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320 results for “ecosystem effects”
Root biomass data: Biodiversity II: Effects of Plant Biodiversity on Population and Ecosystem Processes
Biodiversity II (E120) is designed to determine how the number of plant species affects the dynamics of ecological processes at the population, community, and ecosystem levels. By experimentally manipulating the number of species and the kinds of species, the amount of plant growth and the change from year to year, that result can be examined. Plots are large (9m x 9m actively maintained) and well-replicated, allowing responses of plant pathogens, insect herbivores, seed predators, soil parameters, invasive plant species and other variables to also be studied. Plots were seeded in May 1994 to have 1, 2, 4, 8, or 16 species, with roughly 30 replicates of each diversity level. The species composition of each plot was chosen by random draw from a pool of 18 grassland perennials that included four warm-season (C4) grasses, four cool-season (C3) grasses, four legumes, four non-legume forbs, and two woody species. All species occur in monoculture allowing comparison of responses of each species in monoculture to combinations of these same species. The experiment was established in 1994 by the lead investigators David Tilman, Peter Reich, Johannes Knops, and David Wedin. Experiment 120 is similar to Experiment 123, but it uses larger plots to provide a large capacity for long-term subexperiments.
Plant aboveground biomass data: Biodiversity II: Effects of Plant Biodiversity on Population and Ecosystem Processes
Biodiversity II (E120) is designed to determine how the number of plant species affects the dynamics of ecological processes at the population, community, and ecosystem levels. By experimentally manipulating the number of species and the kinds of species, the amount of plant growth and the change from year to year, that result can be examined. Plots are large (9m x 9m actively maintained) and well-replicated, allowing responses of plant pathogens, insect herbivores, seed predators, soil parameters, invasive plant species and other variables to also be studied. Plots were seeded in May 1994 to have 1, 2, 4, 8, or 16 species, with roughly 30 replicates of each diversity level. The species composition of each plot was chosen by random draw from a pool of 18 grassland perennials that included four warm-season (C4) grasses, four cool-season (C3) grasses, four legumes, four non-legume forbs, and two woody species. All species occur in monoculture allowing comparison of responses of each species in monoculture to combinations of these same species. The experiment was established in 1994 by the lead investigators David Tilman, Peter Reich, Johannes Knops, and David Wedin. Experiment 120 is similar to Experiment 123, but it uses larger plots to provide a large capacity for long-term subexperiments.
Soils Bulk Density: Biodiversity II: Effects of Plant Biodiversity on Population and Ecosystem
Biodiversity II (E120) is designed to determine how the number of plant species affects the dynamics of ecological processes at the population, community, and ecosystem levels. By experimentally manipulating the number of species and the kinds of species, the amount of plant growth and the change from year to year, that result can be examined. Plots are large (9m x 9m actively maintained) and well-replicated, allowing responses of plant pathogens, insect herbivores, seed predators, soil parameters, invasive plant species and other variables to also be studied. Plots were seeded in May 1994 to have 1, 2, 4, 8, or 16 species, with roughly 30 replicates of each diversity level. The species composition of each plot was chosen by random draw from a pool of 18 grassland perennials that included four warm-season (C4) grasses, four cool-season (C3) grasses, four legumes, four non-legume forbs, and two woody species. All species occur in monoculture allowing comparison of responses of each species in monoculture to combinations of these same species. The experiment was established in 1994 by the lead investigators David Tilman, Peter Reich, Johannes Knops, and David Wedin. Experiment 120 is similar to Experiment 123, but it uses larger plots to provide a large capacity for long-term subexperiments.
Soils Organic Matter: Biodiversity II: Effects of Plant Biodiversity on Population and Ecosystem
Biodiversity II (E120) is designed to determine how the number of plant species affects the dynamics of ecological processes at the population, community, and ecosystem levels. By experimentally manipulating the number of species and the kinds of species, the amount of plant growth and the change from year to year, that result can be examined. Plots are large (9m x 9m actively maintained) and well-replicated, allowing responses of plant pathogens, insect herbivores, seed predators, soil parameters, invasive plant species and other variables to also be studied. Plots were seeded in May 1994 to have 1, 2, 4, 8, or 16 species, with roughly 30 replicates of each diversity level. The species composition of each plot was chosen by random draw from a pool of 18 grassland perennials that included four warm-season (C4) grasses, four cool-season (C3) grasses, four legumes, four non-legume forbs, and two woody species. All species occur in monoculture allowing comparison of responses of each species in monoculture to combinations of these same species. The experiment was established in 1994 by the lead investigators David Tilman, Peter Reich, Johannes Knops, and David Wedin. Experiment 120 is similar to Experiment 123, but it uses larger plots to provide a large capacity for long-term subexperiments.
Soils pH: Biodiversity II: Effects of Plant Biodiversity on Population and Ecosystem
Biodiversity II (E120) is designed to determine how the number of plant species affects the dynamics of ecological processes at the population, community, and ecosystem levels. By experimentally manipulating the number of species and the kinds of species, the amount of plant growth and the change from year to year, that result can be examined. Plots are large (9m x 9m actively maintained) and well-replicated, allowing responses of plant pathogens, insect herbivores, seed predators, soil parameters, invasive plant species and other variables to also be studied. Plots were seeded in May 1994 to have 1, 2, 4, 8, or 16 species, with roughly 30 replicates of each diversity level. The species composition of each plot was chosen by random draw from a pool of 18 grassland perennials that included four warm-season (C4) grasses, four cool-season (C3) grasses, four legumes, four non-legume forbs, and two woody species. All species occur in monoculture allowing comparison of responses of each species in monoculture to combinations of these same species. The experiment was established in 1994 by the lead investigators David Tilman, Peter Reich, Johannes Knops, and David Wedin. Experiment 120 is similar to Experiment 123, but it uses larger plots to provide a large capacity for long-term subexperiments.
Cover of ground lichens, bryophytes, and cyanobacteria: Biodiversity II: Effects of Plant Biodiversity on Population and Ecosystem Processes
Biodiversity II (E120) is designed to determine how the number of plant species affects the dynamics of ecological processes at the population, community, and ecosystem levels. By experimentally manipulating the number of species and the kinds of species, the amount of plant growth and the change from year to year, that result can be examined. Plots are large (9m x 9m actively maintained) and well-replicated, allowing responses of plant pathogens, insect herbivores, seed predators, soil parameters, invasive plant species and other variables to also be studied. Plots were seeded in May 1994 to have 1, 2, 4, 8, or 16 species, with roughly 30 replicates of each diversity level. The species composition of each plot was chosen by random draw from a pool of 18 grassland perennials that included four warm-season (C4) grasses, four cool-season (C3) grasses, four legumes, four non-legume forbs, and two woody species. All species occur in monoculture allowing comparison of responses of each species in monoculture to combinations of these same species. The experiment was established in 1994 by the lead investigators David Tilman, Peter Reich, Johannes Knops, and David Wedin. Experiment 120 is similar to Experiment 123, but it uses larger plots to provide a large capacity for long-term subexperiments.
Nutrient effects on a detritus-based stream ecosystem at the Coweeta Hydrologic Laboratory from 1998 to 2003
To determine the effects of nutrient enrichment in a detritus-based stream, we have continuously enriched a headwater stream with N and P for 4.5 years and quantified the response at different scales of stream structure and function: microbial, metazoan, and ecosystem. The effects of enrichment in the treatment stream (Watershed 54, WS54) were compared to conditions in the reference stream (Watershed 53, WS53) and one year of comprehensive baseline sampling was conducted in both streams prior to enrichment. Our first objective was to assess the effects of nutrient enrichment on growth and production of organisms. Our second objective was to determine the effects of nutrients on the fate of carbon resources, which were altered via increased microbial metabolism and invertebrate consumption.
PSC01 Exploring effects on stream ecosystem properties by two size classes of prairie stream cyprinids
Losses in freshwater fish diversity might produce a loss in important ecological services provided by fishes in particular habitats. An important gap in our understanding of ecosystem services by fishes is the influence of individuals from different size classes, which is predicted based on known ontogenetic shifts in habitat and diet. I used twenty experimental stream mesocosms located on Konza Prairie Biological Station (KPBS), KS, USA to assess the influence of fish size on ecosystem properties. Mesocosms included two macrohabitats: one riffle upstream from one pool filled with consistent pebble and gravel substrate. There were four experimental and one control treatment, each replicated four times (N = 20). I used two size classes of Central Stonerollers (Campostoma anomalum) and Southern Redbelly Dace (Chrosomus erythrogaster). Five ecosystem properties were assessed: algal filament length (cm), benthic chlorophyll a (µg/cm2), benthic organic matter (g/m2), macroinvertebrate biomass (g/m2), and stream metabolism (g O2/m2/day1). Size structure of fish populations affected some, but not all, ecosystem properties and these effects were dependent upon species identity. Size structure of both species had effects on algal filament lengths where stonerollers of both size classes reduced algal filaments, but only small redbelly dace kept filaments short. A better understanding of the relationship between these prairie stream minnows and their small stream habitats could be useful to both predict changes in stream properties if species are lost or size structure shifts, and to redbelly dace populations, a Species In Need of Conservation.
Data from: An effective method for ecosystem-scale manipulation of bird abundance and species richness
Manipulation experiments are a cornerstone of ecological research, but can be logistically challenging to execute – particularly when they are intended to isolate the ecological role of large, vagile species, like birds. Despite indirect evidence that birds are influential in many ecosystems, large-scale, multi-year bird manipulation experiments are rare. When these studies are conducted, they are typically realized with caged or netted exclosures, an approach that can be expensive, risky for wildlife, and difficult to maintain. In cases where caged exclosures are not appropriate, alternate approaches are needed to allow rigorous empirical studies on the ecological role of birds. Here, we present and validate a method for experimentally increasing the abundance and richness of birds at the scale of entire aquatic ecosystems. Unlike bird exclusion, this approach is experimentally tractable, appealing to land managers, and possible to deploy over large spatial scales. We tested the efficacy of our approach for increasing bird abundance and species richness at 16 central California ponds. Based on bird visitation data obtained by summer camera trapping, our approach significantly increased bird species richness and abundance at manipulated ponds compared to control ponds. Attractant treatments mitigated the negative effects of a major drought on bird species richness, and generated a near-doubling of bird abundance in the presence of attractants. Treatments had no effect on most mammal species, with the exception of ground squirrels, which increased in abundance in the presence of attractants. These results suggest that attractants are effective in increasing bird abundance and richness. We encourage researchers to consider this approach for experimentally isolating the ecological role of birds in aquatic and open terrestrial ecosystems, especially in cases where cost or logistical constraints preclude the use of caged or netted exclosures.
Mitigation of urbanisation effects on aquatic ecosystems by synchronous ecological restoration
<p>Ecosystem degradation and biodiversity loss have been caused by economic booms in developing countries over recent decades. In response, ecosystem restoration projects have been advanced in some countries but the effectiveness of different approaches and indicators at large spatio-temporal scales (i.e., whole catchments) remains poorly understood. Our datasets with a diverse array of 440 aquatic restoration projects including wastewater treatment, constructed wetlands, plant/algae salvage, and dredging of contaminated sediments implemented and maintained from 2007 to 2017 across more than 2000km2 of the northwest Taihu basin (Yixing, China). Synchronized investigations of water quality and invertebrate communities were conducted before and after restoration. Our datasets showed that even though there was rapid urbanization at this time, nutrient concentrations (NH<sub>4</sub><sup>+</sup>-N, TN, TP) and biological indices of benthic invertebrates (taxonomic richness, Shannon diversity, sensitive taxon density) improved significantly across most of the study area. Improvements were associated with the type of restoration project, with projects targeting pollution sources leading to the clearest ecosystem responses compared with those remediating pollution sinks. However, in some locations, the recovery of biotic communities appears to lag behind nutrients (e.g. nitrogen and phosphorus), likely reflecting long-distance re-colonization routes for invertebrates given the level of pre-restoration degradation of the catchment.</p>
Cumulative effects doubled the drought impacts for one-fifth of ecosystems exposed to recurrent droughts during Australia's Millennium Drought
<p><strong>Drought-induced vegetation declines have been reported across the globe and may have widespread implications for ecosystem composition, structure, and functions. Thus, it is critical to maximizing our understanding of how vegetation has responded to recent drought extremes. To date, most drought assessments have focused on the impact of a single drought event, emphasizing the importance of drought intensity for vegetation responses. However, drought timing, duration, and repeat exposure may all be important aspects of ecosystem response with the potential for non-linear effects. Cumulative effects are one such phenomenon, representing the additional decline due to repeated or prolonged exposure to drought, and indicating gradual loss of ecosystem resistance. This study quantifies the frequency and magnitude of cumulative effects among Australian ecosystems as they responded to the Millennium Drought. Three distinct biophysical variables derived from satellite remote sensing were analyzed, including fraction of photosynthetically absorbed radiation, photosynthetic vegetation cover, and canopy density derived from passive microwave data. While cumulative effects were detected in only 20% or less of the landscape exposed to repeat or long-duration drought, they approximately doubled drought impacts in the areas where they occurred. Cultivated lands and grasslands were the most susceptible to cumulative effects from recurrent droughts. Despite being relatively infrequent in forests and savannas, cumulative effects from repeated or long-duration drought caused larger additional declines in these ecosystems. Overall, our study demonstrates that the temporal sequence of drought events can strongly influence the magnitude of drought impacts, which provides important insights into modeling vegetation response to recurrent drought events</strong></p>
Data and code – Effects of climate on salmonid productivity: A global meta-analysis across freshwater ecosystems
<p>Salmonids are of immense socio-economic importance in much of the world but are threatened by climate change. This has generated a substantial literature documenting effects of climate variation on salmonid productivity in freshwater ecosystems, but there has been no global quantitative synthesis across studies. We conducted a systematic review and meta-analysis to gain quantitative insight into key factors shaping the effects of climate on salmonid productivity, ultimately collecting 1,321 correlations from 156 studies, representing 23 species across 24 countries. Fisher's Z was used as the standardized effect size, and a series of weighted mixed-effects models were compared to identify covariates that best explained variation in effects. Patterns in climate effects were complex, and were driven by spatial (latitude, elevation), temporal (time-period, age-class), and biological (range, habitat type, anadromy) variation within and among study populations. These trends were often consistent with predictions based on salmonid thermal tolerances. Namely, warming and decreased precipitation tended to reduce productivity when high temperatures challenged upper thermal limits, while opposite patterns were common when cold temperatures limited productivity. Overall, variable climate impacts on salmonids suggest that future declines in some locations may be counterbalanced by gains in others. In particular, we suggest that future warming should (1) increase salmonid productivity at high latitudes and elevations (especially >60° and >1,500m), (2) reduce productivity in populations experiencing hotter and dryer growing season conditions, (3) favor non-native over native salmonids, and (4) impact lentic populations less negatively than lotic ones. These patterns should help conservation and management organizations identify populations most vulnerable to climate change, which can then be prioritized for protective measures. Our framework enables broad inferences about future productivity that can inform decision-making under climate change for salmonids and other taxa, but more widespread, standardized, and hypothesis-driven research is needed to expand current knowledge.</p>
Fig. 3 in Diet and trophic structure of the fish fauna in a subtropical ecosystem: impoundment effects
Fig. 3. Proportion in number and biomass (CPUE) of the trophic guilds along the longitudinal gradient of the Salto Caxias Reservoir, Iguaçu River, before and after the impoundment. (1 = upstream; 2 = middle region; 3 = dam; 4 = downstream) (Alg = algivores; Det = detritivores; Her = herbivores; Ain = aquatic insectivores; Tin = terrestrial insectivores; Inv = invertivores; Omn = omnivores; Pis = piscivores; Pla = planktivores; Car = carcinophages).
Fig. 1 in Diet and trophic structure of the fish fauna in a subtropical ecosystem: impoundment effects
Fig. 1. Location of sampling sites along the longitudinal gradient of the Iguaçu River, in the area influenced by the Salto Caxias Reservoir, Paraná State. a) before the impoundment; b) after the impoundment. (site 1 = upstream; site 2 = middle region; site 3 = dam; site 4 = downstream).
Fig. 2 in Diet and trophic structure of the fish fauna in a subtropical ecosystem: impoundment effects
Fig. 2. Graphical representation of the first two axes of the Nonmetric multidimensional scaling (nNMDS), demonstrating the food resources used by the fish fauna in the different sites and phases, in the area influenced by the Salto Caxias Reservoir, Iguaçu River. FR = Food resources (AI = aquatic insects; TI = terrestrial insects; DE = decapods; MC = microcrustaceans; MA = macroinvertebrates; MI = microinvertebrates; FI = fish; FS = fish scales; AP = aquatic plants; TP = terrestrial plants; AL = algae; DS = detrit/sediment); B = before impoundment, A = after impoundment; 1 to 4 = sampling sites.
Fig. 5. Emys orbicularis habitat 3 in P R O J E C T S O N E M Y S O R B I C U L A R I S (R E P T I L I A: Testudines: Emydidae) In Latvia For Thirty Years (1984 - 2014): Biological Aspects, Results And Effect On Population And Ecosystems
Fig. 5. Emys orbicularis habitat 3 in Silene Nature Park before restoration (Google Earth service, SAS services).
Fig. 4. Emys orbicularis habitats 1 and 2 in P R O J E C T S O N E M Y S O R B I C U L A R I S (R E P T I L I A: Testudines: Emydidae) In Latvia For Thirty Years (1984 - 2014): Biological Aspects, Results And Effect On Population And Ecosystems
Fig. 4. Emys orbicularis habitats 1 and 2 in Silene Nature Park before (a) and after (b) restoration (Google Earth service, SAS services).
Fig. 2 in P R O J E C T S O N E M Y S O R B I C U L A R I S (R E P T I L I A: Testudines: Emydidae) In Latvia For Thirty Years (1984 - 2014): Biological Aspects, Results And Effect On Population And Ecosystems
Fig. 2. Old Emys orbicularis female, found in 1984 in Daugavpils living for 20 years in a zooculture (Photo: 2005).
Fig. 6. Emys orbicularis habitat 3 in P R O J E C T S O N E M Y S O R B I C U L A R I S (R E P T I L I A: Testudines: Emydidae) In Latvia For Thirty Years (1984 - 2014): Biological Aspects, Results And Effect On Population And Ecosystems
Fig. 6. Emys orbicularis habitat 3 in Silene Nature Park after restoration (Google Earth service, SAS services).
Figure 5. Sentinel 3 in Marine mucilage in the Sea of Marmara and its effects on the marine ecosystem: mass deaths
Figure 5. Sentinel 3 imagery of the chlorophyll-a concentration in the study area on April 22, 2021.
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Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.