The demonstration of sexual dimorphism in the fossil record can provide vital information about the role that sexual selection has played in the evolution of life. However, statistically robust inferences of sexual dimorphism in fossil organisms are exceedingly difficult to establish, owing to issues of sample size, experimental control, and methodology. This is particularly so in the case of dinosaurs, for which sexual dimorphism has been posited in many species, yet quantifiable data are often lacking. This study presents the first statistical investigation of sexual dimorphism across Dinosauria. It revisits prior analyses that purport to find quantitative evidence for sexual dimorphism in nine dinosaur species. After the available morphological data were subjected to a suite of statistical tests (normality and unimodality tests and mixture modeling), no evidence for sexual dimorphism was found in any of the examined taxa, contrary to conventional wisdom. This is not to say that dinosaurs were not sexually dimorphic (phylogenetic inference suggests they may well have been), only that the available evidence precludes its detection. A priori knowledge of the sexes would greatly facilitate the assessment of sexual dimorphism in the fossil record, and it is suggested that unambiguous indicators of sex (e.g., presence of eggs, embryos, medullary bone) be used to this end.

The extinction of endemic brachiopods in North America at the end of the Ordovician and recolonization by European species has been related to glacio-eustatic lowering of sea level which disrupted conditions in epicontinental seas. North American species may have been narrowly adapted to relatively stable conditions of broad, tropical shallow seas. European invaders may have been less specialized because they were adapted to conditions in both the open ocean and in narrow European epicontinental seas. Being less narrowly adapted, European species probably were better able to cope with changing environmental conditions than were North American species.

During the Lower and Middle Llandovery, shallow water, low diversity communities of Pentamerus Community depth were unstable and characterized by repeated extinctions and invasions. Following the crisis at the Ordovician-Silurian boundary 3 to 5 million years were needed to reestablish communities that were persistent in geologic time.

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.

The Upper Jurassic Morrison Formation has yielded one of the richest dinosaur faunas of the world. Morrison sediments are distributed over more than a million square kilometers in the western United States and represent a mosaic of riverine, lacustrine and floodplain environments developed on a vast alluvial plain nourished by debris from the ancestral Rocky Mountains. Plant productivity must have been reasonably high to support abundant large-bodied herbivores, but the absence of coals, scarcity of small aquatic vertebrates, the abundance of oxidized sediments, and presence of calcretes lead us to believe that water was periodically in short supply. A strongly seasonal climate may have necessitated annual large-scale movements of large herbivores, accounting in part for their remarkably broad and uniform geographic distribution. Dinosaur diversity is lower in the Morrison than in the Late Cretaceous, and taphonomic alteration is higher. Massed accumulations of thousands of bones are characteristic of the Morrison. Morrison dinosaurs were not confined to specific depositional environments but were distributed across the complete spectrum of available habitats, from lakes to dry floodplains; this type of distribution is similar to that of large terrestrial mammals such as elephants and rhinos and is different from that of hippos and crocodiles. Common Morrison taxa were Camarasaurus, Apatosaurus, Diplodocus, Allosaurus and Stegosaurus; these genera probably constituted a true dinosaur community. Stegosaurus may have been partially segregated from the other genera, and Camptosaurus more strongly so. Camarasaurus and Diplodocus were gregarious, with juveniles and subadults of the former particularly common; Apatosaurus was less abundant and more solitary in its habits. Juveniles and subadults are known for a number of dinosaurs.

This paper presents scaling equations relating suspension-feeding rates to body size for articulate brachiopods and bivalve molluscs, two classes which represent a significant component of the fossil record of marine benthic communities. Clearance (feeding) rates of five species of living articulate brachiopods and three species of epifaunal suspension-feeding bivalve molluscs collected from mid-latitude fjords of Newfoundland and New Zealand were measured in similar experimental conditions. In comparisons within and between the two classes, we found that both plectolophous and spirolophous brachiopods had significantly lower feeding rates than mytilids, which are filibranchs, but that a sympatric primitive eulamellibranch veneroid bivalve had rates comparable to the brachiopods. Articulate brachiopods do not appear to feed effectively at the high algal concentrations which bivalves can exploit. The data on comparative suspension-feeding rates support the hypothesis that past changes in diversity and distribution of bivalves and brachiopods may be related to an overall increase in energy flux and escalation of metabolic rates during the Phanerozoic.

Brachiopods generally have not been considered to be typical or significant faunal components of modern or ancient hydrothermal vent and cold-seep settings. The Early Cretaceous (Neocomian) rhynchonellide brachiopod Peregrinella has long been viewed as a paleontological curiosity because of its distinctive morphology, status as the largest Mesozoic brachiopod, anomalous stratigraphic associations, and widespread, yet discontinuous paleogeographic distribution. Examination of all worldwide Peregrinella occurrences (14) indicates restriction of this brachiopod to ancient cold-seeps. It is probable that Peregrinella grew to large sizes in such great abundances at fossil cold-seep sites because of a richly organic food supply generated by localized fluid seepage and bacterial chemosynthetic activity. Living brachiopods are not known to harbor chemosymbiotic bacteria in their tissues; however, direct chemoautotrophic utilization of reduced fluids by Peregrinella cannot be rejected or demonstrated at present. Peregrinella occurs at widely separated cold-seeps of Neocomian age (e.g., California, Mexico, Tibet, Europe), yet its mode of dispersal and larval development is unknown. In modern hydrothermal vents of the deep-sea, organism dispersal occurs along oceanic ridges, where benthic faunas display both planktotrophic and nonplanktotrophic larval-mode types. Peregrinella may represent a Mesozoic relic of a long-lived “lineage” of vent-seep associated rhynchonellides from the Paleozoic (e.g., ?Eoperegrinella, Dzieduszyckia), but major gaps in the stratigraphic record between these rhynchonellide occurrences, and the lack of rigorous phylogenetic analysis for these groups preclude a clear resolution of the origin(s) of vent-seep brachiopods at present.

Scanning electron microscope (SEM) examination of bone surfaces from the Pleasant Lake mastodon, excavated in southern Michigan, documents features indicative of butchery. These features are identified by comparison with modern bones modified by human and natural processes. We report new studies of (1) marks made by bone tools during removal of meat from and disarticulation of carcasses and (2) use wear developed on bone tools. We also apply previously developed criteria for recognizing stone tool cutmarks and stages in the burning of bone. The Pleasant Lake site, dated to between 10,395 ± 100 and 12,845 ± 165 b.p., provides compelling evidence of mastodon butchery and bone tool use. Another site, near New Hudson, Michigan, provides replication of much of this evidence. Together these sites offer new examples of patterns of bone modification and extend the geographic and temporal representation of the much discussed, but still controversial, late Pleistocene bone technology.

In recent years several authors have questioned the reality of a widely accepted and apparently large increase in marine biodiversity through the Cenozoic. Here we use collection-level occurrence data from the rich and uniquely well documented New Zealand (NZ) shelfal marine mollusc fauna to test this question at a regional scale. Because the NZ data were generated by a small number of workers and have been databased over many decades, we have been able to either avoid or quantify many of the biases inherent in analyses of past biodiversity. In particular, our major conclusions are robust to several potential taphonomic and systematic biases and methodological uncertainties, namely non-uniform loss of aragonitic faunas, biostratigraphic range errors, taxonomic errors, choice of time bins, choice of analytical protocols, and taxonomic rank of analysis.

The number of taxa sampled increases through the Cenozoic. Once diversity estimates are standardized for sampling biases, however, we see no evidence for an increase in marine mollusc diversity in the NZ region through the middle and late Cenozoic. Instead, diversity has been approximately constant for much of the past 40 Myr and, at the species and genus levels, has declined over the past ~5 Myr. Assuming that the result for NZ shelfal molluscs is representative of other taxonomic groups and other temperate faunal provinces, then this suggests that the postulated global increase in diversity is either an artifact of sampling bias or analytical methods, resulted from increasing provinciality, or was driven by large increases in diversity in tropical regions. We see no evidence for a species-area effect on diversity. Likewise, we are unable to demonstrate a relationship between marine temperature and diversity, although this question should be re-examined once refined shallow marine temperature estimates become available.

Analysis of two independent data sets with increased taxonomic resolution (genera rather than families) using the revised 2012 timescale reveals that an extinction periodicity first detected by Raup and Sepkoski (1984) for only the post-Paleozoic actually runs through the entire Phanerozoic. Although there is not a local peak of extinction every 27 Myr, an excess of the fraction of genus extinction by interval follows a 27-Myr timing interval and differs from a random distribution at the p ∼ 0.02 level. A 27-Myr periodicity in the spectrum of interval lengths no longer appears, removing the question of a possible artifact arising from it. Using a method originally developed in Bambach (2006) we identify 19 intervals of marked extinction intensity, including mass extinctions, spanning the last 470 Myr (and with another six present in the Cambrian) and find that ten of the 19 lie within ±3 Myr of the maxima in the spacing of the 27-Myr periodicity, which differs from a random distribution at the p = 0.004 level. These 19 intervals of marked extinction intensity also preferentially occur during decreasing diversity phases of a well-known 62-Myr periodicity in diversity (16 of 19, p = 0.002). Both periodicities appear to enhance the likelihood of increased severity of extinction, but the cause of neither periodicity is known. Variation in the strength of the many suggested causes of extinction coupled to the variation in combined effect of the two different periodicities as they shift in and out of phase is surely one of the reasons that definitive comparative study of the causes of major extinction events is so elusive.

This paper tests whether the most common fossil brachiopod, gastropod, and bivalve genera also have intrinsically more durable shells. Commonness was quantified using occurrence frequency of the 450 most frequently occurring genera of these groups in the Paleobiology Database (PBDB). Durability was scored for each taxon on the basis of shell size, thickness, reinforcement (ribs, folds, spines), mineralogy, and microstructural organic content. Contrary to taphonomic expectation, common genera in the PBDB are as likely to be small, thin-shelled, and unreinforced as large, thick-shelled, ribbed, folded, or spiny. In fact, only six of the 30 tests we performed showed a statistically significant relationship between durability and occurrence frequency, and these six tests were equally divided in supporting or contradicting the taphonomic expectation. Thus, for the most commonly occurring genera in these three important groups, taphonomic effects are either neutral with respect to durability or compensated for by other factors (e.g., less durable taxa were more common in the original communities). These results suggest that biological information is retained in the occurrence frequency patterns of our target groups.

Geographical restriction to refuges implies the regional extinction of taxa in areas of the previous range falling outside the refuge. A comparison of the circumstances in the refuge with those in areas from which the taxa were eliminated is potentially informative for pinpointing the causes of extinction. A synthesis of data on the geographical and stratigraphical distributions of cool-water molluscs of the North Pacific and North Atlantic Oceans during the late Neogene reveals four patterns of geographical restriction, at least two of which imply that climatic cooling was not the only cause of extinction during the last several million years. These four patterns are (1) the northwestern Pacific restriction, involving 15 taxa whose amphi-Pacific distributions during the late Neogene became subsequently restricted to the Asian side of the Pacific; (2) the northwestern Atlantic restriction, involving six taxa whose early Pleistocene distribution is inferred to have been amphi-Atlantic, but whose present-day and late Pleistocene ranges are confined to the northwestern Atlantic; (3) a vicariant Pacific pattern, in which many ancestral amphi-Pacific taxa gave rise to separate eastern and western descendants; and (4) the circumboreal restriction, involving six taxa whose early Pleistocene distribution, encompassing both the Atlantic and Pacific Oceans, became subsequently limited to the North Pacific. Like the Pliocene extinctions in the Atlantic, previously studied by Stanley and others, the vicariant Pacific pattern is most reasonably interpreted as having resulted from regional extinction of northern populations in response to cooling. The northwestern Pacific and Atlantic restrictions, however, cannot be accounted for in this way. In contrast to the northeastern margins of the Pacific and Atlantic, the northwestern margins are today characterized by wide temperature fluctuations and by extensive development of shore ice in winter. Northeastern, rather than northwestern, restriction would be expected if cooling were the overriding cause of regional extinction. Among the other possible causes of extinction, only a decrease in primary productivity can account for the observed northwestern and circumboreal patterns of restriction. Geographical patterns of body size and the distribution of siliceous deposits provide supporting evidence that primary productivity declined after the Miocene in the northeastern Pacific, but remained high in the northwestern Pacific, and that productivity in the Pacific is generally higher than it is in the Atlantic. The patterns of geographical restriction in the northern oceans thus provide additional support to previous inferences that reductions in primary productivity have played a significant role in marine extinctions.

To understand how well fossil assemblages represent original communities, paleoecologists seek comparisons between death assemblages and their source communities. These comparisons have traditionally used nearshore, marine invertebrate assemblages for their logistical ease, high abundance, and comparable census data from living communities. For large marine vertebrates, like cetaceans, measuring their diversity in ocean ecosystems is difficult and expensive. Cetaceans, however, often beach or strand themselves along the coast, and archived data on stranded cetaceans have been recorded, in some areas, over several decades. If the stranding record is interpreted as a death assemblage, then the stranding record may represent a viable alternative for measuring diversity in living communities on directly adjacent coastlines. This study assessed the fidelity of the cetacean stranding record in the eastern North Pacific Ocean. The living community in this region has been studied for over 100 years and, recently, extensive and systematic live transect surveys using ship-based observing platforms have produced a valuable source of live diversity data. Over this same period, the U.S. Marine Mammal Stranding Program has collected and archived a record of cetacean strandings along the U.S. Pacific coastline, providing an ideal death assemblage for comparison. Using fidelity metrics commonly used in marine invertebrate taphonomy, I determined that the stranding record samples the living cetacean community with high fidelity, across fine and coarse taxonomic ranks, and at large geographic scales (>1000 km of coastline). The stranding record is also richer than the live surveys, with live-dead ratios between 1.1 and 1.3. The stranding record recovers similar rank-order relative abundances as live surveys, with statistical significance. Also, I applied sample-based rarefaction methods to generate collector's curves for strandings along the U.S. Pacific Coast to better evaluate the spatiotemporal characteristics of the stranding record. Results indicate that saturation (i.e., sampling >95% assemblage) at species, genus, and family levels occurs in less than five years of sampling, with families accumulating faster than species, and larger geographic regions (i.e., longer coastlines) accumulating taxa the most rapidly. The high fidelity of the stranding record, measured both in richness and by ranked relative abundance, implies that ecological structure from living cetacean communities is recorded in the death assemblage, a finding that parallels marine invertebrate assemblages, though at far larger spatial scales. These results have implications for studying cetacean ecology in both modern and ancient environments: first, these results imply that the stranding record, over sufficiently long time intervals, yields a richer assemblage than using line-transect methods, and faithfully records aspects of community structure; and second, these results imply that geochronologically well-constrained fossil cetacean assemblages might preserve ecologically relevant features of community structure, depending on depositional and taphonomic conditions.

This analysis examines the evolution of the greater diversity of species with non-planktonic larval types relative to species with planktonic larval types in the turritellid gastropods. This sort of trend has been documented in both the fossil and recent biota of several gastropod families. Two mechanisms for generating diversity gradients in larval types have been proposed in the literature. The first, species selection, focuses on the population biology of larval types. The second proposes that factors in development that are mediated by organismal adaptation are responsible. Turritellids have been cited as a classic example of species selection. In order to examine the relevance of these two proposed mechanisms, a phylogenetic analysis of the turritellids using molecular sequence data was performed to determine the evolution of larval types in this clade. The resultant phylogeny suggests that species selection is not the only process driving the trend toward increasing numbers of non-planktonic species through time. Developmental processes, apart from those involving organismal adaptation (except in the trivial sense), are implicated as playing a role in this trend. In particular, these processes may involve changes in the timing of germ-line sequestration in organisms. Germ-line sequestration governs how accessible organisms are to heritable variation during ontogeny. Embryological evidence from gastropods suggests that non-planktonic species have early germ-line sequestration relative to planktonic species, making them more resistant to developmental change. Thus, non-planktonic lineages will only rarely revert to a planktonic larval mode.

Lambeosaurine dinosaur crests are judged to have been conducive to resonation on the basis of an acoustic analysis of the structure of the nasal cavity. Size and shape of the nasal cavity suggest low vocal frequencies in adults, as does information on potential auditory acuity in these animals. Lateral diverticula (present in all but juvenile specimens) acted to suppress portions of the vocal spectrum. Juveniles vocalized at higher frequencies than adults and potential auditory sensitivity at high frequencies in adults suggests a high degree of parent-offspring vocal communication. Sexual variation and causes of selection for low frequency vocalization are also examined.

The significant impact of extant carnivores, particularly spotted hyenas, on the depositional history and physical characteristics of archaeofaunal and paleontological assemblages is well recognized. We focus on the behavioral ecology of extant spotted hyenas (Crocuta crocuta) in relation to bone accumulations produced by one East African clan at communal dens. Limbs and skulls of prey animals more frequently appear at dens than do other carcass portions. These items reflect the relative abundance of prey species near dens; carnivore remains are poorly represented. Comparative analysis reveals that bones are deposited far more slowly (<7 carcass portions per month) and accumulations tend to be smaller at Crocuta dens than at dens of either brown (Parahyaena brunnea) or striped (Hyaena hyaena) hyenas. We propose that extant Crocuta bone accumulation rates and sizes are likely affected by prey species abundance, clan size, social interactions within the clan, and the type and availability of den sites. We also suggest that the potential for intraspecific behavioral variability in bone accumulation patterns is important when comparisons are made among spotted hyena populations and across hyena species. For example, accumulation patterns may be dramatically influenced by the temporal span, potentially ranging from days to hundreds or thousands of years, in which bones are collected, depending on the species-specific history of occupation at a given site. Understanding the behavioral and ecological variability likely to influence bone accumulation patterns at dens used by different hyaenids will allow taphonomists and zooarchaeologists to refine their knowledge of mechanisms underlying site formation processes and potential causes of variability in deeper-time den assemblages.

Morphologic discrimination of species of scleractinian reef corals has long been plagued by a shortage of independent characters and by high ecophenotypic plasticity. Because of these two factors, many species appear to intergrade morphologically. We outline a newly developed protocol for the morphometric recognition of species, which uses size and shape coordinates derived from landmark data. The landmarks consist of spatially homologous points digitized in three dimensions on upper calical surfaces. The approach is more powerful than linear measurements at detecting subtle distinctions among species; and the distinctions are easy to visualize and interpret biologically, which increases the accuracy and resolution of subsequent phylogenetic and large-scale faunal analyses.

As an example, we distinguish morphospecies in collections of Porites made at three Caribbean locations. Size and shape coordinates are analyzed using principal component analysis, average linkage cluster analysis, and a series of iterative discriminant analyses. Positions of different corallites from the same colonies are examined on cluster dendrograms to determine cutoffs for group recognition, and discriminant classifications for different corallites from the same colonies are compared to maximize group assignments. The results yield seven morphospecies, which are generally in 90% agreement with classification of the same animals using allozyme electrophoresis. Measures of corallite size and the relative heights and locations of the pali and septal denticles all reveal unique patterns of variation among morphospecies.

Taxonomic diversity and morphological disparity are different measures of biodiversity that together can describe large-scale evolutionary patterns. Diversity measures are often corrected by extending lineages back in time or adding additional taxa necessitated by a phylogeny, but disparity analyses focus on observed taxa only. This is problematic because some morphologies required by phylogeny are not included, some of which may help fill poorly sampled time bins. Moreover the taxic nature of disparity analyses makes it difficult to compare disparity measures with phylogenetically corrected diversity or morphological evolutionary rate curves. We present a general method for using phylogeny to correct measures of disparity, by including reconstructed ancestors in the disparity analysis. We apply this method to discrete character data sets focusing on Triassic archosaurs, Cenozoic carnivoramorph mammals, and Cretaceous-Cenozoic euarchontogliran mammals. Phylogenetic corrections do not simply mirror the taxic disparity patterns, but affect the three analyses in heterogeneous ways. Adding reconstructed ancestors can inflate morphospace, and the amount and direction of expansion differs depending on the taxonomic group in question. In some cases phylogenetic corrections give a temporal disparity curve indistinguishable from the taxic trend, but in other cases disparity is elevated in earlier time intervals relative to later bins, due to the extension of unsampled morphologies further back in time. The phylogenetic disparity curve for archosaurs differs little from the taxic curve, supporting a previously documented pattern of decoupled disparity and rates of morphological change in dinosaurs and their early contemporaries. Although phylogenetic corrections should not be used blindly, they are helpful when studying clades with major unsampled gaps in their fossil records.

Using a conservative definition of the hominid taxon Homo erectus, the sample of specimens known at this time, 92 individuals in all, is examined to determine whether the species exhibited significant temporal trends or evolutionary stasis. The sample is divided into three low-resolution time spans, and it is shown that significant change characterizes a number of cranial, mandibular, and dental features. Rates of change are comparable to or above rates reported for other fossil vertebrate lineages sampled over a similar duration. The often repeated assertion that Homo erectus is an example of a species in evolutionary stasis is incorrect.

The concept of heterochrony has long had a central place in evolutionary theory. During their long history, heterochrony and several associated concepts such as paedomorphosis and neoteny have often been contentious and they continue to be criticized. Despite these criticisms, we review many examples showing that heterochrony and its associated concepts are increasingly cited and used in many areas of evolutionary study. Furthermore, major strides are being made in our understanding of the underlying genetic and developmental mechanisms of heterochrony, and in the methods used to describe heterochronic changes. A general theme of this accumulating research is that some of the simplistic notions of heterochrony, such as terminal addition, simple rate genes, and “pure” heterochronic categories are invalid. However, this research also shows that a more sophisticated view of the hierarchical nature of heterochrony provides many useful insights and improves our understanding of how ontogenetic changes are translated into phylogenetic changes.

The extent to which perceived patterns of evolution are affected by the use of single characters versus overall morphology or measured versus counted and coded characters is explored empirically, employing multiple-character data from closely spaced sequential populations of the Neogene bryozoan Metrarabdotos. In all nine species examined, the pattern of evolution in overall morphology revealed by discriminant analysis is so highly punctuated that changes within species do not vary significantly from zero. Among the 46 single characters in the nine species, a few statistically significant temporal trends do occur, as apparent departures from the static pattern in overall morphology. However, these exceptions are so poorly related to the morphology that distinguishes inferred ancestor and descendant species from each other, and are so few in number, that they can be interpreted as chance variation from a general condition of no change within species. There is no difference in behavior between measured characters and counted or coded ones, in part because the distinction between the two types of characters can be artificial in bryozoans and other modular organisms. The results suggest that interpretation of single-character changes, in isolation rather than as statistical samples of the change in overall morphology, should be made with caution.