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Figure 9 from: Carvalho FL, Magalhães C, Mantelatto FL (2014) Molecular and morphological differentiation between two Miocene-divergent lineages of Amazonian shrimps, with the description of a new species (Decapoda, Palaemonidae, Palaemon). In: Wehrtmann IS, Bauer RT (Eds) Proceedings of the Summer Meeting of the Crustacean Society and the Latin American Association of Carcinology, Costa Rica, July 2013. ZooKeys 457: 79-108. https://doi.org/10.3897/zookeys.457.6771
Figure 9 - Type locality of Palaemon yuna sp. n. Lago Tupé beach, lower Rio Negro tributary, Manaus, Amazonas, Brazil (003°02'42"S, 060°15'10"W).
Figure 8 from: Carvalho FL, Magalhães C, Mantelatto FL (2014) Molecular and morphological differentiation between two Miocene-divergent lineages of Amazonian shrimps, with the description of a new species (Decapoda, Palaemonidae, Palaemon). In: Wehrtmann IS, Bauer RT (Eds) Proceedings of the Summer Meeting of the Crustacean Society and the Latin American Association of Carcinology, Costa Rica, July 2013. ZooKeys 457: 79-108. https://doi.org/10.3897/zookeys.457.6771
Figure 8 - Palaemon yuna sp. n. Figures i and m holotype; figures a–e, g, h, j–l paratype (CCDB 4866, male, CL 5.5 mm); figure f paratype (CCDB 4866, female, CL 5.5 mm). a left third pereiopod, lateral view b left fourth pereiopod, lateral view c distal portion of the left fifth pereiopod, lateral view d left fifth pereiopod, lateral view e left first pleopod, posterior view f left first pleopod, posterior view g left second pleopod, posterior view h left appendix masculina and appendix interna, posterior view i right posterior part of the abdomen, lateral view j pre-anal fig, ventral view k telson and uropods, dorsal view l distal part of the telson, dorsal view m left distal portion of the exopod of the uropod, dorsal view. Scale bar: a, b, d–g, i, k equal to 1 mm; c, j, m equal to 0.5 mm; h, l equal to 0.25 mm.
Figure 7 from: Carvalho FL, Magalhães C, Mantelatto FL (2014) Molecular and morphological differentiation between two Miocene-divergent lineages of Amazonian shrimps, with the description of a new species (Decapoda, Palaemonidae, Palaemon). In: Wehrtmann IS, Bauer RT (Eds) Proceedings of the Summer Meeting of the Crustacean Society and the Latin American Association of Carcinology, Costa Rica, July 2013. ZooKeys 457: 79-108. https://doi.org/10.3897/zookeys.457.6771
Figure 7 - Palaemon yuna sp. n. Figure a holotype; figures b–n paratype (CCDB 4866, male, CL 5.5 mm). a anterior part of the carapace b right eye, dorsal view c left scaphocerite, ventral view d left mandible, ventral view e left maxillula, ventral view f left maxilla, ventral view g left second maxilliped, ventral view h left first maxilliped, ventral view i left first maxilliped, dorsal view j right third maxilliped, ventro-lateral view k right second pereiopod, ventro-lateral view l right first pereiopod, ventro-lateral view m right first chela, mesial view n right second chela, mesial view. Scale bar: a, c, k equal to 1 mm; others equal to 0.5 mm.
Figure 6 from: Carvalho FL, Magalhães C, Mantelatto FL (2014) Molecular and morphological differentiation between two Miocene-divergent lineages of Amazonian shrimps, with the description of a new species (Decapoda, Palaemonidae, Palaemon). In: Wehrtmann IS, Bauer RT (Eds) Proceedings of the Summer Meeting of the Crustacean Society and the Latin American Association of Carcinology, Costa Rica, July 2013. ZooKeys 457: 79-108. https://doi.org/10.3897/zookeys.457.6771
Figure 6 - Commonest shape of the rostrum. Palaemon carteri (a MPEG 787), Palaemon ivonicus (b INPA 128) and Palaemon yuna sp. n. (c CCDB 4866).
Figure 4 from: Carvalho FL, Magalhães C, Mantelatto FL (2014) Molecular and morphological differentiation between two Miocene-divergent lineages of Amazonian shrimps, with the description of a new species (Decapoda, Palaemonidae, Palaemon). In: Wehrtmann IS, Bauer RT (Eds) Proceedings of the Summer Meeting of the Crustacean Society and the Latin American Association of Carcinology, Costa Rica, July 2013. ZooKeys 457: 79-108. https://doi.org/10.3897/zookeys.457.6771
Figure 4 - Intralineage and interlineage uncorrected genetic distance values for the "ivonicus/yuna" and "carteri" lineages.
Figure 5 from: Carvalho FL, Magalhães C, Mantelatto FL (2014) Molecular and morphological differentiation between two Miocene-divergent lineages of Amazonian shrimps, with the description of a new species (Decapoda, Palaemonidae, Palaemon). In: Wehrtmann IS, Bauer RT (Eds) Proceedings of the Summer Meeting of the Crustacean Society and the Latin American Association of Carcinology, Costa Rica, July 2013. ZooKeys 457: 79-108. https://doi.org/10.3897/zookeys.457.6771
Figure 5 - Commonest shape of the antennular peduncle. Palaemon carteri (a MPEG 787), Palaemon ivonicus (b INPA 128) and Palaemon yuna sp. n. (c CCDB 4866).
Figure 2 from: Carvalho FL, Magalhães C, Mantelatto FL (2014) Molecular and morphological differentiation between two Miocene-divergent lineages of Amazonian shrimps, with the description of a new species (Decapoda, Palaemonidae, Palaemon). In: Wehrtmann IS, Bauer RT (Eds) Proceedings of the Summer Meeting of the Crustacean Society and the Latin American Association of Carcinology, Costa Rica, July 2013. ZooKeys 457: 79-108. https://doi.org/10.3897/zookeys.457.6771
Figure 2 - Bayesian (GTR+Γ+I and HKY+Γ models) and maximum likelihood 50% majority-rule consensus tree. Numbers in the nodes represent posterior probabilities (GTR+Γ+I and HKY+Γ, respectively), and bootstrap value for maximum likelihood and parsimony analyses, respectively. c1–Bragança, Pará; c2–Santa Maria do Pará, Pará; c3–National Forest of Amapá, Amapá; c4–Belém, Pará; i1–Solimões River, near Manaus, Amazonas; i2–Xingu River, Altamira, Pará; i3 and i4–Itacoatiara, Amazonas. MYBP–million years before present.
Figure 11 from: Carvalho FL, Magalhães C, Mantelatto FL (2014) Molecular and morphological differentiation between two Miocene-divergent lineages of Amazonian shrimps, with the description of a new species (Decapoda, Palaemonidae, Palaemon). In: Wehrtmann IS, Bauer RT (Eds) Proceedings of the Summer Meeting of the Crustacean Society and the Latin American Association of Carcinology, Costa Rica, July 2013. ZooKeys 457: 79-108. https://doi.org/10.3897/zookeys.457.6771
Figure 11 - Putative current distribution of the "carteri" and "ivonicus/yuna" lineages. [Pebas system during the Late Miocene (~11.8 to 10 Ma) according to Lundberg et al. 1998.]
Figure 10 from: Carvalho FL, Magalhães C, Mantelatto FL (2014) Molecular and morphological differentiation between two Miocene-divergent lineages of Amazonian shrimps, with the description of a new species (Decapoda, Palaemonidae, Palaemon). In: Wehrtmann IS, Bauer RT (Eds) Proceedings of the Summer Meeting of the Crustacean Society and the Latin American Association of Carcinology, Costa Rica, July 2013. ZooKeys 457: 79-108. https://doi.org/10.3897/zookeys.457.6771
Figure 10 - Historical context for the proposed divergence time between the "carteri" and "ivonicus/yuna" lineages.
Figure 1 from: Carvalho FL, Magalhães C, Mantelatto FL (2014) Molecular and morphological differentiation between two Miocene-divergent lineages of Amazonian shrimps, with the description of a new species (Decapoda, Palaemonidae, Palaemon). In: Wehrtmann IS, Bauer RT (Eds) Proceedings of the Summer Meeting of the Crustacean Society and the Latin American Association of Carcinology, Costa Rica, July 2013. ZooKeys 457: 79-108. https://doi.org/10.3897/zookeys.457.6771
Figure 1 - Sample sites of Palaemon carteri, Palaemon ivonicus and Palaemon yuna sp. n. c1–Bragança, Pará; c2–Santa Maria do Pará, Pará; c3–National Forest of Amapá, Amapá; c4–Belém, Pará; i1–Solimões River, near Manaus, Amazonas; i2–Xingu River, Altamira, Pará; i3 and i4–Itacoatiara, Amazonas; AC-Acre; AM-Amazonas; AP-Amapá; MS-Mato Grosso do Sul; MT-Mato Grosso; PA-Pará and RO-Rondônia.
Figure 9 from: Hong X, Wang Q, Han X, Xue X (2014) Three new species of eriophyoid mites (Acari, Eriophyoidea) associated with Lauraceae in China. ZooKeys 406: 81-100. https://doi.org/10.3897/zookeys.406.6897
Figure 9 - Dechela phoebe sp. n.: AL lateral view of anterior body LO lateral view of annuli PM lateral view of posterior opisthosoma CGF female coxae and genitalia GM male genital region.
Figure 7 from: Hong X, Wang Q, Han X, Xue X (2014) Three new species of eriophyoid mites (Acari, Eriophyoidea) associated with Lauraceae in China. ZooKeys 406: 81-100. https://doi.org/10.3897/zookeys.406.6897
Figure 7 - Phyllocoptes setalsolenidion sp. n.: A prodorsal shield B male genitalia C coxae and female genitalia D female internal genitalia E empodium F leg I and leg II.
Figure 5 from: Hong X, Wang Q, Han X, Xue X (2014) Three new species of eriophyoid mites (Acari, Eriophyoidea) associated with Lauraceae in China. ZooKeys 406: 81-100. https://doi.org/10.3897/zookeys.406.6897
Figure 5 - Phyllocoptes setalsolenidion sp. n.: D dorsal view of female em empodium IG female internal genitalia CGF female coxae and genitalia.
Figure 8 from: Hong X, Wang Q, Han X, Xue X (2014) Three new species of eriophyoid mites (Acari, Eriophyoidea) associated with Lauraceae in China. ZooKeys 406: 81-100. https://doi.org/10.3897/zookeys.406.6897
Figure 8 - Dechela phoebe sp. n.: D dorsal view of female IG female internal genitalia em empodium L1 Leg I L2 leg II.
Figure 6 from: Hong X, Wang Q, Han X, Xue X (2014) Three new species of eriophyoid mites (Acari, Eriophyoidea) associated with Lauraceae in China. ZooKeys 406: 81-100. https://doi.org/10.3897/zookeys.406.6897
Figure 6 - Phyllocoptes setalsolenidion sp. n.: V ventral view of female GM male genital region L1 leg I L2 leg II.
Figure 2 from: Hong X, Wang Q, Han X, Xue X (2014) Three new species of eriophyoid mites (Acari, Eriophyoidea) associated with Lauraceae in China. ZooKeys 406: 81-100. https://doi.org/10.3897/zookeys.406.6897
Figure 2 - Gammaphytoptus striatilobus sp. n.: D dorsal view of female em empodium IG female internal genitalia GM male genital region.
Figure 4 from: Hong X, Wang Q, Han X, Xue X (2014) Three new species of eriophyoid mites (Acari, Eriophyoidea) associated with Lauraceae in China. ZooKeys 406: 81-100. https://doi.org/10.3897/zookeys.406.6897
Figure 4 - Gammaphytoptus striatilobus sp. n.: A coxae and female genitalia B prodorsal shield C female internal genitalia D leg I and leg II E male genitalia F empodium.
Figure 3 from: Hong X, Wang Q, Han X, Xue X (2014) Three new species of eriophyoid mites (Acari, Eriophyoidea) associated with Lauraceae in China. ZooKeys 406: 81-100. https://doi.org/10.3897/zookeys.406.6897
Figure 3 - Gammaphytoptus striatilobus sp. n.: AL lateral view of anterior body region LO lateral view of annuli PM lateral view of posterior opisthosoma CGF female coxae and genitalia L1 leg I L2 leg II.
Figure 10 from: Hong X, Wang Q, Han X, Xue X (2014) Three new species of eriophyoid mites (Acari, Eriophyoidea) associated with Lauraceae in China. ZooKeys 406: 81-100. https://doi.org/10.3897/zookeys.406.6897
Figure 10 - Dechela phoebe sp. n.: A prodorsal shield B coxae and female genitalia C leg I and leg II D female internal genitalia E male genitalia F tarsal solenidion of leg I G empodium.
Figures 92-95 from: Shimbori E, Shaw S (2014) Twenty-four new species of Aleiodes Wesmael from the eastern Andes of Ecuador with associated biological information (Hymenoptera, Braconidae, Rogadinae). ZooKeys 405: 1-81. https://doi.org/10.3897/zookeys.405.7402
Figures 92-95 - Aleiodes onyx sp. n. 92 habitus 93 host mummy after parasitoid emergence 94 mesopleuron 95 mesosoma and metasomal terga 1–2, dorsal.
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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
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International Brain Laboratory public data
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OpenNeuro
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