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412 results for “pest species”
Figure 1 in Key to Florida Alydidae (Hemiptera: Heteroptera) and selected exotic pest species
Figure 1. Images of diagnostic characters for couplets 1 and 2. (a) Hyalymenus sp., hind femur; (b) Stenocoris tipuloides, hind femur; (c) Stenocoris tipuloides, scent gland evaporative area; (d) Esperanza texana, scent gland evaporative area.
Figures 13–18. Female genitalia. 13 in Two species of Compsus Schoenherr, new citrus pests from Colombia (Coleoptera: Curculionidae: Entiminae)
Figures 13–18. Female genitalia. 13) C. obliquatus–sternum VIII. 14) C. obliquatus–spermatheca. 15) C. viridivittatus–sternum VIII. 16) C. viridivittatus–spermatheca. 17) C. viridivittatus–ovipositor, dorsal view. 18) C. viridivittatus–ovipositor, lateral view.
Figures 5–8. Habitus. 5 in Two species of Compsus Schoenherr, new citrus pests from Colombia (Coleoptera: Curculionidae: Entiminae)
Figures 5–8. Habitus. 5) C. viridivittatus–male dorsal. 6) C. viridivittatus–male lateral. 7) C. viridivittatus–female dorsal. 8) C. viridivittatus–female lateral.
Figures 1–4. Habitus. 1 in Two species of Compsus Schoenherr, new citrus pests from Colombia (Coleoptera: Curculionidae: Entiminae)
Figures 1–4. Habitus. 1) C. obliquatus–male dorsal. 2) C. obliquatus–male lateral. 3) C. obliquatus–female dorsal. 4) C. obliquatus–female lateral.
Figures 9–12. Male median Lobe. 9 in Two species of Compsus Schoenherr, new citrus pests from Colombia (Coleoptera: Curculionidae: Entiminae)
Figures 9–12. Male median Lobe. 9) C. obliquatus–dorsal. 10) C. obliquatus –lateral. 11) C. viridivittatus–dorsal. 12) C. viridivittatus–lateral.
Figs 22–31 in Determination of sexual dimorphism in the puparia of four whitefly pest species from India (Hemiptera: Aleyrodidae)
Figs 22–31. Sexual dimorphism in puparia of Dialeurodes delhiensis David & Sundararaj, 1992. 22, 26, 31 – males; 23, 27 – male vasiform orifice and caudal furrow; 24, 28, 30 – females; 25, 29 – female vasiform orifice and caudal furrow.
Figs 1–3 in Determination of sexual dimorphism in the puparia of four whitefly pest species from India (Hemiptera: Aleyrodidae)
Figs 1–3. Morphometric measurements considered for sexual dimorphism in whitefly puparia. 1 – puparium, dorsal view; 2, 3 – enlarged view, vasiform orifice and caudal furrow. LP – puparium length; BP – puparium width; AL – antennal length; L7AS – seventh abdominal segment length, WVO – vasiform orifice width; LVO – vasiform orifice length; WO – operculum width; LO – operculum length; LL – lingula length; LCF – caudal furrow length.
Figs 12–21 in Determination of sexual dimorphism in the puparia of four whitefly pest species from India (Hemiptera: Aleyrodidae)
Figs 12–21. Sexual dimorphism in puparia of Bemisia tabaci (Gennadius, 1889). 12, 14, 20 – males; 13, 15 – male vasiform orifice and caudal furrow; 16, 18, 21 – females; 17, 19 – female vasiform orifice and caudal furrow.
Figs 4–11 in Determination of sexual dimorphism in the puparia of four whitefly pest species from India (Hemiptera: Aleyrodidae)
Figs 4–11. Sexual dimorphism in puparia of Aleyrodes sp. 4, 6 – males; 5, 7 – male vasiform orifice and caudal furrow; 8, 10 – females; 9, 11 – female vasiform orifice and caudal furrow.
Figs 48–55 in Determination of sexual dimorphism in the puparia of four whitefly pest species from India (Hemiptera: Aleyrodidae)
Figs 48–55. Scatter plots generated through PCA using ratios of puparium morphometric characters and differentiating sexes. 48, 49 – Aleyrodes sp.; 50, 51 – Bemisia tabaci (Gennadius, 1889); 52, 53 – Dialeurodes delhiensis Dialeurodes delhiensis David & Sundararaj, 1992; 54, 55 – Trialeurodes vaporariorum Westwood, 1856.
Fig. 2 in Community structure of termites in a hill dipterocarp forest of Belum- Temengor Forest Complex, Malaysia: emergence of pest species
Fig. 2. The composition of termite assemblages in the natural forest and disturbed forest areas of the Belum–Temengor Forest Complex.
Fig. 1 in Community structure of termites in a hill dipterocarp forest of Belum- Temengor Forest Complex, Malaysia: emergence of pest species
Fig. 1. Map of Belum–Temengor Forest Complex and location of study sites. Sites: SK = Sungai [=River] Kejar; SM = Sungai Mes; ST = Sungai Telang; SG = Sungai Gadong; SKJBC = Sungai Kejar Base Camp; SKNBC = Sungai Kenarong Base Camp; PB = Pulau [=Island] Bendong; PP = Pulau Pertanian.
Fig. 3 in Community structure of termites in a hill dipterocarp forest of Belum- Temengor Forest Complex, Malaysia: emergence of pest species
Fig. 3. The different compositions of termite feeding groups in natural forest and disturbed forest areas within the Belum–Temengor Forest Complex.
Figure 2 in Predatory mites, a green pesticide, and an entomopathogenic compound: A proposed IPM tactic based on pest species diversity indices and population dynamics
Figure 2. Schematic diagram of the experiment's plantation and IPM methodology, C.n: Cydnoseius negevi, A.s: Amblyseius swirskii, and P.p Phytoseiulus persimilis. (Photo credits: Dr. Zidan has created this diagram on www.biorender.com).
Figure 1 in Predatory mites, a green pesticide, and an entomopathogenic compound: A proposed IPM tactic based on pest species diversity indices and population dynamics
Figure 1. Google Earth map photography of the experimental locations (pointed with pin) – i) Om Sabir, Kom Hamada, El Beheira Governorate (30° 29' 50.6" N, 30° 46' 18.8" E), and ii) Kom Oshim, Fayoum Governorate (29° 34' 40.9" N, 30° 55' 38.3" E).
Data from: DNA metabarcoding for biodiversity monitoring in a national park: screening for invasive and pest species
Open the record for dataset details and reuse information.
Simulation models from: Can CRISPR-mediated gene drive work in pest and beneficial haplodiploid species?
<p>Gene drives based on CRISPR/Cas9 have the potential to reduce the enormous harm inflicted by crop pests and insect vectors of human disease, as well as to bolster valued species. In contrast with extensive empirical and theoretical studies in diploid organisms, little is known about CRISPR gene drive in haplodiploids, despite their immense global impacts as pollinators, pests, natural enemies of pests, and invasive species in native habitats. Here we analyze mathematical models demonstrating that, in principle, CRISPR homing gene drive can work in haplodiploids, as well as at sex-linked loci in diploids. However, relative to diploids, conditions favoring the spread of alleles deleterious to haplodiploid pests by CRISPR gene drive are narrower, the spread is slower, and resistance to the drive evolves faster. By contrast, the spread of alleles that impose little fitness cost or boost fitness was not greatly hindered in haplodiploids relative to diploids. Therefore, altering traits to minimize damage caused by harmful haplodiploids, such as interfering with transmission of plant pathogens, may be more likely to succeed than control efforts based on introducing traits that reduce pest fitness. Enhancing fitness of beneficial haplodiploids with CRISPR gene drive is also promising.</p>
Data from: Introgression between divergent corn borer species in a region of sympatry: implications on the evolution and adaptation of pest arthropods
The Asian corn borer, Ostrinia furnacalis, and European corn borer, O. nubilalis (Lepidoptera: Crambidae), cause damage to cultivated maize in spatially distinct geographies, and have evolved divergent hydrocarbons as the basis of sexual communication. The Yili area of Xinjiang Uyghur Autonomous Region in China represents the only known region where O. furnacalis has invaded a native O. nubilalis range, and these two corn borer species have made secondary contact. Genetic differentiation was estimated between Ostrinia larvae collected from maize plants at 11 locations in Xinjiang Province, and genotyped using high throughput SNP and microsatellite markers. Maternal lineages were assessed by direct sequencing of mitochondrial cytochrome c oxidase subunit I and II haplotypes, and a high degree of genotypic diversity was demonstrated between lineages based on SNP genotypes. Furthermore, historical introgression was predicted among SNP genotypes only at sympatric locations in the Yili area, whereas in Xinjiang populations wherein only O. furnacalis haplotypes were detected no analogous introgressed genotypes were predicted. Our detection of putative hybrids and historical evidence of introgression defines Yili area as a hybrid zone between the species in normal ecological interactions, and furthermore might indicate that adaptive traits could spread even between seemingly divergent species through horizontal transmission. Results of this study indicate there may be a continuum in the degree of reproductive isolation between Ostrinia species, and that the elegance of distinct and complete speciation based on modifications to the pheromone communication might need to be reconsidered.
Thermal requirements for egg development of two endemic Wiseana pest species (Lepidoptera: Hepialidae) of economic importance
<p>Raw and analyzed data for our paper title "Thermal requirements for egg development of two endemic <em>Wiseana</em> pest species (Lepidoptera: Hepialidae) of economic importance". </p>
Pest species preyed upon by bats and the crop types affected by them.
<p>This database compiles the pest species consumed by bats and the crop types they attack, as part of the supplementary material of the article entitled "<strong>Pest suppression by bats and management strategies to favour it: a global review</strong>", published in the journal Biological Reviews.</p> <p>The crop types were classified into several categories this work: cereals (e.g. wheat, maize, corn, rice, barley, sorghum); forest (e.g. beech, oak, poplar, willow); fruit crops (e.g. apple, pear, apricot, strawberry, cranberry); grasses (e.g. sugarcane, turfs, pastures); legumes (e.g. pea, bean, alfalfa, soybean); ornamental (e.g. garden species); other (cotton, tea, tobacco, hop, flax, rubber tree, hemp, peppermint, jute, rapeseed, kenaf, ashwagandha, mushrooms, honeybees); stored products (e.g. stored cereals, stored tobacco, dried fruits); and vegetables (e.g. tomato, lettuce, spinach, potato, onion).</p>
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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.