Short and long distance translocations: Movement and survival in eastern box turtles (_Terrapene carolina carolina_)

*Background/Question/Methods*

Human development represents a serious threat to wildlife populations through continued habitat loss and incidental mortality from construction activities. Resource managers responsible for protecting species with legal status or high public profile are faced with difficult decisions on how to best manage populations located in construction zones. One approach to mitigate mortalities is to relocate individuals. The effectiveness of translocation for reptiles and amphibians has been questioned, with studies often reporting higher mortality and increased movements of translocated individuals. Translocations of reptiles and amphibians have primarily involved moving animals long distances, well beyond an individual’s home range. For reptiles this means finding new nesting, foraging, and overwintering sites, which may be problematic. Moving individuals only short distances, within their home range, may reduce those problems. As part of the mitigation plan for a highway construction project in central Maryland, groups of eastern box turtles (Terrapene carolina carolina) were translocated both short distances (<0.5km), and long distances (~5km). To investigate differences in survival and movement patterns among long distance translocation, short distance translocation, and non-translocation groups, I tracked 94 turtles (31 long distance translocation, 29 short distance translocation, and 34 non-translocation) using radio telemetry. 

*Results/Conclusions*

Eleven animals died during the first activity season after translocation (April through November 2008). The mortalities included two long distance translocation, six short distance translocation, and three non-translocation animals. The causes of mortality included road kill, construction activity, and unknown (1, 4, and 6 mortalities respectively). All construction related mortalities were a result inadequate exclusion fencing to keep turtles from trespassing back onto the construction site. All mortalities due to construction were either non-translocation or short distance translocation animals. Eleven other individuals were located at least once within the construction zone, suggesting that without our intervention mortality rates would have been much higher. Preliminary results for movement show that turtles in the non-translocation group had the lowest average movements while long distance translocation animals had the greatest average movements. Long distance translocation turtles also chose overwintering sites farther away from their initial overwintering sites than either short distance translocation or non-translocation turtles (average distance from original site of 261.8m, 155.6m, and 124.3m respectively). This suggests that movement patterns of short distance translocation turtles are more like native turtles.
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Transcriptional role of cyclin D1 in development revealed by a “genetic-proteomic” screen

Author manuscript: 2010 September 22.Cyclin D1 belongs to the core cell cycle machinery, and it is frequently overexpressed in human cancers[superscript 1, 2]. The full repertoire of cyclin D1 functions in normal development and oncogenesis is unclear at present. Here we developed Flag- and haemagglutinin-tagged cyclin D1 knock-in mouse strains that allowed a high-throughput mass spectrometry approach to search for cyclin D1-binding proteins in different mouse organs. In addition to cell cycle partners, we observed several proteins involved in transcription. Genome-wide location analyses (chromatin immunoprecipitation coupled to DNA microarray; ChIP-chip) showed that during mouse development cyclin D1 occupies promoters of abundantly expressed genes. In particular, we found that in developing mouse retinas—an organ that critically requires cyclin D1 function[superscript 3, 4]—cyclin D1 binds the upstream regulatory region of the Notch1 gene, where it serves to recruit CREB binding protein (CBP) histone acetyltransferase. Genetic ablation of cyclin D1 resulted in decreased CBP recruitment, decreased histone acetylation of the Notch1 promoter region, and led to decreased levels of the Notch1 transcript and protein in cyclin D1-null (Ccnd1-/-) retinas. Transduction of an activated allele of Notch1 into Ccnd1-/- retinas increased proliferation of retinal progenitor cells, indicating that upregulation of Notch1 signalling alleviates the phenotype of cyclin D1-deficiency. These studies show that in addition to its well-established cell cycle roles, cyclin D1 has an in vivo transcriptional function in mouse development. Our approach, which we term ‘genetic–proteomic’, can be used to study the in vivo function of essentially any protein

Effectiveness of Action in India to Reduce Exposure of Gyps Vultures to the Toxic Veterinary Drug Diclofenac

Contamination of their carrion food supply with the non-steroidal anti-inflammatory drug diclofenac has caused rapid population declines across the Indian subcontinent of three species of Gyps vultures endemic to South Asia. The governments of India, Pakistan and Nepal took action in 2006 to prevent the veterinary use of diclofenac on domesticated livestock, the route by which contamination occurs. We analyse data from three surveys of the prevalence and concentration of diclofenac residues in carcasses of domesticated ungulates in India, carried out before and after the implementation of a ban on veterinary use. There was little change in the prevalence and concentration of diclofenac between a survey before the ban and one conducted soon after its implementation, with the percentage of carcasses containing diclofenac in these surveys estimated at 10.8 and 10.7%, respectively. However, both the prevalence and concentration of diclofenac had fallen markedly 7–31 months after the implementation of the ban, with the true prevalence in this third survey estimated at 6.5%. Modelling of the impact of this reduction in diclofenac on the expected rate of decline of the oriental white-backed vulture (Gyps bengalensis) in India indicates that the decline rate has decreased to 40% of the rate before the ban, but is still likely to be rapid (about 18% year−1). Hence, further efforts to remove diclofenac from vulture food are still needed if the future recovery or successful reintroduction of vultures is to be feasible

Tissue-Specific Target Analysis of Disease-Associated MicroRNAs in Human Signaling Pathways

MicroRNAs are a large class of post-transcriptional regulators that bind to the 3′ untranslated region of messenger RNAs. They play a critical role in many cellular processes and have been linked to the control of signal transduction pathways. Recent studies indicate that microRNAs can function as tumor suppressors or even as oncogenes when aberrantly expressed. For more general insights of disease-associated microRNAs, we analyzed their impact on human signaling pathways from two perspectives. On a global scale, we found a core set of signaling pathways with enriched tissue-specific microRNA targets across diseases. The function of these pathways reflects the affinity of microRNAs to regulate cellular processes associated with apoptosis, proliferation or development. Comparing cancer and non-cancer related microRNAs, we found no significant differences between both groups. To unveil the interaction and regulation of microRNAs on signaling pathways locally, we analyzed the cellular location and process type of disease-associated microRNA targets and proteins. While disease-associated proteins are highly enriched in extracellular components of the pathway, microRNA targets are preferentially located in the nucleus. Moreover, targets of disease-associated microRNAs preferentially exhibit an inhibitory effect within the pathways in contrast to disease proteins. Our analysis provides systematic insights into the interaction of disease-associated microRNAs and signaling pathways and uncovers differences in cellular locations and process types of microRNA targets and disease-associated proteins

Evaluation of translocation as a tool for mitigating development threats to great crested newts (Triturus cristatus) in England, 1990-2001

Great crested newts (Triturus cristatus) are protected under European and UK legislation, but are frequently the subject of conflict between development and conservation in England. When this occurs, the developer is legally obliged to instigate a mitigation plan to reduce the impacts on the newts. This usually involves the translocation of newts coupled with habitat enhancement and creation. We reviewed mitigation projects carried out in England between 1990 and 2001 by (1) analysing licensing information collected by the governmental licensing authorities; and (2) a questionnaire survey of a sample of mitigation projects. Over half of the licensed projects on file contained no report of the work undertaken. There was an increase in the number of new translocation projects from less than 10 a year in the early 1990s to over 80 a year by 2000. This translates into about 1.5 million per year currently being spent on grew: crested newt mitigation projects. Most of these projects involved in situ translocations of newts to areas within or adjacent to the development site. The number of newts translocated per project declined over the same period, and was related to the total area of habitat destroyed and work effort. About 27% of great crested newt terrestrial habitat was destroyed during the developments along with about half of all ponds. Although the number of new ponds created compensated for the number of known great crested newt ponds lost, there was a net loss in terms of overall area of aquatic habitat. Where follow-up monitoring of translocations was conducted, there was evidence of breeding at most sites one-year post-development, but it is unclear whether these populations were sustainable in the long-term. (C) 2004 Elsevier Ltd. All rights reserved