Symbioses are often regarded as an important means for the creation of evolutionary novelty as well as a trigger for the abrupt appearance of higher taxa. The fossil record of foraminifer-algal symbiosis suggests that the appearance of this ecological association contributed to the radiation of Paleogene planktic foraminifera. Isotopic evidence shows that photosymbiosis evolved in synchrony with a major diversification of trochospiral planktic foraminifera about 3.5 m.y. after the end-Cretaceous extinction. In modern planktic foraminifera, photosymbiotic species tend to have more cosmopolitan distributions than asymbiotic foraminifera and a greater ability to withstand periods of nutrient stress. The simultaneous taxonomic radiation and acquisition of photosymbiosis are evidence that the ecological strategy permitted Paleocene foraminifera to expand their niche in pelagic environments by diversifying into low-nutrient surface waters.

A comparison of the species longevities of Neogene and Paleogene symbiotic clades suggests that photosymbiosis does not regulate the characteristic rate of taxonomic turnover in clades after they appear. Species longevities are much shorter in Paleocene and Eocene photosymbiotic morphospecies than they are among photosymbiotic Neogene clades; apparently photosymbiosis does not exert a significant control over long-term evolutionary rates. In addition, the absence of a characteristic morphology associated with photosymbiosis in Cenozoic planktic foraminifera suggests that morphology, as with rate of evolutionary turnover, is linked to symbiosis only because of common inheritance instead of a functional relationship. Although the coincidence between the acquisition of photosymbiosis and generic diversification does suggest a linkage between this ecology and the appearance of foraminiferal higher taxa, there is little indication at the present that symbioses control long-term morphological or ecological patterns within these groups after their appearance. Photosymbiosis, and other evolutionary innovations, may be more a catalyst for the differentiation of major groups than a predictable governor on evolutionary rates.

The Brontotheriidae (Perissodactyla, Mammalia) are often used as an illustration of vertebrate macroevolutionary trends because their morphological evolution includes significant size increases accompanied by the disproportionate lengthening of bony frontonasal horns. The positive phylogenetic allometry for horn length vs. skull length is among the strongest known of such relationships in vertebrate phylogeny. Hypotheses explaining the change from small, incipient horns in Eocene ancestors to longer horns in Oligocene descendants have included two heterochronic mechanisms, hypermorphosis (extrapolation) and predisplacement (earlier onset time of horn growth). These proposed peramorphic mechanisms derive from interpretation of adult intergeneric allometries in logarithmic data spaces. Analysis of the raw (unlogged) data shows that the simple allometric model previously used is not an appropriate model for this specific problem. The heterochronic interpretations derived from them are therefore unsupported (but not disproven) by the allometries. A more appropriate allometric model for the data (full model) does not support any heterochronic interpretation. Previously unaccounted for in the heterochronic hypotheses is a complication due to body-size scaling effects on life history stage lengths. Neontological scaling patterns suggest that brontothere size increases were probably accompanied by increasing life spans and longer developmental stages. This effect broadens the types of heterochronies that may be postulated. Semiquantitative analyses comparing brontotheres with similarly sized extant ungulates show the hypothesized effect of larger size on brontothere life history stages. A scaled descendant ontogeny introduces the problem of relative vs. absolute time frames within which to view ontogenetic onset times. Thus, predisplacements, postdisplacements, or nondisplacements may be viewed as relative or absolute with respect to ancestral ontogenies. This raises a fundamental question about how development scales, which in turn affects how heterochronies are interpreted. A scaling effect suggests that brontothere horns are more likely postdisplaced in the traditional absolute time sense. Paradoxically then, while the descendant adult horn is peramorphic, its onset time may have shifted in a paedomorphic direction. Data for two Oligocene juvenile brontotheres suggest that most horn growth occurred late in their longer (i.e., descendant) ontogenies (hypermorphosis), and that the horns probably grew at faster rates (acceleration) than in Eocene taxa.

Dorsal sails supported by hyperelongate neural spines of dorsal vertebrae were evolved by various tetrapods, but most work on their function has centered on the pelycosaur Dimetrodon, in which the sail has generally been interpreted as a thermoregulatory structure that would permit rapid warming in the morning and cooling during the hot midday. The pelycosaur Edaphosaurus differed from other sailed tetrapods in that the neural spines supporting the sail had laterally directed tubercles or cross-bars. Past interpretations of Edaphosaurus suggested that the cross-bars were embedded in a thick fat-storage structure or extended from a thin sail to enhance its utility for intraspecific display. However, wind tunnel modeling of air flow over a thin sail with laterally projecting cross-bars supports a thermoregulatory interpretation of the sail of Edaphosaurus. The cross-bars would produce a turbulent flow, which would increase the effectiveness of convective cooling. Measurements of heat flow in an instrumented model show that cross-bars increase heat loss from the sail. The cross-bars may have enabled Edaphosaurus to thermoregulate effectively with a smaller and lower dorsal sail than would have been required without them.

Steneofiber, an early Miocene European beaver, showed evidence of a K-strategy model of reproduction and important morphological modifications for better adaptation to a semiaquatic way of life. At the same time, a North American branch of Castoridae developed not only a parental care system but also a series of cranial and postcranial osteological adaptations to a burrowing way of life. As the North American and the European Castoridae evolved independently from each other for at least fifteen m.y., these behavioral trends seem to have been inherent in the family for a long time and have apparently promoted, up to the present time, the spread of semiaquatic forms on the two continents; on the contrary, the burrowing branch of the Castoridae rapidly vanished.

We report quantitative paleoecologic data on the large mammal assemblage preserved in lower Pleistocene deposits at Venta Micena (Orce, Granada, southeastern Spain). Taphonomic studies show that bones were collected mainly by hyaenids, which transported and deposited them near shallow dens. Differential fragmentation of major long bones was produced by hyaenas as a function of their density and marrow content. Strong selection of prey by carnivores—which preferentially killed juveniles, females, and individuals with diminished locomotor capabilities among ungulate prey species of larger body size—is indicated by (1) the abundance of remains of juvenile ungulates in relation to the average weight of adult individuals in each species, (2) attritional mortality profiles for ungulate species deduced from crown height measurements, (3) the presence of many metapodials with different osteopathologies in their epiphyses, such as arthrosis, and (4) a biased intersexual ratio of large bovids. Comparison of the frequencies with which modern African carnivores kill and scavenge ungulates from various size classes with the abundance of these size categories in the assemblage suggests that the Venta Micena hyaena (Pachycrocuta brevirostris) was a bone-cracking scavenger that fed largely on carcasses of ungulates preyed upon and partially consumed by fresh meat-eating carnivores such us saber-toothed felids (Homotherium latidens and Megantereon whitei) and wild dogs (Canis falconeri).

Eocene lake beds of Horsefly, British Columbia, are preserved in varves, or discrete yearly layers representing seasonal changes in the lake. These varves allow study of temporal variation and rates of change in morphological and ecological characters on a very short time scale. One of the most sensitive indicators of the paleoenvironmental conditions on the floor of the lake may be the taphonomic condition of the fishes, which vary between perfectly articulated and completely disarticulated skeletons. Patterns of disarticulation correspond to those produced by scavengers. The taphonomy supports the hypothesis that the lake was warm monomictic, circulating in the winter, at which time scavengers could gain access to the bottom of the lake. Larger-scale environmental events (on the order of hundreds of years) are suggested by the fact that the proportion of well-preserved specimens reached two peaks within the seven centuries of deposition, one peak during the second century and another during the fifth and sixth centuries. These results clearly demonstrate two principles: that taphonomy can be a sensitive indicator of paleoenvironmental conditions, and that temporal averaging can affect the taphonomic properties of this fossil site, and presumably of others with equal or lower time resolution.

Study of the assemblage of encrusting organisms on co-occurring disarticulated valves of the bivalves Crassostrea virginica and Mercenaria mercenaria in Bogue Sound, North Carolina, indicates that there is little or no substrate specificity among the encrusting organisms but that the shape of the shells has an important influence on how extensively members of each higher taxon collectively inhabit the shells. Encrusting bryozoans, a dense low mat composed of many species from diverse phyla, and a unicellular film cover most of the area of both exterior and interior surfaces. The encrusting bryozoans most extensively cover both surfaces of C. virginica but are in second place behind the multispecies mat on exterior surfaces of M. mercenaria and behind the unicellular film on its interior surfaces. These differences are inferred to result from different physical stability of valves of the two bivalve species, which exhibit different frequencies of circumrotatory growth.

Degradation of the assemblage by sodium hypochlorite, to simulate loss of organic matter during fossilization, results in the complete loss of encrusting sponges, erect hydrozoans, erect bryozoans, and ascidians. Loss of these taxa results in overexposure and more apparently uniform distribution of skeletal taxa with respect to their surface representation in living assemblages and also in complete loss of the higher tiers present in the living assemblage. However, indications of the original structural organization of the living assemblage is indicated by preservation of the most abundant taxa in the lower tiers and by the retention in the reduced treated assemblage of the patterns of distribution that characterized the living assemblage.