Global conservation policy and action have largely neglected protecting and monitoring genetic diversity—one of the three main pillars of biodiversity. Genetic diversity (diversity within species) underlies species’ adaptation and survival, ecosystem resilience, and societal innovation. The low priority given to genetic diversity has largely been due to knowledge gaps in key areas, including the importance of genetic diversity and the trends in genetic diversity change; the perceived high expense and low availability and the scattered nature of genetic data; and complicated concepts and information that are inaccessible to policymakers. However, numerous recent advances in knowledge, technology, databases, practice, and capacity have now set the stage for better integration of genetic diversity in policy instruments and conservation efforts. We review these developments and explore how they can support improved consideration of genetic diversity in global conservation policy commitments and enable countries to monitor, report on, and take action to maintain or restore genetic diversity.
Reported in this study are the initial results from studies to develop rabbit models of systemic lupus erythematosus (SLE) by immunizations using two distinct peptides on branched polylysine backbones (multiple Ag peptide)-peptides. Eleven rabbits received a peptide from the Sm B/B′ spliceosomal complex previously shown to be immunogenic in rabbits, and 13 rabbits received a peptide from the rabbit N-methyl-d-aspartate receptor NR2b. All 24 animals in different generations of pedigreed, noninbred rabbits produced peptide-specific responses. Anti-nuclear autoantibody responses, including anti-dsDNA, were seen in 17 of 24 rabbits. To date, two rabbits have been observed to have seizure-like events and a third nystagmus. A model for eliciting development of SLE in genetically related yet heterogeneous rabbits may more closely resemble development of human SLE than do some models in inbred mice. Through selective breeding, it may also ultimately provide additional information about the genetics and etiology of SLE and serve as a model for assessing new treatment options.
1. Genetic diversity is one of the three main levels of biodiversity recognised in the Convention on Biological Diversity (CBD). Fundamental for species adaptation to environmental change, genetic diversity is nonetheless under-reported within global and national indicators. When it is reported, the focus is often narrow and confined to domesticated or other commercial species.2. Several approaches have recently been developed to address this shortfall in reporting on genetic diversity of wild species. While multiplicity of approaches is helpful in any development process, it can also lead to confusion among policy makers and heighten a perception that conservation genetics is too abstract to be of use to organisations and governments.3. As the developers of five of the different approaches, we have come together to explain how various approaches relate to each other and propose a scorecard, as a unifying reporting mechanism for genetic diversity. 4. Policy implications. We believe the proposed combined approach captures the strengths of its components and is practical for all nations and subnational governments. It is scalable and can be used to evaluate species conservation projects as well as genetic conservation projects.
1. Fire drives animal population dynamics across many ecosystems. Yet, we still lack an understanding of how most species recover from fire and the effects of fire severity and patchiness on recovery processes. This information is crucial for firemediated biodiversity conservation, particularly as fire regimes change globally.2. We conducted an experiment to test whether post-fire recovery is driven by in situ survival or recolonisation, and to determine whether this varies with fires of increasing percentage area burnt (burn cover) and severity. We used the pale field rat Rattus tunneyi as a model, because it represents the extinction process for a suite of mammal species suffering population collapse across Australia's northern savannas. Our treatments spanned a gradient from patchy, low severity fires (simulating early dry season management burns) to thorough, high severity fires (simulating wildfires). We performed capture-mark-recapture, vegetation and aerial surveys before, 6 weeks after and 1 year after fire.3. Six weeks after fire, pale field rats were only captured in unburnt patches of vegetation, and capture rates were proportional to the amount of unburnt habitat.One year later, both vegetation and pale field rat populations recovered across all sites. However, population recovery after low severity fires was likely achieved through in situ survival and reproduction in unburnt micro-refuges, compared to recolonisation driving recovery after high severity fires. Synthesis and applications.Pale field rat persistence is strongly dependent on the retention of unburnt habitat patches within fire-affected areas. Management strategies that increase micro-refugia within burnt areas may facilitate pale field rat population recovery. Globally, building recovery mechanisms into fire management will be vital for supporting the long-term persistence of fire-affected species.
An important aspect of any meaningful public discussion about developments in gene technology is the provision of opportunities for interested publics to engage in sociable public discourse with other lay people and with experts. This article reports on a series of peer group conversations conducted in late 1996 and early 1997 with sixteen community groups in Perth, Western Australia, interested in gene therapy technology. With the case of cystic fibrosis as a particular focus, and using background resource material as a stimulus for discussion, the participating groups explored a range of value issues arising from the new genetic medicine. This more discursive context enabled participants to express a number of background or life-world concerns about genetic medicine, concerns that are often obscured by the dominant biomedical and bioethical discourses.
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