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Fig. 11 in Reproductive biology of Cetengraulis edentulus (Cuvier, 1829), the major fishery resource in Guanabara Bay, Brazil
Fig. 11. Relation between the oocytes mean diameter with the gonadosomatic index (A) and with the condition factor (B) of Cetengraulis edentulus in Guanabara Bay. Lines represent the generalized additive models selected by the Akaike information criterion.
Fig. 10 in Reproductive biology of Cetengraulis edentulus (Cuvier, 1829), the major fishery resource in Guanabara Bay, Brazil
Fig. 10. Relation between fecundity with total length (A) and fullness index (B) and between fecundity residuals (after controlling for the length effect) with gonadosomatic index (C) for Cetengraulis edentulus in Guanabara Bay. Lines represent the generalized additive models selected by the Akaike information criterion.
Fig. 7 in Reproductive biology of Cetengraulis edentulus (Cuvier, 1829), the major fishery resource in Guanabara Bay, Brazil
Fig. 7. Mean values (± standard error) of the condition factor among months and seasons (black square = females; white circle = males) of Cetengraulis edentulus in Guanabara Bay.
Fig. 4 in Reproductive biology of Cetengraulis edentulus (Cuvier, 1829), the major fishery resource in Guanabara Bay, Brazil
Fig. 4. Mean values (± standard error) of gonadosomatic index (GSI) among months and seasons (black square = females; white circle = males) of Cetengraulis edentulus in Guanabara Bay.
Fig. 6 in Reproductive biology of Cetengraulis edentulus (Cuvier, 1829), the major fishery resource in Guanabara Bay, Brazil
Fig. 6. Variation of the index of reproductive activity (IRA) for female Cetengraulis edentulus among months and seasons in Guanabara Bay.
Fig. 3 in Reproductive biology of Cetengraulis edentulus (Cuvier, 1829), the major fishery resource in Guanabara Bay, Brazil
Fig. 3. Seasonal variation in percent (%) frequency of occurrence of gonad maturation stages (GMS) for females (white column) and males (black column) of Cetengraulis edentulus in Guanabara Bay.
Figure 2. A–G, Madagascan Scarabaeini species. A, B in Rediscovery of Scarabaeus sevoistra Alluaud, 1902 (Coleoptera: Scarabaeinae): biological notes and IUCN Red Listing
Figure 2. A–G, Madagascan Scarabaeini species. A, B, holotype male of Scarabaeus sevoistra Alluaud, 1902 and the associated labels from the MNHN; C, habitus drawing of a female S. sevoistra (from Paulian & Lebis (1960: 14)) for comparison; note the dimorphism in the shape and form of the protibiae of the male (A) and female (C); D, Scarabaeus radama Fairmaire, 1895; E, F, Scarabaeus viettei (Paulian, 1953), holotype female and the associated labels from the MNHN. Scale bar is 10 mm.
Figure 1. A–F in Rediscovery of Scarabaeus sevoistra Alluaud, 1902 (Coleoptera: Scarabaeinae): biological notes and IUCN Red Listing
Figure 1. A–F, Recent photographic observations of Scarabaeus sevoistra Alluaud, 1902. A, B, C, photographed by Joseph Thompson, 04 November 2015; D, photographed by Bitty Roy, 17 November 2019; E, F, photographed by Maxim Nuraliev, 01 August 2015.
Figure 3 in Rediscovery of Scarabaeus sevoistra Alluaud, 1902 (Coleoptera: Scarabaeinae): biological notes and IUCN Red Listing
Figure 3. Map showing the ecoregions of Madagascar with the Madagascan spiny thickets in the southwest.
Figure 2 in Trichoderma: biological control efficiency and perspectives for the Brazilian Midwest states and Tocantins
Figure 2. Interaction mechanisms of Trichoderma spp. and phytopathogens. (A) Yellow, red, and blue correspond to the antagonistic actions of Trichoderma from contact with phytopathogens; (B) Contact of fungal hyphae (Trichoderma spp. in green and phytopathogens in orange). Elements in pink correspond to the process of competition for space (long base) and nutrients (rectangles). Blue circles correspond to the metabolites produced by Trichoderma. Yellow stars represent the enzymes produced by Trichoderma in the mycoparasitic process.
Figure 5. B in Phytochemical and biological attributes of Bauhinia variegata L. (Caesalpiniaceae)
Figure 5. B. variegata extracts result forα-amylase inhibition assay. The standard drug used is Acarbose IC50 33.43 ± 0.28 µg/mL. All procedures are repeated three times and results are mentioned as mean ± SD. nH = n-hexane; EA = ethyl acetate; MeOH = methanol; DW = distilled water; IC 50 = concentration for 50% inhibition; (S) = stem; (L) = leaf; (F) = flower; (B) = bark; (R) = root.
Figure 4 in Phytochemical and biological attributes of Bauhinia variegata L. (Caesalpiniaceae)
Figure 4. Brine shrimp lethality assay of B. variegata extracts. Doxorubicin is used as a standard with an LC50 5.63 ± 0.25 µg/ mL. All values are obtained thrice and shown as mean ± SD. nH = n-hexane; EA = ethyl acetate; MeOH = methanol; DW = distilled water; LC50 = concentration for 50% lethality; (S) = stem; (L) = leaf; (F) = flower; (B) = bark; (R) = root.
Figure 3. B in Notes on the biological development of the darkling beetle Blaps nefrauensis nefrauensis Seidlitz, 1893 (Coleoptera: Tenebrionidae)
Figure 3. B. nefrauensis life cycle: (a) Eggs and newly hatched larva (1st instar). (b) 2nd instar larva beside eggs. (c) Larvae in the last instar. (d) Prepupa. (e) Pupa. (f) Adults. (g) Newly moulted 2ndand 4th instar larvae. (h) Moulted 2nd and 6th instar larva began to yellowish. (i) Newly moulted larva beside its old yellow cuticle. (j) Newly moulted larva compared with larva in the 8th instar. Diagram representation of the life cycle of B. nefrauensis (k).
Figure 5 in Notes on the biological development of the darkling beetle Blaps nefrauensis nefrauensis Seidlitz, 1893 (Coleoptera: Tenebrionidae)
Figure 5. Light microscopy of some structure of the newly hatched egg larva of B. nefrauensis: (a) Ligula (ventral view). (b) Lacinia teeth (ventral view). (c) Ligula, and Labial and Maxillary palpi (dorsal view). (d) Ocelli (lateral view). (e) Nerves across ligula. (f) Nerve across third antennomere. Light microscopy on the antennal protection in the embryo of B. nefrauensis (g) Larva just before egg hatching. (h) Cylindrical membrane covering apically the antennae.
Figure 4 in Notes on the biological development of the darkling beetle Blaps nefrauensis nefrauensis Seidlitz, 1893 (Coleoptera: Tenebrionidae)
Figure 4. Newly egg hatched larva: (a) First instar larva compared with egg, scale = 1 mm. (b) First instar larva compared with 8th instar larva. (c) Head (dorsal view). (d) Head (ventral view). (e-g) Pygopods and urogomphi in first instar larva
Figure 1. Oyster hangings with T in Biological control of incrusting organisms and sediments in Chilean oyster cultures
Figure 1. Oyster hangings with T. atra presence and absence for incrusting organisms and sediments removal.
Fig. 1 in New data on the biology and chorology of the tribe Gonocerini (Hemiptera: Heteroptera: Coreidae) in the Canary Islands.
Fig. 1.-. Plinachtus imitator (Reuter, 1891). a.-Adult on leaves of Schinus molle. b.- Late instar nymph on leaves of Maytenus canariensis. c.- Early instar nymph on fruits of Maytenus canariensis.
Fig. 2.- Monthly D in Dryocosmus kuriphilus Yasumatsu, 1951 (Hymenoptera: Cynipidae) in Galicia (NW Spain): pest dispersion, associated parasitoids and first biological control attempts.
Fig. 2.- Monthly D. kuriphilus phenology (E: egg; L1: first-instar larvae; L2: intermediate instar larvae; L3: terminal-instar larvae; Pp: pre pupae stage; P: pupae stage; A: adult). *: punctual presence; +: sterile eggs. Sweet chestnut fruit phenology is given for orientation (§: fructification and burr development).
WT, Delta and Omicron RBDs Adsorption onto Hydrophobic, Hydrophilic Surfaces and Biological Interfaces
<p>Simulations (trajectories) and analysis of the 3 VoCs RBDs of the SARS-CoV-2.</p> <p>For more information go to this article: https://doi.org/10.1021/acs.jcim.4c00460</p>
Fig. 1 in Sugarcane stem borers of the Colombian Cauca River Valley: current pest status, biology, and control
Fig. 1. Male adults of 4 Diatraea species present in Colombia. A. D. saccharalis; B. D. indigenella; C. D. tabernella; D. D. busckella. In general, moths are difficult to distinguish, and clear species identification requires the dissection of male genitalia (photos L. A. Lastra).
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.