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Litterfall on the elevational gradient (Group 6) from the Coweeta Hydrologic Laboratory from 1995 to 1996
Null Hypothesis: Litterfall weights not statistically different between plots on the altitudinal gradient.
Fall 2000 grasshopper monitoring -- mid-marsh grasshopper abundance and species diversity at GCE LTER sampling sites 1, 3, 4, 5, and 6
Grasshopper abundance and species diversity were investigated at five sampling sites within the Georgia Coastal Ecosystems (GCE) LTER study area in August 2000. Visual surveys were conducted along 10 2m by 10m transects randomly allocated within the mid-marsh zone at each site. All grasshoppers observed within each transect were counted and identified to species, if possible. This survey was conducted as part of the GCE invertebrate monitoring program, and will be performed annually to assess long-term changes in relative species abundances across the GCE study area.
Root Decomposition and root in-growth rates for GCE marsh sites 6-9 from June 2003 to June 2004
Rates of decomposition and root in-growth were measured in four tidal marshes of the Georgia coast (USA) that vary in freshwater input. Replicate nylon mesh bags containing roots of dominant plant species were buried 20cm deep in marsh sediments at stream-side levee and marsh plain locations within GCE sampling sites 6, 7, 8 and 9 in June 2003. Dry weight, carbon, nitrogen and phosphorus content, and root in-growth were measured initially and every three months to evaluate the effects of freshwater input on root decomposition and growth rates. This study was part of the GCE-LTER soil monitoring program.
Hubbard Brook Experimental Forest: Seedling bank – watershed 1 and watershed 6 (2018)
The understory layer is complex and includes groups of stems with distinctly different chances of survival and recruitment to the sapling size class. We explored how calcium amendment has impacted the trajectory of the seedling bank at Hubbard Brook Experimental Forest. The density of all tree stems in the seedling bank in 2018 (19 years after treatment) was greater in CAL (Watershed 1; calcium treatment) than REF (Waterhsed 6; reference) and beech was more abundant than sugar maple in both watersheds. In terms of relative abundance, the treatment had the opposite effects on the two species: the relative density of sugar maple was significantly greater in CAL than REF while the relative density of beech was significantly less. In terms of beech stem origin, Beech sprouts were more abundant than seedlings on both watersheds; however, beech stems of seed origin were more abundant on CAL (mean±1SE: 4.06±0.49 seedlings m-2) than REF (2.98±0.42), while sprouts were fewer (CAL: 14.4±1.30; REF: 20.5±1.47) resulting in the seedling to sprout ratio on CAL (1:3.5) being half that on REF (1:7). The influence on the seedling bank on future composition of these forests remains to be seen. These data were gathered as part of the Hubbard Brook Ecosystem Study (HBES). The HBES is a collaborative effort at the Hubbard Brook Experimental Forest, which is operated and maintained by the USDA Forest Service, Northern Research Station.
Hubbard Brook Experimental Forest: Soil Acid-Base Properties and Microbial Activity, Watershed 1 and West of Watershed 6 (2015-2016)
In summer 2015 and spring 2016, researchers collected soils from the CaSiO3-enriched watershed at Hubbard Brook (W1) and from a nearby site west of the reference watershed at Hubbard Brook (W6). These soils were sampled throughout the hardwood zone of each watershed, and the sampling scheme explicitly examined pit-and-mound microtopographic gradients. These soils were analyzed for acid-base properties, net and gross N cycling rates, microbial biomass, and C cycling rates. These data were gathered as part of the Hubbard Brook Ecosystem Study (HBES). The HBES is a collaborative effort at the Hubbard Brook Experimental Forest, which is operated and maintained by the US Forest Service, Northern Research Station.
Figure 6 in New endemic species of freshwater crayfish Parastacus Huxley, 1879 (Crustacea: Decapoda: Parastacidae) from the Atlantic forest in southern Brazil
Figure 6. Parastacus pilicarpus sp. nov., habitat and living specimens. A, B, Typical habitat, a first order stream in the municipality of Morro Grande, state of Santa Catarina; C, living specimen. Photographs by Caio R. M. Feltrin. No available information of scale in photograph C.
Figure 6 in Revision of Cataulax Spinola, with Architas Distant as a New Synonymy (Heteroptera: Pentatomidae: Discocephalini)
Figure 6. Phallus, dorsal, ventral, and lateral views respectively for each species. A-C) C. eximius Stål, 1860; D-F) C. pudens (Distant, 1889); G-I) C. subtiliterconspersus, n. sp. (bpl = basal plate, dc1 = dorsal connectives 1, dc2 = dorsal connectives 2, ds = ductus seminis distalis, me = membramblase, pc = processus capitati, ph = phallotheca, prph = processus phallothecae, prv1 = processus vesicae 1, prv2 = processus vesicae 2, pt = ponticulus transversalis, sg = second gonopore, v = vesica).
Example Eiger data with 6 virtual data sets dereferencing images
<p>Standard Eiger data set from Diamond Light Source I04, consisting of 180° of rotation data from a cubic insulin crystal, with 6 virtual data sets each corresponding to 30° of data, to illustrate how multi-trigger Eiger data sets could be structured efficiently. </p> <p> </p> <p>Virtual data sets made with </p> <p> </p> <p><a href="https://github.com/graeme-winter/NXmxtools/blob/master/vdsmaker.py">https://github.com/graeme-winter/NXmxtools/blob/master/vdsmaker.py</a></p> <p> </p> <p>Key feature is that the underlying data type (UINT16) corresponds to the virtual data set type. </p> <p> </p> <p>This will require HDF5 1.10 series to read. </p> <p> </p> <p>Files:</p> <p>insu_d200_1.nxs - NXmx formatted data with internal VDS</p> <p>insu_d200_1_000001.h5 - real data 1/2</p> <p>insu_d200_1_000002.h5 - real data 2/2</p> <p>insu_d200_1_1.nxs - VDS subset of data 1/6</p> <p>...</p> <p>insu_d200_1_6.nxs - VDS subset of data 1/6</p> <p>insu_d200_1_master.h5 - DECTRIS style master file</p> <p>insu_d200_1_meta.h5 - metadata</p> <p>insu_d200_1_meta_pack.h5 - repacked metadata (not used)</p>
FIG. 6. — Lepthyphantes imazigheni Barrientos n in The high complexity of Micronetinae Hull, 1920 (Araneae, Linyphiidae) evidenced through ten new cave-dweller species from the Morocco
FIG. 6. — Lepthyphantes imazigheni Barrientos n. sp., carapace and genital organs: A, carapace; B, C, epigyne, ventral view (B), lateral view (C). Abbreviations: see Material and methods. Scale bars: 0.5 mm.
Fig. 6 in A new species of Paralithoxus (Siluriformes: Loricariidae: Ancistrini) from the highlands of Serra da Mocidade, Roraima State, Brazilian Amazon
Fig. 6. Type-locality of Paralithoxus mocidade in Ajarani River, tributary of the Branco River basin, located immediately downstream of a large waterfall. Photo by Marcos Amend.
Fig. 6 in Revision of the Eurybrachidae (XV). The Oriental genus Purusha Distant, 1906 with two new species and a key to the genera of Eurybrachini (Hemiptera: Fulgoromorpha: Eurybrachidae)
Fig. 6. Purusha paradoxa (Gerstaecker, 1895), ♂ from Sumatra (RMNH). A. Habitus, dorsal view. B. Habitus, ventral view. C. Head and thorax, dorsal view. D. Normal view of frons. C–D not to scale.
Map of 15 Ecoclimatic Arid and Semi-Arid zones in Africa (6°S-39°N)
<p>Ecoclimatic Arid and Semi-Arid zones in Africa (6°S-39°N) based were derived from a multiway analysis of the WorldClim database (1950-2000). See details in the paper:<em> Leibovici DG,<strong> </strong>Quillevere G and Desconnets J-C (2007) A method to Classify Ecoclimatic Arid and Semi-Arid Zones in Circum-Saharan Africa Using Dynamics of Multiple Indicators. <strong>IEEE Transaction in Geoscience And Remote Sensing, 45(12), 4000-4007. </strong></em>doi:<a href="https://doi.org/10.1109/TGRS.2007.908878">10.1109/TGRS.2007.908878</a></p> <p>A follow up paper is part of the zip archive for multiscale consideration (Leibovici, D. G., & Jackson, M. (2011). Multi-scale integration for spatio-temporal ecoregioning delineation. <strong><em>International Journal of Image and Data Fusion</em>, <em>2</em>(2), 105-119</strong>. doi:<a href="https://doi.org/10.1080/19479832.2010.542893">10.1080/19479832.2010.542893</a>)</p>
Fig. 6 in Unravelling the foraging behavior of the southern stingray, Hypanus americanus (Myliobatiformes: Dasyatidae) in a Southwestern Atlantic MPA
Fig. 6. Illustrations of species-typical patterns of foraging behavior performed by Hypanus americanus in the FNA in phase 5 entitled as final phase. The sub-phases are named as (a) active take-off; (b) drift take-off; (c) rest; (d) bury. The arrow indicates the direction of the movement. The figures were drawn using original still photographs.
Fig. 6. Prochilodus costatus swimming speeds measured a in Upstream and downstream migration speed of Prochilodus costatus (Characiformes: Prochilodontidae) in upper São Francisco basin, Brazil
Fig. 6. Prochilodus costatus swimming speeds measured a. in this study in stretch 2 and b. in the laboratory by Santos et al. (2012). Central points are medians, boxes represent percentiles 25 and 75 and whiskers represent amplitude. Dashed lines separate different kinds of fish movements. BL/s = swimming velocity in standard length of fish per second.
Fig. 6 in The bony fishes (Teleostei) caught by industrial trawlers off the Brazilian North coast, with insights into its conservation
Fig. 6. Species of the order Clupeiformes, family Clupeidae, (A) Lile piquitinga MPEG 35023, 95 mm TL, family Engraulidae, (B) Anchoa filifera MPEG 35122, 31 mm TL, (C) Anchoa pectoralis not cataloged, 100 mm TL, (D) Anchovia clupeoides not cataloged, 94 mm TL, (E) Anchoviella lepidentostole MPEG 35240, 118 mm TL, family Pristigasteridae, (F) Chirocentrodon bleekerianus MPEG 35674, 108 mm TL, (G) Odontognathus mucronatus MPEG 35048, 142 mm TL, (H) Pellona harroweri MPEG 35700, 136 mm TL, ordem Siluriformes, family Ariidae, (I) Amphiarius phrygiatus MPEG 35077, 345 mm TL, (J) Notarius grandicassis MPEG 35204, 410 mm TL, (K) Sciades couma not cataloged, 423 mm TL.
Figura 6 in Revisión del género Microogenius Gutiérrez (Coleoptera: Scarabaeidae: Rutelinae: Rutelini), con descripción de dos nuevas especies altoandinas
Figura 6. Microogenius arroaei (Ohaus). a–b) Lectotipo de Lasiocala arroaei Ohaus. c) Etiquetas lectotipo. d) Macho de Microogenius arroaei (Ohaus). e–f) Aedeago, vista lateral y dorsal. g) Maxila izquierda. h) Labio y palpos labiales. i) Maxila derecha. j–k) Holotipo hembra de Eremophygus calƲus Gutiérrez (= Microogenius arroaei). l) Etiquetas holotipo
Figures 1–6 in Records of tiger beetles (Coleoptera: Cicindelidae) collected in Cambodia, with description of a new species. 149. Contribution towards the knowledge of the Cicindelidae
Figures 1–6. Cambodian tiger beetles. All scale bars = 5 mm. 1) Tricondyla (Tricondyla) macrodera abruptesculpta Horn, 1925 from Phnom Samkos. 2) Neocollyris (Neocollyris) moesta moesta (Schmidt-Goebel, 1846) from Phnom Aural. 3) Neocollyris (Pachycollyris) bipartita unicolor (Horn, 1935) from Phnom Samkos. 4) Prothyma (Genoprothyma) heteromalla (Macleay, 1825) from Be Treed. 5) Heptodonta eugenia Chaudoir, 1865 from Phnom Aural. 6) Therates laotiensis Sawada and Wiesner, 1999 from Bokor N. P.
Fig. 6. a in Use of a nursery area by cownose rays (Rhinopteridae) in southeastern Brazil
Fig. 6. a. Number of Rhinoptera bonasus and R. brasiliensis according to disc width (DW) and b. individuals <50 cm and> 50 cm in the months sampled in Bertioga, São Paulo, southeastern Brazil (November 2015 – May 2017).
Fig. 6 in Two new species of Odontostilbe historically hidden under O. microcephala (Characiformes: Cheirodontinae)
Fig. 6. Southern South America showing the distribution of Odontostilbe avanhandava (green diamonds), O. microcephala (yellow squares) and O. weitzmani (red circle). Type localities represented by star of respective colors.
Figures 1–6 in Onciderini Thomson, 1860 (Coleoptera: Cerambycidae: Lamiinae) types of the Museu de Zoologia, Universidade de São Paulo (MZSP), with a brief history of the Coleoptera collection
Figures 1–6. Six species of Onciderini. Fig. 1. Bucoides montana Martins and Galileo (a, dorsal habitus; b, labels). Fig. 2. Cacostola acuticauda Marinoni and Martins (a, dorsal habitus; b, labels). Fig. 3. Cacostola bimaculata Martins, Galileo, and Limeira-de-Oliveira (a, dorsal habitus; b, labels). Fig. 4. Cacostola carinata Martins, Galileo, and Santos-Silva (a, dorsal habitus; b, labels). Fig. 5. Cacostola colombiana Martins and Galileo (a, dorsal habitus; b, labels). Fig. 6. Cacostola exilis Martins, Galileo, and Limeira-de-Oliveira (a, dorsal habitus; b, labels).
ScienceDex guides
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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.