Research Article |
Corresponding author: Sergei Zonstein ( serzon56@gmail.com ) Academic editor: Shuqiang Li
© 2021 Sergei Zonstein, Yuri M. Marusik.
This is an open access article distributed under the terms of the Creative Commons Attribution License (CC BY 4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Citation:
Zonstein S, Marusik YM (2021) The first Western Palearctic record of Euprosthenops Pocock (Araneae, Pisauridae), with description of a new species from Israel. ZooKeys 1065: 13-27. https://doi.org/10.3897/zookeys.1065.74119
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The primarily Afrotropical genus Euprosthenops Pocock, 1897 is recorded in the Western Palearctic for the first time. A diagnosis and an illustrated description of E. insperatus sp. nov., based on a single male from southern Israel, are provided. Considering the structure of the male palp, the holotype of E. insperatus sp. nov. resembles males of two widespread African species, E. australis Simon, 1898 and E. proximus Lessert, 1916; it differs from them by colouration pattern as well as by the different shapes of the retrolateral tibial apophysis and the palpal sclerites. A short survey of the regional insect and spider genera of the paleotropical origin is also presented.
Afrotropical, Arava Valley, new species, paleotropical, spiders, taxonomy
The spider genus Euprosthenops Pocock, 1897 currently includes nine species and one subspecies distributed within the mainland Sub-Saharan Africa except one species known from India and Pakistan (
SMNH Steinhardt Museum of Natural History, Tel-Aviv, Israel.
Comparative material: Euprosthenops sp. aff. australis Simon, 1898 – 1♂ (
Photographs were taken using an Olympus SZX16 stereomicroscope with a Canon EOS 7D camera and prepared using the Helicon Focus 7.6.2 Pro (http://www.heliconsoft.com). Measurements were taken through the above-mentioned stereomicroscope to an accuracy of 0.01 mm. All measurements are given in millimetres.
ALE anterior lateral eye(s);
AME anterior median eye(s);
PLE posterior lateral eye(s);
PME median lateral eye(s).
Other used abbreviations are explained in the text and in the captions.
Podophthalma bayonianna Brito Capello, 1867, by subsequent designation (
The genus and its characters were comprehensibly described by
According to
Holotype ♂ (SMNH), Israel, Southern District: Arava Valley, Hahal Shezaf 5 km S. Hazeva (Hatseva) Village, 30°43'N, 35°16'E, –120 m (below sea level), 26.03.2006 (S. Zonstein). The spider was collected within the Aqaba–Jordan section of the East African – Syrian rift zone, in a few kilometres to the west from the midline of fault. The holotype specimen is in a relatively good condition, only the left leg III is completely missed being evidently lost prior to sampling and preservation.
The sole male of the new species most closely resembles the males of E. australis and E. proximus in a number of similarly shaped structures: the distal tegular apophysis (Dt), the tegular prolateral projection (Pp), the median apophysis (Ma) and the retrolateral tibial apophysis (Ta). Euprosthenops insperatus sp. nov. differs from these similar species in having relatively longer prolateral tegular projection (length of tegulum/length of projection ratio 1.4 to 1.5 vs. 1.6), in the localization of the embolus origin (posteriorly from posterior edge of distal tegular apophysis vs. anteriorly in E. australis), and in the shape of the distal part of the distal tegular apophysis, as well as by shorter palpal tibia (length/width ratio 1.5 vs. 1.6 to 1.7). Structure of male palp differs in many details from that in E. proximus and E. australis (Figs
Male. Habitus as in Fig.
Euprosthenops insperatus sp. nov., holotype male, structures of left (A, B) and right (C, D) palp A entire palp, retrolateral B palpal tibia and cymbium, dorsal C, D distal palpal tibia and basal embolus close up, retrolateral and ventral. Abbreviations: Co – conductor, Dt – distal tegular process, Ma –– median apophysis, Ta – retrolateral tibial apophysis. Scale bars: 0.5 mm (A, B); 0.2 mm (C, D).
Carapace (Fig.
Ventral pairs of spines on tibiae I–IV: 4, 4, 3, 4, respectively. Paired claws on tarsi I–IV with 6–7 teeth each.
Palp and leg measurements as follows:
Femur | Patella | Tibia | Metatarsus | Tarsus | Total | |
Palp | 2.74 | 0.85 | 0.96 | — | 2.91 | 7.46 |
Leg I | 11.31 | 2.90 | 11.84 | 12.77 | 5.66 | 44.48 |
Leg II | 10.74 | 2.89 | 10.53 | 11.84 | 5.29 | 41.29 |
Leg III | 9.13 | 2.18 | 7.98 | 8.27 | 3.71 | 31.27 |
Leg IV | 11.28 | 2.54 | 11.01 | 11.15 | 4.89 | 40.87 |
Male palp (Figs
Euprosthenops insperatus sp. nov., holotype male (A–D) and E. proximus Lessert, 1916, male (E–G), separated copulatory bulb A, E retrolateral B, F retrodorsal C ventral D, G frontal. Small teeth of embolus are indicated with arrows. Abbreviations: Co – conductor, Dt – distal tegular process, El – embolus loop, Em – embolus, Ma – median apophysis, Pp – prolateral projection, St – subtegulum, Tp – prolateral tegular pouch. Scale bars: 0.2 mm.
Female. Unknown.
From the Latin adjective of the masculine gender “insperatus” for “unforeseen”, alluding to the unexpected discovery of a species belonging to the previously paleotropical genus Euprosthenops in Israel.
Euprosthenops insperatus sp. nov., holotype male (A, C), and males of E. australis Simon, 1898 (B) and E. proximus Lessert, 1916 (D); comparison of copulatory bulbs schematically depicted in the same position. The differences in their structure are indicated with arrows. Abbreviations: Co – conductor, Dt – distal tegular process, Em – embolus, Ma –– median apophysis, Pp – prolateral projection.
Known only from the type locality (Fig.
Distribution of Euprosthenops spp. Records of Afrotropical congeners are presented as circles (localities) and quadrangles (country records) according to numbers: 1 E. australis Simon, 1898 2 E. bayaonianus (Brito Capello, 1867) 3 E. proximus maximus Blandin, 1976 4 E. wuehlischi Roewer, 1955 5 E. biguttatus Roewer, 1955 6 E. proximus proximus Lessert, 1916 7 E. pavesii Lessert, 1928 8 E. schenkeli (Roewer, 1955) 9 E. benoiti Blandin, 1976. Records of Asian E. ellioti (O. Pickard-Cambridge, 1877) and E. insperatus sp. nov. are indicated as triangles (? means questionable record) and diamond, respectively.
Since the 1960s, the territory belonging to the modern Israel is known as the “crossroads” for different plant and animal taxa penetrating the country from the north, south and east (
Regarding the spiders (Araneae), the genus Levymanus Zonstein & Marusik, 2013 (Palpimanidae) originally was established as a monotypic taxon known only from the desert rift zone in south Israel (see
Two widespread paleotropical genera, Calommata Lucas, 1837 (Atypidae) and Cambalida Simon, 1909 (Corinnidae) are represented in Israel by a single species each (
The similar situation is observed in two Afrotropical spider genera. Within eight species of Festucula Simon, 1901 (Salticidae) known from Sub-Saharan Africa, the generotype E. vermiformis Simon, 1901 has been recorded also in Sudan, Egypt and Israel (
A similar disjunct distribution is recorded for the mostly Afrotropical huntsman spider genus Pseudomicrommata Järvi, 1912 (Sparassidae). Here, the distribution of four congeners is restricted to the western, eastern and southern regions of the mainland Africa (Moramand 2015). However, one species, P. mocranica Moramand, Zamani & Jäger, 2019 has been recently found in the Sistan & Baluchistan Province of Iran (see Moramand et al. 2019).
Among the insects (Hexapoda), the distribution of a paleotropical (predominantly, of an Afrotropical) taxon having its northernmost limit in Israel or very close to it can be observed in several insect orders. According to
In the tiger beetle subfamily Cicindelinae (Carabidae), East African Cephalota littorea (Forskål, 1775) spreads northward almost achieving the Egypt-Israeli border at the northwestern coast of the Gulf of Aqaba, while Asian records of Habrodera nylotica (Dejean, 1825) distributed throughout the mainland Africa and recorded also for the Canary Islands, are limited to the Sinai mountains (
Within the weevil family Curculionidae, the paleotropical (and mostly Afrotropical) genus Aorus Schoenherr, 1835 is represented in Israel by A. anthracinus Brancsik, 1898, and this sole Palearctic record is the northernmost point of the genus distribution (
In the mayfly family Baetidae (Ephemeroptera), Cloeon perkinsi Barnard, 1932, previously known only from the western, eastern and southern regions of the mainland Africa, has been very recently found in Yemen, western Saudi Arabia and Israel (
Among the taxa of Diptera, a disjunctive fruit fly genus Hyalotephritis Freidberg, 1979 includes only two species: H. planiscutellata (Becker, 1903), originally described from Egypt and then found in Ethiopia and Israel, and H. complanata (Munro, 1929) known from South and South-Western Africa (
Similar paleotropical relations are also known for some Israeli taxa of moths and butterflies (Lepidoptera). Since description, the tiger moth genus Olepa Watson, 1980 (Erebidae, Arctiinae) has been considered as restricted to South and South-Eastern Asia (see
All the above-noted examples indicate that the disjunctive range of Euprosthenops is only a particular case of a more common pattern. In the future, either E. insperatus sp. nov. itself or related species, could well be found in Egypt, Yemen, Saudi Arabia and other regions of the Middle East. It is possible, however, that for various reasons, the former connections have disappeared and the gap will remain unfilled.
We thank Alireza Zamani (currently at Zoological Museum, the University of Turku) who kindly checked an early version of the manuscript. We also appreciate Dragomir Dimitrov (University of Barcelona, Spain) and Xiaoqi Mi (Tongren University, China) for their constructive comments. Special thanks to Seppo Koponen who arranged our stay in Turku and provided us with the museum facilities. The senior co-author was supported by the Ministry of Absorption, Israel.