The evolutionary and dispersal history of the following freshwater mollusc species of the northern Levant has been reconstructed as an example by using new records and an analysis of the subspecific arrangement: Unio elongatulus, Unió terminális, Coibicula fluminalis, Leguminaia saulcyi, Leguminaia wheatleyi, Potomida littoralis, Maigaritifera homsensis (Bivalivia), Theodoxus joidani, Melanopsis piaemoisa (Gastropoda). The patterns of distribution confirm and complement the general geological and paleogeographical theories concerning the Levant region

Kinzelbach, R. K.

Roth, G.

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Fol. Hist.-nat. Mus. Matr. 9. 1984. Patterns of distribution of some freshwater molluscs of the Levant region* UMB3 BUDAPEST R. K. KINZELBACH and G. ROTH Institut für Zoologie, Tehcnische Hochschule Darmstadt, FRG ABSTRACT: The evolutionary and dispersal history of the following freshwater mol-lusc species of the northern Levant has been reconstructed as an example by using new records and an analysis of the subspecific arrangement: Unio elongatulus, Unió ter-minális, Coibicula fluminalis, Leguminaia saulcyi, Leguminaia wheatleyi, Potomida littoralis, Maigaritifera homsensis (Bivalivia), Theodoxus joidani, Melanopsis piaemoi-sa (Gastropoda). The patterns of distribution confirm and complement the general geo-logical and paleogeographical theories concerning the Levant region. INTRODUCTION The Levant, situated at the intersection of several faunal regions, de-serves, also in malacological, view, a particular attention. BOURGUIG-NAT (1825), LEA (1863, 1864), ROLLE et KOBELT (1895-1897), BLANC-KENHORN (1897), TCHERNOV (1973, 1975 a, b), SCHUTT (1982) stand for the large number of authors who worked in this field. Above all re-cent specialists pointed out clearly the still existing gaps in our knowled-ge, chiefly regarding the colonizationary and evolutionary history of this region. Filling them up will lead to results of general interest. As a basis of further research in this field collecting travels to the Le-vantine rift valley and its surroundings were carried out by KINZELBACH and his students during the years 1975—83, supported by Stiftung Volks-wagenwerk and Deutsche Forschungsgemeinschaft. SCHUTT (1982) al-ready revised to some extent the 60 species of freshwater molluscs collec-ted so far. Great importance was attached to the requirement, that the collec-ting sites cover the freshwater systems in question as densely as pos-sible. Additionally the subspecific arrangement of the species collected was investigated. From this procedure we expect information about the establishment of isolates and pathways of dispersal. In the following patterns of distribution of some selected bivalve and gastropod species will be presented and discussed. * Results of the travels of R. Kinzelbach to the countries of the Middle East, no. 70. U S PATTERNS OF DISTRIBUTION OF SOME SELECTED SPECIES i. Unio elongatulus eucinus (BOURGUIGNAT, 1857) (Fig. 1). Middle Eastern subspecies of Unio elognatulus C. PFEIFFER, 1825, for-merly Unio mancus (LAMARCK), which is known from the western Me-diterranean since the Pliocene and which spread eastward through sout-hern Greece (e. g. Lake of Kopias) and Anatolia (e. g. Lake Sugla near Konya) as far as Iran. Starting from the Çukurova region this species co-lonized many of the Levantine coastal rivers down to Palestine but was unable to invade the Levantine rift valley. Further south it reached the Nile, where it is represented by the subspecies dembeae SOWERBY (MO-DELL 1951). Its occurence in the lower course of the Orontes river indicates, that this part of the Orontes was a coastal river in the past. The rivers Quwaiq and Sagur were colonized by this mussel from the Euphrates system, af-ter their being separated from the Orontes. 2. L7m'o terminális terminális (BOURGUIGNAT, 1852) (Fig. 2). According to MODELL (1951) Unio terminális originated from the Lower Danube and reached the Levant region through the Vardar depression and the Levant region throught the Vardar depression and the Egean lakes. As an easily distinguishable subspecies, U. t. terminális, it appeared within the Antakya basin (Amik Gölü) and the Gab rift valley during the Pliocene and disappeared from there during the Pleistocene. In the southern Levan-tine rift valley this subspecies still exists,- it invaded the Nahal Quison, using the Yisrce'l plain as a pathway. 3. Unio terminális delicatus (LEA, 1863) (Fig. 2). After the extinction of 17. t. terminális in the northern Levantine rift valley the region was colonized by L7. t. delicatus from southern Anato-lia. At this time there were no connections from the Orontes to the Qu-waiq nor to the Euphrates. A short termed connection between the upper Orontes and the Mediterranean Sea via the Gate of Horns during the la-te Pleistocene allowed U. t. delicatus to penetrate into the Nahr al-Kabir (S) and several temporarily connected rivulets north of its mouth. An iso-lated occurence in the Lake of Muzairib was caused by recent introducti-on, maybe by fishes of the genus Tilapia from fish-hatcheries of the Gab. The two taxa listed here as subspecies are possibly already isolated at the specific level. 4. Corbicula fluminalis (O. F. MÜLLER, 1774) (Fig. 3). Within the Levant this species, which already during the Tertiary was widely spread in Africa and the Middle East, was originally restricted to the entire Levantine rift valley. Apparently, it invaded this area coming from the Euphrates system. During the Pleistocene it dispersed into the 116 coastal rivers of Palestine, the Nahr al-Kabir (S) through the Gate of Horns and finally into the lower courses of the Orontes and the Ceyhan rivers. 5. Leguminaia saulcyi (BOURGUIGNAT, 1852] (Fig. 4). The pathway of dispersal of this species, which represents a Pliocene im-migrant from the Euphrates system, cannot yet be reconstructed accura-tely. On its way along the coast it spread as fas as southern Palestine down to Jaffa (MODELL 1951). During the Pleistocene it lived for a short period of time within the Jordan valley ( = L.chantrei according to TCHERNOV !973)/ which it probably reached through the Yisrce'l plain. 6. Leguminaia wheatleyi (LEA, 1862) (Fig. 4). This species dispersed from the Euphrates system towards the southwest into the Orontes river. By invading the lower Orontes and the Nahr al-Kabir (S) it reached areas already colonized by its neighbouring species L. saulcyi. Both taxa coexist there without hybridizing. 7. Potomida littomlis delesserti (BOURGUIGNAT, 1852) (Fig. 5). According to MODELL (1951) Potomida littomlis came from the Lower Danube region to southern Anatolia during the Pliocene by way of the Vardar depression and the Egean lakes. In that region the subspecies P. I. tracheae (KOBELT, 1895) occurs down to Iskenderun. It is only slightly different from the subspecies delesserti, which lives in the rivers of the coastal plain between the lower course of the Orontes and Haifa. 8. Potomida littoralis semirugata (LAMARCK, 1819) (Fig. 5). Still during the Pliocene Potomida littomlis invaded the Levantine rift valley and further the Gabbiil basin. Here a particular subspecies, semiru-gata, developed. As the result of the Pleistocene fusion of the central Orontes with its present lower course semirugata reached the Amik Gö-lü. It immigrated further through the Gate of Horns into the Nahr al-Ka-bïr (S), which was already occupied by P. I. delesserti. The existence of shells with intermediate characters in both of these areas confirms their subspecific status. 9. Margaritifera homsensis (LEA, 1864) (Fig. 6). 1864 Unio homsensis LEA, Proc. Acad. nat. Sei. Philad. 8: 285. 1865 Unio episcopalis TRISTRAM, Proc. Zool. Soc. London iS6y. 544. 1893 Unio barroisi DROUET, Rev. Biol. Nord France 5: 285, F. i ; J. de Conch. 41: 36. 1929 Margaritana syriaca PALLARY, Mém. Inst. Egypte 12; 34. 1951 Potomida littoralis homsensis, — MODELL, Rev. Fac. Sei. Instanbul (B) 16: 357, 361. 1964 Margaritifera cf. auricularia, — MODELL, Arch. Moll. 83: 97. A very large mussel (up to 15 cm in length) is found in the Orontes river mainly at the same localities as P. J. semirugata. It is absent from the Qu-117 waiq river and the Gabbül basin. Fossil records from the Jordan area are still to be confirmed. Until present the mussel in question was conside-red to be a subspecies of Potomida littoralis,, namely Potomida littoialis homsensis. According to MODELL (1964), however, this taxon belangs to the genus Maigaiitifeia; it is therefore considered here as a valid species, Mar-gaiitifeia homsensis. During the Pliocene it spread from the lower Danu-be through the Vardar depression and the Egean lakes into the Orontes system. The closely related Margaritifera auricularia occurs in southwest and central European rivers. Because of its thick pink nacreous layers this shell served as jewelry since lang ago. A piece of shell was found near Polmyra. ro. Theodoxus jordani (SOWERBY, 1832) (Fig. 7}. Coming from the north, the Ponto-Caspian area, the ancestors of the wi-despread, quite polymorphic snail Theodoxus jordani penetrated into Middle East, where they are known to occur since the Pliocene (TCHER-NOV, Г973). It has not yet been possible to establish clearly distinct sub­species. However, comparative studies on the radula teeth indicate a gene­tic heterogeneousness between different geographical units (ROTH, 1983), namely a) the southern part of the Levantine rift valley, where one out of two possible morphological types of the first lateral tooth, the „J-form" pre­dominates (with exception of the springs arround the Dead Sea), b) the coastal rivers except for the Nahr al-Kabïr (N), where solely the second type, the „A-form" occurs, and a) the southern part of the Levantine rift valley, where one out of two gether. It is not very easy to explain this varying but orderly distribution of radu-la types within the populations. Probably the A-form represents a gene-rally distributed original state. On the other hand, the J-form may have developed in an isolated population, most likely in the area of the Jordan valley, and later invaded the Orontes system and the Euphrates. This would at least help to explain its absence from the coastal rivers. n . Melanopsis praemorsa (L., 1758) (Fig. 8). In this context only a few principal features of the subspecific arrange-ment of the snail Melanopsis praemorsa can be outlined. The basic pattern of distribution, which is exhibited by the mussels, applies in this case as well despite quite different means of dispersal. 1. The first group consists of mainly smooth shelled or, rarely finely rib-bed specimens without shouldered whorls. It is distributed in Anato-lia, in the tributaries to the upper Euphrates and the,coastal rivers of the Levant region. It reaches the Quwaiq river and Gabül basin, the Damascus basin, the Biqâc plain and parts of the Jordan system. It may be subdivided into the chiefly black Melanopsis, praemorsa ferus-saci (ROTH, 1839) of the Levantine coast and Palestine and the yello-wish or ochre coloured M. pr. olivieri (BOURGUIGNAT, 1884) of eas-tern Anatolia. 118 2. A second group are the mainly costated or, rarely smooth shelled spe-cimens which always possess a stepped outline. They occur in the Oron-tes river incl. Krasu and Afrin, the Quwaiq river, the Jordan river incl. Nähr az-Zarqä and at isolated localities of the Syrian Plateau. It is named M. pi. costata (OLIVIER, 1804); another distinct subspecies of the water boides of Palmyra is M. pi. obsolete (DAUTZENBERG, 1894). 3. The third group comprises individuals of the Euphrates river, probably representatives of a species of its own, Melanopsis nodosa FÉRUSSAC, 1823. Specimens of similar morphology are known from Pleistocene si-tes in the Orontes and Jordan valleys. These groups do apparently not represent local varieties or morphs but true genetic units, the status of which will have to be clarified in the future. The natural limis of distribution are frequently broken through by former or recent displacement. PALEOGOGRAPHICAL CONCLUSIONS The patterns of distribution even of he few species discussed here show principal agreement, hus their evolution may be explained by the same paleogeographical situations. These are in detail: 1. A north-south junction along the Levantine coast during the Pliocene or earlier, which allowed the spreading of Unio elongatulus eucinus, Leguminaia saulcyi, Potomida littoialis delesserti and L/ш'о tigridis (not treated here); the latter and L/ш'о elongatulus reached the Nile. 2. The particular development of the Levantine rift valley with the ende­mic species Dreissena bouiguignati and Vivipaius apameae, which are not treated here as well as the subspecies Potomida littoialis semiiuga-ta and Unio teiminalis teiminalis. 3. A clear cut separation of the northern and southern part of the Le­vantine rift valley; connections existed only for a short period of time by way of the Biqâc plain (which was used as a pathway by Coibicula fluminalis) and the Damascus basin,- Maigaiitifeia homsensis and Unio teiminalis delicatus for instance are forms restricted to the northern part. 4. A connection between the northern Levantine rift valley and the Euphrates by way of the Quwaiq river and the Gabbűl basin during the Pliocene and perhaps even later; possibly also the Amik Gölü basin and the upper courses of Afrin and Karasu rivers discharged to the east; this was used by the genera Leguminaia, Potomida and Coibicula. 5. The present lower Orontes was formerly a short and unimportant ri­ver of the Mediterranean coastal plain which shares till now serveral faunal elements such as Potomida littoialis delesseiti, Leguminaia sa­ulcyi, Unio elongatulus euciirus with the other coastal rivers. 6. The close junction between the lower course of the Orontes and the Ceyhan river during a period of marine regression during the Pleis­tocene, which led to a faunal exchange: Coibicula fluminalis and Me­lanopsis piaemoisa femssaci invaded the Ceyhan, the reverse way was used by Unio terminális, delicatus. 119 7- A passage to the Nahr al-Kabïr (S) in the area of the Gate of Horns, which was blacked again later by basaltic extrusions; this way was used by Potomida littoralis semirugata, Maigaritifera homsensis, Cor-bicula fluminalis, Leguminaia wheatleyi, Unió terminális delicatus. These findings support the geological theories of the Levant (WEU-LERSSE 1940, VAUMAS 1957, 1961, HOROWITZ 1979) and add beyond that some details. They may be confirmed and differenciated by conside-ring all mollusc species and also species of other taxonomical units. DISCUSSION At present only relative dating of the above mentioned paleogeograp-hical events is possible. It is our intention to establish an absolute chrono-logy by consulting exactly dated fossil sites, thus allowing to date evolu-tionary events. Therefore additional materials from the dried-up lake ba-sins of the Syrian Plateau and from right tributaries of the Euphrates are necessary. Because of occasional displacement, routes of dispersal of the one or the other species might be misleading, but in connection with the results obtained in other species this may easily be revognized. A better knowledge of the subspecific division may be achieved ma-inly in gastropods by using additional anatomical and serological charac-ters. LITERATURE: BLANCKENHORN, M., 1897, Zur Kenntniss der Süsswasserablagerungen und Mollosken Syriens. Palaeontographica, 44: 71—144, pl. 7—10 — BOURGUIGNAT, J. R., 1852, Testacea novissima qoae Cl. de Saulcy in itinere per orientem annis 1850 et 1851 collegit. Lutetiae, 31 pp. — HOROWITZ, A., 1979, The Quaternary of Israel. Acade-mic Press, New York, London, 394 pp. — LEA, I., 1863, Description of Eleven New Spe-cies of Exotic Unionidae. Proc. Acad. nat. Sei. Philad., 7: 189—190. — LEA, I., 1864, Des-cription of six new species of Western Asiatic Unionidae. Proc. Asiat, nat. Sei. Philad., 8: 285—286. — MODELL, H., 1951, ön Asyanin tatlisu miyeleri hakkinda — Die Najaden Vorderasiens. Rev. Fac. Sei. Univ. Istanbul Ser. В., i6 (4): 351—366. — MODELL, H., 1964, Das natürliche System der Najaden. 3. Arch. Moll., 93: 71—126. — ROLLE, H. et KOBELT, W., 1859—97, Beiträge zur Molluskenfauna des Orients. 1. Suppl. Bd. zu ROSSMÄSSLERs Ikonogr., Wiesbaden. — ROTH, G, 1983, Intraspezifische Variabilität von Gehäuse, Operculum und Radula bei Theodoxus (Neritaea) jordani in den Levante-ländern (Gastropoda: Neritidae). Mitt. dtsch. malak. Ges. (in print) — SCHUTT, H., 1982, Die Molluskenfauna der Süsswässer im Einzugsgebiet des Orontes unter Berück-sichtigung benachbarter Fluss-systeme Arch. Moll., 113: 17—91, 225—228. — TCHER-NOV, E., 1973, On the Pleistocene Molluscs of the Jordan Valley. Pubis. Isr. Acad. Sei. Hum., Jerusalem, 50 pp., 7 pis. — TCHERNOV, E., 1975a, The Early Pleistocene Molluscs of cErq el-Ahmar. Pubis. Isr. Acad. Sei. Hum., Jerusalem, 36 pp., 4 pis. — TCHERNOV, E., 1975b, The Molluscs of the Sea of Galilee. Mallacologia, 15 (1): 147—184. — VAU-MAS, E. de, 1957, Plateaux, plaines et dépressions de la Syrie intérieure septentrionale (Du parallèle d'Alep au parallèle de Homs). Etude morphologique. Bull. Soc. Roy. Géogr. Egypte, Kairo, 30: 97—235 — VAUMAS, E. de, 1961, Structure et morphologie du Proche-Orient. Nouvel essai de synthèse et orientation de recherche. Rev. Géogr. Alpine, Gre-noble, 49: 225—274, 433—509, 645—739. — WEULERSSE, 1940, L'Oronte. Etude de fleu-ve. (Institut Français de Damas). Tours, 90 pp. R. K. KINZELBACH und G. ROTH Institut für Zoologie, Technische Hochshule 6100 DARMSTADT Schnittspahn str. 3, GFR 120 1 2 1 123 124 126 Fig. 7: Patterns of distribution of different types of the first lateral radula tooth within the populations of Theodoxus joidani. 

Patterns of distribution of some freshwater molluscs of the Levant region

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