Iheringia On a new species of the genus Simlops ( Araneae , Oonopidae ) from Guyana , with notes on the bodanus group of species

A new species of Simlops Bonaldo, Ott & Ruiz, 2014, S. kartabo sp. nov., from Guyana is described. The new species belongs to the putatively basal bodanus species group, sharing with other species of the group a relatively simple embolar distal third. The presence of a fi liform accessory process on the conductor, previously evidenced only for S. guatopo Brescovit, 2014 is also identifi ed here for S. bodanus (Chickering, 1968), S. guyanensis Santos, 2014 and S. kartabo sp. nov. and may support the monophyly of the bodanus group.

recently proposed Simlops Bonaldo, Ott & Ruiz for 15 oonopid species of which only one was previously described. Simlops shares with other Neotropical genera grouped in the Scaphiella complex (sensu Platnick & Dupérré 2009, 2010a,b, 2011 characteristic sexual dimorphism, in which the males have fully sclerotized abdomens, with a large dorsal scutum, while the females are less sclerotized, generally without the dorsal abdominal scutum. The monophyly of Simlops was based on the tripartite distal end of the male endites ( Fig. 8; Bonaldo et al., 2014, fi gs 275-289), a condition that seems to be exclusive within the Scaphiella complex. Bonaldo et al. (2014) recognized fi ve informal groups of species in Simlops, based mainly in the shape of the embolus and conductor. One of these groups, the bodanus group, is composed by three putatively basal species that share a relatively simple embolar distal third, without the modifi cations present in other groups of species.
Here, we describe a new species of the genus that represents the fourth known member of the bodanus group, since it also has a simple embolar distal third. The distribution of Simlops species is typically Amazonian, with most species occurring in the Amazon Basin, from Colombia to the State of Pará, northern Brazil. However, the bodanus group has a more peripheral distribution, being known from southern Caribbean and Guyanas. The new species is based on a single specimen collect 93 years ago in the small village of Kartabo, Guyana, the same locality in which the types of S. guyanensis Santos, 2014 were collected.

MATERIAL AND METHODS
The material examined belongs to the Arachnida collection of the American Museum of Natural History, New York (AMNH, curator L. Prendini). Our description methods were those described by Bonaldo et al. (2014) and included an extensive use of the descriptive database made available by the Planetary Biodiversity Inventory (PBI-Oonopidae). This database allows entering descriptive data in a highly structured format, aiming the direct use of that information in formal descriptions. To make the description of S. kartabo sp. nov. comparable to those of other species presented by Bonaldo et al. (2014), a genus description was generated with the available information of all 16 species in the database. Then, species descriptions devoid of those characters common to all species were generated for each of the 16 species. In order to make the species descriptions more concise, the formal generic description of Simlops by Bonaldo et al. (2014) included a few characters that were not observed in all species (noted as exceptions). Thus, the automatically generated species description obtained for S. kartabo sp. nov. was further shortened to match those of previously described species. Google Earth was used to estimate locality coordinates. The images were flipped for consistency when necessary. High-resolution versions of the images and distribution maps for all species of Simlops will be available at the PBI-Oonopidae page (http://research.amnh.org/oonopidae). Etymology. The specific name is a noun in apposition taken from the type locality.

Simlops kartabo
Diagnosis. Males of Simlops kartabo sp. nov. are similar to those of S. bodanus (Chickering, 1968) in the short, wide-based needle-like process on palpal conductor (see Bonaldo et al., 2014: fig. 315), but are readily recognized by this process being basally inserted and by the shorter embolus, strongly bent proximally, with truncate apex (Figs 12-15).
Female: Unknown. Other material examined. None. Distribution. Known only from the type locality.

DISCUSSION
Based on the relatively unmodified embolus, Bonaldo et al. (2014) suggested that species of the bodanus group could be regarded as basal taxa in the genus. Other features that could support that claim, such as the presence of a welldeveloped posterior receptaculum in the female genitalia (also present in Pescennina Simon, 1903) and even the presence of a small (S. bodanus) or rudimental (S. guyanensis) female dorsal scutum, cannot be addressed here since no female forms are known for either S. guatopo Brescovit, 2014 and S. kartabo sp. nov. However, the discovery of S. kartabo sp. nov. permitted the reinterpretation of some details of the conductor morphology, leading to the recognition of further informative characters. The conductor in Simlops species is variable in shape, position and degree of sclerotization. Some species, such as S. cristinae Santos, 2014 andS. cachorro Ruiz, 2014, have extremely complex conductors, while the three species of the juruti group have simple hyaline ones. The pennai group is characterized by the presence of a lamellar expansion inserted in the base of a tapering or filiform conductor. Our present findings indicated that the conductor of the species in the bodanus group is more complex than previously described. Bonaldo et al. (2014) indicated that S. guatopo present two accessory processes on the conductor, a filiform, needle-like basal process and a stout sub-basal process. It is now clear that the needle-like process is also present in all other species of the group (Figs 15-18, white arrows), being short, wide-based in S. kartabo sp. nov. (Fig. 15) and S. bodanus (Fig. 16) and long, narrow-based in S. guyanensis (Fig. 17) and S. guatopo (Fig. 18). The exclusive presence of the needle-like process may be regarded as a putative synapomorphy of the bodanus group, and the conductor morphology may also provide some clues regarding the relationships of the species within the group. The short, wide-based needle-like process in S. kartabo sp. nov. and S. bodanus may represent a synapomorphy supporting a sister group relationship between these two species. On the other hand, the shape and position of the sub-basal process of S. guatopo indicated that this structure could be regarded as homologous with the lamellar expansion found in the conductor of the pennai group (Bonaldo et al., 2014, figs 290-297). If so, the sub-basal process in S. kartabo sp. nov., S. bodanus and S. guyanensis would either be lost or represented as a conspicuous, elongated sclerotized strip running in parallel to the distal hyaline portion of the conductor (Figs 15-18, black arrows; Bonaldo et al., 2014, fig. 240). We favor the homology of the sub-basal process of S. guatopo and the sclerotized strip of the remaining species because both structures are inserted in the same unsclerotized area of the conductor base. Besides, the hypothesis of non-homology of these structures would require an instance of loss of the stout process as well as an instance of gain of the sclerotized strip in S. kartabo sp. nov., S. bodanus and S. guyanensis. If our homology assumptions are correct, the stout condition in S. guatopo could be regarded as symplesiomorphic, leading to the recognition of a monophyletic group composed by the three species in the bodanus group that share the sclerotized strip condition.  : abdomen: 9, dorsal; 10, lateral; 11, ventral; palp: 12, prolateral; 13, dorsal; 14, retrolateral; distal portion of the palp: 15, retro-ventral; Simlops bodanus (Chickering, 1968): 16, distal portion of palp, retrolateral. Simlops guyanensis Santos, 2014: 17, distal portion of palp, retrolateral. Simlops guatopo Brescovit, 2014: 18, distal portion of palp, retroventral. Black arrows: conductor, sub-basal process. White arrows: conductor, needle-like process.