Two methods are discussed for assessing the contributions of subgroups to the morphological disparity of the larger group containing them. (1) Given an ordination of points representing specimens or species in morphological space, morphological disparity of the entire group is measured as the average squared distance of points from the centroid. The contribution that a subgroup makes to morphological disparity is measured as the average squared distance of its points from the overall centroid (not the subgroup centroid), weighted by the subgroup sample size relative to the total group sample size. Thus, morphological disparity of a group can be additively partitioned into the disparity components of its subgroups, and the relative contributions of these subgroups can be assessed quantitatively. (2) An alternative approach is to compare morphological disparity of a group to the disparity it would have if a certain subgroup were omitted. If the resulting disparity differs substantially from the original disparity, then the subgroup in question is considered to have a significant effect on morphological disparity. Because some subgroups are very centralized in morphological space, omitting them can cause an increase in morphological disparity when disparity is measured as the average dissimilarity among species. In general, relatively large subgroups that are located peripherally in morphospace make the greatest contributions to morphological disparity, and failure to sample smaller groups often has little effect on disparity estimates. The two methods are applied to morphological disparity in trilobites, partitioned at different levels in the taxonomic hierarchy. Results of the two methods are intuitively reasonable and largely in agreement, and point to the predominance of Early Cambrian olenelloids, Cambro-Ordovician Libristoma, Ordovician Asaphina and Cheirurina, Siluro-Devonian Phacopida and Phacopina, and Devonian Proetida.

Rapid shell closure in articulate brachiopods occurs by a twitch contraction of the “quick” adductor muscles. Rapid accelerations and decelerations of the valves induce large accelerations of the surrounding fluid, placing constraints on the speeds of closure; inertial forces govern the mechanics of the closing mechanism. The position, size, and physiological properties of the muscles, and the size and shape of the shell, govern the properties of the shell closing system. A numerical model predicts that, for given muscle and shell characteristics, there is a location of the adductor muscle which maximizes the shell's closing velocity, and that this position shifts allometrically with size. Positive allometry in the muscle's moment arm length is observed in both living and fossil brachiopods, although the observed coefficients are less than those predicted by the model.

The brachiopod closing mechanism provides a model for understanding the biomechanical interrelationships between components of dynamic skeletal systems. Dynamic systems, where the muscles induce resisting inertial reactions, are characterized by mechanical feedback loops, or couplings. Mechanical couplings may represent an important class of constraints on the evolution of skeleto-muscular architecture.

We studied mammal and bird track formation at the northern edge of Lake Manyara, Tanzania, to develop models for interpreting fossil tracks and trackways. Lake Manyara is a closed-basin, alkaline lake in the East African Rift System. The area has a high vertebrate diversity, allowing us to investigate tracks in an environment similar to that of many ancient track-bearing sequences. Three study sites, two on mud flats adjacent to the lake margin and a third on a delta floodplain, provided contrasting environments in which to assess the types of biological data that can potentially be extracted from fossil trackways.

Our censuses of mammals and their tracks revealed that most species that occur within the study area leave a track record, and that common species leave abundant tracks, although numbers of trackways are not proportional to numbers of individuals. Logarithmic increases in track sampling area yield a linear increase in the proportion of both the medium and large-sized local mammals represented in a track record. Transect vs. area mapping methods produced different censusing results, probably because of differences in monitoring periods and areal coverage.

We developed a model of expected track production rates that incorporates activity budget and stride length data in addition to abundance data. By using these additional variables in a study of diurnal birds, we obtained a much better estimator relating track abundance to trackmaker abundance than that provided by census data alone. Proportions of different types of tracks predicted by the model differ significantly from the observed proportions, almost certainly because of microenvironmental differences between the censusing and track counting localities. Censuses of fossil tracks will be biased toward greater numbers of depositional-environment generalists and away from habitat-specific species.

Trackways of migratory animals were dominantly shoreline-parallel, whereas trackways of sedentary species were more variable. A strong shoreline-parallel environmental zonation at the Alkaline Flats site exerted an influence on trackmaker distribution patterns, initial track formation, and track preservation. Variations in habitat usage by different species, as well as species abundance and directionality of movement, were all important in determining the number of preservable tracks a species produced within a given environmental zone.

Fossil trackways are time-averaged, although over entirely different temporal scales than are bones. Unlike bones, tracks are not space-averaged. Therefore, wherever possible, fossil track and bone studies should be used to complement each other, as they provide fundamentally different pictures of paleocommunities. Tracks provide “snapshot” views of localized assemblages of organisms useful in reconstructing autecological relationships, whereas bones yield a broader image of a local fauna in which seasonal and microenvironmental variation are more commonly smoothed out.

Pterobranchs are the closest living relatives of graptolites. Their skeleton is constructed from the same material, and in a homologous manner. Growth rates of the pterobranch Cephalodiscus gracilis are described for the first time and, along with rhabdopleuran growth rates, they are used to estimate the amount of time invested by a graptolite colony in growing its rhabdosome. This is a measure of minimum age. The significance of age calculations is shown for individuals and large communities of graptoloids. Large individuals can be shown to be much older than the time it would have taken them to settle through seawater and so it is shown that graptoloids moved up, as well as down, through the water column. Life tables constructed for biserial graptoloids from the Utica shale in Quebec, Canada, suggest that these graptoloids died from constant environmental stress. Graptoloid length can thus be a function of environment and should only cautiously be considered to be of taxonomic significance.

Predatory marine snails and their prey provide a unique look at many aspects of predation events, allowing behavioral inference and studies of coevolution. This study examines differential predation patterns, rates, and success of two co-occurring gastropod predator families which drill two co-occurring species of Turritella (Turritellidae: Gastropoda) in the Gulf of California. Both naticid and muricid predators, identified by the shapes of their respective boreholes, attacked the thinner-shelled Turritella leucostoma more frequently than the thicker-shelled Turritella gonostoma. Both species were drilled more frequently and more successfully by naticid, as compared to muricid, predators. Naticids drilled prey in the 40- to 70-mm size class most frequently. Prey over 100 mm in length were relatively safe from all drilling predators. Predator size (estimated by borehole diameter) in naticids was correlated with prey size in both species, but for a given-sized prey, predators on T. gonostoma were proportionally larger. There was no size correlation for muricid predators. Unsuccessful attempts (incomplete drilling) were started on the suture more often than were completed holes, for both predator families on both prey species. Naticids began drilling T. leucostoma on the suture significantly less than expected by chance. We looked for possible changes over evolutionary time by analyzing prey shells from Pleistocene and Recent storm deposits. We found no evidence of change in any aspect of implied predatory behavior over the past 100 k.y.

The incidences of selected features of dicotyledonous wood that are believed to be of ecologic and/or phylogenetic significance (distinct growth rings, narrow and wide vessel diameter, high and low vessel frequencies, scalariform perforations, tangential vessel arrangement, ring porosity, and helical wall thickenings) were plotted through time (Cretaceous–Recent). There are marked differences between the Cretaceous and Tertiary in the frequency of all wood anatomical features. Incidences of features that are associated with markedly seasonal climates in extant floras do not approach modern levels until the Neogene. Correlations of wood anatomical features with ecology do not appear to have been constant through time, because in the Cretaceous different features provide conflicting information about the climate. Throughout the Tertiary the southern hemisphere/tropical and the northern hemisphere/temperate regions differed in the incidences of ecologically significant features and these differences are similar to those in the Recent flora. Possibilities for reliably using dicotyledonous wood for climatic reconstructions appear restricted to the Tertiary and Quaternary. However, at present the fossil wood record for most epochs and regions is too limited to permit detailed reconstructions of their past climate.

Climatic change has long been regarded as an important factor in evolutionary history. In particular, periods of enhanced extinction in marine taxa (especially those from warmer waters) have frequently been linked to decreases in seawater temperature. Studies of the physiology of marine invertebrates and fish alive today have revealed well-developed abilities to cope with temperature change, and there would thus appear to be a dichotomy between the rates of temperature change associated with extinction in geological history and the very much faster rates (by several orders of magnitude) with which many marine organisms can cope today. Nevertheless, evidence from ecology and biogeography indicates that temperature, or some temperature-associated factor, does play a significant role in determining the limits to performance, and hence distribution. The resolution of the dichotomy between the evidence from paleontology and physiology may come through a consideration of the role of the previous evolutionary history of the fauna, the influence of sudden temperature events, or the impact of climatic change on individual competitive ability, community structure, and ecosystem functioning. Studies of the energetics of marine invertebrates in relation to temperature and the evolutionary history of polar faunas indicate that we should beware of anthropocentric judgements in attempting to understand the role of climatic change in evolutionary history, and be critical in distinguishing the role of temperature per se from temperature-associated ecological factors. Present evidence suggests that climatic change in the sea, at least at the rates currently believed to be typical, is unlikely to cause extinction by direct physiological impact. It is more likely that extinction is caused by ecological factors; temperature change is thus only one of several factors that may promote those ecological changes that are currently the best candidates for the proximate cause of extinction in the sea.