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2,507 results for “Species list”
Fig. 1 in Phylogenetics and historical biogeography of Encyclia (Laeliinae: Orchidaceae) with an emphasis on the E. adenocarpos complex, a new species, and a preliminary species list for the genus
Fig. 1 Major biogeographical areas for the distribution of Encyclia. See section of Materials and Methods for details
List of references for species from Argentina with IMTA potential
<p>This is a list of bibliographical references about the aquaculture potential of four species native to the Beagle Channel. This list comprises 175 references with data on the finfish <em>Galaxias maculatus</em>, the mussel <em>Mytilus chilensis</em>, the red sea urchin <em>Loxechinus albus</em> and the halophyte <em>Sarcocornia magellanica</em>.</p>
Figure 6 in The family Dolichopodidae (Diptera) of the Arabian Peninsula: identification key, an updated list of species and new records from Saudi Arabia
Figure 6. Dolichopodid species habitus: a – Micromorphus albipes (Zetterstedt); b – Condylostylus longicornis (Fabricius); c – Sympycnus basilaris (Curran); e – Syntormon pallipes (Fabricius); d – Syntormon pumilus (Meigen).
Figure 5 in The family Dolichopodidae (Diptera) of the Arabian Peninsula: identification key, an updated list of species and new records from Saudi Arabia
Figure 5. Dolichopodid species habitus: a – Thinophilus indigenus Becker; b – Thinophilus ochripalpis Becker; c – Thinophilus promotus Becker; d – Thinophilus spinulosus Parent; e – Medetera grisescens De Meijere; f – Micromorphus aereus (Vaillant).
Figure 3 in The family Dolichopodidae (Diptera) of the Arabian Peninsula: identification key, an updated list of species and new records from Saudi Arabia
Figure 3. Dolichopodid species habitus: a – Asyndetus albifrons Parent; b – Chrysotus suavis Loew; c – Cryptophleps buttikeri Grichanov; d – Diaphorus hoffmannseggi Meigen.
Figure 4 in The family Dolichopodidae (Diptera) of the Arabian Peninsula: identification key, an updated list of species and new records from Saudi Arabia
Figure 4. Dolichopodid species habitus: a – Argyrochlamys cavicola (Parent); b – Hercostomus plagiatus (Loew); c – Tachytrechus brittoni Grichanov; d – Tachytrechus notatus (Stannius).
Figure 1 in The family Dolichopodidae (Diptera) of the Arabian Peninsula: identification key, an updated list of species and new records from Saudi Arabia
Figure 1. The most sampled sites: a – Jazan, Abu Aresh, Al-Mahdag village (Photo by Habib Khemira); b – Jazan, Um Al-Raq Island; c – Asir, Maraba, Al-Hudaithy Fruit Farm; d – Asir, Karatha, Al-Ethrebany Fruit Farm; e – Asir, Abha, Hay Al-Nusub; f – Asir, Al-Souda, Al-Muqtha Dam (Photos by Othman M. Abdullah).
Cannot see the diversity for all the species: evaluating inclusion criteria for local species lists when using abundant citizen science data
Abundant citizen science data on species occurrences is becoming increasingly available and enables identifying composition of communities occurring at multiple sites with high temporal resolution. However, for species displaying temporary patterns of local occurrences, i.e. that are transient to some sites, biodiversity measures are clearly dependent on the criteria used to include species into local species lists. Using abundant opportunistic citizen science data from frequently visited wetlands we investigated the sensitivity of α- and β-diversity estimates to the use raw vs. detection-corrected data and to the use of inclusion criteria for species presence reflecting alternative site use. We tested 7 inclusion criteria (with varying number of days required to be present) on time series of daily occurrence status during a breeding season of 90 days for 77 wetland bird species. We show that even when opportunistic presence-only observation data is abundant, raw data may not produce reliable local species richness estimates and rank sites very differently in terms of species richness. Furthermore, occupancy model based - and - diversity estimates were sensitive to the inclusion criteria used. Total species lists (all species observed at least once during a season) may therefore mask diversity differences among sites in local communities of species, by e.g. including vagrant species on potentially breeding communities and change the relative rank order of sites in terms of species richness. Very high sampling effort does not necessarily free opportunistic data from its inherent bias and can produce a pattern in which many species are observed at least once almost everywhere, thus leading to a possible paradox: the large amount of biological information may hinder its usefulness. Therefore, when prioritizing among sites to manage or preserve species diversity estimates need to be carefully related to relevant inclusion criteria depending on the diversity estimate in focus.
Figure 7 in First record of the genus Stenotus Jakovlev from Australia, with two new species, and a list of mirine species from Witchelina Nature Reserve (Insecta: Heteroptera: Miridae: Mirinae: Mirini)
Figure 7. Habitus view of other Mirini, found in Witchelina Nature Reserve: Chimsunchartella schwartzi, Creontiades dilutus and Taylorilygus apicalis (male and female of each species).
Figure 1 in First record of the genus Stenotus Jakovlev from Australia, with two new species, and a list of mirine species from Witchelina Nature Reserve (Insecta: Heteroptera: Miridae: Mirinae: Mirini)
Figure 1. Habitus view of Stenotus gressitti, Stenotus witchelina and Stenotus binotatus (male and female of each species).
Figure 5 in First record of the genus Stenotus Jakovlev from Australia, with two new species, and a list of mirine species from Witchelina Nature Reserve (Insecta: Heteroptera: Miridae: Mirinae: Mirini)
Figure 5. Male genitalia. Stenotus binotatus: (A) inflated aedeagus, dorsal view; (B) right paramere, dorsal view; (C) left paramere, posterior view; (D) left paramere, dorsal view; (E) genital capsule, dorsal view.
Figure 4 in First record of the genus Stenotus Jakovlev from Australia, with two new species, and a list of mirine species from Witchelina Nature Reserve (Insecta: Heteroptera: Miridae: Mirinae: Mirini)
Figure 4. Male genitalia. Stenotus gressitti: (A) inflated aedeagus, dorsal view; (B) right paramere, dorsal view; (C) left paramere, posterior view; (D) left paramere, dorsal view; (E) genital capsule, dorsal view. Stenotus witchelina: (F) inflated aedeagus, dorsal view; (G) right paramere, dorsal view; (H) left paramere, posterior view; (I) left paramere, dorsal view; (J) genital capsule, dorsal view.
Figure 6 in First record of the genus Stenotus Jakovlev from Australia, with two new species, and a list of mirine species from Witchelina Nature Reserve (Insecta: Heteroptera: Miridae: Mirinae: Mirini)
Figure 6. Female genitalia. Stenotus gressitti: (A) dorsal labiate plate; (D) posterior wall of bursa copulatrix. Stenotus witchelina: (B) dorsal labiate plate; (E) posterior wall of bursa copulatrix. Stenotus binotatus: (C) dorsal labiate plate; (F) posterior wall of bursa copulatrix.
Figure 3 in First record of the genus Stenotus Jakovlev from Australia, with two new species, and a list of mirine species from Witchelina Nature Reserve (Insecta: Heteroptera: Miridae: Mirinae: Mirini)
Figure 3. Scanning electron micrographs. Stenotus gressitti: (A) hind tarsus; (C) pretarsus, lateral view; (D) abdomen, lateral view; (F) pretarsus, dorsal view; (G) pretarsus, ventral view; (H) evaporatorium. Stenotus witchelina: (B) hind tarsus; (E) abdomen, lateral view; (I) evaporatorium.
Figure 2 in First record of the genus Stenotus Jakovlev from Australia, with two new species, and a list of mirine species from Witchelina Nature Reserve (Insecta: Heteroptera: Miridae: Mirinae: Mirini)
Figure 2. Scanning electron micrographs. Stenotus gressitti: (A) head of male, anterior view; (B) head and pronotum of male, dorsal view; (E) head and pronotum of female, lateral view; (I) vestiture on hemelytra. Stenotus witchelina: (C) head and pronotum of male, dorsal view; (D) head of male, anterior view; (F) head and pronotum of female, lateral view; (G) head of female, anterior view; (H) head of female, lateral view.
Figures 9–11 in Three new species of Yponomeutinae (Lepidoptera: Yponomeutidae) from China with faunistic supplements and an updated list of the Chinese species of the subfamily
Figures 9–11. (9) Adult of Zelleria japonicella Moriuti. Notes: Scale bar = 3 mm, (10) Male genitalia and aedeagus (a) of Zelleria japonicella Moriuti. Note: Scale bar = 0.5 mm, (11) Female genitalia of Zelleria japonicella Moriuti. Note: Scale bar = 1 mm.
Figures 5–8 in Three new species of Yponomeutinae (Lepidoptera: Yponomeutidae) from China with faunistic supplements and an updated list of the Chinese species of the subfamily
Figures 5–8. (5) Adult of Euhyponomeutoides spadix Sohn and Wu, n. sp. Note: Scale bar = 5 mm, (6) Adult ofYponomeuta zebra Sohn and Wu, n. sp. Note: Scale bar = 5 mm, (7) Female genitalia of Euhyponomeutoides spadix Sohn and Wu, n. sp. Note: Scale bar = 1 mm, (8) Female genitalia Yponomeuta zebra Sohn and Wu, n. sp. Note: Scale bar = 2 mm.
Figures 1–4 in Three new species of Yponomeutinae (Lepidoptera: Yponomeutidae) from China with faunistic supplements and an updated list of the Chinese species of the subfamily
Figures 1–4. (1) Adult of Cedestis leucopterostigmatis Sohn and Wu, n. sp. Note: Scale bar = 3 mm, (2) Adult of Cedestis exiguata. Note: Scale bar = 3 mm, (3) Female genitalia of Cedestis leucopterostigmatis Sohn and Wu, n. sp. Note: Scale bar = 1 mm, (4) Female genitalia of Cedestis exiguata Note: Scale bar = 1 mm.
FIGURE 2. Anacroneuria bahiensis nymph. A in Perlidae (Plecoptera) from Bahia State, Brazil: description of the nymphs of Anacroneuria bahiensis Righi-Cavallaro & Lecci, notes on Anacroneuria debilis (Pictet), and updated list of the species
FIGURE 2. Anacroneuria bahiensis nymph. A. head and pronotum, dorsal view; B. mesonotum and metanotum, dorsal view; C. abdominal segments 5–10, dorsal view; D. labium, ventral view; E. mandible and maxilla, dorsal view; F. foreleg; G. cercus in proximal, medial and distal sections. Scales: 1 mm for A–F and 0.5 mm for G.
FIGURE 3 in Perlidae (Plecoptera) from Bahia State, Brazil: description of the nymphs of Anacroneuria bahiensis Righi-Cavallaro & Lecci, notes on Anacroneuria debilis (Pictet), and updated list of the species
FIGURE 3. Adult head and pronotum. Anacroneuria bahiensis: A. adult male; B. adult female; C. adult teneral male; A. debilis: D. adult male; E. nymph. Scale: 1 mm.
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.