Find research datasets worth reusing
Search datasets from major research repositories and use ShareScore to quickly assess how well each record supports discovery, access, and reuse.
11
datasets available to search
ShareScore release 0.9.0
Dataset results
11 results for “leaf length”
Eriophorum vaginatum leaf length 2015-2017 from 2014 common gardens established at Toolik Lake, Coldfoot, and Sagwon - Alaska
Data on Eriophorum vaginatum leaf length collected from common gardens established at Toolik Lake, Coldfoot, and Sagwon in 2014 with tussocks from Coldfoot, Toolik Lake, and Sagwon. Data collected during the growing seasons of 2015, 2016, and 2017
Toolik Lake 2011 common garden leaf length phenology 2015-2016 Alaska
Data on Eriophorum vaginatum leaf length collected from a common garden established at Toolik Lake in 2011 with tussocks from No Name Creek, Coldfoot, Eagle Creek, Toolik Lake, Sagwon, and Prudhoe Bay. Data collected during the growing seasons of 2015 and 2016. Results published in Parker, T. C., J. Tang, M. B. Clark, M. M. Moody, and N. Fetcher. 2017. Ecotypic differences in the phenology of the tundra species Eriophorum vaginatum reflect sites of origin. Ecology and Evolution 7: 9775-9786. doi: 10.1002/ece3.3445
Increases in vein length compensate for leaf area lost to lobing in grapevine
<p><span></span></p> <p>There is considerable variation in leaf lobing and leaf size, including among grapevines, some of the most well-studied leaves. We examined the relationship between leaf lobing and leaf size across grapevine populations which varied in extent of leaf lobing. We used homologous landmarking techniques to measure 2,632 leaves across two years in 476 unique, genetically distinct grapevines from 5 biparental crosses which vary primarily in the extent of lobing. We determined to what extent leaf area could explain variation in lobing, vein length, and vein to blade ratio. Although lobing was the primary source of variation in shape across the leaves we measured, leaf area varied only slightly as a function of lobing. Rather, leaf area increases as a function of total major vein length, total branching vein length, and decreases as a function of vein to blade ratio. These relationships are stronger for more highly lobed leaves, with the residuals for each model differing as a function of distal lobing. For a given leaf area, more highly lobed leaves have longer veins and higher vein to blade ratios, allowing them to maintain similar leaf areas despite increased lobing. These findings show how more highly lobed leaves may compensate for what would otherwise result in a reduced leaf area, allowing for increased photosynthetic capacity through similar leaf size.</p>
Fig. 2. Full length d in Low Genetic Variability In The Recovering Urban Banded Leaf Monkey Population Of Singapore
Fig. 2. Full length d- loop of Presbytis melalophos (1.08kbp) and target region of d-loop (variable site for P. femoralis is position 190). The complete mitochondrial genome of this specimen is published under Sterner et al. (2006), and the specimen is identified as P. melalophos following Groves (2001) and Brandon-Jones et al. (2004).
Increases in vein length compensate for leaf area lost to lobing in grapevine
Open the record for dataset details and reuse information.
Scaling the leaf length-times-width equation to predict total leaf area of shoots
<p><strong>Background and Aims:</strong> An individual plant consists of different-sized shoots, each of which consists of different-sized leaves. To predict plant-level physiological responses from the responses of individual leaves, modelling this within-shoot leaf size variation is necessary. Within-plant leaf trait variation has been well investigated in canopy photosynthesis models but less so in plant allometry. Therefore, integration of these two different approaches is needed.</p> <p><strong>Methods:</strong> We focused on an established leaf-level relationship that the area of an individual leaf lamina is proportional to the product of its length and width. The geometric interpretation of this equation is that different-sized leaf laminas from a single species share the same basic form. Based on this shared basic form, we synthesized a new length-times-width equation predicting total shoot leaf area from the collective dimensions of leaves that comprise a shoot. Furthermore, we showed that several previously established empirical relationships, including the allometric relationships between total shoot leaf area, maximum individual leaf length within the shoot and total leaf number of the shoot, can be unified under the same geometric argument. We tested the model predictions using five species, all of which have simple leaves, selected from diverse taxa (Magnoliids, monocots and eudicots) and from different growth forms (trees, erect herbs and rosette herbs).</p> <p><strong>Key Results:</strong> For all five species, the length-times-width equation explained within-species variation of total leaf area of a shoot with high accuracy (R2 &gt; 0.994). These strong relationships existed despite leaf dimensions scaling very differently between species. We also found good support for all derived predictions from the model (R2 &gt; 0.85).</p> <p><strong>Conclusions:</strong> Our model can be incorporated to improve previous models of allometry that do not consider within-shoot size variation of individual leaves, providing a cross-scale linkage between individual leaf-size variation and shoot-size variation.</p>
Scaling the leaf length-times-width equation to predict total leaf area of shoots
Open the record for dataset details and reuse information.
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
dataset for paper entitled "Effect of Moringa Oleifera Leaf Extract On Body Length, Malondialadehyd and Interleukin-6 Levels in Zebrafish Larvae (Danio Rerio) Induced Stunting Model with Rotenone"
<p>The dataset consist of:</p> <p>1. Appendices of tools and material used for laboratory research</p> <p>2. Certificate of ethical test </p> <p>3. Data of moringa oleifera controls</p> <p>4. Data of zebrafish growth </p>
High-resolution time series of leaf length and leaf thickness of strawberry and tomato measured in a growth chamber
<p>This dataset captures leaf thickness and leaf length of two strawberry plants and one tomato seeding. Leaf thickness measurements are only available of the strawberry plants. Additional data included light intensity data, soil water content (of one plant), relative humidity and temperature data. All sensors were read every second over a period of two weeks.</p>
Data from: Functional correlations between specific leaf area and specific root length along a regional environmental gradient in Inner Mongolia grasslands
Open the record for dataset details and reuse information.
ScienceDex guides
Understand access before you commit
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.