Population genetic structure and gene flow in a gleaning bat,Plecotus auritus

During summer the brown long-eared bat Plecotus auritus (Vespertilionidae) forms stable colonies, comprised of both adult females and males and young of the year. A long-term ringing study conducted in north-east Scotland has established that little movement occurs among colonies and that both sexes are recruited into their natal colony. The aim of the present study was to investigate, using microsatellite DNA markers, if genetic structure within the population reflects the spatial structure indicated by ringing. Inter-colony F_ST estimates obtained for all colony members, and for females and males separately, were low (0.019, 0.026 and 0.011, respectively), but all values differed significantly from zero. These data indicate high gene flow between colonies, although some coancestry among colony members is evident in both sexes. On combining the ringing and genetic data, it is concluded that gene flow occurs via extra-colony copulation, rather than natal dispersal, and that each colony behaves as a distinct subpopulation. Microgeographical genetic isolation by distance was demonstrated for, to our knowledge, the first time in a bat species, and found to be apparent both across the entire study area and along one river valley. The results suggest that extensive macrogeographical population genetic structure may be evident across the species'' range.     

A journey through time: exploring temporal patterns amongst digitized plant specimens from Australia

Online access to species occurrence records has opened new windows into investigating biodiversity patterns across multiple scales. The value of these records for research depends on their spatial, temporal, and taxonomic quality. We assessed temporal patterns in records from the Australasian Virtual Herbarium, asking: (1) How temporally consistent has collecting been across Australia? (2) Which areas of Australia have the most reliable records, in terms of temporal consistency and inventory completeness? (3) Are there temporal trends in the completeness of attribute information associated with records? We undertook a multi-step filtering procedure, then estimated temporal consistency and inventory completeness for sampling units (SUs) of 50?km ×?50?km. We found temporal bias in collecting, with 80% of records collected over the period 1970–1999. South-eastern Australia, the Wet Tropics in north-east Queensland, and parts of Western Australia have received the most consistent sampling effort over time, whereas much of central Australia has had low temporal consistency. Of the SUs, 18% have relatively complete inventories with high temporal consistency in sampling. We also determined that 25% of digitized records had missing attribute information. By identifying areas with low reliability, we can limit erroneous inferences about distribution patterns and identify priority areas for future sampling.     

Distal Val346Ile mutation in inducible NO synthase promotes substrate-dependent NO confinement

The function of inducible NO synthase (WT iNOS) depends on the release of NO from the ferric heme before the enzyme is reduced. Key parameters controlling ligand dynamics include the distal and proximal heme pocket amino acids, as well as the inner solvent molecules. In this work, we tested how a point mutation in the distal heme side of WT iNOS affected the geminate rebinding of NO by ultrafast kinetics and molecular dynamics simulations. The mutation sequestered much of the photodissociated NO close to the heme compared to WT iNOS, with a main picosecond phase accounting for 78% of the rebinding to the arginine-bound Val346Ile protein. Consequently, the probability of NO release from Val346Ile decreased as compared to that from WT iNOS, provided the substrate binding site is filled. These data are rationalized by a steric effect of the Ile methyl group inducing events mediated by the substrate, transmitted via the propionates to the NO and the protein. This model is consistent with the role of the H-bonding network involving the heme, the substrate, and the BH4 cofactor in controlling NO release, with a key role of the heme propionates [Gautier et al. (2006) Nitric Oxide 15, 312]. These data support the effect of Val346Ile mutation in decreasing NO release and slowing down NO synthesis compared to WT iNOS determined by single turnover catalysis [Wang et al. (2004) J. Biol. Chem. 279, 19018].