scholarly journals Synopsis of the genus Drosera (Droseraceae) in Angola and the Democratic Republic of the Congo

Author(s):  
A. Rjosk ◽  
C. Neinhuis ◽  
M. Monizi ◽  
T. Lautenschläger

While some African Floras were continuously revised and several are now almost completed, the Flora of Angola’s ‘Conspectus Florae Angolensis’ still remains incomplete. This applies also for Droseraceae and the genus Drosera. Our study aims to provide an identification key for Drosera of Angola and the Democratic Republic of the Congo, including all morphological characters of the different Angolan and Congolese taxa. Loans from different herbaria were studied. A list of important morphological characters was combined with data obtained by observations and measurements. Beside the identification key, nine species descriptions with drawings of the main characteristics, distribution maps and SEM-pictures of pollen and seed morphology are provided. The possibility of hybridisation is discussed. Despite difficulties such as varying morphology or hybridisation in some species, the identification key enables researchers to identify specimens by morphological characters.

Zootaxa ◽  
2011 ◽  
Vol 3011 (1) ◽  
pp. 45 ◽  
Author(s):  
KIRSTIN S. MEYER ◽  
NEIL CUMBERLIDGE

The taxonomy of the freshwater crabs living in the rivers draining from the mountains in the eastern Democratic Republic of the Congo and Rwanda into Lake Kivu is revised. Four species are recognized: Potamonautes perparvus (Rathbun, 1921), P. minor Bott, 1955, P. gonocristatus Bott, 1955, and P. semilunaris Bott, 1955. Updated diagnoses, illustrations, and distribution maps are provided for the species. The four species are compared to each other, and an identification key to all eight species found in Lake Kivu and its drainage basin is included.


Zootaxa ◽  
2019 ◽  
Vol 4630 (1) ◽  
pp. 1-619 ◽  
Author(s):  
MASSIMO OLMI ◽  
ROBERT S. COPELAND ◽  
SIMON VAN NOORT

An updated revision of Afrotropical Dryinidae is presented. Nine subfamilies, 23 genera and 430 species (including 60 new species) are treated. Six new species-level synonymies and three new combinations are proposed. Descriptions, geographic distribution, known hosts, natural enemies and type material of each species are presented, together with illustrations of the main morphological characters and keys to the subfamilies, genera and species. A complete list of references concerning the Afrotropical Dryinidae and their hosts is provided. The following new species are described: Anteon ambrense, sp. nov. (Madagascar), Anteon beankanum, sp. nov. (Madagascar), Anteon elongatum, sp. nov. (Madagascar), Anteon hoekense, sp. nov. (South Africa), Anteon mabibiense, sp. nov. (South Africa), Anteon majunganum, sp. nov. (Madagascar), Anteon malagasy, sp. nov. (Madagascar), Anteon musmani, sp. nov. (Kenya), Anteon nigropictum, sp. nov. (South Africa), Anteon nimbense, sp. nov. (Guinea), Anteon pseudohova, sp. nov. (Madagascar), Anteon sakalavense, sp. nov. (Madagascar), Anteon tulearense, sp. nov. (Kenya, Madagascar), Aphelopus sequeirai, sp. nov. (Kenya), Apoaphelopus fisheri, sp. nov. (Madagascar), Apoaphelopus wallacei, sp. nov. (Kenya), Bocchus forestalis, sp. nov. (Madagascar), Bocchus granulatus, sp. nov. (South Africa), Bocchus harinhalai, sp. nov. (Madagascar), Bocchus nigroflavus, sp. nov. (Madagascar), Bocchus parkeri, sp. nov. (Madagascar), Bocchus ruvidus, sp. nov. (Madagascar), Conganteon hawleyi, sp. nov. (Kenya), Conganteon sensitivum, sp. nov. (Madagascar), Crovettia afra, sp. nov. (Kenya, Madagascar), Deinodryinus ambrensis, sp. nov. (Madagascar), Deinodryinus granulatus, sp. nov. (South Africa), Deinodryinus nigropictus, sp. nov. (South Africa), Deinodryinus piceus, sp. nov. (Madagascar), Dryinus bellicosus, sp. nov. (Madagascar), Dryinus dentatiforceps, sp. nov. (South Africa), Dryinus erenianus, sp. nov. (Ivory Coast), Dryinus milleri, sp. nov. (Kenya), Dryinus mobotensis, sp. nov. (Madagascar), Dryinus nigrithorax, sp. nov. (Ivory Coast), Dryinus teres, sp. nov. (Madagascar), Dryinus tulearensis, sp. nov. (Madagascar), Dryinus whittleorum, sp. nov. (Kenya), Gonatopus avontuurensis, sp. nov. (South Africa), Gonatopus bellicosus, sp. nov. (Madagascar), Gonatopus comorensis, sp. nov. (Union of the Comoros), Gonatopus costalis, sp. nov. (South Africa), Gonatopus flavotestaceus, sp. nov. (Madagascar), Gonatopus gumovskyi, sp. nov. (Democratic Republic of the Congo), Gonatopus hantamensis, sp. nov. (South Africa), Gonatopus harinhalai, sp. nov. (Madagascar), Gonatopus karooensis, sp. nov. (South Africa), Gonatopus koebergensis, sp. nov. (South Africa), Gonatopus marojejyanus, sp. nov. (Madagascar), Gonatopus minutus, sp. nov. (Madagascar), Gonatopus nigropictus, sp. nov. (South Africa), Gonatopus ranomafanensis, sp. nov. (Madagascar), Gonatopus robertsoni, sp. nov. (South Africa), Gonatopus rugithorax, sp. nov. (South Africa), Gonatopus scholtzi, sp. nov. (South Africa), Gonatopus wikstrandae, sp. nov. (Kenya), Lonchodryinus madagascolus, sp. nov. (Madagascar), Madecadryinus ranomafanensis, sp. nov. (Madagascar), Neodryinus bimaculatus, sp. nov. (Madagascar), Neodryinus keleboensis, sp. nov. (Democratic Republic of the Congo). The ♀ of Deinodryinus danielssoni Olmi, 1998, is described for the first time. The following new synonymies are presented: Anteon fiorii Olmi, 1984 (=A. proteicolum Olmi, 2006, syn. nov.); Anteon madagascolum (Benoit, 1954) (=Anteon brooksi Olmi, 2003, syn. nov.); Anteon zairense Benoit, 1951 (=A. terminale Olmi, 2007, syn. nov.); Aphelopus incisus Olmi, 1984 (=A. himyarita Olmi & van Harten, 2006, syn. nov.); Bocchus watshami Olmi, 1987 (=Bocchus simoni Olmi, 2005, syn. nov.); Dryinus ugandanus Olmi, 1984 (=Dryinus constantiae Olmi, 2006, syn. nov.). The following new combinations are presented: Dryinus luweli (Benoit, 1951) new comb. in place of Lestodryinus luweli Benoit, 1951; Gonatopus africanus (Benoit, 1951) new comb. in place of Aphelopus africanus Benoit, 1951; Gonatopus ghanensis (Olmi, 1987) new comb. in place of Pseudogonatopus ghanensis Olmi, 1987. Gynander specimens of Deinodryinus rusticus Olmi, 2004 and Deinodryinus steineri Olmi, 1994 are described (first gynander specimens of Dryinidae from the Afrotropical region). The authors provide well-illustrated identification keys to all species of Afrotropical Dryinidae. Online Lucid Phoenix and Lucid matrix interactive keys are provided at http://www.waspweb.org. 


Phytotaxa ◽  
2016 ◽  
Vol 279 (1) ◽  
pp. 1 ◽  
Author(s):  
MICHAEL H.J. BARFUSS ◽  
WALTER TILL ◽  
ELTON M.C. LEME ◽  
JUAN P. PINZÓN ◽  
JOSÉ M. MANZANARES ◽  
...  

A taxonomic revision of Bromeliaceae subfam. Tillandsioideae is presented based on a multi-locus DNA sequence phylogeny (viz., plastid DNA loci rpoB-trnC-petN, trnK-matK-trnK, and ycf1, and the nuclear DNA gene PHYC) and new or re-evaluated morphology (e.g., leaf, inflorescence, sepal, petal, ovary, stigma, stamen, pollen, ovule, and seed morphology). This enables the circumscription of monophyletic units using synapomorphic combinations of diagnostic morphological characters. Stigma morphology has proven to be indicative for super-specific taxa in Tillandsioideae. One new stigma type and several subtypes of previously described stigmas were found. The four tribes proposed earlier are mostly confirmed, but Catopsideae replaces the formerly used name Pogospermeae for the monotypic tribe of Catopsis. In addition, the two new subtribes Cipuropsidinae and Vrieseinae are proposed within tribe Vrieseeae. Several new genera are established to render taxonomic units monophyletic and morphologically well circumscribed. They represent segregates of either Mezobromelia (Gregbrownia: 4 spp.), Tillandsia (viz., Barfussia: 3 spp., Josemania: 5 spp., Lemeltonia: 7 spp., Pseudalcantarea: 3 spp., and Wallisia: 4 spp. and 1 hybrid), or Vriesea (viz., Goudaea: 2 spp., Jagrantia: 1 sp., Lutheria: 4 spp., Stigmatodon: 18 spp., and Zizkaea: 1 spp.). The new subgenera Tillandsia subg. Pseudovriesea and T. subg. Viridantha are established, and T. subg. Aerobia is resurrected. An identification key to all accepted genera of Bromeliaceae subfam. Tillandsioideae is provided. Furthermore, to clarify nomenclatural uncertainties, typifications are proposed for Catopsis subg. Tridynandra, Thecophyllum [unranked] Biflorae, Tillandsia subg. Aerobia, T. sect. Caricifoliae, T. sect. Conostachys, T. sect. Cyathophora, T. sect. Eriophyllum, T. sect. Macrocyathus, T. sect. Platystachys Baker auct. non al., Tillandsia sect. Strepsia, Vriesea subg. Conostachys Mez auct. non al., T. lindenii K. Koch auct. non al., and T. macropetala.


Author(s):  
Renata Asprino ◽  
André Márcio Amorim

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.


Zootaxa ◽  
2021 ◽  
Vol 4970 (3) ◽  
pp. 401-452
Author(s):  
MUHAMMAD ASGHAR HASSAN ◽  
XINGYUE LIU

Taxonomic notes are presented on the former Ascalaphidae (owlflies), now subfamily Ascalaphinae of the family Myrmeleontidae from Pakistan. An updated checklist of new records is provided that accounts for all known 15 genera and 22 species from Pakistan, excluding the species of the tribe Palparini. Geographical distribution maps and an updated identification key to all known genera and species from Pakistan are also given. We synonymized two monotypic genera, Horischema Mészáros & Ábrahám, 2003 and Perissoschema Mészáros & Ábrahám, 2003 both as junior synonyms of Ogcogaster Westwood, 1847 based on very similar male genitalia and external morphological characters. Moreover, Perissoschema evae Mészáros & Ábrahám, 2003 is treated as a junior synonym of Ogcogaster segmentator Westwood, 1847. We recorded three genera for the first time from Pakistan, i.e., Acheron Lefèbvre, 1842, Glyptobasis McLachlan, 1873, and Suphalomitus van der Weele, 1909. To more completely resolve the generic or specific status of those poorly known species from Pakistan, broader sampling throughout the country is needed. 


Zootaxa ◽  
2020 ◽  
Vol 4799 (1) ◽  
pp. 1-80
Author(s):  
BRUNO V. B. RODRIGUES ◽  
CRISTINA A. RHEIMS

A taxonomic revision of exclusively African genera of Prodidominae (Gnaphosidae), with the exception of Theuma, is provided. Austrodomus Lawrence, 1947 is revised. The type species A. zuluensis Lawrence, 1947 is redescribed, the male of A. scaber (Purcell, 1904) is described for the first time, and one new species, A. gamsberg sp. nov. (♂), is described from Namibia. Katumbea Cooke, 1964 is considered a junior synonym of Austrodomus and A. oxoniensis (Cooke, 1964) comb. nov. from Tanzania is redescribed. Eleleis Simon, 1893 is revised. The type species, E. crinita Simon, 1893, is redescribed and eight new species are described: E. limpopo sp. nov. (♂♀) from South Africa and Zambia, E. okavango sp. nov. (♂♀) from Botswana and Namibia, E. etosha sp. nov. (♂♀), E. himba sp. nov. (♂) and E. luderitz sp. nov. (♀) from Namibia, E. leleupi sp. nov. (♂) and E. haddadi sp. nov. (♀) from South Africa, and E. solitaria sp. nov. (♀) from Cape Verde. Purcelliana Cooke, 1964 is revised. The type species, P. problematica Cooke, 1964, is redescribed and three new species are described: P. kamaseb sp. nov. (♂♀) and P. khabus sp. nov. (♂♀) from Namibia, and P. cederbergensis sp. nov. (♂) from South Africa. Plutonodomus Cooke, 1964 is redescribed based solely on the type species, P. kungwensis Cooke, 1964. In addition, three new genera are described: Kikongo gen. nov., to include K. ruwenzori sp. nov. (♂♀) and K. buta sp. nov. (♂♀) from the Democratic Republic of the Congo (D.R. Congo), and K. rutshuru sp. nov. (♂♀) from D.R. Congo and Kenya; Kituba gen. nov., to include K. mayombensis sp. nov. (♂♀) and K. langalanga sp. nov. (♀) from D.R. Congo; and Yoruba gen. nov., to include Y. ibadanus sp. nov. (♂♀) from Nigeria and Y. toubensis sp. nov. (♂♀) from Ivory Coast. Distribution maps are provided for the species discussed in this study and an identification key is provided for all twelve genera of Prodidominae recorded in Africa. 


Phytotaxa ◽  
2014 ◽  
Vol 181 (1) ◽  
pp. 47 ◽  
Author(s):  
Faik Ahmet Karavelioğulları ◽  
Ebru YÜCE ◽  
Birol Başer

Verbascum duzgunbabadagensis (Scrophulariaceae) is described and illustrated as a new species endemic to eastern Anatolia, Turkey. In this study, diagnostic morphological characters of this and closely related species (V. luciliae and V. rupicola) are discussed. Pollen and seed morphology of the new species and of similar taxa are documented. The seeds of this group are brown in color and oblong in V. luciliae and V. rupicola, whereas they are dark brown in color and ovate in shape in V. duzgunbabadagensis. Furthermore, distribution maps for the three taxa are provided.


Zootaxa ◽  
2018 ◽  
Vol 4399 (4) ◽  
pp. 451
Author(s):  
FERNANDO HENRIQUE CARNIMEO ◽  
FERNANDO BARBOSA NOLL

The Neotropical thynnine genus Scotaena is revised and a cladistic analysis is presented. The analysis, conducted from 75 morphological characters of 31 terminal taxa, returned a single tree under equal weighting. The monophyly of Scotaena was not recovered. Three new genera and five new species are described: Kaysara gen. nov., Pseudoscotaena gen. nov. and Pampathynnus gen. nov., Scotaena reversa sp. nov., Kaysara laterolata sp. nov., Kaysara apiciconcava sp. nov., Kaysara marginoplicata sp. nov. and Kaysara levicrenata sp. nov. Three species are transferred to other genera as follows: Eucyrtothynnus rosenbergi (Turner, 1910) comb. nov., Glottynoides genisei Kimsey, 1991 comb. nov., Ornepetes clypearis Durán-Moya, 1941 comb. nov. Scotaena now comprises four species: S. trifasciata Klug, 1810; S. horni (Turner, 1927); S. vetusta Turner, 1909; and S. reversa. An identification key and geographical distribution maps for the studied species are also provided. 


2006 ◽  
Vol 85 (1) ◽  
pp. 209 ◽  
Author(s):  
Olof Biström ◽  
Anders N. Nilsson

The genus <em>Canthyporus</em> Zimmermann, 1919, is revised. A total of 35 species are recognized, all of them distributed within the Ethiopian Region, and with a centre of diversity in the South African Western Cape province. Descriptions of all species are given together with illustrations of habitus and male and female genitalia. A key to species (males), distribution maps, and ecological information are provided. Four new species are described from South Africa: <em>Canthyporus aenigmaticus</em> n.sp., <em>C</em>. <em>nimius</em> n.sp., <em>C. turneri</em> n.sp., and <em>C. wewalkai</em> n.sp. The species <em>C. congener</em> Omer-Cooper, 1956, is regarded as valid and not as a junior synonym of<em> C. canthydroides</em> (Régimbart, 1895). Lectotypes are designated for the following ten names:<em> C. alvei</em> Omer-Cooper, 1965, <em>C. consuetus </em>Omer-Cooper, 1965, <em>C. latus</em> Omer-Cooper, 1965, <em>C. lowryi </em>Omer-Cooper, 1965, <em>C. nebulosus</em> Omer-Cooper, 1965, <em>C. similator</em> Zimmermann, 1923, <em>C. simulator</em> Guignot, 1959, <em>C. testaceus</em> Zimmermann, 1923, <em>Hydroporus collaris</em> Boheman, 1848, and <em>Hydroporus hottentottus</em> Gemminger &amp; Harold, 1868. A parsimony analysis based on 32 morphological characters found 28 shortest trees. Monophyly of the genus <em>Canthyporus</em> is supported mainly by the presence of an anterior ligula on the ventral side of the elytron. Four species groups are recognized within the genus: (1) <em>canthydroides</em> group, including ten species in Namibia and South Africa; (2) <em>exilis</em> group, including four species in Lesotho and South Africa; (3) <em>hottentottus</em> group, including 18 species from the Democratic Republic of the Congo, Ethiopia, Kenya, Lesotho, Madagascar, South Africa, Swaziland, Tanzania, and Zimbabwe; and (4) <em>lateralis</em> group, including three species from South Africa.


2011 ◽  
Vol 24 (6) ◽  
pp. 405 ◽  
Author(s):  
C. A. Lehnebach

Morphology of New Zealand hook sedges Uncinia angustifolia Hamlin, U. rupestris Raoul and U. zotovii Hamlin overlaps considerably, making species identification difficult. All three species have a complicated taxonomic history. U. angustifolia has been considered a variety of U. rupestris, which, in turn, has been considered a variety of U. caespitosa Boot or included in two other species. As for U. zotovii, this was originally part of U. caespitosa along with the grassland species U. viridis (C.B.Clarke) Edgar. The present study re-examines historical and recently collected material, and re-evaluates species limits for these five species using multivariate statistic analyses of morphological characters. Results confirm the circumscription of U. caespitosa s.str. and the segregation of U. viridis and U. zotovii from U. caespitosa s.lat., but they also indicate that current species descriptions are inaccurate and based on material of mixed identity. Results also suggest that U. angustifolia, U. rupestris and U. zotovii should be considered as three different species. U. viridis and U. rupestris are conspecific; the latter name has priority and should be maintained. An identification key, revised descriptions, new synonymy and distribution maps for the species recognised here are also presented.


Sign in / Sign up

Export Citation Format

Share Document