[p. 83] ON SOME EARLY TRIASSIC PECTINACEA (BIVALVIA) FROM THE EASTERN PRE-CAUCASUS AND MANGYSHLAK V. A. Gavrilova* Information is presented on the range of bivalves of superfamily Pectinacea, discovered in Lower Triassic deposits of the Eastern Pre-Caucasus and Mangyshlak, as well as descriptions of eight species: Eumorphotis telleri, E. multiformis, Leptochondria minima, L. bittneri, L. (?) dagestana sp. nov., Ornithopecten temirbabensis, Palaeontolium microtis and Entolioides ussuricus, and also illustration of one taxon, Claraia cf. punjabiensis is given. Ammonoids have the greatest value for the biostratigraphic partition of the Lower Triassic in the regions being studied. At that, in Mangyshlak in sections of the Tyururpinskiy Series, uncovered and revealed along the core of deep drill holes, the currently most detailed sequence of changes of complexes of late Dzhelamian [Olenekian?] ammonoids are seen, allowing the distinguishing of five biostrata [7].1 One should emphasize that here marine Upper Dzhelamian sediments lie under and are covered by red-colored and terrigenous formations without ammonoids. In the Eastern Pre-Caucasus, Triassic sediments have been established only as a result of deep drilling for oil and gas. In a stratigraphic chart of 1979, the Kultayskaya and Dem’yanovskaya Svitas are included in the Dzhelamian stage [8]. According to the complexes of ammonoids observed in them, the former is assigned to the Lower Dzhelamian substage, and the latter to the Upper Dzhelamian. However, poor preservation of the rock material and weak paleontological description do not allow accomplishing a more detailed partition of the Upper Dzhelamian according to ammonoids in this region. In frequency and preservation, especially in the core of the drill hole, they are far inferior in numbers to bivalves. The presence of the latter is as well an important index of a definite facies environment which allows them to be used for reconstructing the conditions of sedimentation. Many species of bivalves had entered into stratigraphic charts of western Central Asia and the Eastern Pre-Caucasus at all only on the basis of preliminary paleontological identifications. Until now, Early Triassic bivalves of the southern regions of SNG remain very poorly studied. Our article is devoted to the results of research of Pectinacea, most widely distributed in in Dzhelamian sediments of the Eastern Pre-Caucasus and Mangyshlak. The collections of T. V. Babicheva (Central Asian Expedition of IGiRGI) 1982, 1984 and those of the author in 1978– 1980 and 1984 are used in this work. The description of Pectinacea given below was done first and is a supplement to the * Original citation: Gavrilova, V. A. 1995. O nekotorykh rannetriasovykh pektinatseiakh predkavkaz’ia i mangyshlaka. Bulletin of the Moscow Society of Naturalists, Geological Series 70(5):83–97. Translated by Rosanne D’Aprile Johnson, Smithsonian Institution, 2004. Scanned and edited by Abree Murch and Matthew Carrano, 2014. 1 The author accepts division of the Lower Triassic into Induan and Dzhelamian stages [9]. paleontological description of the Parsymurunskaya, Uzen’skaya, and Tartalinskaya Svitas of Mangyshlak, and is its [p. 84] paleontological foundation for Dem’yanovskaya Svita of the Eastern Pre-Caucasus [2, 6, 7, 8]. The monographic study of Dzhelamian complexes of Pectinacea of the regions being examined allowed establishing their systematic composition and stratigraphic range. Three families are represented here: Pterinopectinidae Newell, 1938, Aviculopectinidae Meek et Hayden, 1864 and Entoliidae Korobkov, 1960. The first family is represented by six taxa: Claraia aurita (Hauer), Claraia orbicularis dagestanica Gavr. subsp. nov., Claraia stavropolica Gavr. sp. nov., Cl. australasiatica kumschokensis Gavr. subsp. nov., Cl. aff. tridentina (Bittn.), Cl. cf. punjabiensis (Witt.), examined in a separate article. Only a photo illustration of the species Cl. cf. punjabiensis (Witt.) is given for comparison in this work. The following species are assigned to Aviculopectinidae: Eumorphotis telleri (Bittn.), E. multiformis (Bittn.), Leptochondria minima (Kipar.), L. bittneri (Kipar.), L. (?) dagestanica Gavr. sp. n., and Ornithopecten temirbabensis Kipar. Only two species of Entoliidae have been studied: Palaeoentolium microtis (Witt.) and Entolioides ussuricus (Bittn.). The oldest representative of Pectinacea is endemic species Ornithopecten temirbabensis Kipar., remains of which have been discovered in the cores of many drill holes in the territory of YuzhnoMangyshlak depression. Finds of it coincide with variegated clay siltstones and calciferous argillites of the Upper Parsymurunskaya Svita, traced through areas in the Zheltybay-Uzen’, Zhazgurla, and Aksu-Kendyrlik zones of lithofacies. Because it lies directly under formations of the Uzen’skaya Svita with Late Dzhelamian ammonoids in all sections, its geological age is conditionally accepted as Early Dzhelamian. The rest of the Pectinacea species were discovered together with remains of ammonoids. Analysis of species composition of studied Pectinacea demonstrated that five species are common to those of southern Primor’ye, established earlier by A. Bittner and L. D. Kiparisova in Dzhelamian sediments but at a lower stratigraphic level (Meekoceras layers–Owenites zone): Leptochondria minima Kiparisova, L. bittneri Kiparisova, Entolioides ussuricus (Bittner), Palaeoentolium microtis (Witt.) and Eumorphotis multiformis (Bittner). Finds of the species mentioned in Upper Dzhelamian sediments of Mangyshlak and the Eastern Pre-Caucasus could be evidence of either their broader stratigraphic range as a whole, or of migration from Primor’ye to regions to the west. With descriptions of studied Pectinacea species, terminology previously suggested by N. I. Kurushin [3] is used. The collection is kept in the F. N. Chernyshev Central Research Geology Museum in St. Petersburg under No. 12682. Superfamily Pectinacea Rafinesque, 1815 Family Aviculopectinidae Meek et Hayden, 1864 Subfamily Aviculopectininae Meek et Hayden, 1864 Genus Eumorphotis Bittner, 1901 Eumorphotis telleri (Bittner, 1899) Pl. 1, Fig. 4 Pseudomonotis telleri: Bittner, 1899a, p. 710, pl. 15, figs. 11–15; 1901a, p. 568, pl. 22, figs. 1–5; Frech, 1909, p. 22, pl. 2, figs. 3, 4; Pseudomonotis (Eumorphotis) telleri: Ogilvie-Gordon, 1927, p. 20, pl. 1, figs. 6a–b; Kiparisova, 1947, pl. 14, fig. 5; Eumorphotis telleri: Ichikawa, 1958, p. 154, pl. 22, figs. 11–13. The lectotype is described in A. Bittner’s work [11, pl. 15, fig. 13]. Alps, Yugoslavia, Lower Triassic, Upper Werfenian strata. D e s c r i p t i o n . Shell is average size (up to 30.5 mm in height and up to 25 mm in length), oval, slightly prosocline, inequilateral, strongly elongate in height. Hinge is straight, long, somewhat less than the overall shell length. Apical angle is 82°. Left valve is strongly convex, the maximum convexity being found in the upper half of its height. The beak is massive, turning slightly forward, hanging like a vulture over the hinge and being approximately one third of the overall valve length distant from anterior margin. Anterior slope of beak is steep, but the posterior and lower are more gently sloping. Anterior auricle is triangular, slightly convex and separated from main field of the valve by a rather deep groove. Posterior auricle is set apart by a gently sloping bend, is flat and larger than anterior. Surface of valve is covered with weak and irregular concentric growth marks. D i m e n s i o n s (mm): Spec. No. 4/12 682 H 30.5 L 24.6 H/L 1.23 Hinge Length 23.8 Hinge Length/L 0.96 Convexity 10.6 Convexity/H 0.30 C o m p a r i s o n . The examined specimen differs from the most closely related species, Eumorphotis iwanovi (Bittner) [1, p. 8, pl. 1, figs. 1–9] from Lower Triassic beds of YuzhnoUssuriyskiy Kray by having valves more elongate in height, a massive beak, turned forward, by greater difference in dimensions of auricles and by the absence of radial ribs. R a n g e . Lower Triassic of Darvaz, Hungary, Yugoslavia; Upper Dzhelamian of Mangyshlak. M a t e r i a l . Single steinkern of left valve of satisfactory preservation. Eumorphotis multiformis (Bittner, 1899) Pl. 1, figs. 2, 3 Pseudomonotis multiformis: Bittner, 1899, p. 10, pl. 2, figs. 15–22; Pseudomonotis (Eumorphotis) multiformis: Spath, 1935, p. 74, pl. 22, fig. 8; Kiparisova, 1947, p. 97, pl. 15, figs. 1–9; 1954, p. 10, pl. 1, figs 11–13; Eumorphotis multiformis: Kiparisova, 1938, p. 224, pl. 2, figs. 4, 9, 12; pl. 3, figs. 2–4; Ciriacks, 1963, p. 77, pl. 15, figs. 13–15; Nakazawa, 1971, p. 117, pl. 23, figs. 7–12; Chen, 1976, p. 184, pl. 30, figs. 34–35; Yin Hongfu et Ho Yuanliang, 1979, pl. 14, fig. 3; Eumorphotis multiformis var. regularaecosta: Kiparisova, 1938, p. 227, pl. 2, figs 10–11; 82° Eumorphotis multiformis var. rara: Kiparisova, 1938, p. 227, pl. 3, fig. 1; Eumorphotis multiformis var. rudaecosta: Kiparisova, 1938, p. 226, pl. 2, figs. 5 & 14; Eumorphotis multiformis regularaecosta: Ciriacks, 1963, p. 77, pl. 15, fig. 14; Chen, 1976, p. 185, pl. 30, fig. 29 Eumorphotis multiformis rudaecosta: Okuneva, 1976, p. 28, pl. 1, figs. 1, 3; Chen, 1976, p. 185, pl. 30, fig. 33. The lectotype is illustrated in Bittner’s work [1, pl. 2, fig. 21]. No. 45/221, TsNIG Museum. Yuzhno, Ussuriyskiy Kray, Shamara River, Lower Triassic. D e s c r i p t i o n . Shell is of average size (up to 39.5 mm in height and 31.5 in length), slightly prosocline, oval, elongate in height, [p. 86] [p. 87] not equilateral. Beak strongly protrudes beyond the long straight hinge, visibly close to anterior margin. Apical angle is equal to 88 - 90°. Left valve is strongly convex with maximum convexity in upper half of its height. Anterior auricle is close to right-angled, convex and set well apart from main field of valve by a narrow groove. Larger, slightly separated auricle, flat, elongate in length, pointed. { sic } Entire surface of the valve, including auricles, is covered with radial ribs of three-four orders, varying in nature of arrangement, length and prominence. Thus, in the Dagestan specimen (Ill. 1, fig. 2), the coarsest ribbing, situated in a three-order system, is visible. Ribs of the first and second orders differ slightly in length and prominence, and ribs of the third order are substantially finer and have an irregular arrangement: on the anterior half of valve surface, interspaces of ribs of first and second orders are developed in twos, but in the posterior margin, they {are developed} either singly or are absent altogether. In the largest outer steinkern of the left valve, without an anterior auricle with ragged surface in the part around the beak (Ill. 1, fig. 3), the radial sculpture is regularly situated and is slightly distinguishable in prominence of ribs of four orders. Distinct concentric, but irregular growth lines are developed as well on valves, as a result of the intersection with which, ribs acquire unevenness or serration. On the auricles, growth lines bend, turned toward the beak with convexity. Pl. 1. Fig. 1. Claraia cf. punjabiensis (Wittenburg, 1909). Spec. No. 11/2682, a – left valve, x1.5; b –view from beak side, x2. Mangyshlak, southwestern slope of Kumshoky Mountain, outcrop 2, layer 7, sample 2–7–78f/80. Upper Dzhelamian, Tartalinskaya Svita. Collections of V. A. Gavrilova, 1980. Figs. 2–3. Eumorphotis multiformis (Bittner, 1899). 2 – Specimen No. 2/12682, left valve, xl. Dagestan, Darginskaya area, drill hole 2, 4126–4116 m depth. Upper Dzhelamian, Dem’yanovskaya Svita. Collections of V. A. Gavrilova, 1984; 3 – Specimen No. 3/12682, left valve, x1. Mangyshlak, southwestern slope of Kumshoky Mountain, outcrop 2, layer 8, specimen 2–8– 79f/80. Upper Dzhelamian, Tartalinskaya Svita, Collections of V .A. Gavrilova, 1980. Fig. 4. Eumorphotis telleri (Bittner, 1899) Specimen No. 4/12682, left valve, x1. Mangyshlak, north slope of Karatauchik Range, region of Dollapa Well, outcrop 3, sample 3–11f/79. Upper Dzhelamian, Tartalinskaya Svita. Collections of V. A. Gavrilova, 1979. Figs. 5, 6. Leptochondria minima (Kiparisova, 1938), 5 – Specimen No. 5/12682, 5a – left valve, x4; 5b – the same, x5; 6 – Specimen No. 6/12682, 6a – left valve, x4; 6b – the same, x5. Mangyshlak, northern slope of Karatauchik Range, Dollapa Well region, outcrop 3, sample 3–24f/79. Upper Dzhelamian, Tartalinskaya Svita. Collections of V. A. Gavrilova, 1979. Figs. 7, 8. Leptochondria bittneri (Kiparisova, 1938). 7 – Specimen No. 7112682, left valve, x3. Mangyshlak, southwestern slope of Kumshoky Mountain, outcrop 2, layer 8, sample 2–8– 79f/80. Collections of V. A. Gavrilova, 1980. 8 – Specimen No. 8/12682, right valve, x2. Northern slope of Karatauchik Range, Dollapa Well region, outcrop 3, sample 3–16f/79. Upper Dzhelamian, Tartalinskaya Svita. Collections of V. A. Gavrilova, 1979. Figs. 9, 10. Leptochondria (?) dagestanica Gavrilova, sp. nov. 9 – Specimen no. 9/12682, left valve, x1. Mangyshlak, northern slope of Karatauchik Range, region of Dollapa Well, outcrop 3, sample 3–16f/79. Upper Dzhelamian, Tartalinskaya Svita. Collections of V. A. Gavrilova, 1979. 10 – holotype No. 10/12682, 10a – left valve, x1; 10b – the same; x2.5. Dagestan, Solonchakovaya area, drill hole 47, 4470–4465 m depth. Upper Dzhelamian, Dem’yanskaya Svita. Collections of V . A. Gavrilova, 1984. Figs. 11, 12. Ornithopecten temirbabensis Kiparisova, 1980. 11 – Specimen No. 11/12682, left valve, x5. Southern Mangyshlak, Zhilandy area, drill hole 4, 3944–3937 m depth. 12 – Specimen No. 12/12682, impression of right valve, x5. Tasbulat area, drill hole 26, 3642–3633 m depth. Lower Dzhelamian, Parsymurunskaya Svita. Collections of T. V. Babicheva, 1982, 1984. [p. 88] D i m e n s i o n s (mm): Spec. No. 23/12 682 2/12 682 3/12 682 H L 19.2 18.l 35.4 27.2 39.5 31.5 H/L Hinge Length Hinge Length/L 1.06 17.3 0.95 1.30 – – 1.25 – – Convexity 7.8 6.4 12.l Convexity/H 0.40 0.18 0.31 88° – 90° C o m p a r i s o n a n d r e m a r k s . The collection of syntypes of species Eumorphotis multiformis (Bittner), which was the basis of study for its designation and the first description carried out by A. Bittner [1], contains 6 left valves. I suggest the largest left valve of these, with slightly damaged auricles, be the lectotype; it has an exceptionally a well-preserved sculptured surface, the most typical for the species being examined. The specimens studied differ from the species Eumorphotis telleri (Bittner) described above in having large dimensions, smaller apical angle and by the presence of radial ribbing. It is distinguished from Eumorphotis iwanovi [1, p. 8, pl. 1, figs. 1-9], described by A. Bittner from Lower Triassic of Yuzhno-Ussuriyskiy Kray, by smaller size of valves elongate in height and multi-order system of radial ribbing, which covers the entire surface of the shell. R a n g e . Lower Dzhelamian of Yuzhnoye Primor’ye, Khabarovskiy Kray; upper Dzhelamian of Dagestan and Mangyshlak; Lower Triassic of Greenland, U.S., China, and Japan. M a t e r i a l . One impression and three steinkerns of left valves in various states of preservation from three localities. Genus Leptochondria Bittner, 1891 Leptochondria minima (Kiparisova, 1938) Pl. 1, Figs. 5, 6 Pecten (Leptochondria?) ex. aff. albertii: Bittner, 1899, p. 6, pl. 2, figs 1,2, 4–10; Pecten (Velopecten) minimus: Kiparisova, 1938, p. 246, pl. 4, figs. 10, 12; pl. 5, figs. 4–6; 1947, p. 113, pl. 21, figs. 3, 6. 9, 10; 1954, p. 12, pl. 3, figs. 3–7; Pecten (Velopecten) minimus var. reticulatus: Kiparisova , I 938, p. 247, pl. 5, figs. 1–2; Pecten (Velopecten) minimus var. laevis: Kiparisova, 1938, p. 247, pl. 5, fig. 3; Leptochondria minima: Nakazawa, 1971, p. 119, pl. 23, figs. 13 &14 ; Chen, 1976, p. 159, pl. 29, figs. 1–3; Yin Hongfu et Ho Yuanliang, 1979, pl. 14, fig. 6. Holotype is illustrated in L. D. Kiparisova’s work [4, pl. 5, fig. 5]. No 42/10909, TsNIG Museum. Ussuriyskiy Kray, Russkiy Island, Karpinskaya Bay; Lower Triassic. D e s c r i p t i o n . Left valves are small (up to 10 mm in height and length), close to round in outline, almost equilateral. Beaks are small, central, slightly protruding beyond the straight hinge. Apical angle is equal to 100-109°. Valve is convex with auricles slightly delimited. Anterior auricle is substantially larger than posterior and is set apart from overall surface of valve by a weak depression. It is slightly convex, and when joining the anterior margin, has an almost right-angled outline. The posterior auricle, in no way separated from the valve surface, gradually is joined to the posterior margin at an obtuse angle. Valve surface is covered with numerous radial thread-like, straight and densely situated riblets of one order, strongly pronounced with the aid of a magnifying glass. In some specimen [p. 89] they are more bold, and in others, they are flatter. Five mm from the beak, the number of riblets reaches 60–70. On the valve, concentric, regularly situated, more feebly marked, fine growth lines and irregular, coarse folds are developed as well; in some specimens, 11–14 such folds are observed. At the intersection with them, the riblets bend and the surface of the valve acquires a concentrically undulating nature. Auricles are covered with radial striae and threadlike growth lines. D i m e n s i o n s (mm): Spec. No. 5/12 682 6/12 682 H 8.5 9.6 L 8.7 10.0 H/L 0.98 0.96 Hinge Length Hinge Length/L 4.9 0.56 0.68 6.8 100° 109° C o m p a r i s o n . The Mangyshlak specimens are very closely related to shells of Leptochondria bittneri [4, p. 243, figs. 5–9, 11, 13] from the Lower Triassic of Ussuriyskiy Kray, being distinguished from the latter by smaller size and more feeble and simple radial sculpture on the left valve. From Leptochondria albertii [3, p. 90, pl. 17, figs. 3–8] from Anisian deposits of northern Central Siberia, it differs not only by substantially smaller dimensions, but also by more convex left valve, as well as by thread-like radial sculpture. R a n g e . Lower Dzhelamian: Ussuriyskiy Kray; Upper Dzhelamian; Mangyshlak; Lower Triassic: China, Japan. M a t e r i a l . Three steinkerns and five impressions of left valves in varying states of preservation from two localities. Leptochondria bittneri (Kiparisova, 1938) Pl. 1, Figs. 7, 8 Pseudomonotis cf. multiformis: Bittner, 1899, p. 10, pl. 2, figs. 11–14; Pecten (Velopecten) bittneri: Kiparisova, 1938, p. 243, pl. 4, figs. 5–9, 11, 13; 1947, p. 113, pl. 21, figs. 4, 5, 7, 8; Leptochondria cf. bittneri: Chen, 1976, pl. 29, fig. 4. Holotype is illustrated in L. D. Kiparisova’s work [4, pl. 4, fig. 11]. No. 38/10909, TsNIG Museum. Ussuriyskiy Kray, Russkiy Island, Lower Triassic. D e s c r i p t i o n . Shells are small (up to 14 mm in height and 13 mm long), from rounded to slightly elongate in height, almost equilateral. Beaks are small, central, protruding slightly over the straight hinge. Apical angle is equal to 105-116°. Left valve is uniformly convex with slightly delimited auricles. Anterior auricle is slightly larger than the posterior one and separated from the overall field of the valve by an outlining groove. Auricles are slightly convex and joined to the anterior and posterior margins at almost identical obtuse angles. Valve surface is covered with fine radial riblets of several orders, concentric growth lines and nicks. At that, several variations in the manner of arrangement of radial riblets on the valves are visible. Between two ribs of the first order, a single rib of the second order proceeds from the beak to the lower margin. Riblets of the third order appear at a distance equal to approximately 1/3 of height from the beak. One more riblet of the fourth order is wedged in from the middle of the valve height, but they are not visible in every rib interspace. Ribs of the first two orders are coarser and more bold, which, in their prominence are visibly distinguished [p. 90] from each other, and the ribs of the third and fourth orders are more smoothed out {softened} and fine, almost identical in prominence. At 5 mm from the beak, the number of ribs reaches 50–55. The concentric sculpture is represented by thread-like growth lines and disorderly nicks. Sometimes, where intersecting with the latter, the radial ribs break down and acquire a somewhat displaced new direction. Auricles are covered with more strongly pronounced concentric growth lines and scarcely visible radial striae. The right valve is slightly convex, not equilateral in outline, with attenuated anterior margin. Anterior auricle is set apart from the main valve field by a groove, which replaces a deep byssal notch. Radial sculpture is more feeble and simpler than in the left valve. D i m e n s i o n s (mm): Spec. No. 7/12 682 8/12 682 24/12 682 l. v. r. v. l. v. H L H/L Hinge length Hinge length/L 11.6 13.l 13.7 11.8 12.5 12.1 0.98 1.04 1.13 7.1 7.6 6.9 0.60 0.60 0.57 116° 110° 105° C o m p a r i s o n . From Leptochondria albertii [3, p. 90, pl. 17, figs. 3–8], from the Anisian of northern Central Siberia, the species being described differs by having smaller dimensions, more complicated differentiated radial ribbing and larger apical angle. R a n g e . Lower Triassic: China; Lower Dzhelamian of Ussuriyskyi Kray; Upper Dzhelamian: Mangyshlak. M a t e r i a l . Two steinkerns of left valves and one inner steinkern of a right valve of satisfactory preservation from two localities. Leptochondria (?) dagestanica2 Gavrilova, sp. nov. Pl. l , Figs. 9, 10 Holotype No. 10/12682, TsNIG Museum. Eastern Pre-Caucasus, Dagestan, Solonchakovaya area, drill hole 47, 4465–4470 m depth. Lower Triassic, upper Dzhelamian substage, Dem’yanovskaya Svita. D e s c r i p t i o n . Shell is of average dimensions (up to 25 mm in height), of oval outlines, elongate in height, acline or slightly prosocline. Apical angle is equal to 82–90°. Left valve is from slightly to moderately convex, the greatest convexity being found on its anterior and central parts . Beak is small, subcentral and does not protrude over the straight hinge. Auricles are sharply delimited from the overall valve field. The anterior slightly convex auricle is triangular with acute (78°) or right external angle. Posterior flat auricle is smaller than the anterior, obtuse-angled one (116°). 2 From the locality of the holotype in the territory of Dagestan. Surface of valve is covered with fine straight radial riblets of two orders. There are around 45 riblets in all with riblets of the second order arising irregularly within the interspaces. The strongly pronounced primary ribs have a triangular section and the rib interspaces substantially exceed them in thickness . Ribs of the second order are smoothed out and shorter than the primary ones, and in the rib interspaces, they occupy a marginal position. In the posterior margin of the valve, radial riblets of two orders are more densely [p. 91] situated and become almost identical in prominence. Fine concentric growth lines, which become more prominent on the anterior and posterior margins, are developed as well on the valve. The auricles are covered with sparse radial striae and densely situated, thread-like growth lines. On the inner steinkern, sculpture appears to be somewhat smoothed out. D i m e n s i o n s (mm): Spec. No. 10/12 682 9/12 682 H 19.5 24.8 L 15.2 - H/L 1.28 - Hinge length 8.1 - Hinge length/L 0.53 - 82° 90° C o m p a r i s o n a n d r e m a r k s . Difficulties arose upon identification of the form being examined with establishing the genus to which it belongs. In the shape and sculpture of the auricles, sharply set apart from the main field of the left valve by straight grooves, as well as in the acute-angled or right apical angle, the specimens examined are similar to shells which are usually attributed to genus Chlamys, which is distinguished by somewhat smaller differences in dimensions of anterior and posterior auricles, by the absence of unevenness on the ribs and complicated cellular sculpture of the rib interspaces. With the almost equilateral, weakly convex left valve with subcentral beak and simpler radial sculpture, the Dagestan specimens are close to shells of genus Leptochondria. However, one should note, that round or oval shell shape with poorly separated auricles, almost identical in size and the obtuse apical angle, is characteristic of the majority of ancient forms of this genus from the Early and partially from Middle Triassic. Only in the younger (Late Triassic) representatives of genus Leptochondria are auricles sharply separated from the overall valve field. Because only left valves are represented in the available collection of specimens being described, and these were discovered together with remains of other pectinids and late Dzhelamian ammonoids, and representatives of genus Chlamys have a higher stratigraphic range in Triassic sediments, then very conditionally, I assign them to genus Leptochondria. It is possible that in the future, this species will be assigned to a new genus, but for now this question is difficult because of the lack of paleontological material. The greatest similarity of the species being described is to Leptochondria pervulgata [10, p. 248, pl. 30, figs. 2–4] from Anisian sediments of Italy, which is distinguished by a higher and more equilateral valve with finer radial ribbing, as well as by sculptured auricles. Some similarity is observed with Pecten venustulus [12, p. 55, pl. 6, fig. 9], which as well is assigned to genus Leptochondria and is known from Carnian Stage of Bakony (Hungary). However, the species being described differs in the left valve being less convex, and having auricles more sharply separated and radial ribs of two orders. From Chlamys (Praechlamys) subalternicostata [10, p. 345, pl. 46, figs. 1–3] from the Carnian Stage of the Southern Alps, the specimens studied are distinguished by smaller size, absence of sinus in anterior auricle, fewer radial ribs and more weakly sculptured auricles. R a n g e . Upper Dzhelamian: Eastern Pre-Caucasus and Mangyshlak. [p. 92] M a t e r i a l . A single outer steinkern of a left valve and its impression in satisfactory condition, and a single inner steinkern of a left valve, lacking posterior part and an auricle from two localities. Genus Ornithopecten Cox, 1962 Ornithopecten temirbabensis Kiparisova, 1980 Pl. 1, Figs. 11, 12 Ornithopecten temirbabensis: Kiparisova, 1980, p. 151, pl. 35, figs. 7, 8. The holotype is illustrated in L. D. Kiparisova’s work [5, pl. 35, fig. 7]. No. 3/11012, TsNIG Museum, South Mangyshlak, Temirbaba area, drill hole 1, 3784–3791 m depth; Lower Triassic, Dolnapinskaya Svita. D e s c r i p t i o n . Shell is small (up to 6–6.5 mm in height and 7 mm in length), slightly elongate, inequivalved, not equilateral, with hinge equal to or somewhat exceeding the overall length of the shell. Apical angle is equal to 114–120°. Left valve is moderately convex. Beak is small, displaced forward, and, being set apart at 1/3 of length from anterior margin, does not protrude beyond the straight hinge. The anterior auricle is large, slightly convex, separated by the steep anterior slope of the valve. The surface of the valve is covered with numerous fine, straight radial riblets of two-three orders, which when approaching the lower margin equalize in thickness. At the lower margin, their number reaches 50–55. Concentric, thread-like growth lines are developed as well and also wrinkles situated irregularly, which become more sharply defined on crossing the auricle. Right valve is compressed, with a small swelling in the area of the beak, and is flat in the lower part. Beak is small, feebly marked. The narrow and long anterior auricle is in the shape of an acute-angled triangle, sharply delimited from the anterior margin of the valve by a deep groove which ends in a small hollow. At the groove it is convex, but when approaching the hinge, it flattens out. Sculpture of the valve is the same as on the left. The posterior auricles of both valves are somewhat more poorly separated, wing-like, with a small hollow on the posterior margin. Besides the wrinkles, feebly marked radial striae are visible on the auricles. In the inner steinkern, sculpture is noticeably smoothed out. D i m e n s i o n s (mm): Spec. No. 12/12 682 11/12 682 H 4.0 5.0 L 5.8 6.6 H/L 0.69 0.76 Hinge Length 6.3 6.9 Hinge Length/L 1.09 1.04 DPCh* 2.2 2.5 DPCh/L* 0.38 0.38 120° 114° C o m p a r i s o n . When comparing with the type species of genus Ornithopecten, 0. bosniae (Bittner) [13, p. 592, pl. 26/9, figs. 16, 17], described from the Anisian deposits of Yugoslavia, a great similarity is not visible, because the Mangyshlak species differs substantially by having smaller shell size, with more distinctly separated auricles, with larger anterior auricle of the right valve, which is the shape of an acute-angled triangle and delimited from the main field of the valve by a deep groove, by having narrow posterior wing-like auricles of both valves * Translator’s note: These mysterious initials occurred in an earlier publication I translated. Here, I think they may refer to “length of anterior portion” and “length of anterior portion/[overall] length.” with small hollow on posterior margin, being covered with visible concentric wrinkles, and the finer radial sculpture being identical on both valves. [p. 93] From species O. schlosseri (Bittner) in the description and illustration of A. Allasinaz [10, p. 264, pl. 32, figs. 6, 7] from Anisian deposits of Yugoslavia, the specimens being described are distinguished not only by smaller dimensions, but also by a more eccentric and blunt, non-protruding beak, different shape of the more sharply separated auricles and different type of sculpture. R a n g e . Lower Dzhelamian: Mangyshlak. M a t e r i a l . A single impression of right valve and three steinkerns of left valves in various states of preservation from four localities. Family Entoliidae Korobkov, 1960 Genus Palaeoentolium Romanov, 1985 Palaeoentolium microtis (Wittenberg, 1908) Pl. 2, Figs. 1–6 Pecten discites var. microtis: Bittner, 1899, p. 2, pl. 1, figs. 12–18; Bittner, 1901, p. 90, pl. 9, figs. 43–54; Pecten discites mut. microtis: Frech, 1904, p. 34, pl. 1 fig. 4; Pecten microtis: Wittenberg, 1908, p. 20, pl. 2, figs. 9–11; Ogilvie-Gordon, 1927, p. 24, pl. 2, fig. l 7a, b. Pecten (Entolium) microtis: Kiparisova, 1954, p. 11, pl. 2, figs. 3, 4; Entolium microtis: Kiparisova, 1938, p. 250; Entolium discites microtis: Chen, 1976, p. 208, pl. 34, figs. 12, 13; Palaeoentolium microtis: Romanov, 1985, p. 35. The lectotype is illustrated in A. Bittner’s work [1, pl. 1, fig. 13]. No.1/221, TsNIG Museum. Yuzhno-Ussuriyskiy Kray, Russkiy Island, Ayaks Bay, Lower Triassic. D e s c r i p t i o n . Shells of average dimensions (up to 28 mm in height and 27 mm in length), from round to elongate in height, sometimes slightly oblique, equivalved, equilateral, and from slightly to moderately convex. Beaks are small, slightly pointed, central and not protruding beyond the straight hinge, which takes up approximately one third of shell length. Small auricles well separated are almost equal, symmetrical, and do not protrude above the hinge. The anterior auricle is close to right-angled in outline, but the posterior is strongly oblique and obtuse-angled. The surface of the valves is covered with fine, numerous concentric growth lines and coarser small folds, more strongly developed in the lower half of the shell. Sometimes, weak radial sculpture is visible, expressed by straight striae. The auricles are covered with thread-like growth lines. On the inner surface of the valves, auricular crura and lateral bolsters [resilial teeth] are well developed. D i m e n s i o n s (mm): Spec. No. 19/12 682 H 10.7 L 10.3 H/L 1.03 Hinge margin 3.4 Hinge margin/L 0.33 115° 20/12 682 21/12 682 22/12 682 23/12 682 24112 682 25/12 682 26/12 682 11.5 11.6 14.l 19.4 22.2 23.7 27.9 9.7 9.8 14.7 17.l 18.6 23.1 26.5 1.18 1.18 0.95 1.13 1.19 1.02 1.05 4.2 3.3 4.3 4.8 5.1 6.7 – 0.43 0.33 0.29 0.24 0.27 0.29 – 92° 98° 116° 118° 104° 108° 112° V a r i a b i l i t y . Outlines of the shells appear to range from round to elongate in height (H/L varies from 0.95 to 1.18). Valve convexity varies from slight to moderate. The prominence and nature of the arrangement of the concentric folds are susceptible to a degree of variability: [p. 94] [p. 95] they vary from coarse wrinkles to less coarse, fine growth lines. In some specimens, they are not numerous and are more strongly developed in the lower half of the shell, while in others, they are more feebly marked and are situated at approximately equal interspaces along the entire height of the valve, and in a third of them, they are completely invisible. The apical angle varies from 92 to 118°. C o m p a r i s o n . The shells being described differ from the most closely related species, Palaeoentolium discites (Schloth.), illustrated by A. Allasinaz [10, p. 284, pl. 35, fig. 8, 9] from the Anisian of Italy, by having shorter hinge, small auricles, and greater apical angle, and more sharply pronounced concentric sculpture. The examined specimens differ from P. hallense (Woehrmann) [10, p. 287, pl. 36, figs. 1–4] from the Carnian of the Alps (Northern Tyrol) by having smaller shells, shorter hinge, and by the presence of coarse concentric folds. R a n g e . Lower Triassic: Spitzbergen, Austria, Hungary, China, and Primorskiy Kray; Upper Dzhelamian: Dagestan, Mangyshlak. M a t e r i a l . 15 steinkerns and impressions of odd pieces of valves in various states of preservation from two localities. Genus Entolioides Allasinaz, 1972 Entolioides ussuricus (Bittner, 1899) Pl. 2, Figs. 7–10 Pecten ussuricus: Bittner, 1899, p. 4 pl. 1, fig. 11; Pecten sichoticus: Bittner, 1899, p. 4, pl. 11, fig. 10; Pecten (Aequipecten) ussuricus: Kiparisova, 1938, p. 251, pl. IV, figs. 14–16; Pecten (Eupecten) ussuricus: Kiparisova, 1947, p. 109, pl. XX, figs. 10–13; 1954, p. 12, pl. III, figs. 1,2; "Pecten" ussuricus: Nakazawa, 1961, pl. 12, figs. 10–12. Holotype is illustrated in A. Bittner’s work [1, pl. I, fig. 11]. Spec. No. 5/221, TsNIG Museum. Ussuriyskiy Kray, Russkiy Island, Paris Bay; Lower Triassic. Description. The shell is of average size (up to 34.5 mm in height and 37 mm in length), from round to slightly elongate, not equilateral, inequivalved. The apical angle is equal to 105–120°. Left valve is moderately convex. Its middle section is the most convex, but the lateral ones are recessed, and only at the boundary with the auricles Pl. 2. Figs 1–6. Palaeoentolium microtis (Wittenburg, 1908). 1 – Spec. No. 13/12682, steinkern of left valve, x3; 2 – Spec. No. 14/12682, steinkern of left valve, x1; 3 – Specimen No. 15/12682, steinkern of left valve, x1. Dagestan, Darginskaya area, drill hole 2, 4077–4072 m depth. 4 – Specimen No. 16/12682, left valve, x2, 4126–4116 m depth. 5 – Sample No. 17/12682, a – steinkern of left valve, x1, b – the same, x3; 4077–4072 m depth. Upper Dzhelamian, Dem’yanovskaya Svita. Collections of V. A. Gavrilova, 1984. 6 – Spec. No. 18/12682, a – steinkern of left valve, x3; b – its impression, x3. Mangyshlak, northern slope of Karatauchik Range, region of Dollapa Well, outcrop 2, Sample 2–198f/75. Upper Dzhelamian, Tartalinskaya Svita. Collections of V. A. Gavrilova, 1975. Figs. 7–10. Entolioides ussuricus (Bittner, 1899). 7 – Specimen No. 19/12682, steinkern of right valve, x2; Mangyshlak, northern slope of Karatauchik Range, region of Dollapa Well, outcrop 3, sample 3– 16f/79; 8 – Spec. No. 20/12682, a – steinkern of left valve, x2; b – its impression, x2, outcrop 3, sample 3–15f/79; 9 – Specimen No. 21/12682, steinkern of left valve, x2; outcrop 3, sample 3–10f/79. Upper Dzhelamian, Tartalinskaya Svita. Collections of V. A. Gavrilova, 1979. 10 – Specimen No. 22/12682, steinkern of left valve, x1. Dagestan, Stepnaya area, drill hole 24, 4950–4940 m depth. Upper Dzhelamian, Dem’yanovskaya Svita. Collections of V. A. Gavrilova, 1984. [p. 96] are small swellings observed again. The anterior swelling is narrower and longer than the posterior one. The beak is subcentral, small, slightly pointed, not protruding over the straight and long hinge. The surface of the inner steinkerns is represented by radial ribs, feebly marked in relief, which proceed straight from the beak to the lower margin, slightly thickening and keeping the rib interspaces wider than they are themselves. Fine, concentric growth lines and irregularly situated wrinkles are developed as well as radial ribbing. Flat and smooth obtuse auricles with rounded apices are distinctly delimited from the main valve field and do not protrude beyond the hinge. Under the anterior auricle, there is a shallow byssal groove. Impressions of short auricular and hinge crura are visible on the surface of the inner steinkern. The right valve is less convex than the left. The sculpture is represented by fine concentric growth lines. Sometimes, scarcely visible radial striation along the anterior margin can be seen on the surface of the valve. On the inner surface of the steinkern, long and narrow lateral bolsters, which proceed for some distance from the anterior and posterior margins are very visible. D i m e n s i o n s (mm): Spec. No. 15/12 682 16/12 682 17/12 682 18/12 682 l. v. l. v. r. v. r. v. H L 11.9 17.3 17.8 34.l 12.7 17.6 19.1 37.0 H/L 0.93 0.98 0.93 0.92 Hinge Length 5.7 8.8 8.0 Hinge Length/L – – 0.44 0.50 0.41 105° 113° 110° 120° V a r i a b i l i t y . Variations in the shell outline, from rounded to slightly elongate, appear (H/L varies from 0.92 to 0.98). The apical angle varies from 105 to 120°. C o m p a r i s o n . From most closely related species Pecten kokeni Wittenburg [14, p. 7, pl. 2, figs. 3, 4], which probably is ascribed to genus Entolioides and is known from Lower Triassic sediments from the Salt [River] Range, the species being described differs in having a flat right valve and finer radial sculpture on the left valve. From species Entolioides zitteli (Woehrmann et Koken), illustrated by A. Allasinaz [10, p. 300, pl. 38, figs 4, 5; pl. 39, figs. 1–6] from the Carnian of Lombardy, the Mangyshlak specimens are distinguished by elongate shell shape, large apical angle and different type of sculpture on both valves. R a n g e . Lower Triassic: Ussuriyskiy Kray and Japan; Upper Dzhelamian: Mangyshlak and Dagestan. M a t e r i a l . One impression and four inner steinkerns of broken valves from two localities. Remains of a fine layer of shell has been preserved on one steinkern. LITERATURE CITED 1. Bittner A. 1899. Fossils from Triassic Deposits of Yuzhno-Ussuriyskiy Territory [Okamenelosti iz triasovykh otlozhenii Iuzhno-Ussuriyskogo kraya]//Tr. Geol. komiteta, vol. 7, no. 4, pp. 1–35. 2. Gavrilova V. A. 1992. Biostratigraphy of the Lower Triassic of Mangyshlak with bivalve mollusks. [Biostratigrafiia nizhnego triasa Mangyshlaka po dvustvorchatym molliuskam]//Izv. RAN [Russian Academy of Sciences]. Ser. geol. no. 4, pp. 151–157. 3. Dagys A. S., Kurushin N. I. 1985. Triassic brachiopods and bivalve mollusks of north Central Siberia. [Triasovye brakhiopody i dvustvorchatye molliuski severa Srednei Sibiri]//Tr. IGiG SO AN SSSR [USSR Academy of Sciences], no. 633. Moscow, 159 pp. 4. Kiparisova L. D. 1938. Lower Triassic Lamellibranchiata of Ussuriyskiy Territory. [Nizhnetriasovye plastinchatozhabernye Ussuriyskogo kraya.]//Tr. Geol. in-ta AN SSSR [USSR Academy of Sciences], vol. 7, pp. 197–311. [Page 97] 5. Kiparisova, L. D. 1980. New Early Triassic Aviculopectinidae from the Eastern Pre-Caucasus and Southern Mangyshlak. [Novye rannetriasovye avikulopektinidy Vost. Predkavkaz’ya i Iu. Mangyshlaka.] Nov. rody i vidy drev. rast. i besposzvon. SSSR [New Genera and Species of Ancient Plants and Invertebrates of the USSR]. Leningrad, pp. 150–152. 6. Regional Stratigraphic Diagram of Triassic Deposits of Southern Mangyshlak. [Regional’naia stratigraficheskaia skhema triasovykh otlozhenii Yuzh. Mangyshlaka]. 1986. Aliev A. M., Alekseeva L. V. et al.//Biul. MOIP. Otd. Geol. vol. 61, no. 6, pp. 35–45. 7. Resolutions of the Interdepartmental Stratigraphic Conference on the Mesozoic of Central Asia (Samarkand, 1971). [Resheniia Mezhvedomstvennogo stratigraficheskogo soveshchaniia po mezozoiu Srednei Azii]. Leningrad, 1977. 48 pp. 8. Resolutions of the Second Interdepartmental Regional Stratigraphic Conference on the Mesozoic of the Caucasus (Triassic) 1977, with Regional Stratigraphic Diagrams. [Resheniia 2-ogo Mezhvedomstvennogo stratigraficheskogo soveshchaniia po mezozoiu Kavkaza (trias), 1977, c regional’nymi stratigraficheskimi skhemami]. Leningrad, 1979. 36 pp. 9. Rostovtsev K. O., Dagys A. S. 1984. Standard of the Lower Triassic [Standart nizhnego triasa]//XXVI MGK. Sek. S.01. Stratigraphy [Stratigrafiia]. Dokl. [Papers], vol. 1, Moscow, pp. 79–86. 10. Allasinaz A. 1972. Revisione dei Pettinide triassici//Riv. Ital. Paleontol. e Stratigr., vol. 78, no. 2, pp. 189–428. 11.Bittner A. 1899 (1898). Beitrage zur Palaontologie, insbesondere der triadischen Ablagerungen centralasiatischer Hochgebirge//Jahrb. Geol. Reichsanst. Wien, vol. 48, no. 3/ 4, S. 689-718. 12. Bittner A. 1901. Lamellibranchiaten aus der Trias des Bakonyer Waldes//Result. Wissenschaftl. Erforsch. Balatonsees, vol. 1(3), pp. 1–107. 12. Bittner A. 1902. Brachiopoden und Lamellibranchiaten aus der Trias von Bosnien, Dalmatien und Venetien//Jahrb. Geol. Reichsanst. Wien, vol. 52, no. 3/4, pp. 495–643. 14. Wittenburg P. 1909. Einige Lamellibranchiaten der Salt-Range, mit Berticksichtigung der Lamellibranchiata des Stid-Ussuri-Gebiets//N. Jahrb. Mineral. Geol. Palaont. vol. 1, pp. 6–13. VSEGEI, Saint Petersburg Submitted for publication 19.04.94