Larisa E. Harding

The Evolution of Maximum Body Size of Terrestrial Mammals

How Mammals Grew in Size Mammals diversified greatly after the end-Cretaceous extinction, which eliminated the dominant land animals (dinosaurs). Smith et al. (p. 1216) examined how the maximum size of mammals increased during their radiation in each continent. Overall, mammal size increased rapidly, then leveled off after about 25 million years. This pattern holds true on most of the continents—even though data are sparse for South America—and implies that mammals grew to fill available niches before other environmental and biological limits took hold. Maximum mammal size increased at the beginning of the Cenozoic, then leveled off after about 25 million years. The extinction of dinosaurs at the Cretaceous/Paleogene (K/Pg) boundary was the seminal event that opened the door for the subsequent diversification of terrestrial mammals. Our compilation of maximum body size at the ordinal level by sub-epoch shows a near-exponential increase after the K/Pg. On each continent, the maximum size of mammals leveled off after 40 million years ago and thereafter remained approximately constant. There was remarkable congruence in the rate, trajectory, and upper limit across continents, orders, and trophic guilds, despite differences in geological and climatic history, turnover of lineages, and ecological variation. Our analysis suggests that although the primary driver for the evolution of giant mammals was diversification to fill ecological niches, environmental temperature and land area may have ultimately constrained the maximum size achieved.

What can multiple phylogenies say about the latitudinal diversity gradient? : a new look at the tropical conservatism, out of the tropics, and diversification rate hypotheses

We reviewed published phylogenies and selected 111 phylogenetic studies representing mammals, birds, insects, and flowering plants. We then mapped the latitudinal range of all taxa to test the relative importance of the tropical conservatism, out of the tropics, and diversification rate hypotheses in generating latitudinal diversity gradients. Most clades originated in the tropics, with diversity peaking in the zone of origin. Transitions of lineages between latitudinal zones occurred at 16–22% of the tree nodes. The most common type of transition was range expansions of tropical lineages to encompass also temperate latitudes. Thus, adaptation to new climatic conditions may not represent a major obstacle for many clades. These results contradict predictions of the tropical conservatism hypothesis (i.e., few clades colonizing extratropical latitudes), but support the out‐of‐the‐tropics model (i.e., tropical originations and subsequent latitudinal range expansions). Our results suggest no difference in diversification between tropical and temperate sister lineages; thus, diversity of tropical clades was not explained by higher diversification rates in this zone. Moreover, lineages with latitudinal stasis diversified more compared to sister lineages entering a new latitudinal zone. This preserved preexisting diversity differences between latitudinal zones and can be considered a new mechanism for why diversity tends to peak in the zone of origin.

The maximum rate of mammal evolution

How fast can a mammal evolve from the size of a mouse to the size of an elephant? Achieving such a large transformation calls for major biological reorganization. Thus, the speed at which this occurs has important implications for extensive faunal changes, including adaptive radiations and recovery from mass extinctions. To quantify the pace of large-scale evolution we developed a metric, clade maximum rate, which represents the maximum evolutionary rate of a trait within a clade. We applied this metric to body mass evolution in mammals over the last 70 million years, during which multiple large evolutionary transitions occurred in oceans and on continents and islands. Our computations suggest that it took a minimum of 1.6, 5.1, and 10 million generations for terrestrial mammal mass to increase 100-, and 1,000-, and 5,000-fold, respectively. Values for whales were down to half the length (i.e., 1.1, 3, and 5 million generations), perhaps due to the reduced mechanical constraints of living in an aquatic environment. When differences in generation time are considered, we find an exponential increase in maximum mammal body mass during the 35 million years following the Cretaceous–Paleogene (K–Pg) extinction event. Our results also indicate a basic asymmetry in macroevolution: very large decreases (such as extreme insular dwarfism) can happen at more than 10 times the rate of increases. Our findings allow more rigorous comparisons of microevolutionary and macroevolutionary patterns and processes.

Predicting the fate of biodiversity using species' distribution models: enhancing model comparability and repeatability.

Species distribution modeling (SDM) is an increasingly important tool to predict the geographic distribution of species. Even though many problems associated with this method have been highlighted and solutions have been proposed, little has been done to increase comparability among studies. We reviewed recent publications applying SDMs and found that seventy nine percent failed to report methods that ensure comparability among studies, such as disclosing the maximum probability range produced by the models and reporting on the number of species occurrences used. We modeled six species of Falco from northern Europe and demonstrate that model results are altered by (1) spatial bias in species’ occurrence data, (2) differences in the geographic extent of the environmental data, and (3) the effects of transformation of model output to presence/absence data when applying thresholds. Depending on the modeling decisions, forecasts of the future geographic distribution of Falco ranged from range contraction in 80% of the species to no net loss in any species, with the best model predicting no net loss of habitat in Northern Europe. The fact that predictions of range changes in response to climate change in published studies may be influenced by decisions in the modeling process seriously hampers the possibility of making sound management recommendations. Thus, each of the decisions made in generating SDMs should be reported and evaluated to ensure conclusions and policies are based on the biology and ecology of the species being modeled.

Effects of allometry, productivity and lifestyle on rates and limits of body size evolution

Body size affects nearly all aspects of organismal biology, so it is important to understand the constraints and dynamics of body size evolution. Despite empirical work on the macroevolution and macroecology of minimum and maximum size, there is little general quantitative theory on rates and limits of body size evolution. We present a general theory that integrates individual productivity, the lifestyle component of the slow–fast life-history continuum, and the allometric scaling of generation time to predict a clades evolutionary rate and asymptotic maximum body size, and the shape of macroevolutionary trajectories during diversifying phases of size evolution. We evaluate this theory using data on the evolution of clade maximum body sizes in mammals during the Cenozoic. As predicted, clade evolutionary rates and asymptotic maximum sizes are larger in more productive clades (e.g. baleen whales), which represent the fast end of the slow–fast lifestyle continuum, and smaller in less productive clades (e.g. primates). The allometric scaling exponent for generation time fundamentally alters the shape of evolutionary trajectories, so allometric effects should be accounted for in models of phenotypic evolution and interpretations of macroevolutionary body size patterns. This work highlights the intimate interplay between the macroecological and macroevolutionary dynamics underlying the generation and maintenance of morphological diversity.

Mustela or Vison? Evidence for the taxonomic status of the American mink and a distinct biogeographic radiation of American weasels

The American minks relationship to the weasels in Mustela has been uncertain. Karyological, morphological, and phylogenetic comparisons to Eurasian Mustela support placing the mink outside the genus as Neovison vison. However, genetic comparisons that incorporate other endemic American Mustela suggest the interpretation of N. visons position to Mustela has been handicapped by biased geographic sampling. Here, we analyzed mitochondrial cytochrome-b from all weasels endemic to the Americas, including two poorly known South American species (M. felipei, M. africana), weasels native to North America (M. vison, M. frenata, M. nigripes), Mustela migrant to North America (M. erminea, M. nivalis), palearctic Mustela, and other American members of Mustelidae. Bayesian and likelihood inference methods were used to construct a phylogeny of Mustela, and relaxed Bayesian phylogenetic techniques estimated ages of divergence within the genus using priors calibrated by fossil ages. Our analyses show that the American mink and the smaller Mustela endemic to the Americas represent a distinct phylogenetic heritage apart from their Eurasian cousins, and biogeographic barriers like the Bering and Panamanian land bridges have influenced the evolutionary history of Mustela in the Americas.

Patterns of maximum body size evolution in Cenozoic land mammals: eco-evolutionary processes and abiotic forcing.

There is accumulating evidence that macroevolutionary patterns of mammal evolution during the Cenozoic follow similar trajectories on different continents. This would suggest that such patterns are strongly determined by global abiotic factors, such as climate, or by basic eco-evolutionary processes such as filling of niches by specialization. The similarity of pattern would be expected to extend to the history of individual clades. Here, we investigate the temporal distribution of maximum size observed within individual orders globally and on separate continents. While the maximum size of individual orders of large land mammals show differences and comprise several families, the times at which orders reach their maximum size over time show strong congruence, peaking in the Middle Eocene, the Oligocene and the Plio-Pleistocene. The Eocene peak occurs when global temperature and land mammal diversity are high and is best explained as a result of niche expansion rather than abiotic forcing. Since the Eocene, there is a significant correlation between maximum size frequency and global temperature proxy. The Oligocene peak is not statistically significant and may in part be due to sampling issues. The peak in the Plio-Pleistocene occurs when global temperature and land mammal diversity are low, it is statistically the most robust one and it is best explained by global cooling. We conclude that the macroevolutionary patterns observed are a result of the interplay between eco-evolutionary processes and abiotic forcing.

Out of the tropics: a phylogeographic history of the long-tailed weasel, Mustela frenata

Abstract The long-tailed weasel (Mustela frenata) has the largest distribution of any mustelid in the Western Hemisphere, yet little is known of its genetic history. As a result of its broad distribution, the species provides an excellent model for identifying potential barriers influencing general phylogeographic patterns shared across multiple taxa. Here we used mitochondrial DNA with phylogenetic, phylogeographic, and molecular dating techniques to investigate molecular and geographical structure, as well as demographic history of M. frenata. Samples encompass 38 of the 42 recognized subspecies ranging from southern Canada to Bolivia. Our results suggest that long-tailed weasels are divided into distinct genetic clades, with eastern and western groups present in North America, 2 distinct lineages in Mexico and Central America separated by the trans-Mexican volcanic belt, and 1 clade in South America. Unlike other Mustela in North America, long-tailed weasels appear to have originated in the tropical areas of Mexico and Central America prior to dispersing 1st to the south before also expanding north in the Pleistocene. Resumen La comadreja de cola larga (Mustela frenata) tiene la distribución más amplia entre todos los mustélidos del hemisferio occidental. Sin embargo, poco se conoce acerca de su historial genético. Dada su amplia distribución geográfica, la especie es un excelente modelo para identificar posibles barreras que influyen en patrones filogeográficos compartidos entre varios taxones. Usamos ADN mitocondrial con técnicas moleculares de datación, filogenia, y filogeografía para investigar la estructura molecular y geográfica así como la historia demográfica de M. frenata. Las muestras incluyen 38 de las 42 subespecies reconocidas desde el sur de Canadá hasta Bolivia. Nuestros resultados sugieren que comadrejas de cola larga se dividen en distintos clados, con grupos orientales y occidentales presentes en América del Norte y dos linajes distintos en México y Centroamérica, separados por el eje transvolcánico mexicano, y finalmente, un clado en América del Sur. A diferencia de otros mustélidos de América del Norte, las comadrejas de cola larga parecen haberse originado en las áreas tropicales de México y América Central previa a dispersión hacia el sur y luego hacia el norte durante el Pleistoceno.