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2,732 results for “Physiology”
Fig. 2 in Physiological and Biochemical Thermoregulatory Responses in Male Chinese Hwameis to Seasonal Acclimatization: Phenotypic Flexibility in a Small Passerine.
Fig. 2. Seasonal variation in body mass (A), resting metabolic rate (B), evaporative water loss (C) and thermal conductance (D) in Chinese hwamei (Garrulax canorus) captured in either summer or winter in Wenzhou, China. Data are shown as mean ± SEM, **p <0.01.
Fig. 5 in Physiological and Biochemical Thermoregulatory Responses in Male Chinese Hwameis to Seasonal Acclimatization: Phenotypic Flexibility in a Small Passerine.
Fig. 5. Correlations between resting metabolic rate (RMR) and state-4 respiration in the pectoral muscle (A), heart (C), liver (E) and kidneys (G), and between RMR and cytochrome c oxidase activity in the pectoral muscle (B), heart (D), liver (F) and kidneys (H), in Chinese hwameis (Garrulax canorus) captured in either summer or winter in Wenzhou, China.
Fig. 3 in Behavioral, physiological and morphological correlates of parasite intensity in the wild Cururu toad (Rhinella icterica)
Fig. 3. Association between locomotor performance and pulmonary parasite intensity in Rhinella icterica (N = 20; r = –0.49, P = 0.03). SVL = snout-vent length.
Fig. 2 in Behavioral, physiological and morphological correlates of parasite intensity in the wild Cururu toad (Rhinella icterica)
Fig. 2. Association between standard metabolic rate and total parasite intensity in Rhinella icterica (N = 22; r = –0.45, P = 0.03).
Fig. 1 in Behavioral, physiological and morphological correlates of parasite intensity in the wild Cururu toad (Rhinella icterica)
Fig. 1. Association between the score of the first component of a PCA on morphological variables (large heart, kidney and intestine masses) and parasite intensities in Rhinella icterica (N = 16). Full circles represent total parasite intensity (r = 0.66, P <0.01), open circles represent pulmonary parasite intensity (r = 0.71, P <0.01), and open triangles represent intestinal parasite intensity (r = 0.51, P = 0.04).
Рис. 1. КоΛичество макрокониΑий грибов роΑа Fusarium (% от общего чисΛа эΛементов морфоΛогии) на органах и в физиоΛогических жиΑкостях картофеΛьной коровки Fig. 1. Number of macroconidia of fungus species from the genus Fusarium (% of the total number of morphological elements) on organs and in physiological fluids of the potato ladybird beetle in On the vector characteristics of the potato ladybird beetle Henosepilachna Vigintioctomaculata (Motsch.) (Coleoptera, Coccinellidae) in the system "phytophagous insect - plant pathogen - plant"
Рис. 1. КоΛичество макрокониΑий грибов роΑа Fusarium (% от общего чисΛа эΛементов морфоΛогии) на органах и в физиоΛогических жиΑкостях картофеΛьной коровки Fig. 1. Number of macroconidia of fungus species from the genus Fusarium (% of the total number of morphological elements) on organs and in physiological fluids of the potato ladybird beetle
The effects of environmental history and thermal stress on coral physiology and immunity
<p>This dataset has all data for the manuscript (Wall CB, CA Ricci, GE Foulds, LD Mydlarz, RD Gates, HM Putnam (2018) The effects of environmental history and thermal stress on coral physiology and immunity. <em>Marine Biology</em>). Data included a zipped archive shape file for creating Kāne'ohe Bay map, physical data (light and temperature) from Kāne'ohe Bay and laboratory experiments, pCO<sub>2</sub> data for Kāne'ohe Bay reef sites dowloaded from NOAA PMEL, and biological responses (PAM fluorometry, physiology, immune activity and oxidative profile). </p>
Slow motion in films and video clips: Music influences perceived duration and emotion, autonomic physiological activation and pupillary responses [data set]
<p>Data set for a study to be published by PLOS ONE.</p>
Data from: Defensive fruit metabolites obstruct seed dispersal by altering bat behavior and physiology at multiple temporal scales.
<p>These data support the publication "Defensive fruit metabolites obstruct seed dispersal by altering bat behavior and physiology at multiple temporal scales".</p>
Nobel Prize winners in Physics, Chemistry and Medicine or Physiology 1994-2018
<p>The lists of Nobel Prize winners in Physics, Chemistry and Medicine or Physiology 1994-2018 + theirs Scopus ID's and theirs affiliations at the time of the award.</p>
Fig. 1. Terrestrial leeches. A in Leeches in the extreme: Morphological, physiological, and behavioral adaptations to inhospitable habitats
Fig. 1. Terrestrial leeches. A) Orobdella sp. out of water after a rainstorm in the Philippines. Leech is estimated to be more than 25 cm in length. Image credit: Will Reeves. B) Haemadipsa zeylanica pursuing the photographer as a host on the Vietnamese forest floor. Leech size approximately 4 cm in length. C) SEM image of the head of a haemadipsid leech. The inset depicts an outline of the same image with the eye spots marked by black dots. D) Caudal sucker of a haemadipsid leech with friction rays on the sucker surface. White arrows indicate the two flaps of the auricle. Scale bars in C and D = 0.5 mm.
Fig. 4. Leech parental care. A in Leeches in the extreme: Morphological, physiological, and behavioral adaptations to inhospitable habitats
Fig. 4. Leech parental care. A) Light microscopy image of a glossiphoniid leech with pink circular eggs gathered on its ventral side for protection. B) Light microscopy image of a glossiphoniid leech with leech hatchlings gathered on the ventral side of the parent leech. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)
Fig. 3. Extreme feeding. A in Leeches in the extreme: Morphological, physiological, and behavioral adaptations to inhospitable habitats
Fig. 3. Extreme feeding. A) Hirudo verbana, a commercially important and frequently traded species of European medicinal leech. B) Several individuals of Hirudo verbana feeding on blood inside a nitrile rubber glove.
Fig. 5 in The effects of light-emitting diode and conventional lighting on sorghum physiology and sugarcane aphid interaction
Fig. 5. Mean ± SE photosynthetic rates (μmol CO2 m−2 s−1) of resistant (TX-7000 and KS-585) and susceptible (TX-2783 and DKS-37-07) sorghum cultivars grown under either conventional or light-emitting diodes. All plants were measured at 15 d afer infestation with sugarcane aphids. Bars with different letters are significantly different (Kruskal-Wallis ANOVA, df = 3; H> 27.14; P <0.01).
Fig. 7 in The effects of light-emitting diode and conventional lighting on sorghum physiology and sugarcane aphid interaction
Fig. 7. Mean ± SE chlorophyll loss at 15 d afer infestation under lightemitting diode and conventional lights (control-infested)/control.Different letters represent significant differences (P <0.001) with a Kruskal-Wallis ANOVA followed by Dunn's multiple comparison test (H = 62.629; df = 7).
Fig. 3 in The effects of light-emitting diode and conventional lighting on sorghum physiology and sugarcane aphid interaction
Fig. 3. Susceptible sorghum variety KS-585 across 4 treatments: (A) control under light-emitting diodes; (B) infested under light-emitting diodes; (C) control under conventional lights; (D) infested under conventional lights. Plants were infested with sugarcane aphids and assessed 15 d post infestation.
Fig. 2 in The effects of light-emitting diode and conventional lighting on sorghum physiology and sugarcane aphid interaction
Fig. 2. Resistant sorghum variety TX-2783 across 4 treatments: (A) control under light-emitting diodes; (B) infested under light-emitting diodes; (C) control under conventional lights; (D) infested under conventional lights. Plants were infested with sugarcane aphids and assessed 15 d post infestation.
Fig. 1 in The effects of light-emitting diode and conventional lighting on sorghum physiology and sugarcane aphid interaction
Fig. 1. Light emission spectrum of the 9 band 60-watt light-emitting diode grow panels over the visible spectrum and into the near infrared.
Fig. 6 in The effects of light-emitting diode and conventional lighting on sorghum physiology and sugarcane aphid interaction
Fig. 6. Mean ± SE stomatal conductance (mol H2O m−2 s−1) at 15 d af- ter infestation under light-emitting diode and conventional lights. Bars with different letters are significantly different (Kruskal-Wallis ANOVA, df = 3; H> 24.13; P <0.01).
Fig. 4 in The effects of light-emitting diode and conventional lighting on sorghum physiology and sugarcane aphid interaction
Fig. 4. Mean ± SE number of sugarcane aphids per plant 15 d afer infestation when grown for resistant (TX-2783 and DKS-37-07) and susceptible (TX-7000 and KS-585) sorghum cultivars grown under either conventional or light-emitting diodes. P-values represent results of a Student's t-test (df = 22) for each variety.
ScienceDex guides
Understand access before you commit
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.