on the spider genus meleon wanless (araneae: salticidae)

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On the Spider Genus Meleon Wanless (Araneae: Salticidae) Author(s): D. P. Wijesinghe Reviewed work(s): Source: Journal of the New York Entomological Society, Vol. 102, No. 1 (Jan., 1994), pp. 56-61 Published by: New York Entomological Society Stable URL: http://www.jstor.org/stable/25010052 . Accessed: 10/05/2012 21:19 Your use of the JSTOR archive indicates your acceptance of the Terms & Conditions of Use, available at . http://www.jstor.org/page/info/about/policies/terms.jsp JSTOR is a not-for-profit service that helps scholars, researchers, and students discover, use, and build upon a wide range of content in a trusted digital archive. We use information technology and tools to increase productivity and facilitate new forms of scholarship. For more information about JSTOR, please contact [email protected]. New York Entomological Society is collaborating with JSTOR to digitize, preserve and extend access to Journal of the New York Entomological Society. http://www.jstor.org

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Page 1: On the Spider Genus Meleon Wanless (Araneae: Salticidae)

On the Spider Genus Meleon Wanless (Araneae: Salticidae)Author(s): D. P. WijesingheReviewed work(s):Source: Journal of the New York Entomological Society, Vol. 102, No. 1 (Jan., 1994), pp. 56-61Published by: New York Entomological SocietyStable URL: http://www.jstor.org/stable/25010052 .Accessed: 10/05/2012 21:19

Your use of the JSTOR archive indicates your acceptance of the Terms & Conditions of Use, available at .http://www.jstor.org/page/info/about/policies/terms.jsp

JSTOR is a not-for-profit service that helps scholars, researchers, and students discover, use, and build upon a wide range ofcontent in a trusted digital archive. We use information technology and tools to increase productivity and facilitate new formsof scholarship. For more information about JSTOR, please contact [email protected].

New York Entomological Society is collaborating with JSTOR to digitize, preserve and extend access toJournal of the New York Entomological Society.

http://www.jstor.org

Page 2: On the Spider Genus Meleon Wanless (Araneae: Salticidae)

J. New York Entomol. Soc. 102(1):56-61, 1994

ON THE SPIDER GENUS MELEON WANLESS (ARANEAE: SALTICIDAE)

D. P. WUESINGHE

Department of Entomology, American Museum of Natural History, Central Park West at 79th Street, New York, New York 10024

Abstract. -The genus Meleon Wanless is restricted to three African species: M. guineensis (Berland and Millot), M. solitaria (de Lessert) and M. kenti (de Lessert). Linus guineensis Berland and Millot is removed from the synonymy of M. solitaria and re-established as a valid species. Portia falcifera Wanless is placed in the synonymy of M. solitaria, while a male previously assigned to M. solitaria is considered the male of M. guineensis. Portia oreophila Wanless is placed in the synonymy of Portia madagascarensis Wanless. Meleon madagascarensis and M. russata (Simon) are shown to be misplaced in Meleon.

The genus Meleon, with Portia kenti de Lessert as type species, was established by Wanless (1984) for six species of jumping spiders which had previously been placed

in Portia (Wanless, 1978; Murphy and Murphy, 1983). These species are (after Wanless, 1984:195):

M. falcifera (Wanless)-d Uganda M. kenti (de Lessert)-8Y Angola, Malawi, South Africa M. madagascarensis (Wanless)-a Madagascar M. oreophila (Wanless)-Q Madagascar M. russata (Simon)-Q Madagascar M. solitaria (de Lessert)-aQ Guinea, Ivory Coast, Zaire

According to Wanless (1984:143) "[the] hyaline socket of the palpal tibial apoph yses (sic) is synapomorphic for Meleon." Refering to the same feature Wanless (1984: 187) stated that "the male palps [of Meleon species are] easily recognised by the

membranous socket of the tibial apophyses." A re-examination of Meleon and related taxa (Salticidae: Spartaeinae) reveals that although a membranous or hyaline tibial apophyseal socket is present in the known males of Wanless's Meleon species, a similar feature is shown also by species of several other spartaeine genera, notably Cyrba, Gelotia and Cocalus. It would thus appear that this character, as formulated by Wanless, cannot serve as a synapomorphy for Meleon. However, evidence from other characters indicates that Meleon kenti and some, but not all, of the other species included by Wanless in Meleon do form a monophyletic (natural) group. These characters include the following: (1) base of retrolateral tibial apophysis (proximal to socket) dorsally directed in the form of an inverted 'L', (2) cymbium proximally

with a vertical retrolateral membranous fissure and (3) epigynal integument mem branous anteriorly around copulatory orifices. In addition, the shape of the carapace in profile is fairly distinctive in M. kenti and close relatives, being elevated, with the highest point at or about the level of the second eye row (not at the level of the third eye row, as in Portia and several other spartaeine genera), with the anterior cephalic declivity much steeper than the posterior thoracic declivity. However, a similar

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1994 ON THE SPIDER GENUS MELEON 57

carapace form is shown by some other taxa, notably Veissella durbanii (Peckham and Peckham) within the Spartaeinae and, outside the Spartaeinae, by Lyssomanes, and thus should be viewed with some caution. Similarly, the shape of the cymbium (dorsal or ventral) in Meleon kenti and close relatives is fairly distinctive but the significance of this, too, is uncertain.

Reexamination of the material studied by Wanless necessitates some nomenclatural changes and reassociation of sexes. In his earlier revision of Portia (=Linus), in which

Meleon species were previously included, Wanless (1978) synonymized Linus gui neensis Berland and Millot, 1941 (female holotype from Kankan, Guinea) with Portia solitaria de Lessert, 1927 (female holotype from Medje, Zaire). As shown below, however, M. guineensis proves to be a valid species quite distinct from M. solitaria. In the same work Wariless described a male from Uganda as a new species, Portia falcifera. Subsequently, Wanless (1984) assigned a male Meleon from the Ivory Coast to the species M. solitaria. With the recognition of M. guineensis as a valid species, and taking into account the locality data of Meleon specimens in collections, it seems likely that the 'solitaria' male of Wanless is in fact conspecific with M. guineensis,

whilefalcifera appears to be the true male of M. solitaria. The synonymy by Wanless

[in Murphy and Murphy (1983)] of Portia cazomboensis Wanless, 1978 (female holotype from Cazombo, Angola) under Portia kenti de Lessert, 1925 (male holotype from Umbilo, Natal, South Africa) is accepted here. Thus the genus Meleon, as restricted above, appears to contain only three species, all known from both sexes:

MV. guineensis (Berland and Millot, 1941), M. kenti (de Lessert, 1925) and M. solitaria (de Lessert, 1927).

In addition to the species discussed above, Wanless (1984) transferred to Meleon three other spartaeine species which had previously been included in Portia: M.

madagascarensis (Wanless, 1978) (male holotype from Mt. Ambohisanga, Mada gascar), M. oreophila (Wanless, 1978) (female holotype from Mt. Ambohisanga,

Madagascar) and M. russata (Simon, 1900) (female holotype from Antongil, Mad agascar). The identical locality data and similar structure of madagascarensis and oreophila (e.g., carapace profile, cheliceral dentition, clypeal setae, leg spination) strongly suggest their conspecificity. Wanless's decision to maintain them as separate species was evidently due to the fact that oreophila (female) has a faint striped dorsal pattern and very short but distinct ventral hair fringes on the anterior legs whereas madagascarensis (male) is uniformly colored and lacks ventral leg hair fringes. Sexual dimorphism is widespread and common among salticids (see Peckham and Peckham, 1 889) but usually involves conspicuous color patterns and structural features in males, females as a rule being less strikingly modified. However, in spite of the more dis tinctive female color pattern, the available evidence favors regarding madagascar ensis and oreophila as the male and female of a single species. This evidence is as follows: (1) leg hair fringes: these are usually better developed in females than in

males among those spartaeine salticids that possess them, thus the difference between madagascarensis and oreophila may not be significant; (2) cheliceral dentition: very similar in both species, consisting of three promarginal teeth with the middle tooth largest and six retromarginal teeth with the first distal smallest and slightly set apart from the rest (absent in right male chelicera); (3) leg spination: the number and

position of leg spines in the two species is very similar, with identical retrolateral and dorsodistal femoral series; (4) carapace form: similar in the two taxa, being

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58 JOURNAL OF THE NEW YORK ENTOMOLOGICAL SOCIETY Vol. 102(1)

Figs. 1-8. Meleon guineensis (Berland and Millot) and Meleon soUitaria (de Lessert), female genitalia and carapace. 1-3, 7. M. guineensis. 4-6 8. M. solitaria. 1, 4. epigynum (ventral view).

2, 5. spermathecae and ducts (dorsal view). 3, 6. spermathecae and ducts (dorsolateral view).

7 8. carapace (lateral view).

moderately high and wide with the dorsum rounded in profile; (5) clypeal setae: the

two pairs of clypeal setae below the anterio}r median eyes are anteriorly directed and

long in both species; (6) carapace guanine deposits: both species show extensive'

whitish subintegumental guanine deposits in the ocular area of the carapace. On the

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1994 ON THE SPIDER GENUS MELEON 59

basis of these features Portia oreophila Wanless is here considered a synonym of Portia madagascarensis Wanless (NEW SYNONYMY). 'Meleon' madagascarensis does not show any of the synapomorphies of Meleon as specified above but instead has a stout, dorsally curved embolus and anteriorly-shifted embolar base as in the south Asian genera Cocalus and Gelotia, a special tibio-cymbial articulation as seen also in some species of Gelotia, and a distinctive epigynum. Similarly, 'Meleon' russata (Simon), known only from the female, shows no features (e.g., carapace shape) justifying its placement in Meleon; its spermathecae are small, hemispherical, with very short copulatory ducts. No derived features are known which associate russata with any other genus and until the male is discovered its systematic position is likely to remain enigmatic.

The format of description follows Wanless (1984). Synonyms listed by Wanless (1978) are not repeated here. Abbreviations of collections are as follows: AMNH

American Museum of Natural History, New York; BMNH-The Natural History Museum, London; MCZC-Museum of Comparative Zoology, Cambridge, Massa chusetts; MHNG-Museum d'Histoire Naturelle, Geneva; MNHN-Museum Na tional d'Histoire Naturelle, Paris; MRAC-Musee Royal d'Afrique Centrale, Ter vuren; NMSA-Natal Museum, Pietermaritzburg.

Meleon guineensis (Berland and Millot) STATUS REVISED (Figs. 1-3, 7)

Linus guineensis Berland and Millot, 1941:399, figs. 92D, G, H (female holotype from Kankan, Guinea, MNHN, examined); Wanless, 1978:91, fig. 3F (as synonym

of Portia solitaria). Meleon solitaria: Wanless, 1984:187 (male, misidentification).

Diagnosis. Females of M. guineensis resemble those of M. solitaria in having a U-shaped anterior epigynal invagination but can be distinguished by the dorsally flexed ducts and the dorsal membranous folds around the copulatory openings. Males

may easily by distinguished from other species by the elongate, curved embolus and the distinctive spiny dorsal cymbial apophysis. Male. Described as Meleon solitaria by Wanless (1984:187). Female (holotype, in fair condition). Carapace: pale reddish orange; sparsely clothed

with recumbent translucent or white hairs with some darker hairs above margins and on thoracic region. Eyes: encircled with black; fringed with pale hairs, tuft-like behind PME. Clypeus: pale reddish orange, margin narrowly blackish; with medial setal triad, single seta below each AME, row of long setae at margin; Chelicerae: pale reddish orange; paturon anteriorly with many long setae and scattered pale hairs; promargin with three teeth, retromargin with four. Maxillae: pale reddish orange, with dark streak basally. Labium: reddish orange. Sternum: buffy yellow with darker margins, clothed with fine erect hairs. Coxae: similar to sternum, smooth. Abdomen: dorsally pale cream or whitish, anteriorly greyish at sides; two pairs of small sigilla; clothed with adpressed amber hairs (mostly rubbed off); ventrally whitish, with greyish median stripe from epigastric furrow to (and encircling) spinneret bases. Legs:

buffy yellow with traces of darker annulations on femora, tibiae and metatarsi; ven trodistal hair fringes on tibiae II slight, marked on tibiae IV; spines numerous, strong. Legs I (both) missing. Palp: slender, whitish, tarsus apically buffy, femur with basal blackish prolateral spot; strong spines only on femur; tibia and tarsus clothed with

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60 JOURNAL OF THE NEW YORK ENTOMOLOGICAL SOCIETY Vol. 102(1)

numerous long white hairs. Epigynum: anterior invagination recurved with numerous dorsal membranous folds; spermathecae elongate-pyriform; ducts strongly flexed dorsally.

Dimensions (mm): total length 6.85; carapace length 2.88, breadth 2.30, height 1.83; abdomen length 3.70; eyes, anterior row 1.56, middle row 1.22, posterior row 1.46; quadrangle length 1.25; diameters, AME 0.54, ALE 0.30, PME 0.23, PLE 0.26; interocular distances AL-PM-PL 0.30-0.45; clypeus 0.23.

Legs 1 2 3 4 Palp

Femur - 2.50 2.20 2.65 1.14 Patella - 1.13 0.98 1.03 0.59 Tibia - 1.86 1.58 2.21 0.75 Metatarsus - 1.90 2.00 3.15 - Tarsus - 0.87 0.80 0.81 1.23

Total - 8.26 7.56 9.85 3.71

Distribution. Tropical West Africa. Material examined. Guinea. Kankan: 19 (MNHN) (holotype of Linus guineensis,

determined as Portia solitaria by Wanless, September 1974); Ivory Coast. Kotiessou (environs of): 16 (J. Jezequel, MNHN: PNB. 145) (determined as Meleon solitaria by

Wanless, 1982).

Meleon solitaria (de Lessert) (Figs. 4-6, 8)

Portia solitaria de Lessert, 1927:425, fig. 14 (inverted!) (holotype female from Medje, Zaire, AMNH, examined).

Portiafalcifera Wanless, 1978:1 1 1, figs. 14B, E-F, 1 5B-D (holotype male from Mpan ga forest, Uganda, BMNH, not examined). NEW SYNONYMY.

Diagnosis. Females of M. solitaria resemble those of M. guineensis in having an anterior epigynal invagination in the form of an inverted 'U' but can be distinguished by the spherical spermathecae and parallel ducts. Males can be distinguished by the stout, moderately long embolus and the apically elongate and strongly curved retro lateral tibial apophysis.

Male. Described as Portia falcifera by Wanless (1978). Female. Described by Wanless (1978) (excluding references to guineensis). Distribution. Central and East Africa. Material examined. Zaire. Medje: 1 Y (AMNH) (holotype of Portia solitaria de

Lessert).

Meleon kenti (de Lessert)

Portia kenti de Lessert, 1925:339, figs. 8A-D (holotype male from Umbilo, Natal, South Africa, NMSA, examined); Wanless, 1978: 111, figs. 14A, C-D,1 SA; Murphy & Murphy, 1983:39.

Portia cazomboensis Wanless, 1978:90, figs. 2A-D (holotype female from Cazombo, Angola, BMNH, not examined); Murphy & Murphy, 1983:39 (as synonym of Portia kenti).

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1994 ON THE SPIDER GENUS MELEON 61

Diagnosis. Males of M. kenti can be distinguished easily by the short embolus. The epigynum of females lacks the recurved anterior invagination seen in the other two species, having this area smooth with a pair of weak folds extending laterally from the copulatory openings; the spermathecae are pyriform, with the narrowed anterior ends (ducts) angled laterally.

Male. Described by Wanless (1978). Female. Described (as Portia cazomboensis) by Wanless (1978). Variation. The copulatory openings of the epigynum are spaced apart in South

African (Natal) specimens but situated closer together in the female from Malawi. Distribution. Southern Africa. Material examined. Malawi. Chintheche, 1 1?5O'S, 3401 3'E: I , I i, January-Feb

ruary 1976 (R. Jocque, MRAC: 147.921); South Africa. Durban, Natal: 1Q (MCZC, in vial of Veissella durbanii); Umbilo, Durban, Natal: LI (Kent, NMSA; palp, MHNG) (holotype of Portia kenti de Lessert); Rosi Bay, Toppin: Ih (NMSA: 9925, ex 1957 part) (paratype of Portia cazomboensis Wanless).

ACKNOWLEDGMENTS

I would like to thank the following curators for the loan of material studied during the course of this work: P. M. Croeser (NMSA, Pietermaritzburg), B. Hauser (MHNG, Geneva), R. Jocque (MRAC, Tervuren), H. W. Levi (MCZC, Cambridge, Massachusetts), N. I. Platnick (AMNH,

New York) and C. Rollard (MNHN, Paris). I am grateful to Dr. N. I. Platnick for providing facilities for work and for reading and commenting on a draft of this paper. I would also like to thank Pablo A. Goloboff (Cornell University, Ithaca) and an anonymous referee for their helpful comments on the manuscript. This work was supported through a graduate student fellowship from the American Museum of Natural History, New York, and a research grant from the Department of Biology, City College of the City University of New York.

LITERATURE CITED

Berland, L. and J. Millot. 1941. Les araign&es de I'Afrique occidentale francaise. I. Les Sal ticides. Mem. Mus. Hist. Nat. Paris (n.s.) 12(2):297-424.

de Lessert, R. 1925. Araignees du Sud de l'Afrique (Suite). Revue Suisse Zool. 32(21):323 365.

de Lessert, R. 1927. Araign&es du Congo. Premiere partie. Revue Suisse Zool. 34(17):405 475.

Murphy, J. and F. Murphy. 1983. More about Portia. Bull. Brit. Arachnol. Soc. 6(1):37-45. Peckham, G. W. and E. G. Peckham. 1889. Observations on sexual selection in spiders of

the family Attidae. Occ. Pap. Nat. Hist. Soc. Wisconsin 1: 1-60. Simon, E. 1900. Descriptions d'arachnides nouveaux de la famille des Attidae. Ann. Soc.

Entomol. Belg. 44:381-407. Wanless, F. R. 1978. A revision of the spider genus Portia (Araneae: Salticidae). Bull. Brit.

Mus. Nat. Hist. (Zool.) 34(3):83-124. Wanless, F. R. 1984. A review of the spider subfamily Spartaeinae nom. n. (Araneae: Saltici

dae) with descriptions of six new genera. Bull. Brit. Mus. Nat. Hist. (Zool.) 46(2):135 205.

Received 4 February 1993; accepted 14 June 1993.