Introduction

The North American harvestman genus Philora Goodnight and Goodnight, 1954 is comprised of 2 remarkable species with scutum completum and low tarsal count 2(1):2(1):4:4 (^{Cruz-López & Francke, 2013b}), characters that are unusual within suborder Laniatores (^{Sharma & Giribet, 2011}). These characters are also present in Sandokanidae, Heteropachylus inexpectabilis (Soares & Soares, 1946) and presumably in Paralola buresi Kratochvíl, 1951 (^{Mendes, 2011}; ^{Sharma & Giribet, 2009}; ^{Ubick, 2007}). The genus Philora was recently revised, rediagnosed and transferred from incertae sedis within Laniatores to the familial assignment in Stygnopsidae (^{Cruz-López & Francke, 2013b}). ^{Cruz-López and Francke (2013b)} also discussed the morphological similarities in male genitalia present in Paramitraceras Pickard-Cambridge, 1905, Philora, and Troglostygnopsis anophthalma Šilhavý, 1974, describing the Paramitraceras-pattern among Stygnopsidae (^{Cruz-López & Francke, 2013b}). Subsequently, ^{Kury and Villarreal (2015)} proposed the first penial setae homology assessment among Gonyleptoidea (^{Kury & Villarreal, 2015}). In that work, the authors described 5 groups of setae based on topological criteria; with respect to Stygnopsidae, these groups were recognized in Hoplobunus boneti (Goodnight & Goodnight, 1942), Karos sp. and the genera with the Paramitraceras-pattern (^{Kury & Villarreal, 2015}). Recently, ^{Cruz-López and Francke (2015)} based on a cladistics analysis, recognized that all members with the Paramitraceras-pattern form a clade, supported by synapomorphies related to characters from the penis, and formally recognized the Paramitraceras genus-group (^{Cruz-López & Francke, 2015}).

Recent collecting trips to the states of Oaxaca and Puebla, Mexico, produced some specimens of 2 epigean and 1 cavernicolous new species of Philora, described in the present work. One of the epigean species and the cavernicolous species show remarkable troglomorphisms, i.e. morphological adaptations associated with life underground, illustrated and discussed below. Additionally, a taxonomic key is provided to identify the 5 known species of Philora.

Materials and methods

The material examined is deposited in the Colección Nacional de Arácnidos (CNAN), UNAM, Mexico. Color images were taken with a Nikon Coolpix S10 VR camera adapted to fit in a Nikon SMZ645 stereoscopic microscope. Drawings were made in Photoshop CS5 software, using assembled photographs to delineate the structures. All plates were edited using the previously mentioned version of Photoshop. Measurements are in mm. External morphology nomenclature was modified from ^{Cruz-López and Francke (2013b)} and ^{Kury (2014)}. Abbreviations: ChH = cheliceral hand height, ScL = scutum length, ScW = scutum width at mesotergal area I. Genitalic nomenclature according to ^{Kury and Villarreal (2015)}. The distribution map was generated using the Mapa Digital de México to desktop software, ver. 6.0.1, using geographic information from WMS service on-line (http://gaia,inegi.org.mx/NLB/mdm5.wms).

Descriptions

Preliminary considerations, genital nomenclature modifications

^{Cruz-López and Francke (2013b)} described the Paramitraceras-pattern, present in at least Paramitraceras, Philora and Troglostygnopsis (Šilhavý, 1974). These authors recognized the position pattern in all macrosetae in pars distalis, named 3 setal groups: dorso-lateral or mesal, laterobasal and ventral microsetae.

^{Kury and Villarreal (2015)} proposed the first hypothesis of homology in macrosetae in Gonyleptoidea. They described 5 setal groups according to topological criteria. Kury & Villarreal identified these groups in Hoplobunus boneti, Karos sp. and the genera with Paramitraceras pattern. According to ^{Kury and Villarreal (2015)}, setal group C is: “short, grouped subapically (as in the Paramitraceras-Troglostygnopsis complex)”, “no common pattern for family is discernible other than the number of 2 pairs C1-C2 and the subdistal insertion.” We adopt herein the hypothesis and nomenclature of Kury & Villarreal, but we consider that setal group C is not recognizable at least in Philora. Group C is easily recognizable in Paramitraceras as a transversal row along the lateral margin of pars distalis, sometimes almost touching E2 setae (^{Cruz-López & Francke, 2012}: figs. 13-15; ^{Cruz-López & Francke, 2013a}: figs. 25-27, 37-39); in Troglostygnopsis these setae are found as a small transversal row of 3 spiniform setae, differing from spatular macrosetae in the A + B groups (^{Cruz-López & Francke, 2013b}: figs. 49, 52). Therefore, in Philora the lateral macrosetae of penis are herein considered as a complex formed by the A + B groups, the 2 ventral pairs conform the E group, and 1 pair of a small D1 setae are present. ^{Cruz-López and Francke (2013b)} showed the small D1 setae in P. quetzalzin (^{Cruz-López & Francke, 2013b}: figs. 28, 31), but they did not describe or mentioned these setae. For the present contribution, a cursory examination of male genitalia of P. tuxtlae exposed the presence of D1 setae, with the same size and position as the other species of the genus described herein.

Philora izel sp. nov. (Figs. 1,2,3,4,5,6)

Diagnosis

This species differs from all others by the presence of the following characters: light orange color (Fig. 1), uniform throughout body and appendages; eyes very reduced and unpigmented; ocularium strong, with the base very wide, anterior face swollen; surface of prosoma posterior to ocularium raised, forming a dome (Fig. 2D).

Description of male holotype. Dorsum: base of ocularium very wide, anterior face swollen, apex forming a small tip, pointing anteriorly. Surface of prosoma posterior to ocularium elevated, forming a dome (Fig. 2D). Eyes very reduced and unpigmented. Prosoma smooth, ocularium covered with few, small, scattered tubercles; mesotergal areas finely granular, with few, small scattered tubercles, stand out on area I (Figs. 2, 5A). Venter: all surface covered by tubercles, on coxae I and II with long spiniform setiferous tubercles; 4 setiferous tubercles on stigmatic area, blunt and contiguous, just behind coxa IV (Fig. 5B). Chelicera: basichelicerite short, bulla well marked with distinct constriction, with 2 acute spiniform teeth, 1 dorso-apical and 1 ventral, just behind notch of bulla; cheliceral hand slightly swollen medially, with 4 spiniform tubercles and few spiniform setae on frontal side; cheliceral fingers: fixed finger with 3 blunt teeth, decreasing in size toward the apical portion, movable finger with basal serrula and 2 small teeth in the middle (Fig. 2A, B). Pedipalp: femur hardly convex dorsally, mesal face feebly concave, ventral face reduced, basally with 2 large setiferous tubercles, these tubercles with strong spiniform sockets, and small sub-apical seta; patella cylindrical, without noticeable ornamentation; tibia quadrangular in cross-section, internal face slightly concave, with rounded projection at the base of ectal border, both edges with 4 setiferous tubercles, similar to those ventrally on femur; tarsus tapering distally, with 3 setiferous tubercles each on ectal and mesal edges (Fig. 3). Male genitalia: lateral margins of pars distalis rolled dorsally, apical margin with 2 paramedian lobes pointed dorsally. 9 pairs of macrosetae A + B forming 2 irregular row across the lateral margin of pars distalis, latero-basally to glans. D1 setae not visible. Setae E ventral subapically, E1 slightly above of E2. Lobes of dorsal bilobular proyection with dotted apices (Fig. 6).

Female. Unknown.

Distribution. Known only from the type locality (Fig. 19).

Taxonomic summary

Type data: male holotype (CNAN-T0939) from Cerro Caballero (18°08′32.28″ N, 96°42′57.491″ W), municipio de San José Tenango, Oaxaca, Mexico. April 10-2014 (O. Francke, J. Cruz, G. Contreras, J. Mendoza, A. Guzmán and S. Davlañtes coll.).

Etymology. Specific name feminine adjetive, from the Nahuatl word “izel”, meaning unique, remarkable; alluding to the unusual troglomorphisms exhibited by this presumably epigean species.

Philora mazateca sp. nov. (Figs. 7,8,9,10,11,12)

Diagnosis

This species is easily recognizable from P. izel sp. nov. and P. nympha sp. nov. by the mostly bicolored body, light brown background with the reticular pattern around the margin of the scutum, central portion of mesotergal areas and on prosoma, and the ocularium very dark, almost black (Fig. 7). This species differs from P. quetzalzin in that the base of ocularium is not widened on P. mazateca, the surface of prosoma posterior to ocularium is not raised, and the dorsum is finely granular, with few scattered blunt tubercles on areas V-VII (Fig. 11A). It differs from P. tuxtlae in following characters: dorso-apical tubercle on metatarsus IV sub-distally rather than apically (Fig. 10F), movable cheliceral finger with small teeth rather than almost smooth (Fig. 8A) and number of macrosetae on penis.

Description of male holotype. Dorsum: ocularium conical, base elliptical, apex forming a blunt tip pointing forward; surface of prosoma posterior to ocularium not elevated. Eyes well pigmented and marked (Fig. 8). Prosoma and ocularium smooth, mesotergal areas finely granular, with blunt scattered tubercles in central portion of areas V-VIII (Fig. 11A). Venter: covered by small scattered tubercles, coxae I and II with small setiferous tubercles; 3 setiferous tubercles on stigmatic area, blunt and contiguous, just behind coxa IV (Fig. 11B). Chelicera: basichelicerite short, bulla well marked, with distinct constriction, with 2 spiniform teeth, the dorso-apical irregular and the ventral 1 slightly distal from the notch of bulla, blunt; cheliceral hand with 4 frontal setiferous tubercles, the apical bigger, also covered by some spiniform setae; fixed finger with 3 middle teeth, blunt and contiguous, basally with small teeth and inconspicuous notches; movable finger with 2 small and contiguous median teeth, and 1 median notch, slightly distal to the teeth (Fig. 8A, B). Pedipalp: femur convex dorsally, mesal face concave, ventral area reduced, with 3 large spiniform setiferous tubercles, the 2 apical tubercles contiguous at their bases; patella cylindrical, unarmed; tibia sub-quadrangular in cross-section, with the internal face concave, ectal edge with 3 setiferous tubercles, mesal with 2, in both edges similar to those ventrally on femur; tarsus tapering distally, with 3 setiferous tubercles on each edge (Fig. 9). Male genitalia: paramedian lobes of apical margin long and rounded, pointed dorsally. Apical margin concave. 7-8 setae A + B forming an irregular group, 3-4 of them surrounding small D1 setae, the remaining in the base of pars distalis. Setae E subapically, both pairs noticeably separated between them, E1 slightly above of E2. Lobes of dorsal bilobular proyection wide, with dotted apices (Fig. 12).

Female paratype. Very similar to male, recognizable only by the absence of 4 ventral light-colored pointed areas (^{Cruz-López & Francke, 2013b}).

Distribution. Known only from the type locality and 1 nearby locality (Fig. 19).

Taxonomic summary

Type data: male holotype (CNAN-T0940) 600 m from Pozo de Águila (18°11′51.792″ N, 96°40′36.552″ W), Municipio de San José Tenango, Oaxaca, Mexico. April 11-2014 (O. Francke, J. Cruz, G. Contreras, J. Mendoza, A. Guzmán and S. Davlañtes coll.). 3 female and 1 juvenile paratypes (CNAN-T0941) same data as holotype.

Other material examined: female DNA voucher (DNA-Op0046) from Cerro Caballero (18°08′8.88” N, 96°41′22.92″ W), Municipio de San José Tenango, Oaxaca, Mexico. September 30-2008 (J. Cruz coll.).

Etymology. The specific name is feminine, a noun used in apposition, derived from the Spanish word “mazateca”, a demonym which refers to the Mexican ethnic group that lives in the region of the type locality.

Philora nympha sp. nov. (Figs. 13,14,15,16,17,18)

Diagnosis

This species is easily recognizable from all the other members of the genus by the following characters: general pale white color throughout body and appendages (Fig. 13); basichelicerite, pedipalp, pedipalpal armature and legs very long (Figs. 14,15,16), femur IV >3.4 mm, tarsus II >2.90 mm.

Description of male holotype. Dorsum: ocularium conical, elongated and finely acute in the apex, pointing dorsally; surface of prosoma posterior to ocularium slightly elevated; eyes well marked and pigmented; prosoma and ocularium smooth, mesotergal areas finely granular, with a central row of small setiferous tubercles on areas II-VII (Figs. 14C, D, 17A). Venter: covered by small scattered tubercles; coxae I and II with long, spiniform setiferous tubercles, these tubercles with the apical setae very long; with 3 setiferous tubercles behind coxa IV, 2 of them very wide and fused, giving blunt dome appearance (Fig. 17B). Chelicera: basichelicerite elongated, bulla subtly marked with shallow constriction, extending more than 3 fourths of the basichelicerite length, dorsoapical spiniform tooth small, ventral absent; cheliceral hand covered only with spiniform setae, near the cheliceral fingers; fixed finger with 4 middle teeth, contiguous, central pair more developed; movable finger with small basal tooth, and serrula covering almost entire length (Fig. 14A, B). Pedipalp: femur quadrangular in cross-section, ventrally with 4 small setiferous tubercles, scattered along the entire length; patella without remarkable ornamentation; tibia quadrangular in cross-section, mesal edge with 3 spiniform setiferous tubercles, ectal with 4; tarsus tapering distally, with 4 setiferous tubercles on each edge; all setae of pedipalpal armature inserted apically on the tubercle, rather than subdistally (Fig. 15). Male genitalia: paramedian lobes acute apically, pointed dorso-internally. With 11-12 A + B setae, forming 2 longitudinal rows, the dorsal row along the lateral margin, the ventral row from the base of pars distalis to ventral position, below to E setae. D1 setae long, in the inner side of lateral margin. E1 setae slightly apical to E2. Lobes of dorsal bilobular projection triangular shape, with dotted apices (Fig. 18).

Female paratype. Very similar to male, barely distinguishable by the absence of 4 ventral light-colored pointed areas (^{Cruz-López & Francke, 2013b}).

Distribution. Known only from the type locality (Fig. 19).

Taxonomic summary

Type data: male holotype (CNAN-T0942) from Chupa Cave (18°18′55.728″ N, 96°52′4.908″ W), Municipio de Tequixtepec, Puebla, Mexico. March 12-2014 (L. Bouchard, M. Archambault coll.). 2 female paratypes (CNAN-T0943) with same data as holotype.

Etymology. Specific name is feminine, a noun in apposition derived from the Greek word “υύμφα” (nymph), in reference to minor divinities in Greco-Roman culture and often represented as beautiful maidens. It was believed that they sometimes lived inside caves.

Discussion

The epigean species P. quetzalzin, P. mazateca and P. tuxtlae have the cryptic coloration of the body, with background color brown with darks areas. This color pattern plus thanatotic behavior suggest specific habits to life in leaf litter, which is where these species have been retrieved from (^{Cruz-López & Francke, 2013b}). On the other hand, P. izel exhibits light orange color, uniform in all body and appendages, and reduced and unpigmented eyes, characters usually correlated with cavernicolous habits (^{Christiansen, 2012}), even though the single known specimen was collected on the surface under a large rock and not inside a cave. However, it is known that some epigean species of harvestmen exhibit light color body, eye reduced or lost, and occasionally legs elongation (^{González-Sponga, 1997}; ^{Kauri, 1989}; ^{Pérez-González & Kury, 2007}; ^{Pinto-da-Rocha & Kury, 2003}). These characters have been associated to the specific ecological niche of these species, which might have similar light and humidity conditions to those found in caves, although this hypothesis has not been tested.

Even though P. izel and P. mazateca are from the same type locality, the specimens of P. mazateca were collected by sifting leaf litter, a technique previosly used to collect epigean P. tuxtlae (^{Cruz-López & Francke, 2013b}). The holotype of P. izel was found by chance inside a small pit in a deeply buried rock, similar micro-habitat to that of the ricinuleid Pseudocellus cruzlopezi ^{Valdez-Mondragón & Francke, 2013} (^{Valdez-Mondragón & Francke, 2013}). Further studies are needed to determine if the “troglomorphisms” in P. izel are due to environmental conditions of its particular ecological niche, or perhaps the male wandered outside a hidden cave through a small crevice in search of mates.

The cavernicolous P. nympha exhibits typical troglomorphic characters: pale color and remarkably long legs, and incredibly delineated and pigmented eyes. The type specimens were found walking in the walls of cave (collectors label) so that, the long legs could represent an adaptative change from inhabiting leaf litter to a wandering habit inside the cave.