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351 results for “Species pair”
Supplementary material 2 from: Liu M-C, Dong T-F, Feng W-W, Qu B, Kong D-L, van Kleunen M, Feng Y-L (2022) Leaf trait differences between 97 pairs of invasive and native plants across China: effects of identities of both the invasive and native species. NeoBiota 71: 1-22. https://doi.org/10.3897/neobiota.71.71385
Table S1, S2, S4
Supplementary material 3 from: Liu M-C, Dong T-F, Feng W-W, Qu B, Kong D-L, van Kleunen M, Feng Y-L (2022) Leaf trait differences between 97 pairs of invasive and native plants across China: effects of identities of both the invasive and native species. NeoBiota 71: 1-22. https://doi.org/10.3897/neobiota.71.71385
Table S3
The contribution of extra-pair paternity to the variation in lifetime and age-specific male reproductive success in a socially monogamous species
<p>In socially monogamous species, extra-pair paternity (EPP) is predicted to increase variance in male reproductive success beyond that resulting from genetic monogamy, thus increasing the 'opportunity for selection' (maximum strength of selection that can act on a trait). This prediction is challenging to investigate in wild populations because lifetime reproduction data are often incomplete. Moreover, age-specific variances in reproductive success have been rarely quantified. We analysed 21 years of near-complete social and genetic reproduction data from an insular population of Seychelles warblers (<em>Acrocephalus sechellensis</em>). We quantified the contribution of EPP to lifetime and age-specific opportunities for selection in males. We also compared the variance in male genetic reproductive success (RS) vs. social ('apparent') reproductive success (RSap) to assess if EPP increased the opportunity for selection over that resulting from genetic monogamy. EPP contributed substantially to the variance in lifetime RS, despite not causing a statistically significant excess of this over the variance in lifetime RSap. Partitioning the opportunity for selection into age-specific (co)variance components, showed that EPP provided a substantial contribution at most ages, varying with age. Therefore, in Seychelles warblers EPP likely provides an age-dependent contribution to the opportunity for selection, which can influence evolutionary processes in age-structured populations.</p>
Fig. 40. Haplochromis squamipinnis Regan, 1921 in From a pair to a dozen: the piscivorous species of Haplochromis (Cichlidae) from the Lake Edward system
Fig. 40. Haplochromis squamipinnis Regan, 1921 (RMCA 2016.035.P.0254; 182.0 mm SL). a. Dorsal view of the lower pharyngeal jaw. b. Lateral view of the lower pharyngeal jaw.
Fig. 33 in From a pair to a dozen: the piscivorous species of Haplochromis (Cichlidae) from the Lake Edward system
Fig. 33. Haplochromis pardus sp. nov. a. Photograph of preserved holotype (RMCA 2016.035.P.0202; 89.2 mm SL). b. X-ray image of holotype. c–d. Photographs of freshly caught specimens. c. Dominant male (RMCA 2017.006.P (HP1463); 81.4 mm SL). d. Female (RMCA 2017.006.P.0342; 75.9 mm SL) to illustrate the live colour patterns. The contrast was slightly enhanced.
Fig. 29 in From a pair to a dozen: the piscivorous species of Haplochromis (Cichlidae) from the Lake Edward system
Fig. 29. Haplochromis curvidens sp. nov., holotype, ♂, 112.0 mm SL (RMCA 2016.035.P.0219). Drawn by N. Vranken.
Fig. 14 in From a pair to a dozen: the piscivorous species of Haplochromis (Cichlidae) from the Lake Edward system
Fig. 14. Haplochromis simba sp. nov., holotype, ♂, 105.8 mm SL (RMCA 2016.035.P.0225). Drawn by N. Vranken.
Fig. 13 in From a pair to a dozen: the piscivorous species of Haplochromis (Cichlidae) from the Lake Edward system
Fig. 13. Haplochromis rex sp. nov. (IRSNB 13480; 154.2 mm SL). a. Dorsal view of the lower pharyngeal jaw. b. Lateral view of the lower pharyngeal jaw.
Fig. 20 in From a pair to a dozen: the piscivorous species of Haplochromis (Cichlidae) from the Lake Edward system
Fig. 20. Haplochromis aquila sp. nov., holotype, ♂, 113.6 mm SL (RMCA 2018.008.P.0355). Drawn by N. Vranken.
FIGURES 203–204. Philonix fulvicollis Fitch. 203, asexual gall. 204 in Pairing of sexual and asexual generations of Nearctic oak gallwasps, with new synonyms and new species names (Hymenoptera: Cynipidae, Cynipini)
FIGURES 203–204. Philonix fulvicollis Fitch. 203, asexual gall. 204, sexual gall.
FIGURES 181–182. Neuroterus niger Gillette. 181, asexual gall. 182 in Pairing of sexual and asexual generations of Nearctic oak gallwasps, with new synonyms and new species names (Hymenoptera: Cynipidae, Cynipini)
FIGURES 181–182. Neuroterus niger Gillette. 181, asexual gall. 182, sexual gall.
FIGURES 119–120 in Pairing of sexual and asexual generations of Nearctic oak gallwasps, with new synonyms and new species names (Hymenoptera: Cynipidae, Cynipini)
FIGURES 119–120. Melikaiella tumifica (Osten Sacken). 119, sexual gall. 120, asexual gall.
FIGURES 224–225 in Pairing of sexual and asexual generations of Nearctic oak gallwasps, with new synonyms and new species names (Hymenoptera: Cynipidae, Cynipini)
FIGURES 224–225. Phylloteras poculum (Osten Sacken). 224, asexual gall. 225, sexual gall.
FIGURES 112–113. Bassettia pallida Ashmead. 112 in Pairing of sexual and asexual generations of Nearctic oak gallwasps, with new synonyms and new species names (Hymenoptera: Cynipidae, Cynipini)
FIGURES 112–113. Bassettia pallida Ashmead. 112, asexual gall, 113, putative sexual gall.
FIGURES 42–43. Amphibolips spinosa Ashmead. 42, asexual gall. 43 in Pairing of sexual and asexual generations of Nearctic oak gallwasps, with new synonyms and new species names (Hymenoptera: Cynipidae, Cynipini)
FIGURES 42–43. Amphibolips spinosa Ashmead. 42, asexual gall. 43, sexual gall.
Figure 2 in Effects of nitrogen and phosphorus availability on the early growth of two congeneric pairs of savanna and forest species
Figure 2. The effect of our four treatments (Com: Complete Hoagland solution; -N: Solution without nitrogen; -P: Solution without phosphorus and -NP: Solution without both macronutrients) in the grow of a congeneric pair of species after 45 days of experiment. The boxes in the left side represent the savanna species (Enterolobium gummiferum), those on the right side, the forest ones (E. contortisiliquum).
FIGURE 32 in Revision of the Old World species of the genus Tephritis (Diptera, Tephritidae) with a pair of isolated apical spots
FIGURE 32. Tephritis theryi—habitus, paratype♀. Scale bar = 1 mm.
FIGURES 18a–b in Revision of the Old World species of the genus Tephritis (Diptera, Tephritidae) with a pair of isolated apical spots
FIGURES 18a–b. Tephritis heiseri: a—habitus ♀; b—abdomen, dorsal.
FIGURES 9a–d in Revision of the Old World species of the genus Tephritis (Diptera, Tephritidae) with a pair of isolated apical spots
FIGURES 9a–d. Tephritis dilacerata dilacerata: a—lectotype ♀ habitus; b–d—wings; bar = 1 mm.
FIGURE 32 in Revision of the Old World species of the genus Tephritis (Diptera, Tephritidae) with a pair of isolated apical spots
FIGURE 32. Tephritis theryi—habitus, paratype♀. Scale bar = 1 mm.
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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.