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129 results for “Cave beetles”
Figure 62 from: Moore MR, Cave RD, Branham MA (2018) Synopsis of the cyclocephaline scarab beetles (Coleoptera, Scarabaeidae, Dynastinae). ZooKeys 745: 1-99. https://doi.org/10.3897/zookeys.745.23683
Figure 62 Country-level distribution of Ruteloryctes species in Africa. Numbers indicate taxa per country.
Supplementary material 1 from: Leray VL, Caravas J, Friedrich M, Zigler KS (2019) Mitochondrial sequence data indicate "Vicariance by Erosion" as a mechanism of species diversification in North American Ptomaphagus (Coleoptera, Leiodidae, Cholevinae) cave beetles. Subterranean Biology 29: 35-57. https://doi.org/10.3897/subtbiol.29.31377
: Data type: statistical data
Supplementary material 2 from: Leray VL, Caravas J, Friedrich M, Zigler KS (2019) Mitochondrial sequence data indicate "Vicariance by Erosion" as a mechanism of species diversification in North American Ptomaphagus (Coleoptera, Leiodidae, Cholevinae) cave beetles. Subterranean Biology 29: 35-57. https://doi.org/10.3897/subtbiol.29.31377
: Data type: statistical data
Supplementary material 3 from: Leray VL, Caravas J, Friedrich M, Zigler KS (2019) Mitochondrial sequence data indicate "Vicariance by Erosion" as a mechanism of species diversification in North American Ptomaphagus (Coleoptera, Leiodidae, Cholevinae) cave beetles. Subterranean Biology 29: 35-57. https://doi.org/10.3897/subtbiol.29.31377
: Data type: phylogenetic data
Figure 5 from: Leray VL, Caravas J, Friedrich M, Zigler KS (2019) Mitochondrial sequence data indicate "Vicariance by Erosion" as a mechanism of species diversification in North American Ptomaphagus (Coleoptera, Leiodidae, Cholevinae) cave beetles. Subterranean Biology 29: 35-57. https://doi.org/10.3897/subtbiol.29.31377
Figure 5 Biogeographic and phylogenetic expectations for a 'vicariance by erosion' scenario as hypothesized for the southern Cumberland Plateau. A–C Karst (gray) erodes and fragments over time, leading to the isolation and divergence of cave populations (colored circles) in the remaining patches of karst D A phylogeny consistent with the vicariance by erosion process, with taxa that diverge early distributed at the periphery of the eroding region.
Figure 3 from: Leray VL, Caravas J, Friedrich M, Zigler KS (2019) Mitochondrial sequence data indicate "Vicariance by Erosion" as a mechanism of species diversification in North American Ptomaphagus (Coleoptera, Leiodidae, Cholevinae) cave beetles. Subterranean Biology 29: 35-57. https://doi.org/10.3897/subtbiol.29.31377
Figure 3 Ultrametric tree for the hirtus-group. Bayesian tree estimated from combined partial mitochondrial sequence data. Branches supported by posterior probability >0.90 are labeled with values or, for branches with posterior probability of 1.0, an asterisk. Blue bars indicate 95% confidence intervals of estimated ages for the nodes. Taxa are labeled with species name and specimen identifier (Table 1). Scale at bottom indicates divergence times in millions of years as estimated by BEAST (Drummond et al. 2012). Branch colors correspond to those in Figure 2A.
Figure 1 from: Leray VL, Caravas J, Friedrich M, Zigler KS (2019) Mitochondrial sequence data indicate "Vicariance by Erosion" as a mechanism of species diversification in North American Ptomaphagus (Coleoptera, Leiodidae, Cholevinae) cave beetles. Subterranean Biology 29: 35-57. https://doi.org/10.3897/subtbiol.29.31377
Figure 1 Eye morphologies in Ptomaphagus. Lateral view of head capsule and compound eye or eyelets (arrowheads) of Ptomaphagus species discussed in this paper. Ptomaphaguscavernicola and P.consobrinus are macrophthalmic and were used as outgroups in this study. Ptomaphagusshapardi, the only soil-dwelling species in the hirtus-group, has reduced eyes and is considered microphthalmic. The other 17 members of the hirtus-group are extremely microphthalmic.
Figure 2B from: Leray VL, Caravas J, Friedrich M, Zigler KS (2019) Mitochondrial sequence data indicate "Vicariance by Erosion" as a mechanism of species diversification in North American Ptomaphagus (Coleoptera, Leiodidae, Cholevinae) cave beetles. Subterranean Biology 29: 35-57. https://doi.org/10.3897/subtbiol.29.31377
Figure 2B Distribution of hirtus-group species. All known sites for members of the South Cumberlands lineage in Tennessee and Alabama. Exposed karst is shown in gray.
Figure 2A from: Leray VL, Caravas J, Friedrich M, Zigler KS (2019) Mitochondrial sequence data indicate "Vicariance by Erosion" as a mechanism of species diversification in North American Ptomaphagus (Coleoptera, Leiodidae, Cholevinae) cave beetles. Subterranean Biology 29: 35-57. https://doi.org/10.3897/subtbiol.29.31377
Figure 2A Distribution of hirtus-group species. All known sites for hirtus-group species in Kentucky, Tennessee, Alabama, and Georgia. P.shapardi sites in Oklahoma and Arkansas are indicated in upper right inset map. A dozen species from the southern Cumberland Plateau in Tennessee and Alabama are combined.
Figure 4 from: Leray VL, Caravas J, Friedrich M, Zigler KS (2019) Mitochondrial sequence data indicate "Vicariance by Erosion" as a mechanism of species diversification in North American Ptomaphagus (Coleoptera, Leiodidae, Cholevinae) cave beetles. Subterranean Biology 29: 35-57. https://doi.org/10.3897/subtbiol.29.31377
Figure 4 Distribution of Ptomaphagus species on the southern Cumberland Plateau, overlaid on a digital elevation model. Higher elevations (to 500 m) are indicated by darker shades, lower elevations (to 180 m) by lighter shades. Ptomaphagus species diverging early in the South Cumberlands lineage are limited to isolated ridges and mountains on the fringes of the plateau. These species are P.loedingi (yellow), P.longicornis (dark gray), P.julius (blue), P.solanum (dark green) and P.hazelae (light blue). The colors used here correspond to those in Figure 2B.
Supplementary material 2 from: Royzenblat S, Kulacic J, Friedrich M (2023) Evidence of ancestral nocturnality, locomotor clock regression, and cave zone-adjusted sleep duration modes in a cave beetle. Subterranean Biology 45: 79-94. https://doi.org/10.3897/subtbiol.45.100717
Activity logs of the two long-term adjusted DD animals
Supplementary material 1 from: Royzenblat S, Kulacic J, Friedrich M (2023) Evidence of ancestral nocturnality, locomotor clock regression, and cave zone-adjusted sleep duration modes in a cave beetle. Subterranean Biology 45: 79-94. https://doi.org/10.3897/subtbiol.45.100717
Activity logs of select non-adjusting DD animals
Supplementary material 3 from: Royzenblat S, Kulacic J, Friedrich M (2023) Evidence of ancestral nocturnality, locomotor clock regression, and cave zone-adjusted sleep duration modes in a cave beetle. Subterranean Biology 45: 79-94. https://doi.org/10.3897/subtbiol.45.100717
Actograms of the long-term adjusted LD animals
Supplementary material 4 from: Royzenblat S, Kulacic J, Friedrich M (2023) Evidence of ancestral nocturnality, locomotor clock regression, and cave zone-adjusted sleep duration modes in a cave beetle. Subterranean Biology 45: 79-94. https://doi.org/10.3897/subtbiol.45.100717
Activity logs of the long-term adjusted LD animals
Fig. 1 – a in Distribution and bioclimatic suitability of Duvalius hartigi, subterranean beetle from the lava caves of Mount Etna (Coleoptera: Carabidae, Trechinae)
Fig. 1 – a, The sampling site "Grotta dei Lamponi", a lava cave formed during the 1614/24 eruption at 1718 m a.s.l.. Photo: F. Fiorenza; b, Pitfall trap placed on the cave floor of "Grotta di Piano Porcaria". Photo: G. Nicolosi; c, Specimen of Duvalius hartigi on the cave floor of "Grotta del Burrò". Photo: M. Isaia.
Figure 8 from: Tian M, Cheng G, Huang S (2021) A contribution to the knowledge of cave-adapted ground beetles from Guiyang, central Guizhou Province, southwestern China (Coleoptera, Carabidae, Trechini). ZooKeys 1075: 175-198. https://doi.org/10.3897/zookeys.1075.73318
Figure 8 Habitus of Zhijinaphaenops zhaofeii sp. nov., holotype, male.
Figure 2 from: Tian M, Cheng G, Huang S (2021) A contribution to the knowledge of cave-adapted ground beetles from Guiyang, central Guizhou Province, southwestern China (Coleoptera, Carabidae, Trechini). ZooKeys 1075: 175-198. https://doi.org/10.3897/zookeys.1075.73318
Figure 2 Habitus of Haixiaphaenops jinxiaohongae gen. nov., sp. nov., holotype, male
Figure 1 from: Tian M, Huang S, Wang D (2017) Discovery of a most remarkable cave-specialized trechine beetle from southern China (Coleoptera, Carabidae, Trechinae). ZooKeys 725: 37-47. https://doi.org/10.3897/zookeys.725.21040
Figure 1 Habitus of Xuedytes bellus Tian & Huang, gen. et sp. n., holotype male.
Figure 2 from: Tian M, Huang S, Wang D (2017) Discovery of a most remarkable cave-specialized trechine beetle from southern China (Coleoptera, Carabidae, Trechinae). ZooKeys 725: 37-47. https://doi.org/10.3897/zookeys.725.21040
Figure 2 Head (ventral) of Xuedytes bellus, a paratype female.
Figure 60 from: Moore MR, Cave RD, Branham MA (2018) Synopsis of the cyclocephaline scarab beetles (Coleoptera, Scarabaeidae, Dynastinae). ZooKeys 745: 1-99. https://doi.org/10.3897/zookeys.745.23683
Figure 60 Country-level distribution of Harposceles paradoxus in South America.
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International Brain Laboratory public data
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OpenNeuro
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