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18 results for “tapia”
Fig. 3 in Selizitapia gen. nov. (Hemiptera: Fulgoromorpha: Flatidae) from tapia woodlands of Madagascar
Fig. 3. Selizitapia pennyi gen. et sp. nov. Holotype, ♂ (CAS CASLOT 044412). SEM photographs. A. Antenna, lateral view. B–C. Hind leg. D. Apical part of metatibia and metatarsus. E. Tegmen, basal part. F. Same, apical part.
Fig. 2 in Selizitapia gen. nov. (Hemiptera: Fulgoromorpha: Flatidae) from tapia woodlands of Madagascar
Fig. 2. Selizitapia pennyi gen. et sp. nov. A–B. Paratype, ♀ (CAS CASLOT 044446). C–F. Holotype, ♂ (CAS CASLOT 044412). SEM photographs. A. Anterior part of body, fronto-dorsal view. B. Same, frontal view. C. Head and pronotum, dorsal view. D. Upper part of head and pronotum, fronto-dorsal view. E. Head and thorax, dorsal view. F. Antenna, frontal view.
Fig. 6 in Selizitapia gen. nov. (Hemiptera: Fulgoromorpha: Flatidae) from tapia woodlands of Madagascar
Fig. 6. Selizitapia pennyi gen. et sp. nov. Paratype, ♀ (CAS CASLOT 044463). SEM photographs. A. Abdomen, ventral view. B. Same, lateral view. C. Abdomen, dorsal view. D. Tergites, central membranous part. E. Gonoplacs, fronto-ventral view. F. Gonoplac teeth.
Fig. 1 in Selizitapia gen. nov. (Hemiptera: Fulgoromorpha: Flatidae) from tapia woodlands of Madagascar
Fig. 1. Selizitapia pennyi gen. et sp. nov. Holotype, ♂ (CAS CASLOT 044412). Habitus. A. Anterior part, dorsal view. B. Same, frontal view. C. Tegmen. Scale bars = 1.0 mm.
Fig. 5 in Selizitapia gen. nov. (Hemiptera: Fulgoromorpha: Flatidae) from tapia woodlands of Madagascar
Fig. 5. Selizitapia pennyi gen. et sp. nov. Holotype, ♂ (CAS CASLOT 044412). Line drawings. A. Terminalia, lateral view. B. Anal tube, dorsal view. C. Periandrium, lateral view. D. Same, dorsal view. E. Aedeagus, lateral view. F. Same, dorsal view. Scale bars = 0.5 mm.
Fig. 7 in Selizitapia gen. nov. (Hemiptera: Fulgoromorpha: Flatidae) from tapia woodlands of Madagascar
Fig. 7. Selizitapia pennyi gen. et sp. nov. Paratype, ♀ (CAS CASLOT 044463). Line drawings. A. Pregenital sternite, flattened, ventral view. B. Anal tube, dorsal view. C. Same, lateral view. D. Gonoplac, lateral view E. Gonapophysis VIII, lateral view. F. Bursa copulatrix with cells, lateral view. G. Spermatheca. H. Gonapophyses IX and gonospiculum bridge, lateral view. I. Same, dorsal view. Scale bars = 0.5 mm.
Fig. 4 in Selizitapia gen. nov. (Hemiptera: Fulgoromorpha: Flatidae) from tapia woodlands of Madagascar
Fig. 4. Selizitapia pennyi gen. et sp. nov. Holotype, ♂ (CAS CASLOT 044412). SEM photographs. A. Abdomen, lateral view. B. Terminalia, lateral view. C. Abdomen, dorsal view. D. Terminalia, dorsal view. E. Terminalia, postero-ventral view. F. Same, fronto-dorsal view.
Pinus kesiya invasions in Tapia woodland Madagascar
<p>Pinus species are among the highly invasive species which have spread outside their plantation area after their introduction in the Southern Hemisphere. The case of <em>Pinus kesiya</em> invasion is observed in the high plateau of Madagascar, inside the sclerophyll Tapia woodland which is dominated by the endemic <em>Uapaca bojeri </em>tree species. The analysis of this invasion was carried out using 375 plots of 100 m2 each in Tapia woodland. Data on the vegetation structure, the plot characteristics and the propagule pressure were collected. We recorded a total of 740 pines distributed in 29.8% of the plots. The generalized linear model revealed that the diminution in frequency of the dominant species <em>Uapaca bojeri</em> with the increasing degree of disturbance of the fragment led to the vulnerability of the Tapia woodland to the abundance of pine. The factors explaining pine occurrence varied according to the pine life-stage. In the seedling stage, the distance of the plot from the propagule source combined with the longitudinal position of the plot explained 18% of the pine invasion success. In the sapling and adult stages, the vegetation structure was the main important factor (22% and 11% of variation explained). The frequency of <em>U. bojeri</em> and the degree of disturbance were the most important factors characterizing this vegetation structure. Based on these results, a strategy to control pine invasion in the Tapia woodland may focus on enrichment with <em>U. bojeri</em> and limitation of the plantation of <em>P. kesiya</em> in proximity.</p>
Pinus kesiya invasions in Tapia woodland Madagascar
Open the record for dataset details and reuse information.
Prevalence of Tapia's Syndrome in Weaning Unit
ClinicalTrials.gov study NCT06033144. IPD Sharing: NO. Countries: 1. Publications: 5.
Figure 4 from: Zaragoza-Tapia F, Pulido-Flores G, Gardner SL, Monks S (2020) Host relationships and geographic distribution of species of Acanthobothrium Blanchard, 1848 (Onchoproteocephalidea, Onchobothriidae) in elasmobranchs: a metadata analysis. ZooKeys 940: 1-49. https://doi.org/10.3897/zookeys.940.46352
Figure 4 Number of species of Acanthobothrium reported from elasmobranchs in each biogeographic region (Last et al. 2016b).
Figure 1 from: Zaragoza-Tapia F, Pulido-Flores G, Gardner SL, Monks S (2020) Host relationships and geographic distribution of species of Acanthobothrium Blanchard, 1848 (Onchoproteocephalidea, Onchobothriidae) in elasmobranchs: a metadata analysis. ZooKeys 940: 1-49. https://doi.org/10.3897/zookeys.940.46352
Figure 1 Type localities of species of Acanthobothrium reported worldwide and the biogeographic regions (Last et al. 2016b) of the geographic distribution of their hosts (see Table 1).
Figure 3 from: Zaragoza-Tapia F, Pulido-Flores G, Gardner SL, Monks S (2020) Host relationships and geographic distribution of species of Acanthobothrium Blanchard, 1848 (Onchoproteocephalidea, Onchobothriidae) in elasmobranchs: a metadata analysis. ZooKeys 940: 1-49. https://doi.org/10.3897/zookeys.940.46352
Figure 3 Families of rays: A number of species of rays per family B number of species of rays parasitized by species of Acanthobothrium. Note: The first number within parentheses corresponds to the number of species of ray that have been reported as hosts of Acanthobothrium and the second is the number of species that have been described from that Family C percentage of species of rays reported to be parasitized within the total number of families of rays- note: Red color = parasitized; Blue color = not parasitized.
Figure 2 from: Zaragoza-Tapia F, Pulido-Flores G, Gardner SL, Monks S (2020) Host relationships and geographic distribution of species of Acanthobothrium Blanchard, 1848 (Onchoproteocephalidea, Onchobothriidae) in elasmobranchs: a metadata analysis. ZooKeys 940: 1-49. https://doi.org/10.3897/zookeys.940.46352
Figure 2 Families of sharks: A number of species of sharks per family B number of species of sharks parasitized by species of Acanthobothrium. Note: The first number within parentheses corresponds to the number of species of shark that have been reported as hosts of Acanthobothrium and the second is the number of species that have been described from that Family C percentage of species of shark reported to be parasitized within the total number of families of sharks- note: Red color = parasitized; Blue color = not parasitized.
Figure 4 from: Zaragoza-Tapia F, Pulido-Flores G, Violante-González J, Monks S (2019) Two new species of Acanthobothrium Blanchard, 1848 (Onchobothriidae) in Narcine entemedor Jordan & Starks, 1895 (Narcinidae) from Acapulco, Guerrero, Mexico. ZooKeys 852: 1-21. https://doi.org/10.3897/zookeys.852.28964
Figure 4 Light microscope photographs of holotype of Acanthobothriumvidali sp. nov. (CNHE-11134). A Scolex B details of bothridium C peduncle cephalic D genitalia. Scale bars: 400 µm (A); 40 µm (B);100 µm (C, D). Abbreviations: vg vagina; cs cirrus sac; gp genital pore.
Figure 3 from: Zaragoza-Tapia F, Pulido-Flores G, Violante-González J, Monks S (2019) Two new species of Acanthobothrium Blanchard, 1848 (Onchobothriidae) in Narcine entemedor Jordan & Starks, 1895 (Narcinidae) from Acapulco, Guerrero, Mexico. ZooKeys 852: 1-21. https://doi.org/10.3897/zookeys.852.28964
Figure 3 Holotype of Acanthobothriumvidali sp. nov. (CNHE-11134). A Scolex B hooks C mature proglottid D genitalia. Scale bars: 400 µm (A); 200 µm (B–D).
Figure 1 from: Zaragoza-Tapia F, Pulido-Flores G, Violante-González J, Monks S (2019) Two new species of Acanthobothrium Blanchard, 1848 (Onchobothriidae) in Narcine entemedor Jordan & Starks, 1895 (Narcinidae) from Acapulco, Guerrero, Mexico. ZooKeys 852: 1-21. https://doi.org/10.3897/zookeys.852.28964
Figure 1 Holotype of Acanthobothriumsoniae sp. nov. (CNHE-11136). A Scolex B hooks C mature proglottid D terminal proglottid E genitalia. Scale bars: 200 µm (A, D); 100 µm (B, E); 150 µm (C).
Figure 2 from: Zaragoza-Tapia F, Pulido-Flores G, Violante-González J, Monks S (2019) Two new species of Acanthobothrium Blanchard, 1848 (Onchobothriidae) in Narcine entemedor Jordan & Starks, 1895 (Narcinidae) from Acapulco, Guerrero, Mexico. ZooKeys 852: 1-21. https://doi.org/10.3897/zookeys.852.28964
Figure 2 Light microscope photographs of holotype of Acanthobothriumsoniae sp. nov. (CNHE-11136). A Scolex B details of bothridium C peduncle cephalic D genitalia. Scale bars: 200 µm (A); 40 µm (B), 100 µm (C, D). Abbreviations: mt microtriches; vg vagina; cs cirrus sac; gp genital pore.
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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)
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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
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.