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14 results for “Alainites”
Figs 31–36 in First record of the genus Alainites Waltz & McCafferty, 1994 (Ephemeroptera, Baetidae) from India with the description of a new species from the North-western Himalayas
Figs 31–36. Alainites neeru sp. nov. 31–32. Paratype (AMC). 33–36. Holotype (AMC). 31. Tergalius I. 32. Tergalius IV. 33. Posterior margin of tergum IV denticulation. 34–35. Paraproct. 36. Closer view of paraproct.
Figs 27–30 in First record of the genus Alainites Waltz & McCafferty, 1994 (Ephemeroptera, Baetidae) from India with the description of a new species from the North-western Himalayas
Figs 27–30. Alainites neeru sp. nov., paratype (AMC), thorax and abdomen of larva. 27. Foreclaw. 28. Hindwing pad (pointed by arrow). 29. Tergal segments III–X. 30. Tergal segments VIII–X.
Figs 14–18 in First record of the genus Alainites Waltz & McCafferty, 1994 (Ephemeroptera, Baetidae) from India with the description of a new species from the North-western Himalayas
Figs 14–18. Alainites neeru sp. nov., paratype (AMC), mouthparts of larva. 14. Labium. 15. Glossae and paraglossae. 16. Closer view of labial palp segment III. 17. Maxilla. 18. Closer view of crown of maxilla.
Figs 19–21 in First record of the genus Alainites Waltz & McCafferty, 1994 (Ephemeroptera, Baetidae) from India with the description of a new species from the North-western Himalayas
Figs 19–21. Alainites neeru sp. nov., paratype (AMC), legs of larva. 19. Forefemur. 20. Middle femur. 21. Hind femur.
Figs 22–26 in First record of the genus Alainites Waltz & McCafferty, 1994 (Ephemeroptera, Baetidae) from India with the description of a new species from the North-western Himalayas
Figs 22–26. Alainites neeru sp. nov., paratype (AMC), legs of larva. 22. Foretibia and foretarsus. 23. Outer marginal setation of foretibia. 24. Inner marginal setation of foretibia. 25. Middle tibia and middle tarsus. 26. Hind tibia and hind tarsus.
Figs 7–13 in First record of the genus Alainites Waltz & McCafferty, 1994 (Ephemeroptera, Baetidae) from India with the description of a new species from the North-western Himalayas
Figs 7–13. Alainites neeru sp. nov. paratypes (AMC), mouthparts of larva. 7. Left mandible. 8. Right mandible. 9. Prostheca and incisor of left mandible. 10. Closer view of left mandible. 11–12. Prostheca and incisor of right mandible. 13. Prostheca of right mandible.
Figs 1–5 in First record of the genus Alainites Waltz & McCafferty, 1994 (Ephemeroptera, Baetidae) from India with the description of a new species from the North-western Himalayas
Figs 1–5. Alainites neeru sp. nov. 1. Holotype, ♀ (AMC), mature larva. 2–6. Paratype (AMC). 2. Immature larva. 3. Antenna. 4. Labrum. 5. Labrum, sub-marginal setae (arrows indicate 1+2 long, simple setae). 6. Setae of the ventral surface of the labrum.
Data from: What ecological factors favor parthenogenesis over sexual reproduction? A study on the facultatively parthenogenetic mayfly Alainites muticus in natural populations
<p>Different reproductive modes are characterized by costs and benefits which depend on ecological contexts. For example, sex can provide benefits under complex biotic interactions, while its costs increase under mate limitation. Furthermore, ecological contexts often vary along abiotic gradients. Here, we study how these factors simultaneously influence the frequency of sex in the facultatively parthenogenetic mayfly Alainites muticus . We first verified that parthenogenesis translates into female-biased population sex ratios. We then measured the density of individuals (a proxy for mate limitation) and community diversity (biotic interaction complexity) for 159 A. muticus populations covering a broad altitudinal gradient and used structural equation modeling to investigate their direct and indirect influences on sex ratios. We found no effect of community diversity or altitude on sex ratios. Furthermore, even when females can reproduce parthenogenetically, they generally reproduce sexually, indicating that the benefits of sex exceed its costs in most situations. Sex ratios only become female-biased under low population densities, as expected if mate limitation was the main factor selecting for parthenogenesis. Mate limitation might be widespread in mayflies because of their short adult lifespan and limited dispersal, which can generate strong selection for reproductive assurance and may provide a stepping-stone towards obligate parthenogenesis.</p>
Data from: What ecological factors favor parthenogenesis over sexual reproduction? A study on the facultatively parthenogenetic mayfly Alainites muticus in natural populations
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FIGURE 12 in First record of Alainites sadati Thomas, 1994 (Ephemeroptera: Baetidae) in Tunisia, description of the larval stage and ecology
FIGURE 12. Map of the distribution of Alainites sadati in North Africa: star: type locality; round: sites hosting A. sadati.
FIGURE 1–6 in First record of Alainites sadati Thomas, 1994 (Ephemeroptera: Baetidae) in Tunisia, description of the larval stage and ecology
FIGURE 1–6. Larval structures of Alainites sadati from Khemis (Algeria) except Fig. 3b from Beja (Tunisia): 1. Labrum (left: ventral, right: dorsal). 2. Right mandible. 3a. Left mandible. 3b. Left prostheca and incisors. 4. Hypopharynx. 5. Right maxilla. 6. Labium (left: ventral, right: dorsal).
FIGURE 7–11 in First record of Alainites sadati Thomas, 1994 (Ephemeroptera: Baetidae) in Tunisia, description of the larval stage and ecology
FIGURE 7–11. Structures of Alainites sadati from Khemis (Algeria): 7a. Foreleg. 7b. Midtibia. 8. Tarsal claw. 9. Distal margin of fourth abdominal tergum. 10. Fourth gill. 11. Paraproct.
Supplementary material 2 from: Yanai Z, Sroka P, Gattolliat J-L (2022) Two new species of Alainites (Ephemeroptera, Baetidae) from the Mediterranean biodiversity hotspot. ZooKeys 1118: 73-95. https://doi.org/10.3897/zookeys.1118.84643
Table S2
Supplementary material 1 from: Yanai Z, Sroka P, Gattolliat J-L (2022) Two new species of Alainites (Ephemeroptera, Baetidae) from the Mediterranean biodiversity hotspot. ZooKeys 1118: 73-95. https://doi.org/10.3897/zookeys.1118.84643
Table S1
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