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662 results for “Rove Beetles”
Figure 3 in Aedeagus evolution promotes speciation? A primary pattern in rove beetle phylogeny
Figure 3. Plotting Paramere-to-Median-lobe Index (PM Index) and the number of species of the selected genera (Y axis) with the divergence time (X axis) estimated. PM Index variations along with divergence time (a, c); species number variations along with evolutionary time (b, d). The abbreviation of geological ages are as follows: Jur—Jurassic; Cre—Cretaceous; Pal—Paleocene; Eoc— Eocene; Oli—Oligocene; Mio—Miocene; Pli—Pliocene.
Figure 2. Figure 2 in Aedeagus evolution promotes speciation? A primary pattern in rove beetle phylogeny
Figure 2. Figure 2. Phylogeny of the subfamily Staphylininae with divergence time estimates based on the concatenated sequence. Blue bars at each node show 95% highest posterior density interval for the main nodes. Colored branches and circled capital letters are as in Figure 1. Circled numbers refer to three main sub-clades within Clade A discussed in text. Circled roman letters represent the calibration points. Capital letter 'A', 'P' and 'N' represent aedeagus, paramere and species number of each corresponding genus respectively. Colored arrows refer to phylogenetic patterns of aedeagus morphology discussed in text. Dot lines with lower case letters refer to divergence times discussed in text. The abbreviation of geological ages are as follows: Jur—Jurassic; Cre—Cretaceous; Pal— Paleocene; Eoc—Eocene; Oli—Oligocene; Mio—Miocene; Pli—Pliocene.
Figure 1 in Aedeagus evolution promotes speciation? A primary pattern in rove beetle phylogeny
Figure 1. Bayesian phylogenetic tree for the partitioned combined analysis of four genes. Only posterior probabilities above 0.60 are shown. Colored branches represent the mainly monophyletic groups resolved in the phylogenetic inference. Verticle bars: thick bars denote the tribes of Staphylinini, thin bars the subtribes, grey bar the outgroup. The capital letters "A" and "B" refer to two main clades discussed in the text.
Additional set of photos for the publication "The oldest case of paedomorphosis in rove beetles: a new genus of Paederinae from Cretaceous amber (Coleoptera: Staphylinidae)"
<p>Additional set of photos of two specimens of extinct <em>Midinudon juvenis</em> Tokareva & Żyła gen. et sp. nov. (Coleoptera: Staphylinidae) in Burmese amber. Accession codes of specimens in the collection of the Leibniz Institute for the Analysis of Biodiversity Change are GPIH05515 and GPIH05516.</p>
Data for: Termite nest evolution fostered social parasitism by termitophilous rove beetles
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Fig 2 in Significant range expansion for the rove beetle genus Deleaster, based on a new species from Papua New Guinea (Coleoptera: Staphylinidae: Oxytelinae)
Fig 2. Distribution of extant Deleaster Erichson, 1839.
Figure 6 in Survey of rove beetles (Coleoptera, Staphylinidae) from Stanley Park, Vancouver, British Columbia, Canada, with new records and description of a new species. Part 2
Figure 6. Sonoma squamishorum, dorsal view (holotype). Apical part of abdomen removed.
Fig. 1 in Ocypus (Pseudocypus) aethiops (Waltl, 1835) - new but not unexpected rove beetle in Canary Islands (Coleoptera, Staphylinidae)
Fig. 1. Ocypus aethiops (Waltl) - a specimen caught by author; scale bar = 2 mm
Figure 1 in Rove beetle communities (Coleoptera: Staphylinidae) in the rock dumps after coal mining
Figure 1. Location of the study site.
Rapid recovery of boreal rove beetle (Staphylinidae) assemblages 16 years after variable retention harvest
<p>Post-harvest recovery<span> of biodiversity is one of the important goals in modern forestry. A variable retention (VR) approach has been of particular interest in North America because it promotes rapid faunal recovery while </span>minimizing the negative lasting impacts of logging on the natural fauna. <span>We studied responses of </span>rove beetles (Coleoptera: Staphylinidae) to a broad range of retention harvests (2, 10, 20, 50, and 75 % retention) in comparison to uncut controls as part of the <span>Ecosystem Management Emulating Natural Disturbance (EMEND) experiment in the boreal mixedwood forest of western Canada. We sampled beetles using pitfall traps 1, 2, 11, and 16 years post-harvest in replicated (n=3) stands representing four cover types (deciduous-dominated, deciduous with spruce understory, mixed, and coniferous-dominated). We collected</span> 74,263 individuals distributed across 99 species (excluding Aleocharinae). <span>Estimated species richness was highest in clear-cuts until year 11, but by year 16 species richness was similar among treatments. Species composition initially varied strongly in relation to the intensity of harvest treatments, but overall variation decreased with time</span>, and by year 16, species composition overlapped among most treatment combinations. Assemblages recovered more quickly in <span>early successional (deciduous-dominated) </span>than in <span>late successional (</span>mixed and <span>conifer-dominated) stands. Overall, our results show that rove beetle assemblages in stands harvested to all VR prescriptions converged more rapidly toward those in fire-origin mature stands than did assemblages in clear-cuts over the first 16 years post-harvest. Thus, it demonstrates that even modest levels of forest retention can facilitate the recovery of staphylinid assemblages in managed landscapes.</span></p>
Rove beetle (Staphylinidae) assemblages following the cumulative effect of wildfire and linear footprint in Boreal treed peatlands of northeastern Alberta (Canada)
<p>Cumulative effects of anthropogenic and natural disturbances have become increasingly relevant in the context of biodiversity conservation. Oil and gas (OG) exploration and extraction activities have created thousands of kilometers of linear footprints in boreal ecosystems of Alberta, Canada. Among these disturbances, seismic lines (narrow corridors cut through the forest) are one of the most common footprints and have become a significant landscape feature influencing the maintenance of forest interior habitats and biodiversity. <a name="_Hlk118288505"></a>Wildfire is a common stand-replacing natural disturbance in the boreal forest, and as such, it is hypothesized that its effects can mitigate the linear footprint associated with OG exploration, but only a few studies have examined its effectiveness. We studied the short-term (1 year post-fire) response of rove beetle assemblages to the combined effects of wildfire and linear footprint in forest, edge and seismic line habitats at burned and unburned peatlands along the southwest perimeter of the 2016 Horse River wildfire (Fort McMurray). While rove beetle species richness was higher in seismic lines in both burned and unburned habitats compared to the adjacent peatland, diversity was greater only in seismic lines of burned areas. Abundance was lower in the burned adjacent peatland but similarly higher in the remaining habitats. Assemblage composition on seismic lines was significantly different from that in the adjacent forest and edge habitats within both burned and unburned sites. Moreover, species composition in burned seismic lines was different to either unburned lines or burned forest and edge. <a name="_Hlk89787659"></a><em>Euaesthethus laeviusculus</em> and <em>Gabrius picipennis</em> were indicator species of burned line habitats, are sensitive to post-fire landscape and can occupy wet habitats with moss cover more efficiently than when these habitats are surrounded by unburned forest. Although these results are based on short-term responses, they suggest that wildfire did not reduce the linear footprint, and instead, the cumulative effect of these two disturbances had a more complex influence on rove beetle recovery at the landscape level than for other invertebrates. Therefore, continued monitoring of these sites can become useful to evaluate changes over time and to better understand longer-term biodiversity responses to the cumulative effects of wildfire and linear disturbances in boreal treed peatlands, given the long-lasting effect of such disturbances.</p>
Rapid recovery of boreal rove beetle (Staphylinidae) assemblages 16 years after variable retention harvest
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Rove beetle (Staphylinidae) assemblages following the cumulative effect of wildfire and linear footprint in Boreal treed peatlands of northeastern Alberta (Canada)
Open the record for dataset details and reuse information.
FIGURES 12–20 in A new species and new record of the intertidal rove beetle genus Bryothinusa Casey (Staphylinidae: Aleocharinae: Myllaenini) from Japan
FIGURES 12–20 Bryothinusa koreana Ahn & Jeon, 2004 from Kyûshû, 12, Labrum; 13, Mandible. lateral view; 14, Lacinia. lateral view; 15, Labium; 16, Mentum; 17, Median lobe, ventral view; 18, Median lobe, lateral view; 19, Paramere; 20, Spermatheca. Scale bars=0.1 mm.
FIGURES 3–11 in A new species and new record of the intertidal rove beetle genus Bryothinusa Casey (Staphylinidae: Aleocharinae: Myllaenini) from Japan
FIGURES 3–11 Bryothinusa japonica sp. nov., 3, Labrum; 4, Mandible. lateral view; 5, Lacinia. lateral view; 6, Labium; 7, Mentum; 8, Median lobe, ventral view; 9, Median lobe, lateral view; 10, Paramere; 11, Spermatheca. Scale bars=0.1 mm.
FIGURE 4 in Cyanocypus gen. nov., a new rove beetle genus of the "Staphylinus-complex" (Coleoptera: Staphylinidae) with one new species from China
FIGURE 4. Cyanocypus leukos He & Zhou, sp. nov.: A. underside of apical portion of paramere; B and D. aedeagus, lateral view; C. aedeagus, ventral view; E. male tergite 10; F. apical portion of median lobe, ventral view, paramere removed; G. male sternite 9; H. male sternite 8. Scale bars = 0.50 mm.
FIGURE 1 in Cyanocypus gen. nov., a new rove beetle genus of the "Staphylinus-complex" (Coleoptera: Staphylinidae) with one new species from China
FIGURE 1. Cyanocypus leukos He & Zhou, sp. nov.: A. habitus, dorsal view (2.0 mm); B. habitus, ventral view (2.0 mm); C. left mandible (0.5 mm); D. right mandible (0.5 mm). Scales in parentheses.
FIGURES 13–18 in A new species and new records of Malagasy Megalopinus Eichelbaum (Coleoptera Staphylinidae, Megalopsidiinae), with notes on the sperm pump in rove beetles
FIGURES 13–18. Megalopinus heissi Puthz, male. Dorsal habitus (13); head, pronotum and elytra in dorsal (14) and lateral (15) views; aedeagus in dorsal (16) and lateral (17) views; close-up of endophallic structures (18).
FIGURES 7–12 in A new species and new records of Malagasy Megalopinus Eichelbaum (Coleoptera Staphylinidae, Megalopsidiinae), with notes on the sperm pump in rove beetles
FIGURES 7–12. Megalopinus lemur Puthz, male. Dorsal habitus (7); head, pronotum and elytra in dorsal (8) and lateral (9) views; aedeagus in dorsal (10) and lateral (11) views; close-up of endophallic structures (12).
FIGURES 19–27 in A new species and new records of Malagasy Megalopinus Eichelbaum (Coleoptera Staphylinidae, Megalopsidiinae), with notes on the sperm pump in rove beetles
FIGURES 19–27. Examples of sperm pumps in Staphylinidae. Euaesthetinae: Edaphus sp. (19); Euaesthetinae: Euaesthetus ruficapillus (Lacordaire) (20); Steninae: Stenus ludyi Fauvel (21); Solieriinae: Solierius obscurus (Solier) (22); Scydmaeninae: Leptochromus laselva Lord et al. (23); Scydmaeninae: Ablepton treforti Frivaldszky (24); Scydmaeninae: Taurablepton sp. (25); Scydmaeninae: Clidicus assymetricus Jałoszyński (26); Scydmaeninae: Stenomastigus longicornis (Boheman), histological cross-section through middle region of sperm pump (27). Abbreviations: aed, aedeagus; de, ductus ejaculatorius; fn, funnel; ms, muscle; spp, sperm pump.
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