On size and area: Patterns of mammalian body size extremes across landmasses

We describe a biogeographic pattern in which mammalian body size extremes scale with landmass area. The relationship between the largest and the smallest mammal species found on different landbridge islands, mountaintops and continents shows that the size of the largest species increases, while that of the smallest species decreases, with increase in the area of the landmass. We offer two possible explanations: (1) that the pattern is the result of sampling artefacts, which we call the ‘statistical artefact hypothesis’, or (2) that the pattern is the result of processes related to the way body size affects the number of individuals that a particular species can pack in a given area, which we call the ‘area-scaling hypothesis’. Our results point out that the pattern is not a statistical artefact resulting from random sampling, but can be explained by considering the scaling of individual space requirements and its effect on population survival on landmasses of different area. This revised version was published online in July 2006 with corrections to the Cover Date.     

Phylogeny of Neotropical Protoneuridae (Odonata: Zygoptera) and a preliminary study of their relationship with related families

Abstract.  A cladistic analysis of Neotropical Protoneuridae was performed on a data matrix of 48 morphological characters and 43 terminal taxa. Representatives of Paleotropical Protoneuridae, Platycnemididae and Isostictidae were included to test their relationships with Neotropical Protoneuridae. Coenagrionidae was chosen as the outgroup, but alternative analyses with Platycnemididae as the outgroup were also performed. Protoneuridae appears as a polyphyletic clade, with its Paleotropical component being more closely related to Platycnemididae and Isostictidae. Neotropical Protoneuridae appear as a monophyletic clade; included genera considered monophyletic or valid monotypic taxa are Epipleoneura Williamson, 1915 ; Idioneura Selys, 1860; Junix Rácenis, 1968; Neoneura Selys, 1860; Peristicta Hagen in Selys, 1860; Roppaneura Santos, 1966; and Lamproneura De Marmels, 2003. A key to the Neotropical Protoneuridae genera is included.     

Effect of host instar on host discrimination of heterospecific‐parasitised hosts by sympatric parasitoids

1. Interspecific competition among hymenopteran parasitoids may shape their behavioural strategies for host resource exploitation. In order to reduce or prevent competition, many parasitoid species have evolved the ability to discriminate between unparasitised hosts and hosts parasitised by another parasitoid species (i.e. heterospecific host discrimination). However, discriminatory ability might be affected by host instar. 2. This study reports the first results on whether host instar can influence the use of heterospecific‐parasitised hosts by sympatric parasitoids of the genus Aphytis (Hymenoptera: Aphelinidae). 3. Aphytis melinus and Aphytis chrysomphali discriminated between unparasitised and heterospecific‐parasitised hosts when they found a third‐instar host (high quality), with a tendency to multi‐parasitise. However, this discrimination was not observed in the second instar (lower size). 4. The behavioural strategies adopted towards multi‐parasitise third‐instar hosts varied between both species. Aphytis chrysomphali reduced its clutch size in heterospecific‐parasitised hosts, whereas A. melinus tended to probe them for longer than healthy hosts. 5. Overall, our results highlight the importance of host instar in the study of intrinsic competition between parasitoids.     

Epithelial-Directed Mesenchyme Differentiation in vitro

To assess the requirement for specific or possibly non-specific epithelial instructions for mesenchymal cell differentiation, we designed studies to evaluate and compare homotypic with heterotypic tissue recombinations across vertebrate species. These studies further tested the hypothesis that determined dental papilla mesenchyme requires epithelial-derived instructions to differentiate into functional odontoblast cells using a serumless, chemically-defined medium. Theiler stage 25 C57BL/6 or Swiss Webster cap stage mandibular first molar tooth organs or trypsin-dissociated, homotypic epithelial-mesenchymal tissue recombinants resulted in the differentiation of odontoblasts within 3 days. Epithelial differentiation into functional ameloblasts was observed within 7 days. Trypsin-dissociated and isolated mesenchyme did not differentiate into odontoblasts under these experimental conditions. Heterotypic recombinants between quail Hamburger-Hamilton stages 22–26 mandibular epithelium and Theiler stage 25 dental papilla mesenchyme routinely resulted in odontoblast differentiation within 3 days in vitro. Odontoblast differentiation and the production of dentine extracellular matrix continued throughout the 10 days in organ culture. Ultrastructural observations of the interface between quail and mouse tissues indicated the reconstitution of the basal lamina as well as the maintenance of an intact basal lamina during 10 days in vitro. Quail epithelial cells did not differentiate into ameloblasts and no enamel extracellular matrix was observed. These results show that quail mandibular epithelium can provide the required developmental instructions for odontoblast differentiation in the absence of serum or other exogenous humoral factors in a chemically-defined medium. They also suggest the importance of reciprocal epithelial-mesenchymal interactions during epidermal organogenesis.