Journal articles on the topic 'Psalmopoeus'

Dupérré, Nadine, Tapia, Elicio (2024): Description of a new Psalmopoeus Pocock, 1895 species (Araneae, Theraphosidae, Psalmopoeinae) from the Chocó region of Ecuador. Zootaxa 5437 (4): 495-509, DOI: 10.11646/zootaxa.5437.4.3, URL: http://dx.doi.org/10.11646/zootaxa.5437.4.3

Cifuentes, Yeimy, Bertani, Rogerio (2022): Taxonomic revision and cladistic analysis of the tarantula genera Tapinauchenius Ausserer, 1871, Psalmopoeus Pocock, 1985, and Amazonius n. gen. (Theraphosidae, Psalmopoeinae). Zootaxa 5101 (1): 1-123, DOI: 10.11646/zootaxa.5101.1.1, URL: http://dx.doi.org/10.11646/zootaxa.5101.1.1

Based on molecular and morphological phylogenetic analyses a new genus of Theraphosidae is described,Pseudoclamorisgen. n.TapinaucheniusgigasandTapinaucheniuselenaeare transferred toPseudoclamorisand a new species ofPseudoclamorisfrom the Amazon Region is described:P.burgessisp. n.Two new species ofTapinaucheniusfrom the Caribbean are described:T.rastisp. n.andT.polybotessp. n.Tapinaucheniussubcaeruleusis considered anomen dubium. Psalmopoeinae subfamily is diagnosed based on molecular and morphological phylogenies, andPseudoclamorisgen. n.andEphebopusSimon, 1892 are included. A taxonomic key for Psalmopoeinae generaTapinauchenius,Pseudoclamoris,Psalmopoeus, andEphebopusis provided.

Based on molecular and morphological phylogenetic analyses a new genus of Theraphosidae is described, Pseudoclamoris gen. n. Tapinauchenius gigas and Tapinauchenius elenae are transferred to Pseudoclamoris and a new species of Pseudoclamoris from the Amazon Region is described: P. burgessi sp. n. Two new species of Tapinauchenius from the Caribbean are described: T. rasti sp. n. and T. polybotes sp. n. Tapinauchenius subcaeruleus is considered a nomen dubium. Psalmopoeinae subfamily is diagnosed based on molecular and morphological phylogenies, and Pseudoclamoris gen. n. and Ephebopus Simon, 1892 are included. A taxonomic key for Psalmopoeinae genera Tapinauchenius, Pseudoclamoris, Psalmopoeus, and Ephebopus is provided.

The tarantula genus Ephebopus Simon 1892 is reviewed and includes the type species, E. murinus (Walckenaer 1837), and E. uatuman Lucas, Silva & Bertani 1992, E. cyanognathus West & Marshall 2000, E. rufescens West & Marshall 2000 and Ephebopus foliatus, sp. nov., from Guyana. Ephebopus violaceus Mello-Leitão 1930 is transferred to Tapinauchenius Ausserer, where it is a senior synonym of Tapinauchenius purpureus Schmidt 1995 new synonymy. Ephebopus fossor Pocock 1903 is considered a nomen dubium. Ephebopus occurs in northeastern South America where it is known only from Brazil, Guyana, Suriname, and French Guiana. Spiders of the genus are generally fossorial; however, Ephebopus murinus has a developmental stage that is arboreal. A cladistic analysis of the Theraphosidae retrieves the Aviculariinae as monophyletic, including Avicularia Lamarck, Iridopelma Pocock 1901, Pachistopelma Pocock 1901, Tapinauchenius, Psalmopoeus Pocock, Ephebopus, Stromatopelma Karsch and Heteroscodra Pocock, having as a synapomorphy the well-developed scopulae on tarsi and metatarsi I–II that is very laterally extended.

Psalmopeotoxin I (PcFK1) is a 33-residue peptide isolated from the venom of the tarantula Psalmopoeus cambridgei. This peptide specifically inhibits the intra-erythrocyte stage of Plasmodium falciparum in vitro. It contains six cysteine residues forming three disulfide bridges and belongs to the superfamily of natural peptides containing the inhibitor cystine knot (ICK) fold. We produced the wild-type and mutated forms of the recombinant peptide to examine the mechanism of action of PcFK1. The purified toxins were consistently produced as two isobaric peptides (r-PcFK1-1 and r-PcFK1-2) with different retention properties but identical anti-plasmodial biological activity. Comparison of 15N-NMR heteronuclear single quantum correlation spectra revealed that although rPcFK1-1 was highly structured, rPcFK1-2 does not have a stable three-dimensional structure. We used high-energy collision-induced fragmentation of the peptides with a matrix-assisted laser desorption/ionization tandem time-of-flight mass spectrometer to further investigate the structure of the native peptides in its natural form and produced in E. coli. The fragmentation spectra of the native peptides were very complex due to the occurrence in the spectrum of ions resulting from (1) cross-linking of fragments through a disulfide bridge and (2) asymmetric fragmentations of the disulfide bridges and (3) multiple neutral losses. The tandem mass spectrometry fragmentation pattern of r-PcFK1-1 was similar to that of the natural peptide isolated from crude venom, but r-PcFK1-2 had a clearly distinct fragmentation pattern, more closely resembling the fragmentation spectra of reduced and alkylated peptides. Observed ions could be attributed to specific fragments by comparing spectra between the wild-type and selected variants with point mutations (Y11W, R20T, Y26W, K28V). The disulfide connections in r-PcFK1-2 differed from those of the native peptide and showed a rare disulfide bridge between vicinal cysteine residues. The r-PcFK1_(R20T) variant showed a very limited fragmentation pattern when analyzed in positive mode but displayed much more fragmentation in negative mode pointing out the importance of the R20 residue in the fragmentation of PcFK1. Using the reductive matrix 1,5-diaminonaphtalene promoted strongly in source decay fragmentation of the peptides in MS mode. Our findings illustrated the critical role of the electronic environment around the central Cys18–Cys19 doublet in PcFK1 in internal fragmentation of the peptide.

The genus Avicularia Lamarck, 1818 is revised and all species are rediagnosed. The type species, described as Aranea avicularia Linnaeus, 1758, is the oldest mygalomorph species described and its taxonomic history is extensive and confusing. Cladistic analyses using both equal and implied weights were carried out with a matrix of 46 taxa from seven theraphosid subfamilies, and 71 morphological and ecological characters. The optimal cladogram found with Piwe and concavity = 6 suggests Avicularia and Aviculariinae are monophyletic. Subfamily Aviculariinae includes Avicularia Lamarck, 1818, Typhochlaena C. L. Koch, 1850, Tapinauchenius Ausserer, 1871, Stromatopelma Karsch, 1881, Ephebopus Simon, 1892, Psalmopoeus Pocock, 1895, Heteroscodra Pocock, 1899, Iridopelma Pocock, 1901, Pachistopelma Pocock, 1901, Ybyrapora gen. n., Caribena gen. n., and Antillena gen. n. The clade is supported by well-developed scopulae on tarsi and metatarsi, greatly extended laterally. Avicularia synapomorphies are juveniles bearing black tarsi contrasting with other lighter articles; spermathecae with an accentuated outwards curvature medially, and male palpal bulb with embolus medial portion and tegulum's margin form an acute angle in retrolateral view. Avicularia is composed of twelve species, including three new species: Avicularia avicularia (Linnaeus, 1818), Avicularia glauca Simon, 1891, Avicularia variegata (F. O. Pickard-Cambridge, 1896) stat. n., A. minatrix Pocock, 1903, Avicularia taunayi (Mello-Leitão, 1920), Avicularia juruensis Mello-Leitão, 1923, Avicularia rufa Schiapelli & Gerschman, 1945, Avicularia purpurea Kirk, 1990, A. hirschii Bullmer et al. 2006, Avicularia merianae sp. n., A. lynnae sp. n., and A. caei sp. n.. Avicularia species are distributed throughout Mexico, Costa Rica, Panama, Trinidad and Tobago, Venezuela, Guyana, Suriname, French Guiana, Colombia, Ecuador, Peru, Bolivia, and Brazil. Three new genera are erected to accommodate former Avicularia species: Caribena gen. n., composed of Caribena laeta (C. L. Koch, 1842), comb. n. and Caribena versicolor (Walckenaer, 1837), comb. n.; Antillena gen. n., with a single species, Antillena rickwesti (Bertani & Huff, 2013), comb. n., both from the Caribbean; and Ybyrapora gen. n., composed of Ybyrapora sooretama (Bertani & Fukushima, 2009), comb. n., Ybyrapora gamba (Bertani & Fukushima, 2009), comb. n. and Ybyrapora diversipes (C. L. Koch, 1842), comb. n. from Brazilian rainforest. The subspecies Avicularia avicularia variegata F. O. Pickard-Cambridge, 1896 is elevated to species status, resulting in the combination Avicularia variegata (F. O. Pickard-Cambridge, 1896) stat. n.. The following new synonymies are established: Avicularia velutina Simon 1889, Avicularia exilis Strand, 1907, Avicularia ancylochyra Mello-Leitão, 1923, Avicularia cuminami Mello-Leitão, 1930, and Avicularia nigrotaeniata Mello-Leitão, 1940 are junior synonyms of A. avicularia; Avicularia bicegoi Mello-Leitão, 1923 is a junior synonym of A. variegata stat. n., and Avicularia urticans Schmidt, 1994 is a junior synonym of Avicularia juruensis Mello-Leitão, 1923. Species transferred to other genera: Avicularia affinis (Nicolet, 1849) is transferred to Euathlus Ausserer, 1875, making the new combination Euathlus affinis (Nicolet, 1849), comb. n.; Avicularia subvulpina Strand, 1906 is transferred to Grammostola Simon, 1892, making the new combination Grammostola subvulpina (Strand, 1906), comb. n.; Avicularia aymara (Chamberlin, 1916) is transferred to Thrixopelma Schmidt, 1994, making the new combination Thrixopelma aymara (Chamberlin, 1916), comb. n.; Avicularia leporina (C. L. Koch, 1841) and Avicularia plantaris (C. L. Koch, 1842) are transferred to Iridopelma Pocock, 1901, making the new combinations Iridopelma leporina (C. L. Koch, 1841), comb. n. and Iridopelma plantaris (C. L. Koch, 1842), comb. n.; the two last species are considered nomina dubia. The following species are considered nomina dubia: Avicularia hirsutissima (C. L. Koch, 1842) nomen dubium; Ischnocolus hirsutum Ausserer, 1875 nomen dubium; Ischnocolus gracilis Keyserling, 1891 nomen dubium; Avicularia arabica (Strand, 1908) nomen dubium; Araneus hirtipes (Fabricius, 1787) nomen dubium; Avicularia ochracea (Perty, 1833) nomen dubium; Avicularia walckenaerii (Perty, 1833) nomen dubium; Avicularia testacea (C. L. Koch, 1841) nomen dubium; Avicularia detrita (C. L. Koch, 1842) nomen dubium; Ischnocolus doleschalli Ausserer, 1871 nomen dubium; Avicularia metallica Ausserer, 1875 nomen dubium; Avicularia rapax (Ausserer, 1875) nomen dubium; Avicularia holmbergi Thorell, 1890 nomen dubium; Avicularia aurantiaca Bauer, 1996 nomen dubium; Avicularia azuraklaasi Tesmoingt, 1996 nomen dubium; Avicularia huriana Tesmoingt, 1996 nomen dubium; Avicularia ulrichea Tesmoingt, 1996 nomen dubium; Avicularia braunshauseni Tesmoingt, 1999 nomen dubium; Avicularia geroldi Tesmoingt, 1999 nomen dubium; Avicularia soratae Strand, 1907 nomen dubium; Avicularia fasciculata Strand, 1907 nomen dubium; Avicularia fasciculata clara Strand, 1907 nomen dubium; and Avicularia surinamensis Strand, 1907 nomen dubium. Avicularia vestiaria (De Geer, 1778) is considered nomen nudum. Keys are provided for identification of all aviculariine genera, as well as to Avicularia, Caribena gen. n., Ybyrapora gen. n. and Antillena gen. n. species. Maps with records and information on species habitat are also presented. Lectotypes are newly designed for A. avicularia, A. variegata stat. n., A. juruensis, C. laeta comb. n., E. affinis comb. n. and a neotype is established for C. versicolor comb. n.

Se describe una especie nueva de tarántula, Psalmopoeus victori sp. nov. (Araneae, Theraphosidae,Aviculariinae) de Veracruz, México. Es la primera especie arborícola descrita en México y la distribución más al norteconocida hasta ahora para el género Psalmopoeus. Se presenta una descripción detallada de la lira.