Arnapa Huber

Huber, Bernhard A. & Carvalho, Leonardo S., 2019, Filling the gaps: descriptions of unnamed species included in the latest molecular phylogeny of Pholcidae (Araneae), Zootaxa 4546 (1), pp. 1-96: 15-16

publication ID

https://doi.org/10.11646/zootaxa.4546.1.1

publication LSID

lsid:zoobank.org:pub:D2C9F49A-9B76-40AE-9A60-CAE9B99BA547

persistent identifier

http://treatment.plazi.org/id/E21587DB-FF96-FFDB-FF11-FB614E9EF9D5

treatment provided by

Plazi

scientific name

Arnapa Huber
status

gen. n.

Arnapa Huber  gen. n.

Type species. Arnapa arfak  sp. n.

Etymology. The genus is named for West Papuan cultural leader and musician Arnold Ap (1946–1984); gender feminine.

Diagnosis. Distinguished from similar Southeast Asian and Australian Arteminae  ( Wugigarra  , Holocneminus  , Trichocyclus  ) by the combination of: (1) male palpal tarsus dorsally with whitish area (e.g., Huber 2001: figs 201, 248, 265; absent in Wugigarra  ); (2) genital bulb without worm-shaped process (present in Wugigarra  and some Holocneminus  ; e.g., Huber 2001: figs 16, 24); (3) legs with curved hairs (absent in Trichocyclus  ); (4) genital bulb without transparent dorsal process (present in most Trichocyclus  , e.g., Huber 2001: figs 191, 203, 252); (5) ALS with only two spigots each ( Figs 96, 97View FIGURES 90–97; 8–9View FIGURES 7–12 spigots in Holocneminus  and Trichocyclus  ; e.g. Huber 2001: figs 195, 209, 224); (6) male clypeus unmodified or with round median process (pair of strong horns in Holocneminus  ; e.g., Deeleman-Reinhold 1995: fig. 2; Beatty et al. 2008: fig. 7); (7) carapace with median and lateral dark bands ( Figs 39–44View FIGURES 39–44; three pairs of marks in most Holocneminus  and Trichocyclus  ; e.g. Huber 2001: fig. 187; Deeleman- Reinhold 1995: fig. 1; Beatty et al. 2008: fig. 34); (8) female chelicerae without stridulatory ridges ( Fig. 92View FIGURES 90–97; present and distinct in Wugigarra  and Holocneminus  ; e.g. Huber 2011: figs 45, 139); (9) epigynum without light median projection ( Figs 75, 78View FIGURES 75–80, 81, 84, 87View FIGURES 81–89; present in Trichocyclus  ; e.g. Huber 2001: figs 200, 213, 240).

Description. Male. MEASUREMENTS. Total body length 2.0–2.3, carapace width 0.9–1.1. Leg 1: ~25–35, tibia 1: 4.9–8.0; tibia 1 L/d: ~70–100. Distance PME-PME 75–110 µm, diameter PME 80–110 µm, distance PME- ALE 60–120 µm, distance AME-AME 15–20 µm, diameter AME 40–50 µm.

COLOR. In general ochre to brown ( Figs 39, 41, 43View FIGURES 39–44). Carapace with dark brown median and lateral marginal bands, never with three pairs of dark marks. Clypeus with pair of brown bands. Legs usually with dark rings on femora subdistally, patellae + tibiae proximally, and tibiae subdistally; tips of femora and tibiae whitish. Abdomen always with dark marks and sometimes also white marks dorsally and laterally; ventrally with dark mark behind gonopore.

BODY. Habitus as in Figs 39, 41, 43View FIGURES 39–44. All eyes on raised ocular area. Carapace with distinct median furrow, without pit. Clypeus unmodified or slightly more prominent than in females, only in A. tinoor  with rounded median projection ( Fig. 68View FIGURES 65–69). Chelicerae with cone-shaped apophyses in species-specific arrangement, always with distinct stridulatory ridges. Gonopore without epiandrous spigots ( Fig. 101View FIGURES 98–104). ALS with one strongly widened and one long pointed spigot each ( Fig. 97View FIGURES 90–97); PMS with two spigots each; PLS without spigots.

PALPS. Large relative to body size. Coxa unmodified. Trochanter barely modified or with short ventral projection. Femur strongly widened, with retrolateral process proximally. Patella on ventral side not closed. Retrolateral trichobothrium of tibia in relatively proximal position. Tarsus dorsally with whitish area, with exposed tarsal organ ( Fig. 102View FIGURES 98–104). Procursus with distinct dorsal process, with species-specific distal sclerotized and membranous elements. Bulb with complex and species-specific process carrying sperm duct opening, never with worm-shaped process.

LEGS. Without spines; few vertical hairs; with curved hairs, especially on tibiae and metatarsi; retrolateral trichobothrium on tibia 1 at 4–11%; prolateral trichobothrium present on all tibiae; tibia 2 and tibia 4 approximately same length; pseudosegmentation of tarsi distally distinct.

Female. In general similar to male ( Figs 40, 42, 44View FIGURES 39–44) but legs shorter (tibia 1: 3.8–6.7), stridulatory files on chelicerae either absent or very fine. Epigynum with weakly sculptured anterior plate and distinct posterior plate, sometimes with dark median sclerite anteriorly.

Monophyly. The recent molecular phylogeny of Pholcidae ( Eberle et al. 2018)  included four representatives of Arnapa  and a total of 12 representatives of Wugigarra  , Holocneminus  , and Trichocyclus  . Arnapa  was recovered with maximum support, but there is no obvious morphological character that is likely to provide a synapomorphy for the genus. The diagnosis above shows that similarities exist with each of the three closely related genera, but in the absence of a comprehensive cladistic analysis it is generally not known which character states are plesiomorphic and which apomorphic.

Generic Relationships. The recent molecular phylogeny of Pholcidae ( Eberle et al. 2018)  supports a close relationship between Arnapa  and three other Southeast Asian and Australian Arteminae  genera ( Wugigarra  , Holocneminus  , Trichocyclus  ). However, relationships among these four genera remain unresolved.

Composition/Diversity. The genus currently includes six species: the five species newly described below, plus Arnapa nigromaculatus ( Kulczyński, 1911)  comb. n. that is newly transferred from Psilochorus  . The latter species originates from Indonesia, West Papua, “Manikion” (~ 1.49°S, 133.94°E). The only known specimen (male holotype) could not be found at the Museum and Institute of Zoology of the Polish Academy of Sciences, Warsaw (W. Wawer, pers. comm. July 2018). Kulczyński’s (1911) reasonably good drawings of the male palp suggest that it is likely to be closely related to the species newly described below but not conspecific with the geographically close A. arfak  , nor with any of the other four species described below.

Several additional species exist in collections (Institut Royal des Sciences Naturelles de Belgique, Brussels; Natural History Museum, London; and Netherlands Centre for Biodiversity Naturalis, Leiden). The Pholcidae  of New Guinea are extremely poorly known and it seems likely that the island is home to many dozen species of this genus.

Distribution. Widely distributed in eastern Indonesia ( Fig. 343View FIGURE 343). Further undescribed species that might belong in this genus are known from the Caroline Islands and from New Guinea east to the Louisiade Archipelago.

Kingdom

Animalia

Phylum

Arthropoda

Class

Arachnida

Order

Araneae

Family

Pholcidae