Speciation patterns in the Forficula auricularia species complex: cryptic and not so cryptic taxa across the western Palaearctic region

2020 ◽  
Vol 190 (3) ◽  
pp. 788-823 ◽  
Author(s):  
Rubén González-Miguéns ◽  
Eva Muñoz-Nozal ◽  
Yolanda Jiménez-Ruiz ◽  
Paloma Mas-Peinado ◽  
Hamid R Ghanavi ◽  
...  
Keyword(s):  
Sequence Data ◽  
Niche Overlap ◽  
Forficula Auricularia ◽  
Evolutionary Trajectory ◽  
Mitochondrial Coi ◽  
Morphometric Analyses ◽  
Cryptic Taxa ◽  
Western Palaearctic ◽  
New Synonymy ◽  
European Earwig

Abstract Forficula auricularia (the European earwig) is possibly a complex of cryptic species. To test this hypothesis, we performed: (1) a phylogeographic study based on fragments of the mitochondrial COI and the nuclear ITS2 markers on a wide geographic sampling, (2) morphometric analyses of lineages present in Spain and (3) niche overlap analyses. We recovered five reciprocally monophyletic ancient phylogroups with unique historical patterns of distribution, climatic niches and diversification. External morphology was conserved and not correlated with speciation events, except in one case. Phylogenetic placement of the morphologically distinct taxon renders F. auricularia paraphyletic. Based on the congruence of the phylogenetic units defined by mtDNA and nuclear sequence data, we conclude that phylogroups have their own historical and future evolutionary trajectory and represent independent taxonomic units. Forficula auricularia is a complex of at least four species: the morphologically diagnosable Forficula aeolica González-Miguéns & García-París sp. nov., and the cryptic taxa: Forficula mediterranea González-Miguéns & García-París sp. nov., Forficula dentataFabricius, 1775stat. nov. and Forficula auriculariaLinnaeus, 1758s.s. We also provide new synonymy for F. dentata.

Morphological and molecular characterization of Mermisnigrescens Dujardin, (Nematoda: Mermithidae) parasitizing the introduced European earwig (Dermaptera: Forficulidae) in New Zealand

2014 ◽  
Vol 89 (3) ◽  
pp. 267-276 ◽  
Author(s):  
B. Presswell ◽  
S. Evans ◽  
R. Poulin ◽  
F. Jorge
Keyword(s):  
New Zealand ◽  
18S Rrna ◽  
Sequence Data ◽  
18S Rrna Gene ◽  
Parasitic Nematodes ◽  
Rrna Gene ◽  
28S Rrna ◽  
Forficula Auricularia ◽  
Adult Females ◽  
European Earwig

AbstractParasitic nematodes of the family Mermithidae were found to be infecting the introduced European earwig Forficula auricularia (Dermaptera: Forficulidae) in Dunedin, South Island, New Zealand. Adult females were later collected from various garden plants while depositing eggs. These mermithid specimens were identified morphologically as Mermis nigrescens Dujardin, 1842. A genetic distance of 0.7% between these specimens and a M. nigrescens isolate from Canada (18S rRNA gene), suggests that they have diverged genetically, but there are currently no available comparable sequences for the European M. nigrescens. Two additional nuclear fragments were also amplified, the 28S rRNA and the ribosomal DNA first internal transcribed spacer (ITS1), providing a basis for future studies. Bearing in mind the morphological similarity with other reported M. nigrescens and the lack of sequence data from other parts of the world, we retain the name M.nigrescens, and suggest that the species may be found to represent a complex of cryptic species when more worldwide data are available. Herein, we present a brief description of the post-parasitic worms and adult females, along with an inferred phylogeny using 18S rRNA gene sequences.

scholarly journals Frequent discordance between morphology and mitochondrial DNA in a species group of European water beetles (Coleoptera: Dytiscidae)

PeerJ ◽  
2017 ◽  
Vol 5 ◽  
pp. e3076
Author(s):  
David T. Bilton ◽  
Lucy Turner ◽  
Garth N. Foster
Keyword(s):  
Mitochondrial Dna ◽  
Sequence Data ◽  
Introgressive Hybridization ◽  
Species Group ◽  
Central Spain ◽  
Water Beetles ◽  
Mitochondrial Coi ◽  
Dna Sequence Variation ◽  
Western Palaearctic ◽  
Evolutionary Lineages

TheHydroporus memnoniusspecies group includes both widespread and range restricted diving beetle taxa in the western Palaearctic, some of which have been divided into a number of geographical subspecies. Of these,Hydroporus necopinatusis distributed in the far west of Europe, from central Spain to southern Britain, and has been split into three subspecies, occurring in Iberia (necopinatussst.), France (robertorum) and England (roni) respectively—the last of these being a rare example of an insect taxon apparently endemic to northern Europe. Here we explore inter-relationships between populations and subspecies ofH. necopinatusand related members of theHydroporus melanariussubgroup, using mitochondrial COI sequence data. We reveal widespread discordance between mitochondrial DNA sequence variation and morphology in areas whereH. necopinatusandH. melanariuscome into contact, consistent with historical introgressive hybridization between these taxa. In light of this discordance, the lack of clear genetic divergence betweenH. necopinatussubspecies, and the fact that bothrobertorumandroniare morphologically intermediate betweenH. necopinatussstr. andH. melanarius, we suggest that these taxa may be of hybridogenic origin, rather than representing discrete evolutionary lineages.

scholarly journals Revision of the West Palaearctic Euura bergmanni and oligospila groups (Hymenoptera, Tenthredinidae)

2021 ◽  
Vol 84 ◽  
pp. 187-269
Author(s):  
Marko Prous ◽  
Andrew Liston ◽  
Marko Mutanen
Keyword(s):  
Southern Hemisphere ◽  
Sequence Data ◽  
Species Discrimination ◽  
The West ◽  
Genetic Sequence ◽  
Mitochondrial Coi ◽  
Incertae Sedis ◽  
Males And Females ◽  
Western Palaearctic ◽  
Group Species

Eight Western Palaearctic Euura species are here assigned to the bergmanni group (bergmanni, brevivalvis, dispar, glutinosae, leptocephalus, respondens, sylvestris, and viridis) and two species to the oligospila group (frenalis and oligospila). Euura pallens (Konow, 1903) (bergmanni group) is removed from the list of West Palaearctic taxa. Euura pyramidalis (Hellén, 1948) is treated as incertae sedis within the bergmanni group. Definitions of the bergmanni and oligospila groups are primarily based on genetic sequence data (mitochondrial COI and nuclear NaK and POL2). We report likely occurrence of heteroplasmy and amplification of NUMTs among some of the treated species, complicating the use of DNA barcoding in species discrimination. Based on morphological and genetic evidence, we establish that the correct name for the invasive willow sawfly in the southern hemisphere (South America, southern Africa, Australia, New Zealand), known there only in the female sex, is Euura respondens (Förster, 1854). The species is probably native to the Palaearctic (or even Holarctic) where males are common: possibly as common as females (examined from Europe and Central Asia). The name Euura oligospila (Förster, 1854) has been incorrectly used for the species in the southern hemisphere. The examination of type material and reliable association of males and females based on genetics revealed that females of E. oligospila are morphologically extremely similar to E. respondens (and to some other E. bergmanni group species), but male penis valves and genetics enable reliable separation of these species. Morphological separation of females of E. oligospila and E. respondens is possible, but challenging. Identification keys for males and females of the bergmanni and oligospila groups are provided. The following 15 new synonymies are proposed: Nematus validicornis Förster, 1854, syn. nov. with Euura bergmanni (Dahlbom, 1835); Pteronidea woollatti Lindqvist, 1971, syn. nov. and Nematus turgaiensis Safjanov, 1977, syn. nov. with Euura brevivalvis (Thomson, 1871); Pteronidea pseudodispar Lindqvist, 1969, syn. nov. with Euura dispar (Zaddach, 1876); Nematus (Pteronidea) fastosus var. ponojense Hellén, 1948, syn. nov. and N. (P.) fastosus var. punctiscuta Hellén, 1948, syn. nov. with Euura frenalis (Thomson, 1888); Nematus declaratus Muche, 1974, syn. nov. and N. desantisi D.R. Smith, 1983, syn. nov. with Euura respondens (Förster, 1854); Pteronidea straminea Lindqvist, 1958, syn. nov., P. angustiserra Lindqvist, 1969, syn. nov., and P. disparoides Lindqvist, 1969, syn. nov. with Euura sylvestris (Cameron, 1884); Pteronidea breviseta Lindqvist, 1946, syn. nov., P. breviseta Lindqvist, 1949, syn. nov., P. abscondita Lindqvist, 1949, syn. nov., and P. lauroi Lindqvist, 1960, syn. nov. with Euura viridis (Stephens, 1835). Lectotypes are designated for 18 nominal taxa: Amauronematus longicornis Konow, 1897; A. spurcus Konow, 1904; Nematus bergmanni Dahlbom, 1835; N. brevivalvis Thomson, 1871; N. curtispina Thomson, 1871; N. (Pteronidea) fastosus var. ponojense Hellén, 1948; N. (P.) fastosus var. punctiscuta Hellén, 1948; N. glutinosae Cameron, 1882; N. microcercus Thomson, 1871; N. polyspilus Förster, 1854; N. prasinus Hartig, 1837; N. respondens Förster, 1854; N. salicivorus Cameron, 1882; N. validicornis Förster, 1854; N. virescens Hartig, 1837; Pteronidea curtispina var. luctuosa Enslin, 1916; Pteronus fastosus Konow, 1904; and P. pallens Konow, 1903.

scholarly journals Systematics of the subfamily Aclyvolvinae (Caenogastropoda: Ovulidae) based on molecular and morphometric analyses

2019 ◽  
Vol 85 (3) ◽  
pp. 336-347
Author(s):  
Bastian T Reijnen ◽  
Sancia E T van der Meij
Keyword(s):  
16S Rrna ◽  
Type Species ◽  
Sequence Data ◽  
Morphological Characters ◽  
Phylogenetic Position ◽  
28S Rrna ◽  
Molecular Analyses ◽  
Mitochondrial Coi ◽  
Morphometric Analyses ◽  
Molecular Phylogenetic

Abstract Molecular phylogenetic research on the octocoral-associated gastropod family Ovulidae is still in its infancy and, as a consequence, the relationships between subfamilies and genera are not well defined. Previous research on various ovulid genera has shown that their conchological characters are often too fluid when dealing with species delimitations. For this study, Ovulidae were collected in Indonesia and Malaysia, with some additional specimens obtained from Thailand and the Red Sea. Relationships between the Aclyvolvinae and other ovulid subfamilies were assessed using sequence data from two mitochondrial genes (cytochrome c oxidase subunit I (COI) and 16S rRNA); the dataset contained ovulid species (including type species) from the subfamilies Eocypraeinae, Ovulinae, Pediculariinae and Simniinae. The type species of the subfamilies Eocypraeinae and Sulcocypraeinae are fossils, and hence could not be included in the analyses. The phylogeny and systematics of the subfamily Aclyvolvinae were assessed based on four DNA gene regions (mitochondrial COI and 16S rRNA, and nuclear 28S rRNA and histone H3) and morphometric analyses. Shell morphological characters were analysed to help clarify species delimitations within the Aclyvolvinae. The results from the molecular analyses showed that the subfamilies Aclyvolvinae, Eocypraeinae and Simniinae are polyphyletic, whereas the Ovulinae and Pediculariinae appear to be monophyletic. Within the subfamily Aclyvolvinae, the type species of Hiatavolva, H. depressa, did not form a clade with the other species of Hiatavolva. Instead, H. rugosa and H. coarctata formed a clade that is sister to the clade comprising Aclyvolva lamyi, A. lanceolata and A. nicolamassierae, and are therefore now considered as belonging to the genus Aclyvolva. Aclyvolva lamyi and A. nicolamassierae were shown to be synonyms of A. lanceolata, and A. rugosa (n. comb.) is a synonym of A. coarctata (n. comb.). The genus Kuroshiovolva could not be retrieved in a fixed phylogenetic position within the Aclyvolvinae, nor did it cluster with H. depressa or Aclyvolva spp. Our morphometric analyses are in agreement with the results of the molecular analyses, and furthermore show that juvenile shells are morphologically significantly different from their adult conspecifics. Photographs of the type material of Ovulum lanceolatum, O. coarctatum, Neosimnia lamyi, Hiata rugosa and A. nicolamassierae are provided, and new information is given on the geographical distribution and host species of Aclyvolvinae. The subfamily Aclyvolvinae is redefined and now includes only A. lanceolata and A. coarctata. The genus Hiatavolva is now monotypic, containing only H. depressa, but the subfamily to which this genus belongs remains unclear. Kuroshiovolva is not part of the Aclyvolvinae, but its subfamily level placement is unclear.

Molecular and Reproductive Characterization of Sibling Species in the European Earwig (Forficula auricularia)

Evolution ◽  
1998 ◽  
Vol 52 (1) ◽  
pp. 260 ◽  
Author(s):  
Thierry Wirth ◽  
Rene Le Guellec ◽  
Michel Vancassel ◽  
Michel Veuille
Keyword(s):  
Sibling Species ◽  
Forficula Auricularia ◽  
European Earwig

Note on Control of the European Earwig, Forficula auricularia L., in Newfoundland With Traps and Attractants

1965 ◽  
Vol 97 (10) ◽  
pp. 1075-1076 ◽  
Author(s):  
Ray F. Morris
Keyword(s):  
Peanut Butter ◽  
Pitfall Traps ◽  
Forficula Auricularia ◽  
Four Corners ◽  
Set Up ◽  
European Earwig

In a test at St. John's from 20 August to 9 September 1964, grooved-board traps captured more specimens of the Eluropean earwig, Forficula auricularia L., than pitfall traps containing attractants. On 19 August two replicates of one grooved-board and eight Legner traps (Fig. 1) containing bran flakes plus an attractant were set up on a city lot. The Legner traps were set in the soil so that their tops were level with the surface. They were protected from rain by a 12 in. × 12 in. board held in position over the opening by short legs at the four corners. The attractants used were: peanut butter, cod oil, sugar, molasses, honey and macerated earwigs. The traps were attended from 21 August to 9 September and all earwigs removed daily and counted in the laboratory.

scholarly journals Revision of Claraeola (Diptera, Pipunculidae) in the Middle East based on morphology and DNA barcodes

ZooKeys ◽  
2019 ◽  
Vol 873 ◽  
pp. 85-111 ◽  
Author(s):  
Behnam Motamedinia ◽  
Jeffrey H. Skevington ◽  
Scott Kelso
Keyword(s):  
Middle East ◽  
Sequence Data ◽  
Morphological Characteristics ◽  
Identification Key ◽  
Dna Barcodes ◽  
Mitochondrial Coi ◽  
Coi Barcoding

The Middle East species of Claraeola Aczél (Diptera, Pipunculidae) are revised based on morphological characteristics and sequence data from the mitochondrial COI barcoding gene, using a novel COI mini-barcode protocol. Four new Claraeola species are described: C. bousynterga Motamedinia & Skevington, sp. nov., C. heidiae Motamedinia & Skevington, sp. nov., C. khuzestanensis Motamedinia & Skevington, sp. nov., and C. mantisphalliga Motamedinia & Skevington, sp. nov.Eudorylas thekkadiensis Kapoor, Grewal & Sharma, 1987 is transferred to Claraeola, C. thekkadiensis (comb. nov.). Diagnoses, illustrations, an identification key, and a distributional map are given for the Middle East species.

Influence of diet on development and oviposition of Forficula auricularia (Dermaptera: Forficulidae)

2001 ◽  
Vol 133 (5) ◽  
pp. 705-708 ◽  
Author(s):  
Ghislain Berleur ◽  
Jean Gingras ◽  
Jean-Claude Tourneur
Keyword(s):  
Food Preference ◽  
Rhopalosiphum Padi ◽  
Soil Surface ◽  
Cold Weather ◽  
Forficula Auricularia ◽  
Content Analyses ◽  
European Earwig ◽  
Preference Tests ◽  
Daylight Period ◽  
Better Than

In North America, the life cycle of the European earwig (Forficula auricularia L.) can be divided into a nesting phase (hypogean phase) and a free-foraging phase (epigean phase) (Crumb et al. 1941; Behura 1956; Lamb and Wellington 1975). Adults spend the nesting phase in the soil; females burrow into the ground at the onset of the cold weather, lay eggs, and then care for the eggs. Hatching occurs in spring; first- or second-instar nymphs move to the soil surface for the free-foraging period. The earwig, a nocturnal insect, spends the entire daylight period of hiding under trash or in dark crevices. Where two broods occur, females reenter the ground a second time (Lamb and Wellington 1975). Stomach content analyses (Crumb et al. 1941; Sunderland and Vickerman 1980) and food preference tests (McLeod and Chant 1952; Buxton and Madge 1976) revealed that the European earwig is omnivorous. Under laboratory conditions, nymphs fed freshly frozen aphids, Rhopalosiphum padi (L.) (Hemiptera: Aphididae), survive better than those fed green algae or carrots, develop faster, and produce heavier females (Phillips 1981; Carrillo 1985).

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