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At least 19 recordsLinked to original sources
USGS2005

Host diversity begets parasite diversity: Bird final hosts and trematodes in snail intermediate hosts

An unappreciated facet of biodiversity is that rich communities and high abundance may foster parasitism. For parasites that sequentially use different host species throughout complex life cycles, parasite diversity and abundance in ‘downstream’ hosts should logically increase with the diversity and abundance of ‘upstream’ hosts (which carry the preceding stages of parasites). Surprisingly, this logical assumption has little empirical support, especially regarding metazoan parasites. Few studies have attempted direct tests of this idea and most have lacked the appropriate scale of investigation. In two different studies, we used time-lapse videography to quantify birds at fine spatial scales, and then related bird communities to larval trematode communities in snail populations sampled at the same small spatial scales. Species richness, species heterogeneity and abundance of final host birds were positively correlated with species richness, species heterogeneity and abundance of trematodes in host snails. Such community-level interactions have rarely been demonstrated and have implications for community theory, epidemiological theory and ecosystem management.

Proceedings of the Royal Society B: Biological Sci↗
USGS2005

Factors affecting plant diversity during post-fire recovery and succession of mediterranean-climate shrublands in California, USA

Plant community diversity, measured as species richness, is typically highest in the early post-fire years in California shrublands. However, this generalization is overly simplistic and the present study demonstrates that diversity is determined by a complex of temporal and spatial effects. Ninety sites distributed across southern California were studied for 5 years after a series of fires. Characteristics of the disturbance event, in this case fire severity, can alter post-fire diversity, both decreasing and increasing diversity, depending on life form. Spatial variability in resource availability is an important factor explaining patterns of diversity, and there is a complex interaction between landscape features and life form. Temporal variability in resource availability affects diversity, and the diversity peak in the immediate post-fire year (or two) appears to be driven by factors different from subsequent diversity peaks. Early post-fire diversity is influenced by life-history specialization, illustrated by species that spend the bulk of their life cycle as a dormant seed bank, which is then triggered to germinate by fire. Resource fluctuations, precipitation in particular, may be associated with subsequent post-fire diversity peaks. These later peaks in diversity comprise a flora that is compositionally different from the immediate post-fire flora, and their presence may be due to mass effects from population expansion of local populations in adjacent burned areas. ?? 2005 Blackwell Publishing Ltd.

Diversity and Distributions↗
USGS2022

Multiple dimensions of functional diversity affect stream fish β-diversity

When investigating metacommunity dynamics, functional differences among species are often assumed to be as important as environmental differences between sites in determining β-diversity. However, few studies have examined the influence of functional diversity on β-diversity. We examine the relative importance of regional functional diversity partitioned by niche dimensions and environmental variation in structuring taxonomic β-diversity of stream fishes using a large dataset of stream fish assemblages (hereafter, simply β-diversity). We predicted that both functional diversity and environmental variation play a role in determining β-diversity. We tested this prediction by modelling the patterns of stream fish β-diversity as a function of environmental variation, functional diversity and γ-richness across 10,220 sites for 329 fish species using a series of conceptual path models. Environmental variation consistently affected β-diversity across all models, whereas functional diversity and γ-richness influenced β-diversity only in some models. We show that including relevant trait differences among species in path models can improve their ability to explain β-diversity, suggesting that functional traits influence β-diversity. The ability of path models to explain β-diversity varied depending on the trait grouping included in the model, demonstrating that specific path models representing different niche dimensions can improve the ability of a model to explain β-diversity. In addition, parsing traits into different niche dimensions revealed alternative patterns of functional diversity–β-diversity relationships that otherwise would have been missed. The selection of relevant traits and linked niche dimensions is critical for detecting relationships between functional diversity and β-diversity. Using traits associated with different niche dimensions allows for the identification of niche dimensions most strongly associated with species sorting and the detection of patterns missed by focusing on a single niche dimension. Determining the niche dimensions that influence β-diversity could provide insights into the processes driving biodiversity and metacommunity dynamics, improving our ability to conserve or restore aquatic communities.

Eastern United States↗
USGS2016

Mississippian coral latitudinal diversity gradients (western interior United States): Testing the limits of high resolution diversity data

Analysis of high resolution diversity data for Mississippian corals in the western interior United States yielded mild latitudinal diversity gradients despite the small geographic area covered by samples and a large influence on diversity patterns by geographic sampling intensity (sample bias). Three competing plate tectonic reconstructions were tested using the diversity patterns. Although none could be forcefully rejected, one reconstruction proved less consistent with diversity patterns than the other two and additional coral diversity data from farther north in Canada would better discriminate the two equivalent reconstructions. Despite the relatively high sampling intensity represented by the analyzed database, diversity patterns were greatly affected by sample abundance and distribution. Hence, some effort at recognizing and accounting for sample bias should be undertaken in any study of latitudinal diversity gradients. Small-scale geographic lumping of sample localities had only small effects on geographic diversity patterns. However, large-scale (e.g., regional) geographic lumping of diversity data may not yield latitudinally sensitive diversity patterns. Temporal changes in coral diversity in this region reflect changes in eustacy, local tectonism, and terrigenous sediment flux, far more than they do shifting latitude. Highest regional diversity occurred during the interval when the studied region occupied the highest latitude. Therefore, diversity data from different regions may not be comparable, in terms of latitudinal inference. Small-scale stratigraphic lumping of the data caused a nearly complete loss of the latitudinal diversity patterns apparent prior to lumping. Hence, the narrowest possible stratigraphic resolution should be maintained in analyzing latitudinal diversity gradients.

Journal of Paleontology↗
USGS2011

Genetic diversity and species diversity of stream fishes covary across a land-use gradient

Genetic diversity and species diversity are expected to covary according to area and isolation, but may not always covary with environmental heterogeneity. In this study, we examined how patterns of genetic and species diversity in stream fishes correspond to local and regional environmental conditions. To do so, we compared population size, genetic diversity and divergence in central stonerollers ( Campostoma anomalum ) to measures of species diversity and turnover in stream fish assemblages among similarly sized watersheds across an agriculture–forest land-use gradient in the Little Miami River basin (Ohio, USA). Significant correlations were found in many, but not all, pair-wise comparisons. Allelic richness and species richness were strongly correlated, for example, but diversity measures based on allele frequencies and assemblage structure were not. In-stream conditions related to agricultural land use were identified as significant predictors of genetic diversity and species diversity. Comparisons to population size indicate, however, that genetic diversity and species diversity are not necessarily independent and that variation also corresponds to watershed location and glaciation history in the drainage basin. Our findings demonstrate that genetic diversity and species diversity can covary in stream fish assemblages, and illustrate the potential importance of scaling observations to capture responses to hierarchical environmental variation. More comparisons according to life history variation could further improve understanding of conditions that give rise to parallel variation in genetic diversity and species diversity, which in turn could improve diagnosis of anthropogenic influences on aquatic ecosystems.

Ohio↗
USGS2011

Defining conservation priorities for freshwater fishes according to taxonomic, functional, and phylogenetic diversity

To date, the predominant use of systematic conservation planning has been to evaluate and conserve areas of high terrestrial biodiversity. Although studies in freshwater ecosystems have received recent attention, research has rarely considered the potential trade-offs between protecting different dimensions of biodiversity and the ecological processes that maintain diversity. We provide the first systematic prioritization for freshwaters (focusing on the highly threatened and globally distinct fish fauna of the Lower Colorado River Basin, USA) simultaneously considering scenarios of: taxonomic, functional, and phylogenetic diversity; contemporary threats to biodiversity (including interactions with nonnative species); and future climate change and human population growth. There was 75% congruence between areas of highest conservation priority for different aspects of biodiversity, suggesting that conservation efforts can concurrently achieve strong complementarity among all types of diversity. However, sizable fractions of the landscape were incongruent across conservation priorities for different diversity scenarios, underscoring the importance of considering multiple dimensions of biodiversity and highlighting catchments that contribute disproportionately to taxonomic, functional, and phylogenetic diversity in the region. Regions of projected human population growth were not concordant with conservation priorities; however, higher human population abundance will likely have indirect effects on native biodiversity by increasing demand for water. This will come in direct conflict with projected reductions in precipitation and warmer temperatures, which have substantial overlap with regions of high contemporary diversity. Native and endemic fishes in arid ecosystems are critically endangered by both current and future threats, but our results highlight the use of systematic conservation planning for the optimal allocation of limited resources that incorporates multiple and complementary conservation values describing taxonomic, functional, and phylogenetic diversity.

Ecological Applications↗
USGS2021

Genetic diversity is considered important but interpreted narrowly in country reports to the Convention on Biological Diversity: Current actions and indicators are insufficient

International agreements such as the Convention on Biological Diversity (CBD) have committed to conserve, and sustainably and equitably use, biodiversity. The CBD is a vital instrument for global conservation because it guides 195 countries and the European Union in setting priorities and allocating resources, and requires regular reporting on progress. However, the CBD and similar policy agreements have often neglected genetic diversity. This is a critical gap because genetic diversity underlies adaptation to environmental change and ecosystem resilience. Here we aim to inform future policy, monitoring, and reporting efforts focused on limiting biodiversity loss by conducting the largest yet evaluation of how Parties to the CBD report on genetic diversity. A large, globally representative sample of 114 CBD National Reports was examined to assess reported actions, progress, values and indicators related to genetic diversity. Although the importance of genetic diversity is recognized by most Parties to the CBD, genetic diversity targets mainly addressed variation within crops and livestock (a small fraction of all species). Reported actions to conserve genetic diversity primarily concerned ex situ facilities and legislation, rather than monitoring and in situ intervention. The most commonly reported status indicators are not well correlated to maintaining genetic diversity. Lastly, few reports mentioned genetic monitoring using DNA data, indigenous use and knowledge of genetic diversity, or development of strategies to conserve genetic diversity. We make several recommendations for the post-2020 CBD Biodiversity Framework, and similar efforts such as IPBES, to improve awareness, assessment, and monitoring of genetic diversity, and facilitate consistent and complete reporting in the future.

Biological Conservation↗
USGS2019

Temporal gamma-diversity meets spatial alpha-diversity in dynamically varying ecosystems

Community measures collected at a single instance or over a short temporal period rarely provide a complete accounting of biological diversity. The gap between such “snapshot” measures of diversity and actual diversity can be especially large in systems that undergo great temporal variation in environmental conditions. To adequately quantify diversity in these temporally varying ecosystems, individual measures of diversity collected throughout the range of environmental variation, i.e., temporal alpha-diversity measures, must be combined to obtain temporal gamma-diversity. Such a time-integrated gamma-diversity measure will be a much closer approximation of a site’s true alpha-diversity and provide a measure better comparable to spatial alpha-diversity measures of sites with lower temporal variation for which a single or a few “snapshot” measures may suffice. We used aquatic-macroinvertebrate community-composition data collected over a 24-year period from a complex of 16 prairie-pothole wetlands to explore the rate that taxa accumulate over time at sites with differing degrees of temporal variation. Our results show that the rate of taxa accumulation over time, i.e., the slope of the species–time relationship, is steeper for wetlands with ponds that frequently dry compared to those with more-permanent ponds. Additionally, we found that a logarithmic function better fit species accumulation data for seasonally ponded wetlands whereas a power function better fit accumulations for permanently and semi-permanently ponded wetlands. Thus, interpretations of ecological diversity measures, and conservation decisions that rely on these interpretations, can be biased if temporal variations in community composition are not adequately represented.

North Dakota↗
USGS2006

Resource availability controls fungal diversity across a plant diversity gradient

Despite decades of research, the ecological determinants of microbial diversity remain poorly understood. Here, we test two alternative hypotheses concerning the factors regulating fungal diversity in soil. The first states that higher levels of plant detritus production increase the supply of limiting resources (i.e. organic substrates) thereby increasing fungal diversity. Alternatively, greater plant diversity increases the range of organic substrates entering soil, thereby increasing the number of niches to be filled by a greater array of heterotrophic fungi. These two hypotheses were simultaneously examined in experimental plant communities consisting of one to 16 species that have been maintained for a decade. We used ribosomal intergenic spacer analysis (RISA), in combination with cloning and sequencing, to quantify fungal community composition and diversity within the experimental plant communities. We used soil microbial biomass as a temporally integrated measure of resource supply. Plant diversity was unrelated to fungal diversity, but fungal diversity was a unimodal function of resource supply. Canonical correspondence analysis (CCA) indicated that plant diversity showed a relationship to fungal community composition, although the occurrence of RISA bands and operational taxonomic units (OTUs) did not differ among the treatments. The relationship between fungal diversity and resource availability parallels similar relationships reported for grasslands, tropical forests, coral reefs, and other biotic communities, strongly suggesting that the same underlying mechanisms determine the diversity of organisms at multiple scales. ?? 2006 Blackwell Publishing Ltd/CNRS.

Ecology Letters↗
USGS1994

Paleocene floral diversities and turnover events in eastern North America and their relation to diversity models

This paper uses angiosperm pollen taxon turnover (first and last appearance) and diversity events as metrics to describe the Paleocene floral history of the eastern Gulf Coast; data are from 64 samples and 67 angiosperm pollen taxa. Angiosperm pollen diversity was very low at the beginning of the Paleocene, rose slowly and then somewhat more rapidly to a maximum for the epoch in the middle of the late Paleoceneas a result of the maximum in rate of first appearances during the late early Paleocene and earliest late Paleocene. Diversity then dropped very rapidly at or near the end of the epoch as the rate of last appearances reached its maximum, resulting in the Terminal Paleocene Extinction Event. The latest Paleocene diversity decline coincided with an increase in mean annual temperature and probably in rainfall, representing the beginning of the climatic maximum for the Tertiary which characterized the early Eocene. The increase in diversity of early Paleocene floras in the eastern Gulf Coast resulted from exploitation of unfilled ecospace originating from (1) low regional diversity following the Terminal Cretaceous Extinction Event, and (2) creation of many new niches during the Paleocene, resulting, according to megafloral evidence, from a change to a new vegetation type (multistratal tropical rainforest) brought about by an increase in rainfall. The slow rate of recovery of earliest Paleocene angiosperm diversity in the eastern Gulf Coast may be explained in part by the diversity-dependence model of Carr and Kitchell (1980). However, additional factors may have contributed to the slow recovery: (1) the adverse terminal Cretaceous climates may have extended into the early Paleocene, (2) the initial Paleocene environment of the eastern Gulf Coast may have contained relatively few niches, (3) some earliest Paleocene angiosperms, particularly trees, may have had inherently poor capabilities for rapid evolution, and (4) there was a lack of significant immigration of new taxa to the region. In contrast, the earliest Eocene angiosperm flora recovered very rapidly from the Terminal Paleocene Extinction Event, and this high recovery rate resulted to a significant degree from immigration of new taxa from Europe; thus, the shape of the earliest Eocene diversity curve supports the immigration-dependence recovery model of Barry et al. (1991). ?? 1994.

Review of Palaeobotany and Palynology↗
USGS2014

Plant diversity predicts beta but not alpha diversity of soil microbes across grasslands worldwide

Aboveground–belowground interactions exert critical controls on the composition and function of terrestrial ecosystems, yet the fundamental relationships between plant diversity and soil microbial diversity remain elusive. Theory predicts predominantly positive associations but tests within single sites have shown variable relationships, and associations between plant and microbial diversity across broad spatial scales remain largely unexplored. We compared the diversity of plant, bacterial, archaeal and fungal communities in one hundred and forty-five 1 m 2 plots across 25 temperate grassland sites from four continents. Across sites, the plant alpha diversity patterns were poorly related to those observed for any soil microbial group. However, plant beta diversity (compositional dissimilarity between sites) was significantly correlated with the beta diversity of bacterial and fungal communities, even after controlling for environmental factors. Thus, across a global range of temperate grasslands, plant diversity can predict patterns in the composition of soil microbial communities, but not patterns in alpha diversity.

Ecology Letters↗
USGS2021

Culturally diverse expert teams have yet to bring comprehensive linguistic diversity to intergovernmental ecosystem assessments

Multicultural representation is a stated goal of many global scientific assessment processes. These processes aim to mobilize a broader, more diverse knowledge base and increase legitimacy and inclusiveness of these assessment processes. Often, enhancing cultural diversity is encouraged through involvement of diverse expert teams and sources of knowledge in different languages. In this article, we examine linguistic diversity, as one representation of cultural diversity, in the eight published assessments of the Intergovernmental Science-Policy Platform on Biodiversity and Ecosystem Services (IPBES). Our results show that the IPBES assessment outputs are disproportionately filtered through English-language literature and authors from Anglophone countries. To incorporate more linguistic diversity into global ecosystem assessment processes, we present actionable steps for global science teams to recognize and incorporate non-English-language literature and contributions from non-Anglophones. Our findings highlight the need for broad-scale actions that enhance inclusivity in knowledge synthesis processes through balanced representation of different knowledge holders and sources.

One Earth↗
USGS2023

Monitoring status and trends in genetic diversity for the Convention on Biological Diversity: An ongoing assessment of genetic indicators in nine countries

Recent scientific evidence shows that genetic diversity must be maintained, managed, and monitored to protect biodiversity and nature's contributions to people. Three genetic diversity indicators, two of which do not require DNA-based assessment, have been proposed for reporting to the Convention on Biological Diversity and other conservation and policy initiatives. These indicators allow an approximation of the status and trends of genetic diversity to inform policy, using existing demographic and geographic information. Application of these indicators has been initiated and here we describe ongoing efforts in calculating these indicators with examples. We specifically describe a project underway to apply these indicators in nine countries, provide example calculations, address concerns of policy makers and implementation challenges, and describe a roadmap for further development and deployment, incorporating feedback from the broader community. We also present guidance documents and data collection tools for calculating indicators. We demonstrate that Parties can successfully and cost-effectively report these genetic diversity indicators with existing biodiversity observation data, and, in doing so, better conserve the Earth's biodiversity.

Conservation Letters↗
USGS2012

Selection indicates preference in diverse habitats: A ground-nesting bird ( Charadrius melodus ) using reservoir shoreline

Animals use proximate cues to select resources that maximize individual fitness. When animals have a diverse array of available habitats, those selected could give insights into true habitat preferences. Since the construction of the Garrison Dam on the Missouri River in North Dakota, Lake Sakakawea (SAK) has become an important breeding area for federally threatened piping plovers ( Charadrius melodus ; hereafter plovers). We used conditional logistic regression to examine nest-site selection at fine scales (1, 3, and 10 m) during summers 2006&ndash;2009 by comparing characteristics at 351 nests to those of 668 random sites within nesting territories. Plovers selected sites (1 m 2 ) that were lower than unused random sites, increasing the risk of nest inundation. Plovers selected nest sites that were flat, had little silt, and at least 1 cobble; they also selected for 3-m radius nest areas that were relatively flat and devoid of vegetation and litter. Ninety percent of nests had <38% coverage of silt and <10% slope at the site, and <15% coverage of vegetation or litter and <31% slope within the 3-m radius. Gravel was selected for at nest sites (11% median), but against in the area 10-m from the nest, suggesting plovers select for patches or strips of gravel. Although elevation is rarely evaluated in studies of ground-nesting birds, our results underscore its importance in habitat-selection studies. Relative to where plovers historically nested, habitat at SAK has more diverse topography, substrate composition, vegetation communities, and greater water-level fluctuations. Accordingly, our results provide an example of how habitat-selection results can be interpreted as habitat preferences because they are not influenced by desired habitats being scarce or absent. Further, our results will be useful for directing habitat conservation for plovers and interpreting other habitat-selection studies.

North Dakota↗
USGS2010

Diverse elevational diversity gradients in Great Smoky Mountains National Park, U.S.A.: Chapter 10

Why does the number of species vary geographically? The earliest naturalists puzzled over this question, as do many biogeographers and macroecologists today. Over the last 200-plus years, the most striking geographic pattern in species richness – the decline in species richness with increasing latitude – has received the most attention. Thanks to many recent theoretical developments, coupled with global-scale databases and satellite technology, the number of candidate mechanisms that shape the latitudinal diversity gradient has been whittled down to a manageable number.

Great Smoky Mountains National Park↗
USGS2001

Early post-fire succession in California chaparral: Changes in diversity, density, cover and biomass

For four consecutive years, following the fires in November 1993, temporal variations in species richness, cover and biomass of component plant groups in early post-fire chaparral succession were monitored on different aspects at the Stunt Ranch Santa Monica Mountains Reserve, southern California. Plant groups were categorized based on growth form, life form, ability to fix nitrogen, geographic origin and regeneration strategies. North-facing slopes exhibited higher species richness, higher species turnover rate over time and faster vegetation recovery in terms of biomass accumulation and return to pre-fire species composition. This was probably due to higher species richness and biomass of nitrogen-fixing species found on north-facing slopes in comparison to south-facing slopes. On both north- and south-facing slopes, annuals had the highest species turnover rate, followed by herbaceous perennials and shrubs. In the first four post-fire years, annual species were the largest floristic group, but herbaceous perennials and shrubs were the major contributors to community biomass. Nitrogen-fixing species and exotics contributed significantly to early post-fire community structure. Although the general trends in post-fire succession are clear in terms of temporal changes in the relative proportions of different plant groups, environmental variation and the nature of plant life histories of component species, especially dominant species, could alter such trends significantly.

Ecological Research↗
USGS2019

Oyster reefs in northern Gulf of Mexico estuaries harbor diverse fish and decapod crustacean assemblages: A meta-synthesis

Oyster reefs provide habitat for numerous fish and decapod crustacean species that mediate ecosystem functioning and support vibrant fisheries. Recent focus on the restoration of eastern oyster ( Crassostrea virginica) reefs stems from this role as a critical ecosystem engineer. Within the shallow estuaries of the northern Gulf of Mexico (nGoM), the eastern oyster is the dominant reef building organism. This study synthesizes data on fish and decapod crustacean occupancy of oyster reefs across nGoM with the goal of providing management and restoration benchmarks, something that is currently lacking for the region. Relevant data from 23 studies were identified, representing data from all five U.S. nGoM states over the last 28 years. Cumulatively, these studies documented over 120,000 individuals from 115 fish and 41 decapod crustacean species. Densities as high as 2,800 ind m −2 were reported, with individual reef assemblages composed of as many as 52 species. Small, cryptic organisms that occupy interstitial spaces within the reefs, and sampled using trays, were found at an average density of 647 and 20 ind m −2 for decapod crustaceans and fishes, respectively. Both groups of organisms were comprised, on average, of 8 species. Larger-bodied fishes captured adjacent to the reef using gill nets were found at an average density of 6 ind m −2 , which came from 23 species. Decapod crustaceans sampled with gill nets had a much lower average density, <1 ind m −2 , and only contained 2 species. On average, seines captured the greatest number of fish species ( n = 33), which were made up of both facultative residents and transients. These data provide general gear-specific benchmarks, based on values currently found in the region, to assist managers in assessing nekton occupancy of oyster reefs, and assessing trends or changes in status of oyster reef associated nekton support. More explicit reef descriptions (e.g., rugosity, height, area, adjacent habitat) would allow for more precise benchmarks as these factors are important in determining nekton assemblages, and sampling efficiency.

Alabama, Florida, Louisiana, Mississippi, Texas↗