Adult Dimorphism Research Articles

Relating antennal sensilla diversity and possible species behaviour in the planthopper pest Lycorma delicatula (Hemiptera: Fulgoromorpha: Fulgoridae).

Antennal sensory units in nymphs and adults of the spotted Lanternfly, Lycorma delicatula (White) (Hemiptera: Fulgoromorpha: Fulgoridae), an economically important plant pest, are studied with scanning electron microscopy. Sensilla trichodea / chaetica type recognition is based on their external morphology and ratio of their size to diameter. The flagellum Bourgoin’s organ is a complex sensory unit with 2–3 internal sensilla coeloconica. During nymphal stages, the sensory surface available for a chemoreceptive function particularly increases with the number and size of sensilla placodea on the antennal pedicel. From first to fourth instar and to adult males and females, plate organ sensory surface is estimated to increase respectively by 33x, 68x and 125x (= 2.72 mm2 and 5.02 mm2 respectively for males and females). The most important increase (5x) occurs between second and third instar. In parallel, a distinctive pair of plate organs on the flagellum decreases in size from first to third instar, and disappears. Sexual dimorphism occurs in sensilla placodea in adults. Diversity, disparity and evolution of nymphal sensilla, and their sexual dimorphism in adults are discussed in the context of the species and planthopper behaviour.

Leaf heteroblasty in eucalypts: biogeographic evidence of ecological function

Leaves that develop on seedlings, young saplings or regenerative shoots of many eucalypt species are strikingly different in morphology from the typical leaves of more mature plants; a developmental pattern known as heteroblasty. We measured dimorphism between juvenile and adult leaves in shape and size, leaf mass per unit area, and vein frequency in a continent-wide sample of Angophora, Corymbia and Eucalyptus species. We tested whether heteroblasty in this group is an adaptation to shading by comparing the degree of juvenile–adult leaf dimorphism with the canopy closure (measured by the leaf area index) of the habitat in which species occurred. No pattern emerged for heteroblasty in leaf shape and size or leaf mass per unit area, but there was a significant relationship (accounting for phylogenetic relationships) between the degree of juvenile–adult dimorphism in vein frequency and habitat leaf area index. Juvenile leaves tended to have more widely spaced veins than adult leaves of the same species, in regions with more closed vegetative canopies. This evidence suggests that eucalypt heteroblasty is, at least in part, a hydraulic adaptation to the different conditions faced by younger and older plants in higher productivity regions with denser vegetation.

Difference in Body Size and Sexual Dimorphism in the Ogasawara Mitten Crab,Eriocheir ogasawaraensis,and the Japanese Mitten Crab,Eriocheir japonica

To highlight adaptation of an endemic species to an oceanic island environment, adult morphological characteristics and growth patterns were compared between a mitten crab endemic to the Ogasawara Islands ( Eriocheir ogasawaraensis ) and a congener from mainland Japan ( E. japonica ). Mean carapace width of E. ogasawaraensis was nearly 1.6 times larger than that of E. japonica in both sexes. A difference was detected in the carapace length versus carapace width relationship between these two species. Comparing chela propodus height versus carapace width, a sexual difference was detected similarly in both species, but males had only one growth phase in E. ogasawaraensis , whereas males of E. japonica were dimorphic due to two growth phases. The regression line obtained for male E. ogasawaraensis (chela propodus height versus carapace width) was nearly on the extending line of small-phase male E. japonica . Female E. ogasawaraensis had relatively larger chelipeds than female E. japonica . As for ambulatory legs, E. japonica males had relatively longer legs than females, but no sexual difference was detected in E. ogasawaraensis. Eriocheir ogasawaraensis had relatively shorter legs than male E. japonica but longer legs than female E. japonica . Therefore, in E. ogasawaraensis sexual dimorphism was not as differentiated as in E. japonica , and the adult male dimorphism recognized in E. japonica was absent. The large body size of E. ogasawaraensis is consistent with island gigantism that is commonly found in response to a lack of large predators on isolated islands. Evolution of dimorphism can be explained by sexual selection, and the differences between the island and mainland species are presumed to be correlated with differences in the mating behavior and/or environmental factors in their habitats.

Female-biased sexual size dimorphism: ontogeny, seasonality, and fecundity of the cliff chipmunk (Tamias dorsalis)

Female-biased sexual dimorphism is uncommon in mammals and is usually attributed to increased fecundity of large females. Moreover, sexual dimorphism is usually described for adults, and the ontogeny of sex differences is poorly documented. We studied cliff chipmunks (Tamias dorsalis), a small mammal with female-biased sexual dimorphism, to describe development of sexual dimorphism in juveniles and to measure sexual dimorphism and seasonal body mass in adults. To test the fecundity hypothesis, we compared body mass of females to litter size and body mass of offspring. Juveniles were not sexually dimorphic at emergence from the nest and did not differ in body mass 2 months after emergence. Adult chipmunks maintained a relatively stable body mass in March– October with females consistently larger than males. Maternal mass did not have an effect on litter size or mass of juveniles. Because females were consistently larger than males, the ontogeny of sexual dimorphism may provide insights into selection pressures that lead to female-biased sexual dimorphism.

Sexual dimorphism using odontometric indexes: Analysis of three statistical techniques

Sex dimorphism is an important part in the identification process. The teeth are an excellent material for anthropological analysis and it can be considerate a valuable tool for sex determination. This study aims to analyze sexual dimorphism through the dental measures in Brazilian adults using three different statistical methods. The sample consists of maxillary and mandibular plaster models of 200 Caucasoid Brazilian individuals (100 male and 100 female), aged between 20 and 30 years. The mesiodistal (MD) and buccolingual (BL) diameters were measured of all teeth, excluding third molars. These measurements were performed directly on the plaster models. For statistical analysis we used the software STATA 12.0. Three techniques were performed to check the sexual dimorphism Logistic Regression, Linear Discriminant Function and Function Discriminant KNN. The significance level for all tests was 5%. The study population was composed of 200 research participants. Of this total, 100 were male and 100 were female. The average age was 24.33 years and the average height of 1.69 m. According to the results presented in this study we can conclude that it is possible to check the sexual dimorphism in Brazilian adults through dental measures. No differences were verified between homologous teeth. Dental elements of the male participants had higher averages than those of female participants. The best indicators for evaluating sexual dimorphism were measures of the canines and molars. Multivariate techniques were more accurate and KNN discriminant analysis showed the best results.

Spatially dense morphometrics of craniofacial sexual dimorphism in 1-year-olds.

Recent advances in the field of geometric morphometrics allow for powerful statistical hypothesis testing for effects of biological and environmental variables on anatomical shape. This study used partial least-squares regression (PLSR) and the recently developed bootstrapped response-based imputation modelling (BRIM) algorithm to test for sexual dimorphism in the craniofacial shape of 1-year-old humans. We observed a recession of the forehead in boys relative to girls, and differences in the nose, consistent with adult dimorphism. Results also suggest that the degree to which individuals express dimorphic traits is continuous throughout the population. This is also seen in adult dimorphism but in 1-year-olds the amount of overlap between groups is much higher, indicating the strength of dimorphism between sexes is lower. Our results demonstrate early sexual dimorphism that is not attributable to the influx of sex hormones at puberty. This highlights the need to look at very early ontogeny for the origins of sexual dimorphism. We suggest that future work look at potential mediating effects of this early dimorphism on the later impact of puberty. The subtle shape differences we have detected, may also be applied to sexing fossilised crania. A common artefact in 3D images of faces of young children is that they often have their mouths open to varying degrees, introducing variability in the data unrelated to anatomy. We describe two PLSR-based methods of correcting this. These methods may facilitate surgical planning and assessment of young children based on 3D images.

Sexual dimorphism across 3 stages of development in polygynous Artiodactyls is not affected by maternal care

In polygynous mammals, mature males are usually much heavier than females. Competition for females is intense, and few males reproduce. Given the importance of the male’s body size for the reproduction and social life of these species, levels of sexual dimorphism were studied in 27 species of polygynous terrestrial cetartiodactyls at the 3 most significant stages of development: birth, 6 months of age, and adulthood. Overall, there were 3 different types of changes in male-to-female (M/F) mass ratios between birth and adulthood, corresponding to the 3 categories of adult dimorphism. The change in mass ratio between birth and 6 months of age was inversely correlated to the degree of dimorphism at birth. Most adult dimorphism was acquired after weaning. On the whole, postnatal maternal care seems to have no or even an inverse effect on the evolution of dimorphism, which is apparently not consistent with the assumption of greater maternal investment in male than in female offspring among polygynous mammals.

Using the 3D Facial Norms Database to investigate craniofacial sexual dimorphism in healthy children, adolescents, and adults.

BackgroundAlthough craniofacial sex differences have been extensively studied in humans, relatively little is known about when various dimorphic features manifest during postnatal life. Using cross-sectional data derived from the 3D Facial Norms data repository, we tested for sexual dimorphism of craniofacial soft-tissue morphology at different ages.MethodsOne thousand five hundred fifty-five individuals, pre-screened for craniofacial conditions, between 3 and 25 years of age were placed in to one of six age-defined categories: early childhood, late childhood, puberty, adolescence, young adult, and adult. At each age group, sex differences were tested by ANCOVA for 29 traditional soft-tissue anthropometric measurements collected from 3D facial scans. Additionally, sex differences in shape were tested using a geometric morphometric analysis of 24 3D facial landmarks.ResultsSignificant (p < 0.05) sex differences were observed in every age group for measurements covering multiple aspects of the craniofacial complex. The magnitude of the dimorphism generally increased with age, with large spikes in the nasal, cranial, and facial measurements observed after puberty. Significant facial shape differences (p < 0.05) were also seen at each age, with some dimorphic features already present in young children (eye fissure inclination) and others emerging only after puberty (mandibular position).ConclusionsSeveral craniofacial soft-tissue sex differences were already present in the youngest age group studied, indicating that these differences emerged prior to 3 years of age. The results paint a complex and heterogeneous picture, with different groups of traits exhibiting distinct patterns of dimorphism during ontogeny. The definitive adult male and female facial shape was present following puberty, but arose from numerous distinct changes taking place at earlier stages.Electronic supplementary materialThe online version of this article (doi:10.1186/s13293-016-0076-8) contains supplementary material, which is available to authorized users.

Peramorphic males and extreme sexual dimorphism in Monodelphis dimidiata (Didelphidae)

The southern short-tailed opossum, Monodelphis dimidiata, is a species known not only for its semelparous life cycle, but also for the extreme sexual dimorphism of adults, where males are not only larger, but also have distinctive morphological characters in their skull. Using geometric morphometrics and a suite of statistical tests, I analyzed the postweaning ontogenetic development of this species in order to evaluate the age-class where sexual dimorphism becomes significant and the amount of change exhibited by both sexes. My results showed that M. dimidiata partly follows the ontogenetic pattern described for didelphids by previous authors. The character that escapes the general pattern is rostral length, which becomes shorter instead of lengthening throughout the development. This change could be related to an increment in the bite force in the anterior part of the dentition. The amount of sexual dimorphism found for this species is larger than the reported previously for other American marsupials, and I also found a higher rate of growth in males at the attaining of sexual maturity. Based on my results and the information available for other didelphids, I can suggest that M. dimidiata males undergo through a process of hypermorphosis, resulting in a peramorphic condition. It is possible that the extreme sexual dimorphism present in this species is related to reproductive success, specially taking into account their semelparous life cycle.

Ontogenetic stage-specific quantitative trait loci contribute to divergence in developmental trajectories of sexually dimorphic fins between medaka populations.

Sexual dimorphism can evolve when males and females differ in phenotypic optima. Genetic constraints can, however, limit the evolution of sexual dimorphism. One possible constraint is derived from alleles expressed in both sexes. Because males and females share most of their genome, shared alleles with different fitness effects between sexes are faced with intralocus sexual conflict. Another potential constraint is derived from genetic correlations between developmental stages. Sexually dimorphic traits are often favoured at adult stages, but selected against as juvenile, so developmental decoupling of traits between ontogenetic stages may be necessary for the evolution of sexual dimorphism in adults. Resolving intralocus conflicts between sexes and ages is therefore a key to the evolution of age-specific expression of sexual dimorphism. We investigated the genetic architecture of divergence in the ontogeny of sexual dimorphism between two populations of the Japanese medaka (Oryzias latipes) that differ in the magnitude of dimorphism in anal and dorsal fin length. Quantitative trait loci (QTL) mapping revealed that few QTL had consistent effects throughout ontogenetic stages and the majority of QTL change the sizes and directions of effects on fin growth rates during ontogeny. We also found that most QTL were sex-specific, suggesting that intralocus sexual conflict is almost resolved. Our results indicate that sex- and age-specific QTL enable the populations to achieve optimal developmental trajectories of sexually dimorphic traits in response to complex natural and sexual selection.

Odontometric sex estimation on three populations of the Iron Age from Abruzzo region (central–southern Italy)

BackgroundIn archaeological contexts, sex identification is a necessary step for a complete reconstruction of the biological profile of the individuals and to know demographic patterns of the population, nutritional stress, diseases, growth and development, and distribution of pathological conditions. MethodsThis study is based on the skeletal remains of 149 individuals from three protohistoric populations in close temporal and geographic proximity in Abruzzo region (central–southern Italy): Opi, Alfedena and Bazzano. It has been possible to develop logistic regression equations based on dental measurements of permanent teeth of adult individuals whose sex had previously been estimated based on pelvic and cranial features. These equations were subsequently applied to the permanent dentition of immature individuals and adult individuals whose sex was estimated as uncertain or unknown in order to estimate their sex. ResultsThe mandibular canine is the tooth with the greatest sexual dimorphism in adults, followed by both maxillary and mandibular first and second molars, providing a correct assignment of sex ranging from 83.7% and 95.9% of cases, depending on the dimensions used for the construction of these equations. Of the 29 individuals in the target sample (14 adultus, 10 juvenilis and 5 infans), sex estimation was possible for 23 (10 adultus, 8 juvenilis and 5 infans), representing an applicability rate of 79.31% of the individuals. ConclusionsThe results indicate that odontometrics is a useful tool for sex estimation and allows to increase the data to perform more complete paleodemographic studies on archaeological populations.

The ontogeny of sexual size dimorphism of a moth: when do males and females grow apart?

Sexual dimorphism in body size (sexual size dimorphism) is common in many species. The sources of selection that generate the independent evolution of adult male and female size have been investigated extensively by evolutionary biologists, but how and when females and males grow apart during ontogeny is poorly understood. Here we use the hawkmoth, Manduca sexta, to examine when sexual size dimorphism arises by measuring body mass every day during development. We further investigated whether environmental variables influence the ontogeny of sexual size dimorphism by raising moths on three different diet qualities (poor, medium and high). We found that size dimorphism arose during early larval development on the highest quality food treatment but it arose late in larval development when raised on the medium quality food. This female-biased dimorphism (females larger) increased substantially from the pupal-to-adult stage in both treatments, a pattern that appears to be common in Lepidopterans. Although dimorphism appeared in a few stages when individuals were raised on the poorest quality diet, it did not persist such that male and female adults were the same size. This demonstrates that the environmental conditions that insects are raised in can affect the growth trajectories of males and females differently and thus when dimorphism arises or disappears during development. We conclude that the development of sexual size dimorphism in M. sexta occurs during larval development and continues to accumulate during the pupal/adult stages, and that environmental variables such as diet quality can influence patterns of dimorphism in adults.

Mechanisms causing variation in sexual size dimorphism in three sympatric, congeneric lizards.

Sexual differences in adult body size (sexual size dimorphism, or SSD) ultimately can be favored by selection because larger males are more likely to be successful competitors for females, because larger females bear larger clutches, or because intersexual size differences reduce resource competition. Natural selection during juvenile development can influence sexual dimorphism of adults, and selection on adults and juveniles may differ. Studies that address the relative contributions of adult body shape dimorphism and sexually dimorphic patterns of growth and maturity are particularly useful in understanding the evolution of size dimorphism, yet they are rare. We investigated three sympatric, congeneric lizard species with different degrees and directions of adult sexual dimorphism and compared their growth patterns, survival probabilities, and intersexual trophic niche differences. Different mechanisms, even within these closely related, sympatric species, acted on juvenile lizards to produce species differences in adult SSD. Both degree and direction of dimorphism resulted from differences between the sexes in either the duration of growth or the rate of growth, but not from differences in rates of survival or selection on juvenile growth rate. Species- and sex-specific trade-offs in the allocation of energy to growth and reproduction, as well as differential timing of maturation, thus caused the growth patterns of the sexes to diverge, producing SSD. The differences that we observed in the direction of SSD among these species is consistent with their different social systems, suggesting that differential selection on adult body size has been responsible for the observed species-specific differences in juvenile growth rates and maturational timing.

Crecimiento postnatal y desarrollo del vuelo en el murciélago Leptonycteris yerbabuenae en Chiapas, México

Introduction: Neonate bats represent 12-43% of postpartum-maternal body mass, but unlike other small mammals with large offsprings, bats are altricial and totally dependent on maternal care for survival. Neonates of several bat species are born naked, with low thermoregulatory ability; therefore their growth and development are affected by factors such as humidity and temperature, likewise by sex and food availability, among others. Phyllostomidae is the most diverse family of bats in the Neotropics, nevertheless, there are few studies on the postnatal growth and development of their offspring and especially of glosophagine bats. For that reason, we described the postnatal growth and development of a population of Leptonycteris yerbabuenae inhabiting “The Laguitos” Cave, in the state of Chiapas, México. This species is distributed from the southern United States, through most of Mexico to Guatemala and El Salvador .In Mexico this species is listed as “threatened” by the Mexican government (SEMARNAT, 2010). Methods: Based on capture-recapture data, we examined the growth trajectories of three morphological variables and flight development of young Leptonycteris yerbabuenae during 1998 and 2001. Sexual variation, and inter-year variation among specimens of the same age category was assessed by a t Student test. The growth of each variable was measured with a lineal regression analysis, meanwhile the growth parameters were derived from a logistic growth equation and from a polynomial model. To describe the flight development in young bats, we classified these as non-volant, semivolant and volant as was done by Stern et al . (1997) in Phyllostomus hastatus . Results: The highest records for ambient and roost temperature were in 2001, and so were the lowest records for relative humidity compared with 1998 conditions (Fig. 1). Male and female young bats (Fig. 2) were morphologically similar in the three variables assessed in both years (Table 1). The body mass and length of the forearm increased linearly the first three weeks in both years, while the length of the epiphysis grew until the second week in 1998 and day 10 in 2001, then the growth rate decreased in all variables (Figure 3, Table 2). The sustained flight was achieved at ages 15 and 20 days in 2001 and 1998, respectively (Table 3). Discussion and conclusions: This study shows that neonates of Leptonycteris yerbabuenae from Chiapas born naked and with the ear meatus closed compared with those of Carbo, Sonora (Gould 1975), what reveals intraspecific variability of these traits. The morphological similarity between male and females young bats was expected; because there is not secondary sexual dimorphism in adults. Neonates of 1998 had lesser body mass and greater length of the fourth metacarpal-phalangeal epiphyseal gap than specimens of 2001. Differences between years were persistent during growth phase, and maybe these results were consequences of different weather conditions that prevailed in each year. The growth parameters derived from the logistic model for forearm length (0.07-0.10) and body mass (0.06-0.10) of L. yerbabuenae were similar to other neotropical phyllostomid bats, but lower than vespertilionid bats. These results may be influenced by phylogenetic distance or by environmental conditions. The sustained flight started five days earlier in 2001 compared with 1998, probably influenced by different environmental conditions that prevailed each year. Therefore the sustained flight was achieved at an age similar to those of other phyllostomid bats. Key words: Cave, Chiroptera, Phyllostomidae, relative humidity, temperature, growth trajectories.

Facial width-to-height ratio relates to alpha status and assertive personality in capuchin monkeys.

Social dominance hierarchies play a pivotal role in shaping the behaviour of many species, and sex differences within these hierarchies often exist. To date, however, few physical markers of dominance have been identified. Such markers would be valuable in terms of understanding the etiology of dominant behaviour and changes in social hierarchies over time. Animals may also use such traits to evaluate the potential dominance of others relative to themselves (i.e. a physical “cue”). Facial width-to-height ratio (fWHR), for example, has been suggested as a cue to dominance in humans, with links to both dominant behaviour and the perception of dominance in other individuals. Whether this association is present in non-human animals is currently not known. Therefore, here we examine within-species links between fWHR and dominant behaviour in 64 brown capuchin monkeys (Sapajus spp.) aged between 2 and 40 years. fWHR was positively associated with alpha status and with a dimensional rating of assertive personality in both males and females. Moreover, fWHR showed significant sexual dimorphism in adults but not juveniles, suggesting a developmental change may occur during puberty. In a sub-sample, sex differences were mediated by weight, suggesting fWHR dimorphism does not exceed what would be expected by differences in body weight. This is the first report of an association between face shape and behaviour in a non-human species. Results are discussed in terms of the role that face-behaviour associations might play within capuchin societies, and the possible selective forces that might have led to the evolution of fWHR-dominance associations in humans.

Sexual Dimorphism and Facial Growth Beyond Dental Maturity in Great Apes and Gibbons

The great apes and gibbons are characterized by extensive variation in degree of body size and cranial dimorphism, but although some studies have investigated how sexual dimorphism in body mass is attained in these species, for the majority of taxa concerned, no corresponding work has explored the full extent of how sexual dimorphism is attained in the facial skeleton. In addition, most studies of sexual dimorphism combine dentally mature individuals into a single “adult” category, thereby assuming that no substantial changes in size or dimorphism take place after dental maturity. We investigated degree and pattern of male and female facial growth in Pan troglodytes troglodytes, Pan paniscus, Gorilla gorilla gorilla, Pongo pygmaeus, and Hylobates lar after dental maturity through cross-sectional analyses of linear measurements and geometric mean values of the facial skeleton and age-ranking of individuals based on molar occlusal wear. Results show that overall facial size continues to increase after dental maturity is reached in males and females of Gorilla gorilla gorilla and Pongo pygmaeus, as well as in the females of Hylobates lar. In male Pongo pygmaeus, adult growth patterns imply the presence of a secondary growth spurt in craniofacial dimensions. There is suggestive evidence of growth beyond dental maturity in the females of Pan troglodytes troglodytes and Pan paniscus, but not in the males of those species. The results show the presence of statistically significant facial size dimorphism in young adults of Pan paniscus and Hylobates lar, and of near statistical significance in Pan troglodytes troglodytes, but not in older adults of those species; adults of Gorilla gorilla gorilla and Pongo pygmaeus are sexually dimorphic at all ages after dental maturity. The presence of sex-specific growth patterns in these hominoid taxa indicates a complex relationship between socioecological selective pressures and growth of the facial skeleton.

Evolution of the Paleocene-Early Eocene larger benthic foraminifera in the Tethyan Himalaya of Tibet, China

The Paleocene-Early Eocene larger benthic foraminifera (LBF) in the far eastern Neo-Tethyan Ocean of Tibet still remain poorly known. Here, we present a novel, high-resolution larger foraminiferal biozonation from the shallow-water limestones in Tibet, which will improve our current understanding of the larger foraminiferal evolution in the eastern Neo-Tethyan Ocean. Based on one continuous section at Tingri and three separate sections at Gamba, ten Shallow Benthic Zones (SBZ 1–10) have been designated in Tibet by following the principle of Oppel Zone. In contrast to those in Europe, the Paleocene LBFs in Tibet are characterized by high diversification of Lockhartia, Kathina, Daviesina, Miscellanea, Ranikothalia, and Operculina and show progressively increasing diversity of genera and species during SBZ 2–5. Adult dimorphism and large shell size of some LBFs as well as differentiation of the diversity between genera and species initiated as early as SBZ 3. It suggests that the occurrence of the Larger Foraminifera Turnover (LFT) was probably not synchronous in the entire Neo-Tethyan Ocean, because in Europe, the LFT was generally thought to occur at the beginning of SBZ 5. During the Early Eocene, the LBFs in Tibet decreased markedly on the generic level and increased on the species level, and some new genera (Alveolina, Orbitolites, Nummulites, Assilina, Discocyclina) have gained predominance in Tibet. It is nearly identical to the evolution of the LBFs in Europe and indicates a high-degree homogenization of the LBFs in the entire Neo-Tethyan Ocean. Furthermore, the Paleocene-Eocene (P-E) boundary in shallow-water environments has been clearly identified by us, and it is situated in the upper part of SBZ 5 and associated with no evident biotic turnover of shallow benthic foraminiferal communities. The possible diachroneity of the LFT in the Neo-Tethyan Ocean and the evident lagging of the Paleocene-Eocene Thermal Maximum (PETM) behind the LFT imply that the LFT could only be the result of a natural evolutionary process and has no linkage with the PETM. Notably, a transient but distinct larger foraminiferal extinction and origination (LFEO) event has been found in Tibet, which is characterized by a sudden disappearance of all Paleocene lamellar-perforate LBFs, such as Lockhartia, Kathina, Daviesina, Miscellanea, Ranikothalia, and Operculina, and the initial dominance of the Early Eocene porcellaneous-walled Alveolina. The LFEO marks the boundary between SBZ 5 and 6, and might only occur in the low-latitude areas of the Neo-Tethyan Ocean. Surprisingly, the LFEO coincides with the initial recovery of the Carbon Isotope Excursion (CIE), and their synchronicity implies that some possible mechanisms causing the rapid recovery of the CIE probably had also led to the LFEO in the shallow-water environments.

The Paleocene-Eocene thermal maximum (PETM) in shallow-marine successions of the Adriatic carbonate platform (SW Slovenia)

The Paleocene-Eocene thermal maximum represents one of the most rapid and extreme warming events in the Cenozoic. Shallow-water stratigraphic sections from the Adriatic carbonate platform offer a rare opportunity to learn about the nature of Paleocene-Eocene thermal maximum and the effects on shallow-water ecosystems. We use carbon and oxygen isotope stratigraphy, in conjunction with detailed larger benthic foraminiferal biostratigraphy, to establish a high-resolution paleoclimatic record for the Paleocene-Eocene thermal maximum. A prominent negative excursion in δ 13 C curves of bulk-rock (∼1‰–3‰), matrix (∼4‰), and foraminifera (∼6‰) is interpreted as the carbon isotope excursion during the Paleocene-Eocene thermal maximum. The strongly 13 C-depleted δ 13 C record of our shallow-marine carbonates compared to open-marine records could result from organic matter oxidation, suggesting intensified weathering, runoff, and organic matter flux. The Ilerdian larger benthic foraminiferal turnover is documented in detail based on high-resolution correlation with the carbon isotopic excursion. The turnover is described as a two-step process, with the first step (early Ilerdian) marked by a rapid diversification of small alveolinids and nummulitids with weak adult dimorphism, possibly as adaptations to fluctuating Paleocene-Eocene thermal maximum nutrient levels, and a second step (middle Ilerdian) characterized by a further specific diversification, increase of shell size, and well-developed adult dimorphism. Within an evolutionary scheme controlled by long-term biological processes, we argue that high seawater temperatures could have stimulated the early Ilerdian rapid specific diversification. Together, these data help elucidate the effects of global warming and associated feedbacks in shallow-water ecosystems, and by inference, could serve as an assessment analog for future changes.

Morphological variation of introduced species: The case of American mink (Neovison vison) in Spain

We studied the morphology of American mink Neovison vison in five out of the six introduced populations in Spain. The spatial and temporal variation of body weight (BW), body length (BL), tail length, hind-foot length and ear length were analysed. Temporal trends in BW and BL in relation to years since mink introduction were also analyzed. In addition, we tested the effect of sex, age (juvenile, subadult and adult) and age–sex interaction, on each parameter. Morphological parameters differed between populations, illustrating the high variability of body size of American mink in different environments, and the phenotypic plasticity of the species. Annual variations were synchronized between populations, suggesting a large-scale effect on all of them. BW and BL showed a decreasing trend in both males and females in relation to years since introduction. This decrease may be related to mink's diet. Differences in sex and age were found, pointing to sexual dimorphism in adults, subadults and juveniles. The dimorphism in non-adult individuals suggests that subadult males may have a competitive advantage from subadult females in feeding and/or hunting on bigger prey from an early age (resource partitioning hypothesis).

Brief communication: Endocranial volumes in an ontogenetic sample of chimpanzees from the taï forest national park, ivory coast

Ontogenetic samples of endocranial volumes (EVs) from great apes and humans are critical for understanding the evolution of the brain growth pattern in the hominin lineage. However, high quality ontogenetic data are scarce, especially for nonhuman primates. Here, we provide original data derived from an osteological collection of a wild population of Pan troglodytes verus from the Taï Forest National Park, Ivory Coast. This sample is unique, because age, sex, and pedigree information are available for many specimens from behavioral observations in the wild. We scanned crania of all 30 immature specimens and 13 adult individuals using high-resolution computed tomography. We then created virtual casts of the bony braincase (endocasts) to measure EVs. We also measured cranial length, width, and height and attempted to relate cranial distances to EV via regression analysis. Our data are consistent with previous studies. The only neonate in the sample has an EV of 127 cm(3) or 34% of the adult mean. EV increases rapidly during early ontogeny. The average adult EV in this sample is 378.7 ± 30.1 cm(3) . We found sexual dimorphism in adults; males seem to be already larger than females before adult EV is attained. Regressions on cranial width and multiple regression provide better estimates for EV than regressions on cranial length or height. Increasing the sample size and compiling more high quality ontogenetic data of EV will help to reconcile ongoing discussions about the evolution of hominin brain growth.