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1,003 results for “darkness”
Fig. 14 in Life in darkness: an overview of cave-adapted japygids (Hexapoda, Diplura)
Fig. 14. Imazighenjapyx marocanus Sendra & Sánchez-García gen. et sp. nov., holotype, ♀ (MHNM). A. Cerci, ventral view. B. Detail of right cercus in ventro-lateral view. C. Right cercus, ventral view. D. Leaft cercus, ventral view.
Fig. 19 in Life in darkness: an overview of cave-adapted japygids (Hexapoda, Diplura)
Fig. 19. Opisthjapyx naledi Sendra & Sánchez-García sp. nov., holotype, ♀ (ISAM). A. Urotergite I. B. Urotergite II. C. Urotergite VII. D. Urotergite VIII.
Fig. 9 in Life in darkness: an overview of cave-adapted japygids (Hexapoda, Diplura)
Fig. 9. Imazighenjapyx marocanus Sendra & Sánchez-García gen. et sp. nov., holotype, ♀ (MHNM). A. Dorsal side of head and anterior part of pronotum. B. Pronotum and anterior part of mesonotum. C. Mesonotum. D. Metanotum. E. Urotergites I and II. F. Urotergites VII and VIII.
Fig. 8 in Life in darkness: an overview of cave-adapted japygids (Hexapoda, Diplura)
Fig. 8. Imazighenjapyx marocanus Sendra & Sánchez-García gen. et sp. nov., holotype, ♀ (MHNM). A. Antennae.B. Central antennomeres. C. Apical antennomere.D. Lateral side of the apical antennomere. E. Detail of apical antennomere. F. Detail of antennal micro-barbed sM setae.
Fig. 5 in Life in darkness: an overview of cave-adapted japygids (Hexapoda, Diplura)
Fig. 5. Austrjapyx wynbergensis Sendra & Sánchez-García sp. nov., 2-paratype, ♀ (AS). A. Lateral organ of urosternite I in B. B. Urosternite I. C. Detail lateral organ of the first urosternite. D. Micropores in posterior part of urosternite I. E. Urosternite II. F. Abdominal segments VII‒X in latero-ventral view.
Fig. 7 in Life in darkness: an overview of cave-adapted japygids (Hexapoda, Diplura)
Fig. 7. Location and habitat of Austrjapyx wynbergensis Sendra & Sánchez-García sp. nov. A. External area at the Table Mountains in the surroundings of the Wynberg cave. B. Wynberg cave interior, general appearance. C. Living specimen of Austrjapyx wynbergensis.
Fig. 4 in Life in darkness: an overview of cave-adapted japygids (Hexapoda, Diplura)
Fig. 4. Austrjapyx wynbergensis Sendra & Sánchez-García sp. nov., holotype, ♀ (ISAM). A. Urotergites V and VI. B. Urotergites VII‒IX.
Fig. 6 in Life in darkness: an overview of cave-adapted japygids (Hexapoda, Diplura)
Fig. 6. Austrjapyx wynbergensis Sendra & Sánchez-García sp. nov., holotype, ♀ (ISAM). A. Abdominal segments IX and X in dorsal view. B. Cerci, dorsal view. C. Abdominal segments VIII‒X in lateroventral view. D. Cerci, ventral view.
Fig. 1 in Life in darkness: an overview of cave-adapted japygids (Hexapoda, Diplura)
Fig. 1. Austrjapyx wynbergensis Sendra & Sánchez-García sp. nov., holotype, ♀ (ISAM). A. Dorsal habitus. B. Head and pronotum in dorsal view. C. Mesonotum. D. End of metatarsus and claws. E. Metanotum and first urotergite.
Fig. 3 in Life in darkness: an overview of cave-adapted japygids (Hexapoda, Diplura)
Fig. 3. Austrjapyx wynbergensis Sendra & Sánchez-García sp. nov., ♀ (AS). A. Head in ventro-lateral view. B. Pro-prosternum (pr-prt) with spine (sp) and prosternum (pr-st). C. Meso-poststernum (mspst), meso-intersternum (ms-ist) and mesosternum (ms-st). D. Metasternum (mt-st). E. Lateral view of metathoracic leg. F. Detail of metathoracic tarsus and claws.
Fig. 2 in Life in darkness: an overview of cave-adapted japygids (Hexapoda, Diplura)
Fig. 2. Austrjapyx wynbergensis Sendra & Sánchez-García sp. nov., holotype, ♀ (ISAM). Distal antennomere. See terminology in the text.
Data from: Human avoidance, selection for darkness and prey activity explain wolf diel activity in a highly cultivated landscape
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Data from: To the top or into the dark? Relationships between elevational and canopy cover distribution shifts in mountain forests
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From darkness to twilight: Morphological divergence between cave and surface-subterranean ecotone Niphargus species
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Data from: A call in the dark: Nocturnal flight calls and their potential to advance the study of avian migration
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Data from: Use of visual display in dark, cluttered environments
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Museum ‘dark data’ show variable impacts on deep-time biogeographic and evolutionary history
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Genome sequence and characterization of a freshwater photoarsenotroph, Cereibacter azotoformans strain ORIO, isolated from sediments capable of cyclic light-dark arsenic oxidation and reduction
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Eight Mile Lake Research Watershed, Carbon in Permafrost Experimental Heating Research (CiPEHR): Half-hourly growing season, chamber-based, CO2 flux data, with dark daytime measurements, 2014
The Carbon in Permafrost Experimental Heating Research (CiPEHR) project addresses the following questions: 1) Does ecosystem warming cause a net release of C from the ecosystem to the atmosphere?, 2) Does the decomposition of old C, that comprises the bulk of the soil C pool, influence ecosystem C loss?, and 3) How do winter and summer warming alone, and in combination, affect ecosystem C exchange? We are answering these questions using a combination of field and laboratory experiments to measure ecosystem carbon balance and radiocarbon isotope ratios at a warming experiment located in an upland tundra field site near Healy, Alaska in the foothills of the Alaska Range. How does warming impact the phenology of dominant plant species? This data contains CO2 fluxes measured using an automated chamber system that measures net CO2 exchange (NEE). Measurements are made every ~1.5 hours and modeled half-hourly. Half hour ecoystem respiration is modeled using an exponential Q10 relationship when light conditions are low (PAR<5umol/m2/s) and using a hyperbolic light relationship when PAR>5umol/m2/s. Addditional dark daytime Reco measurements were used to define the Q10 model. GPP is calculated as the difference between NEE and Reco.
Eight Mile Lake Research Watershed, Carbon in Permafrost Experimental Heating Research (CiPEHR): Weekly dark CO2 fluxes, 2014
The Carbon in Permafrost Experimental Heating Research (CiPEHR) project addresses the following questions: 1) Does ecosystem warming cause a net release of C from the ecosystem to the atmosphere?, 2) Does the decomposition of old C, that comprises the bulk of the soil C pool, influence ecosystem C loss?, and 3) How do winter and summer warming alone, and in combination, affect ecosystem C exchange? We are answering these questions using a combination of field and laboratory experiments to measure ecosystem carbon balance and radiocarbon isotope ratios at a warming experiment located in an upland tundra field site near Healy, Alaska in the foothills of the Alaska Range. How does warming impact the phenology of dominant plant species? This data contains manual CO2 flux measurements collected using a dark, portable CO2 flux chamber. These measurements are intended to estimate daytime ecosystem respiration to provide some validation for ecosystem respiration modeled with an exponential temperature response from clear, automated CO2 flux chambers at this same site. Dark flux measurements were taken weekly from 25 April 2014 to 23 Sep 2014.
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Allen Brain Atlas
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International Brain Laboratory public data
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OpenNeuro
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