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22,455 results for “Diversion”
FIGURE 1 Phylogenetic relationships within the genus Longidorus. Bayesian 50 in Molecular phylogenetic analysis and comparative morphology reveals the diversity and distribution of needle nematodes of the genus Longidorus (Dorylaimida: Longidoridae) from Spain
FIGURE 1 Phylogenetic relationships within the genus Longidorus. Bayesian 50% majority rule consensus tree as inferred from D2 and D3 expansion domains of 28S rRNA sequence alignment under an SYM model with invariable sites and a gamma-shaped distribution (SYM + I + G). Posterior probabilities greater than 0.70 are given for appropriate clades. Newly obtained sequences in this study are shown in bold. Scale bar = expected changes per site. ** = Branches collapsed, indicating clustered Longidorus species. For a more specific detail of collapsed clades, see supplementary fig. S1.
FIGURE 2 Phylogenetic relationships within the genus Longidorus. Bayesian 50 in Molecular phylogenetic analysis and comparative morphology reveals the diversity and distribution of needle nematodes of the genus Longidorus (Dorylaimida: Longidoridae) from Spain
FIGURE 2 Phylogenetic relationships within the genus Longidorus. Bayesian 50% majority rule consensus tree as inferred from ITS1 rRNA sequence alignment under a 3-parameter model with invariable sites and a gamma-shaped distribution (TPM3 µf + I + G). Posterior probabilities greater than 0.70 are given for appropriate clades. Newly obtained sequences in this study are shown in bold. Scale bar = expected changes per site. Downloaded from Brill.com08/29/2023 05:44:51PM via free access
Figure 5 in Species Composition, Diversity and Length Frequency of By-Catch Sharks from the Syrian Coast
Figure 5. Geographic distribution of possible nursery areas for three species (H. griseus; +, C. plumbeus; ×, M. mustelus; *, black circles; main cities) in Syrian marine waters.
Figure1 in Species Composition, Diversity and Length Frequency of By-Catch Sharks from the Syrian Coast
Figure1. Changes of diversity indices seasonally for by-catch sharks: (a); diversity index H, (b); qualitative richness factor D, (c); evenness factor
Figure 3 in Species Composition, Diversity and Length Frequency of By-Catch Sharks from the Syrian Coast
Figure 3. Size (TL) variations of abundant and common of by-catch sharks per season off Syria coast. Males (gray), females (white): (a); H. griseus,(b); H. perlo, (c); C. plumbeus, (d); M. mustelus (e); G. melastomus, (f); S. blainvillei, (g); C. granulosus, (h); C. uyato
Figure 4 in Species Composition, Diversity and Length Frequency of By-Catch Sharks from the Syrian Coast
Figure 4. Total length (TL) frequency distributions (percent of species catch) of the abundant and common bycatch sharks off Syrian coast. Males (black), females (white). Vertical lines indicate maturity size of males (sporadic) and females (continuous) following literature: (a); H. griseus,(b); H. perlo, (c); C. plumbeus, (d); M. mustelus (e); G. melastomus, (f); S. blainvillei, (g); C. granulosus, (h); C. uyato
Figure 2 in Species Composition, Diversity and Length Frequency of By-Catch Sharks from the Syrian Coast
Figure 2. Changes of caught specimens number per season; (a) H. griseus,(b); H. perlo, (c); C. plumbeus, (d); M. mustelus (e); G. melastomus, (f); S. blainvillei, (g); C. moluccensis, (h); C. granulosus
Fig. 13 in Diversity And Density Of Mollusca (Gastropoda And Bivalvia) Population In The Euphrates River At Al-Nasiriyah, Southern Iraq
Fig. 13. Dominance values of Mollusca species from July 2018 to June 2019 in the study stations at the Euphrates River.
Fig. 14 in Diversity And Density Of Mollusca (Gastropoda And Bivalvia) Population In The Euphrates River At Al-Nasiriyah, Southern Iraq
Fig. 14. Evenness values of Mollusca species from July 2018 to June 2019 in the study stations at the Euphrates River.
Fig. 1 in Diversity And Density Of Mollusca (Gastropoda And Bivalvia) Population In The Euphrates River At Al-Nasiriyah, Southern Iraq
Fig. 1. Shows the three study stations on the Euphrates River within Al-Nasiriyahcity. Yelow circle: station 1; blue circle: station 2; red cicle: station 3.
Fig. 11 in Diversity And Density Of Mollusca (Gastropoda And Bivalvia) Population In The Euphrates River At Al-Nasiriyah, Southern Iraq
Fig. 11. Shannon index values of Mollusca species from July 2018 to June 2019 in the study stations at the Euphrates River.
Fig. 12 in Diversity And Density Of Mollusca (Gastropoda And Bivalvia) Population In The Euphrates River At Al-Nasiriyah, Southern Iraq
Fig. 12. Richness values of Mollusca species from July 2018 to June 2019 in the study stations at the Euphrates River.
FIG. 1 in Epiphyllous bryophyte diversity in lowland rain forest and lowland cloud forest of French Guiana
FIG. 1. ― Species accumulation curves and estimated total number of species (*) of epiphyllous bryophytes in the understory of lowland cloud forest (LCF) and lowland rain forest (LRF) at Nouragues, French Guiana.
Maintaining habitat diversity at small scales benefits wild bees and pollination services in mountain apple orchards
<p>In 2021, we conducted our study in apple orchards in South Tyrol, an Alpine region in Italy, using pan-traps, direct observations of visitation frequency, and a pollinator exclusion experiment. We investigated the scale-dependent effects of landscape heterogeneity and other parameters on wild bee assemblages and the related pollination service they provide at five spatial scales (radius 100 – 2,000 m).</p>
Supporting dataset for manuscript "Estimating the microarthropod diversity in cropping systems by comparing ecological indices across Europe" by Bigiotti et al. 2025
<p>This dataset contains counts of mesofauna individuals classified as Biological Forms (BF). It represent the raw data used for all indices calculation in the manuscript entitled "Microarthropod communities' diversity for soil health assessment: comparing several ecological indices across Europe" by authors Gaia Bigiotti, Francesco Vitali, Stefano Mocali, Giovanni L’Abate, Eligio Malusà, Dawid Kozacki, Irena Bertoncelj, Morgane Ourry, Massimo Pugliese, Heinrich Maisel, Expedito Olimi, Maria Grazia Tommasini, Carlo Jacomini, and Lorenzo D’Avino.</p>
Fig. 20 in Taxonomic diversity of marine planktonic 'y-larvae' (Crustacea: Facetotecta) from a coral reef hotspot locality (Japan, Okinawa), with a key to y-nauplii
Fig. 20. Relative abundance of lecithotrophic y-nauplii at Sesoko Island (Okinawa, Japan) during field work in 2018 and 2019. Grey bars denote the number of lecithotrophic nauplii of each morphospecies that survived until the last naupliar stage during laboratory rearing. Blue bars show the numbers of cyprids that successfully molted from these last-stage nauplii. Images of all lecithotrophic y-naupliar morphospecies obtained during those two years are shown to the same scale.
Fig. 19 in Taxonomic diversity of marine planktonic 'y-larvae' (Crustacea: Facetotecta) from a coral reef hotspot locality (Japan, Okinawa), with a key to y-nauplii
Fig. 19. Last-stage nauplii of four different morphospecies of y-larvae (Facetotecta) from Sesoko Island (Okinawa, Japan). A–E. Y-nauplius Type AK. F–G. Y-nauplius Type AO. H. Y-nauplius Type AM. I–K. Y-nauplius Type AN. Shown either in life (A–B, H) or as slide-mounted exuviae (C–G, I–K). Abbreviations: A1 = first antenna; A2 = second antenna; Md = mandible.
Fig. 16 in Taxonomic diversity of marine planktonic 'y-larvae' (Crustacea: Facetotecta) from a coral reef hotspot locality (Japan, Okinawa), with a key to y-nauplii
Fig. 16. Last-stage nauplii of two different morphospecies of y-larvae (Facetotecta) from Sesoko Island (Okinawa, Japan). A–E. Y-nauplius Type Y. F–J. Y-nauplius Type O*. Shown either in life (A, F–G) or as slide-mounted exuviae (B–E, H–J). Abbreviations: A1 = first antenna; A2 = second antenna; Md = mandible.
Fig. 18 in Taxonomic diversity of marine planktonic 'y-larvae' (Crustacea: Facetotecta) from a coral reef hotspot locality (Japan, Okinawa), with a key to y-nauplii
Fig. 18. Last-stage nauplii of two different morphospecies of y-larvae (Facetotecta) from Sesoko Island (Okinawa, Japan). A–F. Y-nauplius Type AL. G–J. Y-nauplius Type AJ. Shown either in life (A–C, G–J) or as slide-mounted exuviae (D–F). Abbreviations: A1 = first antenna; A2 = second antenna; Md = mandible.
Fig. 17 in Taxonomic diversity of marine planktonic 'y-larvae' (Crustacea: Facetotecta) from a coral reef hotspot locality (Japan, Okinawa), with a key to y-nauplii
Fig. 17. Last-stage nauplii of three different morphospecies of y-larvae (Facetotecta) from Sesoko Island (Okinawa, Japan). A–E. Y-nauplius Type AF. F–K. Y-nauplius Type N*. L. Y-nauplius Type AP. Shown either in life (A–C, F–G) or as slide-mounted exuviae (D–E, H–L). Abbreviations: A1 = first antenna; A2 = second antenna; Md = mandible. L from Grygier et al. (2019).
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)
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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.