Amazonia area described. Miconia amapaënsis has been collected in the Brazilian state of Amapá and in nearby locations in northern Pará and southern French Guiana. It has remarkable seeds, with both the appendix and seed coat covered with long papillae. Miconia forzzae has been collected on the Brazilian side of the Neblina Massif, in the Brazilian state of Amazonas, close to the border with Venezuela. It has 4-merous flowers, with a terete hypanthium, yellow stamens, the ovary apex with unbranched trichomes, and a punctiform stigma. This species may be endangered, considering its narrow distribution, and the fact that it was collected between 2000 and 2100 m elevation in an isolated mountain range with no neighboring mountains with similar height, but we assess its conservation status as “data deficient”, due to a lack of knowledge on the situation of the populations and the number of individuals. | ||||||||||||||||||||||||||||||
20 | Melastomataceae | Miconia rondoniensis (Melastomataceae), a new species from the Southern Amazon of Brazil | Julia Meirelles, Carlos Renato Boelter & Renato Goldenberg | artigo | Brittonia | 69 | 470-476 | 2017 | Miconieae, terra firme, Rondônia, Mato Grosso, Amazonas | não | Springer | https://link.springer.com/article/10.1007/s12228-017-9480-6 | Miconia rondoniensis occurs in secondary upland (terra firme) moist open forest in the Brazilian states of Rondônia, Mato Grosso and Amazonas. It can be recognized by the tree habit, large leaves with rounded to obtuse or subcordate bases and 5+2 basal veins (five main veins plus a faint submarginal pair), large inflorescences with proximal paraclades bearing quaternary branches and distal paraclades bearing tertiary branches, persistent hemi-elliptic bracteoles, short persistent calyx lobes, and capitate stigmas. The most striking feature of this new species is the thick pubescence on the branches and petioles, composed of trichomes having a long axis and short arms at the base, but inflated and lacking arms at the apex, resulting in a sorus-like surface covered with globose structures. | ||||||||||||||||||||||||||||||||
21 | Melastomataceae | Flora das cangas da Serra dos Carajás, Pará, Brasil: Melastomataceae | Keila Cristina de Jesus Rocha, Renato Goldenberg, Julia Meirelles & Pedro Lage Viana | artigo | Rodriguesia | 68 | 3 | 997-1034 | 2017 | Miconia, Clidemia, Brasilianthus, Pleroma, Mouriri, Rhynchanthera, Aciotis, Nepsera, Acisanthera, Ernestia, Pterolepis, Macairea, Tibouchina, Desmoscelis, Tococa, Leandra, Bellucia, Henriettea, afloramentos ferruginosos, Amazônia, endemismo | sim | Scielo | http://www.scielo.br/scielo.php?script=sci_arttext&pid=S2175-78602017000500997 | temos a dissertação | português | Apresenta-se um tratado taxonômico para a família Melastomataceae nas áreas de cangas da Serra dos Carajás. Foram registradas 42 espécies distribuídas em 18 gêneros, sendo Miconia o mais rico, com 20 espécies, seguido de Clidemia com três espécies. O gênero monotípico Brasilianthus (B. carajensis) é considerado endêmico da região de Carajás, assim como uma espécie de Pleroma. Este trabalho apresenta descrições morfológicas, chaves de identificação para gêneros e espécies, ilustrações, distribuição geográfica e comentários para as espécies tratadas. | |||||||||||||||||||||||||||||
22 | Melastomataceae | Pleroma carajasense (Melastomataceae), a new species endemic to ironstone outcrops in the Brazilian Amazon | Keila Cristina de Jesus Rocha, Renato Goldenberg, Pedro Lage Viana & Fabrício Schmitz Meyer | artigo | Phytotaxa | 329 | 3 | 233-242 | 2017 | Canga, Melastomeae, solo ferruginoso, afloramento ferruginoso, Tibouchina caatingae | não | Phytotaxa | https://www.biotaxa.org/Phytotaxa/article/view/phytotaxa.329.3.4 | A new species of Pleroma from Serra dos Carajás, Pará state, Brazil, is described. Pleroma carajasense occurs in southeastern Amazonia, northern Brazil, in canga vegetation, on ironstone outcrops. It is morphologically related to Tibouchina caatingae, because both are shrubs with elliptic to oval leaves, conspicuous petioles (3–17 mm and 10–15 mm, respectively), a pair of elliptic bracteoles, and purple petals, anthers (both cycles) and style. Pleroma carajasense differs from T. caatingae by its chartaceous leaves (versus coriaceous in T. caatingae), with an obtuse to cuneate base (vs. obtuse to subcordate), hypanthium 4–7 × 1.2–4 mm (vs. 10–15 × 3–5 mm). According to IUCN criteria, this species should be considered endangered (EN). A morphological description, illustrations, photos in the field, scanning electronic micrographs of the leaf indumentum and seeds, information on conservation status and distribution are presented. | |||||||||||||||||||||||||||||||
23 | Melastomataceae | Systematics and phylogeny of Siphanthera (Melastomataceae) | Frank Almeda & Orbélia R. Robinson | Monografia | Systematic Botany Monographs | 93 | 1-101 | 2011 | generic and species limits, South America, Siphanthera, macromorphology, pollen, seed micromorphology, chromosome cytology, cladistic analysis, geographic distribution, phylogeny, Farringtonia, Amazon Basin | não | ResearchGate (Download full-text) / JSTOR (read online) | https://www.researchgate.net/publication/263383427_Systematics_and_phylogeny_of_Siphanthera_Melastomataceae | https://www.jstor.org/stable/23210353?seq=1 | inglês | This study represents the first attempt to evaluate generic and species limits in the South American genus Siphanthera by incorporating new information from macromorphology, pollen and seed micromorphology, chromosome cytology, a cladistic analysis, and distributional information. Available data provide a rationale for recognizing Siphanthera as a monophyletic genus of fifteen species with a bicentric distribution centered in the Brazilian Planalto, and the Guayana Highlands and contiguous areas. The monotypic genus Farringtonia has been merged with Siphanthera during this study and two new species are proposed here, S. todziae from the Amazon Basin and S. wurdackii from the Brazilian Planalto. The recent assignment of Siphanthera to the broadly defined tribe Melastomeae is called into question pending the results of a forthcoming family-wide multigene phylogenetic analysis. An evaluation of taxonomic characters used to recognize previous infrageneric groups has led to the abandonment of a formal sectional classification of the genus. Some major evolutionary trends in Siphanthera include: change from a perennial to an annual life cycle; change in foliar venation from basal acrodromous to loss of secondaries in one direction and change in the prominence of secondary veins and their pattern of divergence from the primary vein in another direction; reduction in inflorescence complexity from branched compound dichasia to congested capituliform inflorescences or few-flowered or solitary flowered inflorescences; change in petal shape from obovate with a rounded to acute base to more or less rotund petals with a clawed base; reduction in stamen number from eight fertile stamens to four fertile stamens; change in anther shape from elongate and subulate or rostrate with a small apical pore to ovoid or subrotund with a broad ventrally or dorsally inclined apical pore; and modification of capsule shape from essentially globose with a rounded apex to laterally compressed with a bilobed or notched apex. Species constituting the first diverging lineage in our cladogram suggest a possible Brazilian Planalto origin for the genus. Pathways to northward migration were opened via large areas of continuous savanna vegetation across the Amazon Basin that connected the Brazilian and Guayana Shields during climatic fluctuations of the Pleistocene. In a less likely alternative, the distribution of Siphanthera can be accounted for by vicariance of a widespread ancestor that spanned the Brazilian and Guayana Shields. In this scenario, the taxa that branch off from the first diverging clade in our phylogenetic tree could represent a geographic sequence of differentiation from the widespread ancestor and not a series of dispersal events. Present-day rain forest dominance of the Amazon Basin with its few and scattered savanna islands has largely isolated northern and southern populations of Siphanthera and appears to explain the prevailing bicentric concentration of species on the South American continent. | ||||||||||||||||||||||||||||||
24 | Melastomataceae | A família “Melastomataceae s.s” Juss. no Parque Nacional do Viruá (Roraima) | Katia Gigliola Cangani | Dissertação | Instituto Nacional de Pesquisas da Amazônia | 102 | 2012 | Melastomataceae, taxonomia, Parque Nacional do Viruá, Roraima | sim | INPA | http://www.files.scire.net.br/atrio/inpa-ppgbot_upl//THESIS/141/dissertao_katia.pdf | OBS: foram enviados dois arquivos deste trabalho, um doc e um pdf | português | O trabalho foi realizado no Parque Nacional do Viruá (PNV), situado dentro na região Amazônica, no Estado de Roraima. Oparqueé citado por concentrar alta biodiversidade, formada pelos mosaicos de vegetações.As coletas foram realizadas durante o ano de 2010 e 2011. Todos os exemplares foram incorporados ao herbário do INPA. Foram registradas 45 espécies no total, pertencentes a 15 gêneros. Dentro das tribos: Microlicia;RhynchantheraDC. (uma espécie), Siphanthera Pohl. (uma espécie); Melastomeae,foram coletadas espécies de Acisanthera P. Br. (duas espécie), AciotisD. Don, (três espécies); Comolia DC. (duas espécies), Macairea DC. (duas espécies)eTibouchina Aubl. (umaespécie),Merianieae foram coletadas Meriania Sw.(uma espécie)e Pachyloma DC.(duas espécies),Miconieae foram registrados os seguintes gêneros: Bellucia Raf.(duas espécies),Clidemia D. Don., (cinco espécies),HenrietteaDC. (quatro espécies), Henriettella Naudin,(uma espécie), Maieta Aubl.,(uma espécie), Miconia Ruiz & Pavon., (14 espécies) e Tococa Aubl. (quatro espécies).Foram registrados dez novos registros para o Estado de Roraima e um novo registro para o Brasil. As espécies foram encontradas emtodas as formações vegetacionais do PNV, especialmente nas áreas de campina e terra firme. Montamos chave de identificação, descrições taxonômicas, glossário para termos técnicos, ilustrações fotográficas, distribuição das espécies dentro do parque, favorecendo assim para o melhor conhecimento das espécies que ocorrem no PNV | |||||||||||||||||||||||||||||||
25 | Melastomataceae | Monograph of Aciotis (Melastomataceae) | Alina Freire-Fierro | Monografia | Systematic Botany Monographs | 62 | 1-99 | 2002 | Tibouchinae, erva, subarbusto, fruto capsular, fruto baga | não? | ResearchGate (Download full-text) / JSTOR (read online) | https://www.researchgate.net/publication/260181404_Monograph_of_Aciotis_Melastomataceae | https://www.jstor.org/stable/25027895?seq=1 | Aciotis (Melastomataceae) is a genus of 13 species of herbs and subshrubs that occur from southern Mexico to northern Bolivia and southeastern Brazil. Traditionally, Aciotis has been placed in Tibouchineae [=Melastomeae s.l.], because it has capsular fruits; yet, some species of Aciotis have also baccate fruits. Most of the Melastomeae have tuberculate seeds, but all species of Aciotis have foveolate seeds. Three species (A. rubricaulis, A. indecora, and A. purpurascens) have thyrsoid inflorescences and indehiscent baccate fruits; four species (A. annua, A. ornata, A. polystachya, and A. wurdackiana) have cymose inflorescences and dry dehiscent capsules. The remaining six species (A. acuminifolia, A. circaeifolia, A. ferreirana, A. olivieriana, A. paludosa, and A. viscida) exhibit several combinations of characters, such as thyrsoid inflorescences with capsular fruits or cymose inflorescences with indehiscent baccate fruits. Illustrations and distribution maps are provided for all species. | |||||||||||||||||||||||||||||||
26 | Melastomataceae | Two new species of Graffenrieda (Melastomataceae, Merianieae) from the Amazon Rainforest | Laíce Fernanda Gomes de Lima, José Fernando Andrade Baumgratz, Eimear Nic Lughadha & João Ubiratan Moreira dos Santos | artigo | Phytotaxa | 267 | 1 | 77-83 | 2016 | Graffenrieda maturaca, Graffenrieda goldenbergii, Serra do Maturacá, Amazonas, Acre, Peru | não | Phytotaxa | https://www.biotaxa.org/Phytotaxa/article/view/phytotaxa.267.1.8 | Two new species of Graffenrieda are described from the Amazon rainforest. Graffenrieda maturaca is characterized mainly by its leaves which are dull on the adaxial surface, chartaceous, narrowly elliptic to oblanceolate, and apparently uni-nerved, with only the median acrodromous vein evident. This species has been collected only at Serra de Maturacá, in the state of Amazonas, Brazil. Graffenrieda goldenbergii is distinguished mainly by the pulverulent, whitish, early caducous indumentum of the rachis, pedicel, hypanthium and calyx, by the abaxial surface of the leaves which is moderately lepidote, with trichomes ca. 0.2 mm diam., by the irregularly valvate calyx, and by the membranaceous, costate, not sulcate fruits. This species has been collected in the state of Acre, Brazil, and in the Province and District of Lama in Peru. Both species are illustrated, compared with similar species, and their conservation status is discussed. | |||||||||||||||||||||||||||||||
27 | Melastomataceae | Os gêneros Adelobotrys e Graffenrieda (Melastomataceae; Merianieae) no Brasil | Laíce Fernanda Gomes de Lima | Tese | Universidade Federal do Pará | 349 | 2016 | Amazônia; Flora do Brasil; Nomenclatura; Taxonomia | sim | ? | Apesar de existir um repositório de dados da instituição, não consegui encontrar a tese | português | A Amazônia, maior e mais diversa floresta tropical do planeta, ainda apresenta grandes lacunas no conhecimento de sua flora. Visando contribuir com o preenchimento dessa lacuna, este trabalho teve o objetivo de realizar o estudo taxonômico do gêneros Adelobotrys DC., Graffenrieda DC. no Brasil. Esses gêneros pertencem a família Melastomataceae, tribo Merianieae e estão centrados preferencialmente na Amazônia. Foram analisadas as coleções dos dois gêneros em 22 herbários nacionais e internacionais, além de material proveniente de coletas de campo. Os resultados são apresentados na forma de dois capítulos. O primeiro referente ao estudo taxonômico das espécies de Adelobotrys no Brasil, representado por 20 espécies e caracterizado principalmente pelo hábito lianescente, tricomas malpighiáceos e conectivo com dois apêndices, um basal, calcarado e outro ascendente linear. E o segundo, ao estudo taxonômico de Graffenrieda no Brasil, representado por 20 espécies e caracterizado principalmente pelo hábito arborescente ou arbustivo, raramente lianescente, indumento variado, estames iguais em tamanho e forma, e apêndice dorsal-basal, calcarado. Para ambos os gêneros são apresentadas descrições morfológicas, chave de identificação, dados de distribuição geográfica e estado de conservação das espécies. A partir deste trabalho já foram submetidos para publicação três artigos científicos. O primeiro com a descrição de duas novas espécies de Graffenrieda para a Amazônia, Graffenrieda maturaca, caracterizada principalmente pelas folhas opacas, estreito-elípticas a oblanceoladas, cartáceas, aparentemente uninervadas, apenas com a nervuras mediana evidente e Graffenrieda goldenbergii que pode ser reconhecida principalmente pelas folhas com moderado indumento lepidoto, deiscência do cálice irregularmente valvar e frutos com hipanto membranáceo, costado, não sulcado. O segundo com a proposição de lectótipos para nove nomes em Adelobotrys. E o terceiro tratando da indicação de lectótipos para 18 nomes em Graffenrieda. The Amazon, the largest and most diverse rainforest in the world, still has large gaps in the knowledge of its flora. To contribute to filling this gap, this study aimed to realize a taxonomic study of Adelobotrys DC. and Graffenrieda DC. in Brazil. These genera belong to Merianieae tribe, Melastomataceae, Merianieae tribe and have the species centered in the Amazon Biome. We analyzed the collections of both genera in 22 national and international herbaria, as well as material from field works. The results are presented in two chapters. The first refers to the taxonomic study of Adelobotrys in Brazil, covering 20 species, and characterized mainly by climbing habit, malpighian hairs and connective with two appendages, a basal, spur, and other ascending, linear. The second chapter refers to the taxonomic study of Graffenrieda in Brazil, also with 20 species, and characterized mainly by the arboreal or shrubby habit, rarely as liana, varied indumentum, equal stamens in size and shape, and a dorsal appendage consisting of a basal calcar. For both genera are given morphological descriptions, identification key, geographical data, comments, illustrations, geographic distribution maps, and conservation status of species. From these studies, we submitted for publication three scientific manuscripts. The first about description of two new species of Graffenrieda to Amazon rainforest, Graffenrieda maturaca, characterized mainly by its leaves which are dull on the adaxial surface, chartaceous, narrowly elliptic to oblanceolate, and apparently uni-nerved, with only the median acrodromous vein evident, and Graffenrieda goldenbergii, distinguished mainly by the pulverulent, whitish, early caducous indumentum of the rachis, pedicel, hypanthium and calyx, by the adaxial surface of the leaves which is moderately lepidote, by the irregularly valvate calyx, and by the membranaceous, costate, not sulcate fruits. The other two manuscripts refer individually to the proposition of lectotypes for nine names of Adelobotrys, and eighteen names of Graffenrieda. | ||||||||||||||||||||||||||||||||
28 | Melastomataceae | Miconia renatogoldenbergii (Miconieae, Melastomataceae), a new species from savanna enclaves in southern Amazonia, Brazil | Julia Meirelles & Lucas F. Bacci | artigo | Phytotaxa | 298 | 2 | 187-193 | 2017 | Miconia renatogoldenbergii, Miconieae, savana, sub-bosque, Pará, Mato Grosso, Rondônia, Miconia punctata, tirso escorpioide | não | Phytotaxa | https://www.biotaxa.org/Phytotaxa/article/view/phytotaxa.298.2.9 | inglês | A new species of Miconia section Miconia, subsection Seriatiflorae from the Brazilian Amazonian region is described. Miconia renatogoldenbergii has a wide distribution in areas of savanna and forest understory in the states of Pará, Mato Grosso and Rondônia. It is similar to M. punctata as both species have chartaceous leaves with rusty lepidote indument on the abaxial surface. The new species can be distinguished by its mucronate leaf apex, a thyrse with short scorpioid branches, and subulate anthers, with round apex, dehiscent through an apical pore and with cordate connective appendages. | ||||||||||||||||||||||||||||||
29 | Melastomataceae | Filogenia de Miconia seção Miconia subseção Seriatiflorae e revisão taxonômica do clado albicans (Melastomataceae, Miconieae) | Julia Meirelles | Tese | Universidade Estadual de Campinas | 200 | 2015 | Seriatiflorae, inflorescência escorpióide, Miconia suberosa, Miconia macuxi, Miconia astrocalyx, Miconia rondoniensis, Miconia albicans, Miconia argyrophylla subsp. gracilis, Miconia mayarae, Miconia cinerea, Miconia stenostachya, Miconia nambyquarae, Miconia herpetica, campina, campinarana, Roraima, Caracaraí, | sim | UNICAMP | http://repositorio.unicamp.br/handle/REPOSIP/315517 | português | Resumo: Com mais de mil espécies, Miconia é um dos o maiores gênero de plantas Neotropicais. Entretanto, as análises filogenéticas recentes evidenciam sua artificialidade, bem como das suas seções e subseções. Consequentemente, faz-se necessária uma nova delimitação taxonômica para a tribo Miconieae como um todo. Na última filogenia do gênero, foram delimitados alguns grupos internos da seções Miconia e Glossocentrum, mais especificamente das espécies com folhas discolores, que são predominatemente brasileiras. A partir desta classificação preliminar, o presente estudo procurou, em primeiro lugar, entender as relações da seção Miconia subseção Seriatiflorae. Em seguida, procurou entender as relações especificas do clado Albicans, através de um tratamento taxonômico. O primeiro capítulo desta tese aborda o estudo das relações filogenéticas e evolução de caracteres morfológicos entre as espécies de Miconia sect. Miconia subseção Seriatiflorae. São apresentadas análises de parcimônia e de inferência bayesiana com 52 terminais. Seriatiflorae é polifilética com as espécies distribuídas em quatro clados e a relação entre eles não é bem resolvida em ambas análises. A presença de espécies apomíticas e poliplóides amplamente distribuídas pode ser indicativa de evolução reticulada e a falta de resolução entre os clado pode estar relacionada a hibridação interespecífica. Cerca de dez novas espécies foram descobertas durante o desenvolvimento desta tese e os manuscritos das quatro primeiras são apresentados no segundo capítulo: Miconia astrocalyx, M. macuxi, M. rondoniensis e M. suberosa. O terceiro capítulo é o tratamento taxonômico das 18 espécies do clado Albicans , todas com hábito arbustivo a arbóreo, folhas discolores com superfície abaxial recoberta por tricomas amorfos e inflorescências com ramos secundifloros e escorpióides. São espécies amplamente distribuídas desde o México ao Paraguai, ou endêmicas da Amazônia. Para tanto, foram analisadas mais de 2500 exsicatas em 18 herbários no Brasil e no exterior (BR, G, G-DC, HUEFS, IAN, INPA, JOI, K, M, MBM, MG, NY, P, RB, UEC, UPCB, US, W). Além das espécies descritas no capítulo 2, foi reconhecida a mudança de status de M. argyrophylla subsp. gracilis e proposto um novo nome, M. mayarae. Duas novas sinonímias foram estabelecidas: M. cinerea sob M. stenostachya, e M. nambyquarae sob M. herpetica. São apresentadas chave de identificação das espécies, descrições, lista completa de materiais examinados, mapas de distribuição geográfica, ilustrações, imagens e comentários das espécies Abstract: With more than a thousand species, Miconia is one of the largest Neotropical plant genus. However, the recent phylogenetic analyses showed its artificiality, as well as from its sections and subsections, then emerging the necessity of a new taxonomic delimitation for the entire tribe Miconieae. In the last genus phylogeny, it was delimited some internal groups from sections Miconia and Glossocentrum, more specifically from the species with discolors leaves, that are predominantly brazilian. From this preliminary classification, the present study aimed first to understand the relationship of section Miconia subsection Seriatiflorae. And second, more specifically, to understand the relations of the Albicans clade in its taxonomy. The first chapter of this thesis adresses the study of phylogenetic's relationships and morphologial chacaters evolution between the species of the section Miconia subsection Seriatiflorae. There are presented parsimony analyses and bayesian inferences with 52 terminals. Seriatiflorae is polyphyletic with it's species distributed in four clades and the relationships between them are not solved in both analyses. The presence of apomictic polyploid and widely distributed species can be indicative of reticulate evolution and the lack of resolution between clades can be related to interespecific hibridization. About ten new species were discovered during the development of this thesis and the manuscripts of four of them are presented in the secod chapter: Miconia astrocalyx, M. macuxi, M. rondoniensis e M. suberosa. The third chapter is the taxonomic treatment of the 18 species in the Albicans clade with shrubby to treelet habit, discolours leaves with abaxial surface covered by amorfous trichomes ans inflorescences with secundiflorous and scorpioid branches. This species are widely distributed from México to Paraguai, or endemics from Amazon. For this, were analysed more than 2500 exsicates in 18 herbaria in Brasil and abroad (BR, G, G-DC, HUEFS, IAN, INPA, JOI, K, M, MBM, MG, NY, P, RB, UEC, UPCB, US, W). Besides the species described in Chapter 2, it was recognized the status change of M. argyrophylla subsp. gracilis and proposed a new name, M. mayarae. Two new synonyms were established: M. cinerea under M. stenostachya, M. nambyquarae under M. herpetica. There are presented species identification key, descriptions, complete list of examined material, geographic distributional maps, ilustrations, images and commentaries about the species | ||||||||||||||||||||||||||||||||
30 | Melastomataceae | Sandemania hoehnei (Melastomataceae: Tibouchineae): taxonomy, distribution, and biology | Susanne S. Renner | artigo | Brittonia | 39 | 4 | 441-446 | 1987 | Sandemania hoehnei, Tibouchineae, arbusto, savana, | não | Springer | https://link.springer.com/article/10.2307/2807327 | Sandemania Gleason, a monotypic melastome genus of Brazil, Venezuela, and Peru, is described and illustrated with accompanying notes on its habitat, distribution, reproductive biology, and tribal and generic relationships.Sandemania belongs in the Tibouchineae tribe where it is related toComolia andMacairea | |||||||||||||||||||||||||||||||
31 | Melastomataceae | Systematic studies in the Melastomataceae: Bellucia, Loreya, and Macairea | Susanne S. Renner | Monografia | Memoirs of The New York Botanical Garden | 50 | 111 | 1989 | taxonomia, classificação, nomenclatura | não | não | https://nybgshop.org/systematic-studies-in-the-melastomataceae-bellucia-loreya-macairea-mem-50/ | inglês | Bellucia, a small neotropical genus of trees and shrub with large 5-8-merous flowers, ranges from Mexico to Bolivia. This treatment recognizes five of the previously described 27 species. A new species is described and illustrated and two new combinations are made. / Loreya is a neotropical genus of trees, mainly of the upper Amazon valley but ranging from Nicaragua to Bolivia. Careful consideration of allied genera shows that Loreya is a distinct taxon. Four new species are described. / Macairea is a neotropical genus of shrubs and subshrubs, most diverse in the Orinoco-Rio Negro drainage and in the Gran Sabana of Venezuela. Twenty of the previously described 43 species are recognized and two new ones are described. All three treatments include keys. | |||||||||||||||||||||||||||||||
32 | Melastomataceae | A revision of Rhynchanthera (Melastomataceae) | Susanne S. Renner | artigo | Nordic Journal of Botany | 9 | 6 | 601-630 | 1990 | Microliceae, | não | Wiley Online Library | https://onlinelibrary.wiley.com/doi/abs/10.1111/j.1756-1051.1990.tb00551.x | The neotropical genus Rhynchanthera (Melastomataceae, Microlicieae) is revised, and 15 of the 84 proposed taxa are recognized; two species are excluded from the genus. The group consists of subshrubs and shrubs with usually purple flowers in thyrsoid inflorescences of uniparous or biparous cymes. It is characterized by androecia with five antepetalous staminodia in addition to the five fertile stamens, and - in most species - dimorphism of the stamens, with one strikingly longer than the other four. The plants always are covered by at least some simple glandular hairs. The majority of the species of Rhynchanthera occur in south-central Brazil, however, the range of the genus extends from southern Mexico to Bolivia and Paraguay. All species grow in wet places in open scrub or savanna vegetation. Micromorphological features of the seeds have been investigated and support the traditional placement of Rhynchanthera in the Microlicieae where it is closest to Microlicia, Lavoisiera, and Trembleya. Two taxa are illustrated with drawings, and the distribution of all is mapped. | |||||||||||||||||||||||||||||||
33 | Melastomataceae | A revision of Pterolepis (Melastomataceae: Melastomeae) | Susanne S. Renner | artigo | Nordic Journal of Botany | 14 | 1 | 73-104 | 1994 | ervas, arbustos,Pterolepis picorondonica, mapas de distribuição | não | Wiley Online Library | https://onlinelibrary.wiley.com/doi/abs/10.1111/j.1756-1051.1994.tb00575.x | Pterolepis consists of herbs and small shrubs with pink, purple, or white (3-)4–5-merous flowers, stamens with basal-ventrally prolonged connectives, and cochleate seeds. The majority of the species occur in central Brazilian cerrado vegetation, but two weedy species have become widespread, one ranging from Bolivia to southern Mexico, the other from Paraguay to the West Indies. Pterolepis appears related to the paleotropical genera Osbeckia, Melastoma, and Dissotis and to the neotropical genus Tibouchina. The main diagnostic feature of the genus are branched emergences in the intercalycine sinuses but these are variable among the species and also occur in many paleotropical and two neotropical species, casting some doubt on their taxonomic value above the species level. Within Pterolepis, 14 of the 80 taxa proposed by previous authors are recognized and eight species are illustrated; one new species, P. picorondonica from Amazonian Brazil, and a new variety, P. parnassiifolia var. piatensis from Bahia, are described. Also provided are scanning electron micrographs of the seeds of most, and distribution maps of all species. | |||||||||||||||||||||||||||||||
34 | Melastomataceae | Estudos taxonômicos no gênero Comolia DC. (Melastomataceae - Melastomeae) no Brasil | Rita Cristina Seco | Tese | Universidade Estadual de Campinas | 113 | 2006 | Comolia, Melastomataceae, Botanica, Classificação, Brasil | sim | UNICAMP | http://repositorio.unicamp.br/jspui/handle/REPOSIP/315632 | português | Resumo: o gênero Comolia DC. (Melastomataceae, Melastomeae), caracterizado por suas espécies com flores tetrâmeras, ovários 2-4-1oculares, estames glabros com conectivos prolongados e apendiculados e sementes cocleadas, ocorre na América do Sul, sendo encontrado no Brasil, na Colômbia, Venezuela, Guianas e Suriname. É no Brasil, onde só não está representado na Região Sul, que este gênero apresenta maior número de espécies, tendo em vista que, das 17 conhecidas até o momento (e aceitas neste estudo), 11 ocorrem aqui e 6 são endêmicas no país. No território nacional, as espécies de Como lia encontram-se distribuídas no cerrado, inclusive em seus campos rupestres, em áreas de restinga e nas savanas arenosas da Região Norte. Contudo, desde o mal do século XIX, Comolia nunca mais foi amplamente estudado no país. Sendo assim, foi realizado um estudo taxônomico das espécies de Comolia representadas no Brasil, baseado, fundamentalmente, em materiais herborizados. As espécies foram descritas, acompanhadas das respectivas ilustrações, a nomenclatura e a distribuição geográfica foram devidamente atualizadas, quando se fez necessário, as sementes foram analisadas através de microscopia eletrônica de varredura e uma chave de identificação foi elaborada. Partindo-se de 40 binômios validamente publicados para os táxons deste gênero ocorrentes no Brasil, onze espécies foram aceitas. São apresentados cinco sinônimos novos e uma nova ocorrência para o Brasil. Não foram adotadas neste trabalho as divisões infragenéricas propostas por autores anteriores, assim como nenhuma categoria infraespecífica foi admitida | ||||||||||||||||||||||||||||||||
35 | Melastomataceae | Melastomataceae | John J. Wurdack | Monografia | Instituto Botánico | Flora de Venezuela | 8 | 824(?) | 1973 | taxonomia, classificação, nomenclatura | não | não, apenas impresso | espanhol | ||||||||||||||||||||||||||||||||
36 | Melastomataceae | Melastomataceae | John J. Wurdack | Monografia | University of Göteborg / Riksmuseum | Flora of Ecuador | 13 | 406 | 1980 | taxonomia, classificação, nomenclatura | não | ? | Abstract: The genus Comolia DC. (Melastomtaceae, Melastomeae) is characterized by plants with 4-merous flowers, 2(3)-4- locular ovary, stamens with prolonged appendiculate connective and cochleate seeds. The species of this South American genus are found in Brazil, Colombia, Venezuela, Guianas and Suriname, showing most diversity in Brazil. From the 20 species here accepted, 11 occur in the country and 7 are endemic to Brazil. However, since the end ofthe 19th century, no revision of the Brazilian species of Comolia was done. The taxonomic study of the species of Comolia represented in Brazil, was based, fundamentally, on herbarium material. The species were described and illustrated, the nomenclature and geographic distribution were updated where it was required, seeds were analyzed through electronic microscopy and a key for the species was created. From 40 validly published names, 11 species were accepted. Five new synonyms and a new occurrence for Brazil were established. | ||||||||||||||||||||||||||||||||
37 | Annonaceae | Taxonomy of Xylopia barbata (Annonaceae) and related species from the Amazon/Orinoco region | Kenneth J. Bagstad & David M. Johnson | artigo | Contributions from the University of Michigan Herbarium | 22 | 21-28 | 1999 | chave de identificação de espécies, Xylopia rigidiflora, Xylopia orinocensis, Xylopia barbata, arbusto, indumento | sim | BHL | https://www.biodiversitylibrary.org/item/45698#page/27/mode/1up | inglês | não possui resumo | |||||||||||||||||||||||||||||||
38 | Malpighiaceae | Notes on Neotropical Malpighiaceae – VII | William R. Anderson | artigo | Contributions from the University of Michigan Herbarium | 22 | 1-19 | 1999 | Banisteriopsis carolina, Banisteriopsis mariae, Byrsonima cordifolia, Byrsonima hirsuta, Byrsonima lanulosa, Byrsonima riparia, Heteropterys guianensis, Heteropterys hatschbachii, Heteropterys marginata | sim | BHL | https://www.biodiversitylibrary.org/item/45698#page/6/mode/1up | não possui resumo | ||||||||||||||||||||||||||||||||
39 | x | Annonaceae | Studies in Annonaceae XXXIII. A revision of Fusaea (Baill.) Saff. | Lars W. Chatrou & Ping He | artigo | Brittonia | 51 | 2 | 181-203 | 1999 | morfologia, anatomia, tricomas, Fusaea longifolia, Fusaea peruviana, árvore, arbusto | não | Springer | https://link.springer.com/article/10.2307/2666627 | inglês | The neotropical genusFusaea is revised on the basis of almost 400 herbarium collections. The number of species is reduced to two, asF. decurrens R. E. Fr. is put into synonymy underF. longifolia (Aubl.) Saff. Three striking, newly observed characters are reported. An unknown type of coherence of styles is described. Wood anatomically, small rhombic crystals in the ray cells of the wood provide a novelty for Annonaceae. The axes of the rhipidiate inflorescence are, unlike other Annonaceae, not oriented in one plane by addorsement of the prophyll, but the angle of displacement is only 80–90°. | |||||||||||||||||||||||||||||
40 | x | Annonaceae | Revision of Malmea alliance: Malmea and three new Neotropical genera: Klarobelia, Mosannona, and Pseudomalmea | Lars W. Chatrou | capítulo livro | Utrecht University | Changing genera: systematic studies in Neotropical and West African Annonnaceae | 105-192 | 1998 | morfologia, anatomia, chave de identificação de gênero, chave de identificação de espécies, Klarobelia peruviana, Klarobelia anomala, Klarobelia napoensis, Klarobelia stipitata, Klarobelia magalocarpa, Klarobelia candida, Klarobelia lucida, Klarobelia inundata, Klarobelia cauliflora, Klarobelia pumila, Malmea dimera, Malmea dielsiana, Malmea obovata, Malmea guianensis, Malmea manausensis, Malmea surinamensis, Mosannona garwoodii, Mosannona discolor, Mosannona hypoglauca, Mosannona vasquezii, Mosannona papillosa, Mosannona pachiteae, Mosannona pacifica, Mosannona raimondii, Mosannona xanthochlora, Mosannona maculata, Mosannona guatemalensis, Mosannona costaricensis, Mosannona depressa subespécie abscondita, Mosannona depressa subespécie depressa, Pseudomalmea diclina, Pseudomalmea boyacana | não | ? | Precursor of Flora Neotropica Monograph | inglês | |||||||||||||||||||||||||||||||
41 | x | Annonaceae | Keys to the genera of Annonaceae | Thomas L.P. Courvreur, Paul J.M. Maas, Svenja Meinke, David M. Johnson & Paul J.A. KeBler | artigo | Botanical Journal of the Linnean Society | 169 | 74-83 | 2012 | chave de identificação de gêneros, Tetrameranthus, Duguetia, Anaxagorea, Guatteria, Tridimeris, Xylopia, Asimina, Diclinannona, Ephedranthus, Oxandra, Pseudomalmea, Klarobelia, Pseudoxandra, Ruizodendron, Onychopetalum, Bocageopsis, Crematosperma, Pseudephedranthus, Unonopsis, Cymbopetalum, Porcelia, Cardiopetalum, Trigynaea, Hornschucia, Bacagea, Mosannona, Duckeanthus, Annona, Fusaea, Desmopsis, Malmea, Sapranthus, Stenanona, Meiocarpidium, Annickia, Dielsiothamnus, Friesodielsia, Uvaria, Artabotrys, Ophyropetalum, Isolona, Monodora, Fenerivia, Hexalobus, Uvariastrum, Mischogyne, Toussaintia, Monocyclanthus, Letestudoxa, Uvariopsis, Boutiquea, Sphaerocoryne, Pseudartabotrys, Afroguatteria, Monanthotaxis, Gilbertiella, Annickia, Sanrafaelia, Asteranthe, Neostenanthera, Cleistopholis, Cananga, Lettowianthus, Piptostigma, Anonidium, Mkilua, Greenwayodenron, Exellia, Polyceratocarpus, Cleistochlamys, Ambavia, Polyalthia, Mwasumbia, Uvariodendron, Fissistigma, Desmos, Schefferomitra, Mitrella, Pyramidanthe, Orophea, Pseuduvaria, Neouvaria, Cyathocalyx, Drepananthus, Stelechocarpus, Maasia, Mezzettia, Dendrokingstonia, Sageraea, Enicosanthum, Dasymaschalon, Disepalum, Mitrephora, Goniothalamus, Meiogyne, Platymitra, Alphonsea, Meiogyne, Monocarpia, Popowia, Trivalvaria, Haplostichanthus, Woodiellantha, Miliusa, Marsypopetalum, Phaeanthus, Phoenicanthus, Melodorum, Sphaerocoryne | sim | Wiley Online Library | https://onlinelibrary.wiley.com/doi/epdf/10.1111/j.1095-8339.2012.01230.x | inglês | Identification keys are provided for all genera currently recognized in Annonaceae. Separate keys are presented for the Neotropics (34 genera), Africa-Madagascar (40 genera) and Asia-Australasia (42 genera). These keys are based on a combination of vegetative and fertile characters. | ||||||||||||||||||||||||||||||
42 | Annonaceae | Estudos taxonômicos do gênero Xylopia L. (Annonaceae) no Brasil extra-amazônico | Marilda Carvalho Dias | Tese | Universidade Estadual de Campinas | 183 | 1988 | taxonomia, morfologia, chave de identificação de espécies extra-amazônicas, Xylopia emarginata, Xylopia sericea, Xylopia frutescens, Xylopia aromatica, Xylopia brasiliensis, Xylopia involucrata, Xylopia ochrantha, Xylopia laevigata, Xylopia langsdorfiana | sim | UNICAMP | http://repositorio.unicamp.br/jspui/handle/REPOSIP/315262 | português | Resumo: O presente trabalho consiste em estudos taxonomicos do genero Xylopia L. (Annonaceae) para o Brasil extra-amazonico. Das 10 (dez) especies e 1 (uma) variedade levantadas, resultaram 8 (oito) especies distintas e 1 (uma) subespecie X. emarginata, X. serices, X. frutescens, X. aromatica, X. brasiliensis, X. ochrantha, X. laevigata e X. langsdorfina subsp. langsdorfiana e subsp. lanceolata, alem da descrição de uma especie nova, X. involucrata ¿Observação: O resumo, na íntegra poderá ser visualizado no texto completo da tese digital Abstract: A taxonomic study of the genus Xylopia L. (Annonaceae) for the Brazilian extra-Amazonian region was made. Among ten species and one variety cited in the literature, eight species and one subspecies were considered valid in this study: X. emarginata, X. serices, X. frutescens, X. aromatica, X. brasiliensis, X. ochrantha, X. laevigata e X. langsdorfina subsp. langsdorfiana and subsp. lanceolata. A new species was also described: X. involucrata...Note: The complete abstract is available with the full electronic digital thesis or dissertations | ||||||||||||||||||||||||||||||||
43 | Annonaceae | Revisions of Ruizodendron and Pseudephedranthus (Annonaceae) including a new species and an overview os most up-to-date revisions of Neotropical Annonaceae genera | Roy H.J. Erkens, Jessica Oosterhof, Lubbert Y.T. Westra & Paul J.M. Maas | artigo | Phytokeys | 86 | 75-96 | 2017 | taxonomia, morfologia, Ruizodendron ovale, chave de identificação de espécie, Pseudephedranthus enigmaticus, Pseudephedranthus fragrans | sim | Phytokeys, Research Gate, Pubmed | https://phytokeys.pensoft.net/article/13773/ | inglês | We present revisions of the Neotropical genera Ruizodendron and Pseudephedranthus (Annonaceae). Ruizodendron includes a single species R. ovale. Pseudephedranthus now comprises two species, with the description of the new species P. enigmaticus sp. nov. extending the range of the genus beyond the Upper Rio Negro region of Brazil (Amazonas) and adjacent Venezuela (P. fragrans), to include Guyana, Suriname, and the Brazilian state of Pará. An overview is provided of current revisions of Neotropical Annonaceae genera that will aid in accessing proper species information for this frequently encountered tropical rain forest family. | |||||||||||||||||||||||||||||||
44 | Annonaceae | Revision der arten einiger Annonaceen-gattungen | Robert E. Fries | Monografia? | Uppsala | Acta Horti Bergiani ? | 341 | 1931 | chave de identificação de gênero, chave de identificação de espécie, Annona muricata, Annona nitida, Annona densicoma, Annona foetida, Annona montana, Annona coriacea, Annona atabapensis, Annona gardneri, Annona aurantiaca, Annona pygmaea, Annona monticola, Annona excellens, Annona purpurea, Annona crassiflora, Annona campicola, Annona dioica, Annona campestris, Annona salzmannii, Annona impressivenia, Annona glabra, Annona crotonifolia, Annona paludosa, Annona tomentosa, Annona burchellii, Annona malmeana, Annona calophylla, Annona angustifolia, Annona paraensis, Annona sericea, Annona trinitensis, Annona spraguei, Annona ionophylla, Annona holosericea, Annona cercocarpa, Annona ulei, Annona jahnii, Annona scandens, Annona longipes, Annona macrocalyx, Annona sanctaecrucis, Annona echinata, Annona billbergii, Annona jamaicensis, Annona hypoglauca, Annona tessmannii, Annona iquitensis, Annona acuminata, Annona spinescens, Annona punicifolia, Annona nutans, Annona vepretorum, Annona cornifolia, Annona paraguayensis, Annona glaucophylla, Annona cacans, Annona amambayensis, Annona duckei, Annona symphyocarpa, Annona amazonica, Annona manabiensis, Annona humilis, Annona acutiflora, Annona haematantha, Annona ambotay, Annona saffordiana, Annona hayesii, Annona squamosa, Annona reticulata, Annona micrantha, Annona lutescens, Annona frutescens, Annona longiflora, Annona urbaniana, Annona praetermissa, Annona cherimolia, Annona acutifolia, Annona cubensis, Annona palmeri, Annona scleroderma, Annona testudinea, Annona pittieri, Annona liebmanniana, Annona diversifolia, Annona macroprophyllata, Annona bullata, Annona crassivenia, Annona oblongifolia, Annona sclerophylla, Annona ekmanii, Annona elliptica, Annona havanensis, Annona cascarilloides, Annona gracilis, Annona salicifolia, Annona haitiensis, Annona globiflora, Annona bicolor, Annona domingensis, Annona dumetorum, Annona rosei, | não | ? | Em sueco com descrições em latim | |||||||||||||||||||||||||||||||||
45 | Annonaceae | Synopsis of the Tribe Bocageeae (Annonaceae), with revisions of Cardiopetalum, Froesiodendron, Trigynaea, Bocagea, and Hornschuchia | David M. Johnson and Nancy A. Murray | artigo | Brittonia | 47 | 3 | 248-319 | 1995 | morfologia, taxonomia, biogeografia, chave de identificação de gêneros, chave de identificação de espécies, Cardiopetalum calophyllum, Cardiopetalum surinamense, Cardiopetalum plicatum, Froesiodendron urceocalyx, Froesiodendron amazonicum, Froesiodendron longicuspe, Trigynaea cinnamomea, Trigynaea triplinervis, Trigynaea oblongifolia, Trigynaea lagaropoda, Trigynaea duckei, Trigynaea lanceipetala, Trigynaea axilliflora, Trigynaea caudata, Bocagea longepedunculata, Bocagea viridis, Hornschuchia lianarum, Hornschuchia citriodora, Hornschuchia myrtillus, Hornschuchia alba, Hornschuchia cauliflora, Hornschuchia obliqua, Hornschuchia bryotrophe, Hornschuchia polyantha, Hornschuchia santosii, Hornschuchia leptandra | não | Springer / Research Gate | https://link.springer.com/article/10.2307/2807118 | inglês | The tribal name Bocageeae Endlicher is reestablished and the tribe is circumscribed on the basis of solitary internodal ebracteate pedicels that are articulated at the base, and pollen shed in polyads of eight or more grains. Septate anther locules, large pollen size, and seed appendages are prevalent in the tribe. Intectate pollen with free-standing columellae, rare in Annonaceae, occurs not only in the genusTrigynaea but also in some species ofBocagea andHornschuchia. As defined here, the Bocageeae include seven neotropical genera:Cymbopetalum, Porcelia, Bocagea, Cardiopetalum, Froesiodendron, Hornschuchia, andTrigynaea. The latter five genera are revised and the treatments include ten new species:Cardiopetalum plicatum, Froesiodendron urceocalyx, Hornschuchia lianarum, H. santosii, H. leptandra, Trigynaea cinnamomea, T. lanceipetala, T. triplinervis, T. lagaropoda, andT. axilliflora, all from tropical South America. A new combination,Froesiodendron longicuspe, changes the rank of that taxon from subspecies to species.Cardiopetalum surinamense is removed fromFroesiodendron and reassigned toCardiopetalum on the basis of its connate petals, dehiscent monocarps, and seeds with bilobed arils. A cladogram provides an explicit hypothesis of intergeneric relationships in the tribe. The new combinationOnychopetalum periquino, based onTrigynaea periquino, is made. | ||||||||||||||||||||||||||||||
46 | Annonaceae | Revision of Oxandra (Annonaceae) | L. Junikka, Paul J. Maas, Hiltje Maas-van de Kramer & Lubbert Y.Th. Westra | artigo | Blumea | 61 | 215-266 | 2016 | taxonomia, morfologia, ecologia, distribuição geográfica, chave de identificação de espécies, Oxandra rheophytica, Oxandra aberrans, Oxandra euneura, Oxandra krukoffii, Oxandra unibracteata, Oxandra reticulata, Oxandra guianensis, Oxandra xylopioides, Oxandra riedeliana, Oxandra polyantha, Oxandra asbeckii, Oxandra saxicola, Oxandra longipetala, Oxandra leucodermis, Oxandra lanceolata, Oxandra surinamensis, Oxandra martiana, Oxandra bolivarensis, Oxandra sessiliflora, Oxandra maya, Oxandra espintana, Oxandra venezuelana, Oxandra sphaerocarpa, Oxandra macrophylla, Oxandra laurifolia, Oxandra mediocris, Oxandra panamensis | sim | Naturalis repository | https://repository.naturalis.nl/pub/620878 | inglês | A taxonomic revision is given of the Neotropical genus Oxandra (Annonaceae). Within the genus 27 species are recognized, 4 of which are new to science. Most of the species are occurring in tropical South America, whereas a few (6) are found in Mexico and Central America and two in the West Indies (Greater and Lesser Antilles). A key to all species is provided. The treatment includes chapters about the history of the genus and morphology. All species are fully described, including full synonymy, notes on distribution and ecology, field observations (when available), vernacular names (when given), and mostly short notes about relationships of the species concerned. For each species a distribution map is made. At the end of the revision a complete list of vernacular names is included. | |||||||||||||||||||||||||||||||
47 | Annonaceae | Flora das Cangas da Serra dos Carajás, Pará, Brasil: Annonaceae | Adriana Quintella Lobão | artigo | Rodriguesia | 67 | 5 | 1205-1209 | 2016 | taxonomia, morfologia, fenologia, distribuição geográfica, chave de identificação de espécies, Guatteria punctata, Xylopia aromatica | sim | Scielo | http://www.scielo.br/scielo.php?script=sci_arttext&pid=S2175-78602016000501205 | português | Annonaceae está representada nas cangas e matas baixas (transição com o campo rupestre) da Serra de Carajás por duas espécies: Guatteria punctata e Xylopia aromatica. Apresentam-se chave de identificação das espécies, descrições e comentários sobre fenologia, distribuição geográfica e hábitats. | ||||||||||||||||||||||||||||||
48 | Annonaceae | Diversidade e caracterização das Annonaceae do Brasil | Jenifer de Carvalho Lopes, Renato Mello-Silva | artigo | Revista Brasileira de Fruticultura | 36 | 125-131 | 2014 | sinopse de gêneros, Anaxagorea, Annona, Duguetia, Guatteria, Xylopia, Diclinanona, Cardiopetalum, Froesiodendron, Bocagea, Hornschuchia, Trigynaea, Cymbopetalum, Porcelia, Tetrameranthus, Bocageopsis, Crematosperma, Ephedranthus, Klarobelia, Malmea, Mosannona, Onychopetalum, Oxandra, Pseudephedranthus, Pseudomalmea, Pseudoxandra, Ruizodendron, Unonopsis, Oxandra | sim | Scielo | http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-29452014000500015 | português | Há, no Brasil, 29 gêneros e 386 espécies de Annonaceae, distribuídas principalmente na Amazônia, mas também na Mata Atlântica e no Cerrado. As Annonaceae estão classificadas em quatro subfamílias, Anaxagoreoideae, Annonoideae, Ambavioideae e Malmeoideae. Anaxagoreoideae inclui apenas Anaxagorea, com 14 espécies no Brasil. Ambavioideae é composto por nove gêneros, mas apenas Tetrameranthus ocorre no Brasil, com três espécies. Annonoideae é a maior subfamília, com 51 gêneros, dos quais 12 ocorrem no Brasil. Estão aqui incluídos Annona, Duguetia, Guatteria e Xylopia, os gêneros mais representativos da família na flora brasileira. Malmeoideae inclui principalmente gêneros asiáticos, e apenas os representantes da tribo Malmeeae, com 13 gêneros, ocorrem no Brasil. | |||||||||||||||||||||||||||||||
49 | Annonaceae | Ephedranthus dimerus (Annonaceae), a new species from the Atlantic Forest of Brazil, with a key to the species o Ephedranthus | Jenifer de Carvalho Lopes, Lars W. Chatrou & Renato Mello-Silva | artigo | Brittonia | 66 | 1 | 70-74 | 2014 | chave de identificação de espécies, Ephedranthus dimerus, Ephedranthus boliviensis, Ephedranthus columbianus, Ephedranthus amazonicus, Ephedranthus guianensis, Ephedranthus parviflorus, Ephedranthus pisocarpus | não | Springer | https://link.springer.com/article/10.1007/s12228-013-9311-3 | inglês | A new species of Ephedranthus from the Brazilian Atlantic Forest is described and illustrated, and a preliminary key to the species of Ephedranthus is presented. Ephedranthus dimerus is the only species of the genus from the Atlantic Forest region and the first species of the genus with dimerous flowers. It is similar to E. guianensis in having narrowly obovate to elliptic leaves with similar dimensions and a cuneate to acute base. Nevertheless, the two species can be distinguished from each other by the number of monocarps per fruit and by the length of the stipe. / Uma nova espécie de Ephedranthus da Mata Atlântica brasileira é descrita e ilustrada e uma chave preliminar de identificação para as espécies de Ephedranthus é apresentada. Ephedranthus dimerus é a única espécie de Ephedranthus da Mata Atlântica e a primeira espécie do gênero com flores dímeras. É similar a E. guianensis por apresentarem as folhas estreitamente obovadas a elípticas, com as mesmas dimensões e base cuneada a aguda. No entanto, as duas espécies podem ser distintas pelo número de monocarpídios do fruto e comprimento dos estipes. | ||||||||||||||||||||||||||||||
50 | Annonaceae | Studies in Annonaceae II. A monograph of the Anaxagorea A.St.Hil. - Part 1 | Paul J. Maas & Lubbert Y.Th. Westra | artigo | Bot. Jahrb. Syst. | 105 | 1 | 73-134 | 1984 | morfologia, anatomia, cariologia, palinologia, distribuição geográfica, ecologia, fenologia, chave de identificação de espécies, Anaxagorea silvatica, Anaxagorea brevipes, Anaxagorea floribunda, Anaxagorea brachycarpa, Anaxagorea brevipedicellata, Anaxagorea angustifolia, Anaxagorea pachypetala, Anaxagorea panamensis, Anaxagorea prinoides, Anaxagorea giganthophylla, Anaxagorea rufa, Anaxagorea phaeocarpa, Anaxagorea petiolata, Anaxagorea dolichocarpa, Anaxagorea acuminata, Anaxagorea manausensis, Anaxagorea macrantha, Anaxagorea allenii, Anaxagorea crassipetala, Anaxagorea guatemalensis | sim | Naturalis repository | https://repository.naturalis.nl/pub/535159 | inglês | Anaxagorea A. St. Hil. is distinct from other Annonaceae by the fruits. Unlike most members of the family, it occurs both in the Neotropics and in the Palaeotropics. Several chapters are devoted to a.o. morphology, anatomy, karyology, palynology, chemistry, pollination and seed dispersal, geography and ecology, economic uses and vernacular names, partly compiled from existing literature or collectors’ notes, partly as a result of own investigations. A cladistic analysis of intrageneric relationships is given. The taxonomic part provides descriptions, synonyms (nomina nuda are not included), dichotomous keys. For practical reasons, separate keys are given for neotropical and palaeotropical taxa. For neotropical species, a synoptic key is also provided. Altogether, 20 neotropical species and 3 palaeotropical species (including 2 varieties) are recognized, and 14 taxa are brought into synonymy. Another two taxa from the Neotropics are apparently new, but are not formally published because of incomplete material, and one palaeotropical species cannot be properly evaluated because of insufficient material. An index to exsiccata is appended. | ||||||||||||||||||||||||||||||
51 | Annonaceae | Studies in Annonaceae II. A monograph of the Anaxagorea A.St.Hil. - Part 2 | Paul J. Maas & Lubbert Y.Th. Westra | artigo | Bot. Jahrb. Syst. | 105 | 2 | 145-204 | 1985 | morfologia, anatomia, cariologia, palinologia, distribuição geográfica, ecologia, fenologia, chave de identificação de espécies, Anaxagorea silvatica, Anaxagorea brevipes, Anaxagorea floribunda, Anaxagorea brachycarpa, Anaxagorea brevipedicellata, Anaxagorea angustifolia, Anaxagorea pachypetala, Anaxagorea panamensis, Anaxagorea prinoides, Anaxagorea giganthophylla, Anaxagorea rufa, Anaxagorea phaeocarpa, Anaxagorea petiolata, Anaxagorea dolichocarpa, Anaxagorea acuminata, Anaxagorea manausensis, Anaxagorea macrantha, Anaxagorea allenii, Anaxagorea crassipetala, Anaxagorea guatemalensis | sim | Naturalis repository | https://repository.naturalis.nl/pub/535220 | inglês | Anaxagorea A. St. Hil. is distinct from other Annonaceae by the fruits. Unlike most members of the family, it occurs both in the Neotropics and in the Palaeotropics. Several chapters are devoted to a.o. morphology, anatomy, karyology, palynology, chemistry, pollination and seed dispersal, geography and ecology, economic uses and vernacular names, partly compiled from existing literature or collectors’ notes, partly as a result of own investigations. A cladistic analysis of intrageneric relationships is given. The taxonomic part provides descriptions, synonyms (nomina nuda are not included), dichotomous keys. For practical reasons, separate keys are given for neotropical and palaeotropical taxa. For neotropical species, a synoptic key is also provided. Altogether, 20 neotropical species and 3 palaeotropical species (including 2 varieties) are recognized, and 14 taxa are brought into synonymy. Another two taxa from the Neotropics are apparently new, but are not formally published because of incomplete material, and one palaeotropical species cannot be properly evaluated because of insufficient material. An index to exsiccata is appended. | ||||||||||||||||||||||||||||||
52 | Annonaceae | Revision of the Neotropical genus Pseudoxandra (Annonaceae) | Paul J. Maas & Lubbert Y.Th. Westra | artigo | Blumea | 48 | 201-259 | 2003 | morfologia, taxonomia, distribuição geográfica, chave de identificação de gênero, Pseudoxandra, Ruizodendron, Onychopetalum, Bocageopsis, Crematosperma, Pseudephedranthus, Oxandra, Unonopsis, Ephedranthus, Klarobelia, Pseudomalmea, Mosannona, Malmea, chave de identificação de espécie, Pseudoxandra pilosa, Pseudoxandra acreana, Pseudoxandra duckei, Pseudoxandra williamsii, Pseudoxandra parvifolia, Pseudoxandra revoluta, Pseudoxandra pacifica, Pseudoxandra leiophylla, Pseudoxandra lucida, Pseudoxandra papillosa, Pseudoxandra sclerocarpa, Pseudoxandra borbensis, Pseudoxandra cauliflora, Pseudoxandra longipes, Pseudoxandra spiritus-sanctii, Pseudoxandra atrata, Pseudoxandra bahiensis, Pseudoxandra vallicola, Pseudoxandra cauliflora, Pseudoxandra cuspidata, Pseudoxandra rionegrensis, Pseudoxandra leiophylla, Pseudoxandra lucida, Pseudoxandra polyphleba, Pseudoxandra obscurinervis | sim | Naturalis repository | https://repository.naturalis.nl/pub/524896 | inglês | A taxonomic revision is made of the Neotropical genus Pseudoxandra. This genus forms part of the Cremastosperma alliance which consists of Bocageopsis, Cremastosperma, Ephedranthus, Klarobelia, Malmea, Mosannona, Onychopetalum, Oxandra, Pseudephedranthus, Pseudomalmea, Pseudoxandra, Ruizodendron, and Unonopsis, all from the Neotropics. Within Pseudoxandra 22 species are recognized, four of which were described quite recently by the first author (Maas et al., 1986). Fourteen species are described here as new. Two dichotomous keys are provided, one for the genera of the Cremastosperma alliance, and the other for the species of Pseudoxandra. The species treatments include descriptions, geographical and ecological notes, distribution maps, synonymy, taxonomic notes, and vernacular names. A complete index of exsiccatae is included. Parallel to the taxonomic revision, a leaf anatomical survey was made by E.-J. van Marle. One of the intriguing features in Pseudoxandra is the frequent presence of minuscule warts on the leaves in dried specimens, while fresh material does not show any such warts. Osteosclereids found in the mesophyll of most species are probably responsible for this feature. This revision is meant as a precursor for a future Flora Neotropica treatment of the integral Cremastosperma alliance. Revisions of Klarobelia, Malmea s.s., Mosannona and Pseudomalmea, once constituting the genus Malmea s.l., were published earlier by Chatrou (1998). Treatments of other genera are under way, or planned for the near future. | |||||||||||||||||||||||||||||||
53 | x | Annonaceae | Rollinia | Paul J. Maas, Lubbert Y.Th. Westra, K.S. Brown Jr., B.J.H. ter Welle, A.C. Webber, A. Le Thomas, M. Waha, E. van der Heijden, F. Bouman, A. Cavé, M. Leboeuf, O. Laprévote, J. Koek-Noorman, W. Morawetz, W. Hemmer | Monografia | New York Botanical Garden Press | Flora Neotropica | 57 | 1-188 | 1992 | morfologia, distribuição geográfica, chave de identificação de gênero, chave de identificação de seção, chave de identificação de espécies, cariologia, palinologia, anatomia, ecologia, Rollinia, Annona, Anonidium, Raimondia, Gamosepalum, Saccosepalum, Rollinia, Rolliniella, Rollinula, Ancorantha, Monantha, Actinothrix, Rollinia amazonica, Rollinia andicola, Rollinia bahiensis, Rollinia boliviana, Rollinia calcarata, Rollinia centrantha, Rollinia chrysocarpa, Rollinia cuspidata, Rollinia danforthii, Rollinia dolabripetala, Rollinia dolichopetala, Rollinia ecuadorensis, Rollinia edulis, Rollinia emarginata, Rollinia exsucca, Rollinia fendleri, Rollinia ferruginea, Rollinia fosteri, Rollinia glomerulifera, Rollinia helosioides, Rollinia herzogii, Rollinia hispida, Rollinia insignis, Rollinia laurifolia, Rollinia leptopetala, Rollinia mammifera, Rollinia membranacea, Rollinia mucosa, Rollinia pachyantha, Rollinia parviflora, Rollinia peruviana, Rollinia pickelii, Rollinia pittieri, Rollinia rufinervis, Rollinia schunkei, Rollinia sericea, Rollinia sylvatica, Rollinia ubatubensis, Rollinia ulei, Rollinia velutina, Rollinia williamsii, Rollinia xylopiifolia | ? | JSTOR (read online) | https://www.jstor.org/stable/pdf/4393831.pdf?seq=1 | inglês | Rollinia, with 44 species currently recognized, takes fourth place among the Neotropical genera of Annonaceae. It stands close to the well-known genus Annona. Rolliniopsis is brought into synonymy with Rollinia. Rollinia annonoides R. E. Fries and R. poeppigii Martius are transferred to Annona, and two new combinations are made accordingly. No new species are proposed in the present monograph, this having been done in an earlier paper. Both synoptical and dichotomous keys are provided for the species. For each species a description, geographical and ecological notes, a distribution map, herbarium specimens, and, whenever applicable, synonymy, chromosome number, taxonomic notes, etc., are given. Overviews are given of the history, gross morphology, geography and ecology, systematics, economic uses, and conservation status of the genus. Vernacular names are also listed. New data are presented in the fields of leaf and wood anatomy, karyology, palynology, seed anatomy, and chemistry. There are field observations on flower biology and some on seed dispersal, all of recent date. One chapter deals with insects, particularly Lepidopters, feeding on Rollinia and the related Annona. / Rollinia, com 44 espécies atualmente reconhecidas, ocupa o quarto lugar entre os gêneros Neotropicais de Annonaceae. Este gênero é próximo do bem conhecido gênero Annona. Rolliniopsis é colocado como sinônimo de Rollinia. Rollinia annonoides R. E. Fries e R. poeppigii Martius são transferidos para o gênero Annona, e consequentemente duas novas combinaçaaes são feitas. Na presente monografia nenhuma nova espécie é proposta, isso foi feito em artigos anteriores. Uma chave sinóptica e uma dicotômica são fornecidas para as espécies. Para cada espécie são apresentados descriçaaes, mapa de distribução, dados sobre distribução geográfica e ecológica, espécimes herborizadas, e sempre que possível, notas taxonômicas, número de cromossomos, sinônimos, etc., são fornecidos. Além disso são apresentados dados sobre história, morfologia, geografia e ecologia, posição sistemática, importância econômica e conservação do gênero. Nomes vulgares também são listados. Novos dados são apresentados sobre anatomia de madeira e foliar, cariologia, palinologia, anatomia de sementes, e química. Tem algumas observaçaaes de campo sobre biologia floral e dispersão de sementes, todos dados recentes. Um capítulo trata de insetos, particularmente Lepidópteros, que alimentam-se de Rollinia e Annona. | |||||||||||||||||||||||||||||
54 | x | Annonaceae | Duguetia (Annonaceae) | Paul J. Maas, Lubbert Y.Th. Westra, Lars W. Chatrou | Monografia | New York Botanical Garden Press | Flora Neotropica | 88 | 1-274 | 2003 | morfologia, taxonomia,anatomia, cariologia, palinologia, ecologia, chave de identificação de espécies, Duguetia sessilis, Duguetia cadaverica, Duguetia flagellaris, Duguetia amplexifolia, Duguetia phaeoclados, Duguetia restingae, Duguetia inconspicua, Duguetia oblanceolata, Duguetia schulzii, Duguetia macrocalyx, Duguetia asterotricha, Duguetia tenuis, Duguetia oligocarpa, Duguetia aberrans, Duguetia rionegrensis, Duguetia granvilleana, Duguetia pycnastera, Duguetia pauciflora, Duguetia arenicola, Duguetia neglecta, Duguetia riparia, Duguetia gentryi, Duguetia chrysocarpa, Duguetia latifolia, Duguetia macrophylla, Duguetia pycnastera, Duguetia paraensis, Duguetia arenicola, Duguetia subcordata, Duguetia decurrens, Duguetia riparia, Duguetia vallicola, Duguetia riberensis, Duguetia longicuspis, Duguetia eximia, Duguetia magnolioidea, Duguetia uniflora, Duguetia manausensis, Duguetia megalocarpa, Duguetia pohliana, Duguetia sooretamae, Duguetia lucida, Duguetia chrysea, Duguetia salicifolia, Duguetia moricandiana, Duguetia stenantha, Duguetia argentea, Duguetia venezuelana, Duguetia confusa, Duguetia sancticaroli, Duguetia furfuracea, Duguetia lepidota, Duguetia marcgraviana, Duguetia odorata, Duguetia echinophora, Duguetia scottmorii, Duguetia aripuanae, Duguetia rotundifolia, Duguetia guianensis, Duguetia colombiana, Duguetia ruboides, Duguetia duckei, Duguetia inconspicua, Duguetia pauciflora, Duguetia ulei, Duguetia glabriuscula, Duguetia lanceolata, Duguetia macrophylla, Duguetia lucida, Duguetia panamensis, Duguetia caniflora, Duguetia quitarensis, Duguetia peruviana, Duguetia spixiana, Duguetia argentea, Duguetia hadrantha, Duguetia bahiensis, Duguetia elliptica, Duguetia riparia, Duguetia calycina, Duguetia dimorphopetala, Duguetia moricandiana, Duguetia trunciflora, Duguetia rigida, Duguetia riedeliana, Duguetia yeshidan, Duguetia salicifolia, Duguetia cauliflora, Duguetia nitida, Duguetia reticulata, Duguetia glabriuscula, Duguetia spixiana, Duguetia megalophylla, Duguetia oblongifolia, Duguetia gardneriana, Duguetia dicholepidota, Duguetia stelechantha, Duguetia microphylla, Duguetia antioquensis, Duguetia tuberculata, Duguetia surinamensis | ? | Research Gate, JSTOR (read online) | https://www.jstor.org/stable/4393920 | https://www.researchgate.net/publication/224969141_Duguetia_Flora_Neotropica_monograph_88 | inglês | Duguetia, now including Pachypodanthium, is a genus with 93 species, 89 of which occur in the Neotropics, and the remaining four in Africa. Duguetia is the third largest genus of Annonaceae in the Neotropics, after Guatteria (265 species) and Annona (150 species). It is closest to the Amazonian genera Fusaea and Duckeanthus. No new species are proposed in the present monograph, but 25 new species have been published by Maas and co-workers in precursory papers over the last years. Two separate dichotomous keys to the species are provided, one for the Neotropics, and one for Africa, respectively. There is also a synoptical key for the Neotropical species. For each species a description, geographical and ecological notes, a distribution map, an illustration (for most of the species), and a list of herbarium specimens (or a representative selection thereof) are given. Whenever applicable, synonymy, chromosome number, notes on taxonomy and other topics are also provided. Overviews are given of the history, gross morphology, geography and ecology, systematics, economic uses, and conservation status of the genus. A collectors index and a list of vernacular names are appended. New data are presented on anatomy of leaf, wood, and bark, as well as on karyology, palynology, chemistry, and phylogeny. Also, there are new observations from the fields of floral biology and seed dispersal. /// El género Duguetia, que ahora incluye a Pachypodanthium, esta formado por 93 especies; de las cuales 89 son neotropicales y cuatro de Africa. Es el tercer género más diverso de Annonaceae en el Neotropico, después de Guatteria (265 spp.) y Annona (150 spp), y está más relacionado con los géneros amazónicos Fusaea y Duckeanthus. En esta monografía no se propone ninguna especie nueva, sin embargo, en los últimos años Maas et al. han publicado 25 novedades taxonómicas. Se elaboró una clave dicotómica y una sinóptica para las especies neotropicales y, además, una clave dicotómica para los taxones africanos. Para cada especie se presenta una descripción, notas geográficas y ecológicas, un mapa de la distribución, una ilustración para la mayoría de los taxones y una lista de los especimenes de herbario. En algunos casos se presenta la sinonimia, el número de cromosomas y notas taxonómicas, entre otros. Para el género se presentan aspectos de la historia taxonómica, morfología, geografía, ecología, usos económicos, y estado de conservación, además, se muestran nuevos datos de anatomía de la hoja, la madera y la corteza; así como de filogenía, cariología, palinología, química, y observaciones de biología floral y dispersión de semillas. Un índice de colectores y una lista de nombres vernáculos aparecen al final del tratamiento. /// Duguetia, Duguetia, incluindo agora Pachypodanthium, é um gênero de 93 especies, 89 das quais crescem nos Neotrópicos e só 4 na Africa. Em tamanho é o terceiro gênero das Annonaceae nos Neotrópicos depois de Guatteria (265 espécies) e Annona (150 espécies), e é mais afim aos gêneros Amazõnicos Fusaea e Duckeanthus. Nesta monografia nenhumo taxon novo é apresentado, desdeque nos últimos anos 25 espécies novas foram publicadas por Maas e sócios em papeis preliminares. Duas chaves dicótomas são fornecidas, uma para as espécies Neotropicais, e outra para as 4 espécies Africanas. Tambem uma chave sinóptica para as espécies Neotropicais é fornecida. Para cada espécie uma descrição completa, com notas geográficas e ecológicas, um mapa de distribuição, uma illustração (para a grande maioria) e uma lista ou seleção representiva de espécimes de herbária é feita. Quando possivel sinonimia, número cromosómico e notícias taxonômicas são dadas. Sumários da história do gênero, sua morfologia geral, distribuição, ecologia, posição sistemática, usos econômicos e estado de conservação são ofericidas. Dados novos são apresentados sôbre anatomia de folhas, madeira e casca, como tambem nas áreas de cariologia, palinologia, química e filogenia. Novas observações sôbre biologia floral e dispersão de sementes são relatadas. Um index de coletores e uma lista de nomes vernaculares concluem a obra. | ||||||||||||||||||||||||||||
55 | Annonaceae | Flora da Reserva Ducke, Amazonas, Brasil: Annonaceae | Paul J. Maas, Hiltje Maas & J.M.S. Miralha | artigo | Rodriguesia | 58 | 3 | 617-662 | 2007 | morfologia, chave de identificação de gêneros, chave de identificação de espécies, Tetrameranthus, Duguetia, Pseudoxandra, Onychopetalum, Bocageopsis, Unonopsis, Anaxagorea, Xylopia, Diclinanona, Ephedranthus, Guatteria, Guatteriopsis, Cymbopetalum, Rollinia, Fusaea, Malmea, Annona, Anaxagorea brevipes, Anaxagorea manausensis, Anaxagorea phaeocarpa, Annona haematantha, Annona densicoma, Annona foetida, Annona amazonica, Annona ambotay, Bocageopsis pleiosperma, Bocageopsis multiflora, Cymbopetalum euneurum, Diclinanona calycina, Duguetia flagellaris, Duguetia trunciflora, Duguetia stelechantha, Duguetia asterotricha, Duguetia surinamensis, Duguetia megalocarpa, Duguetia pycnastera, Duguetia riparia, Duguetia arenicula, Duguetia calycina, Ephedranthus amazonicus, Fusaea longifolia, Guatteria meliodora, Guatteria guianensis, Guaterria aff. decurrens, Guatteriopsis blepharophylla, Guatteria discolor, Guatteria megalophylla, Guatteriopsis hispida, Guatteriopsis friesiana, Guatteria citriodora, Guatteria foliosa, Guatteria scytophylla, Guatteria procera, Guatteria anthracina, Guatteria olivacea, Malmea manausensis, Pseudoxandra obscurinervis, Pseudoxandra duckei, Rollinia insignis, Rollinia mucosa, Tetrameranthus duckei, Unonopsis stipitata, Unonopsis duckei, Unonopsis guatterioides, Xylopia benthamii, Xylopia emarginata var. duckei, Xylopia spruceana, Xylopia neglecta, Xylopia crinita, Xylopia nitida, Xylopia calophylla, Xylopia amazonica, Xylopia polyantha | sim | Scielo | https://www.scielo.br/scielo.php?script=sci_arttext&pid=S2175-78602007000300617&lng=en&nrm=iso | inglês | não possui resumo | ||||||||||||||||||||||||||||||
56 | Annonaceae | Revision of the Neotropical genera Bocageopsis, Onychopetalum, and Unonopsis (Annonaceae) | Paul J. Maas, Lubbert Y.Th. Westra & Marloes Vermeer | artigo | Blumea | 52 | 413-554 | 2007 | morfologia, anatomia, chave de identificação de gênero, chave de identificação de espécies, Bocageopsis mattogrossensis, Bocageopsis canescens, Bocageopsis multiflora, Bocageopsis pleiosperma, Onychopetalum periquino, Onychopetalum amazonicum, Unonopsis osae, Unonopsis elegantissima, Unonopsis theobromifolia, Unonopsis bullata, Unonopsis peruviana, Unonopsis aviceps, Unonopsis esmeraldae, Unonopsis penduliflora, Unonopsis panamensis, Unonopsis colombiana, Unonopsis costaricensis, Unonopsis cauliflora, Unonopsis glaucopetala, Unonopsis asterantha, Unonopsis monticola, Unonopsis magnifolia, Unonopsis heterotricha, Unonopsis pacifica, Unonopsis storkii, Unonopsis sessilicarpa, Unonopsis spectabilis, Unonopsis guatterioides, Unonopsis mexicana, Unonopsis hammelii, Unonopsis darienensis, Unonopsis longipes, Unonopsis aurantiaca, Unonopsis perrottetii, Unonopsis rufescens, Unonopsis floribunda, Unonopsis pittieri, Unonopsis bauxitae, Unonopsis sanctae-teresae, Unonopsis sericea, Unonopsis megalophylla, Unonopsis macrocarpa, Unonopsis bahiensis, Unonopsis stipitata, Unonopsis onychopetaloides, Unonopsis renati, Unonopsis duckei, Unonopsis riedeliana, Unonopsis veneficiorum, Unonopsis costanensis, Unonopsis stevensii, Unonopsis megalosperma, Unonopsis silvatica, Unonopsis umbilicata | sim | Naturalis repository | https://repository.naturalis.nl/pub/525887 | inglês | (Annonaceae). The closeness of these three genera was expressed by Fries when he placed them in his (informal) Unonopsis group (Fries, 1959), and the close relationship is supported by more recent phylogenetic research as well. Four species are recognized in Bocageopsis and two species in Onychopetalum. Unonopsis is by far the largest of the three genera with close to 50 species, of which no less than 23 species are here described as new. One species (Unonopsis umbilicata) had to be shelved as insufficiently known for lack of data, and another, obviously new, species from Colombia is too incomplete and is described provisionally as Unonopsis spec. A. Several keys are provided, one for the genera and one each for the species of Bocageopsis and Onychopetalum. For the species of Unonopsis a key to all species and, in addition, a key to the species of Mexico and Central America are provided. The species treatments include full descriptions, geographical and ecological notes, distribution maps, synonymy, taxonomic notes, and vernacular names. A complete list of exsiccatae is appended. Parallel to the taxonomic revision, a leaf anatomical survey was made by E.-J. van Marle, and is included here. | |||||||||||||||||||||||||||||||
57 | x | Annonaceae | Confronting a morphological nightmare: revision of the Neotropical genus Guatteria (Annonaceae) | Paul J. Maas, Lubbert Y.Th. Westra, S. Arias Guerrero, Adriana Q. Lobão, U. Scharf, N.A. Zamora & R.H.J. Erkens | artigo | Blumea | 60 | 1-219 | 2015 | morfologia, anatomia, cariologia, palinologia, distribuição geográfica, ecologia, fenologia, chave de identificação de espécies, Guatteria aberrans, Guatteria acrantha, Guatteria aeruginosa, Guatteria alata, Guatteria alba, Guatteria allenii, Guatteria alta, Guatteria alticola, Guatteria amapaensis, Guatteria amplifolia, Guatteria anteridifera, Guatteria antioquensis, Guatteria araracuarae, Guatteria arenicola, Guatteria argentea, Guatteria atabapensis, Guatteria australis, Guatteria auyantepuiensis, Guatteria ayangannae, Guatteria beckii, Guatteria beniensis, Guatteria bernardii, Guatteria blainii, Guatteria blepharophylla, Guatteria brevipetiolata, Guatteria campestris, Guatteria campinensis, Guatteria candolleana, Guatteria capixabae, Guatteria carchiana, Guatteria caribaea, Guatteria castilloi, Guatteri chasmantha, Guatteria chiriquiensis, Guatteria chrysophylla, Guatteria citriodora, Guatteria clusiifolia, Guatteria confusa, Guatteria conspicua, Guatteria costaricensis, Guatteria crassipes, Guatteria crassinervia, Guatteria cryandra, Guatteria cuatrecasasii, Guatteria cuscoensis, Guatteria darienensis, Guatteria decurrens, Guatteria delicatula, Guatteria denudata, Guatteria discolor, Guatteria dolichopoda, Guatteria dotana, Guatteria duckeana, Guatteria duodecima, Guatteria dura, Guatteria elata, Guatteria elegans, Guatteria elegantissima, Guatteria elongata, Guatteria emarginata, Guatteria eriopoda, Guatteria esmeraldae, Guatteria eugeniifolia, Guatteria ferruginea, Guatteria flabellata, Guatteria flagelliflora, Guatteria flexilis, Guatteria foliosa, Guatteria fractiflexa, Guatteria friesiana, Guatteria galeottiana, Guatteria gentryi, Guatteria goudotiana, Guatteria grandiflora, Guatteria grisefolia, Guatteria guianensis, Guatteria herrerana, Guatteria heteropetala, Guatteria hirsuta, Guatteria hispida, Guatteria insculpta, Guatteria intermedia, Guatteria inundata, Guatteria japurensis, Guatteria jefensis, Guatteria latifolia, Guatteria leucotricha, Guatteria liesneri, Guatteria longicuspis, Guatteria lucens, Guatteria macropus, Guatteria maguirei, Guatteria maypurensis, Guatteria megalocarpa, Guatteria megalophylla, Guatteria meliodora, Guatteria microcarpa, Guatteria minutiflora, Guatteria modesta, Guatteria monticola, Guatteria myriocarpa, Guatteria narinensis, Guatteria notabilis, Guatteria novogranatensis, Guatteria oblinga, Guatteria oblongifolia, Guatteria odorata, Guatteria oligocarpa, Guatteria oliviformis, Guatteria oriximinae, Guatteria ouregou, Guatteria pachycarpa, Guatteria pachyphylla, Guatteria pacifica, Guatteria pakaraimae, Guatteria paludosa, Guatteria panamensis, Guatteria pannosa, Guatteria partangensis, Guatteria pastazae, Guatteria peruviana, Guatteria pichinchae, Guatteria pittieri, Guatteria pogonopus, Guatteria pohliana, Guatteria polyantha, Guatteria procera, Guatteria pudica, Guatteria punctata, Guatteria ramiflora, Guatteria reinaldii, Guatteria revoluta, Guatteria richardii, Guatteria rigida, Guatteria rostrata, Guatteria rotundata, Guatteria ruboides, Guatteria rubrinervis, Guatteria rufotomentosa, Guatteria rupestris, Guatteria sabuletorum, Guatteria saffordiana, Guatteria sanctae-crucis, Guatteria scalarinervia, Guatteria scandens, Guatteria schombugkiana, Guatteria scytophylla, Guatteria sellowiana, Guatteria sessilicarpa, Guatteria slateri, Guatteria spectabilis, Guatteria stenocarpa, Guatteria stenopetala, Guatteria stenophylla, Guatteria stipitata, Guatteria subsessilis, Guatteria synsepala, Guatteria tacarcunae, Guatteria talamancana, Guatteria tenera, Guatteria terminalis, Guatteria tomentosa, Guatteria trichocarpa, Guatteria trichostemon, Guatteria ucayalina, Guatteria vallensis, Guatteria venezuelana, Guatteria venosa, Guatteria verrucosa, Guatteria verruculosa, Guatteria vilosissima, Guatteria wachenheimii, Guatteria wokomungensis, Guatteria zamorae, | sim | Naturalis repository | https://repository.naturalis.nl/pub/588490 | inglês | A taxonomic revision of the genus Guatteria, including the former genera Guatteriella, Guatteriopsis and Heteropetalum is given. Within the genus Guatteria 177 species are recognized, 25 of which are new. Included are chapters on the history of the taxonomy of the genus, morphology, wood anatomy, karyology, palynology, chemistry, flower biology and pollination, dispersal, distribution and ecology, phylogeny and molecular studies, conservation, and uses. A synoptical key to all species is included, as well as two dichotomous keys, one for the species of Central America and Mexico, and one for the species of NE, E and SE Brazil. The species treatments include descriptions, full synonymy, geographical and ecological notes, vernacular names and taxonomic notes. For all species distribution maps are made. A complete identification list with all exsiccatae studied, an index to vernacular names and an index of scientific names is included at the end. | ||||||||||||||||||||||||||||||
58 | Annonaceae | Annonaceae from central-eastern Brazil | Paul J. Maas, Hiltje Maas, Leo Junikka, Renato Mello Silva, Heimo Rainer | artigo | Rodriguesia | 52 | 80 | 65-98 | 2001 | chave de identificação de gênero, Anaxagorea dolichocarpa, Anaxagorea silvatica, Annona acutiflora, Annona aurantiaca, Annona burchellii, Annona cacans, Annona cherimola, Annona coriacea, Annona cornifolia, Annona crassiflora, Annona crotonifolia, Annona dioica, Annona gardneri, Annona glabra, Annona impressinervia, Annona malmeana, Annona montana, Annona monticola, Annona muricata, Annona reticulata, Annona saffordiana, Annona salzmannii, Annona spinescens, Annona squamosa, Annona tomentosa, Annona vepretorum, Annona warmingiana, Bocagea longepedunculata, Bocagea viridis, Bocageopsis mattogrossensis, Cardiopetalum calophyllum, Cymbopetalum brasiliense, Duguetia bahiensis, Duguetia chrysocarpa, Duguetia dicholepidota, Duguettia flagellaris, Duguetia furfuracea, Duguetia lanceolata, Duguetia magnolioidea, Duguetia marcgraviana, Duguetia microphylla, Duguetia moricandiana, Duguetia pohliana, Duguetia restingae, Duguetia reticulata, Duguetia riedeliana, Duguetia rotundifolia, Duguetia salicifolia, Duguetia scottmorii, Duguetia sessilis, Duguetia sooretamae, Ephedranthus, Guatteria acutiflora, Guatteria acutipetala, Guatteria australis, Guateria blanchetiana, Guatteria burchellii, Guatteria campestris, Guatteria candolleana, Guatteria clavigera, Guatteria curvinervia, Guatteria densicoma, Guatteria dimorphopetala, Guatteria elliptica, Guatteria ferruginea, Guatteria fruticosa, Guatteria glabrescens, Guatteria gomeziana, Guatteria hookeri, Guatteria klotzschiana, Guatteria latifolia, Guatteria lutea, Guatteria macropus, Guatteria mexiae, Guatteria minarum, Guatteria mosenii, Guatteria notabilis, Guatteria odontopetala, Guatteria oligocarpa, Guatteria peckoltiana, Guatteria penduliflora, Guatteria pogonopus, Guatteria pohliana, Guatteria psilopus, Guatteria reflexa, Guatteria riedeliana, Guatteria rupestris, Guatteria sellowiana, Guatteria silvatica, Guatteria umbrosa, Guatteria villosissima variedade villosissima, Guatteria xylopioides, Guatteriopsis blepharophylla, Hornschuchia alba, Hornschuchia bryotrophe, Hornschuchia cauliflora, Hornschuchia citriodora, Hornschuchia leptandra, Hornschuchia lianarum, Hornschuchia myrtillus, Hornschuchia obliqua, Hornschuchia polyantha, Hornschuchia santosii, Malmea obovata, Oxandra martiana, Oxandra nitida, Oxandra reticulata, Porcelia macrocarpa, Pseudoxandra bahiensis, Rollinia bahiensis, Rollinia dolabripetala, Rollinia emarginata, Rollinia exsucca, Rollinia ferruginea, Rollinia laurifolia, Rollinia leptopetala, Rollinia mucosa, Rollinia parviflora, Rollinia sericea, Rollinia sylvatica, Rollinia ubatubensis, Rollinia xylopiifolia, Trigynaea axilliflora, Trigynaea oblongifolia, Unonopsis lindmanii, Unonopsis riedeliana, Xylopia aromatica, Xylopia brasiliensis, Xylopia emarginata, Xylopia frutescens, Xylopia involucrata, Xylopia laevigata, Xylopia langsdorffiana, Xylopia ochrantha, Xylopia sericea | sim | Scielo | https://www.scielo.br/scielo.php?pid=S2175-78602001000100065&script=sci_arttext | inglês | An annotated checklist of the Annonaceae from Central-Eastern Brazil, comprising the Distrito Federal and the States of Bahia, Espírito Santo, Goiás, Minas Gerais, Rio de Janeiro, São Paulo, and Tocantins is presented. Nineteen genera and 153 species are listed for this region. An identification key for genera, information about most recent revisions, short descriptions, notes on geographical distribution, and comments are provided. | ||||||||||||||||||||||||||||||
59 | Annonaceae | Revision of Cymbopetalum and Porcelia (Annonaceae) | Nancy A. Murray | Monografia | American Society of Plant Taxonomists | Systematic Botany Monographs | 40 | 121 | 1993 | chave de identificação de gêneros, chave de identificação de espécies, morfologia, anatomia, biogeografia, Cymbopetalum baillonii, Cymbopetalum hintonii subespécies hintonii, Cymbopetalum hintonii subespécie septentrionale, Cymbopetalum steyermarkii, Cymbopetalum costaricense, Cymbopetalum mayanum, Cymbopetalum alkekengi, Cymbopetalum physaloides, Cymbopetalum parviflorum, Cymbopetalum sanchezii, Cymbopetalum longipes, Cymbopetalum loretoyacuense, Cymbopetalum coriaceum, Cymbopetalum oppositiflorum, Cymbopetalum lanugipetalum, Cymbopetalum stenophyllum, Cymbopetalum brasiliense, Cymbopetalum gracile, Cymbopetalum penduliflorum, Cymbopetalum mirabile, Cymbopetalum abacophyllum, Cymbopetalum schunkei, Cymbopetalum tessmannii, Cymbopetalum torulosum, Cymbopetalum rugulosum, Cymbopetalum euneurum, Cymbopetalum aequale, Porcelia macrocarpa, Porcelia steinbachii, Porcelia nitidifolia, Porcelia ponderosa, Porcelia mediocris, Porcelia magnifructa, Porcelia venezuelensis | ? | JSTOR (read online) | https://www.jstor.org/stable/pdf/25027830.pdf?seq=1 | inglês | The neotropical genera Cymbopetalum and Porcelia (Annonaceae) are revised on the basis of herbarium and field studies. Twenty-seven species are recognized in Cymbopetalum; 14 of them are described here as new: C. abacophyllum, C. aequale, C. alkekengi, C. coriaceum, C. euneurum, C. fosteri, C. loretoyacuense, C. oppositiflorum, C. parviflorum, C. physaloides, C. rugulosum, C. sanchezii, C. schunkei, and C. steyermarkii. In addition, one new subspecies, C. hintonii subsp. septentrionale, is described. Studies of the floral biology of several species revealed numerous adaptations, both structural and physiological, to pollination by scarab beetles of the genus Cyclocephala. Fruit maturation and seed dispersal were observed in Cymbopetalum baillonii, which, like other species of Cymbopetalum, has a suite of characteristics that promote dispersal of its seeds by birds. Seven species of Porcelia are recognized; one of them, P. mediocris of Ecuador and Colombia, is described here as new. Porcelia exhibits a pollination syndrome analogous to that of Cymbopetalum; its seeds are adapted for dispersal by mammals. | ||||||||||||||||||||||||||||||
60 | Annonaceae | Estudo taxonômico dos gêneros Ephedranthus S. Moore e Pseudephedranthus Aristeg. - Annonaceae | Jorge Oliveira, Margareth F. Sales | artigo | Boletim do Museu Paraense Emilio Goeldi, sér. bot. | 15 | 2 | 117-184 | 1999 | biogeografia, morfologia, chave de identificação de gênero, chave de identificação de espécies, plantas androdióicas, árvores, Ephedranthus amazonicus, Ephedranthus guianensis, Ephedranthus columbianus, Ephedranthus parviflorus, Ephedranthus pisocarpus, Pseudephedranthus fragrans | sim | repositorio.museu-goeldi.br | https://repositorio.museu-goeldi.br/handle/mgoeldi/689 | português | Este trabalho apresenta um estudo taxonômico dos gêneros Ephedrantlms S. Moore e Pseudephedrantltus Aristeg. (Annonaceae), baseado fundamentalmente em análise morfológica comparativa de espécimes de herbário, provenientes de instituições nacionais e estrangeiras. Foram elaboradas chaves para a identificação dos gêneros e das espécies, descrições, ilustrações, relação de material examinado, distri buição geográfica e comentários sobre os taxa. Para o reconhecimento das espécies, os caracteres morfológicos mais relevantes foram: forma da base e consistência da lâmina folial; número de brácteas, forma e consistência das pétalas. O gênero Ephedranthus está composto por E.amazoniclls R.E. Fries, E. colllmbiallus Maas & Setten, R. guianensis R.E. Fries, E. parviflorus S.Moore e E. Pisocarpus. R.E.Fries. Pseudephedrallthus é um gênero monoespecífico, constutuído por P. fragans (R.E. Fries) Aristeg. Ambos os gêneros apresentam distribuição neotropical no domínio amazônico, sendo que algumas espécies de E.phedranthus ocorrem também em outros domínios. | ||||||||||||||||||||||||||||||
61 | Annonaceae | Crematosperma (and other evolutionary digressions): molecular phylogenetics, biogeographic, and taxonomic studies in Neotropical Annonaceae | Michael David Pirie | Tese | Febodruck bv (?) | Enschede/Utrecht | 256 | 2005 | Filogenia, biogeografia, relógio molecular, morfologia, revisão taxonômica, árvores, arbustos, chave de identificação de espécies, Cremastosperma longipes, Cremastosperma bullatum, Cremastosperma novogranatense, Cremastosperma westrae, Cremastosperma venezuelanum, Cremastosperma cauliflorum, Cremastosperma napoense, Cremastosperma chococola, Cremastosperma cenepense, Cremastosperma gracilipes, Cremastosperma microcarpum, Cremastosperma dolichocarpum, Cremastosperma westrae, Cremastosperma stenophyllum, Cremastosperma antioquense, Cremastosperma awaense, Cremastosperma pendulum, Cremastosperma yamayakatense, Cremastosperma monospermum, Cremastosperma peruvianum, Cremastosperma macrocarpum, Cremastosperma pedunculatum, Cremastosperma pacificum, Cremastosperma magdalenae, Cremastosperma megalophyllum, Cremastosperma leiophyllum, Cremastosperma oblongum, Cremastosperma longicuspe, Cremastosperma brevipes, Cremastosperma panamense | sim | Research Gate | https://www.researchgate.net/publication/27686699_Cremastosperma_and_other_evolutionary_digressions_Molecular_phylogenetic_biogeographic_and_taxonomic_studies_in_Neotropical_Annonaceae | inglês | Results are presented of research on a family of flowering plants, the Annonaceae, species of which are found in tropical rainforest across the world. The project focussed on one group of species, the genus Cremastosperma, which is found in the South and Central American tropics. A taxonomic revision of Cremastosperma was made. Most of the species of Cremastosperma are found along the foothills of the Andes. Twenty-nine species were recognised, 13 of which were new to science. They are often narrow endemics, found only in areas such as the valleys of the Magdalena River in Colombia (e.g. C. magdalenae), and Marañon in Peru (e.g. C. bullatum). A resolved phylogeny can be used to infer the ancestral distributions of a clade, and possible factors behind its radiation. DNA sequences were compared in order to reconstruct the phylogeny of 19 of the 29 species of Cremastosperma. A number of clades were revealed. These included species distributed either west or east of the Andes mountain chain, providing further evidence to suggest the importance of the Andean orogeny as a vicariance event in the history of the evolution of Cremastosperma. Many other groups of plants share this ‘Andean-centred’ distribution, and the rising of the Andean mountain chain has thus been hypothesised to have caused the origin of a large proportion of the high biodiversity of the New World tropics. DNA sequences were used to reconstruct the relationships between species of four Andean-centred genera of Annonaceae, Cremastosperma, Klarobelia, Malmea and Mosannona, and to estimate how long ago those species shared common ancestors. The conclusion was drawn that the Andean-centred distribution patterns as observed are not the arbitrary result of the definition of poly-or paraphyletic groups. The timing of species diversifications in these groups was shown to coincide with the rise of the northern Andes, within the last 20-30 million years. Further research compared the timing of diversifications in Cremastosperma and Mosannona with those in two more widely distributed and species rich genera, Duguetia and Guatteria. The effects of taxon and character sampling on date estimates in these genera were assessed and compared. Higher sampling of crown group taxa of the species-rich genus Guatteria resulted in significantly older age estimations, representing a potentially serious bias in a widely used molecular dating method (nonparametric rate-smoothing). Molecular dating techniques should be assessed for sensitivity to levels of taxon sampling under differing conditions. Finally, an ancient paralogue of the widely used chloroplast marker trnL-F was discovered, the origin of which was inferred to have taken place in a common ancestor of the Annonaceae. The paralogue discovered evolves at a faster rate and appears to have complementary phylogenetic signal. It may be a useful phylogenetic marker. Although the exon appears to be intact, some intron sequences show signs of disruption of the secondary structure which is otherwise conserved across land plants. Function may thus have been lost. Future research should attempt to determine both the whereabouts and origin of both copies of trnL-F in the Annonaceae genome | |||||||||||||||||||||||||||||||
62 | Annonaceae | Annonaceae | José Eduardo L.S. Ribeiro, Paul J. Maas, Hiltje Maas, J.M.S. Miralha | capítulo livro | ? | Manaus | Flora da Reserva Ducke: guia de identificação das plantas vasculares de uma floresta de terra firme na Amazônia central | 816 | 1999 | sim? | PDF livro | http://www.botanicaamazonica.wiki.br/labotam/doku.php?id=reservaducke:pfrd:guia:inicio | Flora da Reserva Ducke | ||||||||||||||||||||||||||||||||
63 | Annonaceae | Tetrameranthus (Annonaceae) revisited including a new species | Lubbert Y.Th. Westra & Paul J. Maas | artigo | Phytokeys | 12 | 1-21 | 2012 | chave de identificação de espécies, Tetrameranthus umbellatus, Tetrameranthus laomae, Tetrameranthus globuliferus, Tetrameranthus guianensis, Tetrameranthus pachycarpus, Tetrameranthus macrocarpus, Tetrameranthus duckei | sim | Phytokeys | https://phytokeys.pensoft.net/article/1422/ | inglês | The taxonomic revision of the infrequently collected genus Tetrameranthus by Westra (1985) is updated. A new species is described from French Guiana and Amapá, Brazil, increasing the number of species in this genus to seven. | |||||||||||||||||||||||||||||||
64 | Bixaceae | Systematics of the genus Bixa and geography of the cultivated annatto tree | Donald Franklin Baer | Tese | University of California | Los Angeles | 240 | 1976 | morfologia, anatomia, ecologia, Bixa orellana, Bixa urucurana, Bixa platycarpa, Bixa arborea, Bixa excelsa, | não? | não, apenas impresso | “Reproduced with permission of the copyright owner. Further reproduction prohibited without permission.” | inglês | ||||||||||||||||||||||||||||||||
65 | Bixaceae | Morphology and ecology of seedlings, fruits and seeds of Panama: Bixaceae and Cochlospermaceae | Nancy C. Garwood | artigo | Bulletin of the Natural History Museum of London (Botany) | 24 | 2 | 161-171 | 1994 | Bixa urucurana, Cochlospermum vitifolium, ecologia, morfologia, ecologia, distribuição geográfica, fenologia, propagação, | sim | BHL | https://www.biodiversitylibrary.org/item/19427#page/62/mode/1up | inglês | Seedlings, saplings, fruits and seeds of Bixa urucurana (Bixaceae) and Cochlospermum vitifolium (Cochlospermaceae) are described, and ecological data on these stages summarized, as part of the ongoing Seedling Flora Project, centred on Barro Colorado Island, Panama. Data from these taxa and new seedling characters are used to discuss the relationship between the two families. The presence of extra-floral nectaries at leaf nodes alongthe stem and 'pearl bodies' on leaves, two ecologically important characters not described in standard floras, are discussed. | ||||||||||||||||||||||||||||||
66 | x | Bixaceae | Systematics, Biogeography, and Ethnobotany of the pantropical family Cochlospermaceae (Malvales) | Susannah Brynn Johnson-Fulton | Tese | Miami University | Oxford (?) | 171 | 2014 | molecular systematics, biogeography, ethnobotany, Cochlospermaceae | sim | Ohio Link | http://rave.ohiolink.edu/etdc/view?acc_num=miami1399054377 | inglês | This dissertation reports on the molecular systematics, biogeography, and ethnobotany of the pantropical plant family, Cochlospermaceae. The goal was to examine its origin, diversification, and evolution of morphology. Ethnobotanical data were also reviewed and compared across species and geographic regions, in light of phylogeny, to explore similar use patterns. The data support the monophyly of Cochlospermaceae and its distinctiveness from its allied families, Bixaceae, Diegodendraceae, and Sphaerosepalaceae. Amoreuxia is monophyletic and is supported by an herbaceous growth form and dimorphic stamens. However Cochlospermum is paraphyletic with two South American species, C. orinocense and C. tetraporum, that occur as separate basal lineages. Morphological character states that appear to be ancestral for the family include an arborescent habit, radially symmetrical flowers, and anthers with two apical pores. Biogeographic analyses support a late Cretaceous origin for the family in South America and subsequent dispersals into Central and North America, the West Indies, Africa, Australia, and Southeast Asia through a combination of long distance dispersal, vicariance, and human introduction. Divergence time estimates using fossil calibrations support dispersal from South America across Antarctica during the Late Paleocene Thermal Maximum and the Early Eocene Climatic Optimum before South America and Australia separated from Antarctica. Ethnobotanical research uncovered Cochlospermaceae to be an ethnobotanically rich family, with diverse uses spanning its pantropical distribution. Many species of Cochlospermaceae are used in similar ways in different geographic regions among diverse cultures. These uses range from food to fiber to medicine, with most of the human uses being medicinal. The most common medicinal uses are treating skin ailments, gastro-intestinal problems, malaria, and liver issues, with C. tinctorium having the most medicinal uses. Closely related species used by cultural groups in different regions to treat the same illnesses, suggests the presence of active compounds with potential biomedical value, since they may represent independent discoveries of similar medicinally-active compounds | ||||||||||||||||||||||||||||||
67 | Chrysobalanaceae | The taxonomy and ecology of the Chrysobalanaceae of the Amazon basin | Ghillean T. Prance | artigo | Conselho Nacional de Pesquisas | Atas do Simpósio sôbre a Biota Amazônica | 4 | 209-228 | 1967 | morfologia, anatomia, palinologia, uso econômico, chave de identificação de gêneros, sinopse de gêneros, Chrysobalanus, Licania, Parinari, Exellodendron, Couepia, Hirtella, Acioa | sim | BHL | https://www.biodiversitylibrary.org/item/193241#page/219/mode/1up | inglês | não possui resumo | ||||||||||||||||||||||||||||||
68 | Chrysobalanaceae | Chrysobalanaceae | Ghillean T. Prance | Monografia | New York Botanical Garden Press | Flora Neotropica | 9 | 1-267 | 1989 | morfologia, anatomia, palinologia, chave de identificação de gêneros, chave de identificação de espécies, Chrysobalanus icaco, Chrysobalanus cuspidatus, Chrysobalanus venezuelanus, Licania michauxii, Licania boliviensis, Licania maritima, Licania durifolia, Licania macrocarpa, Licania salzmanii, Licania klugii, Licania guianensis, Licania retifolia, Licania longipedicellata, Licania tomentosa, Licania pyrifolia, Licania leucosepala, Licania angustata, Licania platypus, Licania gonzalezii, Licania egleri, Licania minutiflora, Licania maranhensis, Licania fritschii, Licania britteniana, Licania unguiculata, Licania longipetala, Licania wurdackii, Licania turbinata, Licania lata, Licania apetala var. apetala, Licania apetala var. aperta, Licania parvifolia, Licania maguirei, Licania gardneri, Licania cuspidata, Licania sparsipilis, Licania emarginata, Licania calvescens, Licania persaudii, Licania sprucei, Licania sclerophylla, Licania albiflora, Licania longistyla, Licania fuchsii, Licania humilis, Licania foveolata, Licania octandra subsp. octandra, Licania octandra subsp. pallida, Licania rigida, Licania arborea, Licania velata, Licania subsrachnophylla, Licania salicifolia, Licania araneosa, Licania silvatica, Licania chacoensis, Licania licaniaeflora, Licania hirsuta, Licania costaricensis, Licania krukovii, Licania lasseri, Licania latifolia, Licania minuscula, Licania operculipetala, Licania reticulata, Licania arachnoidea, Licania oblongifolia, Licania macrophylla, Licania caudata, Licania latistipula, Licania divaricata, Licania glabriflora, Licania intrapetiolaris, Licania heteromorpha var. subcordata, Licania heteromorpha var. glabra, Licania heteromorpha var. perplexans, Licania heteromorpha var. heteromorpha, Licania glazioviana, Licania littoralis var. littoralis, Licania littoralis var. cuneata, Licania fanshawei, Licania irwinii, Licania cyathodes, Licania polita, Licania silvae, Licania densiflora, Licania cuprea, Licania impressa, Licania dealbata, Licania pallida, Licania gracilipes, Licania parvifructa, Licania cymosa, Licania ternatensis, Licania membranacea, Licania piresii, Licania hypoleuca var. hypoleuca, Licania hypoleuca var. foveolata, Licania boyanii, Licania buxifolia, Licania orbicularis, Licania niloi, Licania coriacea, Licania urseolaris, Licania affinis, Licania glauca, Licania davillaefolia, Licania elliptica, Licania canescens, Licania couepifolia, Licania trigonioides, Licania cordata, Licania foldatsii, Licania hebantha, Licania steyermarkii, Licania subrotundata, Licania crassivenia, Licania majuscula, Licania alba, Licania hitchcockii, Licania sandwithii, Licania laxiflora, Licania rufescens, Licania kunthiana, Licania bellingtonii, Licania compacta, Licania ovalifolia, Licania caldasiana, Licania savannarum, Licania microphylla, Licania triandra, Licania discolor, Licania apiculata, Licania micrantha, Licania pruinosa, Licania nitida, Licania riedelii, Licania bracteata, Licania parviflora, Licania robusta, Licania lanceolata, Licania spicata, Licania stricta, Licania leptostachya, Licania incana, Licania paraensis, Licania vaupesiana, Licania bahiensis, Licania maxima, Licania mollis, Licania blackii, Licania rodriguesii, Licania indurata, Licania hoehnei, Licania cruegeriana, Licania belemii, Licania splendens, Licania veneralensis, Licania amapaensis, Licania tepuiensis, Licania naviculistipula, Licania obtusifolia, Licania roraimensis, Parinari campestris, Parinari montana, Parinari rodolphii, Parinari excelsa, Parinari occidentalis, Parinari sprucei, Parinari pachyphylla, Parinari brasiliensis, Parinari klugii, Parinari maguirei, Parinari littoralis, Parinari parvifolia, Parinari cardiophylla, Parinari parilis, Parinari chocoensis, Parinari obtusifolia, Parinari romeroi, Exellodendron cordatum, Exellodendron coriaceum, Exellodendron barbatum, Exellodendron gardneri, Exellodendron gracile, Maranthes corymbosa, Couepia guianensis, Couepia glandulosa, Couepia paraensis subsp. paraensis, Couepia paraensis subsp. glaucescens, Couepia paraensis subsp. cerradoana, Couepia leptostachya, Couepia maguirei, Couepia sandwithii, Couepia parillo, Couepia steyermarkii, Couepia canomensis, Couepia foveolata, Couepia magnoliifolia, Couepia exflexa, Couepia habrantha, Couepia spicata, Couepia bracteosa, Couepia subcordata, Couepia belemii, Couepia caryophylloides, Couepia excelsa, Couepia uiti, Couepia cataractae, Couepia macrophylla, Couepia krukovii, Couepia latifolia, Couepia ovalifolia, Couepia schottii, Couepia grandiflora, Couepia elata, Couepia racemosa, Couepia martinii, Couepia bondarii, Couepia insignis, Couepia recurva, Couepia obovata, Couepia williamsii, Couepia chrysocalyx, Couepia eriantha, Couepia trapezioana, Couepia stipularis, Couepia reflexa, Couepia longipendula, Couepia cognata var. cognata, Couepia cognata var. major, Couepia cognata var. membranacea, Couepia multiflora, Couepia ulei, Couepia comosa, Couepia venosa, Couepia polyandra, Couepia platycalyx, Couepia rufa, Couepia robusta, Couepia impressa, Couepia meridionalis, Couepia pernambucensis, Couepia froesii, Couepia parvifolia, Hirtella myrmecophila, Hirtella physophora, Hirtella vesiculosa, Hirtella dorvalii, Hirtella guainiae, Hirtella duckei, Hirtella macrosepala, Hirtella ulei, Hirtella glabrata, Hirtella carbonaria, Hirtella araguariensis, Hirtella cordifolia, Hirtella insignis, Hirtella tocantina, Hirtella piresii, Hirtella davisii, Hirtella subglanduligera, Hirtella ciliata, Hirtella hoehnei, Hirtella glandulosa, Hirtella bullata, Hirtella americana, Hirtella guatemalensis, Hirtella eriandra, Hirtella paniculata, Hirtella deflexa, Hirtella tentaculata, Hirtella macrophylla, Hirtella adderleyi, Hirtella punctillata, Hirtella corymbosa, Hirtella pendula, Hirtella barrosoi, Hirtella leonotis, Hirtella mutisii, Hirtella triandra subsp. triandra, Hirtella triandra subsp. punctulata, Hirtella triandra subsp. media, Hirtella bahiensis, Hirtella latifolia, Hirtella suffulta, Hirtella elongata, Hirtella rodriguesii, Hirtella obidensis, Hirtella cowanii, Hirtella orbicularis, Hirtella guyanensis, Hirtella lightioides, Hirtella aramangensis, Hirtella rasa, Hirtella scabra, Hirtella bicornis var. bicornis, Hirtella bicornis var. pubescens, Hirtella angustissima, Hirtella tenuifolia, Hirtella pilosissima, Hirtella gracilipes, Hirtella brachystachya, Hirtella racemosa var. racemosa, Hirtella racemosa var. hexandra, Hirtella racemosa var. glandipedicellata, Hirtella juruensis, Hirtella kuhlmannii, Hirtella standleyi, Hirtella longifolia, Hirtella lemsii, Hirtella schultesii, Hirtella paraensis, Hirtella sprucei, Hirtella lancifolia, Hirtella burchellii, Hirtella mucronata, Hirtella longipedicellata, Hirtella glandistipula, Hirtella martiana, Hirtella pimichina, Hirtella subscandens, Hirtella hispidula, Hirtella silicea, Hirtella excelsa, Hirtella adenophora, Hirtella caduca, Hirtella fasciculata, Hirtella couepiflora, Hirtella tubiflora, Hirtella floribunda, Hirtella angustifolia, Hirtella rugosa, Hirtella scaberula, Hirtella hebeclada, Hirtella enneandra, Hirtella pauciflora, Hirtella glaziovii, Acioa guianensis, Acioa somnolens, Acioa schultesii, Acioa edulis | ? | JSTOR (read online) | https://www.jstor.org/stable/i399895 | 2 arquivos | inglês | Since the Flora Neotropica account of the Chrysobalanaceae was published in 1972, much new material has been collected. This supplement to the earlier monograph has studied 6170 new collections and includes the descriptions of 67 new taxa that have been described since the monograph, 64 of which are published as new species in this work. Full descriptions are given of all new species and they are numbered next to their closest relatives in the original monograph. New generic keys are provided to incorporate all the new species and other minor changes in taxonomy that were made in the light of the better material of many species. /// Depois a publicação da familia Chrysobalanaceae (1972) em Flora Neotropica muito material botânica foi coletada. Foram estudadas 6170 coleções novas e descritas 67 taxa novas, incluido 64 apresentadas nesta obra. Descrições de tudos espécies descritas desde 1972 e chaves novas para cada gênero são fornicidas. | |||||||||||||||||||||||||||||
69 | Chrysobalanaceae | Taxonomic novelties in Neotropical Chrysobalanaceae: towards a monophyletic Couepia | Cynthia Sothers, Ghillean T. Prance, Sven Buerki, Rogier de Kok, Mark W. Chase | artigo | Phytotaxa | 172 | 2 | 176-200 | 2014 | Acioa, Hirtella, Licania | não pela revista | Research Gate, Semantic Scholar | https://www.semanticscholar.org/paper/Taxonomic-novelties-in-Neotropical-towards-a-Sothers-Prance/bb0d27f0ea0a70b339e24c2baed81b0240671114 | https://www.researchgate.net/publication/263181035_Taxonomic_novelties_in_Neotropical_Chrysobalanaceae_Towards_a_monophyletic_Couepia | inglês | Recent molecular phylogenetic studies in Chrysobalanaceae as well as new analyses presented in this study cast doubt on the monophyly of the three largest genera in the family, Couepia, Hirtella and Licania. Couepia, a Neotropical genus, had species appearing in four separate clades, the majority of species sequenced, however, form a highly supported clade, re-ferred to here as core Couepia (including the type species). These results lend support to a revised taxonomy of the genus, and to resolve Couepia as monophyletic the following taxonomic changes are here proposed: Couepia recurva should be transferred to Hirtella, C. platycalyx transferred to Licania, C.longipendula and C. dolichopoda transferred to Acioa, and a new genus, Gaulettia, is proposed to accommodate species of the Gaulettia clade and allies. | |||||||||||||||||||||||||||||
70 | Chrysobalanaceae | Rosaceae | Anthonia Kleinhoonte | capítulo livro | Kon. Ver. Koloniaal Instituut te Amsterdam | Amsterdam | Flora of Suriname (Netherlands Guyana) | 2 | 1 | 426-456 | 1939 | morfologia, chave de identificação de gênero, chave de identificação de espécies, Prunus myrtifolia, Chrysobalanus icaco var. icaco, Chrysobalanus icaco var. pellocarpa, Licania macrophylla, Licania hostmanni, Licania divaricata, Licania heteromorpha, Licania leptostachya var. leptostachya, Licania leptostachya var. axilliflora, Licania cymosa, Licania grisea, Licania incana, Licania stricta, Licania gracilis, Licania densiflora, Licania poeppigii, Licania affinis, Licania robusta, Licania micrantha, Licania ovalifolia, Licania stahelii, Licania apetala, Hirtella cotticaensis, Hirtella strigulosa, Hirtella manigera, Hirtella racemosa, Hirtella obidensis, Hirtella lanceolata, Hirtella triandra, Hirtella caudata, Hirtella paniculata, Couepia glandulosa, Couepia cognata, Couepia versicolor, Couepia caryophylloides, Parinari campestris, Parinari excelsa, | JPG | não | não, apenas impresso | 32 arquivos de imagem | inglês | ||||||||||||||||||||||||||||
71 | Chrysobalanaceae | Flora da Bahia: Hirtella (Chrysobalanaceae) | Renata Aspirino, André Márcio Amorim | artigo | Sitientibus série Ciências Biológicas | 16 | 1-20 | 2016 | morfologia, chave de identificação de gêneros, chave de identificação de espécies, Hirtella angustifolia, Hirtella bahiensis, Hirtella bicornis, Hirtella ciliata, Hirtella corymbosa, Hirtella glandulosa, Hirtella gracilipes, Hirtella insignis, Hirtella martiana, Hirtella prancei, Hirtella racemosa, Hirtella santosii, Hirtella sprucei, Hirtella triandra | sim | periodicos.uefs.br | http://periodicos.uefs.br/index.php/sitientibusBiologia/article/view/1099 | português | The taxonomic treatment of Hirtella (Chrysobalanaceae) from Bahia State, Brazil, is presented. We recognize 14 species; H. bicornis is recorded for the first time in the state and H. prancei was originally described from this study. The treatment includes an identification key to species, descriptions and comments on taxa, as well as illustrations and geographic distribution maps of species in Bahia. An identification key to the genera of Chrysobalanaceae in the state is also provided. | |||||||||||||||||||||||||||||||
72 | Chrysobalanaceae | Comparative leaf morphological analysis of 20 species of Chrysobalanaceae | Marcos Melo Corrêa, Veridiana Vizoni Scudeller, Maria Gracimar Pacheco de Araújo | artigo | Acta Amazônica | 45 | 1 | 13-20 | 2015 | Reserva Floresta Adolpho Ducke, morfologia foliar, chave de identificação de espécies, Couepia canomensis, Couepia guianensis subsp. guianensis, Couepia longipendula, Couepia robusta, Couepia ulei, Licania adolphoduckei, Licania apetala var. aperta, Licania bracteata, Licania canescens, Licania heteromorpha var. heteromorpha, Licania impressa, Licania laevigata, Licania micrantha, Licania niloi, Licania oblongifolia, Licania octandra subsp. pallida, Licania prismatocarpa, Licania sandwithii, Licania unguiculata, Parinari excelsa | sim | acta.inpa.gov.br | https://acta.inpa.gov.br/fasciculos/45-1/PDF/AA-2014-0098.pdf | inglês | Morphological studies focusing on vegetative traits are useful in identifying species when fertile material is not available. The aim of this study was to assess the application of comparative leaf morphology to identify species of the Chrysobalanaceae family. The morphological observations were made with a stereomicroscope. We used the diaphanization technique for viewing venation details. It is shown the descriptions of the leaf morphology, illustrations and an identification key for 20 species from genera Couepia, Licania and Parinari (Chrysobalanaceae) occurring in the Adolpho Ducke Forest Reserve, Manaus, AM, Brazil. The key was constructed using the DELTA (DEscription Language for TAxonomy) software. Leaf traits such as the presence of intersecondary venation and the type of insertion of secondary veins were recorded for each species. These morphological leaf traits are reliable for identifying species of Chrysobalanaceae. | ||||||||||||||||||||||||||||||
73 | Malpighiaceae | Malpighiales | Klaus Kubitzki (ed.), Maria do Carmo E. do Amaral, Harvey E. Ballard Jr., Clemens Bayer, Volker Bittrich, William C. Dickinson, Stefan Dressler, Geofrey A. Levin, Juliana de Paula-Souza, Ghillean T. Prance, Miriam Repplinger, Andrea Schwarzbach, Gregory Wahlert, Grady L. Webster | livro | Springer | Heidelberg, New York, Dordrecht, London | The Families and Genera of Vascular Plants - K. Kubitzki (ed.) | 11 | 332 | 2014 | chave de identificação de famílias, Achariaceae, Balanopaceae, Bonnetiaceae, Calophyllaceae, Caryocaraceae, Centrolepidaceae, Centroplacaceae, Chrysobalanaceae, Clusiaceae, Ctenolophonaceae, Dichapetalaceae, Elatinaceae, Erythroxylaceae, Euphorbiaceae, Euphroniaceae, Goupiaceae, Humiriaceae, Hypericaceae, Irvingiaceae, Ixonanthaceae, Linaceae, Lophopyxidaceae, Malesherbiaceae, Malpighiaceae, Medusagynaceae, Ochnaceae, Pandanaceae, Passifloraceae, Podostemaceae, Putranjivaceae, Quiinaceae, Rafflesiaceae, Rhizophoraceae, Salicaceae, Trigoniaceae, Turneraceae, Violaceae | não | não | ||||||||||||||||||||||||||||||||
74 | Chrysobalanaceae | Flora da Reserva Ducke, Amazonas, Brasil: Chrysobalanaceae | Ghillean T. Prance | artigo | Rodriguesia | 58 | 3 | 493-531 | 2007 | morfologia, chave de identificação de gênero, chave de identificação de espécies, Chrysobalanus venezuelanus, Couepia bracteosa, Couepia canomensis, Couepia elata, Couepia excelsa, Couepia guianensis subsp. guianensis, Couepia guianensis subsp. glandulosa, Couepia guianensis subsp. divaricata, Couepia habrantha, Couepia longipendula, Couepia magnoliifolia, Couepia obovata, Couepia parillo, Couepia racemosa, Couepia robusta, Couepia ulei, Hirtella bicornis, Hirtella bicornis var. pubescens, Hirtella duckei, Hirtella fasciculata, Hirtella hispidula, Hirtella myrmecophila, Hirtela physophora, Hirtella piresii, Hirtella racemosa var. racemosa, Hirtella racemosa var. hexandra, Hirtella rodriguesii, Licania adolphoduckei, Licania apetala var. aperta, Licania bracteata, Licania canescens, Licania caudata, Licania coriacea, Licania egleri, Licania gracilipes, Licania heteromorpha var. heteromorpha, Licania heteromorpha var. prismatocarpa, Licania heteromorpha var. reticulata, Licania heteromorpha var. laevigata, Licania heteromorpha var. sothersiae, Licania hirsuta, Licania hypoleuca, Licania impressa, Licania laevigata, Licania lata, Licania latifolia, Licania laxiflora, Licania longistyla, Licania macrophylla, Licania micrantha, Licania niloi, Licania oblongifolia, Licania octandra subsp. octandra, Licania octandra subsp. pallida, Licania pallida, Licania prismatocarpa, Licania reticulata, Licania rodriguesii, Licania sandwithii, Licania sothersiae, Licania sprucei, Licania unguiculata, Parinari excelsa, Parinari montana, Parinari parvifolia | sim | Scielo | https://www.scielo.br/scielo.php?pid=S2175-78602007000300493&script=sci_arttext | inglês | não possui resumo | ||||||||||||||||||||||||||||||
75 | Chrysobalanaceae | Chrysobalanaceae I: Chrysobalanus to Parinari | Ghillean T. Prance, Cynthia A. Sothers | Monografia? | Species Plantarum: Flora of the World | 9 | 1-319 | 2003 | morfologia, distribuição geográfica, chave de identificação de gênero, chave de identificação de espécies, Chrysobalanus icaco subsp. icaco, Chrysobalanus icaco subsp. atacorensis, Chrysobalanus cuspidatus, Chrysobalanus venezuelanus, Grangeria borbonica, Grangeria porosa, Licania michauxii, Licania retifolia, Licania riverae, Licania boliviensis, Licania maritima, Licania veneralensis, Licania corniculata, Licania durifolia, Licania filomenoi, Licania celiae, Licania vasquezii, Licania grandibracteata, Licania macrocarpa, Licania gentryi, Licania cabrerae, Licania fasciculata, Licania montana, Licania hedbergii, Licania longicuspidata, Licania belloi, Licania salzmannii, Licania klugii, Licania guianensis, Licania longipedicellata, Licania espinae, Licania tomentosa, Licania pyrifolia, Licania leucosepala, Licania dodsonii, Licania megalophylla, Licania angustata, Licania anneae, Licania platypus, Licania gonzalezii, Licania cariae, Licania egleri, Licania imbaimadaiensis, Licania minutiflora, Licania chiriquiensis, Licania kallunkiae, Licania guatemalensis, Licania maranhensis, Licania fritschii, Licania jaramilloi, Licania brittoniana, Licania cecidiophora, Licania unguiculata, Licania longipetala, Licania tachirensis, Licania wurdackii, Licania turbinata, Licania lata, Licania apetala var. apetala, Licania apetala var. aperta, Licania granvillei, Licania bullata, Licania undulata, Licania parvifolia, Licania maguirei, Licania gardneri, Licania cuspidata, Licania jefensis, Licania morii, Licania sparsipilis, Licania cuatrecasasii, Licania mexicana, Licania stevensii, Licania diegogomezii, Licania emarginata, Licania joseramosii, Licania calvescens, Licania persaudii, Licania sprucei, Licania sclerophylla, Licania albiflora, Licania longistyla, Licania cardiophylla, Licania fuchsii, Licania humilis, Licania foveolata, Licania octandra subsp. octandra, Licania octandra subsp. grandifolia, Licania octandra subsp. pallida, Licania rigida, Licania arborea, Licania velata, Licania amapaensis, Licania subarachnophylla, Licania tambopatensis, Licania salicifolia, Licania araneosa, Licania silvatica, Licania chocoensis, Licania licaniiflora, Licania splendens, Licania palawanensis, Licania fusicarpa, Licania hirsuta, Licania costaricensis, Licania krukovii, Licania lasseri, Licania latifolia, Licania hispida, Licania minuscula, Licania operculipetala, Licania reticulata, Licania adolphoduckei, Licania pakaraimensis, Licania arachnoidea, Licania oblongifolia, Licania macrophylla, Licania caudata, Licania miltonii, Licania latistipula, Licania divaricata, Licania conferruminata, Licania glabriflora, Licania intrapetiolaris, Licania heteromorpha var. subcordata, Licania heteromorpha var. glabra, Licania heteromorpha var. perplexans, Licania heteromorpha var. heteromorpha, Licania heteromorpha var. revoluta, Licania laevigata, Licania occultans, Licania sothersiae, Licania prismatocarpa, Licania glazioviana, Licania littoralis var. lottoralis, Licania littoralis var. cuneata, Licania fanshawei, Licania irwinii, Licania marleneae, Licania cyathodes, Licania polita, Licania silvae, Licania densiflora, Licania cuprea, Licania arianeae, Licania impressa, Licania dealbata, Licania santosii, Licania pallida, Licania gracilipes, Licania parvifructa, Licania cymosa, Licania ternatensis, Licania membranacea, Licania piresii, Licania furfuracea, Licania hypoleuca var. hypoleuca, Licania hypoleuca var. foveolata, Licania boyanii, Licania buxifolia, Licania orbicularis, Licania niloi, Licania coriacea, Licania cuyabenensis, Licania urceolaris, Licania affinis, Licania teixeirae, Licania glauca, Licania davillifolia, Licania elliptica, Licania canescens, Licania couepiifolia, Licania naviculistipula, Licania trigonioides, Licania cordata, Licania foldatsii, Licania hebantha, Licania steyermarkii, Licania subrotundata, Licania crassivenia, Licania majuscula, Licania jimenezii, Licania alba, Licania hitchcockii, Licania sandwithii, Licania laxiflora, Licania rufescens, Licania kunthiana, Licania bellingtonii, Licania compacta, Licania ovalifolia, Licania caldasiana, Licania savannarum, Licania stewardii, Licania microphylla, Licania triandra, Licania tocantina, Licania discolor, Licania apiculata, Licania micrantha subsp. micrantha, Licania micrantha subsp. atabapoensis, Licania roraimensis, Licania pruinosa, Licania nitida, Licania aracaensis, Licania riedelii, Licania bracteata, Licania parviflora, Licania robusta, Licania lamentanda, Licania lanceolata, Licania pittieri, Licania spicata, Licania stricta, Licania leptostachya, Licania incana, Licania nelsonii, Licania paraensis, Licania vaupesiana, Licania bahiensis, Licania maxima, Licania mollis, Licania velutina, Licania blackii, Licania rodriguesii, Licania cidii, Licania indurata, Licania hoehnei, Licania harlingii, Licania ferreirae, Licania cruegeriana, Licania belemii, Licania tepuiensis, Licania obtusifolia, Afrolicania elaeosperma, Parastemon urophyllus, Parastemon versteeghii, Parastemon grandifructus, Bafodeya benna, Exellodendron coriaceum, Exellodendron cordatum, Exellodendron barbatum, Exellodendron gardneri, Exellodendron gracile, Hunga gerontogea, Hunga lifouana, Hunga longifolia, Hunga mackeeana, Hunga minutiflora, Hunga novoguineensis, Hunga papuana, Hunga rhamnoides, Hunga myrsinoides, Hunga guillauminii, Hunga cordata, Neocarya macrophylla, Parinari argenteosericea, Parinari canarioides, Parinari elmeri, Parinari parva, Parinari rodolphii, Parinari hypochrysea, Parinari alvimii, Parinari campestris, Parinari obtusifolia, Parinari capensis subsp. capensis, Parinari capensis subsp. incohata, Parinari littoralis, Parinari maguirei, Parinari leontopitheci, Parinari montana, Parinari parvifolia, Parinari cardiophylla, Parinari romeroi, Parinari congensis, Parinari congolana, Parinari nonda, Parinari papuana subsp. papuana, Parinari papuana subsp. salomonensis, Parinari papuana subsp. whitei, Parinari oblongifolia, Parinari parilis, Parinari chocoensis, Parinari gigantea, Parinari brasiliensis, Parinari metallica, Parinari curatellifolia, Parinari prancei, Parinari sumatrana, Parinari anamensis, Parinari rigida, Parinari occidentalis, Parinari klugii, Parinari insularum, Parinari sprucei, Parinari pachyphylla, Parinari excelsa, Parinari costata subsp. costata, Parinari costata subsp. rubiginosa, Parinari costata subsp. polyneura, | sim | speciesplantarum.net, Research Gate | https://www.researchgate.net/publication/277949824_Species_Plantarum_Flora_of_the_World_Part_9_Chrysobalanaceae_1_Chrysobalanus_to_Parinari_and_Species_Plantarum_Flora_of_the_World_Part_10_Chrysobalanaceae_2_Acioa_to_Magnistipula | dois arquivos | inglês | não possui resumo | ||||||||||||||||||||||||||||||
76 | Chrysobalanaceae | Chrysobalanaceae II: Acioa to Magnistipula | Ghillean T. Prance, Cynthia A. Sothers | Monografia? | Species Plantarum: Flora of the World | 10 | 1-268 | 2003 | morfologia, distribuição geográfica, chave de identificação de gênero, chave de identificação de espécies, Acioa edulis, Acioa guianensis, Acioa schultesii, Acioa somnolens, Couepia guianensis subsp. guianensis, Couepia guianensis subsp. glandulosa, Couepia guianensis subsp. divaricata, Couepia paraensis subsp. paraensis, Couepia paraensis subsp. glaucescens, Couepia paraensis subsp. cerradoana, Couepia maguirei, Couepia sandwithii, Couepia bernardii, Couepia monteclarensis, Couepia parillo, Couepia steyermarkii, Couepia canescens, Couepia canomensis, Couepia foveolata, Couepia magnoliifolia, Couepia exflexa, Couepia habrantha, Couepia scottmorii, Couepia carautae, Couepia spicata, Couepia bracteosa, Couepia subcordata, Couepia belemii, Couepia caryophylloides subsp. caryophylloides, Couepia caryophylloides subsp. glabra, Couepia morii, Couepia excelsa, Couepia uiti, Couepia cataractae, Couepia macrophylla, Couepia krukovii, Couepia latifolia, Couepia ovalifolia, Couepia leitaofilhoi, Couepia schottii, Couepia grandiflora, Couepia elata, Couepia racemosa, Couepia amaraliae, Couepia martinii, Couepia bondarii, Couepia insignis, Couepia cidiana, Couepia recurva, Couepia obovata, Couepia williamsii, Couepia glabra, Couepia marleneae, Couepia joaquinae, Couepia chrysocalyx, Couepia eriantha, Couepia trapezioana, Couepia stipularis, Couepia reflexa, Couepia longipendula, Couepia dolichopoda, Couepia cognata var. cognata, Couepia cognata var. membranacea, Couepia cognata var. major, Couepia multiflora, Couepia ulei, Couepia comosa, Couepia venosa, Couepia polyandra, Couepia nutans, Couepia hondurasensis, Couepia platycalyx, Couepia rufa, Couepia robusta, Couepia impressa subsp. impressa, Couepia impressa subsp. cabraliae, Couepia meridionalis, Couepia coarctata, Couepia longipetiolata, Couepia pernambucensis, Couepia froesii, Couepia rankiniae, Couepia parvifolia, Maranthes aubrevillei, Maranthes chrysophylla subsp. chrysophylla, Maranthes chrysophylla subsp.coriacea, Maranthes corymbosa, Maranthes floribunda, Maranthes gabunensis, Maranthes glabra, Maranthes goetzeniana, Maranthes kerstingii, Maranthes panamensis, Maranthes polyandra, Maranthes robusta, Maranthes sanagensis, Atuna racemosa subsp. racemosa, Atuna racemosa subsp. excelsa, Atuna elliptica, Atuna latifrons, Atuna nannodes, Atuna penangiana, Atuna cordata, Atuna indica, Atuna travancorica, Dactyladenia smeathmannii, Dactyladenia ndjoleensis, Dactyladenia scabrifolia, Dactyladenia letestui, Dactyladenia whytei, Dactyladenia gilletii, Dactyladenia librevillensis, Dactyladenia bellayana, Dactyladenia hirsuta, Dactyladenia campestris, Dactyladenia floretii, Dactyladenia jongkindii, Dactyladenia icondere, Dactyladenia floribunda, Dactyladenia barteri, Dactyladenia sapinii, Dactyladenia pallescens, Dactyladenia buchneri, Dactyladenia staudtii, Dactyladenia dewevrei, Dactyladenia laevis, Dactyladenia lehmbachii, Dactyladenia mannii, Dactyladenia pierrei, Dactyladenia eketensis, Dactyladenia dichotoma, Dactyladenia dinklagei, Dactyladenia cinerea, Dactyladenia johnstonei, Dactyladenia chevalieri, Hirtella myrmecophila, Hirtella physophora, Hirtella vesiculosa, Hirtella dorvalii, Hirtella guainiae, Hirtella duckei, Hirtella revillae, Hirtella macrosepala, Hirtella ulei, Hirtella glabrata, Hirtella confertiflora, Hirtella carbonaria, Hirtella araguariensis, Hirtella barnebyi, Hirtella margae, Hirtella liesneri, Hirtella cordifolia, Hirtella insignis, Hirtella tocantina, Hirtella piresii, Hirtella davisii, Hirtella subglanduligera, Hirtella ciliata, Hirtella hoehnei, Hirtella glandulosa, Hirtella bullata, Hirtella americana, Hirtella santosii, Hirtella aequatoriensis, Hirtella guatemalensis, Hirtella trichotoma, Hirtella papillata, Hirtella eriandra, Hirtella paniculata, Hirtella castilloana, Hirtella deflexa, Hirtella tentaculata, Hirtella macrophylla, Hirtella adderleyi, Hirtella punctillata, Hirtella corymbosa, Hirtella pendula, Hirtella barrosoi, Hirtella leonotis, Hirtella beckii, Hirtella mutisii, Hirtella triandra subsp. triandra, Hirtella triandra subsp. punctulata, Hirtella triandra subsp. media, Hirtella bahiensis, Hirtella latifolia, Hirtella suffulta, Hirtella elongata, Hirtella magnifolia, Hirtella rodriguesii, Hirtella obidensis, Hirtella cowanii, Hirtella orbicularis, Hirtella guyanensis, Hirtella lightioides, Hirtella aramangensis, Hirtella rasa, Hirtella scabra, Hirtella bicornis var. bicornis, Hirtella bicornis var. pubescens, Hirtella tenuifolia, Hirtella radamii, Hirtella pilosissima, Hirtella maguirei, Hirtella gracilipes, Hirtella brachystachya, Hirtella arenosa, Hirtella conduplicata, Hirtella racemosa var. racemosa, Hirtella racemosa var. hispida, Hirtella racemosa var. hexandra, Hirtella juruensis, Hirtella kuhlmannii, Hirtella standleyi, Hirtella longifolia, Hirtella lemsii, Hirtella schultesii, Hirtella paraensis, Hirtella sprucei, Hirtella lancifolia, Hirtella burchellii, Hirtella mucronata, Hirtella longipedicellata, Hirtella glandistipula, Hirtella martiana, Hirtella zanzibarica subsp. zanzibarica, Hirtella zanzibarica subsp.megacarpa, Hirtella thouarsiana subsp. thouarsiana, Hirtella thouarsiana subsp. parvifolia, Hirtella thouarsiana subsp. abrupte-acuminata, Hirtella thouarsiana subsp. obtusifolia, Hirtella parviunguis, Hirtella pimichina, Hirtella subscandens, Hirtella hispidula, Hirtella silicea, Hirtella excelsa, Hirtella adenophora, Hirtella caduca, Hirtella fasciculata, Hirtella couepiiflora, Hirtella tubiflora, Hirtella floribunda, Hirtella angustifolia, Hirtella rugosa, Hirtella scaberula, Hirtella hebeclada, Hirtella enneandra, Hirtella pauciflora, Hirtella glaziovii, Kostermanthus heteropetalus, Kostermanthus robustus, Kostermanthus malayanus, Magnistipula zenkeri, Magnistipula devriesii, Magnistipula cuneatifolia, Magnistipula conrauana, Magnistipula bimarsupiata, Magnistipula glaberrima, Magnistipula cupheiflora subsp. cupheiflora, Magnistipula cupheiflora subsp. leonensis, Magnistipula sapinii, Magnistipula butayei subsp. butayei, Magnistipula butayei subsp. youngii, Magnistipula butayei subsp. montana, Magnistipula butayei subsp. glabriuscula, Magnistipula butayei subsp. bangweolensis, Magnistipula butayei subsp. ituriensis, Magnistipula butayei subsp. sargosii, Magnistipula butayei subsp. greenwayi, Magnistipula butayei subsp. tisseranti, Magnistipula tessmannii, Magnistipula tamenaka, Magnistipula cerebriformis | sim | speciesplantarum.net, Research Gate | https://www.researchgate.net/publication/277949824_Species_Plantarum_Flora_of_the_World_Part_9_Chrysobalanaceae_1_Chrysobalanus_to_Parinari_and_Species_Plantarum_Flora_of_the_World_Part_10_Chrysobalanaceae_2_Acioa_to_Magnistipula | dois arquivos | inglês | não possui resumo | ||||||||||||||||||||||||||||||
77 | x | Chrysobalanaceae | The genera of Chrysobalanaceae: a study in practical and theoretical taxonomy and its relevance to evolutionary biology | Ghillean T. Prance, F. White | artigo | Philosophical Transactions of the Royal Society of London Biological Sciences | 320 | 1-184 | 1988 | filogenia, nomenclatura, biogeografia, morfologia, revisão taxonômica, anatomia, citologia, química, palinologia, embriologia, ecologia, polinização, dispersão, usos, chave de identificação de gêneros, chave de identificação de espécies, Chrysobalanus cuspidatus, Chrysobalanus icaco, Grangeria borbonica, Grangeria porosa, Licania elaeosperma, Licania palawanensis, Licania splendens, Parastemon urophyllus, Parastemon versteeghii, Bafodeya benna, Exellodendron coriaceum, Hunga gerontogea, Hunga lifouana, Hunga longifolia, Hunga mackeeana, Hunga minutiflora, Hunga novoguineensis, Hunga papuana, Hunga rhamnoides, Hunga myrsinoides, Hunga guillauminii, Hunga cordata, Neocarya macrophylla, Parinari capensis, Parinari congensis, Parinari congolana, Parinari curatellifolia, Parinari excelsa, Parinari hypochrysea, Acioa edulis, Acioa guianensis, Acioa schultesii, Acioa somnolens, Couepia, Maranthes aubrevillei, Maranthes chrysophylla, Maranthes corymbosa, Maranthes floribunda, Maranthes gabunensis, Maranthes glabra, Maranthes goetzeniana, Maranthes kerstingii, Maranthes panamensis, Maranthes polyandra, Maranthes robusta, Maranthes sanagensis, Atuna, Atuna latifrons, Dactyladenia barteri, Dactyladenia bellayana, Dactyladenia campestris, Dactyladenia chevalieri, Dactyladenia cinerea, Dactyladenia dewevrei, Dactyladenia dichotoma, Dactyladenia dinklagei, Dactyladenia eketensis, Dactyladenia floribunda, Dactyladenia gilletti, Dactyladenia hirsuta, Dactyladenia icondere, Dactyladenia johnstonei, Dactyladenia laevis, Dactyladenia lehmbachii, Dactyladenia letestui, Dactyladenia librevillensis, Dactyladenia lujae, Dactyladenia mannii, Dactyladenia pallescens, Dactyladenia pierrei, Dactyladenia sapinii, Dactyladenia scabrifolia, Dactyladenia smeathmannii, Dactyladenia staudtii, Dactyladenia whytei, Hirtella, Hirtella zanzibarica, Kostermanthus heteropetalus, Kostermanthus malayanus, Magnistipula zenkeri, Magnistipula cuneatifolia, Magnistipula conrauana, Magnistipula bimarsupiata, Magnistipula glaberrima, Magnistipula cupheiflora, Magnistipula sapinii, Magnistipula butayei, Magnistipula tessmannii, Magnistipula tamenaka, Magnistipula cerebriformis | sim | The Royal Society Publishing | https://royalsocietypublishing.org/doi/pdf/10.1098/rstb.1988.0071 | inglês | This account is a generic monograph of a medium-sized (494 species) pantropical plant family. Its rank, circumscription and relationships to other families are examined. An attempt is made to provide an objective and repeatable taxonomy and to formulate evolutionary hypotheses consistent with the facts presented. The monograph is also used to test the general application of certain relatively new and still controversial theoretical approaches to descriptive and evolutionary biology, notably numerical taxonomy, cladistics and vicariance biogeography. The practical value of some potentially useful sources of taxonomic information, especially electron microscopy and phytochemical analysis, is also examined. This is possibly the first time that non-traditional approaches to taxonomy have been so comprehensively evaluated within the framework of a worldwide monograph. Based mainly on original investigations, the morphology, anatomy, reproductive biology, distribution and ecology of each of the 17 genera are described and illustrated. Published works by others on chemistry, embryology and chromosome cytology are summarized. The delimitation and arrangement of the genera included here depart somewhat from those of earlier systems. Most of the new taxa have been formally published elsewhere but the following are proposed here for the first time: tribus Chrysobalaneae, tribus Parinarieae Prance & F. White, tribus Couepieae Prance & F. White, tribus Hirtelleae Prance & F. White, Licania subgenus Angelesia (Korth.) Prance & F. White and Atuna latifrons (Kosterm.) Prance & F. White. All Chrysobalanaceae are woody. They vary greatly in size but are uniform in their vegetative architecture. By contrast, the structure of the inflorescence, flower and fruit is much more diverse; detailed examination has revealed a multitude of previously overlooked characters of classificatory importance. Individually these characters are small, but they are well correlated and belong to character complexes of high diagnostic value which are also functional syndromes related to pollination, dispersal and germination. Each genus is unique in the precise way in which its stigmatic and polliniferous surfaces are presented to pollen vectors and in the structure of its fruit, although within a genus there may be more than one principal pollinator or disperser. Except for a few anomalous species, each genus is distinct in its general appearance. Membership of a genus can be detected by intuitive perception, based on rapid inspection ‘ by eye ’ of herbarium specimens with flowers. This is possible because of the underlying structural uniformity of the inflorescence and the similar proportions of the flower in all congeneric species. For two genera, Couepia and Hirtella, their objectivity and ease of identification by rapid visual means was demonstrated by simple experiments involving colleagues with little experience of taxonomy and no previous knowledge of the group. The characteristics these ‘subjects’ had subconsciously used were then explicitly formulated in taxonomic terms and their individual diagnostic values calculated. Some methods of numerical taxonomy were found to be useful, although less so than their advocates frequently claim. This is because of problems associated with the detection, selection and weighting of characters. Attempts to apply cladistic analysis to the Chrysobalanaceae were largely unsuccessful because of parallelism and the difficulty of identifying sister groups. The occurrence and extent of parallelism was shown by using a ‘principle of discordant characters’, which is defined and discussed. The ideas underlying it are widely known but the principle itself does not seem to have been previously used as an analytical tool in taxonomic research. In the Chrysobalanaceae, parallelism is so rife that convincing cladograms cannot be constructed; for this reason, among others, the methods of vicariance biogeography are inappropriate. Aspects of evolution other than branching patterns, however, are more relevant to general biology, and monographic studies should help to identify them. Examples from Chrysobalanaceae include: ( a) the response in growth-form to geomorphological and climatic change; (b) the biological consequences of dispersal across faunistic barriers; and (c) the evolution of ocean-dispersed, obligate strand plants. It is concluded that monographers cannot afford to ignore fine structure and chemistry, though there is no evidence that they are more fundamental in practical taxonomy than other sources of information. The Chrysobalanaceae and other families show that parallelism is as likely to occur in fine structure and chemistry (at least of secondary compounds) as in gross morphology, and it is much more expensive to detect. At present, for tropical plants, some currently fashionable approaches to taxonomy are of limited relevance. It is much more important to develop objective methods of visual analysis for dealing with the copious material that monographic work entails. It is equally necessary to understand the central role of ecology in biology. Without ecological understanding taxonomy is lifeless and dull, and taxonomically important information and interesting evolutionary situations go undetected. | ||||||||||||||||||||||||||||||
78 | Euphorbiaceae | O gênero Manihot Mill. (Euphorbiaceae) na Amazônia brasileira | Priscila Orlandini | Dissertação | Universidade Estadual de Campinas | Campinas | 105p | 2016 | Euphorbiaceae, Malpighiales, Manihot, taxonomia, mandioca | sim | Repositório Unicamp | http://repositorio.unicamp.br/jspui/handle/REPOSIP/321161 | português | Resumo: A família Euphorbiaceae é uma das mais complexas da ordem Malpighiales Mart., sendo amplamente distribuída, porém mais diversa em regiões tropicais, apresentando cerca de 6300 espécies distribuídas em 218 gêneros, dentre os quais, Manihot Mill. é o sétimo mais numeroso, com cerca de 150 espécies. O gênero possui grande importância econômica devido à sua espécie mais cultivada: M. esculenta Crantz, que é a base alimentar de muitos povos. Para a confecção deste trabalho foram realizadas viagens a campo e visitas aos herbários que continham coleções significativas de materiais amazônicos. A área de estudo inclui a região compreendida pelo Bioma Amazônia, restrito aos limites do território brasileiro. Foram reconhecidas 13 espécies de Manihot para esta região: M. allemii M.J. Silva, M. anomala Pohl, M. baccata Allem, M. brachyloba Müll. Arg., M. caerulescens Pohl, M. esculenta Crantz, M. leptophylla Pax, M. quinquepartita Müll. Arg., M. tripartita (Spreng.) Müll. Arg., M. tristis Müll. Arg., M. xavantinensis Rogers & Appan, além de duas prováveis espécies novas. Foi realizada uma descrição morfológica para o gênero de acordo com as plantas analisadas e realizada uma breve explanação de características morfológicas gerais como o caule, tronco, metabólitos secundários, folhas, flores, frutos e sementes, além de aspectos relacionados à importância econômica. Para a separação dos táxons foram utilizadas características vegetativas e reprodutivas, com destaque para a ampla variabilidade morfológica apresentada pelas folhas do grupo, que podem ser inteiras ou lobadas ou ambas no mesmo indivíduo / Abstract: The Euphorbiaceae family is one of the most complex of Malpighiales Mart. order, widely distributed, however, is more diverse in tropical regions, presenting 6300 species distributed in 218 genera, among them, Manihot Mill. is the seventh more numerous, with about of 150 species. The genus has such a great economic importance due to its most cultivated species: M. esculenta Crantz, which is the food base for many people. For this study, field trips were necessary and also visits to herbarium which contained significant scientific collections of Amazonian region material. The research was held in the comprised region by the Amazon Biome, restrict to the limit of the Brazilian territory. They were recognized 13 species of Manihot for this region: M. allemii M.J. Silva, M. anomala Pohl, M. baccata Allem, M. brachyloba Müll. Arg., M. caerulescens Pohl, M. esculenta Crantz, M. leptophylla Pax, M. quinquepartita Müll. Arg., M. tripartita (Spreng.) Müll. Arg., M. tristis Müll. Arg., M. xavantinensis Rogers & Appan, and two probable new species. It was realized a morphological description of the genus according to the analysed plants and a brief explanation of the general morphological features as the stem, trunk, secondary metabolites, leaves, flowers, fruits and seeds, as well as aspects related to economic importance. For the separation of the taxa were used vegetative and reproductive features, highlighting the wide morphological variability of the leaves of the group, which may be whole or lobed or both in the same individual | |||||||||||||||||||||||||||||||
79 | Euphorbiaceae | Taxonomia do gênero Sapium Jacq. (Hippomaneae, Euphorbiaceae) no Brasil | Wesley Patrício Freire de Sá Cordeiro | Dissertação | Universidade Federal Rural de Pernambuco | Recife | 152 | 2017 | Euphorbioideae, Nomenclatura, Sapium, Tipificação | sim | Repositório UFRPE | http://www.pgb.ufrpe.br/sites/ww4.pgb.ufrpe.br/files/documentos/wesley_cordeiro_2017_dissertacao.pdf | português | SapiumJacq. é um gênero da tribo Hippomaneae (Euphorbiaceae) composto por espécies neotropicais com ocorrência desde o sul do México ao Uruguai. É bem delimitado e pode ser reconhecido pela presença de glândulas acropeciolares, tirsos espiciformes, grãos de pólen tricolporados com anel equatorial e sementes com arilo vermelho. Entretanto, apresenta problemas na delimitação das espéciese nomenclaturais. Dessa forma, o presente trabalho objetivou realizar um estudo taxonômico das espécies ocorrentes no Brasil. Para isso, foram analisadas populações em campoecerca de 1000 espécimes, provenientes de 56herbários brasileiros e estrangeiros. Os resultados são apresentados na forma de dois capítulos: O primeiro trata do restabelecimento de Sapium sceleratumque estava sob sinonímia de S. argutum, desta forma, o gênero Sapiumpassou de 21 para 22 espécies. Neste capítulo, foram apresentados ainda, um novo sinônimo para S. sceleratum,comentários sobre a distribuição geográfica e caracteres distintivos entre as espécies, bem como uma chave de identificaçãopara os táxonsocorrentes na região Nordeste, além de ilustrações e imagens de tipos. O segundo capítulo consiste no estudo taxonômico deSapiumpara o Brasil. Doze espécies foram reconhecidas, as quais foram diferenciadas com base na persistência/deiscência das estípulas, arquitetura foliar, morfologia das glândulas acropeciolares e no arranjo e disposição das inflorescências. Três espécies são endêmicas: Sapium pallidum(Müll. Arg.) Huber, com ocorrência nos leitos dos rios do Norte, Nordeste e Centro-Oeste; S. sceleratumRidll., exclusiva das Caatingas do Nordeste e para a ilha de Fernando de Noronha; e S. sellowianumKlotzsch ex Baill. referida paraasflorestas estacionais, tabuleiro e Cerrado. As demais ocorrem às margens de corpos d’água (S. haematospermumMüll. Arg.,S. obovatumKlotzsch ex Müll.Arg. e S. laurifolium(A.Rich.) Griseb.), em florestas de terra firme da Amazônia (S. ciliatumHemsl., S. jenmaniiHemsl,S. marmieriHuber eS. paucinerviumHemsl.) ou em bordas e interiores de matas perturbadas (S. glandulosum(L.) Morong). Sãofornecidas ilustrações, chave de identificação e comentários sobre a distribuição das espécies, e dois lectótipos foram propostos. | |||||||||||||||||||||||||||||||
80 | Fabaceae | Silk tree, guanacaste, monkey’s earring. a generic system for the synandrous Mimosaceae of the Americas. Part I. Abarema, Albizia and allies | Rupert C. Barneby, James W. Grimes | Monografia | Memoirs of the New York Botanical Garden | 74 | 1 | 1-292 | 1996 | Mimosoideae, Americas, Ingeae, Fabaceae, Classification, phylogenetic analyses, taxonomic revision, Abarema, Albizia, Acacia, Affonsea, Anneslia, Archidendron, Archidendropsis, Arthrosamanea, Balizia,Hydrochorea, Hesperalbizia, Pseudosamanea, Samanea, Blanchetiodendron, Leuchocloron, Chloroleucon, Sphinga, Havardia, Ebenopsis, Painteria, Macrosamanea, Cedrelinga, Falcataria, Paraserianthes, Enterolobium, Lysiloma | sim | Mertz Digital NYBG | http://mertzdigital.nybg.org/digital/collection/p9016coll16/id/5993/rec/8 | inglês | Presented here are (a) definitions, new or confirmed, of the genera of Mimosaceae tribe Ingeae either native or naturalized in the Americas; (b) phylogenetic analyses and taxonomic revision of Hydrochorea Barneby & Grimes (4spp.), Balizia Baneby & Grimes (3 spp.), Abarema Pittier (45 spp.), Hesperalbizia Barneby & Grimes (1 sp.)Pseudosamanea Harms (2 spp.), Samanea Merrill (3 spp.), Blanchetiodendron Barneby & Grimes (1 sp.), Leuchocloron Barneby & Grimes (4 spp.), Chloroleucon (Bentham) Britton & Rose (10 spp.), Sphinga Barneby & Grimes (3 spp.), Havardia Small (5 spp.), Ebenopsis Britton & Rose (3 spp.), Painteria Britton & Rose (3 spp.), and Macrosamanea Britton & Killip (11 spp.); (c) alpha-taxonomic revision of Albizia Durazzini (23 spp.), Cedrelinga Ducke (1 sp.), Falcataria (Nielsen) Barneby & Grimes (1 sp.), and Paraserianthes Nielsen (1 sp.); and (d) summaries of Enterolobium Martius (11 spp.) and Lysiloma Bentham (8 spp.). Cladistic analyses and revision of the genera Calliandra Bentham, Cojoba Britton & Rose, Pithecellobium Martius (s.str.), and Zygia P.Browne will appear in Part II. | ||||||||||||||||||||||||||||||
81 | Fabaceae | Silk tree, guanacaste, monkey’s earring. a generic system for the synandrous Mimosaceae of the Americas. Part II. Pithecellobium, Cojoba, and Zygia | Rupert C. Barneby, James W. Grimes | Monografia | Memoirs of the New York Botanical Garden | 74 | 2 | 1-161 | 1997 | Pithecellobium, Cojoba, Zygia, phylogenetic analysis | sim | Mertz Digital NYBG | http://mertzdigital.nybg.org/digital/collection/p9016coll16/id/6171/rec/3 | inglês | This paper is Part II of our revision on the Pithecellobium-complex, or those members of tribe Igeae ever referred to Pithecellobium Martius. We present revisions of Pithecellobium Martius, Cojoba Britton & Rose, and Zygia P. Browne, along with phylogenetic analyses of the first two. The number of incompletely known species of Zygia precludes cladistic analysis. | ||||||||||||||||||||||||||||||
82 | Fabaceae | Silk tree, guanacaste, monkey’s earring. a generic system for the synandrous Mimosaceae of the Americas. Part III. Calliandra | Rupert C. Barneby, James W. Grimes | Monografia | Memoirs of the New York Botanical Garden | 74 | 3 | 1998 | Calliandra | sim | Mertz Digital NYBG | http://mertzdigital.nybg.org/digital/collection/p9016coll16/id/6412/rec/12 | inglês | This alphataxonomic revision of genus Calliandra Bentham continues systematic work on tribe Ingeae of the New World recently published (Barneby & Grimes, 1996). No comprehensive account of the genus has appeared since 1875, and its definition and content have become incoherent, an obstacle to floristic work presently in preparation. As redefined, the genus is endemic to the Americas, extending from New Mexico to Chile, the so-called calliandras of Africa and Asia being excluded, as is the recently segregated American genus Zapoteca H. Hernández. The genus comprises 132 species, some composed of several varieties, that are assigned to five sections and 14 series, all newly described. Of 168 specific and varietal taxa recognized, 36 are new. Each taxon is fully described, its nomenclature is analyzed in the context of current rules of nomenclature, and its distribution recorded verbally or in a map. Thirty-four taxa are illustrated, and a list of exsiccatae examined is provided. | |||||||||||||||||||||||||||||||
83 | Fabaceae | Dimorphandra (Caesalpiniaceae) | Marlene Freitas da Silva | Monografia | New York Botanical Garden Press | Flora Neotropica | 44 | 1-127 | 1986 | não | não | existe uma entrada no JSTOR, mas não parece estar disponível | não possui resumo | ||||||||||||||||||||||||||||||||
84 | x | Fabaceae | Revisão taxonômica de Peltogyne Vog. (Leguminosae-Caesalpinioideae) | Marlene Freitas da Silva | artigo | Acta Amazônica | 6 | 1 | 1-61 | 1976 | Leguminosas, revisão taxonômica, botânica, sistemática | sim | Scielo | https://www.scielo.br/scielo.php?script=sci_arttext&pid=S0044-59671976000500005 | português | RESUMO Revisão taxonômica do gênero Peltogyne Vog. (Leguminosae-Caesalpiniodeae), característico da região amozônica, com distribuição geográfica no Continente Americano. Muitas de suas espécies atingem porte elevado e podem ser encontradas em vários tipos de vegetação, produzindo a maioria madeira de valor econômico, conhecida vulgarmente no Brasil pelo nome de "pau-roxo". Uma chave para a determinação das espécies é apresentada e duas novas espécies da região amazônica são descritas. Em decorrência desta revisão, o gênero passa a ter 23 espécies, 3 subespécies e 2 variedades até agora conhecidas. Uma grande coleção de espécimes pertencentes a 20 herbários nacionais e estrangeiros foi examinada. Ilustram o trabalho 11 fotografias, 12 figuras com a distribuição geográfica dos espécies e detalhes da forma das flores e dos frutos, e 3 tabelas com informações sobre as espécies do gênero estudado. SUMMARY Peltogyne is a genus of the subfamily Caesalpinioideae (Leguminosae) in the tribe Amherstiae. This genus occupies an important place among the other representative trees of the Amazon area because of this frequent occurence and exceptional development in tropical América. Its valuable wood, which is violet or purple in colour, gives the genus its local name "purpleheart" (pau roxo). Some species have studied phytochemichally by other workers, and among important substances, one with antimicrobial properties was found in Peltogyne recifensis. At present the genus has 23 known species that occur from México through Central América, Panamá to the Southeast of South América. The Amazon region is the center of Its distribution. The genera Hymenaea and Cynometra have the same center of distribution, the Central Amazonia. Hymenaea and Peltogyne have great morphological similarity, but are diverse in the geographical limits of their distribution. Hymenaea has a striking disjunction in distribution between the African and South América continents; Peltogyne is distributed continuously from the Caribean region through Central América to the Southeastern region of South American continent. These taxa were relicts of the time when the Amazonian evergreen forest was more extensive than it is today. It is probable that Peltogyne, Hymenaea and Cynometra could have migrated to the North of South América into Central América, too. Phytogeographically, the genus Peltogyne occurs in many kinds of habitats. For example P. catingae subsp. catingae is typical of the "catinga" of the Rio Negro (Amazonas), while P. catingae subsp. glabra is found well developed in the high forest near Manaus. This shows the great adaptability of the specie to different ecological habitats. After the original description of the genus Peltogyne by Vogel (1837), the first study of the genus was Bentham's (1870) and the last was Ducke's (1938) in which only the Amazonian species are treated. Actually we found after consulting a large representative collection of herbarium material (Colombia, Venezuela, Panamá, Suriname, México, Brasil, etc.) that it was not possible to base, some taxonomic decisions on specimens from such a restricted area as Amazonia, but that a much wider geographical view must be taken. The genus Peltogyne previously had a total of 29 recognised species. These are now reduced here to 23 species, including 2 new species, 3 subspecies, and 2 varieties giving a total of 28 taxa. | |||||||||||||||||||||||||||||
85 | Fabaceae | Revisão taxonômica do gênero Vataireopsis Ducke (Leg. Fab.) | Haroldo Cavalcanti de Lima | artigo | Rodriguesia | 32 | 54 | 21-40 | 1980 | Dalbergieae, taxonomia, Vataireopsis | sim | Scielo | https://www.scielo.br/scielo.php?script=sci_arttext&pid=S2175-78601980000300021 | português | RESUMO O presente trabalho consiste em uma revisão taxonômica do gênero Vataireopsis Ducke (Leg. Fab.), exclusivo da faixa neotropical, cujas espécies estão distribuídas pela formação denominada Floresta Perenifólia Latifoliada Higrófíla Hileana. O tratamento taxonômico inclui descrições, ilustrações, discussões sobre o grau de afinidade entre as espécies, distribuição geográfica e dados fenológicos. O autor elaborou um quadro com os caracteres diferenciais dos gêneros Vatairea, Vataireopsis (Dalbergieae) e Luetzelburgia (Sophoreae) além de outros sobre os estudos fenológicos. Também acrescentou uma nova espécie e excluiu uma do gênero. Uma chave dicotômica para a identificação das espécies é também apresentada. Os caracteres mais significativos na delimitação das espécies foram a morfologia do cálice, androceu, brácteas, bractéolas e frutos. SUMMARY This work is a taxonomic revision of the species in the genus Vataireopsis Ducke (Leg. Fab.). This genus is found only in the neotropical region and is limited to Perenial Broadleaf Evergreen Hylean Forest. The taxonomic treatment includes descriptions, illustrations, discussions about the degree of affinity, the geographic distribution and fenological data. The most significant characters in delimitation of species are the morphology of calyx, androecium, bracteas, bracteolas and fruits. A dichotomic key for identification of species has also been presented. A new species has been included and another excluded. Also included is a table showing differential characteristic among the genus Vatairea, Vataireopsis (Dalbergieae) and Luetzelburgia (Sophoreae). | ||||||||||||||||||||||||||||||
86 | Fabaceae | Swartzia (Leguminosae, Caesalpinioideae, Swartzieae) | Richard S. Cowan | Monografia | New York Botanical Garden Press | Flora Neotropica | 1 | 1-228 | 1967 | Swartzia, Leguminosae | ? | JSTOR (read online) | https://www.jstor.org/stable/4393651?seq=1 | não possui resumo | |||||||||||||||||||||||||||||||
87 | Fabaceae | Sensitivae censitae: A description of the genus Mimosa Linnaeus (Mimosaceae) in the New World | Rupert C. Barneby | Monografia | Memoirs of the New York Botanical Garden | 54 | 1-835 | 1991 | taxonomia, morfologia, evolução, classificação, Mimosa, Leguminosae, Fabaceae, New World, systematics | sim | Mertz Digital NYBG | http://mertzdigital.nybg.org/digital/collection/p9016coll16/id/5690 | inglês | In this survey of American Mimosa 479 species and 225 subspecies or varieties (a total of 704 taxa) are aligned in five major groups termed sections, these in turn divided into 78 serial or subserial divisions. The primary emphasis is on species native to South America and West Indies, those of continental North America being treated in less exhaustive detail. Significant departures from the classic taxonomy of the genus proposed by G. Bentham in 1875 are: recognition of an ostensibly primitive sect. Mimadenia, characterized by the presence of leaf-nectaries; the division of sect. Habbasia into two sections of equal rank; the reduction of genera Schrankia Willd. And Schranckiastrum Hassler to seria within Mimosa sect. Batocaulon; and the reordering into subgroups of the very large and complex, haplostemonous sect. Mimosa. These innovations are required to accommodate the numerous additions (+- 30% of the presently known total) that have been discovered in the past century, especially in Brazil south of Amazonia. An introductory chapter provides a rationale for the proposed classification and a set of hypothetical evolutionary sequences on which it is based. All taxa are keyed and described. Sixty-seven distribution maps and 27 pages of line-drwuings are provided. Appendices dealing with doubrful names, a selected bibliography, a list of numbered exsiccatae studied, and an index to epithets follow the main text. | |||||||||||||||||||||||||||||||
88 | x | Fabaceae | A taxonomic revision of the South American papilionoid genus Luetzelburgia (Fabaceae) | Domingos Benício Oliveira Silva Cardoso, Luciano Paganucci de Queiroz & Haroldo Cavalcanti de Lima | artigo | Botanical Journal of the Linnean Society | 175 | 328-375 | 2014 | taxonomic revision, leguminosae, biogeography, phylogeny, morphological evolution | não | não | https://onlinelibrary.wiley.com/doi/abs/10.1111/boj.12153 | A taxonomic revision of the monophyletic vataireoid genus Luetzelburgia (Fabaceae, Papilionoideae) is presented, including comments on the biogeography, phylogeny and morphological evolution derived from a combined phylogenetic analysis of morphology and seven DNA regions. The genus is characterized by the unique combination of crimped petals, sericeous on outer surface and biauriculate at the base, oblong to obovate standard petal, lateral and abaxial petals undifferentiated in shape, nearly free filaments and a samara with an indistinct endocarp, usually bearing a small wing on each side of the seed chamber. Luetzelburgia spp. are often confined to disjunct patches of South American seasonally dry tropical forests and woodlands (succulent biome). Our revision involved the examination of about 500 specimens from 56 herbaria. Species circumscription in Luetzelburgia has been a source of confusion because of the difficulty of finding complete herbarium material. All but one species was studied in the field and our extensive field work was critical for arriving at species circumscriptions that relied in large part on floral morphologies. In our revision, four names are lectotypified and one is synonymized, one species is newly described and 13 species are recognized: L. amazonica, L. andina, L. andrade-limae, L. auriculata, L. bahiensis, L. guaissara, L. guianensis, L. harleyi, L. neurocarpa, L. praecox, L. purpurea, L. sotoi and L. trialata. This revision comprises morphological descriptions and illustrations, synonymies, nomenclatural notes, phenology, phylogenetic affinities, distribution maps and preliminary conservation assessments for each species. | |||||||||||||||||||||||||||||||
89 | Fabaceae | A taxonomic revision of the genus Macrolobium (Leguminosae-Caesalpinioideae) | Richard S. Cowan | Monografia | Memoirs of the New York Botanical Garden | 8 | 4 | 257-342 | 1953 | não | não, apenas impresso | ||||||||||||||||||||||||||||||||||
90 | Fabaceae | A monograph of the genus Eperua (Leguminosae: Caesalpinioideae) | Richard S. Cowan | Monografia | Smithsonian Institution Press | Washington | Smithsonian Contributions to Botany | 28 | 1-45 | 1975 | morphology, anatomy, leaf epidermis, palynology, taxonomy | sim | Repositório Smithsonian | https://repository.si.edu/bitstream/handle/10088/6949/scb-0028.pdf?sequence=1&isAllowed=y | inglês | All available data are brought together in a monographic treatment of the legume genus Eperua. Eighteen taxa are considered of which four are described as new: E . duckeana, E . obtusata, E . grandiflora ssp. guyanensis, and E. j e n m a n i i ssp. sandwithii. Also one new combination is made: E. glabriflora (Ducke) Cowan. I n addition to gross morphology, anatomy of leaf epidermis and palynology of most of the species are presented for the first time. Pollen morphology is particularly instructive with respect to the classification derived principally from vegetative and floral morphology. | |||||||||||||||||||||||||||||
91 | Fabaceae | A monograph of the genus Clitoria | Fantz | Monografia | 1977 | systematic treatment, phylogeny, morphology, Fabaceae | sim | Repositório University of Florida | https://ufdc.ufl.edu/AA00003919/00001/pdf | inglês | This monographic treatment of the genus Clitoria L. (Leguminosae: Glycineae) is the first since that of George Bentham in 1858. The genus is treated on a world-wide basis. The study is based upon examination of approximately 7000 specimens from thirty-three lending institutions, and from field studies of United States Species. Clitoria includes fifty-eight species and fifty-one nontypical Subspecific taxa. A history of Clitoria is provided. A systematic treatment is given which recognizes three subgenera and eight sections. Phylogenetic considerations are given based upon the interpretation of morphological data presented in this Study. | ||||||||||||||||||||||||||||||||||
92 | Fabaceae | Macrolobium Schreb. (Leguminosae) no Brasil | Maria Maricélia Félix da Silva | Tese | Universidade Federal do Pará | Belém | 253 | 2016 | Amazônia, Arapari, Detarieae, Neotrópico, Taxonomia | sim | Repositório Universidade Federal do Pará | http://bionorte.propesp.ufpa.br/ARQUIVOS/teses/Tese_Maria-Silva_Para-2012-2016_vs-FINAL.pdf | português | O Brasil possui a maior cobertura de florestas tropicais do mundo, especialmente concentrada na Região Amazônica. Dentre os 221 gêneros da família Leguminosae estimados para o país está Macrolobium Schreb., com distribuição neotropical, atualmente incluído na subfamília Caesalpinioideae, tribo Detarieae, que possui cerca de 70-80 espécies, ocorrentes em formações florestais e arbustivas em geral relacionadas a margens de rios, com o centro de diversidade na Amazônia. O presente trabalho teve o objetivo de realizar um estudo taxonômico das espécies de Macrolobium ocorrentes no Brasil. Foram inventariadas as coleções de 52 herbários nacionais e estrangeiros. Os resultados obtidos são organizados em dois capítulos. O primeiro referente ao estudo taxonômico das espécies de Macrolobium no Brasil, representado por 48 táxons, sendo 35 específicos e 13 infraespecíficos, incluindo chave para identificação, descrições morfológicas, comentários, ilustrações e mapas de distribuição dos táxons. O segundo capítulo consiste na proposição de sinonimização do grupo Macrolobium campestre Huber, caracterizado principalmente pelo hábito arbustivo ou arbóreo, 2-4-pares de folíolos, flor unipétala, 3-estames livres, fruto deiscente. | |||||||||||||||||||||||||||||||
93 | Fabaceae | Parkia (Leguminosae: Mimosoideae) | Helen C.F. Hopkins | Monografia | New York Botanical Garden Press | New York | Flora Neotropica | 43 | 1-123 | 1986 | não | JSTOR (read online) | https://www.jstor.org/stable/pdf/4393790.pdf?seq=1 | Monografia do gênero Parkia. | |||||||||||||||||||||||||||||||
94 | Fabaceae | The American Cassiinae: a synoptical revision of Leguminosae tribe Cassieae subtribe Cassiinae in the New World | Howard S. Irwin, Rupert C. Banerby | Monografia | Memoirs of the New York Botanical Garden | 35 | 1 | 1-454 | 1982 | taxonomia, morfologia, Cassia, Senna, Chamaecrista, chave de identificação | sim | Mertz Digital NYBG | http://mertzdigital.nybg.org/digital/collection/p9016coll16/id/3901 | inglês | Revisão da subtribo Casiinae no Novo Mundo | ||||||||||||||||||||||||||||||
95 | Fabaceae | The American Cassiinae: a synoptical revision of Leguminosae tribe Cassieae subtribe Cassiinae in the New World | Howard S. Irwin, Rupert C. Banerby | Monografia | Memoirs of the New York Botanical Garden | 35 | 2 | 455-918 | 1982 | taxonomia, morfologia, Cassia, Senna, Chamaecrista, chave de identificação | sim | Mertz Digital NYBG | http://mertzdigital.nybg.org/digital/collection/p9016coll16/id/4841/rec/4 | inglês | Revisão da subtribo Casiinae no Novo Mundo | ||||||||||||||||||||||||||||||
96 | x | Fabaceae | Revision of Martiodendron (Cassieae, Caesalpinioideae) | Robert Koeppen, Hugh H. Iltis | artigo | Brittonia | 14 | 2 | 191-209 | 1962 | Saffron, wood specimen, wood anatomy, Terra Firme, Forest Product Laboratory, Fabaceae | não | Springer | https://link.springer.com/article/10.2307/2805226 | Revision of the genus Martiodendron (Cassieae, Caesalpiniaceae). | ||||||||||||||||||||||||||||||
97 | x | Fabaceae | Revision of Dicorynia (Cassieae, Caesalpiniaceae) | Robert C. Koeppen | artigo | Brittonia | 19 | 1 | 42-61 | 1967 | wood specimen, wood anatomy, lower epidermis, Terra Frima, silica body, Fabaceae | não | Springer | https://link.springer.com/article/10.2307/2805082 | https://www.jstor.org/stable/2805082?seq=1 | A combined taxonomic revision and wood anatomical study ofDicorynia, a South American genus of legumes that is unusual in both its floral and wood anatomy, is presented. Two possible evolutionary pathways leading to the unique 8-to 10-thecate anthers are discussed, and it is concluded that apical proliferation of the thecal primordia is the more likely. Gross and microscopic features of this silica-accumulating wood are given in detail and contrasted with other legume woods especially those containing silica. Economic uses of the trees, especially the wood ofD. guianensis, are discussed particularly in regard to marine construction. It is suggested that the high resistance of this wood to marine borers lies not so much in its silica content as to the presence of some other chemical. Based on the similarity of floral and fruit structures, the number of species is reduced from 7 to 2:D. guianensis in the Guianas andD. paraensis in the Amazonian region. Vegetative variations in the Amazonian population, previously given species rank, are reduced to 5 new varieties ofD. paraensis. | |||||||||||||||||||||||||||||
98 | Fabaceae | Diplotropis Bentham (Leguminosae - Faboideae) - estudos taxonômicos infragenéricos | Haroldo Cavalcanti de Lima | artigo | Acta Amazônica | 15 | 1-2 | 61-75 | 1985 | chave de identificação de espécies, Fabaceae | sim | Scielo | https://www.scielo.br/scielo.php?script=sci_arttext&pid=S0044-59671985000100061 | português | No presente trabalho, são analisados e discutidos os táxons infragenéricos de Diplotropis Bentham (Leguminosae - Faboideae) - Tribo Sophoreae s. lato. Uma nova seção (Sect. Racemosae lima) é descrita e são apresentadas chaves para identificação das seções, espécies e variedades. / In this work the infrageneric taxa of Diplotropis Benth. (LEG. FAB.) - Tribe So -phoreae s. lato are analised and discussed. A new secion (Sect. Racemosae Lima) is described and keys for identification of the sections, species and varieties ore provided. | ||||||||||||||||||||||||||||||
99 | x | Fabaceae | O gênero Copaifera (Leguminosae - Caesalpinioideae) na Amazônia brasileira | Regina C.V. Martins-da-Silva, Jorge Fontella Pereira, Haroldo Cavalcanti de Lima | artigo | Rodriguesia | 59 | 3 | 455-476 | 2008 | Copaíba; medicinal; óleo-resina; taxonomia; Cesalpiniaceae; oleoresin; taxonomy; Fabaceae | sim | Scielo | https://www.scielo.br/scielo.php?pid=S2175-78602008000300455&script=sci_arttext | português | O gênero Copaifera está presente na África (4 spp.), América Central (4 spp.), América do Sul (cerca de 37 spp.) e, provavelmente, na Ásia (1 sp.). Foram reconhecidas nove espécies de Copaifera na Amazônia brasileira: Copaifera duckei, C. glycycarpa, C. guyanensis, C. martii, C. multijuga, C. paupera, C. piresii, C. pubiflora e C. reticulata, representadas tanto por arbustos ou árvores que chegam a atingir até 40 metros de altura, fornecendo tanto madeira como o óleo-resina, extraído de seu tronco, utilizada na preparação de medicamentos, cosméticos, tintas e revelação de fotografias. O presente trabalho apresenta uma chave para identificação das espécies que ocorrem na Amazônia brasileira, incluindo ilustrações, descrições e comentários sobre morfologia e taxonomia. / Copaifera occurs in Africa (4 spp.), Central America (4 spp.), South America (about 37 spp.) and probably in Asia (1 sp.). Nine species were recognized within the Brazilian Amazon: Copaifera duckei, C. glycycarpa, C. guyanensis, C. martii, C. multijuga, C. paupera, C. piresii, C. pubiflora e C. reticulata. Their habit varies between shrubby and tree-like, with some species forming 40 m tall trees. Copaifera is economically important as a timber source, and increasingly as the source of an oleoresin used as a component of medicines, cosmetics, ink and film-development. The present treatment includes an identification key for the species, illustrations, descriptions and comments regarding the morphology, taxonomy and distribution of the species treated. | |||||||||||||||||||||||||||||
100 | Fabaceae | Monograph of Andira (Leguminosae - Papilionoideae) | R. Toby Pennington | Monografia | American Society of Plant Taxonomists | Systematic Botany Monographs | 64 | 1-143 | 2003 | Fabaceae, taxonomy, phylogeny, biogeography, dispersal biology, character evolution | ? | JSTOR (read online) | https://www.jstor.org/stable/pdf/25027903.pdf?seq=1 | https://www.researchgate.net/publication/260181406_Monograph_of_Andira_Leguminosae-Papilionoideae | The principally Neotropical genus Andira Lam. (Leguminosae) comprises 29 species; one species, A. inermis, includes three subspecies, two of which occur in Africa. Chloroplast DNA restriction site analysis allows phylogenetic placement of 21 species of Andira, including five species that were not previously studied. These data are also used to investigate intraspecific chloroplast DNA polymorphism and to identify accessions of A. humilis with plastomes derived from probable introgressive hybridization. A cladistic analysis of 12 morphological characters provides little phylogenetic resolution in comparison with a simultaneous analysis of cpDNA restriction site data and morphology. Although some of the clades discovered by this analysis are "cryptic," i.e., they are supported only by molecular characters and have no morphological synapomorphies, the results provide a reasonable estimate of the phylogeny of Andira and are used as the basis of discussions of character evolution, infrageneric classification, and biogeography. Previous infrageneric classifications of Andira were based on the nature of the indumentum of the gynoecium, but glabrous ovaries have evolved in parallel at least three times. Detailed analysis of fruit wall anatomy provides phylogenetically informative characters and insights into dispersal biology. There have been at least five instances of independent evolution of large, putatively rodent-dispersed fruits and three of large, persistent stipules. The frequent changes in stipule morphology are perhaps due to mutation in a single gene. Evidence points to a relatively recent (possibly Pleistocene) radiation of species of Andira in eastern Brazil. All species are fully described and their ranges are mapped, and 15 are illustrated. Five new species and one new subspecies are proposed: A. chigorodensis, A. jaliscensis, A. macrocarpa, A. praecox, A. taurotesticulata, and A. inermis subsp. glabricalyx. |