RESUMO
The genera Psalmopoeus Pocock, 1895, Tapinauchenius Ausserer, 1871 and Pseudoclamoris Hüsser, 2018 are revised and cladistics analyses carried out including most species of these genera. In order to test the monophyly of Aviculariinae and Psalmopoeinae, species of all genera in these two subfamilies were included, as well as of Harpactirinae, Selenocosmiinae, Theraphosinae, Stromatopelmatinae, Ischnocolinae, Schismatothelinae, Poecilotherinae, and a barychelid was used to root the cladogram. The matrix with 50 terminal taxa, 1 continuous and 85 discrete characters was analysed with TNT 1.5. The results show a monophyletic Psalmopoeinae as sister group of Aviculariinae. Psalmopoeus comprises 9 species: Psalmopoeus cambridgei Pocock, 1895 (type species), Psalmopoeus ecclesiasticus Pocock, 1903, Psalmopoeus emeraldus Pocock, 1903, Psalmopoeus irminia Saager, 1994, Psalmopoeus langenbucheri Schmidt, Bullmer & Thierer-Lutz, 2006, Psalmopoeus plantaris Pocock, 1903, Psalmopoeus pulcher Petrunkevitch, 1925, Psalmopoeus reduncus (Karsch, 1880), and Psalmopoeus victori Mendoza, 2014. Psalmopoeus intermedius Chamberlin, 1940 is considered a junior synonym of P. reduncus. Psalmopoeus copanensis Gabriel & Sherwood, 2020, P. sandersoni Gabriel & Sherwood, 2020 and P. petenensis Gabriel & Sherwood, 2020 are considered junior synonyms of P. victori. Psalmopoeus maya Witt, 1996 is considered nomen nudum. Tapinauchenius comprises 8 species: Tapinauchenius plumipes (C. L. Koch, 1842) (type species), Tapinauchenius sanctivincenti (Walckenaer, 1837), Tapinauchenius latipes L. Koch, 1875, Tapinauchenius brunneus Schmidt, 1995, Tapinauchenius cupreus Schmidt & Bauer, 1996, Tapinauchenius polybotes Hüsser, 2018, Tapinauchenius rasti Hüsser, 2018, and T. gretae n. sp. The female of T. brunneus is described for first time. Tapinauchenius violaceus (Mello-Leitão, 1930), T. purpureus Schmidt, 1995, T. concolor (Caporiaccco, 1947), and T. gigas Caporiacco, 1954 are considered junior synonyms of T. plumipes. With the synonymy of T. gigas (type species of Pseudoclamoris Hüsser, 2018), it was necessary to describe a new genus for the two species formerly included in it. Thus, the new genus Amazonius n. gen. is erected to include A. elenae (Schmidt, 1994) n. comb., A. burgessi (Hüsser, 2018) n. comb. as well as two new species A. giovaninii n. gen. n. sp. and A. germani n. gen. n. sp. A discussion on the relationship of Psalmopoeinae and Aviculariinae and maps with the distributions of all species are provided.
RESUMO
The genera Psalistops Simon, 1889, Trichopelma, Simon, 1888 and Cyrtogrammomma Pocock, 1895 are revised and included in cladistics analyses including almost all species of these genera. In order to test previous morphological hypotheses on the relationships of Barychelidae, Paratropididae and Theraphosidae and because of the controversial taxonomic position of Psalistops and Trichopelma, a set of terminal taxa representing all subfamilies of Paratropididae (Paratropidinae, Glabropelmatinae), Barychelidae (Barychelinae, Sasoninae, Trichopelmatinae) and most theraphosid subfamilies were included, as well as a diplurid, a nemesiid, and a pycnothelid, the later used to root the cladogram. The matrix with 66 terminal taxa, 2 continuous and 93 discrete characters was analysed with TNT 1.5. We found that Trichopelmatinae is not a monophyletic group, and Psalistops is transferred to Theraphosidae, as well as the barychelid genus Cyrtogrammomma and the paratropidid genus Melloina Brignoli. Cyrtogrammomma was retrieved as the sister group of Trichopelma, and Melloina as the sister group of Holothele Karsch. Psalistops was retrieved as the sister group of Reichlingia Rudloff, and the clade with these two genera is the most basal in Theraphosidae. Barychelidae was found to be monophyletic and the sister group of Theraphosidae. Paratropididae was retrieved as the sister group of Barychelidae + Theraphosidae. The relationship and possible synapomorphies of the three families are herein discussed. This is the first time since Raven (1985) that representatives of all barychelid (Barychelinae, Sasoninae, Trichopelmatinae), paratropidid (Paratropidinae, Glabropelmatinae) and most theraphosid subfamilies have been included in a morphological cladistic analysis. Psalistops comprises two species, P. melanopygius Simon, 1889 (type species) and P. colombianus sp. nov. Psalistops montigena Simon, 1889, P. tigrinus Simon, 1889 and P. zonatus Simon, 1889 are synonymized with P. melanopygius Simon, 1889. Psalistops fulvus Bryant, 1948, P. hispaniolensis Wunderlich, 1988 (fossil), P. maculosus Bryant, 1948, P. venadensis Valerio, 1986 and P. steini (Simon, 1889) are transferred to Trichopelma. Psalistops gasci Maréchal, 1996 is transferred to Hapalopus Ausserer (Theraphosidae); P. opifex (Simon, 1889) and P. solitarius (Simon, 1889) are transferred to Schismatothele Karsch, 1879 (Theraphosidae). Schismatothele solitarius (Simon, 1889) n. comb. is synonymized with Schismatothele lineata Karsch, 1879, n. syn. Psalistops nigrifemuratus Mello-Leitão, 1939 is probably a nemesiid or pycnothelid, and herein considered as nomen dubium in Pycnothelidae. Trichopelma comprises 22 species: Trichopelma nitidum Simon, 1888 (type species), T. coenobita (Simon, 1889), T. steini (Simon, 1889), T. affine (Simon, 1892), T. cubanum (Simon, 1903), T. maculatum (Banks, 1906), T. zebra (Petrunkevitch, 1925), T. banksia Özdikmen Demir, 2012, T. insulanum (Petrunkevitch, 1926), T. fulvus (Bryant, 1948) n. comb., T. laselva Valerio, 1986, T. venadensis (Valerio, 1986) n. comb., T. huffi sp. nov., T. gabrieli sp. nov., T. tostoi sp. nov., T. goloboffi sp. nov., T. juventud sp. nov., T. laurae sp. nov., T.bimini sp. nov., T. loui sp. nov., T. platnicki sp. nov., and T. hispaniolensis Wunderlich, 1988 n. comb. (fossil). Trichopelma maculosus (Bryant, 1948) n. comb. is synonymized with P. fulvus Bryant, 1948; T. corozalis (Petrunkevitch, 1929) is synonymized with T. insulanum (Petrunkevitch, 1926). Trichopelma astutum Simon, 1889 is transferred to Euthycaelus Simon, 1889, and T. maddeni Esposito Agnarsson, 2014 to Holothele Karsch, 1879 (Theraphosidae). Trichopelma flavicomum Simon, 1891 is transferred to Neodiplothele (Barychelidae, Sasoninae). The species T. illetabile Simon, 1888, T. spinosum (Franganillo, 1926), T. scopulatum (Fischel, 1927) and T. eucubanum Özdikmen Demir, 2012 are considered as nomina dubia. Cyrtogrammomma comprises two species: C. monticola Pocock, 1895 (type species) and C. raveni sp. nov.
Assuntos
Aranhas , Distribuição Animal , Animais , FósseisRESUMO
The genera Psalistops Simon, 1889, Trichopelma, Simon, 1888 and Cyrtogrammomma Pocock, 1895 are revised and included in cladistics analyses including almost all species of these genera. In order to test previous morphological hypotheses on the relationships of Barychelidae, Paratropididae and Theraphosidae and because of the controversial taxonomic position of Psalistops and Trichopelma, a set of terminal taxa representing all subfamilies of Paratropididae (Paratropidinae, Glabropelmatinae), Barychelidae (Barychelinae, Sasoninae, Trichopelmatinae) and most theraphosid subfamilies were included, as well as a diplurid, a nemesiid, and a pycnothelid, the later used to root the cladogram. The matrix with 66 terminal taxa, 2 continuous and 93 discrete characters was analysed with TNT 1.5. We found that Trichopelmatinae is not a monophyletic group, and Psalistops is transferred to Theraphosidae, as well as the barychelid genus Cyrtogrammomma and the paratropidid genus Melloina Brignoli. Cyrtogrammomma was retrieved as the sister group of Trichopelma, and Melloina as the sister group of Holothele Karsch. Psalistops was retrieved as the sister group of Reichlingia Rudloff, and the clade with these two genera is the most basal in Theraphosidae. Barychelidae was found to be monophyletic and the sister group of Theraphosidae. Paratropididae was retrieved as the sister group of Barychelidae + Theraphosidae. The relationship and possible synapomorphies of the three families are herein discussed. This is the first time since Raven (1985) that representatives of all barychelid (Barychelinae, Sasoninae, Trichopelmatinae), paratropidid (Paratropidinae, Glabropelmatinae) and most theraphosid subfamilies have been included in a morphological cladistic analysis. Psalistops comprises two species, P. melanopygius Simon, 1889 (type species) and P. colombianus sp. nov. Psalistops montigena Simon, 1889, P. tigrinus Simon, 1889 and P. zonatus Simon, 1889 are synonymized with P. melanopygius Simon, 1889. Psalistops fulvus Bryant, 1948, P. hispaniolensis Wunderlich, 1988 (fossil), P. maculosus Bryant, 1948, P. venadensis Valerio, 1986 and P. steini (Simon, 1889) are transferred to Trichopelma. Psalistops gasci Maréchal, 1996 is transferred to Hapalopus Ausserer (Theraphosidae); P. opifex (Simon, 1889) and P. solitarius (Simon, 1889) are transferred to Schismatothele Karsch, 1879 (Theraphosidae). Schismatothele solitarius (Simon, 1889) n. comb. is synonymized with Schismatothele lineata Karsch, 1879, n. syn. Psalistops nigrifemuratus Mello-Leitão, 1939 is probably a nemesiid or pycnothelid, and herein considered as nomen dubium in Pycnothelidae. Trichopelma comprises 22 species: Trichopelma nitidum Simon, 1888 (type species), T. coenobita (Simon, 1889), T. steini (Simon, 1889), T. affine (Simon, 1892), T. cubanum (Simon, 1903), T. maculatum (Banks, 1906), T. zebra (Petrunkevitch, 1925), T. banksia Özdikmen & Demir, 2012, T. insulanum (Petrunkevitch, 1926), T. fulvus (Bryant, 1948) n. comb., T. laselva Valerio, 1986, T. venadensis (Valerio, 1986) n. comb., T. huffi sp. nov., T. gabrieli sp. nov., T. tostoi sp. nov., T. goloboffi sp. nov., T. juventud sp. nov., T. laurae sp. nov., T.bimini sp. nov., T. loui sp. nov., T. platnicki sp. nov., and T. hispaniolensis Wunderlich, 1988 n. comb. (fossil). Trichopelma maculosus (Bryant, 1948) n. comb. is synonymized with P. fulvus Bryant, 1948; T. corozalis (Petrunkevitch, 1929) is synonymized with T. insulanum (Petrunkevitch, 1926). Trichopelma astutum Simon, 1889 is transferred to Euthycaelus Simon, 1889, and T. maddeni Esposito & Agnarsson, 2014 to Holothele Karsch, 1879 (Theraphosidae). Trichopelma flavicomum Simon, 1891 is transferred to Neodiplothele (Barychelidae, Sasoninae). The species T. illetabile Simon, 1888, T. spinosum (Franganillo, 1926), T. scopulatum (Fischel, 1927) and T. eucubanum Özdikmen & Demir, 2012 are considered as nomina dubia. Cyrtogrammomma comprises two species: C. monticola Pocock, 1895 (type species) and C. raveni sp. nov.
RESUMO
One new genus and eight new species of anilline carabids are described from southern Mexico. The new genus, Zapotecanillus gen. n., is established for Z. oaxacanus (type species) sp. n., Z. nanus sp. n., Z. iviei sp. n., Z. ixtlanus sp. n., Z. montanus sp. n., and Z. kavanaughi sp. n. from the Sierra Madre de Oaxaca, Z. pecki sp. n. from the Sierra Madre del Sur, and Z. longinoi sp. n. from the Sierra Madre de Chiapas. A taxonomic key for all described species of Zapotecanillus and a cladistic analysis, based on morphological data, are provided. Morphological, behavioral and biogeographical aspects of the speciation in the genus obtained from the resulting cladogram are discussed.
RESUMO
The genera Cohniella, Lophiarella, Lophiaris, and Trichocentrum are included in the Trichocentrum-clade. These genera are distributed from Florida and Northern Mexico to Southern Brazil and Northern Argentina, growing in tropical deciduous forests or tropical rain forests and thorn scrub forests to pine-oak forest, from sea level to 1 700m. The leaf anatomical structure of 23 members of the Trichocentrum-clade was explored as a source of taxonomic and phylogenetic characters. A total of 11 species of Cohniella, three species of Lophiarella, seven species of Lophiaris, two species of Trichocentrum, and other four species were included as outgroup. Anatomical characters were studied by cross sections and paradermic observations of the middle portion of fresh leaves. Although anatomical characters were fairly homogeneous throughout the clade, twelve vegetative anatomical, phylogenetically informative characters were selected and coded for an analysis that was performed using an exhaustive search implicit enumeration implemented through TNT. The strict consensus of 2 692 most parsimonious trees resulted in a poorly resolved polytomy, which however recovers the Trichocentrum-clade with a monophyletic, strongly supported Cohniella nested within it with unifacial leaves and the presence of cellular inclusions in the epidermis as synapomorphies. We concluded that the anatomy characters alone are insufficient to assess the relationships amongst the genera of the Trichocentrum-clade. However, the two synapomorphies recovered for Cohniella strongly support its monophyly when these are analyzed in conjunction with other data sources e.g., molecular and morphological characters.
El clado-Trichocentrum incluye los géneros Cohniella, Lophiarella, Lophiaris y Trichocentrum s.s. Estos géneros se distribuyen desde Florida y el Norte de México hasta el Sur de Brasil y Norte de Argentina, creciendo desde bosques caducifolios, bosques húmedos tropicales hasta matorrales espinosos y bosques de pino-encino, desde el nivel del mar hasta los 1 700m. En este estudio se exploró el valor taxonómico y filogenético de la estructura anatómica de las hojas de 23 especies del clado-Trichocentrum, repartidos en 11 especies de Cohniella, tres de Lophiarella, siete de Lophiaris y dos de Trichocentrum s.s., y de otras cuatro especies incluidas como grupo externo. Se realizaron secciones transversales y observaciones paradérmicas de la porción media de hojas frescas para el estudio de los caracteres anatómicos. Doce caracteres anatómico foliares fueron seleccionados y codificados para el análisis filogenético que se realizó mediante el uso de una búsqueda exhaustiva enumeración implícita con el programa TNT. El consenso estricto de 2 692 árboles más parsimoniosos dio lugar a una politomía que recupera dentro del clado-Trichocentrum a Cohniella como un clado monofilético fuertemente apoyado con sinapomorfías de las hojas unifaciales y la presencia de inclusiones celulares en la epidermis.
Assuntos
Orchidaceae/anatomia & histologia , Orchidaceae/classificação , Folhas de Planta/anatomia & histologia , Brasil , México , Orchidaceae/genética , Panamá , Peru , Filogenia , Folhas de Planta/genética , VenezuelaRESUMO
Comparative leaf anatomy and phylogenetic relationships of 11 species of Laeliinae with emphasis on Brassavola (Orchidaceae). Brassavola inhabits a wide altitude range and habitat types from Northern Mexico to Northern Argentina. Classification schemes in plants have normally used vegetative and floral characters, but when species are very similar, as in this genus, conflicts arise in species delimitation, and alternative methods should be applied. In this study we explored the taxonomic and phylogenetic value of the anatomical structure of leaves in Brassavola; as ingroup, seven species of Brassavola were considered, and as an outgroup Guarianthe skinneri, Laelia anceps, Rhyncholaelia digbyana and Rhyncholaelia glauca were evaluated. Leaf anatomical characters were studied in freehand cross sections of the middle portion with a light microscope. Ten vegetative anatomical characters were selected and coded for the phylogenetic analysis. Phylogenetic reconstruction was carried out under maximum parsimony using the program NONA through WinClada. Overall, Brassavola species reveal a wide variety of anatomical characters, many of them associated with xeromorphic plants: thick cuticle, hypodermis and cells of the mesophyll with spiral thickenings in the secondary wall. Moreover, mesophyll is either homogeneous or heterogeneous, often with extravascular bundles of fibers near the epidermis at both terete and flat leaves. All vascular bundles are collateral, arranged in more than one row in the mesophyll. The phylogenetic analysis did not resolve internal relationships of the genus; we obtained a polytomy, indicating that the anatomical characters by themselves have little phylogenetic value in Brassavola. We concluded that few anatomical characters are phylogenetically important; however, they would provide more support to elucidate the phylogenetic relantionships in the Orchidaceae and other plant groups if they are used in conjunction with morphological and/or molecular characters. Rev. Biol. Trop. 59 (3): 1047-1059. Epub 2011 September 01.
Brassavola crece en un amplio rango altitudinal y de tipos de hábitat desde el Norte de México hasta el Norte de Argentina. En los sistemas de clasificación de las plantas se utilizan normalmente caracteres vegetativos y florales, pero cuando las especies son muy similares, como es el caso de este género, los conflictos surgen en la delimitación de las especies, por lo tanto deben ser aplicados métodos alternativos de identificación. En este trabajo se exploró el valor taxonómico y filogenético de la estructura anatómica de las hojas de Brassavola, se consideró como grupo interno a siete especies de este género y como grupo externo a Guarianthe skinneri, Laelia anceps, Rhyncholaelia digbyana y Rhyncholaelia glauca. Entonces se realizaron secciones transversales de hojas frescas para el estudio de los caracteres anatómicos. Diez caracteres anatómicosvegetativos fueron seleccionados y codificados para el análisis filogenético. La reconstrucción filogenética se llevó a cabo bajo el principio de máxima parsimonia utilizando el programa NONA a través de WinClada. Todas las especies son anatómicamente similares, no obstante, difieren en algunos rasgos como presencia o no: de papilas epidérmicas, de hipodermis, de células con engrosamientos espiralados en la pared secundaria de las células del mesofilo, de inclusiones cristalinas; además en el tipo de hoja de acuerdo al arreglo del mesofilo; en la organización de los haces vasculares y de los paquetes de fibras extravasculares. En el árbol de consenso estricto se obtuvo una politomía. Asimismo, fue evidente que los caracteres anatómicos analizados son filogenéticamente poco informativos; sin embargo, en conjunción con caracteres morfológicos y/o moleculares, podrían dilucidar las relaciones filogenéticas.
Assuntos
Orchidaceae/anatomia & histologia , Orchidaceae/genética , Argentina , Filogenia , Folhas de Planta/anatomia & histologia , Folhas de Planta/genéticaRESUMO
We revalidate the theraphosid genus Pterinopelma Pocock 1901, describe the female of P. vitiosum for first time and Pterinopelmasazimai sp. nov. from Brazil. These two species were included in a matrix with 35 characters and 32 taxa andwere analyzed both with all characters having same weight and with implied weights. Searches considering all charactersnon-additive or some additive were also carried out. The preferred tree, obtained with implied weights, concavity 6 andall characters non-additive shows that Pterinopelma is a monophyletic genus sister to the clade Lasiodora (Vitalius +Nhandu). The presence of denticles on the prolateral inferior male palpal bulb keel is a synapomorphy of the genus.
Assuntos
Feminino , Animais , Aranhas/classificação , Especificidade da EspécieRESUMO
A cladistic analysis using 63 characters and 30 genera of the Neotropical tribe Ochlerini Rolston was performed to test their monophyletic condition and to establish a relationship hypothesis. Janeirona Distant, 1911 (Pentatomini) and the tribes Discocephalini and Halyini were included in the ingroup to test their relationship with Ochlerini; Marghita Ruckes, 1964 and Stictochilus Bergroth, 1918 (Pentatomini) were used as outgroups. The obtained strict consensus cladograms indicate that Ochlerini and Discocephalinae are monophyletic groups, but Pentatominae, Halyini+Ochlerini, Pentatomini+Ochlerini, Ochlerus Spinola, 1837, Stalius Rolston, 1992 and Alitocoris Sailer, 1950 are merophyletic groups. Discocephalini and Ochlerini share three synapomorphies: first rostral segment long, attaining prosternum; metasternum with a mesial, longitudinal carina, and dorsal surface of basal third of male proctiger membranous. Ochlerini is supported by one synapomorphy, the flattened dorsal surface of third tarsal segment of hind legs, in females. Biogeographical analysis based on consensus cladograms shows congruent patterns with several vicariant events proposed for the Neotropical region.
Neste trabalho foi realizada uma análise cladística, utilizando 63 caracteres, dos 30 gêneros da tribo Neotropical Ochlerini Rolston, no intuito de testar seu monofiletismo e estabelecer uma hipótese de parentesco. Janeirona Distant, 1911 (Pentatomini) e as tribos Discocephalini e Halyini foram incluídas no grupo-interno para testar seu relacionamento com Ochlerini; Marghita Ruckes, 1964 e Stictochilus Bergroth, 1918 (Pentatomini) foram utilizados como grupos-externos. Os cladogramas de consenso estrito obtidos indicam que Ochlerini e Discocephalinae são grupos monofiléticos, mas Pentatominae, Halyini+Ochlerini, Pentatomini+Ochlerini, Ochlerus Spinola, 1837, Stalius Rolston, 1992 e Alitocoris Sailer, 1950 são grupos merofiléticos. Discocephalini e Ochlerini compartilham três sinapomorfias: primeiro segmento do rostro longo, alcançando o prosterno; metasterno carenado longitudinalmente; e superfície dorsal do segmento X do macho membranosa no terço basal. Ochlerini é sustentada por uma sinapomorfia, a superfície dorsal do terceiro artículo metatarsal das fêmeas aplainada. Uma análise biogeográfica a partir dos cladogramas de consenso mostrou padrões congruentes com eventos vicariantes propostos para a região Neotropical.
RESUMO
A cladistic analysis using 63 characters and 30 genera of the Neotropical tribe Ochlerini Rolston was performed to test their monophyletic condition and to establish a relationship hypothesis. Janeirona Distant, 1911 (Pentatomini) and the tribes Discocephalini and Halyini were included in the ingroup to test their relationship with Ochlerini; Marghita Ruckes, 1964 and Stictochilus Bergroth, 1918 (Pentatomini) were used as outgroups. The obtained strict consensus cladograms indicate that Ochlerini and Discocephalinae are monophyletic groups, but Pentatominae, Halyini+Ochlerini, Pentatomini+Ochlerini, Ochlerus Spinola, 1837, Stalius Rolston, 1992 and Alitocoris Sailer, 1950 are merophyletic groups. Discocephalini and Ochlerini share three synapomorphies: first rostral segment long, attaining prosternum; metasternum with a mesial, longitudinal carina, and dorsal surface of basal third of male proctiger membranous. Ochlerini is supported by one synapomorphy, the flattened dorsal surface of third tarsal segment of hind legs, in females. Biogeographical analysis based on consensus cladograms shows congruent patterns with several vicariant events proposed for the Neotropical region.
Neste trabalho foi realizada uma análise cladística, utilizando 63 caracteres, dos 30 gêneros da tribo Neotropical Ochlerini Rolston, no intuito de testar seu monofiletismo e estabelecer uma hipótese de parentesco. Janeirona Distant, 1911 (Pentatomini) e as tribos Discocephalini e Halyini foram incluídas no grupo-interno para testar seu relacionamento com Ochlerini; Marghita Ruckes, 1964 e Stictochilus Bergroth, 1918 (Pentatomini) foram utilizados como grupos-externos. Os cladogramas de consenso estrito obtidos indicam que Ochlerini e Discocephalinae são grupos monofiléticos, mas Pentatominae, Halyini+Ochlerini, Pentatomini+Ochlerini, Ochlerus Spinola, 1837, Stalius Rolston, 1992 e Alitocoris Sailer, 1950 são grupos merofiléticos. Discocephalini e Ochlerini compartilham três sinapomorfias: primeiro segmento do rostro longo, alcançando o prosterno; metasterno carenado longitudinalmente; e superfície dorsal do segmento X do macho membranosa no terço basal. Ochlerini é sustentada por uma sinapomorfia, a superfície dorsal do terceiro artículo metatarsal das fêmeas aplainada. Uma análise biogeográfica a partir dos cladogramas de consenso mostrou padrões congruentes com eventos vicariantes propostos para a região Neotropical.