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154 results for “stag beetle”
FIGURE 1 in A checklist of stag beetles (Coleoptera: Scarabaeoidea: Lucanidae) from Iran
FIGURE 1. Map of Iran showing the province boundaries.
FIGURE 68 in Revision of the stag beetle genus Ryssonotus MacLeay (Coleoptera: Lucanidae), with descriptions of a new genus and three new species
FIGURE 68. Eastern Australia, distribution of Ryssonotus nebulosus (Kirby, 1819).
Fig. 18 in Description Of A New Genus And Species Of Stag Beetle (Coleoptera: Lucanidae: Lucaninae) From The Peruvian Andes
Fig. 18. Map of the known distributions for the species of Arnaudius.
Fig. 3 in Contribution to the Knowledge of the Australian Stag Beetles, with Description of a New Species ofLissotesWestwood, 1855 (Coleoptera: Lucanidae)
Fig. 3. Lissotes krakei, female, head and prothorax.
Figs. 4–6. Lissotes krakei, aedeagus. 4 in Contribution to the Knowledge of the Australian Stag Beetles, with Description of a New Species ofLissotesWestwood, 1855 (Coleoptera: Lucanidae)
Figs. 4–6. Lissotes krakei, aedeagus. 4) Dorsal view; 5) Ventral view; 6) Lateral view.
FIGURE 4 in A checklist of stag beetles (Coleoptera: Scarabaeoidea: Lucanidae) from Iran
FIGURE 4. Female of Lucanus xerxes, antenna.
FIGURE 2 in A checklist of stag beetles (Coleoptera: Scarabaeoidea: Lucanidae) from Iran
FIGURE 2. Female of Lucanus xerxes, habitus.
FIGURE 3 in A checklist of stag beetles (Coleoptera: Scarabaeoidea: Lucanidae) from Iran
FIGURE 3. Female of Lucanus xerxes, head and pronotum.
Supplementary material 2 from: Romiti F, Redolfi De Zan L, Rossi de Gasperis S, Tini M, Scaccini D, Anaclerio M, Carpaneto G (2017) Latitudinal cline in weapon allometry and phenology of the European stag beetle. In: Campanaro A, Hardersen S, Sabbatini Peverieri G, Carpaneto GM (Eds) Monitoring of saproxylic beetles and other insects protected in the European Union. Nature Conservation 19: 57-80. https://doi.org/10.3897/natureconservation.19.12681
Monthly total precipitations and temperatures : Data type: еnvironment data
Supplementary material 1 from: Della Rocca F, Bogliani G, Milanesi P (2017) Patterns of distribution and landscape connectivity of the stag beetle in a human-dominated landscape. In: Campanaro A, Hardersen S, Sabbatini Peverieri G, Carpaneto GM (Eds) Monitoring of saproxylic beetles and other insects protected in the European Union. Nature Conservation 19: 19-37. https://doi.org/10.3897/natureconservation.19.12457
Additional information :
Supplementary material 1 from: Zhang M, Ruan Y, Wan X, Tong Y, Yang X, Bai M (2019) Geometric morphometric analysis of the pronotum and elytron in stag beetles: insight into its diversity and evolution. ZooKeys 833: 21-40. https://doi.org/10.3897/zookeys.833.26164
: Data type: morphometric data
Figure 7 from: Zhang M, Ruan Y, Wan X, Tong Y, Yang X, Bai M (2019) Geometric morphometric analysis of the pronotum and elytron in stag beetles: insight into its diversity and evolution. ZooKeys 833: 21-40. https://doi.org/10.3897/zookeys.833.26164
Figure 7 Differences in elytron shape among each branch and ancestor, on the basis of principal component analysis. Empty dots indicate the number of the node on the phylogenetic tree; solid dots indicate the average shape of the extant subfamily/tribe of each branch.
Figure 6 from: Zhang M, Ruan Y, Wan X, Tong Y, Yang X, Bai M (2019) Geometric morphometric analysis of the pronotum and elytron in stag beetles: insight into its diversity and evolution. ZooKeys 833: 21-40. https://doi.org/10.3897/zookeys.833.26164
Figure 6 Differences in pronotum shape among each branch and ancestor, on the basis of principal component analysis. Empty dots indicate the number of the node on the phylogenetic tree; solid dots indicate the average shape of the extant subfamily/tribe of each branch.
Figure 5 from: Zhang M, Ruan Y, Wan X, Tong Y, Yang X, Bai M (2019) Geometric morphometric analysis of the pronotum and elytron in stag beetles: insight into its diversity and evolution. ZooKeys 833: 21-40. https://doi.org/10.3897/zookeys.833.26164
Figure 5 Reconstruction of ancestral groundplans of the elytron in Lucanidae and the outgroups. The splines indicate the deformation of the shapes relative to the reference configuration. The phylogenetic tree was summarized and reconstructed from earlier molecular results (Kim and Farrell 2015).
Figure 3 from: Zhang M, Ruan Y, Wan X, Tong Y, Yang X, Bai M (2019) Geometric morphometric analysis of the pronotum and elytron in stag beetles: insight into its diversity and evolution. ZooKeys 833: 21-40. https://doi.org/10.3897/zookeys.833.26164
Figure 3 Differences in elytron shape between outgroups and Lucanidae, on the basis of principal component analysis at the species level. The four circles are 90%-equal frequency ellipses of Lucanidae subfamilies.
Figure 4 from: Zhang M, Ruan Y, Wan X, Tong Y, Yang X, Bai M (2019) Geometric morphometric analysis of the pronotum and elytron in stag beetles: insight into its diversity and evolution. ZooKeys 833: 21-40. https://doi.org/10.3897/zookeys.833.26164
Figure 4 Reconstruction of ancestral groundplans of the pronotum in Lucanidae and the outgroups. The splines indicate deformation of the shapes relative to the reference configuration. The phylogenetic tree was summarized and reconstructed from earlier molecular results (Kim and Farrell 2015).
Figure 2 from: Zhang M, Ruan Y, Wan X, Tong Y, Yang X, Bai M (2019) Geometric morphometric analysis of the pronotum and elytron in stag beetles: insight into its diversity and evolution. ZooKeys 833: 21-40. https://doi.org/10.3897/zookeys.833.26164
Figure 2 Differences in pronotum shape between outgroups and Lucanidae, on the basis of principal component analysis at the species level. The four circles are 90%-equal frequency ellipses of Lucanidae subfamilies.
Figure 1 from: Zhang M, Ruan Y, Wan X, Tong Y, Yang X, Bai M (2019) Geometric morphometric analysis of the pronotum and elytron in stag beetles: insight into its diversity and evolution. ZooKeys 833: 21-40. https://doi.org/10.3897/zookeys.833.26164
Figure 1 Description of the curves used in geometric morphometric analysis. The positions selected for the pronotum and elytron curves are represented by Prosopocoilus sp. in dorsal view. The curves were resampled in 25 or 50 semi-landmarks (SLM).
Fig. 1. Falcicornis mellianus, male habitus. A in First Country Record of the Stag Beetle Species Falcicornis mellianus (Kriesche, 1921) (Coleoptera: Lucanidae) from Laos
Fig. 1. Falcicornis mellianus, male habitus. A) Dorsal view, B) Ventral view. Scale bar: 1.0 cm.
Data From: Genetic structure of recently fragmented suburban populations of European stag beetle
<p>Habitat loss and fragmentation due to urbanisation can negatively affect metapopulation persistence when gene flow among populations is reduced and population sizes decrease. Inference of patterns and processes of population connectivity derived from spatial genetic analysis has proven invaluable for conservation and management. However, a more complete account of population dynamics may be obtained by combining spatial and temporal sampling. We, therefore, performed a genetic study on European stag beetle (<i>Lucanus cervus</i> L.) populations in a suburban context using samples collected in three locations and during the period 2002-2016. The sampling area has seen recent landscape changes which resulted in population declines. Through the use of a suite of FST, clustering analysis, individual assignment, and relatedness analysis we assessed fine scale spatiotemporal genetic variation within and among habitat patches using 283 individuals successfully genotyped at 17 microsatellites. Our findings suggested the three locations to hold demographically independent populations, at least over time scales of relevance to conservation, though with higher levels of gene flow in the past. Contrary to expectation from tagging studies, dispersal appeared to be mainly female-biased. Although the life cycle of stag beetle suggests its generations to be discrete, no clear temporal structure was identified, which could be attributed to the varying duration of larval development. Since population bottlenecks were detected and estimates of effective number of breeders were low, conservation actions are eminent which should include the establishment of suitable dead wood for oviposition on both local and regional scales to increase (re)colonisation success and connectivity among current populations.</p>
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