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106 results for “Borealis”

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zenodo32/100

Data for "Borealis: An Advanced Digital Hardware and Software Design for SuperDARN Radar Systems"

<p>Clyde River SuperDARN data for 2022-02-07, 18:00-20:00UT.</p> <p>Included are the RAWACF and FITACF files, the latter of which was used to produce Figure 6 in the partner paper: &quot;Borealis: An Advanced Digital Hardware and Software Design for SuperDARN Radar Systems&quot;.</p> <p>Data can be processed&nbsp;further using the Radar Software Toolkit (RST: https://github.com/SuperDARN/rst), or plotted using pyDARN (https://github.com/SuperDARN/pydarn).</p>

opencc-by-4.0Feb 2023View details →
zenodo32/100

FIGURES 67–70. Macrorrhyncha borealis n in The Nearctic species of Asindulum Latreille and Macrorrhyncha Winnertz (Diptera: Keroplatidae)

FIGURES 67–70. Macrorrhyncha borealis n. sp., holotype male, terminalia. 67. Dorsal. 68. Ventral. 69. Lateral. 70. Posterior. Scale bar = ca. 0.25 mm. Abbreviations: bl, basal lobe of gonostylus; ce, cercus; dp, dorsal process of gonocoxite; gc, gonocoxite; gs, gonostylus; t9, tergite 9.

opennotspecifiedSep 2023View details →
zenodo32/100

FIGURES 73–74. Macrorrhyncha borealis n in The Nearctic species of Asindulum Latreille and Macrorrhyncha Winnertz (Diptera: Keroplatidae)

FIGURES 73–74. Macrorrhyncha borealis n. sp.? (female, tentatively associated), female terminalia. 73. Dorsal. 74. Ventral. Scale = ca. 0.25 mm. Abbreviations: ce, cercus; sp, spermathecae; s8, sternite 8; t7, tergite 7.

opennotspecifiedSep 2023View details →
zenodo32/100

FIGURES 71–72. Macrorrhyncha borealis n in The Nearctic species of Asindulum Latreille and Macrorrhyncha Winnertz (Diptera: Keroplatidae)

FIGURES 71–72. Macrorrhyncha borealis n. sp., holotype male, terminalia including sperm pump. 71. Ventral. 72. Lateral. Scale = ca. 0.25 mm. Abbreviations: ea, ejaculatory apodeme; gc, gonocoxite; t9, tergite 9.

opennotspecifiedSep 2023View details →
zenodo32/100

FIGURES 64–65. Macrorrhyncha borealis n in The Nearctic species of Asindulum Latreille and Macrorrhyncha Winnertz (Diptera: Keroplatidae)

FIGURES 64–65. Macrorrhyncha borealis n. sp., holotype male. 64. Habitus. Scale = ca. 1.0 mm. 65. Head, anterolateral. Scale = ca. 0.5 mm. Abbreviations: cx1, coxa 1; lbl, labellum.

opennotspecifiedSep 2023View details →
dryad32/100

Data from: Genetically distinct populations of northern shrimp, Pandalus borealis, in the North Atlantic: adaptation to different temperatures as an isolation factor

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publicMar 2015View details →
dryad32/100

Data from: "Genome-wide microsatellite marker development from next-generation sequencing of two non-model bat species impacted by wind turbine mortality: Lasiurus borealis and L. cinereus (Vespertilionidae)" in Genomic Resources Notes accepted 1 October 2013 to 30 November 2013

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publicJan 2014View details →
dryad32/100

Data from: High frequency of multiple paternity in Eastern red bats, Lasiurus borealis, based on microsatellite analysis

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publicSep 2020View details →
dryad32/100

Variation in isotopic trophic niche of sablefish (Anoplopoma fimbria) and shortraker rockfish (Sebastes borealis) in the Northeast Pacific

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publicAug 2024View details →
dryad28/100

Data from: A method for deducing neck mobility in plesiosaurs, using the exceptionally preserved Nichollssaura borealis

The elongate-necked aquatic plesiosaurs existed for 135 million years during the Mesozoic. The function of this elongate neck is a point of debate. Using computed tomography (CT) and 3-dimensional (3D) modelling, the range of motion (ROM) of the plesiosaur *Nichollssaura borealis* neck was assessed. To quantify the ROM, the intervertebral mobility was measured along the cervical vertebral column. This was done by manipulating the 3D models in the lateral and dorso-ventral directions during two trials. The first assessed the mean intervertebral ROM between pairs of cervical vertebrae along the entire column, and the second assessed ROM with reduced intervertebral spaces. The results suggest that there may be preference for lateral neck movements in *N. borealis*, which could correspond to an ecological function related to prey capture. This study demonstrates that 3D modelling is an effective tool for assessing function morphology for structures where no good modern analogue exists.

opencc-zeroDec 2017View details →
zenodo28/100

FIGURE 19.Metopa borealis Sars, 1883 in A redescription of Metopa species (Amphipoda, Stenothoidae) based on the type material. 3. Natural History Museum, Oslo (NHM) 2465

FIGURE 19.Metopa borealis Sars, 1883, photo of F13738 syntype, female 4 mm (A), male 4 mm (B).

opennotspecifiedMay 2010View details →
dryad28/100

DNA-metabarcoding reveals the importance of gelatinous zooplankton in the diet of Pandalus borealis, a keystone species in the Arctic

<p>Information about the dietary composition of species is crucial to understand their position and role in the food web. Stomach content analysis (SCA) and stable isotope analysis (SIA) are commonly used to study marine trophic relationships. SCA can provide high taxonomic resolution but requires taxonomic expertise and frequently underestimates digestible taxa. SIA provides a time-integrated view of the dietary sources but often lacks in taxonomic resolution. The use of molecular approaches such as DNA-metabarcoding may alleviate these problems. Here, we used DNA-metabarcoding with universal primers for cytochrome c oxidase I (COI), to study the diet composition of the Northern shrimp (<i>Pandalus borealis</i>) from the Barents Sea, a keystone species in the Arctic region with large socio-economic importance. Across locations, jellyfish and chaetognaths were the most important components in the diet of <i>P. borealis</i>, jointly accounting for 40-60% of the total read abundance. This dietary importance of gelatinous zooplankton contrasts sharply with published results based on SCA. At the same time, diet composition differed between fjord and shelf locations, pointing to different food webs supporting <i>P. borealis</i> in these two systems. Our study underscores the potential of molecular approaches to provide important new insights into the diet of marine invertebrates that are difficult or impossible to obtain with traditional methods, and calls for a revision of the role of gelatinous zooplankton in the diet of the key Arctic species <i>P. borealis</i>, and in extension, Arctic food webs.</p>

opencc-zeroJan 2022View details →
zenodo28/100

Fig. 1 in Discovery of the First Nearctic Moss-Eating Flea Beetle, Distigmoptera borealis Blake, 1943 (Coleoptera: Chrysomelidae: Galerucinae: Alticini)

Fig. 1. Distigmoptera borealis, dorsal habitus.

opennotspecifiedSep 2019View details →
zenodo28/100

Figure 11. Amphiura borealis postlarval development. A, B, 0.7 in Who's who among baby brittle stars (Echinodermata: Ophiuroidea): postmetamorphic development of some North Atlantic forms

Figure 11. Amphiura borealis postlarval development. A, B, 0.7 mm dd postlarvae; A, dorsal; B, ventral, note the infradental papillae (IP = MP2); C, D, E, 0.8 mm dd postlarvae; C, dorsal; D, ventral; E, jaw, note that the IP form on the dental plate (DP); F, G, 1.1 mm dd postlarvae; F, dorsal; G, ventral; H, I, 2 mm dd postlarva; H, dorsal, note the radial shields (RS); I, ventral, note the IP on the oral plates; J, K, 2.5 mm dd juvenile; J, arm ventral, note the hatchet-shaped spine (arrow); K, ventral. Abbreviations: as in Figs 1–3, 5. Scale bars in millimetres.

opencc-by-4.0Apr 2005View details →
zenodo28/100

Figure 2 in Barbronia borealis sp. nov., the first salifid leech discovered in Russia, with a global checklist of this genus

Figure 2. Maximum likelihood phylogeny of the Salifidae based on partial sequences of the COI and 18S rRNA genes (Appendix 1). The black numbers near nodes are bootstrap support values of IQ-TREE v. 1.6.12. The scale bar indicates the branch length. The new species name is red. The geographic affinities of subclades/lineages are blue. Outgroup is not shown.

opencc-by-4.0Jun 2023View details →
zenodo28/100

Figure 6 in Barbronia borealis sp. nov., the first salifid leech discovered in Russia, with a global checklist of this genus

Figure 6. Type locality of Barbronia borealis sp. nov.: Kiparisovka River, 43.4578°N, 131.9017°E, Razdolnaya (Suifun) River basin, Primorye Region, Russia, September 05, 2020. Photo: Olga V. Aksenova.

opencc-by-4.0Jun 2023View details →
dryad28/100

Data from: A method for deducing neck mobility in plesiosaurs, using the exceptionally preserved Nichollssaura borealis

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publicJul 2018View details →
dryad28/100

DNA-metabarcoding reveals the importance of gelatinous zooplankton in the diet of Pandalus borealis, a keystone species in the Arctic

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publicJan 2022View details →
zenodo24/100

Fig. 3. Himantolophus borealis, FAKU 140000, 179.1 in First Records of a Rare Deep-sea Anglerfish, Himantolophus azurlucens, from the Western North Pacific, with Comments on the DNA Barcodes of the Genus (Lophiiformes: Himantolophidae)

Fig. 3. Himantolophus borealis, FAKU 140000, 179.1 mm SL, female (in fresh condition).

opencc-by-4.0Oct 2022View details →
zenodo20/100

Subspecies and Distribution. U. c. cinereoargenteus Schreber, 1775 — E USA. U. c. borealis Merriam, 1903 — SE Canada and USA (New England). U. c. californicus Mearns, 1897 — SW USA (S California). U. c. costaricensis Goodwin, 1938 — Costa Rica. U. c. flornidanus Rhoads, 1895 — Gulf of Mexico. U. c. fraterculus Elliot, 1896 — Mexico (Yucatan). U. c. furvus G. M. Allen & Barbour, 1923 — Panama. U. c. guatemalae G. S. Miller, 1899 — S Mexico S to Nicaragua. U. c. madrensis Burt & Hooper, 1941 — Mexico (S Sonora, SW Chihuahua & NW Durango). U. c¢. nigrirostris Lichtenstein, 1830 — SW Mexico. U. c. ocythous Bangs, 1899 — USA (Central Plains) and adjoining S Canada. U. ¢. orinomus Goldman, 1938 — S Mexico (Isthmus of Tehuantepec). U. c. perunsularis Huey, 1928 — NW Mexico (Baja California). U. c. scottit Mearns, 1891 — N Mexico and SW USA. U. c. townsend: Merriam, 1899 — W USA (California & Oregon). U. c. venezuelae]. A. Allen, 1911 — Colombia, Venezuela. in Canidae

Subspecies and Distribution. U. c. cinereoargenteus Schreber, 1775 — E USA. U. c. borealis Merriam, 1903 — SE Canada and USA (New England). U. c. californicus Mearns, 1897 — SW USA (S California). U. c. costaricensis Goodwin, 1938 — Costa Rica. U. c. flornidanus Rhoads, 1895 — Gulf of Mexico. U. c. fraterculus Elliot, 1896 — Mexico (Yucatan). U. c. furvus G. M. Allen &amp; Barbour, 1923 — Panama. U. c. guatemalae G. S. Miller, 1899 — S Mexico S to Nicaragua. U. c. madrensis Burt &amp; Hooper, 1941 — Mexico (S Sonora, SW Chihuahua &amp; NW Durango). U. c¢. nigrirostris Lichtenstein, 1830 — SW Mexico. U. c. ocythous Bangs, 1899 — USA (Central Plains) and adjoining S Canada. U. ¢. orinomus Goldman, 1938 — S Mexico (Isthmus of Tehuantepec). U. c. perunsularis Huey, 1928 — NW Mexico (Baja California). U. c. scottit Mearns, 1891 — N Mexico and SW USA. U. c. townsend: Merriam, 1899 — W USA (California &amp; Oregon). U. c. venezuelae]. A. Allen, 1911 — Colombia, Venezuela.

opennotspecifiedJan 2009View details →

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