Lasionycta phoca Crabo & Lafontaine, 2009, sp. n.

Lasionycta phoca sub-group The L . phoca sub-group contains seven mostly medium-size (expanse 30–36 mm) species from alpine or subarctic habitats. Most occur in western North America, with two in the Northeast. Th e forewing is gray to brown gray with dark basal, antemedial, and postmedial lines; th...

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Main Authors: Crabo, Lars, Lafontaine, Donald
Format: Text
Language:unknown
Published: Zenodo 2009
Subjects:
Online Access:https://dx.doi.org/10.5281/zenodo.3790165
https://zenodo.org/record/3790165
id ftdatacite:10.5281/zenodo.3790165
record_format openpolar
institution Open Polar
collection DataCite Metadata Store (German National Library of Science and Technology)
op_collection_id ftdatacite
language unknown
topic Biodiversity
Taxonomy
Animalia
Arthropoda
Insecta
Lepidoptera
Noctuidae
Lasionycta
Lasionycta phoca
spellingShingle Biodiversity
Taxonomy
Animalia
Arthropoda
Insecta
Lepidoptera
Noctuidae
Lasionycta
Lasionycta phoca
Crabo, Lars
Lafontaine, Donald
Lasionycta phoca Crabo & Lafontaine, 2009, sp. n.
topic_facet Biodiversity
Taxonomy
Animalia
Arthropoda
Insecta
Lepidoptera
Noctuidae
Lasionycta
Lasionycta phoca
description Lasionycta phoca sub-group The L . phoca sub-group contains seven mostly medium-size (expanse 30–36 mm) species from alpine or subarctic habitats. Most occur in western North America, with two in the Northeast. Th e forewing is gray to brown gray with dark basal, antemedial, and postmedial lines; the orbicular and reniform spots are weakly defined, evident mostly due to pale filling, and the claviform spot is absent; in several species the forewing is mottled with white, blue gray, or yellow. Th e dorsal hindwing is typically dark with a pale fringe. Th e ventral hindwing, often useful for diagnosis, is white to pale gray (rarely brownish gray) with dark chevron- or arrowhead-shaped discal spot, postmedial line, and marginal band. A small species from the Sierra Nevada ( Lasionycta mono sp. n.) with a hindwing resembling species in the L . staudingeri sub-group is associated with this sub-group by the shape of the valve. The male valve is elongate with a weak to moderate narrowing at the base of the cucullus. The cucullus is fairly stout and similar to those of the L . leucocycla sub-group in shape. The corona is variable, simple with partial double row near the apex in most species, but comprised of several rows in two species. Th e digitus is cylindrical. The female genitalia are similar to those of the L . leucocycla sub-group. Th e corpus bursae is ovoid with a 50 % medial constriction and an appendix bursae of similar size to the corpus bursae. The male antennae are biserrate with triangular individual segments 1.5–2.1× as wide as the central shaft. Species in this sub-group are among the most diffi cult to identify in the genus. The genitalia are only helpful in a few of the species and the male antennae are generally indistinguishable. Most species resemble each other and several are variable to the point where individuals approach other species in appearance. For this reason, a definitive diagnosis is easiest when series can be examined. Identification is simplified by narrowing the possibilities by locality since no more than three species occur in a region (see Table 1). Th e habitus, especially the ventral hindwing pattern, can then be used for definitive diagnosis. Species status was determined by lack of evidence of intergradation in areas of sympatry together with genital and DNA differences in most cases. Assessment of species limits was most difficult in L . uniformis , a variable widely distributed species with many local forms and several CO1 haplotypes. The rationale for treating it as one species are discussed under L . uniformis . The CO1 DNA sequences of all phoca sub-group species except L . caesia are similar (that of L . mono is unknown), clustering with those of L. lagganata , L . quadrilunata , and L . dolosa (Fig. 248). Th e sequences of L . caesia , L . brunnea , L . gelida sp. n., L . discolor (Smith), and L . phoca are fairly uniform, although this could be an artifact of small sample sizes. In contrast, many haplotypes exist for several L . uniformis subspecies which are intermixed with those of the other species in the DNA tree (Fig. 248). Despite this overlap, CO1 distance analysis was useful for determining the number of taxa in a region. For example, comparison of all L . phoca sub-group DNA samples from the Canadian Rocky Mountains identifies two dominant haplotype clusters that correlate with L . u . uniformis and L . brunnea . Similarly, two main haplotypes from the central United States Rocky Mountains correspond to L . discolor and L . uniformis fusca . However, more haplotypes than identifiable species exist in the Pacific Northwest. Two of the haplotypes correspond to L . gelida and L . caesia . Th e other three major clusters are similar but variable and cannot be sorted by appearance to more than one taxon in L . uniformis multicolor . : Published as part of Crabo, Lars & Lafontaine, Donald, 2009, A Revision of Lasionycta Aurivillius (Lepidoptera: Noctuidae) for North America and notes on Eurasian species, with descriptions of 17 new species, 6 new subspecies, a new genus, and two new species of Tricholita Grote, pp. 1-156 in ZooKeys 30 (30) on page 66, DOI: 10.3897/zookeys.30.308, http://zenodo.org/record/576576
format Text
author Crabo, Lars
Lafontaine, Donald
author_facet Crabo, Lars
Lafontaine, Donald
author_sort Crabo, Lars
title Lasionycta phoca Crabo & Lafontaine, 2009, sp. n.
title_short Lasionycta phoca Crabo & Lafontaine, 2009, sp. n.
title_full Lasionycta phoca Crabo & Lafontaine, 2009, sp. n.
title_fullStr Lasionycta phoca Crabo & Lafontaine, 2009, sp. n.
title_full_unstemmed Lasionycta phoca Crabo & Lafontaine, 2009, sp. n.
title_sort lasionycta phoca crabo & lafontaine, 2009, sp. n.
publisher Zenodo
publishDate 2009
url https://dx.doi.org/10.5281/zenodo.3790165
https://zenodo.org/record/3790165
geographic Pacific
geographic_facet Pacific
genre Subarctic
genre_facet Subarctic
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spelling ftdatacite:10.5281/zenodo.3790165 2023-05-15T18:28:42+02:00 Lasionycta phoca Crabo & Lafontaine, 2009, sp. n. Crabo, Lars Lafontaine, Donald 2009 https://dx.doi.org/10.5281/zenodo.3790165 https://zenodo.org/record/3790165 unknown Zenodo http://zenodo.org/record/576576 http://publication.plazi.org/id/896847397B71FFD6FF8EE829912DFFF8 http://zoobank.org/C26E1A82-0DD4-48EF-865C-9D8AA788B739 https://zenodo.org/communities/biosyslit https://dx.doi.org/10.3897/zookeys.30.308 http://zenodo.org/record/576576 http://publication.plazi.org/id/896847397B71FFD6FF8EE829912DFFF8 https://dx.doi.org/10.5281/zenodo.3769247 http://zoobank.org/C26E1A82-0DD4-48EF-865C-9D8AA788B739 https://dx.doi.org/10.5281/zenodo.3790166 https://zenodo.org/communities/biosyslit Open Access Creative Commons Zero v1.0 Universal https://creativecommons.org/publicdomain/zero/1.0/legalcode cc0-1.0 info:eu-repo/semantics/openAccess CC0 Biodiversity Taxonomy Animalia Arthropoda Insecta Lepidoptera Noctuidae Lasionycta Lasionycta phoca article-journal ScholarlyArticle Text Taxonomic treatment 2009 ftdatacite https://doi.org/10.5281/zenodo.3790165 https://doi.org/10.3897/zookeys.30.308 https://doi.org/10.5281/zenodo.3769247 https://doi.org/10.5281/zenodo.3790166 2022-03-10T14:36:23Z Lasionycta phoca sub-group The L . phoca sub-group contains seven mostly medium-size (expanse 30–36 mm) species from alpine or subarctic habitats. Most occur in western North America, with two in the Northeast. Th e forewing is gray to brown gray with dark basal, antemedial, and postmedial lines; the orbicular and reniform spots are weakly defined, evident mostly due to pale filling, and the claviform spot is absent; in several species the forewing is mottled with white, blue gray, or yellow. Th e dorsal hindwing is typically dark with a pale fringe. Th e ventral hindwing, often useful for diagnosis, is white to pale gray (rarely brownish gray) with dark chevron- or arrowhead-shaped discal spot, postmedial line, and marginal band. A small species from the Sierra Nevada ( Lasionycta mono sp. n.) with a hindwing resembling species in the L . staudingeri sub-group is associated with this sub-group by the shape of the valve. The male valve is elongate with a weak to moderate narrowing at the base of the cucullus. The cucullus is fairly stout and similar to those of the L . leucocycla sub-group in shape. The corona is variable, simple with partial double row near the apex in most species, but comprised of several rows in two species. Th e digitus is cylindrical. The female genitalia are similar to those of the L . leucocycla sub-group. Th e corpus bursae is ovoid with a 50 % medial constriction and an appendix bursae of similar size to the corpus bursae. The male antennae are biserrate with triangular individual segments 1.5–2.1× as wide as the central shaft. Species in this sub-group are among the most diffi cult to identify in the genus. The genitalia are only helpful in a few of the species and the male antennae are generally indistinguishable. Most species resemble each other and several are variable to the point where individuals approach other species in appearance. For this reason, a definitive diagnosis is easiest when series can be examined. Identification is simplified by narrowing the possibilities by locality since no more than three species occur in a region (see Table 1). Th e habitus, especially the ventral hindwing pattern, can then be used for definitive diagnosis. Species status was determined by lack of evidence of intergradation in areas of sympatry together with genital and DNA differences in most cases. Assessment of species limits was most difficult in L . uniformis , a variable widely distributed species with many local forms and several CO1 haplotypes. The rationale for treating it as one species are discussed under L . uniformis . The CO1 DNA sequences of all phoca sub-group species except L . caesia are similar (that of L . mono is unknown), clustering with those of L. lagganata , L . quadrilunata , and L . dolosa (Fig. 248). Th e sequences of L . caesia , L . brunnea , L . gelida sp. n., L . discolor (Smith), and L . phoca are fairly uniform, although this could be an artifact of small sample sizes. In contrast, many haplotypes exist for several L . uniformis subspecies which are intermixed with those of the other species in the DNA tree (Fig. 248). Despite this overlap, CO1 distance analysis was useful for determining the number of taxa in a region. For example, comparison of all L . phoca sub-group DNA samples from the Canadian Rocky Mountains identifies two dominant haplotype clusters that correlate with L . u . uniformis and L . brunnea . Similarly, two main haplotypes from the central United States Rocky Mountains correspond to L . discolor and L . uniformis fusca . However, more haplotypes than identifiable species exist in the Pacific Northwest. Two of the haplotypes correspond to L . gelida and L . caesia . Th e other three major clusters are similar but variable and cannot be sorted by appearance to more than one taxon in L . uniformis multicolor . : Published as part of Crabo, Lars & Lafontaine, Donald, 2009, A Revision of Lasionycta Aurivillius (Lepidoptera: Noctuidae) for North America and notes on Eurasian species, with descriptions of 17 new species, 6 new subspecies, a new genus, and two new species of Tricholita Grote, pp. 1-156 in ZooKeys 30 (30) on page 66, DOI: 10.3897/zookeys.30.308, http://zenodo.org/record/576576 Text Subarctic DataCite Metadata Store (German National Library of Science and Technology) Pacific