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1,552 results for “moorings”
SWOT 2019-2020 Prelaunch Oceanography Field Campaign SIO Mooring WireWalker (WW)
This dataset provides the conductivity, temperature and depth (CTD) measurements from the CTD sensors on a WireWalker profiler on a full-depth mooring deployed by the SWOT prelaunch field campaign. The campaign was designed to test the performance of several instruments/platforms in meeting the SWOT Calibration/Validation (CalVal) requirement. It was conducted near the SWOT CalVal crossover location, about 300 kilometers west of Monterey, California between September, 2019 and January, 2020. The WW samples the upper 500 m of the water column, while the deep ocean below 500 m are measured by fixed-depth CTDs https://doi.org/10.5067/SWTPR-CTD01. The campaign also deployed another two CTD moorings, a slocum glider, one bottom pressure recorder and one Pressure Inverted Echo Sounder. Details can be found in the user guide and the journal reference given in the documentation section.
SWOT 2019-2020 Prelaunch Oceanography Field Campaign SIO Moored Fixed-Depth CTDs
This dataset provides the conductivity, temperature and depth (CTD) measurements from the fixed-depth CTD sensors mounted on a full-depth mooring deployed by the SWOT prelaunch field campaign. The campaign was designed to test the performance of several instruments/platforms in meeting the SWOT Calibration/Validation (CalVal) requirement. It was conducted near the SWOT CalVal crossover location, about 300 kilometers west of Monterey, California between September, 2019 and January, 2020. These fixed-depth CTDs are below 500 m while the upper part of the mooring has a WireWalker (WW) profiler. The CTD data from WW is available here https://doi.org/10.5067/SWTPR-WW001. The campaign also deployed another two CTD moorings, a slocum glider, one bottom pressure recorder and one Pressure Inverted Echo Sounder. Details can be found in the user guide and the journal reference given in the documentation section.
Figure 5 from: Sabbatini Peverieri G, Mitroiu M-D, Bon M-C, Balusu R, Benvenuto L, Bernardinelli I, Fadamiro H, Falagiarda M, Fusu L, Grove E, Haye T, Hoelmer K, Lemke E, Malossini G, Marianelli L, Moore MR, Pozzebon A, Roversi P-F, Scaccini D, Shrewsbury P, Tillman G, Tirello P, Waterworth R, Talamas EJ (2019) Surveys of stink bug egg parasitism in Asia, Europe and North America, morphological taxonomy, and molecular analysis reveal the Holarctic distribution of Acroclisoides sinicus (Huang & Liao) (Hymenoptera, Pteromalidae). Journal of Hymenoptera Research 74: 123-151. https://doi.org/10.3897/jhr.74.46701
Figure 5 Boxplot of pair-wise molecular distances between (left) the Acroclisoides haplotypes evidenced in this study, (center) conspecific individuals in the Pteromalinae, (right) individuals from different species of the same genus in the Pteromalinae.
Figure 4 from: Sabbatini Peverieri G, Mitroiu M-D, Bon M-C, Balusu R, Benvenuto L, Bernardinelli I, Fadamiro H, Falagiarda M, Fusu L, Grove E, Haye T, Hoelmer K, Lemke E, Malossini G, Marianelli L, Moore MR, Pozzebon A, Roversi P-F, Scaccini D, Shrewsbury P, Tillman G, Tirello P, Waterworth R, Talamas EJ (2019) Surveys of stink bug egg parasitism in Asia, Europe and North America, morphological taxonomy, and molecular analysis reveal the Holarctic distribution of Acroclisoides sinicus (Huang & Liao) (Hymenoptera, Pteromalidae). Journal of Hymenoptera Research 74: 123-151. https://doi.org/10.3897/jhr.74.46701
Figure 4 Haplotype network of the 49 Acroclisoides sinicus barcodes analyzed in this study. Each circle corresponds to one haplotype; circle size gives the proportion of individuals belonging to the haplotype. The color of the circles represents the geographical origin. Numbers correspond to the haplotype numbers. Hash marks symbolize the number of mutations between haplotypes.
Figure 1 from: Sabbatini Peverieri G, Mitroiu M-D, Bon M-C, Balusu R, Benvenuto L, Bernardinelli I, Fadamiro H, Falagiarda M, Fusu L, Grove E, Haye T, Hoelmer K, Lemke E, Malossini G, Marianelli L, Moore MR, Pozzebon A, Roversi P-F, Scaccini D, Shrewsbury P, Tillman G, Tirello P, Waterworth R, Talamas EJ (2019) Surveys of stink bug egg parasitism in Asia, Europe and North America, morphological taxonomy, and molecular analysis reveal the Holarctic distribution of Acroclisoides sinicus (Huang & Liao) (Hymenoptera, Pteromalidae). Journal of Hymenoptera Research 74: 123-151. https://doi.org/10.3897/jhr.74.46701
Figure 1 Typical shapes of exit holes produced by egg parasitoids of Halyomorpha halys in Europe: Anastatus bifasciatus male (A) and female (B) (NE-Italy); Acroclisoides sinicus (C, D) (NE-Italy); Trissolcus mitsukurii (E) (NE-Italy) and Trissolcus japonicus (F) (Switzerland).
Figure 3 from: Sabbatini Peverieri G, Mitroiu M-D, Bon M-C, Balusu R, Benvenuto L, Bernardinelli I, Fadamiro H, Falagiarda M, Fusu L, Grove E, Haye T, Hoelmer K, Lemke E, Malossini G, Marianelli L, Moore MR, Pozzebon A, Roversi P-F, Scaccini D, Shrewsbury P, Tillman G, Tirello P, Waterworth R, Talamas EJ (2019) Surveys of stink bug egg parasitism in Asia, Europe and North America, morphological taxonomy, and molecular analysis reveal the Holarctic distribution of Acroclisoides sinicus (Huang & Liao) (Hymenoptera, Pteromalidae). Journal of Hymenoptera Research 74: 123-151. https://doi.org/10.3897/jhr.74.46701
Figure 3 Acroclisoides sinicus: paratype of A. solus ♀ (U.S.A.), habitus in lateral view (A); idem, head in frontal view (B); ♂ (Switzerland), habitus in lateral view (C); idem, head in frontal view (D).
Figure 2 from: Sabbatini Peverieri G, Mitroiu M-D, Bon M-C, Balusu R, Benvenuto L, Bernardinelli I, Fadamiro H, Falagiarda M, Fusu L, Grove E, Haye T, Hoelmer K, Lemke E, Malossini G, Marianelli L, Moore MR, Pozzebon A, Roversi P-F, Scaccini D, Shrewsbury P, Tillman G, Tirello P, Waterworth R, Talamas EJ (2019) Surveys of stink bug egg parasitism in Asia, Europe and North America, morphological taxonomy, and molecular analysis reveal the Holarctic distribution of Acroclisoides sinicus (Huang & Liao) (Hymenoptera, Pteromalidae). Journal of Hymenoptera Research 74: 123-151. https://doi.org/10.3897/jhr.74.46701
Figure 2 Acroclisoides sinicus, ♀ (Italy, Cordenons): habitus in dorso-lateral view (A); head in frontal view (B); head in dorsal view (C); fore wing (D); antennae (E); mesosoma in dorsal view (F); mesosoma in lateral view (G).
Supplementary material 2 from: Galanos CJ (2020) Bionomics of Freyeria trochylus (Freyer, 1844) and Zizeeria karsandra (Moore, 1865) (Lepidoptera, Lycaenidae) on Rodos Island, Greece. Nota Lepidopterologica 43: 139-150. https://doi.org/10.3897/nl.43.48535
Video S2
Supplementary material 1 from: Galanos CJ (2020) Bionomics of Freyeria trochylus (Freyer, 1844) and Zizeeria karsandra (Moore, 1865) (Lepidoptera, Lycaenidae) on Rodos Island, Greece. Nota Lepidopterologica 43: 139-150. https://doi.org/10.3897/nl.43.48535
Video S1
Supplementary material 4 from: Galanos CJ (2020) Bionomics of Freyeria trochylus (Freyer, 1844) and Zizeeria karsandra (Moore, 1865) (Lepidoptera, Lycaenidae) on Rodos Island, Greece. Nota Lepidopterologica 43: 139-150. https://doi.org/10.3897/nl.43.48535
Figures S5–S15
Supplementary material 3 from: Galanos CJ (2020) Bionomics of Freyeria trochylus (Freyer, 1844) and Zizeeria karsandra (Moore, 1865) (Lepidoptera, Lycaenidae) on Rodos Island, Greece. Nota Lepidopterologica 43: 139-150. https://doi.org/10.3897/nl.43.48535
Video S3
FIGURE 4 in A new species of the genus Dahira Moore (Lepidoptera: Sphingidae) from Sichuan, China
FIGURE 4. Habitat of D. sichuanica sp. nov., altitude 1580 m, Mabian, Leshan, C. Sichuan.
Figure 7 in Seasonal changes in the population structure of dominant planktonic copepods collected using a sediment trap moored in the western Arctic Ocean
Figure 7. Seasonal changes in the flux of adult females, lipid accumulation (upper panels) and gonad maturation (lower panels) composition (stage I−III) of C6F (a, d) Calanus hyperboreus; (b, e) Metridia longa; and (c, f) Paraeuchaeta glacialis.
Figure 4 in Seasonal changes in the population structure of dominant planktonic copepods collected using a sediment trap moored in the western Arctic Ocean
Figure 4. Seasonal changes in the copepod flux and species composition at St. NAPt from October 2010 to September 2012.
Figure 6 in Seasonal changes in the population structure of dominant planktonic copepods collected using a sediment trap moored in the western Arctic Ocean
Figure 6. Seasonal changes in the flux and copepodid stage composition of the four large calanoid copepods: (a) Calanus hyperboreus; (b) Metridia longa; (c) Paraeuchaeta glacialis; and (d) Heterorhabdus norvegicus.
Figure 2 in Seasonal changes in the population structure of dominant planktonic copepods collected using a sediment trap moored in the western Arctic Ocean
Figure 2. Seasonal changes in depth (a) and temperature (b) of the sediment trap at St. NAPt from October 2010 to September 2012. The current velocity at 188 and 275 m at St. NAPt (c) was estimated by a physical ocean general circulation model.
Figure 1 in Seasonal changes in the population structure of dominant planktonic copepods collected using a sediment trap moored in the western Arctic Ocean
Figure 1. The location of St. NAPt (Northwind Abyssal Plain) in the western Arctic Ocean where the sediment trap was moored at a depth of approximately 184–260 m from October 2010 to September 2012.
Figure 5 in Seasonal changes in the population structure of dominant planktonic copepods collected using a sediment trap moored in the western Arctic Ocean
Figure 5. (a) Seasonal changes in the flux and copepodid stage composition of the dominant copepod Oncaea parila (Poecilostomatoida). *C6F with egg sacs occurred. (b) The relationship between O. parila flux and the total mass flux. A positive relationship was detected in 2010–2011 (first year).
Figure 28 from: Zhao TT, Han HL (2020) Four new species of the genus Diduga Moore, [1887] (Lepidoptera, Erebidae, Arctiinae) from China and Malaysia. ZooKeys 985: 127-141. https://doi.org/10.3897/zookeys.985.54047
Figure 28 Collecting sites of Diduga spp. Key: D. simianshana sp. nov.: China, Chongqing, Mt Simian (blue dot); D. chebalinga sp. nov.: China, Prov. Guangdong, Shaoguan, Chebaling (red dot); D. chewi sp. nov. and D. hollowayi sp. nov.: Malaysia, Borneo (both green dot).
Figures 22-27 from: Zhao TT, Han HL (2020) Four new species of the genus Diduga Moore, [1887] (Lepidoptera, Erebidae, Arctiinae) from China and Malaysia. ZooKeys 985: 127-141. https://doi.org/10.3897/zookeys.985.54047
Figures 22-27 Female genitalia of Diduga spp. 22D. simianshana sp. nov., paratype, genit. prep. No. ztt-073-2 23D. chebalinga sp. nov., paratype, genit. prep. No. ztt-077-2 24D. quinquicornuta (after Bayarsaikhan and Bae 2019) 25D. chewi sp. nov., paratype, genit. prep. No. ztt-102-2 26D. hollowayi sp. nov., paratype, genit. prep. No. ztt-083-2 27D. kohkongensis (after Bayarsaikhan & Bae, 2018). Scale bars: 0.5 mm.
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