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373 results for “herbaceous”
Data from: Nitrogen acquisition of Central European herbaceous plants that differ in their global naturalization success
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Data from: Influence of Myrmecophytic Acacia drepanolobium on the composition and growth of surrounding herbaceous vegetation
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Herbaceous vegetation responses to experimental fire in savannas and forests depend on biome and climate
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Opposing community assembly patterns for dominant and non-dominant plant species in herbaceous ecosystems globally
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Data from: Grazing herbivores reduce herbaceous biomass and fire activity across African savannas
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Plant Species Composition percent cover:Nutrient Network: A cross-site investigation of bottom-up control over herbaceous plant community dynamics and ecosystem function.
This experiment is one implementation of a globally distributed experiment, known as the Nutrient Network. At Cedar Creek, as in over 70 other sites in grasslands around the world, the experiment aims to describe impacts of increased nutrients (nitrogen, phosphorus, potassium, sulfur and other metals) and decreased herbivory (removal of mammals by fencing). Two overarching questions are being explored with these manipulations: 1. To what extent are plant production and diversity co-limited by multiple nutrients in herbaceous-dominated communities? 2. Under what conditions do grazers or fertilization control plant biomass, diversity, and composition? By utilizing identical protocols at diverse grassland sites around the world, NutNet aims to uncover both the generalities in ecosystem functioning, and the contingencies or differences which can obscure those common mechanisms. In addition to the standard NutNet protocol, e247 includes an additional low Nitrogen gradient (1 gram Nitrogen per meter squared per year and 5 grams Nitrogen per meter squared per year in addition to the standard 10 grams Nitrogen per meter squared per year).
Light Availability:Nutrient Network: A cross-site investigation of bottom-up control over herbaceous plant community dynamics and ecosystem function.
This experiment is one implementation of a globally distributed experiment, known as the Nutrient Network. At Cedar Creek, as in over 70 other sites in grasslands around the world, the experiment aims to describe impacts of increased nutrients (nitrogen, phosphorus, potassium, sulfur and other metals) and decreased herbivory (removal of mammals by fencing). Two overarching questions are being explored with these manipulations: 1. To what extent are plant production and diversity co-limited by multiple nutrients in herbaceous-dominated communities? 2. Under what conditions do grazers or fertilization control plant biomass, diversity, and composition? By utilizing identical protocols at diverse grassland sites around the world, NutNet aims to uncover both the generalities in ecosystem functioning, and the contingencies or differences which can obscure those common mechanisms. In addition to the standard NutNet protocol, e247 includes an additional low Nitrogen gradient (1 gram Nitrogen per meter squared per year and 5 grams Nitrogen per meter squared per year in addition to the standard 10 grams Nitrogen per meter squared per year).
Aboveground Standing Crop Biomass:Nutrient Network A cross-site investigation of bottom-up control over herbaceous plant community dynamics and ecosystem function
This experiment is one implementation of a globally distributed experiment, known as the Nutrient Network. At Cedar Creek, as in over 70 other sites in grasslands around the world, the experiment aims to describe impacts of increased nutrients (nitrogen, phosphorus, potassium, sulfur and other metals) and decreased herbivory (removal of mammals by fencing). Two overarching questions are being explored with these manipulations: 1. To what extent are plant production and diversity co-limited by multiple nutrients in herbaceous-dominated communities? 2. Under what conditions do grazers or fertilization control plant biomass, diversity, and composition? By utilizing identical protocols at diverse grassland sites around the world, NutNet aims to uncover both the generalities in ecosystem functioning, and the contingencies or differences which can obscure those common mechanisms. In addition to the standard NutNet protocol, e247 includes an additional low Nitrogen gradient (1 gram Nitrogen per meter squared per year and 5 grams Nitrogen per meter squared per year in addition to the standard 10 grams Nitrogen per meter squared per year).
Plant and soil organic matter responses to ten years of nutrient enrichment in the Nutrient Network:Nutrient Network. A cross-site investigation of bottom-up control over herbaceous plant community dynamics and ecosystem function
This experiment is one implementation of a globally distributed experiment, known as the Nutrient Network. At Cedar Creek, as in over 70 other sites in grasslands around the world, the experiment aims to describe impacts of increased nutrients (nitrogen, phosphorus, potassium, sulfur and other metals) and decreased herbivory (removal of mammals by fencing). Two overarching questions are being explored with these manipulations: 1. To what extent are plant production and diversity co-limited by multiple nutrients in herbaceous-dominated communities? 2. Under what conditions do grazers or fertilization control plant biomass, diversity, and composition? By utilizing identical protocols at diverse grassland sites around the world, NutNet aims to uncover both the generalities in ecosystem functioning, and the contingencies or differences which can obscure those common mechanisms. In addition to the standard NutNet protocol, e247 includes an additional low Nitrogen gradient (1 gram Nitrogen per meter squared per year and 5 grams Nitrogen per meter squared per year in addition to the standard 10 grams Nitrogen per meter squared per year).
Plant above and belowground biomass across an N fertilization gradient after 13 years of fertilization:Nutrient Network. A cross-site investigation of bottom-up control over herbaceous plant community dynamics and ecosystem function
This experiment is one implementation of a globally distributed experiment, known as the Nutrient Network. At Cedar Creek, as in over 70 other sites in grasslands around the world, the experiment aims to describe impacts of increased nutrients (nitrogen, phosphorus, potassium, sulfur and other metals) and decreased herbivory (removal of mammals by fencing). Two overarching questions are being explored with these manipulations: 1. To what extent are plant production and diversity co-limited by multiple nutrients in herbaceous-dominated communities? 2. Under what conditions do grazers or fertilization control plant biomass, diversity, and composition? By utilizing identical protocols at diverse grassland sites around the world, NutNet aims to uncover both the generalities in ecosystem functioning, and the contingencies or differences which can obscure those common mechanisms. In addition to the standard NutNet protocol, e247 includes an additional low Nitrogen gradient (1 gram Nitrogen per meter squared per year and 5 grams Nitrogen per meter squared per year in addition to the standard 10 grams Nitrogen per meter squared per year).
Net ecosystem exchange measurements throughout the 2020 growing season across an N fertilization gradient:Nutrient Network. A cross-site investigation of bottom-up control over herbaceous plant community dynamics and ecosystem function.
This experiment is one implementation of a globally distributed experiment, known as the Nutrient Network. At Cedar Creek, as in over 70 other sites in grasslands around the world, the experiment aims to describe impacts of increased nutrients (nitrogen, phosphorus, potassium, sulfur and other metals) and decreased herbivory (removal of mammals by fencing). Two overarching questions are being explored with these manipulations: 1. To what extent are plant production and diversity co-limited by multiple nutrients in herbaceous-dominated communities? 2. Under what conditions do grazers or fertilization control plant biomass, diversity, and composition? By utilizing identical protocols at diverse grassland sites around the world, NutNet aims to uncover both the generalities in ecosystem functioning, and the contingencies or differences which can obscure those common mechanisms. In addition to the standard NutNet protocol, e247 includes an additional low Nitrogen gradient (1 gram Nitrogen per meter squared per year and 5 grams Nitrogen per meter squared per year in addition to the standard 10 grams Nitrogen per meter squared per year).
Post-burn study of herbaceous understory plots at Jacobs Branch and Devils Den burn sites, 1992
Establishment and maintenance of pitch pine/hardwood ecosystems in the southern Appalachians depends on intense wildfire. These ecosystems typically have a substantial evergreen shrub component (Kalmia latifolia) which limits regeneration of future overstory species. Wildfires provide microsite conditions conducive to pine regeneration and reduce Kalmia competition. Recent droughts in the region have resulted in significant acreages of southern pine beetle killed pine/hardwood stands. Site conditions are amenable to the high intensity fires needed to regenerate pine; however, fire suppression limits the role of wildfire in these ecosystems. Research shows that pines will not regenerate in the absence of severe disturbance, such as a high intensity fire, and mixed pine/hardwood ecosystem will not be maintained. On three sites in the southern Appalachians, stands characterized by sparse overstories and dense Kalmia latifolia L. shrub layers were felled in early summer and burned in early fall. Amounts of aboveground vegetation and forest floor mass, nitrogen (N), and carbon (C) were measured before and after treatment by sampling wood, foliage, herbs, grasses, and forest floor (Oi and Oe + Oa layers). This data set constitutes the post-burn study of herbaceous understory plots at Jacobs Branch and Devil's Den burn sites, 1992.
Post-burn survey of Blazed Creek herbaceous understory plots, 1991
Recent declines in the yellow pine component of pine-hardwood stands in the southern Appalachian Mountains has prompted managers to increase the use of fire as a silviculture tool. The fell and burn treatment is designed to remove competing vegetation (hardwoods and mountain laurel [Kalmia latifolia]) to ensure successful establishment of planted eastern white pine (Pinus strobus). Two years after burning, mountain laurel had accumulated more biomass than any other species and accounted for 43% of total biomass in year 1 and 20% in year 2. By year 4, mountain laurel ranked fifth (8.9% of total) in total biomass among hardwood species behind Allegheny serviceberry (Amalanchier arborea, 14.3%), chestnut oak (Quercus prinus, 13.7%), red maple (Acer rubrum, 12.4%), and scarlet oak (Q. coccinea, 9.3%). Across sites, woody species richness ranged from 19-24 in year 1 and 14-22 in year 4. Species richness varied across sites and years, and there were substantial changes in the distribution of biomass among species. The introduction of fire allowed the once dominant pitch pine (P. rigida) to successfully reestablish. On sites, pine accounted for 25% of pretreatment stem density, but <1% and 2% in the first and fourth growing seasons after burning, respectively. However, in year 1, pines had increased in density 20-fold compared to pretreatment levels, and by year 4, had maintained a 17-fold increase compared to pretreatment. The use of fire in forest management has been the subject of considerable criticism. In light of current public concerns over the loss of critical or unique habitats, fire may gain public support for use as a restoration tool.
Post-burn study of herbaceous understory plots at Jacobs Creek and Devils Den burn sites, 1990
Recent declines in the yellow pine component of pine-hardwood stands in the southern Appalachian Mountains has prompted managers to increase the use of fire as a silviculture tool. The fell and burn treatment is designed to remove competing vegetation (hardwoods and mountain laurel [Kalmia latifolia]) to ensure successful establishment of planted eastern white pine (Pinus strobus). Two years after burning, mountain laurel had accumulated more biomass than any other species and accounted for 43% of total biomass in year 1 and 20% in year 2. By year 4, mountain laurel ranked fifth (8.9% of total) in total biomass among hardwood species behind Allegheny serviceberry (Amalanchier arborea, 14.3%), chestnut oak (Quercus prinus, 13.7%), red maple (Acer rubrum, 12.4%), and scarlet oak (Q. coccinea, 9.3%). Across sites, woody species richness ranged from 19-24 in year 1 and 14-22 in year 4. Species richness varied across sites and years, and there were substantial changes in the distribution of biomass among species. The introduction of fire allowed the once dominant pitch pine (P. rigida) to successfully reestablish. On sites, pine accounted for 25% of pretreatment stem density, but <1% and 2% in the first and fourth growing seasons after burning, respectively. However; in year 1, pines had increased in density 20-fold compared to pretreatment levels, and by year 4, had maintained a 17-fold increase compared to pretreatment. The use of fire in forest management has been the subject of considerable criticism. In light of current public concerns over the loss of critical or unique habitats, fire may gain public support for use as a restoration tool.
Mating compatibility and fertility studies in an herbaceous perennial undergoing de novo domestication
<p>De novo domestication has received recent attention because of the potential to produce new crop species with niche agroecosystem functions and useful products for climate-resilient agricultural systems of the future. However, there are often deficiencies in wild species that make them difficult to domesticate, including a mating system that is incompatible with preferred plant breeding methods and the lack of standing variation for certain traits requiring improvement. We evaluated a continuum of mating from self-pollination to interspecific hybridization in <em>Silphium integrifolium</em> and <em>S. perfoliatum</em> to determine the extent of possible gene flow between the species, and the potential for fixation of favorable domestication genes by self-pollination. Our results indicate that interspecific hybrids can be developed, potentially facilitating movement of traits from one species to another. Further, self-pollination is also possible in both species and their interspecific hybrids, but the rate is variable based on genotype. This has profound implications for using standard plant breeding and plant genetic methods in the study and improvement of these species.</p>
Data from: Savannas after afforestation: assessment of herbaceous community responses to wildfire versus native tree planting
<p>Afforestation and fire exclusion are pervasive threats to tropical savannas. In Brazil, laws limiting prescribed burning hinder the study of fire in the restoration of Cerrado plant communities. We took advantage of a 2017 wildfire to evaluate the potential for tree cutting and fire to promote the passive restoration of savanna herbaceous plant communities after destruction by exotic tree plantations. We sampled a burned pine plantation (Burned Plantation); a former plantation that was harvested and burned (Harvested & Burned); an unburned former plantation that was harvested, planted with native trees, and treated with herbicide to control invasive grasses (Native Tree Planting); and two old-growth savannas which served as reference communities. Our results confirm that herbaceous plant communities on post-afforestation sites are very different from old-growth savannas. Among post-afforestation sites, Harvested & Burned herbaceous communities were modestly more similar in composition to old-growth savannas, had slightly higher richness of savanna plants (3.8 species per 50-m2), and supported the greatest cover of native herbaceous plants (56%). These positive trends in herbaceous community recovery would be missed in assessments of tree cover: whereas canopy cover in the Harvested & Burned site was 6% (less than typical of savannas of the Cerrado), the Burned Plantation and Native Tree Planting, supported 34% and 19% cover, respectively. By focusing on savanna herbaceous plants, these results highlight that tree cutting and fire, not simply tree planting and fire exclusion, should receive greater attention in efforts to restore savannas of the Cerrado.</p>
Data from: Foundation species promote local adaptation and fine-scale distribution of herbaceous plants
<p><span><span><span>1) Interactions among neighbors can alter demography and traits of commingled species via adaptation or plasticity in phenotypic expression and understanding these two mechanisms in diverse communities is important for determining the ecological and evolutionary consequences of plant–plant interactions. </span></span></span></p> <p><span><span><span>2) We reciprocally transplanted perennial species (<i>Arenaria armerina</i> and <i>Festuca indigesta</i>) among patches of two foundation shrub species and open ground to assess whether origin microsite (defined as the spatially distinct abiotic and biotic conditions associated with the two shrubs and open ground) determines germination, recruitment and growth that, in turn, promotes fine-scale distribution of species among microsites. In addition, we tested the effect of origin microsite on traits, competitive ability, drought tolerance and outlier loci to assess whether origin microsite conditions drove differences in traits, strategies and adaptive loci.</span></span></span></p> <p><span><span><span>3) Germination was consistently greater for seeds planted back into their origin microsite relative to seeds sourced from foreign microsites, although this effect was weakened for recruitment. Plant growth was best in open sites regardless of origin microsite. In the greenhouse, <i>A.</i> <i>armerina</i> had conserved traits within origin microsite but distinct trait values among microsite conditions, specifically for plants originating from the most productive microsite (e.g. sufficient light and high nutrients and water availability). <i>Festuca indigesta</i> had conserved trait responses among microsites while within microsite, individuals had significant trait plasticity to different environmental conditions. The combined field and greenhouse results suggest that fine-scale distributions are supported by local adaptation among microsites of <i>A.</i> <i>armerina </i>and phenotypic plasticity of <i>F.</i> <i>indigesta</i>.</span></span></span></p> <p><span><span><span><i>Synthesis </i>Adaptation or plasticity in phenotypic expression have different implications for demographic rate and persistence of species in changing environments. Local adaptation to neighbors suggests that reductions in foundation species diversity could concomitantly lead to reduced genetic diversity of commingled species while a plastic response indicates a more robust and broad response to changing climatic and biotic conditions.</span></span></span></p>
Optimal resource allocation and prolonged dormancy strategies in herbaceous plants
<p>1. Understanding the fitness consequences of different life histories is critical for explaining their diversity and for predicting effects of changing environmental conditions. However, current theory on plant life histories relies on phenomenological, rather than mechanistic, models of resource production.</p> <p>2. We combined a well-supported mechanistic model of ontogenetic growth that incorporates differences in the size-dependent scaling of gross resource production and maintenance costs with a dynamic optimization model to predict schedules of reproduction and prolonged dormancy (plants staying below ground for ≥ 1 growing season) that maximize lifetime offspring production.</p> <p>3. Our model makes three novel predictions: First, maintenance costs strongly influence the conditions under which a monocarpic or polycarpic life history evolves and how resources should be allocated to reproduction by polycarpic plants. Second, in contrast to previous theory, our model allows plants to compensate for low survival conditions by allocating a larger proportion of resources to storage and thereby improving overwinter survival. Incorporating this ecological mechanism in the model is critically important because without it our model never predicts significant investment into storage, which is inconsistent with empirical observations. Third, our model predicts that prolonged dormancy may evolve solely in response to resource allocation tradeoffs.</p> <p>4. Significance: Our findings reveal that maintenance costs and the effects of resource allocation on survival are primary determinants of the fitness consequences of different life history strategies, yet previous theory on plant life history evolution has largely ignored these factors. Our findings also validate recent arguments that prolonged dormancy may be an optimal response to costs of sprouting. These findings have broad implications for understanding patterns of plant life history variation and predicting plant responses to changing environments.</p>
The timing of leaf senescence relates to flowering phenology and functional traits in 17 herbaceous species along elevational gradients
1. Leaf senescence is a major event in a plant's life history as autumn marks the end of the growing season. The optimal timing of leaf senescence is crucial to both, minimize risks of low temperature events and maximize carbon gain during the growing season. As abiotic conditions are currently changing at unprecedented rates, it is important to study how leaf senescence of different species is responding to these changes in order to forecast future growing season length and carbon sequestration potentials. In contrast to flowering phenology, data on autumn events is scarce and even more so for herbaceous than for woody plants, thus more information on this phenological stage is urgently needed. 2. We studied leaf senescence of 632 populations from 17 herbaceous species located along elevational gradients. We focussed on the beginning (5% of the population senesce, LS5) and peak (50% senesce, LS50) of leaf senescence. To see whether we can predict species-specific changes, we studied the link between LS5 and LS50 and flowering phenology as well as leaf functional traits related to plant performance. We looked at first and last flowering day and flowering duration as well as the traits specific leaf area, leaf dry matter content, area based leaf nitrogen and carbon content, carbon isotope discrimination (Δ13C), and the stomatal pore area index. 3. We found species-specific slopes of the beginning of leaf senescence along the elevational gradient. The peak of leaf senescence was uniformly delayed with increasing elevation across all species. Flowering phenology as well as leaf functional traits had a close relationship with leaf senescence and thus can be used to forecast species-specific responses to changes in abiotic conditions. High SLA and high leaf nitrogen were related to earlier senescence while high LDMC, high Δ13C and high SPI to later senescence. 4. Synthesis: The link between senescence, flowering phenology and plant functional traits will help to fine-tune predictions of future growing season length and ecosystem function. To date, most analyses are based on spring phenology and traits, for which data is more abundant than data on autumn senescence.
Data from: A multilayer network in an herbaceous tropical community reveals multiple roles of floral visitors
<p>Flower visitation does not necessarily mean pollination. In this sense, floral visitors can either act as mutualists (pollinators) or antagonists (floral robbers/thieves), indicating that these interactions are part of a continuum and that a visitor species can present multiple behaviours. We included both mutualistic and antagonistic interactions between plants and floral visitors in a multilayer network to explore the consequences (at the community level) of the dual roles played by flower visitors. The multilayer network of interactions was formed by herbaceous plants (12 species) and insects that visited their flowers (21 species) in an area of Atlantic Forest in Brazil from Jul 2015 to May 2016. The two layers presented similar structures, with high overlap between them. Similar to what was expected, the antagonistic layer was more modular and specialized than the mutualistic layer. Some visitor species exhibited highly central, dual roles, acting as both antagonists and mutualists. Most behaved consistently as mutualists in all their visits, especially bees, which formed a predominantly mutualistic group. Butterflies represented a mixed group in relation to their visits and flies made more antagonistic visits. This research represents an important step towards understanding the role of mutualisms and antagonisms in the structure of interaction networks between herbaceous plants and floral visitors in tropical environments.</p>
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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
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.