scholarly journals Ecological and zoogeographical groups of rove beetles (Staphylinidae, Coleoptera, Insecta) of Subalpine Belt of Northeastern macroslope of Ukrainian Carpathians

2019 ◽  
Vol 13 (1) ◽  
pp. 107-116
Author(s):  
M. P. Lutska ◽  
Keyword(s):  
Rove Beetles ◽  
Subalpine Belt

Predator release from invertebrate generalists does not explain geometrid moth (Lepidoptera: Geometridae) outbreaks at high altitudes

2013 ◽  
Vol 145 (2) ◽  
pp. 184-192 ◽  
Author(s):  
Tino Schott ◽  
Lauri Kapari ◽  
Snorre B. Hagen ◽  
Ole Petter L. Vindstad ◽  
Jane U. Jepsen ◽  
...  
Keyword(s):  
Carabid Beetles ◽  
Birch Forest ◽  
Generalist Predators ◽  
Tree Line ◽  
High Altitudes ◽  
Lower Altitude ◽  
Rove Beetles ◽  
Northern Norway ◽  
Winter Moth ◽  
Underlying Mechanisms

AbstractOutbreaks of geometrid defoliators in subarctic birch forest in Fennoscandia often occur at high altitude in a distinct zone along the tree line. At the same time, moth larvae may not have an impact on the forest at lower altitude. Directly adjacent outbreak and nonoutbreak areas offer unique opportunities for studying the underlying mechanisms of outbreaks. Within two altitudinal gradients in coastal northern Norway, we investigated whether altitudinal outbreaks might be caused by release from pupal predation by ground-dwelling invertebrates such as harvestmen (Opiliones), spiders (Araneae), rove beetles (Coleoptera: Staphylinidae), carabid beetles (Coleoptera: Carabidae), and other beetles (Coleoptera). We predicted a consistently higher abundance of such generalist predators at low versus high altitudes. Our results did not support this prediction. There was no consistent altitudinal variation in the abundance of predators that could be related to zonal moth outbreaks in the birch forest slopes. In addition, none of the predator groups investigated showed any numerical response to a distinct outbreak of winter moth that took place during the course of the study. Consequently, localised moth outbreaks at the altitudinal tree line in northern Norway cannot be explained by the release from pupal predation by the predator groups examined here.

Adaptations of Coleoptera to the marine environment. II. Observations on rove beetles (Staphylinidae) from rocky shores

1988 ◽  
Vol 66 (11) ◽  
pp. 2469-2474 ◽  
Author(s):  
Werner Topp ◽  
Richard A. Ring
Keyword(s):  
Oxygen Consumption ◽  
Spring Tide ◽  
Salinity Range ◽  
Laboratory Population ◽  
Rocky Shores ◽  
Temperature Dependent ◽  
Rove Beetles ◽  
Dry Conditions ◽  
Lethal Time ◽  
Rate Of Evaporation

Two common rove beetles inhabit the intertidal rocky shores of British Columbia: Liparocephalus cordicollis Le Conte and Diaulota densissima Casey. Liparocephalus cordicollis, the more abundant of the two, is a predator that feeds preferentially on small chironomid larvae. Adults and larvae of this species can withstand submergence in seawater at 10 °C for more than 2 weeks. Thus they are able to survive continuous inundation from one spring tide to the next, just above lowest tide levels. Adults of L. cordicollis are osmotic regulators and can stabilize their body weight at salinities varying from 2 to 45‰. Both of these staphylinid species respire above and below water. Oxygen consumption of L. cordicollis in air at 10 °C was 376 ± 59 μL O2∙g−1∙h−1, but when the beetles were immersed in seawater at the same temperature the respiration rate was reduced to 45 ± 8 μL O2∙g−1∙h−1. During submersion, temperature-dependent reactions were observed (Q10 = 2). Respiration was constant within the salinity range of 2–30‰, but at higher levels (45‰) oxygen consumption increased to 55 ± 5 μL∙g−1∙h−1. When L. cordicollis was exposed to warm, dry conditions (simulating low tide on a warm summer day) the rate of evaporation from the cuticle was very high, calculated at 175 μg H2O loss per cm2 body surface per hour per mm Hg saturation deficit. The LT50 (mean lethal time) for a laboratory population was 2.5 h at a vapor pressure deficit of 7 mm Hg. In the larvae of beetles of the two species, asynchrony of growth in the population occurs because submerged larvae stop feeding and growing. Consequently, the development of individuals living near the low tide line is protracted compared with that of individuals living in the midlittoral zone.

Rove beetles (Coleoptera Staphylinidae) – Their abundance and competition with other predatory groups in Bt maize expressing Cry34Ab1, Cry35Ab1, Cry1F and CP4 EPSPS proteins

2016 ◽  
Vol 80 ◽  
pp. 87-93 ◽  
Author(s):  
Zoltán Pálinkás ◽  
Mihály Zalai ◽  
Ágnes Szénási ◽  
Ferenc Kádár ◽  
Zita Dorner ◽  
...  
Keyword(s):  
Bt Maize ◽  
Rove Beetles ◽  
Cp4 Epsps

Corrigendum to: Cladistic analysis and revision of Piestus Gravenhorst with remarks on related genera (Coleoptera : Staphylinidae : Piestinae)

2013 ◽  
Vol 27 (1) ◽  
pp. 129
Author(s):  
Edilson Caron ◽  
Cibele S. Ribeiro-Costa ◽  
Alfred F. Newton
Keyword(s):  
Cladistic Analysis ◽  
Taxonomic Revision ◽  
Sister Group ◽  
Morphological Characters ◽  
Valid Species ◽  
Phylogenetic Position ◽  
Neotropical Forests ◽  
Rove Beetles ◽  
New Synonyms ◽  
Branch Support

Rove beetles of the genus Piestus Gravenhorst, 1806 are commonly captured under the bark of or inside decaying logs from Neotropical forests. Piestus belongs to the subfamily Piestinae, historically an ill-defined dumping-ground for Staphylinidae defined by plesiomorphic characters, but which has gradually been restricted in concept and currently includes only six additional extant genera worldwide. Piestinae in this restricted sense has been considered a probably monophyletic subfamily, but its status and phylogenetic position, as a possible sister-group of Osoriinae within the recently proposed Oxyteline group of staphylinid subfamilies, are uncertain and need confirmation. The main aim of the present study was to provide a morphological cladistic analysis and complete taxonomic revision of Piestus, which, as the type and most speciose genus of Piestinae, is critical for future phylogenetic studies involving the subfamily. In our study, the monophyly of Piestus is established and phylogenetic relationships among its species are proposed based on 70 adult morphological characters. Piestus is supported by 11 synapomorphies and high branch support. All species of Piestus are revised and the genus is redefined. The genus contains 43 species, including 13 species described here for the first time. The previously proposed subgenera Antropiestus Bernhauer, 1917, Eccoptopiestus Scheerpeltz, 1952, Elytropiestus Scheerpeltz, 1952, Lissopiestus Scheerpeltz, 1952, Piestus s. str., Trachypiestus Scheerpeltz, 1952 and Zirophorus Dalman, 1821 have not been confirmed, as they were found to be poly- or paraphyletic, or are here removed from Piestus, and therefore subgenera are not used. The main taxonomic changes are as follows. Lissopiestus, syn. nov. is proposed as new synonym of Eleusis Laporte, 1835 and its species, E. interrupta (Erichson, 1840), comb. rest., is transferred again to that genus. Antropiestus, syn. nov. and Eccoptopiestus, syn. nov. are proposed as new synonyms of Hypotelus Erichson, 1839 and their species, H. laevis (Solsky, 1872), comb. nov. and H. andinus (Bernhauer, 1917), comb. nov., are transferred to Hypotelus. Fourteen new synonymies are proposed (valid species listed first): P. lacordairei Laporte, 1835 = Z. furcatus Sharp, 1887, syn. nov.; P. capricornis Laporte, 1835 = P. frontalis Sharp, 1876, syn. nov.; P. pennicornis Fauvel, 1864 = P. plagiatus Fauvel, 1864, syn. nov.; P. rectus Sharp, 1876, syn. nov.; P. pygialis Fauvel, 1902, syn. nov.; P. surinamensis Bernhauer, 1928, syn. nov.; P. minutus Erichson, 1840 = P. nigrator Fauvel, 1902, syn. nov.; P. sulcatus Gravenhorst, 1806 = P. sanctaecatharinae Bernhauer, 1906, syn. nov.; P. condei Wendeler, 1955, syn. nov.; P. gounellei Fauvel, 1902 = P. wasmanni Fauvel, 1902, syn. nov.; P. mexicanus Laporte, 1835 = P. alternans Sharp, 1887, syn. nov.; P. aper Sharp, 1876 = P. schadei Scheerpeltz, 1952, syn. nov.; P. angularis Fauvel, 1864 = P. crassicornis Sharp, 1887, syn. nov.; H. andinus (Bernhauer, 1917) = P. strigipennis Bernhauer, 1921, syn. nov. One species is revalidated: P. fronticornis (Dalman, 1821), stat. rev., and one synonym is restored: P. penicillatus (Dalman, 1821) = P. erythropus Erichson, 1840, syn. rest. Neotypes are designated for P. lacordairei Laporte, 1835 and Oxytelus bicornis Olivier, 1811, and lectotypes are designated for P. puncticollis Fauvel, 1902, P. capricornis variety muticus Fauvel, 1902, P. zischkai Scheerpeltz, 1951, P. pennicornis Fauvel, 1864, P. plagiatus Fauvel, 1864, P. pygmaeus Laporte, 1835, P. niger Fauvel 1864, P. minutus Erichson, 1840, P. nigratror Fauvel, 1902, P. sulcatus Gravenhorst, 1806, P. sanctaecatharinae Bernhauer, 1906, P. sulcipennis Scheerpeltz, 1952, P. aper Sharp, 1876, P. schadei Scheerpeltz, 1952 and P. andinus Bernhauer, 1917.

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