Expanding marine protected areas to include degraded coral reefs

Marine protected areas (MPAs) are a commonly applied solution to coral reef degradation, yet coral reefs continue to decline worldwide. We argue that expanding the range of MPAs to include degraded reefs (DR‐MPA) could help reverse this trend. This approach requires new ecological criteria for MPA design, siting, and management. Rather than focusing solely on preserving healthy reefs, our approach focuses on the potential for biodiversity recovery and renewal of ecosystem services. The new criteria would help identify sites with the highest potential for recovery and the greatest resistance to future threats (e.g., increased temperature and acidification) and sites that contribute to MPA connectivity. The DR‐MPA approach is a compliment rather than a substitute for traditional MPA design approaches. We believe that the DR‐MPA approach can enhance the natural, or restoration‐assisted, recovery of DRs and their ecosystem services; increase total reef area available for protection; promote more resilient and better‐connected MPA networks; and improve conditions for human communities dependent on MPA ecosystem services.     

The impact of economic factors and governance on greenhouse gas emission

Environmental Economics and Policy Studies - Governance is a basic factor explaining the poor economic, social and environmental performance of many developing countries. Since good governance...     

Regional consequences of the way land users respond to future water availability in Murcia, Spain

Agricultural development in the Murcia autonomous region, Spain, has led to overexploitation of groundwater resources, and climate change will further increase pressures. Policy options to tackle the current unsustainable situation include the development of inter-basin water transfer (IBWT) schemes from wetter regions in the north and the introduction of taxation to further control groundwater abstraction. Under these scenarios, farmers with current access to water could face higher water cost, whereas farmers in areas where water was previously not available could see first time availability of water resources. In this paper, we combine discrete choice-based interviews with farmers in the Torrealvilla catchment, in which they indicate how they would adapt their land use under different scenarios, with an input–output model to assess the aggregate effects of individual land use decisions on the economy and water consumption of the Murcia region. The paper presents steps taken in the development of an input–output table for Murcia, including disaggregation of the agricultural sector, accounting for sector water use and consideration of back- and forward linkages. We conclude that appropriate taxation can lead to better water use efficiency, but that this is delicate as relatively small changes in prices of agricultural products can have significant impacts on land use and water consumption. Although new IBWT schemes would enable water to be used more efficiently, they would considerably increase regional water consumption and the regional economy’s dependence on water. As this is not sustainable under future climate change, water saving development pathways need to be explored.     

Farmer typology, future scenarios and the implications for ecosystem service provision: a case study from south-eastern Spain

Farming communities are increasingly expected to manage their agricultural activities in ways that ensure sustainable flows of a wide range of ecosystem services for society. The land use and management choices that farmers make are dependent upon their socio-economic characteristics and background, and in turn have important implications for the landscape and associated ecosystem services. Thus, a better understanding about the linkages between the characteristics of farmers, farm management and land use is important for managing multifunctional agro-ecosystems. In this paper, we first develop a typology of farmers for Torrealvilla catchment in Murcia, Spain, according to the characteristics of their households and farm management (e.g. the farmer’s age, household income, water access, land tenure and farm labour). This analysis distinguishes six types of farmers. Secondly, we analyse the link between farmer typology and the farmers’ responses to a number of scenarios. The scenarios describe different likely changes to agriculture in the catchment in terms of environmental constraints (irrigation water availability and rainfall pattern) and environmental policy regulation (water taxation and subsidies). This exercise enables us to explore the range of future land use changes that are likely to occur in the study area. The results indicate that: rain-fed agriculture is expected to experience gradual but extensive abandonment; vegetable/fruit farming and pig/animal rearing are likely to stagnate or even decline; and growing of grapes is likely to expand. Thirdly, we qualitatively evaluate how future land use changes are likely to affect key ecosystem services in the study area including future agricultural production and associated local income generation, erosion control, maintenance of the groundwater table and various cultural services associated with a heterogeneous agro-ecosystem. Particular changes such as expansion of grape production will increase food production and local income at the cost of further depletion of the aquifer and increased risk of salinisation. The outcomes of the study highlight that, to be effective, the design of agri-environmental schemes and other government interventions (e.g. specific compulsory regulations on farming practices and associated water use) should carefully take into account the characteristics of the farmers within the area of interest, their land uses and the possible diversity of responses to policy and environmental drivers. Opportunities exist for future studies quantifying the extent of the impacts of ecosystem service provision through formal models combining farmers’ land use decision-making and spatially explicit modelling of landscape processes.     

Neutral lipids in macroalgal spores and their role in swimming

We followed changes in the neutral lipid content of actively swimming zoospores of the palm kelp Pterygophora californica in a laboratory experiment to investigate the degree to which spore swimming is fueled by endogenous lipid reserves. The neutral lipid content of individual zoospores during the experiment was measured by flow cytometry using Nile Red, a fluorescent stain that is specific for neutral lipid. Results showed that photosynthesis greatly influenced lipid consumption during zoospore swimming. We found no detectable change in the neutral lipid content of zoospores after 30 h of swimming under conditions where light was near the optimum for photosynthesis. By contrast, neutral lipid declined by ≃43% over 30 h in zoospores kept in the dark. To evaluate whether lipid reserves are generally related to spore motility in macroalgae, we surveyed spore lipid-content and composition in species with motile spores and non-motile spores using thin-layer chromatography (TLC), and flame-ionization detection (FID). We observed substantial differences in lipid content and composition among the 20 species examined. Spores high in total lipid (as estimated by the ratio of lipid:carbon) generally had a large amount of neutral lipid; motile spores had significantly more lipid and a significantly larger neutral lipid fraction than non-motile spores. The kelps as a group had the highest total lipid content and the largest neutral lipid fraction, while non-motile spores of red algae were generally low in total lipid and in the proportional abundance of neutral lipid. Phospholipids accounted for more than half of all lipid in 14 of the 20 species examined, while neutral lipid accounted for the majority of lipid in all five species of kelp examined. Triacylglycerols, which function primarily in energy storage, were the primary form of neutral lipid in all but one species of kelp (Agarum fimbriatum), whereas free fatty acids were the dominant form of neutral lipid in most red algae and in brown algae that had a small neutral lipid fraction. Our results are largely consistent with the hypothesis that macroalgae use endogenous lipid reserves to fuel spore-swimming. The small amounts of triacylglycerols observed in the motile spores of several species of brown and green algae, however, indicate that the amount of lipid reserves needed to fuel spore-swimming may be influenced by a variety of factors including swimming behavior, photosynthetic efficiency, and the light environment inhabited by spores. Received: 8 September 1998 / Accepted: 8 January 1999     

Correlates of Population Recovery Goals in Endangered Birds

Abstract: Endangered species recovery plans commonly set goals for population size that are used to define the success of recovery efforts. We examined variation in these population recovery goals for bird species listed under the U. S. Endangered Species Act to determine whether there were simple predictors of recovery population size. The median population sizes that must be met for a species to be removed from the list or downlisted to the threatened category are 4000 and 1500 respectively, but the thresholds varied considerably. Most variation in population recovery goals ( ≥75%) was explained by the population size when the recovery plan was written. Species listed when their population's size was relatively large have higher population recovery goals, whereas those listed when populations were small have lower population goals. Population sizes set for recovery also increased over time and were higher for species listed throughout the United States rather than for part of the country. In combination, these three variables explained 86% of the variance in population goals for delisting and 94% of the variance in goals for downlisting. Body mass, annual fecundity, maximum lifespan, whether the population was listed as threatened or endangered, and whether a formal population viability analysis was conducted were variables not significantly associated with population recovery goals. Thus, we found that variables relating to the circumstances under which the populations were listed could explain almost all of the variance in recovery population goals, and that biological traits of the endangered birds explained little of the variance.