Ummidiinae Ortiz, 2007

Decae, Arthur E., Schwendinger, Peter J. & Hongpadharakiree, Komsan, 2021, Descriptions of four new trapdoor spider species in the subfamily Ummidiinae from Thailand (Araneae, Mygalomorphae, Halonoproctidae), Zootaxa 4984 (1), pp. 300-323 : 301-303

publication ID

https://doi.org/ 10.11646/zootaxa.4984.1.22

publication LSID

lsid:zoobank.org:pub:26314FBC-18A7-4EBA-B0CF-5ADD5B03F5FD

DOI

https://doi.org/10.5281/zenodo.5205977

persistent identifier

https://treatment.plazi.org/id/FB3B8783-2520-FFBF-FF7E-FB44FF37F976

treatment provided by

Plazi

scientific name

Ummidiinae Ortiz, 2007
status

 

Ummidiinae Ortiz, 2007

Pachilomerinae Simon 1889: 178–179 (sub Pachylomeri; type genus Pachylomerus Ausserer, 1871 ).

Notes. On grounds of preoccupation replaced with Pachilomerides Strand, 1934, now considered a junior synonym of Ummidia Thorell, 1875 ( Ortiz 2007) . For a detailed review of the nomenclatural history see Cameron (2005).

Diagnosis. Ummidiinae are readily distinguished from Halonoproctinae by the presence of clavate dorsal trichobothria on the tarsi of legs and palps ( Decae 2010: fig. 1), by the fused, folium-shaped central sternal sigilla, and by the absence of lateral sternal sigilla ( Figs 2 View FIGURES 2 D−F).

Description. Ummidiinae are medium-sized trapdoor spiders. Total body lengths in a sample containing representatives from all three genera ( Ummidia , Conothele , Latouchia ) show lengths of females ranging from 7.3 to 26.9 (n = 45) and lengths of males ranging from 8.9 to 16.6 (n = 23). Prosoma: Carapace of females and juveniles longer than wide (average CW/CL = 0.87, SD = 0.05, n = 45), surface smooth, shining as if polished, bristles sparse or absent; cephalic part strongly elevated, with or without a depression behind eye group; all eyes on a distinct ocular tubercle near anterior margin of carapace; fovea deep, strongly procurved. Carapace of males rounded in dorsal view, slightly longer than wide (average CW/CL = 0.94, SD = 0.04, n = 23), surface dull, coriaceous; cephalic part slightly or strongly elevated, bristles, eye group and fovea as in females. Eye group wider than long (EL/PR ranging between 0.5 and 0.6 in 24 species representing all three genera); arrangement of eyes, relative eye sizes and distances between eyes variable between species and species groups. Chelicerae with apical rastellum on proximal article; cheliceral furrow with rows of teeth on both sides; fangs with smooth or serrated ventral keel. Palpal coxa with cuspules compactly grouped or scattered in proximal half; prolateral-distal lobe small, rounded or absent. Labium semi-dome-shaped, proximally wider than long, with or without cuspules. Sternum longer than wide, with diagnostic fused and folium-shaped central sigilla. Palps of females and juveniles leg-like, with dense bands of curvy spines along lateral sides of tarsi and tibiae, ventral and dorsal spines absent, few clavate trichobothria on dorsal side of tarsi, claws with a strong proximal tooth; palps of males with aspinose cymbium and with clavate dorsal trichobothria. Legs: Posterior legs stronger than anterior ones; dense bands of mainly curvy spines along lateral sides of tarsi, metatarsi and tibiae of anterior legs, males with straight spines arranged in compact groups on leg III and rarely on leg IV; scopulae ventrally on leg tarsi in males (absent in females), scopulae on anterior tarsi more strongly developed than on posterior tarsi, scopulae generally absent on leg IV; no apophyses, spurs or clasping hooks (as found in males of some Halonoproctinae , i.e. Hebestatis and Bothriocyrtum ) present; leg III very stout in females and juveniles, less so in males, variable in shape between genera and species groups; tibia III of Ummidia and Conothele more than half as long as femur III (average TibIII/FemIII = 0.6, n = 30), and with a glabrous, strongly sclerotized saddle-shaped depression situated between two unpigmented crescent-shaped zones (here further referred to as ‘saddle crescents’) dorsally on tibia III ( Figs 3A–B View FIGURES 3 ), and with a conical prodorsal protuberance on trochanter III ( Figs 3 View FIGURES 3 D−E); tibia III of Latouchia shorter than half the length of femur III (average TibIII/FemIII = 0.4, n = 17), saddle-shaped depression, saddle crescents and trochanter protuberance usually absent ( Figs 3C, F View FIGURES 3 ), however, the Latouchia species described in here have a more or less distinctly pronounced proximal constriction of tibia III (here referred to as ‘demi-saddle’) suggesting an intermediate evolutionary stage between lineages with a fully developed saddle ( Ummidia and Conothele ) and those without saddle or constriction ( Fig. 3C View FIGURES 3 cf. Figs 9 View FIGURES 9 B−C, 11B−C) (in Latouchia sensu stricto, as represented by the type species of the genus, L. fossoria , tibia III is cylindrical, without a constriction; Decae & Caranhac 2020: fig. 3); leg IV being the longest leg, with or without dense concentration of short spines on dorsal side of patella in females. Tarsal claws: PTC with one or few large proximal teeth with or without small auxiliary teeth; 3 rd claw smooth. Spine patterns: sexually dimorphic, spines in males mostly spread out over articles of legs and palps, in females mostly tightly grouped; location, presence or absence of spines and spine-groups presumably of diagnostic value at genus or species level. Opisthosoma soft, ovoid, dorsal surface with or without small wart-shaped bristle sockets. Spinnerets very short, PMS with distinct apical spigot field, PLS composed of three articles with or without macro-spigots. Genital organs: spermathecae in Ummidia and Conothele typically tripartite, with membranous, tube-shaped proximal part, sclerotized median part, and membranous, globular distal part ( Figs 5 View FIGURES 5 F−K, 7F−H); spermathecae in Latouchia are either monopartite or bipartite ( Ono 2010: fig. 21; Decae 2019: figs 18, 38, 39, 46, 47; Decae & Caranhac 2020: figs 11, 26), ranging from simple membranous columnar or knob-shaped structures to more complex racemose structures with clusters of vesicles ( Figs 9 View FIGURES 9 E−J, 11E−L; palpal organs in Ummidia , Conothele and most Latouchia species proximally pyriform, with an elongated, usually sharply pointed embolus ( Figs 4 View FIGURES 4 H−L, 6H−L, 8F−J, 10F−J); emboli in Ummidia and Conothele very slender and more or less flexible ( Figs 4 View FIGURES 4 H−K, 6H−K), in Latouchia stronger and more sturdy ( Figs 8 View FIGURES 8 F−I, 10F−I).

Sexual dimorphism. As in most fossorial mygalomorph spiders, sexual dimorphism in Ummidiinae is very pronounced. Females and juveniles are sturdy, short-legged spiders. Males, in contrast, are more long-legged. The differences reflect morphological adaptations to markedly different ways of life: females and juveniles of both sexes are sedentary burrow dwellers, whereas adult males abandon their burrows and roam in search for mates.

Taxonomy. In the current taxonomical system the Ummidiinae are recognized as a subfamily within the family Halonoproctidae ( Pocock 1903) . Recent phylogenetic analyses have indicated that the Halonoproctidae constitute a monophyletic family-level unit distinct from the family Ctenizidae in which it had formerly been included. The Halonoproctidae were redefined to include the subfamilies Halonoproctinae (genera Bothriocyrtum Simon, 1891b ; Hebestatis Simon, 1903 ; Cyclocosmia Ausserer, 1871 ) and Ummidiinae (genera Ummidia , Conothele , Latouchia ) ( Godwin et al. 2018).

Included genera. Ummidia Thorell, 1875 ; Conothele Thorell, 1878 ; Latouchia Pocock, 1901 ( Godwin et al. 2018).

Kingdom

Animalia

Phylum

Arthropoda

Class

Arachnida

Order

Araneae

Family

Halonoproctidae

Loc

Ummidiinae Ortiz, 2007

Decae, Arthur E., Schwendinger, Peter J. & Hongpadharakiree, Komsan 2021
2021
Loc

Pachylomerus

Ausserer 1871
1871
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