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372 results for “hawaii”
Figure 2 in First Field Collection of the Rough Sweetpotato Weevil, Blosyrus asellus (Olivier) (Coleoptera: Curculionidae), on Hawaii Island, with Notes on Detection Methods
Figure 2. Locations on Hawaii island (marked with filled circles) where adult rough sweetpotato weevils have been recovered (map developed using ArcGIS [ESRI 2012]).
Figure 3 in First Field Collection of the Rough Sweetpotato Weevil, Blosyrus asellus (Olivier) (Coleoptera: Curculionidae), on Hawaii Island, with Notes on Detection Methods
Figure 3. Trap used for rough sweetpotato weevil detection ('Treatment 9'). (A) Flash picture taken at night to show the sweetpotato root section held underneath the green light and the water container inside the trap holding a sweetpotato leaf. (B) Picture taken without flash to show the appearance of the trap at night.
Figure 3. D in Dichromothrips smithi (Zimmermann), a New Thrips Species Infesting Bamboo Orchids Arundina graminifolia (D. Don) Hochr. and Commercially Grown Orchids in Hawaii
Figure 3. D. smithi (adults females and larvae) and two unidentified Orius predators (lower right area of picture) washed from a bamboo orchid flower blossom and stored in ethanol. Note that predators are similar in length to D. smithi adults. Note also orange-colored second instar larva of D. smithi (middle left). Large secondinstar larvae are distinctly orange in life.
Figure 16 in Unusual Dark Forms of the Solanum Fruit Fly Bactrocera latifrons (Hendel) in Hawaii (Tephritidae: Dacini)
Figure 16. Lateral views showing the difference in the width of the mesopleural stripe. A. Bactrocera latifrons ex USDA fruit fly lab, Honolulu, Hawaii. B. Holotype of B. citima, Chiangdao, Chiangmai prov., Thailand.
Figures 1–15 in Unusual Dark Forms of the Solanum Fruit Fly Bactrocera latifrons (Hendel) in Hawaii (Tephritidae: Dacini)
Figures 1–15. Lateral, dorsal views and abdomen close-ups of five specimens of Hawaiian Bactrocera latifrons with varying degrees of dark markings on the abdomen and the scutum and legs. 1–3: female collected on Oahu, Kahuku, Fukuyama farm, leg. S. Graham (no date on labels), with typical 'textbook' orange-brown abdomen and absence of dark markings. 4–6: UHIM2015.04242 male collected on Maui, Kula, Howard Harada coffee, 26.vii–4.viii-06. leg. L. Leblanc. 7–9: female collected on Oahu, 2017, leg. S. Graham. 10–12: UHIM2015.04243 collected on Maui, Kula, Flora Umeno's coffee plot, 16–23.vi.06, leg. L. Leblanc. 13–15: UHIM2016.25466 female collected on Oahu, Ala Wai, garden, 5.ii.90 ex wild tomatoes, leg. M. M. Ramadan.
Figure 17 in Unusual Dark Forms of the Solanum Fruit Fly Bactrocera latifrons (Hendel) in Hawaii (Tephritidae: Dacini)
Figure 17. Dorsal view drawing of the aculeus (piercer) of the ovipositor, which is needle shaped (above) in Bactrocera citima and trifurcate (below) in B. latifrons and B. parvula.
Figure 1 in New State Record of the Psyllid Heterotrioza chenopodii (Reuter, 1876) (Hemiptera: Psylloidea: Triozidae) for Hawaii
Figure 1. Heterotrioza chenopodii specimens collected on Oahu (imaged after preservation in ethanol); A, male dorsum; B, male lateral; C, female lateral.
Figure 3 in Entomopathogenic Fungi as Mortality Factors of Macadamia Felted Coccid, Eriococcus ironsidei (Hemiptera: Eriococcidae) in Hawaii
Figure 3. Mean (±SEM) length of time E. ironsidei continued to reproduce following treatment with different conidial concentrations of B. bassiana. Bars with different letters differ significantly (α = 0.05) by LSD.
Figure 2 in Recovery of Sweetpotato Vine Borer, Omphisa anastomosalis (Lepidoptera: Crambidae), in Sweetpotato Fields in Hawaii Through Field Collections and Detection Trapping
Figure 2. The three trap types tested for relative effectiveness of detection/monitoring of sweetpotato vine borer field populations: A. Delta trap; B. Wing trap; and C. Heliothis trap. Red arrows point to the locations of the binary sex pheromone in each of the trap types. Blue arrow points to the netted cylinder in the Heliothis trap from which attracted moths were recovered.
Figure 4 in Recovery of Sweetpotato Vine Borer, Omphisa anastomosalis (Lepidoptera: Crambidae), in Sweetpotato Fields in Hawaii Through Field Collections and Detection Trapping
Figure 4. Frass pushed out of a sweetpotato root by a sweetpotato vine borer caterpillar feeding inside the root.
Figure 8 in Recovery of Sweetpotato Vine Borer, Omphisa anastomosalis (Lepidoptera: Crambidae), in Sweetpotato Fields in Hawaii Through Field Collections and Detection Trapping
Figure 8. Posterior ventral abdominal surfaces of sweetpotato vine borer adults showing the absence (female) or presence (male) of a pair of clasper like structures on the last abdominal segment. A. adult female; B. adult male.
Figure 10 in Recovery of Sweetpotato Vine Borer, Omphisa anastomosalis (Lepidoptera: Crambidae), in Sweetpotato Fields in Hawaii Through Field Collections and Detection Trapping
Figure 10. Average weekly catch of adult male sweetpotato vine borer moths in delta traps baited with binary sex pheromone lure consisting of a 2.5 mg: 5.0 mg ratio of Type 1: Type 2 lure components and positioned at different heights above sweetpotato foliage. See text for further description of the Type 1 and Type 2 components. Bars followed by the same letters are not significantly different at the α = 0.05 level.
Figure 9. Average total 3 in Recovery of Sweetpotato Vine Borer, Omphisa anastomosalis (Lepidoptera: Crambidae), in Sweetpotato Fields in Hawaii Through Field Collections and Detection Trapping
Figure 9. Average total 3-week catch of male sweetpotato vine borer adult moths in three different types of traps baited with binary sex pheromone lure consisting of a 2.0 mg: 4.0 mg ratio of Type 1: Type 2 lure components. See text for further description of the Type 1 and Type 2 components. Columns with the same letters above are not significantly different at the α = 0.05 level.
Figure 11 in Recovery of Sweetpotato Vine Borer, Omphisa anastomosalis (Lepidoptera: Crambidae), in Sweetpotato Fields in Hawaii Through Field Collections and Detection Trapping
Figure 11. Average weekly catch of adult male sweetpotato vine borer moths in delta traps baited with binary sex pheromone lure consisting of a 2.0 mg: 4.0 mg ratio of Type 1: Type 2 lure components and positioned at different locations in or around a sweetpotato field. Columns with the same letters above are not significantly different at the α = 0.05 level.
Figure 6 in Recovery of Sweetpotato Vine Borer, Omphisa anastomosalis (Lepidoptera: Crambidae), in Sweetpotato Fields in Hawaii Through Field Collections and Detection Trapping
Figure 6. Posterior ventral surface of sweetpotato vine borer pupae showing the presence (A. female) or absence (B. male) of a prominent notch (indicated by red arrow) on the 9th segment.
Figure 7 in Recovery of Sweetpotato Vine Borer, Omphisa anastomosalis (Lepidoptera: Crambidae), in Sweetpotato Fields in Hawaii Through Field Collections and Detection Trapping
Figure 7. Eggs laid by female sweetpotato vine borer on a sweetpotato root within a screen-walled cubical.
Data from: Pace and shape of life differences drive invasion trajectory in introduced lizards in Hawaii
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Semi‐quantitative metabarcoding reveals how climate shapes arthropod community assembly along elevation gradients on Hawaii Island
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Mesophotic corals in Hawaii maintain autotrophy to survive low-light conditions: Stable isotope dataset
<p>In mesophotic coral ecosystems, reef-building corals and their photosynthetic symbionts can survive with less than 1% of surface irradiance. How depth-specialist corals rely upon autotrophically and heterotrophically-derived energy sources across the mesophotic zone remains unclear. We analyzed the stable carbon (δ<sup>13</sup>C) and nitrogen (δ<sup>15</sup>N) isotope values of a <em>Leptoseris </em>community from the ʻAuʻau Channel, Maui, Hawaiʻi (65-125 m) including four coral host species living symbiotically with three algal haplotypes. We characterized the isotope values of hosts and symbionts across species and depth to compare trophic strategies. Symbiont δ<sup>13</sup>C was consistently 0.5‰ higher than host δ<sup>13</sup>C at all depths. Mean colony host and symbiont δ<sup>15</sup>N differed by up to 3.7‰ at shallow depths and converged at deeper depths. These results suggest that both heterotrophy and autotrophy remained integral to colony survival across depth. The increasing similarity between host and symbiont δ<sup>15</sup>N at deeper depths suggests that nitrogen is more efficiently shared between mesophotic coral hosts and their algal symbionts to sustain autotrophy. Isotopic trends across depth did not generally vary by host species or algal haplotype, suggesting that photosynthesis remains essential to <em>Leptoseris </em>survival and growth despite low light availability in the mesophotic zone.</p>
Dataset for The Effects of COVID-19 Vaccine Mandates in Hawaii
<p>This is the data used for the paper: <em>The Effects of COVID-19 Vaccine Mandates in Hawaii</em> published in Vaccines (2022). It includes the following: (1) foot-traffic data provided by SafeGraph; (2) COVID-19 positive case data provided by the State of Hawaii Department of Health; (3) Population data from the United States Census Bureau estimates from the 2020 Census; (4) Weekly vaccination data provided by the State of Hawaii Department of Health.</p>
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Allen Brain Atlas
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DANDI Archive for NWB datasets
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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.