Xim trenzado, Ibarra-Núñez & Chamé-Vázquez & Maya-Morales, 2021

Ibarra-Núñez, Guillermo, Chamé-Vázquez, David & Maya-Morales, Julieta, 2021, A new spider genus (Araneae: Linyphiidae: Erigoninae) from a tropical montane cloud forest of Mexico, European Journal of Taxonomy 731, pp. 97-116 : 102-110

publication ID

https://doi.org/ 10.5852/ejt.2021.731.1207

publication LSID

lsid:zoobank.org:pub:0EFF0D93-EF7D-4943-BEBF-995E25D34544

DOI

https://doi.org/10.5281/zenodo.4452622

persistent identifier

https://treatment.plazi.org/id/0386965E-2C31-FFE1-711C-FAFC0937D3C6

treatment provided by

Plazi

scientific name

Xim trenzado
status

gen. et sp. nov.

Xim trenzado View in CoL gen. et sp. nov.

urn:lsid:zoobank.org:act:62BE28C7-8A47-4053-B6CD-EA2F7E5EA83B

Figs 1–5 View Fig View Fig View Fig View Fig View Fig

Diagnosis

Monotypic genus, see genus diagnosis.

Etymology

The specific epithet is a noun in apposition taken from the Spanish word meaning ‘braided’, referring to the interweaved macrosetae on the femur I of the male.

Type material

Holotype MEXICO • ♁; Chiapas, Municipio de Unión Juárez, Ejido Talquián ; 15°05′15″ N, 92°05′56″ W; 2010 m a.s.l.; 4 Mar. 2009; Maya, Ibarra, López and Sentíes leg.; tropical montane cloud forest, in low understory; beating; ECOTAAR-005030 . GoogleMaps

Allotype

MEXICO • ♀; same collection data as for holotype; ECOTAAR-005030 . GoogleMaps

Paratypes MEXICO • 1 ♂, 1 ♀; same collection data as for holotype; 22 Jan. 2009; Maya, Ibarra, López and Sentíes leg.; ECOTAAR-004936 GoogleMaps 1 ♂, 1 ♀; same collection data as for preceding; AMNH GoogleMaps 1 ♂, 1 ♀; same collection data as for preceding; 4 Feb. 2009; CNAN GoogleMaps 1 ♂, 1 ♀; same collection data as for preceding; CAS GoogleMaps 1 ♂, 1 ♀; same collection data as for preceding; 18 Mar. 2009; MNHN AR16055 GoogleMaps 1 ♂, 1 ♀; same collection data as for preceding; MACN GoogleMaps 1 ♂, 1 ♀; same collection data as for preceding; 1 Apr. 2009; USNM GoogleMaps 1 ♂, 1 ♀; same collection data as for preceding; 15 Jul. 2009; Maya, Ibarra and López leg.; ZMB Arach 49468 GoogleMaps .

Other material

MEXICO • 2 ♂♂, 8 ♀♀, 1 subadult ♂, 1 subadult ♀, 1 juv.; Chiapas, Municipio de Unión Juárez, Ejido Talquián ; 15°05′15″ N, 92°05′56″ W; 2010 m a.s.l.; 22 Jan. 2009; Maya, Ibarra, López and Sentíes leg.; tropical montane cloud forest, in low understory; beating; ECOTAAR-004937 GoogleMaps 1 ♂; same collection data as for preceding; 4 Feb. 2009; ECOTAAR-004950 GoogleMaps 1 ♀, 2 juvs; same collection data as for preceding; ECOTAAR-004949 GoogleMaps 6 ♂♂, 6 ♀♀, 1 subadult ♂, 2 juvs; same collection data as for preceding; ECOTAAR-004952 GoogleMaps 6 ♂♂, 7 ♀♀, 5 subadult ♂♂; same collection data as for preceding; ECOTAAR-004974 GoogleMaps 2 ♂♂, 6 ♀♀, 2 subadult ♂♂, 1 subadult ♀, 2 juvs; same collection data as for preceding; 4 Mar. 2009; ECOTAAR-005029 GoogleMaps 1 ♀; same collection data as for preceding; 18 Mar. 2009; ECOTAAR-005063 GoogleMaps 6 ♂♂, 2 ♀♀, 2 subadult ♂♂; same collection data as for preceding; 1 Apr. 2009; ECOTAAR-005177 GoogleMaps 1 ♀; same collection data as for preceding; ECOTAAR-005183 GoogleMaps 1 ♀; same collection data as for preceding; 12 Aug. 2009; Maya, Ibarra, López and Chamé leg.; ECOTAAR-005435 GoogleMaps 1 ♂; same collection data as for preceding; hand collecting; ECOTAAR-005438 GoogleMaps 1 ♂; same collection data as for preceding; 15°05′38″ N, 92°06′06″ W; 2044 m a.s.l.; 5 Feb. 2009; beating; ECOTAAR-004962 GoogleMaps 1 ♀; Chiapas, Municipio de Motozintla, Cerro Boquerón ; 15°13′55″ N, 92°18′22″ W; 2332 m a.s.l.; 27 Feb. 2015; Campuzano, Montaño and Moreno leg.; tropical montane cloud forest, in low understory; beating; ECOTAAR-011462 GoogleMaps .

Description

Male HABITUS. Carapace, chelicerae and endites light brown with some suffused grey on thoracic part, labium and sternum brown, distal half of labium light brown. Legs, coxae to femora yellow-cream with distal half of femur I and II light-brown, tibiae to tarsi yellow brown. Opisthosoma light brown with sparse yellow spots and slender yellow chevrons on the rear half of dorsum ( Fig. 1 View Fig A–C, G).

MEASUREMENTS. Total length 1.68. Carapace 0.71 long, 0.59 wide.

PROSOMA. Carapace with conical post-ocular lobe, about as high as clypeus in lateral view, apex crowned with few hairs. Eye diameters and interdistances: AME 0.039, ALE 0.052, PME 0.039, PLE 0.039, AME–AME 0.026, AME–ALE 0.065, PME–PME 0.065, PME–PLE 0.065; AER in frontal view almost straight, slightly recurved, PER in dorsal view almost straight, slightly recurved. Clypeus 0.13 high with few short setae below AME. Chelicerae with five promarginal ( Fig. 1G View Fig ) and four retromarginal teeth; lateral face of chelicerae with scaly striae, widely and evenly spaced. Sternum 0.40 long, 0.44 width, produced between coxae IV posterior tip truncated; coxae IV 1.4 times their width apart ( Fig. 1C View Fig ).

OPISTHOSOMA. Elliptical, slightly narrowed towards posterior end ( Fig. 1 View Fig A–C).

LEGS. Femur I with distal half modified, bent ventrad, prolaterally enlarged, with hemispherical bulge about three quarters from femur base ( Figs 1 View Fig A–B, 4A–F). Distal, prolateral side of femur I with two longitudinal, parallel series of conspicuous macrosetae beginning at femoral turn, finishing at base of the hemispherical bulge ( Fig. 4 View Fig A–G). Dorso-lateral series of macrosetae composed of nine, spaced, erect, macrosetae gently curved, ventro-lateral series composed of 18 (17 on right femur I) macrosetae closely spaced, recumbent, strongly curved, interweaved forming a braid ( Fig. 4 View Fig A–G). Tibiae I to II without dorsal macrosetae, tibiae III with one very short, proximal dorsal macroseta, tibiae IV with one short proximal, dorsal macroseta, without distal, dorsal macroseta; metatarsi and tarsi without macrosetae. Leg formula: 1423. Legs measurements: I 2.52 (0.70, 0.21, 0.61, 0.58, 0.42), II 2.36 (0.71, 0.19, 0.57, 0.53, 0.36), III 1.80 (0.56, 0.16, 0.38, 0.43, 0.27), IV 2.49 (0.66, 0.17, 0.56, 0.68, 0.42); TmI 0.40, TmIV absent.

PALPUS. Distal half of femur ventrally slightly enlarged; tibia with conspicuous plate-like, slanting, higher than long, prolateral apophysis pointed in distal corner ( Figs 1B View Fig , 2 View Fig A–D, F–G); with a small, rounded, distal retrolateral apophysis touching paracymbium ( Fig. 2C View Fig , E–F); with one retrolateral trichobothrium ( Figs 2F View Fig , 4I View Fig ), lacking on prolateral side ( Fig.2D View Fig ).Cymbium with deep retrolateral groove wider in proximal part ( Fig. 2C View Fig , F–H), with an elongated, prolateral, basal process touching palpal tibia ( Fig. 2 View Fig A–B, D–E, G) and a large slanted, pointed dorsal process with retrolateral face slightly concave, glabrous from apex till retrolateral cymbial groove, its prolateral face convex and hirsute as most of cymbium ( Figs 1B View Fig , 2A View Fig , C–D, F–H). Alveolus nearly as long as cymbium. ( Figs 2B, E View Fig , 3A View Fig ). Paracymbium large with scale-like papillae, connected to cymbium by a membrane, longer than wide (wider distally), about half as long as cymbium, extended proximally to fit the RTA, distally overlapping proximal part of tegulum and about half of subtegulum, with few small setae near base and tip forming a straight hook touching retrolateral cymbial groove ( Figs 2 View Fig B–C, E–F, 3A). Subtegulum ectal to tegulum. Tegulum elliptical, with scale-like papillae, slightly sclerotized at mesal border, with small membranous protegulum in distal-mesal corner ( Figs 2 View Fig B–C, E–F, H, 3A); sperm duct with tight kink in tegulum ( Fig. 3A View Fig ). Suprategulum curved, continuous with tegulum, visible on prolateral side of alveolus, touching the cymbium, distally turned retrolaterally and ending in a short distal suprategular apophysis, concealed in ventral view by embolic membrane and distal part of protegulum. ( Figs 2 View Fig A–B, D–E, H–I, 3A–B). Radix as long as cymbium, with a spiral tailpiece and heavily sclerotized distal part with a serrated radical ridge ( Figs 2 View Fig A–B, D–E, H–I, 3B), ending in a short spine-like anterior radical process, at origin (in a slightly closed angle) of a very short, straight, less sclerotized embolus, directed proximally ( Figs 2B, E View Fig , H–I, 3B). Column arising from suprategulum, with embolic membrane developed as an ectal outgrowth from column, both visible among tegulum, tailpiece and radix ( Figs 2E View Fig , H–I, 3B).

Female

HABITUS. Carapace, chelicerae and endites light brown with some suffused grey on thoracic part, a narrow diffuse grey band on border of thoracic part, labium and sternum brown. Legs yellow cream, slightly darker from distal half of femur (I and II) or tibiae (III and IV) to tarsi. Opisthosoma yellow cream on the dorsum with a diffused central longitudinal light brown stripe over the 4/5 anterior part, sides and venter light brown; epigastrium and spinnerets yellow-cream ( Fig. 1 View Fig D–F, H).

MEASUREMENTS. Total length 1.73, carapace 0.75 long, 0.59 wide.

PROSOMA. Carapace similar shape to male, except a lower and rounded post-ocular lobe, about half the clypeus height in lateral view, with few sparse hairs ( Fig. 1E View Fig ). Eye diameters and interdistances: AME 0.052, ALE 0.052, PME 0.039, PLE 0.039, AME–AME 0.026, AME–ALE 0.078, PME–PME 0.052, PME–PLE 0.065; AER in frontal view almost straight, slightly recurved, PER in dorsal view almost straight, slightly recurved. Clypeus 0.143 high. Chelicerae with five promarginal ( Fig. 1H View Fig ) and four retromarginal teeth. Sternum 0.44 long, 0.44 width, produced between coxae IV, posterior tip truncated; coxae IV 1.4 times their width apart ( Fig. 1F View Fig ).

OPISTHOSOMA. Elliptical ( Fig. 1 View Fig D–F). Trachea desmitracheate.

LEGS. Femur I without prolateral macrosetae. Legs I to IV with one proximal, dorsal macrosetae on each tibia (longer than those of male), without distal, dorsal macroseta; metatarsi and tarsi without macrosetae. Leg formula 1423. Legs measurements: I 2.90 (0.82, 0.23, 0.69, 0.69, 0.47), II 2.77 (0.77, 0.21, 0.64, 0.68, 0.47), III 2.18 (0.62, 0.18, 0.43, 0.56, 0.39), IV 2.80 (0.79, 0.19, 0.66, 0.71, 0.45). TmI 0.377, TmIV absent.

EPIGYNUM. With large ventral plate with scattered hairs, with anterior semicircular concavity (ACV) whose rear margin forms a sclerotized border ( Fig. 5A View Fig , G–H). Dorsal plate in ventral view small, rectangular and transverse, occupying only posterior border of epigynum, with a big anterior lobe, flush with ventral plate, ovoid and slightly wider than long, with a narrowing forming a neck at the level of anterior end of copulatory opening slits, where the anterior lobe joins the ventral plate ( Fig. 5 View Fig A–B, G). Ventral and dorsal plates slightly darker than venter; anterior lobe of dorsal plate yellow-whitish, membranous in appearance ( Figs 1F View Fig , 5G View Fig ). Copulatory openings as narrow slits between ventral plate and anterior lobe of dorsal plate ( Fig. 5 View Fig A–B, G). Spermathecae visible ventrally through integument ( Figs 1F View Fig , 5G View Fig ). In dorsal view, copulatory duct wide and very short, connected to an asymmetrical, u-shaped, oblong spermatheca with one mesal and one ectal branch, both branches of spermatheca anteriorly directed, ectal branch longer and larger than mesal one, which is almost round ( Fig. 5 View Fig C–F, H). Spermathecae covered by numerous small glandular pores, with bigger pores in base of ectal branch ( Fig. 5 View Fig C–F). Fertilization duct barely visible, arising from postero-mesal part of ectal branch and posteriorly oriented ( Fig. 5H View Fig ).

Subadult morphology

Subadult males show enlarged palpal cymbium, palpal tibia with a dorsal protuberance corresponding, in position and shape, to forthcoming prolateral apophysis; carapace with a low post-ocular conical lobe, similar in height to that of adult females; femur I with distal half enlarged and bent to ventral side (less than in adult males), with one series of 9–10 prolateral recumbent macrosetae pointing distally (not interweaved among them), and some subadult males with another series of 2–3 macrosetae located dorsally to first series. In subadult females, carapace shows the post-ocular area slightly higher than the ocular area, and the epigastrium slightly swollen.

Variation

Males (n = 6). Same color pattern as holotype. Total length 1.49–1.68. Carapace 0.67–0.73 long, 0.56– 0.60 wide, clypeus 0.12–0.16 high. AME diameter 0.039 –0.052, ALE 0.039 –0.052, PME 0.033 –0.039, PLE 0.033 –0.039, AME separation 0.026 –0.039, AME–ALE separation 0.052 –0.078, PME separation 0.052 –0.078, PME–PLE separation 0.065 –0.078. Sternum 0.38–0.51 long, 0.41–0.52 wide. Coxae IV separation 0.13–0.19. Leg total length: I 2.34–2.57, II 2.27–2.57, III 1.75–2.00, IV 2.31–2.62. Females (n = 6). Same color pattern as allotype. Total length 1.57–1.91. Carapace 0.67–0.76 long, 0.57–0.62 wide, clypeus 0.10–0.17 high. AME diameter 0.039 –0.052, ALE 0.039 –0.052, PME 0.039 –0.039, PLE 0.039 –0.039, AME separation 0.013 –0.039, AME–ALE separation 0.052 –0.078, PME separation 0.052 –0.065, PME–PLE separation 0.052 –0.078. Sternum 0.40–0.44 long, 0.43–0.48 wide. Coxae IV separation 0.14–0.21. Leg total length: I 2.61–290, II 2.48–2.75, III 1.97–2.29, IV 2.55–2.84.

Distribution and ecology

Known only from a small area in the south of Chiapas State, Mexico, the type locality and from Cerro Boquerón, Municipio de Motozintla. One male and one female of this species were collected for the first time by pitfall trap (in January and March 2007, respectively) in a year-round sampling for soil spiders in the type locality. Two years later (2009), when sampling the understory vegetation in the same locality, numerous specimens of both sexes were collected by beating low understory, showing that this species is associated normally to low understory vegetation and was found accidentally on the soil in 2007 ( Ibarra-Núñez et al. 2011; Maya-Morales et al. 2012; cited as “ Erigoninae sp1”). They were collected from January to August but were more abundant during the dry and cold season (January to beginning of March), when adult numbers were about twice that of juveniles. Human disturbances also affect negatively the abundance of this species ( Maya-Morales et al. 2012). Other surveys for spiders were made later in three other cloud forests in the same mountain range (Sierra Madre de Chiapas), but only one female of this species was collected in the nearest of the three studied localities (Cerro Boquerón, 27 km distance from the type locality, by beating low understory). This makes Xim trenzado gen. et sp. nov. a micro-endemic species, and consequently highly vulnerable to habitat destruction.

Remarks

In the ventral plate of the epigynum of Xim trenzado gen. et sp. nov., the anterior semicircular concavity ( Fig. 5A, G View Fig ) is very similar to that of Tutaibo velox (Keyserling, 1886) as described and illustrated by Miller (2007: 179, fig. 138f).

AMNH

USA, New York, New York, American Museum of Natural History

MACN

Argentina, Buenos Aires, Museo Argentina de Ciencias Naturales

USNM

USA, Washington D.C., National Museum of Natural History, [formerly, United States National Museum]

AMNH

American Museum of Natural History

CAS

California Academy of Sciences

MACN

Museo Argentino de Ciencias Naturales Bernardino Rivadavia

USNM

Smithsonian Institution, National Museum of Natural History

Kingdom

Animalia

Phylum

Arthropoda

Class

Arachnida

Order

Araneae

Family

Linyphiidae

Genus

Xim

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