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569 results for “morphological comparison”
Figure 6 in Morphological comparison and description of five new species of Hyalella (Crustacea: Amphipoda) from Veracruz and Mexico City
Figure 6. Hyalella alvarezi sp. nov. male holotype, 4.4 mm; female paratype, 5 mm. (a) Male gnathopod 1; (b) male gnathopod 2; (c) female gnathopod 1; (d) female gnathopod 2. Male pereiopods: (e) pereiopod 3; (f) pereiopod 4; (g) pereiopod 5; (h) pereiopod 6; (i) pereiopod 7. Scale bars: 100 µm.
Figure 10 in Morphological comparison and description of five new species of Hyalella (Crustacea: Amphipoda) from Veracruz and Mexico City
Figure 10. Hyalella viviannae sp. nov. male holotype, 4.9 mm: (a) uropod 1; (b) uropod 2; (c) uropod 3; (d) telson; (e) pleopod 1. Scale bars: 100 µm.
Figure 5 in Morphological comparison and description of five new species of Hyalella (Crustacea: Amphipoda) from Veracruz and Mexico City
Figure 5. Hyalella alvarezi sp. nov. lateral habitus. (a) Male holotype 4.4 mm. (b) Antenna 1; (c) antenna 2. Buccal parts: (d) maxilla 1; (e) maxilla 2; (f) upper lip; (g) lower lip; (h) left mandible; (i) right mandible; (j) maxilliped. Scale bars: 100 µm.
Figure 9 in Morphological comparison and description of five new species of Hyalella (Crustacea: Amphipoda) from Veracruz and Mexico City
Figure 9. Hyalella viviannae sp. nov. male holotype, 4.9 mm; female paratype, 4 mm. (a) male gnathopod 1; (b) male gnathopod 2; (c) female gnathopod 1; (d) female gnathopod 2. Male pereiopods: (e) pereiopod 3; (f) pereiopod 4; (g) pereiopod 5; (h) pereiopod 6; (i) pereiopod 7. Scale bars: 100 µm.
Figure 4 in Morphological comparison and description of five new species of Hyalella (Crustacea: Amphipoda) from Veracruz and Mexico City
Figure 4. Hyalella sarukhani sp. nov. male holotype, 7.7 mm: (a) uropod 1; (b) uropod 2; (c) uropod 3; (d) telson; (e) pleopod 1. Scale bars: 100 µm.
Figure 13 in Morphological comparison and description of five new species of Hyalella (Crustacea: Amphipoda) from Veracruz and Mexico City
Figure 13. Hyalella villalobosi sp. nov. male holotype, 5.4 mm. (a) Uropod 1; (b) uropod 2; (c) uropod 3; (d) telson; (e) pleopod 1. Scale bars: 100 µm.
Figure 2 in Morphological comparison and description of five new species of Hyalella (Crustacea: Amphipoda) from Veracruz and Mexico City
Figure 2. Hyalella sarukhani sp. nov. lateral habitus: (a) male holotype 7.7 mm; (b) antenna 1; (c) antenna 2. Buccal parts: (d) maxilla 1; (e) maxilla 2; (f) upper lip; (g) lower lip; (h) left mandible; (i) right mandible; (j) maxilliped. Scale bars: 100 µm.
Figure 1 in Morphological comparison and description of five new species of Hyalella (Crustacea: Amphipoda) from Veracruz and Mexico City
Figure 1. Study area. (a) Mexico City: Lake of Chapultepec, canals of Xochimilco, Lake of Chalco; (b) State of Veracruz: Lake San Julian; (c) State of Veracruz: Lake La Encantada and Lake Catemaco. Triangles represent type localities. The figure was created using QGIS version 3.10.0 and assembled from the data sources (shapefiles) of the Instituto Nacional de Estadísitica y Geografía.
Figure 8 in Morphological comparison and description of five new species of Hyalella (Crustacea: Amphipoda) from Veracruz and Mexico City
Figure 8. Hyalella viviannae sp. nov. lateral habitus. (a) male holotype, 4.9 mm. (b) antenna 1; (c) antenna 2. Buccal parts: (d) maxilla 1; (e) maxilla 2; (f) upper lip; (g) lower lip; (h) left mandible; (i) right mandible; (j) maxilliped. Scale bars: 100 µm.
Figure 12 in Morphological comparison and description of five new species of Hyalella (Crustacea: Amphipoda) from Veracruz and Mexico City
Figure 12. Hyalella villalobosi sp. nov. male holotype, 5.4 mm; female paratype, 5.5 mm. (a) male gnathopod 1; (b) male gnathopod 2; (c) female gnathopod 1; (d) female gnathopod 2. Male pereiopods: (e) pereiopod 3; (f) pereiopod 4; (g) pereiopod 5; (h) pereiopod 6; (i) pereiopod 7. Scale bars: 100 µm.
FIGURE 3 in A new subspecies of Short-toed Snake-eagle from Wallacea determined from morphological and DNA comparison
FIGURE 3. Lesser Sundas and Palearctic specimens of C. gallicus. The specimens pictured in Figure 2A are male: the left two are from Flores in the Lesser Sundas, while the rightmost specimen is from Romania. The specimen in the center is the holotype of our new C. gallicus sacerdotis. Two female and one unsexed C. gallicus are shown in Figure 2B. The leftmost specimen is a female from Romania, the center specimen is a female from Roti island, while the rightmost specimen is an unsexed individual from Flores.
FIGURE 2 in A new subspecies of Short-toed Snake-eagle from Wallacea determined from morphological and DNA comparison
FIGURE 2. Boxplots of wingspan and tail lengths across both sexes in Lesser Sundas Short-toed Snake-eagle populations as compared to Palearctic populations. The boxes mark out the 25th–75th percentiles. Palearctic birds are consistently larger than individuals from the Lesser Sundas. Additionally, in Palearctic populations females are larger than males, whereas in the Lesser Sundas populations, female-biased dimorphism is absent, both sexes being of similar size.
FIGURE 1 in A new subspecies of Short-toed Snake-eagle from Wallacea determined from morphological and DNA comparison
FIGURE 1. Maximum Likelihood (ML) tree showing placement of the Timor individual of C. gallicus within the Circaetus clade, with H. novaeguineae used as the outgroup. Maximum Parsimony (MP), ML, and Bayesian inference methods produce the same consensus tree. Node labels sequentially represent branch support values for the ML, Bayesian, and MP trees, respectively, with only bootstrap/posterior probabilities greater than 80/0.8 shown. Branch lengths indicate percent divergence, with the scale bar corresponding to 2% divergence. The Timor individual clusters with Palearctic C. gallicus from Israel and France with high bootstrap and posterior probability values, indicating about 0.4% divergence.
FIGURE 3 in Morphological comparison of tympanal organs between Phycitinae and Pyralinae (Lepidoptera: Pyralidae)
FIGURE 3. Ventral view of the tympanal organs of moths before preparation (con: conjunctivum, ft: fornix tympany, prs: processus spiniforme, rgo: rugae odontinae, spn: spinula, tym: tympanum, tymc.: tympanalcilia, zgt: zona glabra tympani) a. Pyralis farinalis b. Hypsopygia glaucinalis c. Endotricha flammealis d. Dioryctria pineae e. Dioryctria mendacella f. Oncocera semirubella g. Etiella zinckenella h. Acrobasis obliqua i. Myelois circumvoluta j. Ematheudes punctellus.
FIGURE 2 in Morphological comparison of tympanal organs between Phycitinae and Pyralinae (Lepidoptera: Pyralidae)
FIGURE 2. Top views of pyralid images. a. Pyralis farinalis b. Hypsopygia glaucinalis c. Endotrichia flammealis d. Dioryctria pineae e. D. mendacella f. Oncocera semirubella g. Etiella zinckenella h. Acrobasis obliqua i. Myelois circumvoluta j. Ematheudes punctellus.
FIGURE 4 in Morphological comparison of tympanal organs between Phycitinae and Pyralinae (Lepidoptera: Pyralidae)
FIGURE 4. Tympanal organs ultrastrukture of the moths after preparation (Blue circle: Intersegmental thoraco abdominal membrane; black circle: pons tympani; black triangle: processus spiniforme; red line: fornix tympani width) a. Pyralis farinalis b. Hypsopygia glaucinalis c. Endotricha flammealis d. Dioryctria pineae e. Dioryctria mendacella f. Oncocera semirubella g. Etiella zinckenella h. Acrobasis obliqua i. Myelois circumvoluta j. Ematheudes punctellus.
FIGURE 1 in Morphological comparison of tympanal organs between Phycitinae and Pyralinae (Lepidoptera: Pyralidae)
FIGURE 1. The tympanal organ and parts of the adult Oncocera semirubella before and after preparation (con: conjunctivum, bt: bulla tympani, ft: fornix tympani, itm: intersegmental thoraco abdominal membrane, prs: processus spiniforme, pt: pons tympani, rgo: rugae odontinae, spn: spinula, tymc: tympanal cilia, ts: tergo sternal sclerite, tym: tympanum, zgt: zona glabra tympani).
Data for "SPH modelling of AGB wind morphology in hierarchical triple systems & comparison to observation of R Aql"
<div> <p>Additional material to Malfait et al. 2024, subm. "SPH modelling of AGB wind morphology in hierarchical triple systems & comparison to observation of R Aql"</p> <p>This contains input files and final output dumps of the Phantom simulations of this paper.</p> <p>The code used to perform the simulations is available at: <a href="https://github.com/danieljprice/phantom">https://github.com/danieljprice/phantom.</a></p> <p>Splash (<a href="https://github.com/danieljprice/splash">https://github.com/danieljprice/splash</a> ) and Plons (<a href="https://github.com/Ensor-code/plons">https://github.com/Ensor-code/plons</a> ) were used to create figures and plots from this data.</p> <p> </p> </div>
Fig. 6 in Histomorphological comparison of testes in species of box jellyfish (Cnidaria; Cubozoa): does morphology differ with mode of reproduction and fertilization?
Fig. 6 Chiropsalmus quadrumanus (from North Carolina State, USA). a Live specimen (scale bar 4 cm) (Image courtesy of Bastian Bentlage). b Male gonad in cross-section stained with toluidine blue (TB) (scale bar 20 μm). c Male gonad in cross-section stained with periodic acid-Schiff + hematoxylin (PAS-H) (scale bar 50 μm). cl cilia, m mesoglea, p pedalia, r rhopalia, sc spermatocyte, sg spermatogonia, t tentacle, v velarium, vl vacuole
Fig. 4 in Histomorphological comparison of testes in species of box jellyfish (Cnidaria; Cubozoa): does morphology differ with mode of reproduction and fertilization?
Fig. 4 Tamoya cf. haplonema from New Jersey State (USA). a– d Male gonad in cross-section stained with hematoxylin-eosin (HE) (scale bars 50 μm). e Male gonad in cross-section stained with Gomori's trichrome + hematoxylin (TG-H) (scale bar 50 μm). f Male gonad in crosssection stained with Toluidine blue (TB) (scale bar 20 μm). g Male gonad in cross-section stained with HE (scale bar 20 μm). Arrows in b-f indicate rupture sites from which sperm are released. sc spermatocyte, sg spermatogonia, sp sperm
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Allen Brain Atlas
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Annotated Behaviour and Observability Dataset (ABODe)
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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
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