Les sclérobiontes des huîtres du Cénomanien supérieur du Mans (Sarthe,France)

Oysters of the Marnes à Pycnodonte biauriculata Formation, Upper Cenomanian (Guerangeri biozone) were significantly sampled in building works within the town of Le Mans (Sarthe, France). They are colonized by episkeletobionts (encrusting organisms) and endoskeletobionts (boring and bioeroding organisms). First ones include bivalves, polychaetes, foraminiferans and bryozoans. Second ones are represented by about fifteen ichnotaxa, the producers of which, when they are known, belong to ten taxa. The oysters, some of which have a large fixation surface, are allochtonous or at least parautochtonous. The settlement of sclerobionts began when the oysters were alive (Entobia isp.) and continued post-mortem on isolated valves, transported in their final depositional environment (Gnathichnus pentax). The significance of the coexistence of both Entobia and Gnathichnus ichnocoenosis is discussed.     

Belichnus Traces Produced on Shells of the Bivalve Lutraria lutraria by Gulls

In February 2011, after a storm, thousands of adult, articulated, and still-living common otter shells Lutraria lutraria (L. 1758) were stranded on the North Sea beach of the Island Texel (NL). These 9 to12 cm long bivalves were rapidly found and consumed by both herring- and lesser black-backed gulls. Holes, irregular in outline, were observed in some 10% of the articulated shells of these bivalves. These holes were always smaller on the outside of the valves than on the inside and varied in size from 1 to 20 mm (outside) to 4 to 22 mm (inside). Often the other valve was crushed indicating consumption by gulls. We concluded that these holes were made by the gulls probing the shells; in a few cases, we observed that valves were broken starting from such a hole. Such traces are described in the literature as the ichnogenus Belichnus and were until now attributed to Stomatopoda only. We also suggest that a separate ichnospecies name for two Belichnus holes in one shell should not be used, as we see them simply as a double injury due to two blows. Our findings stress once more the importance of avoiding premature phylogenetic interpretation of traces and the use of a separate ichnotaxonomy.     

The bivalve boring Cuenulites amygdaloides nov. isp. in siliceous sponges from the Upper Cretaceous of Germany

Lower Campanian siliceous sponges from epicontinental deposits of the Subhercynian Cretaceous Basin in Germany contain amygdaloidal depressions which are distinguished as a new ichnospecies of the ichnogenus Cuenulites. These bioerosion traces are interpreted as borings of semi-endolithic bivalves, produced without significant rotation movement, probably mostly by chemical action. As there are no signs of tissue reaction in the bored sponges, the structure is considered to be produced post mortem to the sponge, probably in a foreshore-shoreface setting, with redeposition offshore.     

Sequence stratigraphic significance of sedimentary cycles and shell concentrations in the Upper Jurassic-Lower Cretaceous of Kachchh, western India

Upper Jurassic and Lower Cretaceous siliciclastic shallow water sediments of the Kachchh Basin, western India, form strongly asymmetric coarsening-upward cycles, which are interpreted as recording changes in relative sea level (deepening-shallowing cycles). These cycles correspond to depositional sequences, in which deposits of the lowstand systems tract are not present, the sequence boundary coinciding with the transgressive surface. Shell concentrations are found in the transgressive lags at the base of the transgressive systems tract (TST), in the maximum flooding zone (MFZ), and at or close to the top of the highstand systems tract. They belong to six assemblages, five of them dominated by large bivalves such as Seebachia, Herzogina, Gryphaea, Gervillella, Megacucullaea, Pisotrigonia and Indotrigonia, the sixth by the coral Amphiastraea. Three types of shell concentrations can be distinguished that differ from each other in a number of ecological and taphonomic features, such as species diversity, preservation quality, orientation in cross-section, percentage of disarticulation, and degree of biogenic alteration. Characteristic features of concentrations at the base of the TSTs are moderate time-averaging, sorting, a preferred convex-up orientation, and nearly total disarticulation of shells. They are suggestive of an environment in which reworking and local transport were frequent events. Similar features are shown by concentrations near the tops of the HSTs, except that there shells were largely concentrated in lenses and in pavements rather than in beds as in the transgressive lags. Associated sedimentary structures indicate deposition above fair weather wave base in a high-energy environment. Concentrations occurring in the MFZ, in contrast, are autochthonous and highly time-averaged, having accumulated during times of low rates of sedimentation below storm wave base. This is supported by their high preservation quality (comparatively high percentage of articulated shells, shells of infaunal organisms commonly preserved in life position), biogenic alteration being the most important taphonomic agent. The dominant elements of these shell concentrations, i.e. Seebachia, Megacuccullaea, and Indotrigonia in the Upper Jurassic, and Pisotrigonia in the Lower Cretaceous, are endemic to the Ethiopean faunal province and belong to lineages that rapidly evolved during this time period.     

The origin and early evolution of metatherian mammals: the Cretaceous record

Metatherians, which comprise marsupials and their closest fossil relatives, were one of the most dominant clades of mammals during the Cretaceous and are the most diverse clade of living mammals after Placentalia. Our understanding of this group has increased greatly over the past 20 years, with the discovery of new specimens and the application of new analytical tools. Here we provide a review of the phylogenetic relationships of metatherians with respect to other mammals, discuss the taxonomic definition and diagnosis of Metatheria, outline the Cretaceous history of major metatherian clades, describe the paleobiology, biogeography, and macroevolution of Cretaceous metatherians, and provide a physical and climatic background of Cretaceous metatherian faunas. Metatherians are a clade of boreosphendian mammals that must have originated by the Late Jurassic, but the first unequivocal metatherian fossil is from the Early Cretaceous of Asia. Metatherians have the distinctive tightly interlocking occlusal molar pattern of tribosphenic mammals, but differ from Eutheria in their dental formula and tooth replacement pattern, which may be related to the metatherian reproductive process which includes an extended period of lactation followed by birth of extremely altricial young. Metatherians were widespread over Laurasia during the Cretaceous, with members present in Asia, Europe, and North America by the early Late Cretaceous. In particular, they were taxonomically and morphologically diverse and relatively abundant in the Late Cretaceous of western North America, where they have been used to examine patterns of biogeography, macroevolution, diversification, and extinction through the Late Cretaceous and across the Cretaceous-Paleogene (K-Pg) boundary. Metatherian diversification patterns suggest that they were not strongly affected by a Cretaceous Terrestrial Revolution, but they clearly underwent a severe extinction across the K-Pg boundary.     

Paläobiogeographie jurassischer Muschelfaunen: Beziehung zwischen Süd- und Nordrand der Tethys

Similarities of mid-Jurassic bivalve faunas between the European and the Ethiopian faunal province are very high at the genus-level. At the species-level, however, it is shown that during the Bathonian and Callovian 35% of the bivalves occurring in the Ethiopian faunal province are restricted to this province. In the region of Kachchh (W-India) in the same time-interval 25% of all bivalves are endemic. In the Ethiopian faunal province a clear tendency of increasing endemism from the Bathonian to the Tithonian/Lower Cretaceous at the genus-level and, even more obviously, at the species-level exists. Endemism and provincialism are most marked within the orders Arcoida, Trigonioida, and Nuculoida. The degree of endemism is lower within the Veneroida, but still very high. The orders Mytiloida, Pterioida, and Pholadomyoida hold the largest portion of cosmopolitan species. The rise of endemism and provincialism in Kachchh and m the Ethiopian faunal province from the Bathonian onwards can be explained only partly by the increasing broadening of the Tethys and its effect as an oceanic barrier. The steep increase of endemism in the Upper Jurassic of Kachchh is essentially caused by a radiation within the astartids and trigoniids, accompanied by a reduction of facies-types, due to a regional regression. The very southerly palaeogeographic position of India, the opening of the ‘South African Seaway’, and a change in the marine current system in the uppermost Jurassic led to an increasing differentiation of the Ethiopian faunal province in an ‘Ethiopian-Tethyan’ subprovince to the north and an ‘Ethiopian-Austral’ subprovince to the south. A migration of bivalves in mid-Jurassic times can be reconstructed along the southern margin of the Tethys mainly from east to west. On the other hand, an easternward migration of bivalves along the northern margin of the Tethys from Europe to China and Japan can be documented especially in the Upper Jurassic. This corroberates the existence of a clock-wise marine current system in the northern hemisphere in the Jurassic. The distribution patterns of bivalves in Kachchh and the Ethiopian faunal province are essentially characterized by ‘migration’ of bivalves. The opening of the ‘Hispanic Corridor’ in the Pliensbachian gave way to the immigration of East Pacific bivalves via the western Tethys as far as Kachchh and Madagascar. The dispersal ofPisotrigonia, Seebachia, Tendagurium, andMegacucullaea in the uppermost Jurassic/lowermost Cretaceous from Kachchh and East-Africa respectively to South-Africa and South-America documents the establishment of a ‘South-African Seaway’ and favours migration. However, ‘migration’ and ‘vicariance’ do not exclude each other. On the contrary, both are important mechanisms for creating distributional patterns of bivalves, although within different geological dimensions. Vicariance events produce faunal provinces which last for a long time and within this time-interval, migration seems to be the more important mechanism affecting palaeobiogeographic distribution of bivalves. There is no evidence that the distribution patterns of bivalves in Kachchh and in the Ethiopian faunal province are governed by eustatic sea-level changes. The dominating factors have been a change of the palaeogeographic constellation as a consequence of the break-up of Gondwana, and the local facies distribution. The number of bivalve species known from Europe is much larger than the number of species of the Ethiopian faunal province. A comparison of rarefaction curves of associations, however, shows that this is not a primary feature, but is a consequence of a greater number of different facies types and is due to a far more intense collecting activity in Europe. The bivalves of the Spiti Shales are unequivocal Ethiopian-Tethyan in character. The composition of the fauna indicates the deposition on the deeper shelf of the southern margin of the Tethys. All occurring ‘European’ faunal elements are not significant because of their more or less cosmopolitan distribution.     

MIDDLE JURASSIC CEMENTED PECTINIDS AND THE MISSING RIGHT VALVES OF EOPECTEN

Large cemented bivalves, previously regarded as oysters, encrustMiddle Jurassic hardgrounds in Southern England, Normandy andBurgundy. Well preserved specimens show auricles and a largeanterior byssal notch indicating that they are, in fact, theright valves of pectinids, apparently assignable to the genusEopecten Douvillé, 1897. Specimens removed from the substratedemonstrate that a prolonged early byssally-attached stage wasfollowed by attachment by cementation. Previously, the lifehabit of Eopecien has been regarded as enigmatic, interpretationshaving been hampered by the museum record of Eopecten whichis remarkably poor in large right valves. Our specimens suggestthat facultative cementation of adults may have been a commonhabit in the genus. (Received 7 May 1992; accepted 30 June 1992)     

Theropod and possible ornithopod track assemblages from the Jurassic–Cretaceous boundary Houcheng Formation,Shangyi, northern Hebei,China

Dinosaur track assemblages from the Houcheng Formation in the small continental Shangyi Basin of northern Hebei Province, China bridge a gap in the record of vertebrates from this unit and enrich our knowledge of ichnofaunas from the Jurassic–Cretaceous boundary. Their stratigraphic position between the Middle Jurassic Yan-Liao Biota and the Lower Cretaceous Jehol Biota gives them a special importance. New discoveries allow a re-assessment of theropod and possible ornithopod tracks that are present with several trackways. Seventy-three footprints were examined and documented. Despite their smaller size, the tridactyl mesaxonic theropod tracks show morphological similarities with the ichnogenus Therangospodus known from the Upper Jurassic deposits of North America, Europe, and Central Asia. The possible ornithopod tracks lack an associated manus imprint, suggesting a bipedal trackmaker. These possible ornithopod tracks from the Houcheng Formation provide evidence for the presence of small basal ornithopods or basal Cerapoda in the Upper Jurassic–Lower Cretaceous in this region. The depositional environment was the margin of an extensive shallow lake with fluctuating water levels under seasonally dry climate.     

Tithonian-Berriasian foraminiferal faunas from the Torinosu-type calcareous blocks of the southern Kanto Mountains, Japan: their implications for post-accretionary tectonics of Jurassic to Cretaceous terranes

The Torinosu-type limestones, having many lithologic characters showing their original deposition on shallow shelves, are widely distributed in the Jurassic to Cretaceous terranes of Japan. The foraminiferal faunas from the Jurassic to the lowermost Cretaceous of Japan were first revealed in the calcareous blocks of the southern Kanto Mountains. Distinguished microfaunas consist of 39 species including many marker species of the Upper Jurassic to Lower Cretaceous in Europe, West Asia, and North Africa such as Melathrokerion spirialis, Charentia evoluta, Freixialina planispiralis, Nautiloculina oolithica, Everticyclammina cf. virguliana, Haplophragmium lutzei and Pseudocyclammina lituus. These faunas suggest a Tithonian to Berriasian age of Torinosu-type limestones. They are contained in four tectonostratigraphic units (Kamiyozawa, Hikawa and Gozenyama Formations; Ogouchi Group) continuously accreted from Middle Jurassic to Late Cretaceous. The younger deposition age of Torinosu-type limestones than the accretion age (Bajocian to Bathonian) in the Kamiyozawa Formation and their older age than the accretion age of the Ogouchi Group (late Albian to middle Maastrichtian) are important to date the post-accretionary tectonics of Jurassic to Cretaceous terranes of Japan and to explain the emplacement process of Torinosu-type limestones.     

Shell mineralogical trends in epifaunal Mesozoic bivalves and their relationship to seawater chemistry and atmospheric carbon dioxide concentration

The Late Triassic-Early Jurassic change from aragonite- to calcite-facilitating conditions in the oceans, which was caused by a decrease of the Mg²⁺/Ca²⁺ ratio of seawater in combination with an increase of the partial pressure of carbon dioxide, also affected the shell mineralogy of epifaunal bivalves. In the “calcite sea” of the Jurassic and Cretaceous, the most diverse and abundant families of epifaunal bivalves had largely calcitic shells. Some of them, such as the Inoceramidae, acquired this shell mineralogy earlier in Earth's history but did not significantly diversify until the onset of “calcite sea” conditions. Others, however, replaced aragonite by calcite in their shell at the beginning of the Jurassic, as shown for the Ostreidae, Gryphaeidae, Pectinidae, Plicatulidae, and Buchiidae. In these families, replacement of aragonite by calcite took place in the middle and inner layer of the shell and was not associated with changes in morphology and life habit. It is therefore proposed that lower metabolic costs rather than higher resistance against dissolution or advantageous physical properties triggered the calcite expansion in their shells. This explanation fits well the observation that clades of thin-shelled bivalves were less affected by the change of seawater chemistry. Thick-shelled clades, by contrast, may suffer a severe decline in diversity until they adapt their shell mineralogy, as demonstrated by the Hippuritoida: The diversity of the Megalodontoidea, which failed to adapt their shell mineralogy to “calcite sea” conditions, dramatically decreased at the end of the Triassic, whereas their descendents became dominant carbonate producers during the Late Mesozoic after they acquired a calcitic outer shell layer in the Late Jurassic. These examples indicate that changes in the seawater chemistry and in the partial pressure of carbon dioxide are factors that influence the diversity of carbonate-secreting animals, and, as in the case of the decline of the Megalodontoidea, may contribute to mass extinctions.     

A new sphenodontian (Lepidosauria: Rhynchocephalia) from the Late Triassic of Argentina and the early origin of the herbivore opisthodontians

Sphenodontians were a successful group of rhynchocephalian reptiles that dominated the fossil record of Lepidosauria during the Triassic and Jurassic. Although evidence of extinction is seen at the end of the Laurasian Early Cretaceous, they appeared to remain numerically abundant in South America until the end of the period. Most of the known Late Cretaceous record in South America is composed of opisthodontians, the herbivorous branch of Sphenodontia, whose oldest members were until recently reported to be from the Kimmeridgian–Tithonian (Late Jurassic). Here, we report a new sphenodontian, Sphenotitan leyesi gen. et sp. nov., collected from the Upper Triassic Quebrada del Barro Formation of northwestern Argentina. Phylogenetic analysis identifies Sphenotitan as a basal member of Opisthodontia, extending the known record of opisthodontians and the origin of herbivory in this group by 50 Myr.     

Ichnocoenoses and taphocoenoses of posidoniid-bearing marl-limestone rhythmites and event beds,Toarcian-Aalenian,Northern Apennines,Italy

The Posidoniid-bearing rhythmic deposits, Toarcian to Aalenian (Early/Middle Jurassic) in age, of the Umbria-Marche basins (Fiuminata Colle Corno and Valdorbia type section) consist of hundred couplets, each composed by two semicouplets, a calcium carbonate-poor bed and a calcium carbonate-rich bed, respectively (CacO₃ between 10% to 85%), where event tempestite beds randomly occurs. The aim of this work is to show ichnocoenoses and taphocoenoses as well as the faunistic variations of each semicouplet and event beds. Each couplet is ∼30 cm thick in the Toarcian Rosso Ammonitico and up to 40 cm in the Aalenian Calcari e Marne a Posidonia Formation, where the sedimentation rate increased. Here, couplets were deposited in the dysaerobic/aerobic transition zone. The clay-rich portion contains abundant thin-shelled poikilaerobic bivalves and benthic foraminifers (whithout radiolarians) and shows oxygen-poor ichnocoenosis with Chondrites, while the taphocoenosis exhibits convex-upward disposition and disarticulated bivalve shells. Conversely, the limestone semicouplet is rich in radiolarians and thin-shelled bivalves, usually more burrowed (ichnocoenosis including Chondrites and few Planolites and Thalassinoides) than the former, with grouping, dispersion, biogenic fragmentation and orientation-reorientation. In all marl-limestone semicouplets, foraminifers and radiolarians exhibit a periodic inverse correlation in abundance, while thin-shelled bivalves are always abundant. Rhythmically disposed within the rhythmites are also event beds indicating an occasional oxygen-rich substrate, fine-grained calcarenitic tempestites with hummocky cross-stratification, and winnowed bed (thin shelled bivalve concentrations). These deposits are intensely bioturbated (ichnocoenosis including Skolithos, Planolites, Trypanites, Chondrites, and Thalassinoides). Taphocoenoses include fragmentation, grouping, surficial burrowing, biogenic reorientation, and deep burrowing. Ichnological and taphonomical features indicate high physical and biogenical reworking affecting sediments. The Jurassic depocenters of Valdorbia and Fiuminata that received rhythmical dilution (clay) or productivity (carbonate) cycles during Toarcian and Aalenian time can therefore strongly contribute to the study of ichnological and taphonomical variations in rhythmic conditions.     

Review of Japanese Dinosaur Track Localities: Implications for Ichnotaxonomy,Paleogeography and Stratigraphic Correlation

Nine dinosaur ichnospecies from the Lower Jurassic to Upper Cretaceous of Japan, including two that are new, are described herein. The new ichnotaxa are Asianopodus pulvinicalx ichnogen. et ichnosp. nov. and Schizograllator otariensis ichnosp. nov. The Japanese ichnotaxa are allied to Lower Jurassic ichnospecies in South China, North America, Western Europe and South Africa, and Upper Jurassic to Lower Cretaceous ichnospecies from Southeast and East Asia. This suggests they were part of a global ichnofauna before continental drift began in the Middle Jurassic, leading to the development of a more endemic dinosaur fauna in the Cretaceous. At least two assemblages, an ornithopod-gracile-toed theropod-dominated community, in northeastern Asia, and a robust theropod- and sauropod-dominated community in the southern part of the continent, existed in the Cretaceous. This parallels North American dinosaur distribution patterns in the Cretaceous and seems to be a reflection of paleolatitudinal controls.     

Crayfish burrows from Late Jurassic–Late Cretaceous continental deposits of Patagonia: Argentina. Their palaeoecological,palaeoclimatic and palaeobiogeographical significance

The trace fossil, Loloichnus baqueroensis igen. and isp. nov., from Late Jurassic–Late Cretaceous continental deposits of Patagonia, Argentina, includes thickly lined, mostly passively-filled, and Y-branched burrows. Other important features of this ichnofossil are the inner surface texture of lining showing transversal, elongated, and adjacent grooves, and less commonly, the pelletal filling of burrows. L. baqueroensis is recorded from the Bajo Grande, Bajo Tigre, Punta del Barco, and Laguna Palacios Formations, which were deposited in different volcaniclastic environments of the Deseado Massif and San Jorge Basin geological provinces, respectively. The described burrows are found in many levels of palaeosols developed in reworked piroclastic deposits, where they are the main component of the ichnofabrics, in association with meniscate and thinly lined burrows and a diffuse and complex boxwork of small diameter burrows. Root traces are also present, and in many cases, occur inside L. baqueroensis. Considering general morphology, surface texture, filling types, palaeoenvironments in which they occur, and comparisons with extant and fossil decapod burrows, the likely trace makers of L. baqueroensis were crayfishes (Decapoda: Astacidea), probably Parastacidae. The producers of L. baqueroensis inhabited soils, where their burrows probably reached the water table, and contained roots that were used for feeding. Considering climatic preferences of extant parastacids, it is proposed a temperate climate for central Patagonia during the deposition of the studied units. The widespread presence of crayfishes during Late Jurassic–Late Cretaceous times in central Patagonia, supports the monophyletic origin of this group during the Triassic, and suggests that the present restricted geographic distribution in southern South America is a relict of a broader one.     

Armored dinosaurs(Ornithischia: Ankylosauria)) from the Middle and Upper Jurassic of England

Hitherto the earliest positive record of ankylosaurs(armored dinosaurs) has been from beds well up in the Lower Cretaceous; in fact, however, specimens referable to the ankylosaurian family Nodosauridae are present in the Middle and Upper Jurassic of England: from the Middle Callovian [partial mandible Sarcolestes leedsiLydekker]], the Upper Oxfordian [femur Cryptodraco eumerus (Seeley)), maxilla Priodontognathus phillipsii (Seeley))], and the Upper Tithonian [caudal vertebra, tooth]. The Tithonian tooth and those of Priodontognathus are large and similar to those of the nodosaurids Priconodon and Sauropelta (Lower Cretaceous, U.S.A.). The incomplete mandible of Sarcolestes is similar to that of Sauropelta with a dermal scute fused to the lateral surface, and a tooth row extending to the anterior end of the jaw; an unusual feature is the caniniform first tooth. The quadrupedal ankylosaurs and stegosaurs probably represent separate evolutionary lines that extend back at least into the Lower Jurassic, and both lines probably evolved from ornithopod dinosaurs that were bipedal. Nodosaurid ankylosaurs occur in Europe from the Middle Jurassic to Late Cretaceous and probably reached North America via a filter route in the early Cretaceous.     

Upper Pliocene bivalve shell concentrations from the Lower Chelif basin (NW Algeria): Systematics,sedimentologic and taphonomic framework

Sedimentologic and palaeontological investigation of the Upper Pliocene Slama Formation in the Lower Chelif Basin (NW Algeria) led us to collect important bivalve assemblages for taxonomic and taphonomic purposes. A rather comprehensive inventory list of Upper Pliocene bivalves from northwestern Algeria is now available and consists of 30 species, 17 of which are extinct ones. Four principal taphonomic attributes were analysed: bioerosion, encrustation, fragmentation, and abrasion. Physical and biogenic sedimentary structures are used for palaeoenvironmental interpretations. The taphonomic, sedimentologic and ichnological characteristics of most of the deposits suggests they originated from discontinuous processes of winnowing and bypassing of sediments, probably due to the action of storms in shallow waters, mainly in the shoreface depositional environment. The bivalve assemblage is dominated by disarticulated valves and displays significant taphonomic alteration in the shells. Sclerobionts traces in shells particulary affect the oyster shells. Bioerosion traces are predominately those of clionid sponges (Entobia isp.), polychaetes (Maeandropolydora isp. and Caulostrepsis isp.), bivalves (Gastrochaenolites isp.), and of predatory gastropods (Oichnus isp.). Among the sclerobionts, the identified encrusters were juvenile oyster recruits, barnacles, polychaetes (serpulid tubeworms), bryozoans (Microporella sp. and Acanthodesia sp.), and vermetid gastropods (Petaloconchus intortus).     

Invasive zebra mussels (Driessena polymorpha) and Asian clams (Corbicula fluminea) survive gut passage of migratory fish species: implications for dispersal

The introduction and spread of invasive species is of great concern to natural resource managers in the United States. To effectively control the spread of these species, managers must be aware of the multitude of dispersal methods used by the organisms. We investigated the potential for survival through the gut of a migrating fish (blue catfish, Ictalurus furcatus) as a dispersal mechanism for two invasive bivalves: zebra mussel (Driessena polymorpha) and Asian clam (Corbicula fluminea). Blue catfish (N = 62) were sampled over several months from Sooner Lake, Oklahoma, transported to a laboratory and held in individual tanks for 48 h. All fecal material was collected and inspected for live mussels. Survival was significantly related to water temperature in the lake at the time of collection, with no mussels surviving above 21.1 C°, whereas 12 % of zebra mussels (N = 939) and 39 % of Asian clams (N = 408) consumed in cooler water survived gut passage. This research demonstrates the potential for blue catfish to serve as a dispersal vector for invasive bivalves at low water temperatures.     

Associations of corals and boring bivalves since the late cretaceous

Summary The fossil record of coral and boring mytilid bivalves IS investigated. Middle Miocene associations from Austria, Hungary, and Turkey are described. As host corals,Montastrea, Porites, Siderastrea, Solenastrea, andTarbellastraea can be noted. Eocene (Waschberg Zone) and Upper Cretaceous (Gosau Formation) examples are presented from Austria only. As host corals,Favia andMontastrea, respectivelyAstrocoenia and an unidentified branching coral are recorded. The associated bivalve species are all mytilidLithophaga, includingL. laevigata (Quoy & Gaimard) inTarbellastraea, a new Middle Miocene species inMontastrea, andL. alpina (Zittel) inAstrocoenia, the latter two from Styria, Austria. Thecharacteristic features of the coral-bivalve relationships include (in massive corals): Boreholes more or less in the direction of coral growth, radially arranged, elongate boreholes, produced by keeping pace with coral growth. Bivalves were not only present near the surface, but deep inside the skeleton, representing successive generations in the same host colony. After the death of borers, their tunnels were closed by coral overgrowth. Cup-shaped false floors in the boreholes are correlated to reduced coral growth, indicating individual longevity of bivalves. The spacing of the floors mirrors the growth rate of the host coral (like its density bands), their number representing the minimal age of the respective bivalve. In branching corals, boreholes of the associated smallsizedLithophaga tended to turn into the axes of branchlets, when space was limited. Elongated boreholes and false floors were usually not developed, as bivalve growth obviously exceeded lateral growth of branchlets and specimens were rather short-lived. References to probable associations of coral and mytilid boring bivalves are given. It is quite likely that they have occurred since Jurassic times and probably since the Upper Triassic. So far, they have been ascertained since the Upper Cretaceous in massive and branching corals.     

Galvechelone lopezmartinezae gen. et sp. nov., a new cryptodiran turtle in the Lower Cretaceous of Europe

Abstract: The Spanish town of Galve (Teruel) is notable because of the abundance of Upper Jurassic and, especially, Lower Cretaceous vertebrates recorded there. Although most groups have been studied in detail, information on turtles is very limited even though the material is relatively abundant. So far, no turtle taxa have been identified at the generic level. The only Lower Cretaceous articulated specimen from Galve is analysed here. It is identified as a representative of Cryptodira, Galvechelone lopezmartinezae gen. et sp. nov. Galvechelone lopezmartinezae is determined as a taxon belonging to the node that groups the turtles traditionally assigned to ‘Macrobaenidae’ and ‘Sinemydidae’, and other taxa such as the members of Panchelonioidea. This node, very abundant in the Lower Cretaceous of Asia, and with a broad subsequent distribution, has recently been recognized in the Lower Cretaceous of Europe. The diversity of basal members of Eucryptodira in the European Late Jurassic (represented by Thalassemydidae, Plesiochelyidae and Eurysternidae) was high. Owing to a relative scarcity of well‐preserved early Cretaceous turtles from Europe, the knowledge of this group of reptiles is limited. The study of the new turtle from Galve, together with the recently described Hoyasemys jimenezi, and the recently completed review of the enigmatic Chitracephalus dumonii demonstrate that members of the cryptodiran node grouping ‘Macrobaenidae’, ‘Sinemydidae’ and Panchelonioidea were also very diverse in this period.     

THE OCCURRENCE OF ANOPAEA (BIVALVIA : INOCERAMIDAE) IN THE ANTARCTIC PENINSULA

The genus Anopaea represents a small but distinctive group ofinoceramid bivalves that apparently remained functionally endobyssate.The somewhat unusual morphology (for an inoceramid) probablyresults from structural modifications tofacilitate sedimentpenetration at a high angle and anchorage by an antero-ventralbyssus. Although never as common as thecontemporary genera Retroceramusand Inoceramus, Anopaea is now known from temperate bivalveassemblages in both the Northern and Southern Hemispheres. Itpersisted from the Late Jurassic (Tithonian) to the Early Cretaceous(Neocomian), and possibly even later. (Received 26 June 1980;