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567 results for “exploitation”

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Fig. 5 in Exploitation status and stock assessment of the smooth clam Callista chione (Linnaeus, 1758) in the northern Alboran Sea (GSA01-W Mediterranean Sea)

Fig. 5: Evolution of catches and CPUE for Callista chione in the northern Alboran Sea between 2001 and 2015.

opencc-by-4.0May 2018View details →
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Fig. 2 in Exploitation status and stock assessment of the smooth clam Callista chione (Linnaeus, 1758) in the northern Alboran Sea (GSA01-W Mediterranean Sea)

Fig. 2: Number and average technical characteristics (gross tonnes, length, and engine power) of artisanal vessels per landing port along the Alboran Sea.

opencc-by-4.0May 2018View details →
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Fig. 3 in Glass Buildings As Bird Feeders: Urban Birds Exploit Insects Trapped By Polarized Light Pollution

Fig. 3. Timing of foraging visits of European magpie (Pica pica) to the northern building of the Eötvös University as detected by a web camera from 17:00 h on 16 May to 20:00 h on 23 May in 2007. Arrow lengths represent the proportion of all visits made during a particular hour over the

opencc-by-4.0Aug 2010View details →
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Fig. 2 in Glass Buildings As Bird Feeders: Urban Birds Exploit Insects Trapped By Polarized Light Pollution

Fig. 2. (A) Hovering white wagtail (Motacilla alba) catching caddis flies from a window. (B) House sparrow (Passer domesticus) capturing caddis flies from a vertical glass surface. (C) Great tit (Parus major) standing on a window's edge and catching caddis flies. (D) European magpie (Pica pica) on

opencc-by-4.0Aug 2010View details →
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Fig. 1 in Glass Buildings As Bird Feeders: Urban Birds Exploit Insects Trapped By Polarized Light Pollution

Fig. 1. (A) The southern (left arrow) and northern (right arrow) building of the Faculty of Natural Sciences of the Eötvös University in Budapest seen from the river Danube. (B) Mass-swarming caddis flies (Hydropsyche pellucidula, white dots) at the vertical glass surfaces of the northern building. (C) "Well-laid table" for urban birds: caddis fly imagoes (black dots) landed on white (untinted) and black (tinted) vertical glass surfaces. (D) An adult caddis fly landed on the outside surface of a window photographed from outside. (E) A copulating caddis fly pair on the outside surface of a window

opencc-by-4.0Aug 2010View details →
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Fig. 3 in Breeding, growth and exploitation of Brachyplatystoma rousseauxii Castelnau, 1855 in the Caqueta River, Colombia

Fig. 3. Standard length (LS) frequency histograms and the corresponding von Bertalanffy growth function for a) females, b) males and c) females, males and unsexed individuals combined of Brachyplatystoma rousseauxii in the Caqueta River during the period 1995-1997.

opencc-by-4.0Sep 2013View details →
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Fig. 4 in Breeding, growth and exploitation of Brachyplatystoma rousseauxii Castelnau, 1855 in the Caqueta River, Colombia

Fig. 4. Standard length at first sexual maturity of Brachyplatystoma rousseauxii males (black dots) and females (white triangles) in the Caqueta River, Colombia.

opencc-by-4.0Sep 2013View details →
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Fig. 1 in Breeding, growth and exploitation of Brachyplatystoma rousseauxii Castelnau, 1855 in the Caqueta River, Colombia

Fig. 1. Map of the Colombian Amazon, its constitutive departments and the principal fishing zones for Brachyplatystoma rousseauxii (based on Agudelo et al., 2000; Murcia et al., 2007).

opencc-by-4.0Sep 2013View details →
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Fig. 2 in Breeding, growth and exploitation of Brachyplatystoma rousseauxii Castelnau, 1855 in the Caqueta River, Colombia

Fig. 2. Monthly percentages of breeding (stages 3 and 4) Brachyplatystoma rousseauxii females (white circles) in the Caqueta River, Colombian Amazon, between 1995 and 1997, in relation to the water level (black line).

opencc-by-4.0Sep 2013View details →
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Figure 1 in Current knowledge of New Caledonian marine and freshwater ichthyofauna, SW Pacific Ocean: diversity, exploitation, threats and management actions

Figure 1. – Location of New Caledonia in the southwest Pacific. Dotted lines: limits of the New Caledonian EEZ, triangles: main seamounts, blue zones: UNESCO world heritage areas, and red hatched zones: fully protected marine areas. Modified from New Caledonian Government, Global seamounts database, The Pew charitable trust.

opencc-by-4.0Dec 2023View details →
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Figure 2 in Life history traits and exploitation of Hampala barb (Hampala macrolepidota - Cyprinidae) in a subtropical reservoir (Lao PDR)

Figure 2. – Transverse section of an otolith (asteriscus) from a 2+-year- old Hampala macrolepidota from the Nam Theun 2 Reservoir. The section was acid etched, stained with toluidine blue and viewed using reflected light: 2 strained translucent zones (white trian- gle) were counted along the sulcus axis. Core (C), translucent stainable zone (TZ), opaque zone (OZ), ventral face (V), dorsal face (D), external face (E) and internal face (I).

opencc-by-4.0Dec 2019View details →
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Figure 5 in Life history traits and exploitation of Hampala barb (Hampala macrolepidota - Cyprinidae) in a subtropical reservoir (Lao PDR)

Figure 5. – Von Bertalanffy growth function adjusted to the age (month)-standard length of Hampala macrolepidota from the Nam Theun 2 Reservoir in Lao PDR between November 2015 and January 2017; at left, all polled and at right, by sex, grey dotted lines show the 95% confident interval.

opencc-by-4.0Dec 2019View details →
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Figure 1 in Life history traits and exploitation of Hampala barb (Hampala macrolepidota - Cyprinidae) in a subtropical reservoir (Lao PDR)

Figure 1. – Map of the Nam Theun 2 Reservoir in Lao PDR at its highest level (surface = 489 km²) and localization of sampling sites by experimental fishing gillnets (black dotes) and of villages (black stars) by landing/fishing effort monitoring. Source: Google Earth.

opencc-by-4.0Dec 2019View details →
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Figure 6 in Life history traits and exploitation of Hampala barb (Hampala macrolepidota - Cyprinidae) in a subtropical reservoir (Lao PDR)

Figure 6. – Percentage of mature Hampala macrolepidota females in 20 mm standard length intervals from the Nam Theun 2 Reservoir in Lao PDR in 2016 fitted to a logistic function.

opencc-by-4.0Dec 2019View details →
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Figure 6 in Life history traits of the exploited Nile Tilapia (Oreochromis niloticus - Cichlidae) in a subtropical reservoir (Lao PDR)

Figure 6. – At left, percentage of mature Oreochromis niloticus females by 20 mm standard length intervals, a fitted to logistic function from the Nam Theun 2 Reservoir in Lao PDR in 2016; at right, percentage of mature Oreochromis niloticus females by age (year), fitted to a logistic function from the Nam Theun 2 Reservoir in Lao PDR in 2016.

opencc-by-4.0Dec 2019View details →
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Fig. 3 in Exploiting parallels between livestock and wildlife: Predicting the impact of climate change on gastrointestinal nematodes in ruminants

Fig. 3. In marginal grazing systems in Europe sheep often occupy separate summer and winter grazing areas, analogous to the summer and winter ranges of migratory ruminants. In the uplands of Wales, UK, (shown here) sheep are often grazed on extensive areas of land at low stocking densities over the summer period, and sent to lowland dairy farms for winter grazing at higher stocking densities. (Photo: Rose, H.).

opencc-by-4.0Aug 2014View details →
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Fig. 2 in Exploiting parallels between livestock and wildlife: Predicting the impact of climate change on gastrointestinal nematodes in ruminants

Fig. 2. The relative seasonal incidence of ovine parasitic gastroenteritis (PGE) in the Southwest of England, UK, based on monthly diagnoses of (a) Nematodosis (NOS = species not otherwise specified), (b) Haemonchosis and (c) Nematodirosis (van Dijk et al., 2008).

opencc-by-4.0Aug 2014View details →
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Fig. 1 in Exploiting parallels between livestock and wildlife: Predicting the impact of climate change on gastrointestinal nematodes in ruminants

Fig. 1. Comparison of the instantaneous daily development rate of Ostertagia ostertagi (grey) and O. gruehneri (black) at a range of constant temperatures. Instantaneous daily development rates were estimated from the time to 50% development of L3, derived from data published in the literature (O. ostertagi: Rose, 1961; Pandey, 1972; Young et al., 1980) and original data (O. gruehneri: Hoar, 2012) as described by Azam et al. (2012).

opencc-by-4.0Aug 2014View details →
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Exploiting the potential of neutron imaging measurements for life sciences applications at the neutron spallation source, ISIS, UK - Crabs X-ray CT

<p>A ZIP file containing slices (in TIFF format) from a X-ray CT scan of crabs from the Eocene of Spain. Specimen was scanned&nbsp;on a Nikon Metrology HMX ST 225 system at the Natural History Museum, London, using a 1.0 mm thick copper filter, 225 kV voltage and 180 &mu;A current, giving a tomographic dataset with a voxel size of 46 &micro;m.</p>

opencc-by-4.0Feb 2018View details →
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Supporting Material to "SIFA: Exploiting Ineffective Fault Inductions on Symmetric Cryptography"

<p>Supplementary material to the paper &quot;SIFA: Exploiting Ineffective Fault Inductions on Symmetric Cryptography&quot; by&nbsp;Christoph Dobraunig, Maria Eichlseder, Thomas Korak, Stefan Mangard, Florian Mendel, and Robert Primas (CHES 2018, <a href="https://eprint.iacr.org/2018/071">https://eprint.iacr.org/2018/071</a>).</p> <p>&nbsp;</p> <p>Ineffectively faulted AES Ciphertexts for different platforms and with different fault countermeasures in place (including infection-based configurations). Files:</p> <ul> <li>*/ct_correct.txt: AES ciphertexts where a fault was induced during the encryption, but did not change the ciphertext (decimal, CSV, 1 row per ciphertext)</li> <li>*/round_keys.txt: 11 expanded AES round keys used for all ciphertexts (decimal, CSV, 1 row per round key)</li> <li>*/sei_hardware.dat: Results of the statistical key-recovery evaluation. Row i lists the SEI of the right key, the SEI of the best wrong key, and the rank of the correct key after using 4*i of the ciphertexts in ct_correct.txt.</li> </ul> <p>Target platforms and setups are described in more detail in the paper.</p>

opencc-by-4.0Jul 2018View details →

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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.

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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.

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

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.

abode-home-cage
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

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.

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

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.

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

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.

openneuro
neuroscienceopenPublished datasets are available on demand over the internet.
Last verified 2026-04-29Open record