Much of the narial anatomy of the enigmatic antelope Saiga tatarica has been described by previous workers. However, the anatomy of the nasal cavity and the causally associated osteological correlates of proboscis structure require closer attention, because these data are integral for both a more comprehensive understanding of saiga functional morphology and more robust reconstructions of proboscis structure in fossil taxa. Saiga and outgroup specimens were subjected to X-ray computed tomographic (CT) imaging, gross dissection and skeletonization. The nasal cavity of saiga is characterized by an enlarged nasal vestibule and basal conchal fold. Many structures (e.g. turbinates, lateral cartilages, mucosal folds, nasolacrimal duct) are retracted caudally to a small area in the caudodorsal part of the nasal cavity proper. The enlarged vestibule is associated laterally and ventrally with paired sacs. The nasal septum is largely membranous and contains a large patch of cavernous tissue that serves as a dynamic baffle modifying the flow of inspired air. Bones comprising the narial margin have modified attachment sites for buccinator group muscles and the reduced lateral cartilages. The premaxilla is greatly modified by the enlarged musculature associated with nasolabial fusion. Maintenance of the topological relationships of narial structures compared to bovid outgroups has resulted in a nasal cavity with much larger area for seromucous glands of the vestibule as well as narial musculature capable of controlling the aperture of the nasal cavity. Maxillolabial muscles and the lateralis nasi act together both to compress the nasal cavity and to control the dilation of the nostrils such that air flow through the cavity is highly modified relative to bovid outgroups. The lateral vestibular recess is an outpocketing of the nasal vestibule that produces supplementary seromucous secretions and seems to have no homologue among outgroups. The enlarged nasal vestibule, lateral vestibular recess, repositioned basal fold, and septal cavernous mass are regarded as a coordinated adaptation to dusty habitats, such that nasal air flow can be dynamically regulated allowing for collection of inspired particulates in the vestibule and thus cleansing of air destined for the lungs.

As a solitary species, giant pandas Ailuropoda melanoleuca have a chemical communication system that allows for avoidance with conspecifics throughout most of the year and facilitates breeding during their brief reproductive period. To date, most studies have focused on adults during the breeding season, but much remains to be learned about developmental and seasonal effects on chemical communication. Here, using odour discrimination methodology, we examine these contextual influences on chemosignalling in giant pandas for the first time. During the breeding season both adult and subadult giant pandas overtly discriminated conspecific sex using chemical cues in urine. Male urine was consistently investigated more than female urine by pandas across all age–sex categories. This preference for male urine was observed for both adult and subadult urine donors, indicating that adult levels of reproductive hormones are not necessary for the production of sex-specific urinary odour cues. By contrast, giant pandas did not overtly discriminate sex during the non-breeding season. This finding underscores that negative results for discrimination studies need to be interpreted with caution, as many contextual factors may influence overt expression of this ability. Evidence points to seasonal changes in motivation, rather than in the availability of sex-specific chemical cues in urine, as the causal factor for changing odour discrimination patterns. These and other findings are discussed in the light of the potential role that discrimination of odour plays in the regulation of competitive and reproductive interactions in nature.

Adult sex change and juvenile sexual differentiation in the protogynous epinepheline Cephalopholis boenak were demonstrated in captivity to be influenced by social factors. Adult sex change in C. boenak occurred in two directions, female to male and male to female. The presence or absence of a larger male plays an important role in adult female sex change; female(s) did not change sex in the presence of a larger male, but sex change occurred after the removal of the larger males in the same social groups. In male pairs, either the larger or the smaller male changed sex. Male to female sex change has not been reported previously in Cephalopholis, and only rarely in epinephelines. This is the first report of direct male sexual differentiation from juveniles (i.e. primary male development), through manipulating the number of juveniles, in a protogynous epinepheline. All isolated, single, juveniles differentiated directly as males, and male to female sex ratios did not differ significantly from 1:1 in all experimental social groups of two to four juveniles. Differentiating males grew significantly faster than differentiating females and undifferentiated juveniles during the 57-week experimental period. The role of growth rate in sex determination in C. boenak is not known but clearly plays a part in juvenile sexual differentiation and merits further investigation. Social factors influencing bi-directional adult sex change and juvenile sexual differentiation are a reflection of plasticity of sexual expression in C. boenak, in particular, and the Serranidae in general.

Predation by wolves Canis lupus on roe deer Capreolus capreolus was studied by scat analysis in five areas of the Province of Arezzo, north-eastern Tuscany, Italy. In the intensive study area (ISA) roe deer represented 19.1% of mean per cent volume (MPV) while in the other areas its use ranged between 10.9% and 53.4% of MPV. A low degree of variation was found in both annual and seasonal use of roe deer, although seasonal differences were more marked in those areas where roe deer use was lower. In ISA, roe deer was negatively selected among species: the Ivlev's electivity index ranged between −0.41 and −0.89. Analysing intra-specific selection, in ISA <1-year-old individuals were preferred by wolves, mainly during the fawns' first months of life. This trend was confirmed in the other areas, where fawns represented more than 50% of the relative number of roe deer prey. In ISA, the use of roe deer (as MPV) was not correlated with its density or with that of the main prey, wild boar, and in almost all the other areas no relation between use and density of roe deer was founded. However, in the one area where both roe deer density and use were the highest, these two variables seemed to exhibit a comparable trend. The use of roe deer was negatively correlated with the percentage of forest cover among all the study areas.

The skin of the emu Dromaius novaehollandiae is described in its entirety by light microscopy for the first time, therefore providing a basis for comparison with the integument of volant birds. The epidermal and dermal layers have a similar arrangement to other avian species. The concentration of lipid spheres in the basal layer of the epidermis is unique to emus. Although no differences in collagen density with depth of the dermis were observed, collagen bundle diameter is significantly smaller in the stratum superficiale compared to the stratum compactum (P=0.001). The extensive stratum laxum, comprised predominantly of adipose tissue, may be an evolutionary adaptation to support the large feathers and also enhance insulation against ambient subzero temperatures. Males have a significantly thicker cellular epidermis (P=0.024) and stratum compactum (P=0.04) than females. In contrast, females have denser collagen (P=0.04) within the stratum superficiale and stratum compactum.

Heterochrony is commonly proposed as a mechanism producing evolutionary changes, and some researchers identify two ways that heterochrony may be conceptualized. ‘Growth heterochrony’ examines ancestor-to-descendant differences in the ontogeny of size relative to shape, while ‘sequence heterochrony’ focuses on differences in the order of occurrence of events during ontogeny. Methods introduced here are allied with sequence heterochrony in that ontogeny is modelled as if it were a sequence of events; however, events are differently defined in this study. Using data from 16 primate species, I demonstrate that discriminant function analysis of data on developmental timing provides an additional tool for exploring the relationship between ontogeny and phylogeny. Patterns in the timing of tooth eruption, craniofacial sutural closure, and postcranial epiphyseal fusion can be used to classify individuals of all ages to their correct taxon. Taxon differences in these patterns can be characterized and described by interpreting correlations between discriminant functions and developmental events. Discriminant analysis has the advantages of: (1) being applicable to taxa for which there are too few individuals to be able to reconstruct ontogenetic sequences, including fossil species; (2) preserving intraspecific developmental variation during analysis; (3) being sensitive to very subtle differences in ontogenetic timing.

The respiratory turbinates of mammals are complex bony plates within the nasal chamber that are covered with moist epithelium and provide an extensive surface area for the exchange of heat and water. Given their functional importance, maxilloturbinate size and structure are expected to vary predictably among species adapted to different environments. Here the first quantitative analysis is provided of maxilloturbinate structure based on high-resolution computed tomography (CT) scans of the skulls of eight canid and seven felid species. The key parameters examined were the density of the maxilloturbinate bones within the nasal chamber and how that density varied along the air pathway. In both canids and felids, total maxilloturbinate chamber volume and bone volume increased with body size, with canids having c. 1.5–2.0 times the volume of maxilloturbinate than felids of similar size. In all species, the volume of the maxilloturbinates varies from rostral to caudal, with the peak volume occurring approximately midway, close to where airway cross-sectional area is greatest. Interspecific differences among canids or felids in maxilloturbinate density were not consistent with adaptive explanations, i.e. the densest maxilloturbinates were not associated with species living in arid or cold habitats. Some of the observed variation in maxilloturbinate form might reflect a need for both low- and high-resistance pathways for airflow under alternative conditions.

Peripatopsis stelliporata sp. nov. from South Africa is described. SEM observations are used to illustrate the similarities and differences between this species and Peripatopsis capensis Grube 1866. The most conspicuous differences in morphology between the two species relate to the structure of the last reduced pair of legs, and the male genital pore, which in P. stelliporata is stellate in shape. Maintaining P. stelliporata in culture allowed timings of births to be recorded and the onset of sexual maturity to be determined. Spermatophores were first noted when the males were c. 4 months old. Females were observed to give birth at 15 months of age. In any female the embryos are all at around the same stage of development, and females gave birth between February and May. Young were born singly or in pairs at intervals of several days. The appearance of the embryos of P. stelliporata and also those of P. capensis collected in 1996 and 1997 was unexpected, as they are transparent apart from the red pigmented gut running from the mouth to the anus. Previously observed embryos of P. capensis were opaque and unpigmented. In appearance these embryos have similarities to those of Opisthopatus cinctipes Purcell 1895, which exhibits a different pattern of embryonic development. Whether or not this difference in appearance of the embryos reflects a transition in the pattern of development is discussed. A modified key for South African Peripatopsidae incorporating P. stelliporata is presented.

Unique features of giraffe Giraffa camelopardalis anatomy are its long neck and slender long limbs. Its neck vertebrae should be light and have low density to make it manoeuvrable while the limb bones should have high density to provide the strength to support the giraffe's mass. Giraffes also have a very high vertical growth rate, a diet with a high Ca:P ratio, and a skeleton that constitutes a high proportion of its body mass. To investigate whether the giraffe skeleton is affected by its anatomy and biology, giraffe bone density and morphology were compared with those of African buffalo Syncerus caffer, an artiodactyl of similar mass, more conventional anatomy, a lower vertical growth rate, and different diet. Our results show that except for minor differences the density of giraffe bones is the same as that of buffaloes. Giraffe limb bones have a slightly greater diameter and much thicker walls than equivalent bones in buffaloes. Giraffe cervical vertebrae, unlike those in buffaloes, decrease in mass with cranial distance. We conclude that giraffe biology and anatomy do not affect bone deposition or density. However, other characteristics of their skeletons seem to be adaptations to their unique anatomy.

The genus Cryptomys contains a number of social, subterranean rodents that are widely distributed throughout sub-Saharan Africa. Specimens of Cryptomys from 23 localities in south-west Zambia were karyotyped using a standard staining protocol. A minimum of five metaphases per specimen was scored for 2n and the fundamental number (NF) was determined in females. Nine new karyotypes, which may represent several new species, were identified: (1) 2n=42, NF=78 (Dongo, Southern Province); (2) 2n=44, NF=76 (Salujinga, North-western Province); (3) 2n=45, NF=78 (Lochinvar, Southern Province); (4) 2n=52, NF=86 (Chinyingi, North-western Province); (5) 2n=54, NF=78 (Monze, Southern Province); (6) 2n=56, NF=76 (Watopa, North-western Province); (7) 2n=58, NF=80 (Livingstone, Southern Province); (8) 2n=58, NF=86 (Senanga, Western Province); (9) 2n=60, NF=82 (Kataba, Western Province; type locality of C. damarensis micklemi). Contrary to previous reports, the specimens from Kataba and Senanga on the left bank of the Zambezi do not correspond to C. damarensis and should be considered a separate species: C. micklemi (as confirmed by molecular analyses; Ingram, Burda & Honeycutt, 2004). According to the karyotype, C. damarensis occurs only on the right bank of the Zambezi River in the Western Province. In contrast to the high karyotypic variability on the right bank of the Kafue River, it was found that C. anselli (2n=68) is widely distributed throughout the Central province on the left bank of the Kafue River. The resulting pattern of occurrence of the different karyotypes correlates well with the extant river system configuration that separates most karyotypes. We hypothesize that geomorphological changes and in particular river system dynamics in recent geological times have played an important role in the chromosomal diversification and may have provided opportunities for speciation to occur.