Search

Although patterns of tooth wear are crucial in palaeo-reconstructions, and dental wear abnormalities are important in veterinary medicine, experimental investigations on the relationship between diet abrasiveness and tooth wear are rare. Here, we investigated the effect of four different pelleted diets of increasing abrasiveness (due to both internal [phytoliths] and external abrasives [sand]) or whole grass hay fed for two weeks each in random order to 16 rabbits (Oryctolagus cuniculus) on incisor and premolar growth and wear, and incisor and cheek tooth length. Wear and tooth length differed between diets, with significant effects of both internal and external abrasives. While diet abrasiveness was linked to tooth length for all tooth positions, whole forage had an additional effect on upper incisor length only. Tooth growth was strongly related to tooth wear and differed correspondingly between diets and tooth positions. At 1.4-3.2 mm per week, the growth of cheek teeth measured in this study was higher than previously reported for rabbits. Dental abnormalities were most distinct on the diet with sand. This study demonstrates that concepts of constant tooth growth in rabbits requiring consistent wear are inappropriate, and that diet form (whole vs. pelleted) does not necessarily affect cheek teeth. Irrespective of the strong effect of external abrasives, internal abrasives have the potential to induce wear and hence exert selective pressure in evolution. Detailed differences in wear effects between tooth positions allow inferences about the mastication process. Elucidating feedback mechanisms that link growth to tooth-specific wear represents a promising area of future research.

Aim Our aims were to test: (1) the extent to which vascular plant associations are related in space to mammalian associations, and (2) whether the plant associations are more closely related than the mammalian associations to climate and to a published environmental stratification of Europe. Location Europe, as defined by the following boundaries: 11� W, 32� E, 71� N and 35� N. Methods The analysis is based on presence/absence records of mammal species and plant species with a resolution of 50 km · 50 km. The similarity of the overall spatial structure was tested using a partial Mantel test while controlling for the effect of geographical proximity. To further identify the main spatial components in the datasets, we used k-means clustering and principal components analysis. The resulting geographical patterns were compared with one another, with climate variables and with the environmental stratification of Europe. Results The clustering of the plant data forms coherent areas that can be interpreted as reflections of floristic regions that are controlled to a large extent by climate and topography. In terms of the correlation between distance matrices, the relationship between plants and mammals is relatively strong. The relationships between mammals and climate, and between plants and climate, are more complex but always statistically significant. There is no evidence that the plant clusters are more closely related than the mammalian clusters to climate, although plant clusters are closer to environmental data than to climate. Main conclusions The clustering patterns of mammals and plants form groups that agree with one another in their spatial extent. The forcing of floristic patterns into coherent entities appears mainly to be caused by climatic variables (temperature, temperature range and rainfall), mediated by elevation differences. The formation of individual plant clusters is also related to species numbers and to local and regional floristic differences. The close correlation between the floristic and faunal patterns suggests that the mammal and plant distributions are controlled by the same environmental variables, although the extent to which the mammals are controlled directly by climate or through the influence of vegetation requires more detailed study.

1. The evolution of high-crowned teeth or hypsodonty in herbivorous mammals is widely interpreted as a species-specific adaptation to increasingly wear-inducing diets and environments at evolutionary time scales, with internal abrasives (such as phytoliths in grasses) and/or external abrasives (such as dust or grit) as putative causative factors. The mesowear score (MS) instead describes tooth wear experienced by individual animals during their lifetime. 2. Under the assumption that the abrasiveness that causes the MS in individuals is the same abrasiveness to which species adapted by evolving hypsodonty, one would expect a close correlation between the MS and the hypsodonty index (HI). Alternatively, if these two measures reflect different aspects of wear, one would expect differences in the way that proxies of diet or environment/climate correlate with each parameter. 3. In order to test these hypotheses, we collated a dataset on the HI, MS, percentage of grass in the natural diet (%grass), habitat (open, intermediate, closed) and annual precipitation (PREC) in extant mammalian herbivores. The availability of a quantitative MS constrained the dataset to 75 species. Data were analysed with and without phylogenetic generalized least squares (PGLS). 4. Correlations with PREC were stronger for HI than for MS, whereas correlations with %grass were similar for HI and MS. Habitat had a significant influence on the relationship with %grass for HI but not for MS. Habitat also had a significant influence on the relationship between HI and MS. MS improved the predictive power of HI for %grass, but not for PREC. 5. These results suggest that while the MS indicates predominantly the wear effect of the diet (internal abrasives), HI represents an adaptation to a wear effect that comprises both diet and environment (external abrasives). The additional environmental wear effect must reduce tooth height without causing macroscopic changes in tooth facet development as described by the MS. 6. The most parsimonious explanation for the apparent discrepancy between HI and MS is that external abrasives of very fine particle size play a major role in naturally occurring tooth wear. The experimental testing of this hypothesis will enhance our understanding of the processes involved in tooth wear.

We outline here an approach for understanding the biology of climate change, one that integrates data at multiple spatial and temporal scales. Taxon-free trait analysis, or "ecometrics," is based on the idea that the distribution in a community of ecomorphological traits such as tooth structure, limb proportions, body mass, leaf shape, incubation temperature, claw shape, any aspect of anatomy or physiology can be measured across some subset of the organisms in a community. Regardless of temporal or spatial scale, traits are the means by which organisms interact with their environment, biotic and abiotic. Ecometrics measures these interactions by focusing on traits which are easily measurable, whose structure is closely related to their function, and whose function interacts directly with local environment. Ecometric trait distributions are thus a comparatively universal metric for exploring systems dynamics at all scales. The main challenge now is to move beyond investigating how future climate change will affect the distribution of organisms and how it will impact ecosystem services and to shift the perspective to ask how biotic systems interact with changing climate in general, and how climate change affects the interactions within and between the components of the whole biotic-physical system. We believe that it is possible to provide believable, quantitative answers to these questions. Because of this we have initiated an IUBS program iCCB (integrative Climate Change Biology).

One of the classic examples of faunal turnover in the fossil record is the Miocene transition from faunas dominated by anchitheriine horses with low-crowned molar teeth to faunas with hipparionine horses characterized by high-crowned teeth. The spread of hipparionine horses is associated with increased seasonality and the expansion of open habitats. It is generally accepted that anchitheriine horses did not display an evolutionary increase in tooth crown height prior to their extinction. Nevertheless, to test whether anchitheriines showed any changes interpretable as adaptation to local conditions, we analyzed molar teeth from multiple populations of Anchitherium in three dimensions. Our results show differences in tooth morphology that suggest incipient hypsodonty in Spain, the first region experiencing increasingly arid conditions in the early Miocene of Europe. Furthermore, analyses of tooth wear show that Spanish specimens cluster with present ungulates that eat foliage together with grasses and shrubs, whereas German specimens cluster with present-day ungulates that eat mostly foliage. Taken together, even a taxon such as Anchitherium, with a long and successful history of forest adaptation, did respond to regional environmental changes in an adaptive manner.

Aim To produce a spatial clustering of Europe on the basis of species occurrence data for the land mammal fauna.

In their technical comment Salesa et al. (2011) raise several issues, including an important topic affecting most, or perhaps all, paleoecological studies—the difficulty of determining a reasonable way to deal with taxonomy. Specifically, Salesa et al. draw our attention to a taxonomic revision of Iberian Anchitherium (Sanchez et al. 1998), that we failed to follow in our study (Eronen et al. 2010), and express concerns that a different handling of Anchitherium taxonomy would have affected our results and conclusions.

In Heikinheimo et al. (Journal of Biogeography, 2007, 34, 1053–1064) we used clustering to analyse European land mammal fauna. Gagne & Proulx criticized our choice of the Euclidean distance measure in the analysis, and advocated the use of the Hellinger distance measure, claiming that this leads to very different clustering results. The criticism fails to take into account the probabilistic nature of the methods used and the fact that in this case the similarity measures correlate strongly. Gagne & Proulx used subjective inspection as the criterion of similarity between clusterings. We show that this is insufficient and misleading. Namely, owing to the local minimum problem, two clustering runs rarely give identical results. In the case of our study, the measured similarity (using the kappa statistic) between the Euclidean- and Hellinger-based clusterings is roughly equal to the similarity between two clusterings that both use the Hellinger distance but different random initialization points.

Book reviewed in this article: Bryan, A. L. (ed.) 1986: New Evidence for the Pleistocene Peopling of the Americas

Kahasa. J. (ed) IY84: Quorrrriury of South Afrierrco and Antarctic Penusula A. A. Balksma. Rotterdam.

Book reviewed in this article: Bjorn Kurttn & Elaine Anderson: Pleistocene Mammals of North America

Subtracting a smoothed version of a digital map image from the unprocessed original leaves a map of the local surface relief. The map in question is obtained by through focussing with a confocal reflection microscope, retaining the focus value for the greatest signal level at each X,Y pixel address as the Z (height/depth) coordinate.