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Tarsal scopula condition and carapace length were studied for eighteen Ischnocolinae species. For cladistic analysis a matrix of 20 terminals and 30 characters of representatives of Ischnocolinae, Theraphosinae, Aviculariinae, Harpactirinae and Trichopelmatinae were analyzed using Nona 2.0 computer software. The matrix was analyzed in four different ways: 1. each tarsal scopula (legs I-IV) coded as separate characters; 2. one character with six ordered states; 3. one character with six independent states; 4. without tarsal scopula character. The first two matrices result in one tree with the same indices (L = 72; CI = 0.54; RI = 0.74) and topology: Part of Ischnocolinae is monophyletic (H. rondoni(S. longibulbi(I. algericus+Catumiri))) and the other representatives (Oligoxystre and Genus 1) form a distinct monophyletic group with Theraphosinae, Harpactirinae and Aviculariinae. There are no homoplasies in tarsal scopula evolution in the second cladogram. The other two cladograms show less resolution for the Ischnocolinae than the two first cladorams. The tarsal scopula condition appears to have no relation to spider size (t =-0.80433; P = 0.438247) and should be used in phylogenetic analysis of Ischnocolinae because it provides information on the character variability within the subfamily.

In this paper, 374 incidents of frog predation by spiders are reported based on a comprehensive global literature and social media survey. Frog-catching spiders have been documented from all continents except for Antarctica (>80% of the incidents occurring in the warmer areas between latitude 30° N and 30° S). Frog predation by spiders has been most frequently documented in the Neotropics, with particular concentration in the Central American and Amazon rain forests and the Brazilian Atlantic forest. The captured frogs are predominantly small-sized with an average body length of 2.76 ± 0.13 cm (usually ≈0.2–3.8 g body mass). All stages of the frogs' life cycle (eggs/embryos, hatchlings, tadpoles, emerging metamorphs, immature post-metamorphs, adults) are vulnerable to spider predation. The majority (85%) of the 374 reported incidents of frog predation were attributable to web-less hunting spiders (in particular from the superfamilies Ctenoidea and Lycosoidea) which kill frogs by injection of powerful neurotoxins. The frog-catching spiders are predominantly nocturnal with an average body length of 2.24 ± 0.12 cm (usually ≈0.1–2.7 g body mass). Altogether >200 frog species from 32 families (including several species of bitter tasting dart-poison frogs) have been documented to be hunted by >100 spider species from 22 families. Our finding that such a high diversity of spider taxa is utilizing such a high variety of frog taxa as prey is novel. The utilization of frogs as supplementary food increases the spiders' food supply (i.e., large diet breadth), and this is presumed to enhance their chance of survival. Studies from Australia and South America indicate that frogs might be a substantial component in the diet of some mygalomorph spiders (i.e., families Atracidae, Idiopidae, and Theraphosidae). Many more quantitative investigations on the natural diets of tropical spiders are needed before reliable conclusions on the importance of frogs as spider food can be drawn.

The infraorder Mygalomorphae (i.e., trapdoor spiders, tarantulas, funnel web spiders, etc.) is one of three main lineages of spiders. Comprising 15 families, 325 genera, and over 2,600 species, the group is a diverse assemblage that has retained a number of features considered primitive for spiders. Despite an evolutionary history dating back to the lower Triassic, the group has received comparatively little attention with respect to its phylogeny and higher classification. The few phylogenies published all share the common thread that a stable classification scheme for the group remains unresolved. We report here a reevaluation of mygalomorph phylogeny using the rRNA genes 18S and 28S, the nuclear protein-coding gene EF-1γ, and a morphological character matrix. Taxon sampling includes members of all 15 families representing 58 genera. The following results are supported in our phylogenetic analyses of the data: (1) the Atypoidea (i.e., antrodiaetids, atypids, and mecicobothriids) is a monophyletic group sister to all other mygalomorphs; and (2) the families Mecicobothriidae, Hexathelidae, Cyrtaucheniidae, Nemesiidae, Ctenizidae, and Dipluridae are not monophyletic. The Microstigmatidae is likely to be subsumed into Nemesiidae. Nearly half of all mygalomorph families require reevaluation of generic composition and placement. The polyphyletic family Cyrtaucheniidae is most problematic, representing no fewer than four unrelated lineages. Based on these analyses we propose the following nomenclatural changes: (1) the establishment of the family Euctenizidae (NEW RANK); (2) establishment of the subfamily Apomastinae within the Euctenizidae; and (3) the transfer of the cyrtaucheniid genus Kiama to Nemesiidae. Additional changes include relimitation of Domiothelina and Theraphosoidea, and the establishment of the Euctenizoidina clade (Idiopidae + Euctenizidae). In addition to these changes, we propose a \"road map\" for future sampling across the infraorder with the aim of solving many remaining questions that hinder mygalomorph systematics.

The theraphosid spider genera Heterophrictus Pocock, 1900 and Neoheterophrictus Siliwal & Raven, 2012 are rediagnosed in this paper and a new genus, Sahydroaraneus gen. nov. is described from Southern Western Ghats. Four new species (two each of Heterophrictus and Neoheterophrictus) and one of Sahydroaraneus gen. nov. are described from the Western Ghats. Plesiophrictus mahabaleshwari Tikader, 1977 is removed from the synonymy of Heterophrictus milleti Pocock, 1900 and is treated as a junior synonym of Heterophrictus blatteri (Gravely, 1935). Plesiophrictus bhori Gravely, 1915 is transferred to the genus Neoheterophrictus, Neoheterophrictus bhori (Gravely, 1915) new combination. The genus, Sahydroaraneus gen. nov., resembles tarantula belonging to the genus, Neoheterophrictus but differs with respect to structure of tibial apophysis and spermathecae. Detailed ultra-structure of setae type of the Indian Eumenophorinae is presented for the first time along with notes on their biogeography. Common elements among Africa, Madagascar and India like the Eumenophorinae and several other mygalomorph spiders advocate mygalomorphae as an important group for evolutionary investigation due to their inability for long distance dispersal rendering the members restrictive in distribution.

According to a recent global literature survey, a total of 39 out of the 129 known spider families (∼30%) contain species capable of capturing vertebrate prey. The finding that the percentage of spider families engaged in vertebrate predation is so high is novel. Two groups of vertebrate-eating spiders are distinguished: “habitual vertebrate-eaters” vs. “occasional vertebrate-eaters”. The habitual vertebrate-eaters comprise ten spider families (Araneidae, Atracidae, Ctenidae, Lycosidae, Nephilidae, Pisauridae, Theraphosidae, Theridiidae, Trechaleidae, and Sparassidae) to which can be attributed 91% of all reported vertebrate predation incidents. The habitual vertebrate-eaters have evolved prey-capture adaptations such as (1) sufficient physical strength coupled with large body size, (2) the use of potent venoms, and (3) the use of highly efficient prey-catching webs. By contrast, unexpected feeding on vertebrates by the occasional vertebrate-eaters (i.e., Actinopodidae, Agelenidae, Amaurobiidae, Anyphaenidae, Barychelidae, Clubionidae, Corinnidae, Ctenizidae, Cyrtaucheniidae, Deinopidae, Desidae, Dipluridae, Eresidae, Filistatidae, Gnaphosidae, Haplonoproctidae, Linyphiidae, Liocranidae, Miturgidae, Oxyopidae, Pholcidae, Porrhothelidae, Salticidae, Selenopidae, Sicariidae, Sparassidae, Tetragnathidae, and Thomisidae) might be considered as chance events that took place when a tiny vertebrate crossed the path of an opportunistic spider. For a few families (e.g., Idiopidae) their status as habitual or occasional vertebrate predators is still unclear. In conclusion, our survey unveiled a large number of spider taxa previously not anticipated to feed on vertebrate prey. These findings improve our general understanding of spider feeding ecology and provide a first assessment of the significance of vertebrate prey as a food source for spiders.

El género Homoeomma presenta 13 especies que se distribuyen en Argentina, Brasil, Colombia, Perú y Uruguay. En Argentina, se citan dos especies, Homoeomma elegans en la provincia de Misiones y H. uruguayense en las provincias de Buenos Aires, Entre Ríos y Santa Fe. El objetivo de este trabajo es reportar el primer registro de Homoeomma uruguayense para las sierras centrales de Argentina, lo cual corresponde al registro más occidental del género en este país. Además, se proveen datos sobre la historia natural de la especie, algunas notas sobre el comportamiento sexual y mediante el modelado de distribución de especies se discute sobre la distribución geográfica de la especie y los factores que pudieron conducir a este patrón. The genus Homoeomma has 13 species distributed in Argentina, Brazil, Colombia, Peru and Uruguay. In Argentina, two species are recorded, Homoeomma elegans in Misiones province and H. uruguayense in Buenos Aires, Entre Ríos and Santa Fe provinces. The objective of this work is to provide the first record of Homoeomma uruguayense in the mountainous system of central Argentina, belonging to western record of the genus in this country. In addition, we provide data on natural history of the species, some notes on its sexual behavior and through the species distribution modeling we discussed about the geographic distribution of the species and factors that could led to this pattern.

We describe and illustrate a new species of tarantula of the genus Euathlus Ausserer, 1875, Euathlus walteri sp. nov. This species represents the first record for the genus in Tarapacá region, being the northernmost limit of its known distribution in Chile. Known and potential distribution are provided. Precipitations and altitude are the most important variables for its distribution. In addition, the conservation status of the new species is discussed, and it is proposed as Endangered (EN) according to IUCN criteria.

In this paper more than 50 incidences of bats being captured by spiders are reviewed. Bat-catching spiders have been reported from virtually every continent with the exception of Antarctica (≈ 90% of the incidences occurring in the warmer areas of the globe between latitude 30° N and 30° S). Most reports refer to the Neotropics (42% of observed incidences), Asia (28.8%), and Australia-Papua New Guinea (13.5%). Bat-catching spiders belong to the mygalomorph family Theraphosidae and the araneomorph families Nephilidae, Araneidae, and Sparassidae. In addition to this, an attack attempt by a large araneomorph hunting spider of the family Pisauridae on an immature bat was witnessed. Eighty-eight percent of the reported incidences of bat catches were attributable to web-building spiders and 12% to hunting spiders. Large tropical orb-weavers of the genera Nephila and Eriophora in particular have been observed catching bats in their huge, strong orb-webs (of up to 1.5 m diameter). The majority of identifiable captured bats were small aerial insectivorous bats, belonging to the families Vespertilionidae (64%) and Emballonuridae (22%) and usually being among the most common bat species in their respective geographic area. While in some instances bats entangled in spider webs may have died of exhaustion, starvation, dehydration, and/or hyperthermia (i.e., non-predation death), there were numerous other instances where spiders were seen actively attacking, killing, and eating the captured bats (i.e., predation). This evidence suggests that spider predation on flying vertebrates is more widespread than previously assumed.

Vertebrate predation by invertebrates has been classically underexplored and thus underestimated, despite the fact that many arthropods consume vertebrates. To shed some light on the relevance that spider predation may have upon lizards in the Neotropical and Andean regions, we compiled the available information in the literature on this trophic interaction. We found 50 reports of spiders consuming lizards in these regions, and the 88% of these were from the Neotropical region. Spiders belong to eight families, but Ctenidae and Theraphosidae were the most frequently reported predators. Lizards belong to 12 families, and the most commonly consumed species corresponded to the families Dactyloidae (all Anolis lizards), Gymnophthalmidae, and Sphaerodactylidae. Data suggest trophic spider–lizard associations between Ctenidae and Dactyloidae, followed by Theraphosidae and Liolaemidae. The body sizes of the spiders and lizards showed a positive relationship, and spiders were smaller than their prey. We conclude that various spider taxa can be considered lizard predators and they may be ecologically important in the Neotropical and Andean regions. However, spiders of prime predation relevance seem to be those of the Ctenidae and Theraphosidae families. In this study, we analyze for the first time the lizard consumption by spiders in the Neotropical and Andean regions, showing that the families Ctenidae and Theraphosidae may be relevant lizard predators in these areas. In addition, we provide the first report on spider predation upon a vertebrate taxon in the Andean region.

Two new species of the genus Chilobrachys Karsh, 1892 are described from China: Chilobrachys dominus Lin & Li, sp. nov. from Yunnan and C. jinchengi Lin & Li, sp. nov. from Tibet. Photos and a morphological description of the new species are given. The type specimens of the new species are deposited in the Institute of Zoology, Chinese Academy (IZCAS) in Beijing.