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37 results for “size class”
FIGURES 53–58. Representative valves from size class 2 in Climate-related morphological changes in Pantocsekiella (Mediophyceae) spanning 0-1.2 Ma in the Lake El'gygytgyn, northeastern Russia including Pantocsekiella elgygytgynensis sp. nov.
FIGURES 53–58. Representative valves from size class 2 (5–10 µm) and size class 3 (10–15 µm). Fig. 53) size class 2 external valve from 1.029 Ma (DC1600)showing flat valve face and large central area with many fovi, Fig. 54) size class 2 external valve 1126 ka (DC1750) with dissolution, Fig. 55) size class 3 external valve from 1.3 ka (LZ31) showing four depressions with small central area, Fig. 56) size class 3 external valve 70.2 ka (LZ688) showing five depressions, Fig. 57) size class 3 external valve 198.2 ka (LZ9-155) with flat valve face, granules, and scattered central fultoportulae, Fig. 58) size class 3 internal valve 214.2 ka (LZ10-65) showing scattered central fultoportulae.
FIGURES 47–52. Representative external valves from size class 2 in Climate-related morphological changes in Pantocsekiella (Mediophyceae) spanning 0-1.2 Ma in the Lake El'gygytgyn, northeastern Russia including Pantocsekiella elgygytgynensis sp. nov.
FIGURES 47–52. Representative external valves from size class 2 (5–10 µm). Fig. 47) Valve from 0.075 ka (LZ23) showing one central fultoportula (cf) and flat valve face with four depressions, Fig. 48) Valve from 29.12 ka (LZ491) showing flat valve face with three depressions, Fig. 49) Valve from 190.5 ka (LZ9-138) showing flat valve face with numerous fovi, Fig. 50) Valve from 198.2 ka (LZ9-155) showing flat valve face with five scattered central fultoportulae (cf), Fig 51) Valve of P. elgygytgynensis from 238.5 ka (LZ10-227), Fig. 52) Valve of P. elgygytgynensis from 417.4 ka (DC570) with white circles highlighting the clusters of central fultoportulae within the large depressions.
FIGURES 59–64. Representative valves from size class 3 in Climate-related morphological changes in Pantocsekiella (Mediophyceae) spanning 0-1.2 Ma in the Lake El'gygytgyn, northeastern Russia including Pantocsekiella elgygytgynensis sp. nov.
FIGURES 59–64. Representative valves from size class 3 (10–15 µm). Fig. 59) external valve of P. elgygytgynensis from 278.8 ka (LZ11- 125), Fig. 60) external valve of P. elgygytgynensis from 333.2 ka (LZ12-176), Fig. 61) external valve of P. elgygytgynensis from 484.1 ka (DC680), Fig. 62) external valve of P. elgygytgynensis from 406.7 ka (DC550), Fig. 63) internal valve of P. elgygytgynensis from 406.7 ka (DC550), Fig. 64) internal valve of P. elgygytgynensis from 302.5 ka (LZ12-54).
FIGURES 41–46. Representative external valves from size class 1 in Climate-related morphological changes in Pantocsekiella (Mediophyceae) spanning 0-1.2 Ma in the Lake El'gygytgyn, northeastern Russia including Pantocsekiella elgygytgynensis sp. nov.
FIGURES 41–46. Representative external valves from size class 1 (3–5 µm). Fig. 41) Valve from 1.029 Ma (DC1600) showing numerous fovi and two central fultoportulae (cf), Fig. 42) Valve from 952.6 ka (DC1480) showing the rimoportula placement, Fig. 43) Valve of P. elgygytgynensis from 406.7 ka (DC550) showing the rimoportula placement,, Fig. 44) Valve of P. elgygytgynensis from 302.5 ka (LZ12- 54) showing three depressions and three central fultoportulae, Fig. 45) Valve from 119.3 ka (LZ6-60) showing less distinct depressions, and Fig. 46) Valve from 8.28 ka (LZ366) showing P. ocellata morphology.
Data from: Nonrandom, diversifying processes are disproportionately strong in the smallest size classes of a tropical forest
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Efficient use of harvest data: A size-class-structured integrated population model for exploited populations
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Annual mortality and growth index for 17 tree species across entire size classes in the Ogawa Forest Reserve, an old-growth deciduous forest, central Japan
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Data from: Shotgun mitogenomics across body size classes in a local assemblage of tropical Diptera: phylogeny, species diversity and mitochondrial abundance spectrum
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Song parameters, repertoire size and song sharing within and across age classes in the saffron finch
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Spat bag deployment location and spat abundance, size class distribution, and associated fauna for a closed area in coastal Maine, USA, from 2013 to 2018.
This data set includes data spanning 2013-2018 describing scallop spat abundance and distribution along the coast of Maine, including closed areas. In recent years, this data includes sampling around Hurricane Island, Maine. This project was initiated as part of a collaborative project, established by fishermen, to understand local larval dynamics of Placopecten magellanicus (sea scallop) and the potential effects of closing an area to scallop fishing for an extended period of time. Spat bags are deployed in the water column in Fall and retrieved in Spring. Once retrieved, the scallop spat is counted and their shell height is measured in millimeters during the months of May to August.
Fig. 2 in An external tag for fish: tagging effects in different fish size classes and its influence on growth performance and hematology of Lophiosilurus alexandri (Siluriformes: Pseudopimelodidae)
Fig. 2. Retention rate of tags for the different size classes of Lophiosilurus alexandri evaluated every 30 days for a period of 90 days. Means followed by different letters (upper- case between days and lowercase between sizes) differ significantly (p <0.05) by two-way ANOVA followed by Tukey test.
Fig. 4 in An external tag for fish: tagging effects in different fish size classes and its influence on growth performance and hematology of Lophiosilurus alexandri (Siluriformes: Pseudopimelodidae)
Fig. 4. Hematological parameters of tagged and untagged Lophiosilurus alexandri on the different days analyzed: a. Er. b. Leuk. c. TPP. d. MCV. e. Htc. Means followed by different capital letters differ significantly (p <0.05) between days by twoway ANOVA followed by Tukey test. Means with different lowercase letters differ significantly (p <0.05) between tagged and untagged fish by Student's t-test.
Fig. 3 in An external tag for fish: tagging effects in different fish size classes and its influence on growth performance and hematology of Lophiosilurus alexandri (Siluriformes: Pseudopimelodidae)
Fig. 3. Photograph of tagged Lophiosilurus alexandri. a. Large-size class animal after 90 days post-tagging. b. Small- -size class animal with wound caused after tag detachment during the experiment. Scale bar = 30 mm.
Morphometrics of taxa in the genus Sphenopsis, recorded from adult male (n = 21) and female (n = 15) study skins in the Academy of Natural Sciences of Drexel University, Philadelphia (ANSP) and Delaware Museum of Nature & Science, Greenville (DMNH) collections. Sample sizes and means (± SD) are given for each taxon, within each sex class (female, male), for the following variables: (WG) wing length, (TR) tarsometatarsus length, (TL) tail length, (BL) bill length, and (BW) bill width. All measurements in mm. in Taxonomic status of the Western Hemispingus Sphenopsis ochracea (Thraupidae) and a review of species limits in the genus Sphenopsis P. L. Sclater, 1861
Morphometrics of taxa in the genus Sphenopsis, recorded from adult male (n = 21) and female (n = 15) study skins in the Academy of Natural Sciences of Drexel University, Philadelphia (ANSP) and Delaware Museum of Nature & Science, Greenville (DMNH) collections. Sample sizes and means (± SD) are given for each taxon, within each sex class (female, male), for the following variables: (WG) wing length, (TR) tarsometatarsus length, (TL) tail length, (BL) bill length, and (BW) bill width. All measurements in mm.
Differential regulation of meristem size, morphology and organization by the ERECTA, CLAVATA and class III HD-ZIP pathways
GEO Series GSE79839. Arabidopsis thaliana. 10 samples. Type: Expression profiling by high throughput sequencing.
Fig. 1 in An external tag for fish: tagging effects in different fish size classes and its influence on growth performance and hematology of Lophiosilurus alexandri (Siluriformes: Pseudopimelodidae)
Fig. 1. Visual tag for fish described in the patent BR1020170075770.
Fish length (TL) vs. otolith length (OL) measurements of selected eleotrids and galaxiids from New Zealand; Size classes of fish otolith specimens from early Miocene Manuherikia section, Otago
<p>Supplement data 1 and 2 to: <strong>The “Gulliver” fish fauna of an early Miocene freshwater system of New Zealand; new insights from otoliths from the Bannockburn Formation</strong>, to be published in the New Zealand Journal of Geology (NZJG).</p>
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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.