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FIGURES 29–35 in Acarine biocontrol agents Neoseiulus californicus sensu Athias-Henriot (1977) and N. barkeri Hughes (Mesostigmata: Phytoseiidae) redescribed, their synonymies assessed, and the identity of N. californicus (McGregor) clarified based on examination of types
FIGURES 29–35. Neoseiulus californicus sensu Athias-Henriot (1977). Male: 29. Dorsal idiosoma (slide lot #26, Table 1); 30. Ventral idiosoma (lot #28); 31. Dorsal and 32. ventrianal shields of a paratype of N. chilenensis (conspecific with specimens of N. californicus sensu Athias-Henriot; lot #43); 33. Sternal shields (lots #25 and 28); 34. Ventrianal shield (lot #26); 35. Chelicerae and spermatodactyls: (a–b) lateral aspect (a: antiaxial, b: paraxial) (c–d) dorsal aspect; specimens from (a–c) lots #40–41 and (d) lot #28. [n.b. Figs 33–35 are at the same scale (shown as 50 µm, between Figs. 33 and 35), but are also at the same scale as Figs 29–30 (scale shown as 100 µm). Figs 31–32 are on the same scale].
FIGURES 19–24 in Acarine biocontrol agents Neoseiulus californicus sensu Athias-Henriot (1977) and N. barkeri Hughes (Mesostigmata: Phytoseiidae) redescribed, their synonymies assessed, and the identity of N. californicus (McGregor) clarified based on examination of types
FIGURES 19–24. Gnathotectum (19, 20) and subcapitulum (21–24). Neoseiulus barkeri: 19, 21. Female, 23. Male (specimens from slide lot #17, Table 1). Neoseiulus californicus sensu Athias-Henriot (1977): 20, 22. Females (from lot #27), 24. Male (lot #28). Legend: dd—deutosternal denticles; im—internal malae; lo—hyaline lobe, present in males only; gt—gnathotectum. All figures at the same scale, shown in Fig. 20.
FIGURES 4–8 in Acarine biocontrol agents Neoseiulus californicus sensu Athias-Henriot (1977) and N. barkeri Hughes (Mesostigmata: Phytoseiidae) redescribed, their synonymies assessed, and the identity of N. californicus (McGregor) clarified based on examination of types
FIGURES 4–8. Males: 4. Chelicerae and spermatodactyls of (a) Neoseiulus californicus holotype; (b) N. barkeri paralectotype (paraxial view); (c) other N. barkeri from Finland (slide lot #16, Table 1); (d) South Korea (dorsal view; slide lot #17). 5–6. Detail of N. barkeri male idiosoma (5) dorsum and (6) venter, based on a specimen from California with similar collection data to that of N. californicus type (slide lot #3, Table 1). 7. Detail of gland opening gv3 (between JV2 setae) on N. barkeri male ventrianal shield region (from slide lot # 15). 8. Detail of N. barkeri gland openings gd4 of (a) paralectotype; (b–e) Finland specimens (slide lot #16, Table 1); (f) South Korea specimens (slide lot #17). [n.b. 8a, c, e present both left and right gd4 of individual males, at different depths, while 8b, d, f present only left gd4; green arrows indicate the point where the gland duct leads deeper into the body. Poroids id5, id2, idm1–6, and idx shown in 5 are based on observations on male from slide lots #15– 17; poroid idm5 is not shown here in 5, being near the posterior edge of the shield, which is curved on the specimen illustrated; poroids ivo, ivp and sigillae in 6 are mostly based on observations on males from slide lots #16 and 17.]
FIGURES 25–28. Neoseiulus barkeri. Legs I–IV in Acarine biocontrol agents Neoseiulus californicus sensu Athias-Henriot (1977) and N. barkeri Hughes (Mesostigmata: Phytoseiidae) redescribed, their synonymies assessed, and the identity of N. californicus (McGregor) clarified based on examination of types
FIGURES 25–28. Neoseiulus barkeri. Legs I–IV, based primarily on the holotype of N. mckenziei (=jun. syn. of N. barkeri; slide lot #9, Table 1). 25–28. includes femora, genua, and tibiae of legs I, II, III, IV, respectively; 28. Basitarsus IV also included. All setae are labelled except dorsals (ad1–2, pd1–2) of genu II–IV to avoid incumbrance.
FIGURES 36–41 in Acarine biocontrol agents Neoseiulus californicus sensu Athias-Henriot (1977) and N. barkeri Hughes (Mesostigmata: Phytoseiidae) redescribed, their synonymies assessed, and the identity of N. californicus (McGregor) clarified based on examination of types
FIGURES 36–41. Neoseiulus californicus sensu Athias-Henriot (1977). Female: 36. Dorsal idiosoma (slide lot #28, Table 1); 37. Ventral idiosoma, metapodal platelets in inset (lot #27); 38–39. Chelicerae (lots #39 and 36); 40. Sternal and 41. ventrianal shields of a paratype of N. chilenensis (= N. californicus sensu Athias-Henriot; lot #43). Legend: MDt—movable digit teeth; pd—pilus dentilis; pr—proximal (paraxial) teeth of fixed digit; su—subapical (antiaxial) teeth of fixed digit.
FIGURE 1 in Acarine biocontrol agents Neoseiulus californicus sensu Athias-Henriot (1977) and N. barkeri Hughes (Mesostigmata: Phytoseiidae) redescribed, their synonymies assessed, and the identity of N. californicus (McGregor) clarified based on examination of types
FIGURE 1. Photographs of the slides of key specimens studied: (a) Holotype of Typhlodromus californicus (male) (verbatim transcription of left label: "Garman says this is prob. a new sp.", "TYPE"; see Table 1, slide lot #1 for info from the right label); (b) Syntypes of T. mungeri (2 females; verbatim transcription of right label: "Garman says this is a n. sp.", "TYPE"; Table 1, lot #2); (c–g) Other specimens from lemon, in southern California (1952–1958) identified by authors as N. barkeri ((c) has a male and female; (d–g) have single females), corresponding to slide lots #3–6, respectively (see Table 1 for label details); (h) A female syntype of N. barkeri Hughes (slide lot #7, Table 1). [n.b. (h) is herein designated as lectotype of N. barkeri (verbatim transcription of left label: "Laelaptidae n. gen.", "Neoseiulus", "type", "barkeri", "sprouting barley", "Barker", "11.5.45"). Slides in (a, b, e–g) were labelled by E.A. McGregor, based on comparison with labels on slides of species that he originally collected and/or described (including types). Slides in (c, d) were most probably labelled by Francis Munger (USDA, Whittier, California), based on comparison with other labels on slides of specimens he collected.]
FIGURES 12–15 in Acarine biocontrol agents Neoseiulus californicus sensu Athias-Henriot (1977) and N. barkeri Hughes (Mesostigmata: Phytoseiidae) redescribed, their synonymies assessed, and the identity of N. californicus (McGregor) clarified based on examination of types
FIGURES 12–15. Neoseiulus barkeri. Female: 12–13. Dorsal and ventral idiosoma of specimen from western Canada (slide lot #12, Table 1); opisthogastric region of specimens from (14) California (lot #5) and (15) New Jersey (N. picketti holotype = jun. syn. of N. barkeri; lot #10). [n.b. green arrows indicate gland openings and poroids of particular interest. All figures at the same scale, shown in 12].
FIGURES 10–11 in Acarine biocontrol agents Neoseiulus californicus sensu Athias-Henriot (1977) and N. barkeri Hughes (Mesostigmata: Phytoseiidae) redescribed, their synonymies assessed, and the identity of N. californicus (McGregor) clarified based on examination of types
FIGURES 10–11. Females: 10. Dorsal and ventral idiosoma of Neoseiulus barkeri lectotype. 11. Spermathecae of N. mungeri lectotypes (a) and paralectotype (b), and of N. barkeri lectotype (c). [n.b. Several setae on 10b appear shorter than they are because they are bent in the Z-axis; arrow on 11c indicates thickened calyx wall]
FIGURE 9 in Acarine biocontrol agents Neoseiulus californicus sensu Athias-Henriot (1977) and N. barkeri Hughes (Mesostigmata: Phytoseiidae) redescribed, their synonymies assessed, and the identity of N. californicus (McGregor) clarified based on examination of types
FIGURE 9. Females: dorsal and ventral idiosoma of (a, b) Neoseiulus mungeri lectotype, and of (c, d) N. barkeri, based on a specimen from California with similar collection data to that of N. mungeri type (slide lot #3, Table 1).
FIGURE 2 in Acarine biocontrol agents Neoseiulus californicus sensu Athias-Henriot (1977) and N. barkeri Hughes (Mesostigmata: Phytoseiidae) redescribed, their synonymies assessed, and the identity of N. californicus (McGregor) clarified based on examination of types
FIGURE 2. Photographs of the type specimens examined: (a) Typhlodromus californicus holotype (male) (slide lot #1, Table 1); (b, c) T. mungeri lectotype and paratype (females), respectively (slide lot #2); (d, e) Neoseiulus barkeri lectotype (female) and paralectotype (male), respectively (slide lot #7); (f) T. chilenensis paralectotype (female) (slide lot #43).
FIGURE 3 in Acarine biocontrol agents Neoseiulus californicus sensu Athias-Henriot (1977) and N. barkeri Hughes (Mesostigmata: Phytoseiidae) redescribed, their synonymies assessed, and the identity of N. californicus (McGregor) clarified based on examination of types
FIGURE 3. Males: (a, c) dorsal shield and ventral idiosoma of Neoseiulus californicus holotype (male); (b, d) and of N. barkeri paralectotype (male).
FIGURE 16 in Acarine biocontrol agents Neoseiulus californicus sensu Athias-Henriot (1977) and N. barkeri Hughes (Mesostigmata: Phytoseiidae) redescribed, their synonymies assessed, and the identity of N. californicus (McGregor) clarified based on examination of types
FIGURE 16. Neoseiulus barkeri (including jun. syn. of N. barkeri). Female chelicerae: (a) Neoseiulus mungeri lectotype; (b) N. barkeri lectotype; N. barkeri females from (c–e) California (c–d: slide lot #3; e: lot #6, Table 1); (f) New Jersey (N. picketti holotype; lot #10); and (g) South Korea (lot #17). [n.b. (c, d) are from the same individual, (a, b, c, f) are in paraxial view, (d, e) in antiaxial view, (g) in dorsal view. Legend: MDt—movable digit tooth; MD L—movable digit length; pr—proximal (paraxial) teeth of fixed digit; pdb—base of pilus dentilis; su—subapical (antiaxial) teeth of fixed digit].
FIGURES 6–9 in Resolving cryptic species with morphology and DNA; thrips as a potential biocontrol agent of Brazilian peppertree, with a new species and overview of Pseudophilothrips (Thysanoptera)
FIGURES 6–9. Pseudophilothrips species. (6) P. ichini pronotum and metanotum. (7) P. gandolfoi pronotum and metanotum. (8) P. gandolfoi holotype head and pronotum. (9) P. gandolfoi holotype pelta and tergites II–III.
FIGURES 1–4 in Resolving cryptic species with morphology and DNA; thrips as a potential biocontrol agent of Brazilian peppertree, with a new species and overview of Pseudophilothrips (Thysanoptera)
FIGURES 1–4. Pseudophilothrips from Schinus terebinthifolius. (1) colony of adults inducing leaf distortion. (2) P. gandolfoi red larvae. (3) P. ichini orange larvae. (4) P. gandolfoi holotype antenna.
FIGURE 5 in Resolving cryptic species with morphology and DNA; thrips as a potential biocontrol agent of Brazilian peppertree, with a new species and overview of Pseudophilothrips (Thysanoptera)
FIGURE 5. Relationships of thrips inferred using the neighbor-joining method and Kimura 2-parameter pairwise distances of mitochondrial COI sequences. Bootstrap values are shown next to the branches.
Data from: Descriptive multi-agent epidemiology via molecular screening on Atlantic salmon farms in the northeast Pacific Ocean
<p>Rapid expansion of salmon aquaculture has resulted in high-density populations that host diverse infectious agents, for which surveillance and monitoring are critical to disease management. Screening can reveal infection diversity from which disease arises, differential patterns of infection in live and dead fish that are difficult to collect in wild populations, and potential risks associated with agent transmission between wild and farmed hosts. We report results from a multi-year infectious-agent screening program of farmed salmon in British Columbia, Canada, using quantitative PCR to assess presence and load of 58 infective agents (viruses, bacteria, and eukaryotes) in 2931 Atlantic salmon (Salmo salar). Our analysis reveals temporal trends, agent correlations within hosts, and agent-associated mortality signatures. Multiple agents, most notably Tenacibaculum maritimum, were elevated in dead and dying salmon. We also report detections of agents only recently shown to infect farmed salmon in BC (Atlantic salmon calicivirus, Cutthroat trout virus-2), detection in freshwater hatcheries of two marine agents (Kudoa thyrsites and Tenacibaculum maritimum), and detection in the ocean of a freshwater agent (Flavobacterium psychrophilum). Our results provide information for farm managers, regulators, and conservationists, and enable further work to explore patterns of multi-agent infection and farm/wild transmission risk.</p>
Genome sequencing of Pachypeltis micranthus Mu et Liu (Hemiptera: Miridae), a potential biological control agent for Mikania micrantha
<p><span>The plant bug, <i>Pachypeltis micranthus</i> Mu et Liu (Hemiptera: Miridae), is a potential biological control agent for <i>Mikania micrantha</i> H.B.K. (Asteraceae; one of the most invasive weeds worldwide). To date, only a few studies have investigated plant bugs. Here, we performed a chromosome-level genome assembly of <i>P. micranthus</i> using MGISEQ-2000 short-read, Nanopore, PacBio long-read, and high-throughput chromosome conformation capture (Hi-C) techniques. The assembled genome was 712.72 Mb in size, with a contig N50 of 16.84 Mb. Using the Hi-C technique, 71 scaffolds were assembled into 15 chromosomes, accounting for 99.96%. We predicted 11,746 protein-coding genes in <i>P. micranthus</i> with 96.20% complete benchmarking universal single-copy orthologs. Phylogenomic analysis showed that <i>P. micranthus</i> and two other Miridae bugs (<i>Apolygus lucorum</i> and <i>Nesidiocoris tenuis</i>) diverged from the common ancestor approximately 200.01 million years ago. Chromosome synteny analysis between <i>P. micranthus</i> and <i>A. lucorum</i> indicated high-level synteny. Many gene families including chemosensory genes and digestive and detoxification enzyme genes—were significantly expanded in the <i>P. micranthus</i> genome. These expanded gene families may indicate the bug to adapt to the single host plant. This high-quality chromosome-level genome assembly provides an invaluable resource for further molecular and evolutionary research on mirid bugs and also provides a basis for further research on biological control mechanisms for<i> M. micrantha</i>.</span></p>
Elemental bioimaging and transcriptomics – no evidence of altered gene expression after single injection of Gadolinium-based contrast agents in mice cerebellum
<p>single read RNA data for GBCA study</p>
IO2 - I am A Change Agent – What R U?
<p>The project outcome <strong>I am A Change Agent – What R U? </strong>is a video documentary co-created by the secondary school student teams. The project movie delivers highly valuable insight into the reactions of the young students that participated in the project towards this new open schooling learning method: <em>what they learned</em>, <em>how they learned</em> <em>it</em>, <em>what went well</em> and <em>what was too complicated</em>.</p>
Supplementary material 1 from: Lahey Z, Chen H, Dowton M, Austin AD, Johnson NF (2023) The genome of the egg parasitoid Trissolcus basalis (Wollaston) (Hymenoptera, Scelionidae), a model organism and biocontrol agent of stink bugs. Journal of Hymenoptera Research 95: 31-44. https://doi.org/10.3897/jhr.95.97654
Genome of the egg parasitoid Trissolcus basalis (Wollaston) (Hymenoptera, Scelionidae), a model organism and biocontrol agent of stink bugs
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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.