Flux estimates from soil methanogenesis and methanotrophy: Landfills,rice paddies,natural wetlands and aerobic soils

Present and future annual methane flux estimates out of landfills, rice paddies and natural wetlands, as well as the sorption capacity of aerobic soils for atmospheric methane, are assessed. The controlling factors and uncertainties with regard to soil methanogenesis and methanotrophy are also briefly discussed.The actual methane emission rate out of landfills is estimated at about 40 Tg yr^–1. Changes in waste generation, waste disposal and landfill management could have important consequences on future methane emissions from waste dumps. If all mitigating options can be achieved towards the year 2015, the CH₄ emission rate could be reduced to 13 Tg yr^–1. Otherwise, the emission rate from landfills could increase to 63 Tg yr^–1 by the year 2025. Methane emission from rice paddies is estimated at 60 Tg yr^–1. The predicted increase of rice production between the years 1990 and 2025 could cause an increase of the CH₄ emission rate to 78 Tg yr^–1 by the year 2025. When mitigating options are taken, the emission rate could be limited to 56 Tg yr^–1. The methane emission rate from natural wetlands is about 110 Tg yr^–1. Because changes in the expanse of natural wetland area are difficult to assess, it is assumed that methane emission from natural wetlands would remain constant during the next 100 years. Because of uncertainties with regard to large potential soil sink areas (e.g. savanna, tundra and desert), the global sorption capacity of aerobic soils for atmospheric methane is not completely clear. The actual estimate is 30 Tg yr^–1.In general, the net contribution of soils and landfills to atmospheric methane is estimated at 180 Tg yr^–1 (210 Tg yr^–1 emission, 30 Tg yr^–1 sorption). This is 36% of the global annual methane flux (500 Tg yr^–1).     

Economic Science, Endangered Species, and Biodiversity Loss

Abstract: Although economic analysis can be used to argue for preservation of species and habitats, many natural assets represent inferior investments in society's asset portfolio. We demonstrate this for the case of ancient temperate rainforests and minke whales (  Balaenoptera acutorostrata ). For both rainforests and whales, we determined their value for harvest and balanced this against society's valuation of the preserved stock. For the market and nonmarket data available, we then determined how much rainforest and how many minke whales global society should keep in its asset portfolio. Although ecologists increasingly attempt to justify preservation of biological assets on economic grounds, we argue that this might be a dangerous approach to take. Ultimately, it may be necessary to reexamine the ethical foundations for conservation of nature and biodiversity, including the economist's use of utilitarianism. We suggest that the safe minimum standard approach may prove useful in practice.     

Overview and recent developments in cell-based noninvasive prenatal testing

Investigators have long been interested in the natural phenomenon of fetal and placental cell trafficking into the maternal circulation. The scarcity of these circulating cells makes their detection and isolation technically challenging. However, as a DNA source of fetal origin not mixed with maternal DNA, they have the potential of considerable benefit over circulating cell-free DNA-based noninvasive prenatal genetic testing (NIPT). Endocervical trophoblasts, which are less rare but more challenging to recover are also being investigated as an approach for cell-based NIPT. We review published studies from around the world describing both forms of cell-based NIPT and highlight the different approaches’ advantages and drawbacks. We also offer guidance for developing a sound cell-based NIPT protocol.     

The relationship between diversity profiles,evenness and species richness based on partial ordering

Problems with the notion of evenness, such as ambiguity, proliferation of indices, choice of indices, etc. can be overcome by a more fundamental, mathematical approach. We show that the Lorenz curve is an adequate representation of evenness. The corresponding Lorenz order induces a partial order in the set of equivalent abundance vectors. Also diversity can adequately be studied through a partial order and represented by a curve derived from the classical Lorenz curve. This curve is known as the intrinsic diversity profile (or k-dominance curve) and was introduced by Patil and Taillie (1979) and Lambshead et al. (1981).     

State Intervention to Protect Endangered Species: Why History and Bad Luck Matter

Abstract: Illegal exploitation threatens the survival of many species, and anti-poaching legislation ("protection on paper") does not protect species. State enforcement is needed to support and supplement the formal status of endangered species, but state enforcement can be a source of instability leading to the demise of species if ad hoc rules are followed blindly. We demonstrate this with a model of poaching, wildlife, and government wildlife enforcement, but our findings apply more generally. Crucial assumptions of the dynamic model are that both poaching and enforcement effort increase or decrease whenever poaching effort and enforcement are relatively profitable or unprofitable activities, respectively. We found that multiple steady states may characterize the system's equilibrium. Depending on initial populations, the initial extent of state involvement, and random events, animal populations may be severely depleted or unexpectedly built up during transition phases. Our findings highlight the importance of history and luck in protecting endangered species.