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Epicadus heterogaster (Guérin-Menéville, 1829). Female (IBSP 08491). A–D epigynum/vulva (A ventral–arrows point the atrium, B dorsal–arrows points tto FD, C sagittal, D frontal—arrow points to FD (left one broken)); E metatarsus I, retrolateral view. Arrows point to bifid setae. Scale bars: 0.5 mm (A, E); 0.2 mm (B–D).  

Epicadus heterogaster (Guérin-Menéville, 1829). Female (IBSP 08491). A–D epigynum/vulva (A ventral–arrows point the atrium, B dorsal–arrows points tto FD, C sagittal, D frontal—arrow points to FD (left one broken)); E metatarsus I, retrolateral view. Arrows point to bifid setae. Scale bars: 0.5 mm (A, E); 0.2 mm (B–D).  

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Article
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All species of Epicadus Simon, 1895 are reviewed and redescribed, including the previously unknown males of E. rubripes Mello-Leitão, 1924 and E. planus Mello-Leitão, 1932. A new diagnosis based on morphological characters is proposed for the genus. Three valid species of Epicadus are recognized: E. heterogaster (Guérin-Méneville, 1829); E. rubripe...

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Context 1
... oriented. Anterior legs distinctively larger and stouter than the posterior ones. Femora I and II armed with two rows of ventral conical tubercles (FeT, Figs 2E, 7E), patellae I and II elongated. Tibiae and metatarsi I and II round in cross-section, armed with short, slightly curved macrosetae, with rounded base and acute edge (sometimes bifid, Fig. 3E). Metatarsi III and IV round in cross-section with distinct setae tuff on the distal third. Anterior tibiae with a concave area on the dorso-retrolateral face (Fig. 6B), where a sensorial pit can be found (SPt, Figs 6C, D) in the proximal part. The same region contains both duster-shaped setae (Fig. 6E) and trichobothria (Figs 6C, D). ...
Context 2
... lowered median area (better seen on SEM, Figs 15B, E, H). Epigynal plate at the same level as the opisthosoma (E. heterogaster, E. rubripes) or slightly elevated (E. planus). Copulatory openings sclerotized ( Figs 3A, 8A, 12A); vestibular edges sclerotized, forming a smooth and rounded atrium (Figs 15B, E, H). Copulatory ducts long, S-shaped ( Fig. 3C) with upper (anterior) curve (CV) enlarged, similar to a secondary spermatheca (see Bonaldo 2000;Machado et al. 2015) at the distal part (Figs 15A, D, G) and getting narrower near the copulatory openings and distant from the spermatheca. Spermathecae rounded or bean-shaped. Fertilization ducts long and thin, oriented dorsally near the ...

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Citations

... The morphological aspects and taxonomic boundaries of Neotropical stephanopines have been extensively studied during the past years (Machado et al. 2015(Machado et al. , 2019aSilva-Moreira & Machado 2016). Meanwhile, phylogenies based on morphological and molecular data were congruent in recovering some close related genera, corroborating classic propositions for the possible existence of tribes or even certain "groups" in this subfamily (Benjamin 2011;Benjamin et al. 2008;Wheeler et al. 2017;Machado et al. 2017Machado et al. , 2019bMachado & Teixeira 2021). ...
... The following species do not share the diagnostic characters proposed for Kryptochroma gen. nov., therefore they are being considered as nomina dubia or transferred to other genera recently revised by Teixeira et al. (2014), Silva-Moreira & Machado (2016) and Machado et al. (2018Machado et al. ( , 2019a. (Petrunkevitch, 1910) Stephanopis aheneus Soares & Soares, 1946: 57, figs 5-6 (male holotype from Rio São José, Colatina, Espírito Santo, Brazil, Soares, B.A.M. leg.,15 September 1942, deposited in MZSP 666, examined). ...
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... While two species of Stephanopis from Central America emerged close to the "cambridgei clade", the remaining Neotropical species were placed inside the "Epicadus group" (Fig. 6), a potential clade suggested by Silva-Moreira and Machado (2016) and partially recovered by Machado et al. (2017). A similar topology was recovered by Wheeler et al. (2017) with considerable support. ...
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Full-text available
We present the first record of Epicadus trituberculatus (Taczanowski, 1872) from the Northeast Region of Brazil. The new record is based on six specimens observed in two areas of montane semi-deciduous tropical forest located in two municipalities: Guaramiranga and Pacatuba, Ceará state, Brazil. Of the six specimens observed we collected manually only three to preserve as voucher material. In Brazil, E. trituberculatus has a wide distribution range, which extends from the Atlantic Forest, Amazon, and Cerrado biomes and the Pampa ecoregion. With the new record there are currently six known species of Epicadus in northeastern Brazil.
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Sri Lankan species of the genus Tmarus are cryptic spiders that live either on greenish moss-covered twigs or brownish dried-out twigs. They have remained taxonomically unrevised. The only known species was misplaced in Peritraeus Simon, 1895, which has never been subjected to phylogenetic evaluation. The present study is designed to investigate the phylogenetic placement of Sri Lankan Tmarus within Thomisidae as well as to assess the validity of Peritraeus and its relationship to Tmarus and Monaeses, if any. Using a multilocus molecular dataset (16S–ND1, 28S, CO1 and H3) we provide evidence that Tmarus and Monaeses are paraphyletic and that Peritraeus is a junior subjective synonym of Tmarus. Four species of Tmarus, including three new species, are now recorded from Sri Lanka. The legacy groups Alcimochthae and Tmarae are confirmed to be polyphyletic. Further, the following new species are described: Tmarus hiyarensis, sp. nov., T. viridomaculatus, sp. nov. and T. manojkaushalyai sp. nov. The following new combination is proposed: Tmarus hystrix (Simon, 1895), comb. nov. (this results in a homonym with Tmarus hystrix Caporiacco, 1954: we rename the species Tmarus caporioccoi Ileperuma Arachchi & Benjamin, replacement name).