The ecosystem-service chain and the biological diversity crisis

The losses that are being incurred of the Earth''s biological diversity, at all levels, are now staggering. The trend lines for future loss are steeply upward as new adverse drivers of change come into play. The political processes for matching this crisis are now inadequate and the science needs to address this issue are huge and slow to fulfil, even though strong advances have been made. A more integrated approach to evaluating biodiversity in terms that are meaningful to the larger community is needed that can provide understandable metrics of the consequences to society of the losses that are occurring. Greater attention is also needed in forecasting likely diversity-loss scenarios in the near term and strategies for alleviating detrimental consequences. At the international level, the Convention on Biological Diversity must be revisited to make it more powerful to meet the needs that originally motivated its creation. Similarly, at local and regional levels, an ecosystem-service approach to conservation can bring new understanding to the value, and hence the need for protection, of the existing natural capital.     

Climate change, biotic interactions and ecosystem services

Climate change is real. The wrangling debates are over, and we now need to move onto a predictive ecology that will allow managers of landscapes and policy makers to adapt to the likely changes in biodiversity over the coming decades. There is ample evidence that ecological responses are already occurring at the individual species (population) level. The challenge is how to synthesize the growing list of such observations with a coherent body of theory that will enable us to predict where and when changes will occur, what the consequences might be for the conservation and sustainable use of biodiversity and what we might do practically in order to maintain those systems in as good condition as possible. It is thus necessary to investigate the effects of climate change at the ecosystem level and to consider novel emergent ecosystems composed of new species assemblages arising from differential rates of range shifts of species. Here, we present current knowledge on the effects of climate change on biotic interactions and ecosystem services supply, and summarize the papers included in this volume. We discuss how resilient ecosystems are in the face of the multiple components that characterize climate change, and suggest which current ecological theories may be used as a starting point to predict ecosystem-level effects of climate change.     

Ecosystem service values and land use change in the opium poppy cultivation region in Northern Part of Lao PDR

Land use change and land-cover impacts ecosystem services and functions. In this paper according to the study area’s land use characteristic and ecosystem type, the Land use category of the study area was divided into seven categories, including Forest, Grassland, Farmland, Water, Wetlands, Urban land and Barren land. The dynamic information of the forest Land use change during 10 years was calculated by the map algebra in ArcGIS 9.2. Both in 1992 and in 2002, Forest and Grassland were two largest Land use category in the study area. Forest took up 44.7% and 39.4% of the total area, and Grassland was 50.13% and 50.72% of the total area in 1992 and 2002. Finally, we valued change in ecosystem services delivered by each land use category using coefficients published by Costanza et al. [5]. Ecosystem services value of study area, the total ecosystem services value of 10.6 million hectares of this study area decreased by 11.74%. From the coefficient of sensitivity (CS) was less than unity in all case, it indicated that the total ecosystem services values was relatively inelastic and the results suggest that we have to pay attention more on land use change and finally, policy for driving forces of land use change were developed.     

Contribution of nematodes to the structure and function of the soil food web

As carbon and energy flow through the soil food web they are depleted by the metabolic and production functions of organisms. To be sustained, a "long" food web, with a large biomass at higher trophic levels, must receive a high rate of rhizodeposition or detrital subsidy, or be top-populated by organisms of slow growth and long life cycle. Disturbed soil food webs tend to be bottom heavy and recalcitrant to restoration due to the slow growth of upper predator populations, physical and chemical constraints of the soil matrix, biological imbalances, and the relatively low mobility and invasion potential of soil organisms. The functional roles of nematodes, determined by their metabolic and behavioral activities, may be categorized as ecosystem services, disservices or effect-neutral. Among the disservices attributable to nematodes are overgrazing, which diminishes services of prey organisms, and plant-damaging herbivory, which reduces carbon fixation and availability to other organisms in the food web. Unfortunately, management to ameliorate potential disservices of certain nematodes results in unintended but long-lasting diminution of the services of others. Beneficial roles of nematodes may be enhanced by environmental stewardship that fosters greater biodiversity and, consequently, complementarity and continuity of their services.     

Global Mapping of Ecosystem Disservices: The Unspoken Reality that Nature Sometimes Kills us

Increasingly, we view nature through a utilitarian lens that leads us to attempt to measure and manage the services that species, habitats and ecosystems provide. Surprisingly, we have tended to consider only the positive values of ecosystems, their ecosystem services. In addition to providing our food and water, Nature also kills us, primarily through disease. If we are to effectively manage the terrestrial Earth, we need to also manage species, habitats and ecosystems so as to minimize such ‘ecosystem disservices’. I consider what we know about the spatial pattern of one disservice, pathogen prevalence and how changes in habitat influence it. I consider the effects of habitat changes on pathogen prevalence and, consequently, ecosystem disservices. In the end, we need to weigh both the costs and the benefits of particular ecosystems, habitats and species – to consider the bad with the good. Doing so requires that we learn much more about the biota than we currently know.     

Assessment of indicator species of butterfly assemblages in coffee–banana farming system in central Uganda

Butterflies are believed to be important pollinators because they are nectar/pollen feeders of both wild and cultivated plant species occurring in natural and managed systems. However, there exist very little knowledge about their spatio‐temporal distribution and diversity in agricultural systems of Sub‐Sahara Africa and in Uganda. There are no protocols to monitor the status of good pollinator species in these systems. The main aim of this study was to collect baseline information about indicator species of butterfly community in coffee–banana farming systems of central Uganda. Data were collected for 1 year (2006) using banana fruit‐bait traps, transect walk‐and‐counts and hand‐nets sampling methods. Indicator species of farmland habitats were identified using indicator value method. Species that emerged as significant (P < 0.05) suitable indicators were Catopsilia florella, Junonia sophia, Bicyclus safitza, Acraea acerata, Eurema hecabe, Ypthima albida, Zizula hylax, Acraea ventura, Eurema brigitta, Neptidopsis ophione, Junonia eonone, Zizeeria kynsna, Cupidopsis cissus, Junonia chorimene and Acrae uvui. These ubiquitous species were recommended to monitoring programmes as indicator species of butterfly communities delivering pollination services to cultivated and wild plants in farmland environments of central Uganda. Transect count was proposed as the best sampling technique to monitor butterfly species that may be involved in successful pollination activities in farmlands. There is a need to develop strategies to protect linear and nonlinear natural and semi‐natural habitats to offer sufficient refugia and breeding sites to butterflies inhabiting farmlands.     

Triploid bumblebees indicate a direct cost of inbreeding in fragmented populations

Hymenopteran species with single-locus complimentary sex-determination (sl-CSD) face an additional cost of inbreeding because of a loss of diversity at the sex-determining locus. Laboratory studies of a range of Hymenoptera have found that a small percentage of diploid males produce viable diploid sperm, and that if these males mate, then the resultant females produce triploid offspring that are sterile. Here, we use microsatellite markers to determine the frequency of triploid individuals of Bombus muscorum and B. jonellus in a model island system. Triploids were found in populations of both species. Observed triploid frequencies of up to 8% were detected, and estimated total frequencies peaked at 20% with respect to normal diploid workers. For both species, triploid frequency was negatively correlated with surrogates of population size, providing direct evidence for inbreeding in small populations. Populations limited to <～15 km(2) of suitable habitat were particularly likely to harbour triploids. Estimated total triploid frequencies were higher in B. muscorum than in B. jonellus, perhaps due to the greater dispersal range of the latter species. Implications for the conservation of rare social hymenopterans are discussed.     

It is getting hotter in here: determining and projecting the impacts of global environmental change on drylands

Drylands occupy large portions of the Earth, and are a key terrestrial biome from the socio-ecological point of view. In spite of their extent and importance, the impacts of global environmental change on them remain poorly understood. In this introduction, we review some of the main expected impacts of global change in drylands, quantify research efforts on the topic, and highlight how the articles included in this theme issue contribute to fill current gaps in our knowledge. Our literature analyses identify key under-studied areas that need more research (e.g. countries such as Mauritania, Mali, Burkina Faso, Chad and Somalia, and deserts such as the Thar, Kavir and Taklamakan), and indicate that most global change research carried out to date in drylands has been done on a unidisciplinary basis. The contributions included here use a wide array of organisms (from micro-organisms to humans), spatial scales (from local to global) and topics (from plant demography to poverty alleviation) to examine key issues to the socio-ecological impacts of global change in drylands. These papers highlight the complexities and difficulties associated with the prediction of such impacts. They also identify the increased use of long-term experiments and multidisciplinary approaches as priority areas for future dryland research. Major advances in our ability to predict and understand global change impacts on drylands can be achieved by explicitly considering how the responses of individuals, populations and communities will in turn affect ecosystem services. Future research should explore linkages between these responses and their effects on water and climate, as well as the provisioning of services for human development and well-being.     

Diverse pollinator communities enhance plant reproductive success

Understanding the functional consequences of biodiversity loss is a major goal of ecology. Animal-mediated pollination is an essential ecosystem function and service provided to mankind. However, little is known how pollinator diversity could affect pollination services. Using a substitutive design, we experimentally manipulated functional group (FG) and species richness of pollinator communities to investigate their consequences on the reproductive success of an obligate out-crossing model plant species, Raphanus sativus. Both fruit and seed set increased with pollinator FG richness. Furthermore, seed set increased with species richness in pollinator communities composed of a single FG. However, in multiple-FG communities, highest species richness resulted in slightly reduced pollination services compared with intermediate species richness. Our analysis indicates that the presence of social bees, which showed roughly four times higher visitation rates than solitary bees or hoverflies, was an important factor contributing to the positive pollinator diversity–pollination service relationship, in particular, for fruit set. Visitation rate at different daytimes, and less so among flower heights, varied among social bees, solitary bees and hoverflies, indicating a niche complementarity among these pollinator groups. Our study demonstrates enhanced pollination services of diverse pollinator communities at the plant population level and suggests that both the niche complementarity and the presence of specific taxa in a pollinator community drive this positive relationship.     

A Genetic Assessment of Ecological Restoration Success in Banksia attenuata

Rarely assessed in the success of ecological restoration projects is the maintenance of genetic variation in restored populations and, critically, their offspring. A founding population sourced from a limited genetic pool of nonlocal provenance seed can result in genetic bottlenecking and inbreeding, potentially reducing future population resilience and restoration success. We used microsatellite markers to assess the genetic variation of natural and restored populations, and their offspring, in Banksia attenuata R.Br. (Proteaceae), a keystone species of Banksia woodlands in south‐west Australia. Both natural and restored populations, and their offspring, displayed similarly high levels of heterozygosity (H_e range = 0.57–0.62) and allelic diversity (N_e range = 6.67–8.86) across 7 microsatellite loci. There was very weak population divergence (F_ST = 0.006) between the restored population and the adjacent natural population, indicating local provenance sourcing of seed. Genetic structuring within the natural population was weak, but detectable at 10 m and more strongly genetically structured than the restored population (Sp = 0.006 and 0.002, respectively). Complete outcrossing, low‐correlated paternity, and very low bi‐parental inbreeding were observed in both populations. Extensive pollen dispersal was observed within and among populations, with >50% of paternity assigned to sires beyond the local population. In a greenhouse experiment, differences in the overall performance of seedlings from natural and restored populations were negligible. Results indicate the successful genetic management of B. attenuata in this restoration project, from which general principles emphasizing the use of diverse local provenance seeds, genetic integration, and delivery of pollinator services are supported.