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Fig. 1 in First report of Trissolcus japonicus parasitizing Halyomorpha halys in North American agriculture
Fig. 1. White and black circles indicate the locations of 2 sentinel egg masses that were parasitized by Trissolcus japonicus within a heterogeneous landscape at 1 of the field sites in New Jersey. Black lines indicate the nearest tree line, and the inset map of New Jersey indicates with a star where this farm was located.
Fig. 2. Statistical parsimony cladogram network representing relationships among the 45 haplotypes for a 615 in Genetic diversity of Halyomorpha halys (Hemiptera, Pentatomidae) in Korea and comparison with COI sequence datasets from East Asia, Europe, and North America
Fig. 2. Statistical parsimony cladogram network representing relationships among the 45 haplotypes for a 615 bp fragment of the COI gene of Halyomorpha halys. Each circle is labeled with haplotype number, and the size of each circle is proportional to the frequency of each haplotype [H3 (n = 353); H1 (n = 285); H22 (n = 43); H8 (n = 34); H33 (n = 23); H2 (n = 16); H32 (n = 8); H7, H9–H13, and H43 (n = 3); H6, H14, H34, H39, and H40 (n = 2); H4–H5, H12, H15–H21, H23, H30–H31, H35–H38, H41, H42, and H44–H51 (n = 1)]. Differing colors indicate countries in which samples were collected.
Fig. 3 in Influence of plant direction, layer, and spacing on the infestation levels of Anthonomus eugenii (Coleoptera: Curculionidae) in open jalapeño pepper fields in North Florida
Fig. 3. Number of infested fruits and presence of weevil larvae in different jalapeño plant parts (means ± SE). Number of infested fruits in 5 directions (A), in 3 layers (C), and at 5 spacings (E). Number of larval A. eugenii within infested fruits in 5 directions (B), in 3 layers (D), and at 5 spacings (F). Different letters indicate significant differences among the treatments (means separated by Tukey's HSD, P <0.05).
Fig. 4 in Influence of plant direction, layer, and spacing on the infestation levels of Anthonomus eugenii (Coleoptera: Curculionidae) in open jalapeño pepper fields in North Florida
Fig. 4. Fruit wall thickness and single weight in different jalapeño plant parts (means ± SE). Fruit wall thickness (A) and single weight (B) in 5 directions, fruit wall thickness (C) and single weight (D) in 3 layers, fruit wall thickness (E) and single weight (F) at 5 spacings. Different letters indicate significant differences among the treatments (means separated by Tukey's HSD, P <0.05).
Fig. 2 in Influence of plant direction, layer, and spacing on the infestation levels of Anthonomus eugenii (Coleoptera: Curculionidae) in open jalapeño pepper fields in North Florida
Fig. 2. Infestation and larval density of pepper weevil in 2017. Vertical bars are standard errors of the means.
Fig. 5 in Influence of plant direction, layer, and spacing on the infestation levels of Anthonomus eugenii (Coleoptera: Curculionidae) in open jalapeño pepper fields in North Florida
Fig. 5. Relationship between the infestation level and the fruit wall thickness (A) and single weight (B). Each data point represents the number of infested fruits per plant in each fruit wall thickness or weight (means ± SE). Line was fitted using linear regression analysis.
Fig. 1 in Influence of plant direction, layer, and spacing on the infestation levels of Anthonomus eugenii (Coleoptera: Curculionidae) in open jalapeño pepper fields in North Florida
Fig. 1. (a) Adult pepper weevil feeding on the stalk of a pepper fruit; (b) young and full grown larvae inside a pepper fruit; (c) pupa inside the fruit; and (d) adult weevil exit holes in pepper fruits.
Fig. 2 in Examining the prevalence of Solenopsis invicta virus 3 (Solinviviridae: Invictavirus) in Solenopsis invicta (Hymenoptera: Formicidae) alates collected in North Florida
Fig. 2. Representative agarose gel depicting detection of Solenopsis invicta virus 3 as determined by polymerase chain reaction using cDNA generated from RNA purified from female alates of Solenopsis invicta. Arrow represents the 258 bp amplicon from Solenopsis invicta virus 3. Lane 1 is a 1 kb DNA ladder and lane 12 is non-template control.
Fig. 1 in Examining the prevalence of Solenopsis invicta virus 3 (Solinviviridae: Invictavirus) in Solenopsis invicta (Hymenoptera: Formicidae) alates collected in North Florida
Fig. 1. Map of Florida illustrating the collection locations and distribution of Solenopsis invicta virus 3 infection rate of female alates of Solenopsis invicta colonies in urban and rural cities of North Florida. Black portions of the pie charts represent the proportion of alates infected with Solenopsis invicta virus 3.
Fig. 4 in Herpetofauna of Marechal Newton Cavalcanti Instruction Center, a hotspot Atlantic Forest fragment in Pernambuco, north-eastern Brazil
Fig. 4. Testudines, amphisbaenians, and crocodilians found in the Marechal Newton Cavalcanti Instruction Center Atlantic Forest fragment. (A) Phrynops geoffroanus (Schweigger, 1812); (B) Kinosternon scorpioides (Linneaus, 1766); (C) Mesoclemmys tuberculata (Lüederwalt, 1926); (D) Amphisbaena vermiculares (Wagler, 1824); (E) Amphisbaena alba (Liennaeus, 1758); (F) Caiman latirostris (Daudin, 1802); (G) Paleosuchus palpebrosus (Cuvier, 1807). Photos: M.A. Freitas.
Fig. 7 in Herpetofauna of Marechal Newton Cavalcanti Instruction Center, a hotspot Atlantic Forest fragment in Pernambuco, north-eastern Brazil
Fig. 7. Comparative evaluation of the sampling methods for anurans and reptiles recorded at Marechal Newton Cavalcanti Instruction Center (CMNIC) Atlantic Forest fragment, from August 2008 through December 2009.
Fig. 3 in Herpetofauna of Marechal Newton Cavalcanti Instruction Center, a hotspot Atlantic Forest fragment in Pernambuco, north-eastern Brazil
Fig. 3. Additional anuran species found in the Marechal Newton Cavalcanti Instruction Center Atlantic Forest fragment. (A) Boana crepitans (Wied-Neuwied, 1824); (B) Leptodactylus troglodytes (A. Lutz, 1926); (C) Leptodactylus natalensis (A. Lutz, 1930); (D) Dendropsophus branneri (Cochran, 1948); (E) Boana faber (Wied-Neuwied, 1821); (F) Boana raniceps (Cope, 1862); (G) Boana semilineatus (Spix, 1824); (H) Boana albomarginatus (Spix, 1824); (I) Leptodactylus latrans (Linneaus, 1758); (J) Leptodactylus marmoratus (Steindachner, 1867); (K) Leptodactylus mystacinus (Burmeister, 1861); (L) Leptodactylus fuscus (Schneider, 1799); (M) Leptodactylus vastus (A. Lutz, 1930); (N) Physalaemus cuvieri (Cruz and Pimenta, 2004); (O) Dendropsophus haddadi (Bastos and Pombal, 1996); (P) Dendropsophus minutus (Peters, 1872). Photos: M.A. Freitas.
Fig. 2 in Herpetofauna of Marechal Newton Cavalcanti Instruction Center, a hotspot Atlantic Forest fragment in Pernambuco, north-eastern Brazil
Fig. 2. Anuran species found in the Marechal Newton Cavalcanti Instruction Center Atlantic Forest fragment. (A) Phyllodytes gyrinaethes (Peixoto, Caramaschi, and Freire, 2003); (B) Phyllodytes edelmoi (Peixoto, Caramaschi, and Freire, 2003); (C) Phyllodytes luteolus (Wied-Neuwied, 1824); (D) Pristimantis ramagii (Boulenger, 1888); (E) Pithecopus nordestinus (Caramaschi, 2006); (F) Dendropsophus elegans (Wied-Neuwied, 1824); (G) Scinax cretatus (Nunes and Pombal, 2011); (H) Scinax eurydice (Bokermann, 1968); (I) Scinax x-signatus (Spix, 1824); (J) Dermatonotus muelleri (Boettger, 1885); (K) Elachistocleis ovalis (Schneider, 1799); (L) Stereocyclops incrassatus (Cope, 1870). Photos: M.A. Freitas.
Fig. 1 in Herpetofauna of Marechal Newton Cavalcanti Instruction Center, a hotspot Atlantic Forest fragment in Pernambuco, north-eastern Brazil
Fig. 1. Atlantic Forest fragment of Marechal Newton Cavalcanti Instruction Center (CIMNIC), Pernambuco, Northeastern Brazil. A few other Ecological Reserves located in Pernambuco State, as well as other states in Northeastern Brazil, are also shown.
Fig. 6 in Herpetofauna of Marechal Newton Cavalcanti Instruction Center, a hotspot Atlantic Forest fragment in Pernambuco, north-eastern Brazil
Fig. 6. Snakes species found in the Marechal Newton Cavalcanti Instruction Center Atlantic Forest fragment. (A) Boa constrictor (Linneaus, 1758); (B) Epicrates cenchria (Linneaus, 1758); (C) Chironius flavolineatus (Jan, 1863); (D) Dendrophidion atlantica (Freire, Caramaschi, and Gonçalves, 2010); (E) Spilotes pullatus (Linneaus, 1758); (F) Tantilla melanocephala (Linneaus, 1758); (G) Erythrolamprus almadensis (Wagler, 1824); (H) Erythrolamprus poecilogyrus (Wied-Neuwied, 1825); (I) Erythrolamprus viridis (Wagler, 1824); (J) Helicops angulatus (Linneaus, 1758); (K) Oxybelis aeneus (Wagler, 1824); (L) Oxyrhopus petolarius (Linneaus, 1758); (M) Oxyrhopus trigeminus (Duméril, Bibron, and Dumeril, 1854); (N) Philodryas olferssi (Lichtenstein, 1823); (O) Philodryas patagoniensis (Girard, 1825); (P) Sibynomorphus neuwiedi (Ihering, 1911); (Q) Siphlophis compressus (Daundin, 1803); (R) Xenodon merremii (Wagler, 1824); (S) Thamnodynastes pallidus (Linneaus, 1758); (T) Micrurus leminiscatus (Linneaus, 1758); (U) Micrurus ibiboboca (Merrem, 1820); (V) Amerotyphlops brongersmianus (Vanzolini, 1976); (W) Crotalus durissus (Linneaus, 1758); (X) Lachesis muta (Linneaus, 1766). Photos: M.A. Freitas.
Fig. 5 in Herpetofauna of Marechal Newton Cavalcanti Instruction Center, a hotspot Atlantic Forest fragment in Pernambuco, north-eastern Brazil
Fig. 5. Lacertid species found in the Marechal Newton Cavalcanti Instruction Center Atlantic Forest fragment. (A) Enyalius catenatus (Wied-Neuwied, 1821); (B) Gymnodactylus aff. darwinii (Gray, 1845); (C) Norops fuscoauratus (D'Orbigny, 1837); (D) Tropidurus hispidus (Spix, 1825); (E) Tropidurus semitaeniatus (Spix, 1825); (F) Ameiva ameiva (Linneaus, 1758); (G) Ameivula ocellifera (Spix, 1825); (H) Salvator merianae (Dumeril and Bíbron, 1839); (I) Kentropyx calcarata (Spix, 1825); (J) Cercosaura ocellata (Weagler, 1830); (K) Hemidactylus mabouia (Moreau de Jonnés, 1818); (L) Iguana iguana (Linneaus, 1758); (M) Coleodactylus meridionalis (Boulenger, 1888); (N) Polychrus marmoratus (Linneaus, 1758); (O) Strobilurus torquatus (Wiegmann, 1834). Photos: M.A. Freitas.
Fig. 1 in Overwintering developmental stages of emerald ash borer in North Carolina
Fig. 1. Length of the terminal process of emerald ash borer (Agrilus planipennis) larvae collected under bark in the winters of 2017 to 2020 (n = 547 total).
Fig. 2 in Overwintering developmental stages of emerald ash borer in North Carolina
Fig. 2. (A) Balcha indica (Eupelmidae); (B) Eurytoma sp. (Eurytomidae); (C) Spathius sp. (Braconidae: Doryctinae); (D) Atanycolus cf. cappaerti (Braconidae: Braconinae); (E) Xorides humeralis (Ichneumonidae: Xoridinae). Not to scale. Photographs by Matt Bertone.
Fig. 4 in Leocrates bitungensis (Hesionidae, Annelida): a new polychaete species from North Sulawesi, Indonesia
Fig. 4. Parapodia and chaetae of Leocrates bitungensis, new species. A, anterior parapodium (chaetiger 3); B, middle parapodium (chaetiger 8); C, posterior parapodium (chaetiger 15); D, close-up of a mid-parapodial neurochaeta (chaetiger 8). Abbreviations: cir = cirrophore; dc = dorsal cirrus; nec = neurochaetae; nel = neuroacicular lobe; neu = neuropodium; noc = notochaetae; nol = notoacicular lobe; not = notopodium; vc = ventral cirrus. Scale bar A, B, C = 200 Mm; D, 25 Mm.
Fig. 2 in Leocrates bitungensis (Hesionidae, Annelida): a new polychaete species from North Sulawesi, Indonesia
Fig. 2. Whole body of Leocrates bitungensis, new species. A, dorsal view; B, ventral view. Scale bar = 1 mm.
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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.
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.