The typical pelecypod form, long thought to be primitively adaptive to burrowing, is likely to have been originally adaptive to a suspension feeding, epifaunal, possibly crawling mode of life. At small body size (< 1 cm), pelecypods possessing typical burrowing features can function as epifaunal crawlers. Pelecypods arose at small body sizes and are part of a molluscan evolutionary sequence in which relative size of the mantle cavity increased to accommodate a few large gills specialized for suspension feeding.

Acquisition of a bivalved shell by ancestral epifaunal suspension feeders may have offered protection from sediment clogging on soft bottoms, additional control over the direction, volume, and rate of water flow through the mantle cavity, more effective protection from predators, and better short-term control of the internal environment. Consideration of invertebrate groups analogous to the pelecypods (Branchiopoda, Cladocera, Ostracoda, Phyllocarida) support the view that the bivalve condition is primarily an adaptation for suspension feeding and predator avoidance in benthic environments.

The earliest known pelecypod, Fordilla troyensis Barrande, was not necessarily infaunal just because it had features similar to much larger, Recent burrowers. The size, shell morphology and environment of preservation of F. troyensis all suggest that it is reasonable to envision Cambrian pelecypods as epifaunal suspension feeders, possibly crawling on sedimentary bottoms. Moreover, the sudden Ordovician expansion of pelecypods and increase in individual size may be explained as a result of invasion of the infaunal adaptive zone.

Marine shelf lagoon deposits of Middle Ordovician age in Tennessee contain the record of repeated ecological successions which began on soft, azoic, terrigenous muds and progressed to a complex bryozoan-brachiopod community. The stages of succession formed a skeletal limestone bed. The process led to an interbedded shale-limestone stratigraphic sequence. The pioneer was the brachiopod Strophomena basilica which paved the soft mud with accumulated shells. Encrusting bryozoans colonized this shell pavement and were followed by ramose bryozoans. The final stages of succession included bryozoans, gastropods, pelecypods, and pelmatozoans but were dominated by the brachiopod Rostricellula rostrata.

Measurements of total length, width, length to growth lines (Strophomena only), and thickness (Rostricellula only) were used to generate growth-rate, and survivorship curves for these two species. Strophomena shows low juvenile mortality, a moderate, linear growth-rate, and increased mortality in later ages. Rostricellula shows relatively higher juvenile mortality, a rapid non-linear growth rate, and nearly constant mortality. These attributes are contrary to expectations derived from theory, but can be understood in the light of autecological factors for each species. Adaptation to soft substrata was the primary factor controlling population dynamics in Strophomena, and crowding was the main factor in Rostricellula.

True muscular articulations, as opposed to ligamentary ones, are reported here for the first time in the biserial arms of advanced inadunate crinoids (Poteriocrinina). The topography of biserial articular surfaces indicates clearly derivation from a uniserial muscular articulation with two muscle scars, a transverse ridge, and other structures considered typical of this articular mode. Biserial muscular articulations extend from the arm base to within a few brachials of the arm tip, although the articulations are more pronounced and better developed proximally. The inadunate facets are compared with those of the biserial arms of camerates, which are shown to be non-muscular and probably were capable of only limited movement. The arm movements of inadunate biserial arms are interpreted to have been ones where alternating muscle bundles on either side of the arm induced twisting motions of the arms so that a planar filtration fan mode of feeding was possible, in contrast to the parabolic feeding fan or other modes of feeding that were probably performed by other Paleozoic crinoids.

Fossil data suggest that the great majority of metazoan classes that existed in the Early Cambrian arose after about 700 my ago. The rectangular model of evolution, which views most evolutionary change as being concentrated in speciation events, can easily accommodate the implied rate of divergence.

If, as some authors believe, the eukaryotic cell arose long before the start of the Cambrian, an explanation is required for the delay of large-scale metazoan divergence. The advent of sexuality may have triggered diversification, not by accelerating phyletic evolution, as traditionally believed, but by making possible speciation and, hence, adaptive radiation. Another important delaying factor may have been the near-saturation of Precambrian algal systems in the absence of cropping by herbivores. Uncropped Precambrian systems should have been self-limiting in terms of diversification. When advanced heterotrophy finally arose, self-propagating feedback systems of diversification should have been set in motion. Even if the eukaryotic cell arose later than commonly envisioned and triggered the radiation of the Metazoa about 700 my ago, the earlier absence of sexuality and cropping may have delayed the transition from the prokaryotic condition to the eukaryotic condition.

The American interchange of land mammals reached its acme during the late Blancan and early Irvingtonian in North America and during the Chapadmalalan and Uquian in South America. It lasted about two million years and included taxa adapted to diverse habitats. It was preceded in the early Hemphillian in North America and the Huayquerian in South America by the interchange of a few heralding genera. The MacArthur-Wilson faunal equilibrium hypothesis correctly predicts a marked increase in originations, number of genera, and turnover rate for the South American fauna during the peak of the interchange. Subsequent further increases were not so predicted but closely resemble patterns also observed in late Pleistocene land mammals of Europe and North America. The continued increase in South American land mammal genera after the interchange had largely ceased resulted principally from autochthonous evolution of northern immigrant stocks. A marked decrease in South American ungulate genera (from thirteen to three) coincided with the appearance of fourteen northern ungulate genera and therefore appears to be a replacement phenomenon. The area/diversity relationship predicts no important change in generic diversity if a maximum of only nine percent of North America is occupied by the interamerican mingled fauna. At the family level, however, diversity is seriously overestimated due to the nomenclatural artifact of increased relative diversity by filtering.

Late Eocene to middle Oligocene floras from the area of the present Rio Grande depression represent a time sequence from the upper part of mixed subtropical forest (Bernalillo flora), to an ecotone between broadleaved sclerophyll and mixed conifer forest (Red Rock Ranch flora), to subalpine conifer forest (Hillsboro and Hermosa floras). The implied difference in mean annual temperature of ~ 11°C suggests that altitude increased 2,000 m in 6–8 my. Construction of the Datil-Mogollon volcanic pile, averaging about 1,200 to 1,500 m thick, is thought to be largely responsible for the forest zonation, but regional doming accompanying volcanism may also be involved. The Oligocene subalpine conifer forests now occur in the piñon-juniper belt 900 and 1,200 m below the present subalpine zone, consistent with the subsidence that formed the Rio Grande rift beginning in the late Oligocene/early Miocene and continuing to the present. Later epeirogenic uplift of ~ 1200 m is implied by fossil plants in the Galisteo (~ 40 my bp), Creede (~ 27 my bp) and Tesuque (~ 14 my bp) Formations that border, or are in the rift.

Genetic and morphologic differentiation in the bryozoan Schizoporella errata parallel each other over a distance of 102 km along the southern shore of Cape Cod. This is seen in the allele frequencies of two marker genes and in the length of the avicularium (a type of defensive polymorph of the bryozoan colony). These changes appear to be part of the continuing evolutionary adaptation to local environmental conditions, perhaps characteristic of marine species whose dispersal ability is very limited. The length scale of significant changes in allele frequencies at the two loci is as low as 10–11 km, and for avicularium length is 13 km.