Morphology of the developmental stages ofHypnogyra angularis (Ganglbauer, 1895) (Coleoptera, Staphylinidae, Staphylininae)

Pietrykowska-Tudruj, Ewa; Staniec, Bernard

doi:10.1002/mmnd.200600007

Cited by 7 publications

(18 citation statements)

References 2 publications

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“…Labium, membranous copula on anterior margin on prementum, length: (0) long, slightly longer than ligula (fig. 18 in Pietrykowska‐Tudruj & Staniec, 2006a); (1) short, shorter than ligula (Fig. 6H).…”

Section: Phylogenetic Analysismentioning

confidence: 99%

“…11F in Solodovnikov & Newton, 2005); (3) ventral ecdysial line entirely forming apotome that is scale‐like, lateral sides slightly convex, without stalk (fig. 6 in Pietrykowska‐Tudruj & Staniec, 2006a); (4) ventral ecdysial line entirely forming apotome that is constricted posteriorly behind pair of posterior setae on apotome, forming stalk (Fig. 4L).…”

Section: Phylogenetic Analysismentioning

confidence: 99%

“…6B); (2) three (fig. 15 in Pietrykowska‐Tudruj & Staniec, 2006a). Mandibles, tooth or lobes on inner margin: (0) absent (fig.…”

Section: Phylogenetic Analysismentioning

confidence: 99%

“…6H); (1) laterally (fig. 18 in Pietrykowska‐Tudruj & Staniec, 2006a). Labium, anterior margin of prementum, membranous copula: (0) absent (fig.…”

Section: Phylogenetic Analysismentioning

confidence: 99%

“…6H); (1) ventroapical (fig. 18 in Pietrykowska‐Tudruj & Staniec, 2006a); (2) ventrolateroapical, near (but not on) inner margin. Ligula, shape: (0) elliptical, base and apex rounded (fig. 22 in Staniec, 2005b); (1) conical, gently narrowed to apex (Fig.…”

Section: Phylogenetic Analysismentioning

confidence: 99%

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Discovery of the Quedius antipodum Sharp larva from New Zealand: phylogenetic test of larval morphology for Staphylinini at the intratribal level (Coleoptera: Staphylinidae)

Pietrykowska-Tudruj

Staniec

Solodovnikov

2011

Systematic Entomology

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Quedius antipodum Sharp is an endemic species from New Zealand. Here we describe its larva, the first of the species‐rich group of the south temperate ‘Quedius’ spp. This finding throws light on the controversy between the conventional systematics of Quedius Stephens and newer phylogenetic analyses, both of which are based on non‐larval characters only. We compare the larva of Q. antipodum with those of the north temperate Quedius (Quediina), where it was traditionally placed, and with the known larvae of Amblyopinina, a group where Q. antipodum was placed by recent phylogenetic studies. Sister‐group relationships of Q. antipodum within the tribe Staphylinini are explored based on larvae by means of parsimony analysis: 77 morphological characters scored for 20 species from 17 genera. Consistent with the adult morphology and DNA sequences, larvae‐based cladistic analysis confirms that Q. antipodum should not be placed in the north temperate genus Quedius. However, larval analysis alone remains dubious with respect to finding the exact sister relationships of that species.

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Section: Phylogenetic Analysismentioning

confidence: 99%

Section: Phylogenetic Analysismentioning

confidence: 99%

“…6B); (2) three (fig. 15 in Pietrykowska‐Tudruj & Staniec, 2006a). Mandibles, tooth or lobes on inner margin: (0) absent (fig.…”

Section: Phylogenetic Analysismentioning

confidence: 99%

“…6H); (1) laterally (fig. 18 in Pietrykowska‐Tudruj & Staniec, 2006a). Labium, anterior margin of prementum, membranous copula: (0) absent (fig.…”

Section: Phylogenetic Analysismentioning

confidence: 99%

Section: Phylogenetic Analysismentioning

confidence: 99%

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Discovery of the Quedius antipodum Sharp larva from New Zealand: phylogenetic test of larval morphology for Staphylinini at the intratribal level (Coleoptera: Staphylinidae)

Pietrykowska-Tudruj

Staniec

Solodovnikov

2011

Systematic Entomology

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Comparative morphology of the eggs of sixteen Central European species of Staphylininae (Coleoptera, Staphylinidae)

Staniec

Pietrykowska-Tudruj

2007

Dtsch. Entomol. Z.

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Morphological characters of the eggs of Bisnius nitidulus, Gabrius osseticus, G. splendidulus, G. trossulus, Gyrohypnus atratus, Heterothops niger, Neobisnius villosulus, Quedius brevicornis, Q. brevis, Q. microps, Philonthus alpinus, Ph. atratus, Ph. corvinus, Ph. lepidus, Ph. micans and Tasgius melanarius are described and illustrated for the first time. Based on the morphology of eggs, species for which eggs were already known and those for which eggs are described here, are divided into 9 groups. Differences in the eggs morphological structure cover: presence or absence and the number of longitudinal ridges; presence or absence of the projection on poles, and structure of its distal end; ratio of egg length to the length of posterior projection; presence or absence of the rostrum-shaped apex and the concave, sloping area on the posterior pole; arrangement, number and structure of aeropyles, and the measurements.

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Potential phylogenetic significance of the number of functional abdominal spiracles in beetle pupae, with focus on Staphylinoidea (Coleoptera)

Newton

2020

Pap. Avulsos Zool.

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The distribution of functional abdominal spiracles in pupae of Coleoptera is reviewed based on published descriptions and original observations. Aquatic Coleoptera typically have strong modifications, generally including dramatic reductions in the number of functional spiracles and often their modification into either spiracular gills or snorkels, as a response to their environment. But pupae of the great majority of Coleoptera, which are terrestrial, show broad stability across higher taxa. Most terrestrial beetles have at least the first five pairs of abdominal spiracles functional, up to and including a full set of eight pairs. However, the number is unexpectedly low in Scarabaeoidea and within Staphyliniformia, where Histeridae and all Staphylinoidea have a confirmed maximum of four pairs of spiracles. The relation between pupal size and number of functional spiracles in terrestrial pupae is explored, and it is suggested that those groups with an unexpectedly small number of functional spiracles may have passed through a “small-size bottleneck” in their ancestry. However, this hypothesis does not explain why several families of very small beetles in other groups of Coleoptera do not show a similar reduction, and little evidence was found to support a strong relation between pupal size and number of functional spiracles at lower taxonomic levels (below family). Whether pupae are exarate or obtect apparently also has little correlation with the number of functional spiracles. However, the consistency and stability of spiracular reductions in the above groups suggests that deep historical factors are involved and thus the reductions may be of phylogenetic significance. It is urged that establishing the number of functional spiracles in beetle pupae become as standard a feature of pupal descriptions as chaetotaxy and whether they are exarate or obtect.

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Morphology of the developmental stages ofHypnogyra angularis (Ganglbauer, 1895) (Coleoptera, Staphylinidae, Staphylininae)

Cited by 7 publications

References 2 publications

Discovery of the Quedius antipodum Sharp larva from New Zealand: phylogenetic test of larval morphology for Staphylinini at the intratribal level (Coleoptera: Staphylinidae)

Discovery of the Quedius antipodum Sharp larva from New Zealand: phylogenetic test of larval morphology for Staphylinini at the intratribal level (Coleoptera: Staphylinidae)

Comparative morphology of the eggs of sixteen Central European species of Staphylininae (Coleoptera, Staphylinidae)

Potential phylogenetic significance of the number of functional abdominal spiracles in beetle pupae, with focus on Staphylinoidea (Coleoptera)

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