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9,671 results for “Leaf”

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edi36/100

Leaf length data: Interactive Effects of Fertility and Distribution on Plant Community Diversity and Structure

There are four levels of nitrogen, corresponding to treatments A, C, F and G in E001, applied at the same time as in that experiment. For a description of fertilizer added to E052, see file fertilization details. There are four levels of soil disturbance designated 1, 2, 3 and 4. Level 1: undisturbed Level 2: 1 pass with a 7 HP Honda rear-tined rototiller with the elevator set to till to a depth of 9 inches Level 3: 2 passes or however many required to produce about 50% bare ground Level 4: 3 passes or however many required to produce 100% bare ground. This requires 3 passes in some plots but 5 or 6 in others. In addition, all woody vegetation not destroyed by tilling is cut at the base. Rototilling is applied in late April. Each fertilization treatment receives each disturbance treatment, for a total of sixteen treatments. There are four replicates of each of the sixteen treatments. In addition, the four extreme ends (lowest N, lowest disturbance; highest N, lowest disturbance, etc. ) are replicated an additional ten times. Treatments are applied in a completely randomized design. Each of the 104 plots is 5m x 5m. Measurements taken at E052 will include: 1) species abundances, 2) community biomass allocation to leaves/roots/stems/flowers, 3) above and below ground net primary production and 4) rates of nitrogen mineralization. For a list of treatments, see the treatment layouts in file trmte52. The plots in E052 are enclosed by a fence to exclude mammalian herbivores. Galvanized welded-wire hardware cloth with 6mm x 6mm openings was buried to a depth of 50cm. Additional hardware cloth extends 60cm above the ground and poultry netting extends to 2m above the ground. In 1990, ten plots of each of four treatments (N1D1, N1D4, N4D1, N4D4, where N is the level of nitrogen added and D is the disturbance treatment) were randomly selected for the competition experiment. The above and belowground effects of neighbors on transplanted grass seedlings were measured using three

openCC0Jan 2018View details →
edi36/100

Specific Leaf Area: BioCON : Biodiversity, Elevated CO2, and N Enrichment

BioCON (Biodiversity, CO2, and Nitrogen) is an ecological experiment started in 1997 at the University of Minnesota's Cedar Creek Ecosystem Science Reserve. BioCON's goal is to explore the ways in which plant communities will respond to three environmental changes that are known to be occurring on a global scale: increasing nitrogen deposition, increasing atmospheric CO2, and decreasing biodiversity. Why Biodiversity, CO2, and Nitrogen? While there are many uncertainties in global change biology, there are also some well documented facts. Some of these are: 1. The amount of carbon dioxide (CO2) in the atmosphere is rising. Since the industrial revolution, the CO2 concentration in the atmosphere has increased from approximately 275 parts per million (ppm) to about 378 ppm today. This has been largely the result of fossil fuel burning. It is expected that CO2 levels will continue to rise, and that by the year 2050 these levels will be approximately 550 ppm. CO2 is the raw material for photosynthesis and is known to affect plant growth and development. 2. The amount of nitrogen moving through terrestrial ecosystems has increased in the recent past. While natural "background" levels of nitrogen fixation have remained constant, human additions to the system through fertilizer production and fossil fuel use have increased dramatically. Nitrogen is a key nutrient for plant growth and plays a critical role in plant community structure and composition in many environments. 3. Biodiversity levels are falling. While the research and data are not as complete as they are for CO2 and nitrogen, data indicate that the number of species globally, is being reduced. Perhaps more important for ecosystem function, diversity levels on local to regional scales have fallen due to land use change, biotic invasion and many other drivers. While much is known about how each of these factors affects ecosystem functioning, many questions remain. There is also little data on how these issues affe

openCC0Jan 2018View details →
edi36/100

Photosynthesis Leaf Carbon and Nitrogen:BioCON : Biodiversity, Elevated CO2, and N Enrichment

BioCON (Biodiversity, CO2, and Nitrogen) is an ecological experiment started in 1997 at the University of Minnesota's Cedar Creek Ecosystem Science Reserve. BioCON's goal is to explore the ways in which plant communities will respond to three environmental changes that are known to be occurring on a global scale: increasing nitrogen deposition, increasing atmospheric CO2, and decreasing biodiversity. Why Biodiversity, CO2, and Nitrogen? While there are many uncertainties in global change biology, there are also some well documented facts. Some of these are: 1. The amount of carbon dioxide (CO2) in the atmosphere is rising. Since the industrial revolution, the CO2 concentration in the atmosphere has increased from approximately 275 parts per million (ppm) to about 378 ppm today. This has been largely the result of fossil fuel burning. It is expected that CO2 levels will continue to rise, and that by the year 2050 these levels will be approximately 550 ppm. CO2 is the raw material for photosynthesis and is known to affect plant growth and development. 2. The amount of nitrogen moving through terrestrial ecosystems has increased in the recent past. While natural "background" levels of nitrogen fixation have remained constant, human additions to the system through fertilizer production and fossil fuel use have increased dramatically. Nitrogen is a key nutrient for plant growth and plays a critical role in plant community structure and composition in many environments. 3. Biodiversity levels are falling. While the research and data are not as complete as they are for CO2 and nitrogen, data indicate that the number of species globally, is being reduced. Perhaps more important for ecosystem function, diversity levels on local to regional scales have fallen due to land use change, biotic invasion and many other drivers. While much is known about how each of these factors affects ecosystem functioning, many questions remain. There is also little data on how these issues affe

openCC0Jan 2018View details →
edi36/100

Leaf carbon, nitrogen and phosphorus:Natural Enemies, Plant Diversity and Plant Community Composition

The purpose of this experiment is to determine the influences of natural enemies, including plant pathogenic fungi and insect pests, influence plant community composition, productivity, and diversity over time. The experiment is being conducted in a subset of plots within the Big Biodiversity field, including monoculture, 2-species, 4-species, 8-species, 16-species, and 32-species plots. There are 5 different treatments: foliar fungicide, soil drench fungicide, foliar insecticide, the combination of all pesticides, and nontreated control. The pesticides are applied repeatedly throughout the growing season. Within the plots, community productivity, species composition, percent cover, and pest damage are being quantified over time.

openCC0Jan 2018View details →
edi36/100

Oak leaf water potential:BioCON: Biodiversity, CO2, and Nitrogen

BioCON (Biodiversity, CO2, and Nitrogen) is an ecological experiment started in 1997 at the University of Minnesota's Cedar Creek Ecosystem Science Reserve. BioCON's goal is to explore the ways in which plant communities will respond to three environmental changes that are known to be occurring on a global scale: increasing nitrogen deposition, increasing atmospheric CO2, and decreasing biodiversity. Why Biodiversity, CO2, and Nitrogen? While there are many uncertainties in global change biology, there are also some well documented facts. Some of these are: 1. The amount of carbon dioxide (CO2) in the atmosphere is rising. Since the industrial revolution, the CO2 concentration in the atmosphere has increased from approximately 275 parts per million (ppm) to about 378 ppm today. This has been largely the result of fossil fuel burning. It is expected that CO2 levels will continue to rise, and that by the year 2050 these levels will be approximately 550 ppm. CO2 is the raw material for photosynthesis and is known to affect plant growth and development. 2. The amount of nitrogen moving through terrestrial ecosystems has increased in the recent past. While natural "background" levels of nitrogen fixation have remained constant, human additions to the system through fertilizer production and fossil fuel use have increased dramatically. Nitrogen is a key nutrient for plant growth and plays a critical role in plant community structure and composition in many environments. 3. Biodiversity levels are falling. While the research and data are not as complete as they are for CO2 and nitrogen, data indicate that the number of species globally, is being reduced. Perhaps more important for ecosystem function, diversity levels on local to regional scales have fallen due to land use change, biotic invasion and many other drivers. While much is known about how each of these factors affects ecosystem functioning, many questions remain. There is also little data on how these issues affe

openCC0Jan 2018View details →
edi36/100

FAB 1 Leaf Herbivory:FAB 1 : Forests and Biodiversity Experiment - High density diversity

A forest biodiversity experiment (FAB) focused on trees of our region investigates the consequences of multiple dimensions of tree diversity for soil, food webs, plant communities and ecosystems. FAB is designed to unravel effects of three forms of biological diversity: species richness (SR), functional diversity (FD), and phylogenetic diversity (PD). We define FD as the representation of multiple traits of leaves, roots, seeds, and the whole organism that are correlated with species positions along gradients of resource supply, growth, and decomposition. PD is the representation of evolutionary lineages measured as the genetic distances between species. While PD and FD are often correlated, convergent evolution and adaptive differentiation can decouple them. When functional traits that drive specific ecosystem functions are not phylogenetically conserved, PD and FD may give contrasting predictions. SR, PD, and FD are not independent, and we posit that PD may help explain SR effects, and FD may help explain both PD and SR effects. Thus FAB is designed to examine the separate and combined effects of all three components of diversity for multiple ecosystem functions and to distinguish between ???sampling??? and ???complementarity??? effects of biodiversity. Due to the long lag between planting tree seedlings and determining effects of tree composition and diversity on ecosystem functioning, fewer experiments have been established to elucidate the role of biodiversity in the functioning of forest ecosystems than grassland experiments. FAB will contribute to this gap and is a member of the IDENT and TreeDiv network of forest biodiversity experiments (www.treedivnet.ugent.be). Hypotheses: 1. PD, FD, and SR will all contribute to increased productivity, stability, and diversity of other trophic levels (herbivores, predators, parasitoids, soil microbes, soil flora and fauna) as well as to greater soil C sequestration. 2. Because PD incorporates both the number of species a

openCC0Nov 2018View details →
edi36/100

Tilia americana leaf senescence phenology:FAB 1 : Forests and Biodiversity Experiment - High density diversity

A forest biodiversity experiment (FAB) focused on trees of our region investigates the consequences of multiple dimensions of tree diversity for soil, food webs, plant communities and ecosystems. FAB is designed to unravel effects of three forms of biological diversity: species richness (SR), functional diversity (FD), and phylogenetic diversity (PD). We define FD as the representation of multiple traits of leaves, roots, seeds, and the whole organism that are correlated with species positions along gradients of resource supply, growth, and decomposition. PD is the representation of evolutionary lineages measured as the genetic distances between species. While PD and FD are often correlated, convergent evolution and adaptive differentiation can decouple them. When functional traits that drive specific ecosystem functions are not phylogenetically conserved, PD and FD may give contrasting predictions. SR, PD, and FD are not independent, and we posit that PD may help explain SR effects, and FD may help explain both PD and SR effects. Thus FAB is designed to examine the separate and combined effects of all three components of diversity for multiple ecosystem functions and to distinguish between ???sampling??? and ???complementarity??? effects of biodiversity. Due to the long lag between planting tree seedlings and determining effects of tree composition and diversity on ecosystem functioning, fewer experiments have been established to elucidate the role of biodiversity in the functioning of forest ecosystems than grassland experiments. FAB will contribute to this gap and is a member of the IDENT and TreeDiv network of forest biodiversity experiments (www.treedivnet.ugent.be). Hypotheses: 1. PD, FD, and SR will all contribute to increased productivity, stability, and diversity of other trophic levels (herbivores, predators, parasitoids, soil microbes, soil flora and fauna) as well as to greater soil C sequestration. 2. Because PD incorporates both the number of species a

openCC0Feb 2021View details →
edi36/100

TeRaCON Leaf Gas Exchange:E141 - BioCON: Biodiversity, CO2, and Nitrogen

BioCON (Biodiversity, CO2, and Nitrogen) is an ecological experiment started in 1997 at the University of Minnesota's Cedar Creek Ecosystem Science Reserve. BioCON's goal is to explore the ways in which plant communities will respond to three environmental changes that are known to be occurring on a global scale: increasing nitrogen deposition, increasing atmospheric CO2, and decreasing biodiversity. Why Biodiversity, CO2, and Nitrogen? While there are many uncertainties in global change biology, there are also some well documented facts. Some of these are: 1. The amount of carbon dioxide (CO2) in the atmosphere is rising. Since the industrial revolution, the CO2 concentration in the atmosphere has increased from approximately 275 parts per million (ppm) to about 378 ppm today. This has been largely the result of fossil fuel burning. It is expected that CO2 levels will continue to rise, and that by the year 2050 these levels will be approximately 550 ppm. CO2 is the raw material for photosynthesis and is known to affect plant growth and development. 2. The amount of nitrogen moving through terrestrial ecosystems has increased in the recent past. While natural "background" levels of nitrogen fixation have remained constant, human additions to the system through fertilizer production and fossil fuel use have increased dramatically. Nitrogen is a key nutrient for plant growth and plays a critical role in plant community structure and composition in many environments. 3. Biodiversity levels are falling. While the research and data are not as complete as they are for CO2 and nitrogen, data indicate that the number of species globally, is being reduced. Perhaps more important for ecosystem function, diversity levels on local to regional scales have fallen due to land use change, biotic invasion and many other drivers. While much is known about how each of these factors affects ecosystem functioning, many questions remain. There is also little data on how these issues affe

openCC0Mar 2021View details →
edi36/100

SGS-LTER CO2 Elevation Study: Leaf water potential, measured with a pressure chamber, from the Open Top Chamber experiment on the Central Plains Experimental Range, Nunn, Colorado, USA 1997 - 2001

This data package was produced by researchers working on the Shortgrass Steppe Long Term Ecological Research (SGS-LTER) Project, administered at Colorado State University. Long-term datasets and background information (proposals, reports, photographs, etc.) on the SGS-LTER project are contained in a comprehensive project collection within the Digital Collections of Colorado (http://digitool.library.colostate.edu/R/?func=collections&collection_id=3429). The data table and associated metadata document, which is generated in Ecological Metadata Language, may be available through other repositories serving the ecological research community and represent components of the larger SGS-LTER project collection. Additional information and referenced materials can be found: http://hdl.handle.net/10217/82454. Leaf water potential of the three major grass species in ambient, elevated open-top-chambers and unchambered controls, was measured nearly weekly, from 1997-2001 using a Scholander-type pressure chamber. Water potential was improved under elevated CO2, very consistently and in all species. This research was conducted at the Central Plains Experimental Range, near Nunn, CO; lat.40degrees 40 minutes N; long. 104 degrees 45 minutes W in the shortgrass steppe region of NE Colorado, USA and as a collaboration between SGS-LTER and USDA-ARS researchers.

openOpenJan 2020View details →
edi36/100

Specific Leaf Area for a chronosquence of Morella cerifera shrub thickets on Hog Island, VA, 2012

Leaf area and mass for Morella cerifera leaves were measured inside and outside shrub thickets of different age (ranging from ~12 to ~50 years old) on Hog Island Virginia and Specific Leaf Area (SLA) was calculated.

openCustomJul 2012View details →
edi36/100

Spartina alterniflora leaf measurements at Site 1 in the Virginia Coast Reserve 1988-1989

Open the record for dataset details and reuse information.

openCustomDec 1996View details →
edi36/100

Spartina alterniflora leaf measurements at Site 2 in the Virginia Coast Reserve 1988-1989

Open the record for dataset details and reuse information.

openCustomDec 1996View details →
edi36/100

Spartina alterniflora leaf measurements at harvest in the Virginia Coast Reserve 1988-1989

Open the record for dataset details and reuse information.

openCustomDec 1996View details →
zenodo32/100

FIGURES 16–19 in A new genus and species of gall midge (Diptera: Cecidomyiidae) inducing leaf galls on Peking lilac, Syringa reticulata subsp. pekinensis (Oleaceae), in China

FIGURES 16–19. Infestation of Syringa reticulata subsp. pekinensis by Pekinomyia syringae. (16) females laying eggs on young leaves, note large number of orange eggs, (17) male resting on leaf, (18) leaf galls, (19) infested leaves, note large number of leaves fallen off to the ground prematurely.

opennotspecifiedFeb 2020View details →
zenodo32/100

FIGURES 1–7 in A new genus and species of gall midge (Diptera: Cecidomyiidae) inducing leaf galls on Peking lilac, Syringa reticulata subsp. pekinensis (Oleaceae), in China

FIGURES 1–7. Pekinomyia syringae. Male. (1) 3rd flagellomere, (2) fore tarsal claw with empodium, (3) palpus, (4) wing, (5) gonostylus, ventral, (6) terminalia, dorsal, (7) terminalia, ventral. Scale bars 0.1 mm in 1, 3, 5, 6; 0.05 mm in 2; 0.5 mm in 4.

opennotspecifiedFeb 2020View details →
zenodo32/100

Supplementary material 4 from: Cumming RT, Bank S, Le Tirant S, Bradler S (2020) Notes on the leaf insects of the genus Phyllium of Sumatra and Java, Indonesia, including the description of two new species with purple coxae (Phasmatodea, Phylliidae). ZooKeys 913: 89-126. https://doi.org/10.3897/zookeys.913.49044

Table S4. Measurements of Phyllium gardabagusi sp. nov., holotype female, paratype males and females

opencc-zeroFeb 2020View details →
zenodo32/100

Supplementary material 5 from: Cumming RT, Bank S, Le Tirant S, Bradler S (2020) Notes on the leaf insects of the genus Phyllium of Sumatra and Java, Indonesia, including the description of two new species with purple coxae (Phasmatodea, Phylliidae). ZooKeys 913: 89-126. https://doi.org/10.3897/zookeys.913.49044

File S1. Concatenated supermatrix of COI, 28S, and 16S sequences from the 21 specimens sampled (18 Phyllium and three outgroups)

opencc-zeroFeb 2020View details →
zenodo32/100

FIGURE 5 in Taxonomy of the leaf beetle genus Exomis Weise (Coleoptera: Chrysomelidae: Clytrini) with description of six new species from China

FIGURE 5. Exomis tanae sp. nov.: (A) male genitalia in dorsal view; (B) apex of male genitalia; (C) male genitalia in lateral view; (D) male genitalia in ventral view; (E) spermatheca; (F) ventral rectal sclerites; (G) dorsal rectal sclerites. Scales = 0.5 mm.

opennotspecifiedMar 2020View details →
zenodo32/100

FIGURE 3 in Taxonomy of the leaf beetle genus Exomis Weise (Coleoptera: Chrysomelidae: Clytrini) with description of six new species from China

FIGURE 3. Exomis pubescens sp. nov.: (A) male genitalia in dorsal view; (B) apex of male genitalia; (C) male genitalia in lateral view; (D) male genitalia in ventral view. Scales = 0.5 mm.

opennotspecifiedMar 2020View details →
zenodo32/100

FIGURE 1 in Taxonomy of the leaf beetle genus Exomis Weise (Coleoptera: Chrysomelidae: Clytrini) with description of six new species from China

FIGURE 1. Exomis deqinensis sp. nov.: (A) male genitalia in dorsal view; (B) apex of male genitalia; (C) male genitalia in lateral view; (D) male genitalia in ventral view; (E) spermatheca; (F) ventral rectal sclerites; (G) dorsal rectal sclerites. Scales = 0.5 mm.

opennotspecifiedMar 2020View details →

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allen-brain-atlas
neuroscienceopenDocumentation, web resources, and API references are available online.
Last verified 2026-04-30Open record

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behavioral-neuroscienceopenThe DataShare record exposes download links for annotations, documentation, license text, and the zipped per-snippet data directory.
Last verified 2026-04-30Open record

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dandi-nwb
electrophysiologyopenPublished Dandiset metadata and archive endpoints are available through the production DANDI API.
Last verified 2026-04-30Open record

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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.

ibl
behavioral-neuroscienceopenPublic sessions can be searched and loaded from the IBL public data server through ONE.
Last verified 2026-04-29Open record

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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.

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neuroscienceopenPublished datasets are available on demand over the internet.
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