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Fig. 5 in Biological control of the twospotted spider mite (Trombidiformes: Tetranychidae) with the predatory mite Neoseiulus californicus (Mesotigmata: Phytoseiidae) in blackberries
Fig. 5. Population of T. urticae (TU) and N. californicus (NC) motiles in N. californicus (A), Abamectin, and unsprayed (control) (B), plots on Arapaho variety in a field experiment. (The arrows on the graph indicate the time of treatment and mite density at that time.)
Fig. 3 in Biological control of the twospotted spider mite (Trombidiformes: Tetranychidae) with the predatory mite Neoseiulus californicus (Mesotigmata: Phytoseiidae) in blackberries
Fig. 3. Population of T. urticae (TU) and N. californicus (NC) eggs stages in N. californicus (A), Abamectin, and unsprayed (control) (B), plots on Arapaho variety in a greenhouse experiment.
Fig. 1 in Biological control of the twospotted spider mite (Trombidiformes: Tetranychidae) with the predatory mite Neoseiulus californicus (Mesotigmata: Phytoseiidae) in blackberries
Fig. 1. Population of T. urticae (TU) and N. californicus (NC) motiles in treatments of N. californicus (A), Abamectin, and unsprayed (control) plots (B), on Arapaho variety in a greenhouse experiment. (The arrows on the graph indicate the time of treatment and mite density at that time.)
Fig. 6 in Biological control of the twospotted spider mite (Trombidiformes: Tetranychidae) with the predatory mite Neoseiulus californicus (Mesotigmata: Phytoseiidae) in blackberries
Fig. 6. Population of T. urticae (TU) and N. californicus (NC) motiles in treatments of N. californicus (A), Abamectin, and unsprayed (control) (B), plots on Navaho variety in a field experiment. (The arrows on the graph indicate the time of treatment and mite density at that time.)
Fig. 10 in Biological control of the twospotted spider mite (Trombidiformes: Tetranychidae) with the predatory mite Neoseiulus californicus (Mesotigmata: Phytoseiidae) in blackberries
Fig. 10. Population of T. urticae (TU) and N. californicus (NC) eggs in treatments of N. californicus (A), Abamectin, and unsprayed (control) (B), plots on Ouachita variety in a field experiment. (The arrows on the graph indicate the time of treatment and mite density at that time.)
Fig. 1 in Predatory behaviors: Pristimantis savagei (Anura: Craugastoridae) as prey of Trechalea sp. spiders (Araneae: Trechaleidae) in a sector of the Piedemonte Llanero, Villavicencio, Colombia
Fig. 1. Site of Pristimantis savagei predation by Trechalea sp., in a sector of Piedemonte Villavicencio-Meta, Colombia. The red dot indicates the exact site of discovery in the Caño Buque.
Fig. 2 in Predatory behaviors: Pristimantis savagei (Anura: Craugastoridae) as prey of Trechalea sp. spiders (Araneae: Trechaleidae) in a sector of the Piedemonte Llanero, Villavicencio, Colombia
Fig. 2. Record of predation of Pristimantis savagei by Trechalea sp., in a sector of Piedemonte, Villavicencio-Meta, Colombia.
Fig. 3 in Predatory behaviors: Pristimantis savagei (Anura: Craugastoridae) as prey of Trechalea sp. spiders (Araneae: Trechaleidae) in a sector of the Piedemonte Llanero, Villavicencio, Colombia
Fig. 3. Warning stance of the spider Trechalea sp. The individual was on a rock at an approximate height of 150 cm, less than 1 m from the water source.
Fig. 1 in Identification of predatory and parasitoid insect species associated with Melanaphis sacchari (Hemiptera: Aphididae), a sorghum pest in Nuevo León, Mexico
Fig. 1. Melanaphis sacchari predators and parasitoids found in Nuevo León, Mexico. (A) Allograpta sp. in adult status, (B) Chilocorus cacti (lef), and Chilocorus stigma (right), (C) Olla v-nigrum, (D) Chrysoperla sp., (E) Allograpta sp. (lef) in larval status, and Cycloneda sanguinea (right), (F) Hippodamia convergens, (G) Ocyptamus dimidiatus, (H) Scymnus sp., (I) Pachyneuron sp., (J) Aphidius sp., (K) Melanaphis sacchari mummies.
Fig. 4 in Assessment of the predatory capacity on mosquito larvae of Jenynsia multidentata (Anablepidae) in presence of vegetation under laboratory conditions
Fig. 4. Daily consumption (mean ±SD) of Jenynsia multidentata (Jenyns, 1842) on 120 Culex pipiens Linnaeus, 1758 fourth-stage larvae. (T1) 20 stems, (TC) without stems, for 5 days.
Fig. 2 in Assessment of the predatory capacity on mosquito larvae of Jenynsia multidentata (Anablepidae) in presence of vegetation under laboratory conditions
Fig. 2. Daily consumption (mean ±SD) of Jenynsia multidentata (Jenyns, 1842) on 60 Culex pipiens Linnaeus, 1758 fourth-stage larvae at different densities of vegetation: (T1) 20 stems, (T2) 10 stems and (TC) without stems, for 5 days.
Fig. 1 in Assessment of the predatory capacity on mosquito larvae of Jenynsia multidentata (Anablepidae) in presence of vegetation under laboratory conditions
Fig. 1. Jenynsia multidentata (Jenyns, 1842) consumption of 60 Culex pipiens Linnaeus, 1758 fourth-stage larvae at different vegetation densities: (T1) 20 stems, (T2) 10 stems and (TC) without stems. Each circle represents the daily consumption of a female specimen and the horizontal bars indicate the average consumption. The letters (a, b) at the top of the figure indicate significant differences between treatments (p <0.05).
Fig. 3 in Assessment of the predatory capacity on mosquito larvae of Jenynsia multidentata (Anablepidae) in presence of vegetation under laboratory conditions
Fig. 3. Jenynsia multidentata (Jenyns, 1842) consumption of 120 Culex pipiens Linnaeus, 1758 fourth-stage larvae at different vegetation densities: (T1) 20 stems and (TC) without stems. Each circle represents the daily consumption of a female specimen and the horizontal bars indicate the average consumption.
Fig. 1. Phyllodytes luteolus Wied, 1824 in Disgusting or delicious? Predatory behavior of the hylid frog Phyllodytes luteolus on sympatric ants
Fig. 1. Phyllodytes luteolus Wied, 1824 manipulating its prey, an ant of the genus Gnamptogenys. Note that the frog has kept the abdominal region of the ant outside of the mouth in order to prevent injuries caused by its sting.
Figure 4 in Description of Prionchulus jonkershoekensis n. sp. (Nematoda: Mononchida), a new predatory species from South Africa
Figure 4: A 50% majority rule Bayesian phylogenetic tree of Mononchidae, including PriOnChUlUS JOnkerShOekenSiS n. sp. from South Africa, based on the partial 18 S rDNA sequences under the GTR + G model. The sequence of the new species is in boldface font.
Figure 3 in Description of Prionchulus jonkershoekensis n. sp. (Nematoda: Mononchida), a new predatory species from South Africa
Figure 3: Scanning electron micrographs of PriOnChUlUS JOnkerShOekenSiS n. sp. female. (A) Lip region (Frontal view); (B) Lateral view showing labial and cephalic papillae and amphidial fovea; (C) Tail; (D) Vulva (ventral view). (L.p- Labial papillae, C.p- Cephalic papillae, Am- Amphidial fovea).
Figure 2 in Description of Prionchulus jonkershoekensis n. sp. (Nematoda: Mononchida), a new predatory species from South Africa
Figure 2: Light micrographs of PriOnChUlUS JOnkerShOekenSiS n. sp. female. (A-B) Anterior region in lateral median view; (C) Neck region; (D) Entire body; (E) Pharyno-intestinal junction; (F) Laterial lip region showing amphidial fovea and cuticle striations; (G-H) Vagina; (I) Caudal region.
Figure 5 in Description of Prionchulus jonkershoekensis n. sp. (Nematoda: Mononchida), a new predatory species from South Africa
Figure 5: A 50% majority rule Bayesian phylogenetic tree of Mononchidae, including PriOnChUlUS JOnkerShOekenSiS n. sp. from South Africa, based on the partial 28 S rDNA sequences under the GTR + G model. The sequence of the new species is in boldface font.
Figure 1 in Description of Prionchulus jonkershoekensis n. sp. (Nematoda: Mononchida), a new predatory species from South Africa
Figure 1: Line drawings of PriOnChUlUS JOnkerShOekenSiS n. sp. female. (A) Head region in lateral view; (B) Entire body; (C) Neck region; (D) Pharyngo-intestinal junction (cardia); (E) Anterior genital branch with egg; (F) Posterior genital branch; (G) Rectal region and tail. (Scale bars: A, D = 20 µm; B, C = 100 µm; E, G = 50 µm; F = 10 µm).
Fig. 7 in A large predatory archosaur from the Late Triassic of Poland
Fig. 7. Comparison of the morphology and sizes of femur bones of the Late Triassic archosaurs (all in anterior views). A. Femur of Smok wawelski gen. et sp. nov., ZPAL V.33/45, Lisowice (Lipie Śląskie clay−pit), Late Triassic (lates Norian–early Rhaetian). B. Femur of Liliensternus liliensterni (Huene, 1934), MB.R.2175.7.1, Grossen Gleichberg, Germany, Late Triassic (early Rhaetian). C. Femur of Postosuchus kirckparicki Chatterjee, 1985, TTU− P9002, Miller's Ranch Quarry, Texas, USA (Norian).
ScienceDex guides
Understand access before you commit
These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
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.