The tortoise and the goat: Interactions on Aldabra island

Endemic giant tortoises and introduced feral goats are the two major terrestrial herbivores on Aldabra atoll and have similar distributions. The tortoises vastly outnumber the goats, however, and the impact of the goats on the tortoises is minimal. Intraspecific competition is a much greater factor for the tortoises than interspecific competition. Feeding habits are significantly different, goats being primarily browsers and tortoises primarily grazers. Both species affect of the growth forms and regeneration of many plant species, but again due to sheer numbers, the tortoises' impact is much greater than the goats. Direct behavioural interactions between tortoises and goats are rare. Goats may, however, indirectly benefit tortoises by depositing heavy loads of faeces at coastal sleeping sites, thus acting as fertilizing agents, moving nutrients from tortoise-inaccessible to tortoise-accessible areas.     

Ecosystem-level dynamics of soil-vegetation features, with implications for conserving a narrowly endemic reptile

Narrow endemism presents challenges to species occurrence modeling particularly when the distribution of key local habitat features changes across space and time as a function of processes operating at larger scales. One need facing conservation in such settings is a better understanding of the biogeographic dynamics of the larger features that govern occurrence of critical local habitat. The Mescalero–Monahans shinnery sands region of western North America is a dynamic landscape where sand shinnery oak interacts with wind-driven sand to establish dune habitat. This ecosystem supports several narrowly endemic dune-dwelling species including the dunes sagebrush lizard. Using near-anniversary satellite and aerial imagery from 1986, 1998, and 2011, we integrated object-based image classification and statistical analysis to develop and validate a spatially explicit estimate of the sand shinnery oak ecosystem, including dynamics associated with its attrition and emergence, at high resolution throughout an 89,849-km² study area encompassing the range of the dunes sagebrush lizard. The spatial estimate of the distribution and extent of the sand shinnery oak soil-vegetation association validated reasonably well (overall accuracy = 0.79; sensitivity = 0.49; specificity = 0.91) and showed that the association declined 10.3 % in extent during the 25-year assessment window. The presence of sand shinnery oak, patch size, and patch isolation were dynamic across space and time; a regression model showed that smaller, isolated patches on the periphery of the system were more likely to be lost over time whereas larger, less isolated, and centrally distributed patches were more likely to persist or expand. This study details broadly applicable methods to accurately delineate landforms throughout large extents, and offers mapping tools specific to issues surrounding Mescalero–Monahans shinnery sands endemics that are readily amenable to testing, refinement, and application in efforts to focus sustainable landscape management including conservation of endemic species.     

Development of real-time PCR assays for the detection and differentiation of Australian and European ranaviruses

Serious systemic disease in fish and amphibians is associated with the ranaviruses, epizootic haematopoietic necrosis virus (EHNV) and Bohle iridovirus (BIV) in Australia, and European sheatfish virus (ESV) and European catfish virus (ECV) in Europe. EHNV, ESV and ECV are recognized causative agents of the OIE (Office International des Epizooties) notifiable systemic necrotizing iridovirus syndrome and are currently identified by protein-based assays, none of which are able to rapidly identify the specific agents. The aim of this study was to develop TaqMan real-time PCR assays that differentiated these viruses using nucleotide sequence variation in two ranavirus genes. A conserved probe representing 100% sequence homology was used as a reference for virus-specific probes. The virus-specific probes produced a similar signal level to the conserved probe while those probes binding to non-target viral DNA produced an altered fluorescent curve. The pattern of probe binding was characteristic for each virus. Sensitivity, specificity and dynamic range of the assay were assessed. The test is currently useful as a research and initial screening tool, with the potential to become a sensitive and specific method for detection and differentiation of ranaviruses with further development.