Biodiversity and Resilience of Ecosystem Functions Oliver, Tom H.; Heard, Matthew S.; Isaac, Nick J.B. ...
Trends in ecology & evolution (Amsterdam),
November 2015, 2015-Nov, 2015-11-00, 20151101, Letnik:
30, Številka:
11
Journal Article
Recenzirano
Odprti dostop
Accelerating rates of environmental change and the continued loss of global biodiversity threaten functions and services delivered by ecosystems. Much ecosystem monitoring and management is focused ...on the provision of ecosystem functions and services under current environmental conditions, yet this could lead to inappropriate management guidance and undervaluation of the importance of biodiversity. The maintenance of ecosystem functions and services under substantial predicted future environmental change (i.e., their ‘resilience’) is crucial. Here we identify a range of mechanisms underpinning the resilience of ecosystem functions across three ecological scales. Although potentially less important in the short term, biodiversity, encompassing variation from within species to across landscapes, may be crucial for the longer-term resilience of ecosystem functions and the services that they underpin.
The reintroduction of livestock grazing to regulate biomass load is being tested for large-scale restoration in Mediterranean landscapes affected by rural abandonment. Concurrently, there is a need ...to develop cost-effective methods to monitor such interventions. Here, we investigate if satellite data can be used to monitor the response of vegetation phenology and productivity to grazing disturbance in a heterogenous forest mosaic with herbaceous, shrub, and tree cover. We identify which vegetation seasonal metrics respond most to grazing disturbances and are relevant to monitoring efforts. The study follows a BACI (Before-After-Control-Impact) design applied to a grazing intervention in a Pyrenean oak forest (Quercus pyrenaica) in central Portugal. Using NDVI time-series from Sentinel-2 imagery for the period between June 2016 and June 2021, we observed that each type of vegetation exhibited a distinct phenology curve. Herbaceous vegetation was the most responsive to moderate grazing disturbances with respect to changes in phenology and productivity metrics, namely an anticipation of seasonal events. Results for shrubs and trees suggest a decline in peak productivity in grazed areas but no changes in phenology patterns. The techniques demonstrated in this study are relevant to a broad range of use cases in the large-scale monitoring of fine-grained heterogeneous landscapes.
Human-driven global change is causing ongoing declines in biodiversity worldwide. In order to address these declines, decision-makers need accurate assessments of the status of and pressures on ...biodiversity. However, these are heavily constrained by incomplete and uneven spatial, temporal and taxonomic coverage. For instance, data from regions such as Europe and North America are currently used overwhelmingly for large-scale biodiversity assessments due to lesser availability of suitable data from other, more biodiversity-rich, regions. These data-poor regions are often those experiencing the strongest threats to biodiversity, however. There is therefore an urgent need to fill the existing gaps in global biodiversity monitoring. Here, we review current knowledge on best practice in capacity building for biodiversity monitoring and provide an overview of existing means to improve biodiversity data collection considering the different types of biodiversity monitoring data. Our review comprises insights from work in Africa, South America, Polar Regions and Europe; in government-funded, volunteer and citizen-based monitoring in terrestrial, freshwater and marine ecosystems. The key steps to effectively building capacity in biodiversity monitoring are: identifying monitoring questions and aims; identifying the key components, functions, and processes to monitor; identifying the most suitable monitoring methods for these elements, carrying out monitoring activities; managing the resultant data; and interpreting monitoring data. Additionally, biodiversity monitoring should use multiple approaches including extensive and intensive monitoring through volunteers and professional scientists but also harnessing new technologies. Finally, we call on the scientific community to share biodiversity monitoring data, knowledge and tools to ensure the accessibility, interoperability, and reporting of biodiversity data at a global scale.
Forest ecosystems have been subjected to continuous dynamics between deforestation and forestation. Assessing the effects of these processes on biodiversity could be essential for conservation ...planning. We analyzed patterns of species richness, diversity and evenness of plants and birds in patches of natural forest of
Quercus spp. and in stands of native
Pinus pinaster and exotic
Eucalyptus globulus in NW Portugal. We analyzed data of forest and non-forest species separately, at the intra-patch, patch and inter-patch scales. Forest plant richness, diversity and evenness were higher in oak forest than in pine and eucalypt plantations. In total, 52 species of forest plants were observed in oak forest, 33 in pine plantation and 28 in eucalypt plantation. Some forest species, such as
Euphorbia dulcis,
Omphalodes nitida and
Eryngium juresianum, were exclusively or mostly observed in oak forest. Forest bird richness and diversity were higher in both oak and pine forests than in eucalypt forest; evenness did not differ among forests. In total, 16 species of forest birds were observed in oak forest, 18 in pine forest and 11 in eucalypt forest. Species such as
Certhia brachydactyla,
Sitta europaea and
Dendrocopos major were common in oak and/or pine patches but were absent from eucalypt stands. Species-area relationships of forest plants and forest birds in oak patches had consistently a higher slope, at both the intra and inter-patch scales, than species-area relationships of forest species in plantations and non-forest species in oak forest. These findings demonstrate the importance of oak forest for the conservation of forest species diversity, pointing the need to conserve large areas of oak forest due to the apparent vulnerability of forest species to area loss. Additionally, diversity patterns in pine forest were intermediate between oak forest and eucalypt forest, suggesting that forest species patterns may be affected by forest naturalness.
Current trajectories of global change may lead to regime shifts at regional scales, driving coupled human–environment systems to highly degraded states in terms of biodiversity, ecosystem services, ...and human well-being. For business-as-usual socioeconomic development pathways, regime shifts are projected to occur within the next several decades, to be difficult to reverse, and to have regional- to global-scale impacts on human society. We provide an overview of ecosystem, socioeconomic, and biophysical mechanisms mediating regime shifts and illustrate how these interact at regional scales by aggregation, synergy, and spreading processes. We give detailed examples of interactions for terrestrial ecosystems of central South America and for marine and coastal ecosystems of Southeast Asia. This analysis suggests that degradation of biodiversity and ecosystem services over the twenty-first century could be far greater than was previously predicted. We identify key policy and management opportunities at regional to global scales to avoid these shifts.
Celotno besedilo
Dostopno za:
BFBNIB, DOBA, IZUM, KILJ, NMLJ, NUK, PILJ, PNG, SAZU, SIK, UILJ, UKNU, UL, UM, UPUK
Aim
Biodiversity hotspots are widely used as conservation priorities to preserve the tree of life. However, many conservation practices identify biodiversity hotspots without considering phylogenetic ...diversity (PD), which reflects total evolutionary history and feature diversity of a region. Moreover, conservation planning rarely distinguishes between neo‐ and palaeo‐biodiversity hotspots despite their differences. Here, we (a) estimated large‐scale patterns in PD of woody plants, (b) identified neo‐ and palaeo‐biodiversity hotspots and (c) demonstrated their implication in conservation planning, with special focus on Hengduan Mountains and southern China.
Location
China.
Methods
Distributions of 11,405 woody species from the Atlas of Woody Plants in China were updated and were transformed into a grid of 50 × 50 km2. By integrating distribution maps with a genus‐level phylogeny of angiosperms, we estimated Faith's PD of each grid cell and evaluated the contribution of species relatedness to PD at given levels of species diversity (i.e. standardized PD, sPD) using regressions and three null models. Then, we identified areas with significantly lower or higher sPD than expected as neo‐ and palaeo‐hotspots and estimated the coverage of protected areas in these regions.
Results
Species diversity and PD decreased towards the north. Southern China had high species diversity, PD and sPD, while Hengduan Mountains had high species diversity and PD but low sPD. The coverage of protected areas in southern China was less than half of that in Hengduan Mountains and entire China.
Main conclusions
Our results identified Hengduan Mountains as a neo‐hotspot and southern China as a palaeo‐hotspot, highlighting their importance for biodiversity conservation. Compared to Hengduan Mountains, southern China has low coverage of protected areas, which calls for more conservation attention. Our study demonstrates a way of incorporating the phylogenetic component in the identification of neo‐ and palaeo‐hotspots, and hence of achieving a more complete perception of biodiversity patterns for conserving the tree of life.
Essential Biodiversity Variables (EBVs) consolidate information from varied biodiversity observation sources. Here we demonstrate the links between data sources, EBVs and indicators and discuss how ...different sources of biodiversity observations can be harnessed to inform EBVs. We classify sources of primary observations into four types: extensive and intensive monitoring schemes, ecological field studies and satellite remote sensing. We characterize their geographic, taxonomic and temporal coverage. Ecological field studies and intensive monitoring schemes inform a wide range of EBVs, but the former tend to deliver short-term data, while the geographic coverage of the latter is limited. In contrast, extensive monitoring schemes mostly inform the population abundance EBV, but deliver long-term data across an extensive network of sites. Satellite remote sensing is particularly suited to providing information on ecosystem function and structure EBVs. Biases behind data sources may affect the representativeness of global biodiversity datasets. To improve them, researchers must assess data sources and then develop strategies to compensate for identified gaps. We draw on the population abundance dataset informing the Living Planet Index (LPI) to illustrate the effects of data sources on EBV representativeness. We find that long-term monitoring schemes informing the LPI are still scarce outside of Europe and North America and that ecological field studies play a key role in covering that gap. Achieving representative EBV datasets will depend both on the ability to integrate available data, through data harmonization and modeling efforts, and on the establishment of new monitoring programs to address critical data gaps.
•Terrestrial biodiversity observations can be organized into four types.•These types differ in taxonomic, geographic, and temporal coverage.•The representativeness of EBV datasets is affected by the underlying types of data.•Global datasets of population abundance are affected by the lack of long-term data.•New monitoring programs must address critical data gaps.
Aim
Plants vary in their hydrological and climatic niches. How these niche dimensions covary among closely related species can help identify co‐adaptations to hydrological and climatic factors, as ...well as predict biodiversity responses to environmental change.
Location
Western United States.
Methods
Relationships between riparian dependence and climate niches of willows (Salix L.) were assessed, incorporating phylogenetics and functional traits to understand the adaptive nature of those relationships. The riparian dependence niche was estimated as the mean distance between georeferenced occurrence records and the nearest stream based on the National Hydrography Database. Results were compared to oaks (Quercus L.), a less riparian‐dependent clade, with the expectation of different niche relationships.
Results
Willows generally occurred closer to streams than expected by chance, but riparian dependence varied substantially among species. Riparian dependence was positively correlated with mean annual temperature and diurnal temperature range niche, both indicators of atmospheric demand on evapotranspiration. Phylogenetic independent contrast correlations for these relationships were significant as well, and the high degree of niche convergence among species indicated evolutionarily labile co‐adaptations to riparian dependence and atmospheric demand. Plant height increased with mean annual temperature niche, and specific leaf area increased with residual variation in height, indicating underlying morphological correlates of niche variation. Oaks, on the other hand, exhibited no relationship between atmospheric demand and riparian dependence, and weaker niche relationships with riparian dependence overall.
Main conclusions
These results support the assertion that hydric‐adapted, woody riparian plants compensate for increased atmospheric demand on transpiration with a reliable supply of water provided by riparian habitats and that this trade‐off may be unique from mesic–xeric woody plants. Conservation of warm‐adapted riparian trees and shrubs under increasing temperatures and atmospheric demand may necessitate reversal of groundwater depletion. Cool‐adapted species may be best conserved through maintenance or expansion of riparian buffers as they become more riparian obligate with warming.
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