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McAfee R.K. 2014. Dental anomalies within extant members of the mammalian Order Pilosa. —Acta Zoologica (Stockholm) 00 :0 00–000 Recent discovery of a supernumerary dental anomaly in two-toed sloths led to an extensive review of extant sloth specimens to look for additional anomalies. In total, 881 museum specimens were examined. These revealed two primary types of anomalies, hyperdontia (extra teeth) and anodontia (loss of teeth), occurring at a rate of 2.4% (n = 21). Two-toed sloths, Choloepus, were more likely to have hyperdontia in the anterior dentition, whereas three-toed sloths, Bradypus ,e xperienced anodontia more frequently with the upper caniniforms. Both genera experienced both anomalies. The majority affected the upper dentition, with only three specimens exhibiting mandibular anomalies. Beyond the patterns of tooth positioning, all anomalies were random with respect to age, sex and geography. A few specimens not counted in the initial assessment expressed incomplete anodontia, indicating that the loss occurred postnatally and was not an embryological anomaly. For Bradypus, the findings provide new support for the hypothesis that the taxon represents a neotenic lineage and opens new possibilities about its relationship to the extinct ground sloths with a suggested rooting above that of the basal position it typically occupies for Folivora.

Typically the number of vertebrae an organism will have post-embryonically is determined during embryogenesis via the development of paired somites. Our research investigates the phenomenon of post-embryonic vertebral addition in salamander tails. We describe body and tail growth, and patterns of postsacral vertebral addition and elongation in context with caudal morphology for four plethodontids (Eurycea), and one ambystomatid. Eurycea nana and A. mexicanum have paedomorphic life cycles; E. cirrigera, E. longicauda and E. quadridigitata are biphasic. Specimens were collected, borrowed and/or purchased, and cleared and stained for bone and cartilage. Data collected include snout-vent length (SVL), tail length (TL), vertebral counts and centrum lengths. Eurycea species with biphasic life cycles had TLs that surpassed SVL following metamorphosis. Tails in paedomorphic species elongated but rarely exceeded body length. Larger TLs were associated with more vertebrae and longer vertebrae in all species. We observed that rates of postsacral vertebral addition varied little amongst species. Regional variation along the tail becomes prominent following metamorphosis in biphasic developers. In all species vertebrae in the posterior one-half of the tail taper towards the tip. We suggest a developmental link might exist between the ability to continually add vertebrae and regeneration in salamanders.

Bever, G.S. 2007. Comparative growth in the postnatal skull of the extant North American turtle Pseudemys texana (Testudinoidea: Emydidae). —Acta Zoologica (Stockholm) 88: 000–000 Postnatal growth is one of the many aspects of developmental morphology that remains distinctly understudied in reptiles. Variation and ontogenetic scaling within the skull of the extant emydid turtle, Pseudemys texana is described based on 25 continuous characters. Results indicate that skull shape in this species changes little during postnatal growth relative to the only cryptodire taxa for which comparable datasets are available (Apalone ferox and Sternotherus odoratus). This relative lack of change results in the paedomorphic retention of a largely juvenile appearance in the adult form of P. texana. The skulls of males and females, despite the presence of distinct sexual dimorphism in size, grow with similar scaling patterns, and the few observed differences appear to reflect alteration of the male growth trajectory. Comparisons with A. ferox and S. odoratus reveal a number of similarities and differences that are here interpreted within a phylogenetic context. These preliminary hypotheses constitute predictive statements that phylogenetically bracket the majority of extant cryptodire species and provide baseline comparative data that are necessary for the future recognition of apomorphic transformations. Plasticity of ontogenetic scaling as a response to the homeostatic needs and behaviour of individuals commonly is evoked as a limitation of ontogenetic scaling as a means to inform phylogenetic studies. These evocations are largely unfounded considering that variability itself can evolve and thus be phylogenetically informative.

Epiphyseal development was investigated on X-rays of flippers from 158 harbour porpoises from Danish waters. Development followed a proximodistal pattern similar to what is known in other cetacean species. Ossification of epiphyses was rare in the phalanges of the first and fifth digits and in the more distal phalanges of the second, third and fourth digits. Along with the morphology of the first metacarpal and the more distal phalanges this suggested paedomorphosis relative to delphinids. Male and female porpoises showed similar progression of epiphyseal development until approximately the sixth year. From then on, female porpoises showed more progressed development than males. This suggests a higher level of paedomorphosis in the male porpoise. The mechanism behind phocoenid paedomorphosis seems to be progenesis, probably as an adaptation towards a high reproductive rate relative to the delphinids.

The larval and post-larval development of Cyclestheria hislopi is examined by SEM. There are at least nine stages (excluding the adult) – six larval and three post-larval stages. The first four stages are passed within the egg-membrane. The larval and the post-larval phase are separated by a profound change in morphology that takes place between stages VI and VII. The larva shifts from a dorso-ventrally flattened ‘larval’ appearance up to stage VI to a laterally flattened, more ‘adult’ appearance from stage VII. New morphological data have been revealed by this study, including (1) a large and globular larval dorsal organ; (2) the carapace starts its development from the segments of the first and second maxillae; (3) the anterior ramus of the second antenna in adult Cyclestheria hislopi is the endopod, and the posterior ramus the exopod. Direct development of the brood in Cyclestheria hislopi– unique among conchostracans – is compared with that of the Cladocera. If Cyclestheria is the sister group to the Cladocera, as favoured in this work, the classical neoteny theory of the Cladocera must be reconsidered, as there is no particular similarity between any adults of the Cladocera and any of the larval stages of Cyclestheria. It is suggested that Cyclestheria displays the type of development present in a cladoceran ancestor. A comparison between Cyclestheria and the Upper Cambrian ‘Orsten’ fossil Rehbachiella kinnekullensis reveals a remarkable similarity in the endite morphology of the trunk limbs.

The Maxillopoda Dahl (1956) was defined primarily by a 5–6–5 body plan; that is, a head supporting five pairs and a thorax six pairs of appendages, and an abdomen of five segments, the first of which may bear a pair of genital limbs and the last of which, the telson, bears caudal rami. Representatives as diverse as ostracods, cirripeds, orstenocarids and skaracarids appear in the Cambrian, so we are dealing with a radiation that in the most part took place over 500 million years ago. A progenetic origin of the maxillopodans, from an ur-malacostracan stock, has been proposed (Newman, W. A. 1983. Crustacean phylogeny—Crustacean Issues, Vol. 1, pp. 105–119). However, new information, including the recently discovered Cambrian forms Skaracarida and Orstenocarida, the structure of spermatozoa, and preliminary results from the sequencing of ribosomal RNA, suggests that the Maxillopoda are more deeply rooted in the crustaceans than previously supposed, likely closer to the ur-crustacean than to the ur-malacostracan.

The Perkinsiana acrosome is elongated, pointed and tapering, strengthened anteriorly by cortical rings of longitudinally running units. The Pseudopotamilla acrosome is cap-like and its apical region contains a laminar body with two electron densities, the laminae crossed by occasional lines of dislocation, as in a crystal. These apparently solid regions are closely followed by peripherally situated lucent zones. The zone in Pseudopotamilla contains tubules, which are very like those in Sabella sperm, except that they lack connections with the acrosome base. Both species are probably broadcast spawners and have nuclei, mitochondria, centrioles and flagella of the primitive type. This may, however, be a secondary reversion through neoteny.