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390 results for “maritime”
Figure 1 from: Gañan M, Contador T, Rendoll J, Simoes F, Pérez C, Graham G, Castillo S, Kennedy J, Convey P (2021) Records of Parochlus steinenii in the Maritime Antarctic and sub-Antarctic regions. ZooKeys 1011: 63-71. https://doi.org/10.3897/zookeys.1011.56833
Figure 1 Map of study area. The red circles correspond to the records of Parochlus steinenii found in this study, the green circles correspond to the bibliographic records.
FIGURE 1 in The checkered beetles (Coleoptera: Cleridae) of the Maritime Provinces of Canada
FIGURE 1. Distribution of Zenodosus sanguineus in the Maritime Provinces.
FIGURE 2 in The checkered beetles (Coleoptera: Cleridae) of the Maritime Provinces of Canada
FIGURE 2. Distribution of Phyllobaenus humeralis and P. lecontei in the Maritime Provinces.
FIGURE 4 in The checkered beetles (Coleoptera: Cleridae) of the Maritime Provinces of Canada
FIGURE 4. Distribution of Thanasimus dubius in the Maritime Provinces.
FIGURE 3 in The checkered beetles (Coleoptera: Cleridae) of the Maritime Provinces of Canada
FIGURE 3. Distribution of Phyllobaenus verticalis and P. pallipennis in the Maritime Provinces.
FIGURE 5 in The checkered beetles (Coleoptera: Cleridae) of the Maritime Provinces of Canada
FIGURE 5. Distribution of Thanasimus undatulus and Cymatodera bicolor in the Maritime Provinces.
FIGURE 8 in The checkered beetles (Coleoptera: Cleridae) of the Maritime Provinces of Canada
FIGURE 8. Distribution of Necrobia violacea and N. rufipes in the Maritime Provinces.
FIGURE 3 in The Mycteridae, Boridae, Pythidae, Pyrochroidae, and Salpingidae (Coleoptera: Tenebrionoidea) of the Maritime Provinces of Canada
FIGURE 3. Distribution of Pedilus lugubris in the Maritime Provinces of Canada.
FIGURE 2 in Introduced leaf beetles of the Maritime Provinces, 7: Cassida rubiginosa Müller and Cassida flaveola Thunberg (Coleoptera: Chrysomelidae)
FIGURE 2. Habitus of Cassida flaveola, dorsal view.
Fig. 1 in Colydiidae (Coleoptera) in the Maritime Provinces of Canada and Maine in the United States
Fig. 1. The distribution of Lasconotus borealis (closed circles) and Synchita fuliginosa
FIGURE 33. Nesostenodontus formosanus Cushman, 1937 in Contribution to the knowledge of the Ichneumoninae (Hymenoptera, Ichneumonidae) from Maritime Southeast Asia
FIGURE 33. Nesostenodontus formosanus Cushman, 1937 ♂. A face-frontal view, B head, dorsal view.
Retrotransposon-based genetic diversity of Deschampsia antarctica Desv. from King George Island (Maritime Antarctic)
<p><span><i>Deschampsia antarctica</i> Desv. can be found in diverse Antarctic habitats which may vary considerably in terms of environmental conditions and soil properties. As a result, the species is characterized by wide ecotypic variation in terms of both morphological and anatomical traits. The species is a unique example of an organism that can successfully colonize inhospitable regions due to its phenomenal ability to adapt to both the local mosaic of microhabitats and to general climatic fluctuations. For this reason, <i>D. antarctica </i>has been widely investigated in studies analyzing morphophysiological and biochemical responses to various abiotic stresses (frost, drought, salinity, increased UV radiation). However, there is little evidence to indicate whether the observed polymorphism is accompanied by the corresponding genetic variation.</span></p> <p>In the present study, retrotransposon-based iPBS markers were used to trace the genetic variation of <i>D. antarctica</i> collected in nine sites of the Arctowski oasis on King George Island (Western Antarctic). The genotyping of 165 individuals from nine populations with seven iPBS primers revealed 125 amplification products, 15 of which (12%) were polymorphic, with an average of 5.6% polymorphic fragments per population. Only one of the polymorphic fragments, observed in population 6, was represented as a private band. The analyzed specimens were characterized by low genetic diversity (uH<sub>e</sub> = 0.021, I = 0.030) and high population differentiation (<i>F<sub>ST</sub></i> = 0.4874). An analysis of Fu's <i>F<sub>S</sub></i> statistics and mismatch distribution in most populations (excluding population 2, 6 and 9) revealed demographic/spatial expansion, whereas significant traces of reduction in effective population size were found in three populations (1, 3 and 5). The iPBS markers revealed genetic polymorphism of <i>D. antarctica</i>, which could be attributed to the mobilization of random transposable elements, unique features of reproductive biology, and/or geographic location of the examined populations.</p>
Supplementary material 1 from: Hatami R, Inglis G, Lane SE, Growcott A, Kluza D, Lubarsky C, Jones-Todd C, Seaward K, Robinson AP (2022) Modelling the likelihood of entry of marine non-indigenous species from internationally arriving vessels to maritime ports: a case study using New Zealand data. NeoBiota 72: 183-203. https://doi.org/10.3897/neobiota.72.77266
Supplementary materials
Figure 5 from: lshishka M, Lazarova S, Radoslavov G, Hristov P, Peneva VK (2017) Biogeography and phylogenetic position of Enchodeloides signyensis (Loof, 1975), gen. n., comb. n. from Maritime Antarctic (Nematoda, Nordiidae). ZooKeys 697: 37-58. https://doi.org/10.3897/zookeys.697.13770
Figure 5 - Enchodeloides signyensis (Loof, 1975), gen. n., comb. n. (= Enchodelus signyensis Loof, 1975). Juveniles (specimens from Livingston Island): A–D Tail ends (J1) E–G Tail ends (J2-J4) Female (specimen from Livingston Island) H Tail end. Scale bar: 50 μm.
Figure 9 from: lshishka M, Lazarova S, Radoslavov G, Hristov P, Peneva VK (2017) Biogeography and phylogenetic position of Enchodeloides signyensis (Loof, 1975), gen. n., comb. n. from Maritime Antarctic (Nematoda, Nordiidae). ZooKeys 697: 37-58. https://doi.org/10.3897/zookeys.697.13770
Figure 9 - Phylogenetic relationships of Enchodeloides signyensis (Loof, 1975), gen. n., comb. n. (= Enchodelus signyensis Loof, 1975) based on 28S rDNA D2-D3 inferred from a Bayesian analysis (GTR+G model) and two Aporcelaimellus species used as an outgroup. * Thonus is currently considered a synonym of Crassolabium (Peña-Santiago & Ciobanu, 2008).
Figure 7 from: lshishka M, Lazarova S, Radoslavov G, Hristov P, Peneva VK (2017) Biogeography and phylogenetic position of Enchodeloides signyensis (Loof, 1975), gen. n., comb. n. from Maritime Antarctic (Nematoda, Nordiidae). ZooKeys 697: 37-58. https://doi.org/10.3897/zookeys.697.13770
Figure 7 - Enchodeloides signyensis (Loof, 1975), gen. n., comb. n. (= Enchodelus signyensis Loof, 1975). Scatter plot of the functional (○) and replacement odontostyle (◊) in relation to the body length of the juvenile stages and females.
Figure 8 from: lshishka M, Lazarova S, Radoslavov G, Hristov P, Peneva VK (2017) Biogeography and phylogenetic position of Enchodeloides signyensis (Loof, 1975), gen. n., comb. n. from Maritime Antarctic (Nematoda, Nordiidae). ZooKeys 697: 37-58. https://doi.org/10.3897/zookeys.697.13770
Figure 8 - Phylogenetic relationships of Enchodeloides signyensis (Loof, 1975), gen. n., comb. n. (= Enchodelus signyensis Loof, 1975) based on 18S rDNA inferred from a Bayesian analysis (GTR+G model) and two Aporcelaimellus species used as an outgroup. * Thonus is currently considered a synonym of Crassolabium (Peña-Santiago and Ciobanu, 2008).
Figure 6 from: lshishka M, Lazarova S, Radoslavov G, Hristov P, Peneva VK (2017) Biogeography and phylogenetic position of Enchodeloides signyensis (Loof, 1975), gen. n., comb. n. from Maritime Antarctic (Nematoda, Nordiidae). ZooKeys 697: 37-58. https://doi.org/10.3897/zookeys.697.13770
Figure 6 - Enchodeloides signyensis (Loof, 1975), gen. n., comb. n. (= Enchodelus signyensis Loof, 1975). Juveniles (specimens from Livingston Island): A–D Anterior ends (J1-J4) F–I Tail ends (J1-J4) Female (specimen from Livingston Island) E Anterior end J Tail end. Scale bar: 10 μm.
Figure 3 from: lshishka M, Lazarova S, Radoslavov G, Hristov P, Peneva VK (2017) Biogeography and phylogenetic position of Enchodeloides signyensis (Loof, 1975), gen. n., comb. n. from Maritime Antarctic (Nematoda, Nordiidae). ZooKeys 697: 37-58. https://doi.org/10.3897/zookeys.697.13770
Figure 3 - SEM micrographs. Enchodeloides signyensis (Loof, 1975), gen. n., comb. n. (= Enchodelus signyensis Loof, 1975). Female: A, D, E Lip region, in face view, amphid aperture B, F Lip region, in sublateral view C Cephalic and labial papillae G–I Vulval region J–L Tail ends. Scale bars: 2 μm (A, C, D, E, F, G); 5 μm (B, I, J); 10 μm (L).
Figure 2 from: lshishka M, Lazarova S, Radoslavov G, Hristov P, Peneva VK (2017) Biogeography and phylogenetic position of Enchodeloides signyensis (Loof, 1975), gen. n., comb. n. from Maritime Antarctic (Nematoda, Nordiidae). ZooKeys 697: 37-58. https://doi.org/10.3897/zookeys.697.13770
Figure 2 - Enchodeloides signyensis (Loof, 1975), gen. n., comb. n. (= Enchodelus signyensis Loof, 1975). Female: A–D Tail ends (A specimen from King George Island; B, C, D specimens from Livingston Island) E–G Tail ends with saccate bodies (E specimen from King George Island F, G specimens from Livingston Island). Scale bar: 10 μm.
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Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
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DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.