Abstract Bivalves first appeared in the Early Cambrian and were virtually cosmopolitan. These very small and insignificant molluscs were probably surface crawlers on the microbial mat floors of the Cambrian sea. They evolved little further in the Mid Cambrian and by the Late Cambrian had apparently disappeared from the fossil record. Their re-appearance in the Early Ordovician coincided with a major diversification in which all the principal bivalve clades evolved, but the class was confined to Gondwana; their habitat was now principally infaunal in siliciclastic sediments. In the Mid Ordovician a few forms reached Baltica and the eastern Laurentian margin, but it was the Late Ordovician before bivalves once again became cosmopolitan. This geographical dispersal allowed bivalves to colonize the low-latitude carbonate platforms and led to the development of diverse epifaunal faunas, although most remained as infaunal forms in siliciclastic sediments. The end-Ordovician regression occasioned by the Hirnantian glaciation caused major extinction of those epifaunal forms restricted to the carbonate platforms. The Silurian faunas were cosmopolitan and the major evolutionary event was caused by the appearance of a Gondwanan cephalopod limestone facies that provided sites for epibyssate praecardiidinid bivalves (=Nepiomorphia) that evolved rapidly and were able to withstand short periods of anoxia.

Abstract Bivalves have a wide distribution in the Lower and to a lesser extent Middle Cambrian rocks, but they have not yet been certainly identified in the Upper Cambrian. Recent discoveries have significantly increased our knowledge of Lower Ordovician bivalve faunas and their explosive radiation from the Early Ordovician apparently coincides with the evolution of the feeding gill. Early Ordovician faunas were confined to the siliciclastic facies of Gondwanan shelf seas; most genera were clearly latitudinally constrained, but others apparently migrated over wide latitudes. By the Mid-Ordovician, bivalves had begun to escape the confines of Gondwana and marked latitudinal differences in the composition of the faunas became apparent, with pteriomorphians showing clear preference for low latitudes, whilst heteroconchs clearly preferred median to high latitudes; surprisingly, nuculoids were both most diverse in terms of species and most abundant as a percentage of individuals within the bivalve populations at low latitudes. It was in the Late Ordovician that bivalves colonized the low-latitude carbonate platforms of Laurentia and Baltica, leading to a second major diversification particularly within the pteriomorphian bivalves, which developed semi-infaunal and epifaunal habits; they became the dominant low-latitude bivalve group. The latest-Ordovician eustatic regression which exposed the low-latitude carbonate platforms resulted in a major reduction in the epifaunal and semi-infaunal bivalves involving extinction of many genera, including the only Ordovician boring bivalves.

Abstract In the 30 years since publication of the bivalve Treatise , (Moore, R. C. (ed.) 1969. Treatise on Invertebrate Paleontology. Part N. Mollusca 6, Bivalvia , Geological Society of America and University of Kansas) important new faunas have been described from the early and mid Cambrian and from the early and mid Ordovician. These contain significant new forms, including some long-ranging intermediate groups, that indicate the relationships between the principal bivalve clades, but lack of fossils from the late Cambrian and earliest Ordovician is a major hindrance. The principal phase of bivalve diversification followed on from the evolution of the filibranch gill in the latest Cambrian or earliest Ordovician. The fundamental division of the class is into two subclasses, Protobranchia and Autolamelli branchiata; links between the two can be demonstrated in the early Ordovician. Major divisions of each subclass are recognized as superorders. Within the Protobranchia, the Nuculoida developed specialist food-gathering palps and an enlarged foot. Diverging early from the protobranch stock were other bivalves that lived symbiotically with sulphur-oxidizing chemoautotrophic bacteria; this allowed colonization of anaerobic substrates and produced two distinct stocks: the deeply infaunal anteriorly elongate Solemyoida and the shallower infaunal Nucinelloida. The Autolamellibranchiata, initially identified by strongly asymmetrical hinges, diversified in three directions, each characterized by distinctive hinges. The Trigonioida were characterized by ligamental nymphs and frequently denticulate teeth, and rapidly regained greater symmetry; the Anomalodesmata also developed a strong ligamental insertion within nymphs and largely lost their dentition, whilst the Heteroconchia, principally with a shell including a complex crossed-lamellar structure, had various combinations of cardinal and lateral teeth. Heteroconch diversifications were mainly in the Mesozoic and Cenozoic, but one Ordovician group, the Glyptarcoidea, is a good ancestor for the Pteriomorphia. The following new taxa are proposed: Cardiolarioidea superfam. nov., Eritropidae fam. nov. and Catamarcaidae fam. nov.