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213 results for “interactive key”
FIGURE 5 in A new group of species of the genus Megalothorax (Collembola, Neelidae) with Gondwanan distribution, and introducing an open interactive identification key of Megalothorax species
FIGURE 5. Megalothorax tasmanterolenis sp. nov. (A) Chaetotaxy of antenna, arrow indicates a facultative chaeta. (B) Claw I. (C) Claw II. (D) Claw III. (E) Furca posterior side.
FIGURE 9 in A new group of species of the genus Megalothorax (Collembola, Neelidae) with Gondwanan distribution, and introducing an open interactive identification key of Megalothorax species
FIGURE 9. Megalothorax tasmanterolenis sp. nov. (A) Integument with secondary granules and area of enlarged primary hexagons devoid of secondary granules, abdominal region dorsal side. (B) Integument, with area of enlarged primary granules, dorso-anterior part of head. (C) Enlarged and clear S-chaeta Sa2 on Ant. IV, compared with (D) normal, dark S-chaetae (e.g. Sb3, Sb4, Sb5) on Ant. IV. Megalothorax zealanterolenis sp. nov. (E) mucro with focus on the smooth and waved internal posterior lamella.
FIGURE 4 in A new group of species of the genus Megalothorax (Collembola, Neelidae) with Gondwanan distribution, and introducing an open interactive identification key of Megalothorax species
FIGURE 4. Megalothorax tasmanterolenis sp. nov. (A) Chaetotaxy of trunk tergites from Th. I to Abd. IV, area of repartition of the secondary granulation represented in grey, (B) Head dorsal side. (C, D) anterior side of the labrum anterior process, (D) labrum posterior side. (E) Maxillary outer lobe. (F) Mandibula. (G) Maxilla.
FIGURE 2 in A new group of species of the genus Megalothorax (Collembola, Neelidae) with Gondwanan distribution, and introducing an open interactive identification key of Megalothorax species
FIGURE 2. Megalothorax anterolenis sp. nov. (A, B) Labrum anterior process, (A) posterior side, (B) anterior side. (C) Maxillary outer lobe internal side. (D) Mandibula. (E) Maxilla. (F, G) Antenna (F) posterior side, (G) anterior side. (H) Abd. VI tergite and sternite, Abd. V and IV sternites, and posterior side of manubrium and dens (furca), chaeta and lobe in dotted line are missing on the figured specimen but normally present. (I) dens anterior side. (J) Mucro.
FIGURE 8 in A new group of species of the genus Megalothorax (Collembola, Neelidae) with Gondwanan distribution, and introducing an open interactive identification key of Megalothorax species
FIGURE 8. (A) Diagram of dorsal head chaetotaxy, chaeta in blue present only in M. tasmanterolenis sp. nov. and M. zealanterolenis sp. nov., channel in blue present only in M. tasmanterolenis sp. nov. (B) Diagram of ventral head chaetotaxy. (C) Diagram of antenna chaetotaxy. (D) Body chaetotaxy diagram, s-chaetae shape based on M. anterolenis sp. nov. (E) Connection of integumentary channels and linea ventralis: (a) crossed, (b) transitional form, (c) circular.
FIGURE 7 in A new group of species of the genus Megalothorax (Collembola, Neelidae) with Gondwanan distribution, and introducing an open interactive identification key of Megalothorax species
FIGURE 7. Megalothorax zealanterolenis sp. nov. (A) chaetae of Abd. IV sternites. (B) Leg I. (C) Leg II. (D) Leg III. (E) Claw I. (F) Claw II. (G) Claw III. (H, I, J) Mucro variations.
FIGURE 10 in A new group of species of the genus Megalothorax (Collembola, Neelidae) with Gondwanan distribution, and introducing an open interactive identification key of Megalothorax species
FIGURE 10. Molecular phylogeny of the genus Megalothorax, with optimization of taxonomically relevant character states. New OTUs names are indicated in bold. Bootstrap node support is shown next to the node, only when below 100 %.
Evidence for maintenance of key components of vocal learning in aging budgerigars despite diminished affiliative social interaction
<p>In some species, the ability to acquire new vocalizations persists into adulthood and may be an important mediator of social interactions. While it is generally assumed that vocal learning persists undiminished throughout the lifespan of these open-ended learners, the stability of this trait remains largely unexplored. We hypothesize that vocal learning exhibits senescence, as is typical of complex cognitive traits, and that this decline may relate to age-dependent changes in sociality. The budgerigar (<em>Melopsittacus undulatus</em>), an open-ended learner which develops new contact call types that are shared with social associates upon joining new flocks, provides a robust assay for measuring the effects of aging on vocal learning ability. We formed captive flocks of 4 previously unfamiliar adult males of the same age class, either "young adults" (6 mo.-1 yr.) or "older adults" (≥ 3 yr.), and concurrently tracked changes in contact call structure and social interactions over time. Older adults exhibited decreased vocal diversity, which may be related to the sparser and weaker affiliative bonds observed in older adults. Older adults, however, displayed equivalent levels of vocal plasticity and vocal convergence compared to young adults, suggesting vocal learning ability is largely maintained into later adulthood in an open-ended learner.</p>
An interaction between host and microbe genotypes determines colonization success of a key bumble bee gut microbiota member
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Data from: Uncovering key metabolic determinants of the drug interactions between trimethoprim and erythromycin in Escherichia coli
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Evidence for maintenance of key components of vocal learning in aging budgerigars despite diminished affiliative social interaction
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Carpophiline-ID: An interactive matrix-based key to the carpophiline sap beetles (Coleoptera, Nitidulidae) of Eastern North America
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Data from: MonotomidGen – A matrix-based interactive key to the New World genera of Monotomidae (Coleoptera, Cucujoidea)
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Data from: Interactions among trees: a key element in the stabilising effect of species diversity on forest growth
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Figure 2 in Development of an interactive identification key for Oncaeidae (Copepoda: Cyclopoida)
Figure 2. Leg armature types of oncaeid copepods, grouped according to the spine counts on the exo- and endopods of swimming legs P1 to P4. The number of oncaeid species per armature type is shown on the y-axis. Leg armature type 1 denotes the typical leg armature of oncaeid copepods (cf. Böttger-Schnack and Schnack 2013, table 4), armature type 2 to 14 differ in spine count on the exo- and/or endopods from type 1 (cf. Böttger-Schnack and Schnack 2013, tables 5 and 6). Question marks denote the estimated number of additional, yet undescribed species of that armature type.
Figure 1 in Development of an interactive identification key for Oncaeidae (Copepoda: Cyclopoida)
Figure 1. Screen shot of the Lucid identification key for Oncaeidae, with morphological characters ('features') presented in the top left window, and the copepod taxa (called 'entities') in the top right window. Features and entities (taxa) are organized in several levels of subgrouping and presented as trees, which are partly expanded.
Figure 8 in Development of an interactive identification key for Oncaeidae (Copepoda: Cyclopoida)
Figure 8. Characteristics of P4 endopod (enlarged) in oncaeid species. (A) Conical process present between the two distal spines of P4 endopod (Triconia minuta [from Böttger- Schnack 1999]); (B) Conical process absent (Oncaea paraclevei [from Böttger- Schnack 2001]).
Figure 3 in Development of an interactive identification key for Oncaeidae (Copepoda: Cyclopoida)
Figure 3. Body length of oncaeid copepod species: illustration of size difference between largesized species (Oncaea venusta f. typica [from Böttger-Schnack 2001]) and small-sized species (O. atlantica [from Boxshall and Böttger 1987]).
Figure 7 in Development of an interactive identification key for Oncaeidae (Copepoda: Cyclopoida)
Figure 7. Form types of maxilliped basis (shaded) in oncaeid species: compact (Oncaea compacta [from Heron 1977]); robust-oblong (O. venusta f. typica [from Böttger-Schnack 2001]); elongate (O. bispinosa [from Böttger-Schnack 2002]); very long and narrow (O. tenuimana [original]).
FIGURE 8 in Description and host interactions of a new species of Exetasis Walker (Diptera: Acroceridae), with a key to species of the genus
FIGURE 8. Exetasis jujuyensis Gillung sp. nov. pupa. A. dorsal view; B. lateral view.
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.