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2,677 results for “LAMS”
FIGURES 8–9 in A remarkable new species of Coeliccia from the Tuyen Lam Lake area, Lam Dong, southern Vietnam (Odonata: Zygoptera: Platycnemididae)
FIGURES 8–9. Coeliccia suoitia holotype genital ligula: (8) ventral view, scale bar 0.2 mm; (9) lateral view terminal segment, scale bar 0.2 mm.
FIGURES 3–7 in A remarkable new species of Coeliccia from the Tuyen Lam Lake area, Lam Dong, southern Vietnam (Odonata: Zygoptera: Platycnemididae)
FIGURES 3–7. Coeliccia suoitia holotype: (3) prothorax, lateral view, scale bar 0.5 mm; (4) prothorax, dorsal view; (5) synthorax, dorsal view; (6) synthorax, lateral view, the small arrow shows the position of the area magnified in Fig. 7; (7) detail of venter of synthorax, lateral view, showing field of setae, scale bar 0.5 mm.
Data from: Annual ryegrass (Lolium multiflorum Lam.) growth response to nitrogen in a sandy soil amended with acidified manure and municipal sludge after "Quick Wash" treatment
<p>The Quick Wash (QW) treatment extracts phosphorus (P) from manure and municipal sludge (MS), producing an organic acidified by-product with adequate nitrogen (N):P ratio to meet crop N requirements. Yet, data on crop response to N using QW by-products are lacking. We evaluated the response of annual ryegrass (<span class="html-italic">Lolium multiflorum</span> Lam.) and potential N leaching in sandy soil to N applications using raw wastes, their corresponding QW by-products, and ammonium sulfate (AMS) fertilizer. Treatments included a control (no amendment added), raw and acid-washed chicken litter, dairy and swine manure, MS, and AMS at 100, 200, and 400 kg N ha<sup>−1</sup>.</p>
Pra Rod lam loon
amulet of thailand Source: Objaverse 1.0 / Sketchfab
FIGURE 6. Asplenium falcatum Lam. Hermann s.n in Taxonomic and nomenclatural notes on Philippine ferns. IV. Asplenium pahli (Polypodiales, Aspleniineae, Aspleniaceae), a new species from Leyte, Philippines
FIGURE 6. Asplenium falcatum Lam. Hermann s.n., BM000621974, Herb. Hermann 3: 47, no. 385 (BM). Note the pinna shape and basal acroscopic tooth, serration and soral arrangement. Courtesy of the Herbarium, British Museum of Natural History, London, England. License CC0-10. Specimen available at: https://plants.jstor.org/stable/10.5555/al.ap.specimen.bm000621974
FIGURE 7 in Alloiothucha artocarpi (Horváth) (Hemiptera: Heteroptera: Tingidae) found on jackfruit, Artocarpus heterophyllus Lam. (Moraceae): first representative of the genus from Laos, and the synonymy of Cetiothucha Drake & Ruhoff
FIGURE 7. Holotype of Alloiothucha constanti, comb. nov.: dorsal view (A); lateral view (B). Arrows mark hood and paranotum. Scale bar: 1.0 mm. Copyright Magnolia Press. Allowed use by Katrina Menard. Modified after Guilbert et al. (2018).
FIGURE 4 in Alloiothucha artocarpi (Horváth) (Hemiptera: Heteroptera: Tingidae) found on jackfruit, Artocarpus heterophyllus Lam. (Moraceae): first representative of the genus from Laos, and the synonymy of Cetiothucha Drake & Ruhoff
FIGURE 4. Male terminalia of Alloiothucha artocarpi, dorsal view: paramere (A) and pygophore (B). Ostiolar peritreme of A. artocarpi, lateral view (C). Scale bars: 0.1 mm.
FIGURE 5 in Alloiothucha artocarpi (Horváth) (Hemiptera: Heteroptera: Tingidae) found on jackfruit, Artocarpus heterophyllus Lam. (Moraceae): first representative of the genus from Laos, and the synonymy of Cetiothucha Drake & Ruhoff
FIGURE 5. Holotype of Alloiothucha philippinensis: dorsal view (A); lateral view (B); labels (C). Arrows mark hood and paranotum. Copyright United States National Museum of Natural History. Allowed use by Thomas J. Henry. Images taken by United States National Museum of Natural History (2022).
FIGURE 2 in Alloiothucha artocarpi (Horváth) (Hemiptera: Heteroptera: Tingidae) found on jackfruit, Artocarpus heterophyllus Lam. (Moraceae): first representative of the genus from Laos, and the synonymy of Cetiothucha Drake & Ruhoff
FIGURE 2. Thoracic structures of Alloiothucha artocarpi: pronotum, dorsal and dorsolateral views (A, B); hemelytra, dorsolateral view (C). Scale bars: 0.2 mm.
FIGURE 1 in Alloiothucha artocarpi (Horváth) (Hemiptera: Heteroptera: Tingidae) found on jackfruit, Artocarpus heterophyllus Lam. (Moraceae): first representative of the genus from Laos, and the synonymy of Cetiothucha Drake & Ruhoff
FIGURE 1. Habitus images of Alloiothucha artocarpi from Laos, dorsal and lateral views (A, B). Scale bar: 1.0 mm.
FIGURE 8 in Alloiothucha artocarpi (Horváth) (Hemiptera: Heteroptera: Tingidae) found on jackfruit, Artocarpus heterophyllus Lam. (Moraceae): first representative of the genus from Laos, and the synonymy of Cetiothucha Drake & Ruhoff
FIGURE 8. Alloiothucha physalia, comb. nov.: dorsal habitus (A); pronotum, lateral view (B); pronotum excluding hood, dorsal view (C). Arrows mark hood and paranotum. Modified after Drake & Ruhoff (1965a).
FIGURE 3 in Alloiothucha artocarpi (Horváth) (Hemiptera: Heteroptera: Tingidae) found on jackfruit, Artocarpus heterophyllus Lam. (Moraceae): first representative of the genus from Laos, and the synonymy of Cetiothucha Drake & Ruhoff
FIGURE 3. Rostrum and sternal laminae of Alloiothucha artocarpi, ventral view (A). Apical part of the abdomen of A. artocarpi, ventral view: male (B) and female (C). Scale bars: 0.2 mm.
FIGURE 6 in Alloiothucha artocarpi (Horváth) (Hemiptera: Heteroptera: Tingidae) found on jackfruit, Artocarpus heterophyllus Lam. (Moraceae): first representative of the genus from Laos, and the synonymy of Cetiothucha Drake & Ruhoff
FIGURE 6. Holotype of Alloiothucha necopinata: dorsal view (A); lateral view (B); labels (C). Arrows mark hood and paranotum. Copyright United States National Museum of Natural History. Allowed use by Thomas J. Henry. Images taken by United States National Museum of Natural History (2022).
Subspecies and Distribution. C. l. latrans Say, 1823 — S Canada and USA (Great Plains region). C. l. cagottis Hamilton-Smith, 1839 — SE Mexico. C. l. clepticus Elliot, 1903 — Mexico (N Baja California) and USA (S California). C. l. dickeyi Nelson, 1932 — Costa Rica, El Salvador, W Honduras, Nicaragua, and Panama. C. l. frustror Woodhouse, 1850 — USA (Missouri, Kansas, parts of Oklahoma & E Texas). C. l. goldmani Merriam, 1904 — Belize, Guatemala, and S Mexico. C. l. hondurensis Goldman, 1936 — E Honduras. C. l. impavidus J. A. Allen, 1903 - W Mexico. C. l. incolatus Hall, 1934 - Alaska and NW Canada. C. l. ¡jamesi Townsend. 1912 - Mexico (Tiburon l. Baia California). c. [l.lestes lam Merriam, 1897 1897 - sw canada Canada and w USA USA Õnzenndunzain Region & NW). v C. l. mearnsi Merriam, 1897 - NW Mexico and SW USA. C. l. mıcrodon Merriam, 1897 — NE Mexico and S USA (S Texas). C. l. ochropus Eschscholtz, 1829 - W USA (W coast). C. l. peninsulaeMerriam, 1897 — Mexico (S Baja California). C. l. texensıs Bailey, 1905 - S USA (W Texas 8c New Mexico). C. l. thamnos Jackson, 1949 - N-C Canada and E USA. C. l. umpquensıs Jackson. 1949 - USA (NW coast). C. l. vigilis Merriam. 1897 — SW Mexico. Coyotes did not originally occur on the USA E coast or Florida. They (probably thamnos) have expanded into the area with the clearing of forests and been introduced to Florida and Georgia (subspecies unknown). in Canidae
Subspecies and Distribution. C. l. latrans Say, 1823 — S Canada and USA (Great Plains region). C. l. cagottis Hamilton-Smith, 1839 — SE Mexico. C. l. clepticus Elliot, 1903 — Mexico (N Baja California) and USA (S California). C. l. dickeyi Nelson, 1932 — Costa Rica, El Salvador, W Honduras, Nicaragua, and Panama. C. l. frustror Woodhouse, 1850 — USA (Missouri, Kansas, parts of Oklahoma & E Texas). C. l. goldmani Merriam, 1904 — Belize, Guatemala, and S Mexico. C. l. hondurensis Goldman, 1936 — E Honduras. C. l. impavidus J. A. Allen, 1903 - W Mexico. C. l. incolatus Hall, 1934 - Alaska and NW Canada. C. l. ¡jamesi Townsend. 1912 - Mexico (Tiburon l. Baia California). c. [l.lestes lam Merriam, 1897 1897 - sw canada Canada and w USA USA Õnzenndunzain Region & NW). v C. l. mearnsi Merriam, 1897 - NW Mexico and SW USA. C. l. mıcrodon Merriam, 1897 — NE Mexico and S USA (S Texas). C. l. ochropus Eschscholtz, 1829 - W USA (W coast). C. l. peninsulaeMerriam, 1897 — Mexico (S Baja California). C. l. texensıs Bailey, 1905 - S USA (W Texas 8c New Mexico). C. l. thamnos Jackson, 1949 - N-C Canada and E USA. C. l. umpquensıs Jackson. 1949 - USA (NW coast). C. l. vigilis Merriam. 1897 — SW Mexico. Coyotes did not originally occur on the USA E coast or Florida. They (probably thamnos) have expanded into the area with the clearing of forests and been introduced to Florida and Georgia (subspecies unknown).
Distribution. NE India (West Bengal and Nagaland), S China (Yunnan), N Thailand, Laos, SW Cambodia (Cardamom Mts), and Vietnam (Ha Tinh, Vin Phuc, Nghe An, Thua Thien-Hue, Dak Lak, and Lam Dong provinces). in Vespertilionidae
Distribution. NE India (West Bengal and Nagaland), S China (Yunnan), N Thailand, Laos, SW Cambodia (Cardamom Mts), and Vietnam (Ha Tinh, Vin Phuc, Nghe An, Thua Thien-Hue, Dak Lak, and Lam Dong provinces).
Subspecies and Distribution. C.h.himalayicaGray,1842—widelydistributedinmiddletohighmountainsinSHimalaya(NW&NEIndia,Nepal,andBhutan),SWC.h.(SETibet[=Xizang],Sichuan,Yunnan,andprobablyGuizhouandGuangxi),NMyanmar,Laos,andN&CVietnam. C. h. varennei Thomas, 1927 — S Vietnam (Kon Tum, Dak Lak, and Lam Dong provinces). in Soricidae
Subspecies and Distribution. C.h.himalayicaGray,1842—widelydistributedinmiddletohighmountainsinSHimalaya(NW&NEIndia,Nepal,andBhutan),SWC.h.(SETibet[=Xizang],Sichuan,Yunnan,andprobablyGuizhouandGuangxi),NMyanmar,Laos,andN&CVietnam. C. h. varennei Thomas, 1927 — S Vietnam (Kon Tum, Dak Lak, and Lam Dong provinces).
Supplementary material 7 from: Lobban CS, Ashworth MP, Camacho T, Lam DW, Theriot EC (2022) Revision of Ardissoneaceae (Bacillariophyta, Mediophyceae) from Micronesian populations, with descriptions of two new genera, Ardissoneopsis and Grunowago, and new species in Ardissonea, Synedrosphenia and Climacosphenia. PhytoKeys 208: 103-184. https://doi.org/10.3897/phytokeys.208.89913
Figure S5. Molecular phylogenetic tree illustrating the results of the ExaBayes Bayesian Inference analysis of the 3-gene dataset
Supplementary material 6 from: Lobban CS, Ashworth MP, Camacho T, Lam DW, Theriot EC (2022) Revision of Ardissoneaceae (Bacillariophyta, Mediophyceae) from Micronesian populations, with descriptions of two new genera, Ardissoneopsis and Grunowago, and new species in Ardissonea, Synedrosphenia and Climacosphenia. PhytoKeys 208: 103-184. https://doi.org/10.3897/phytokeys.208.89913
Figure S4. Molecular phylogenetic tree illustrating the results of the IQTREE Maximum Likelihood analysis of the 3-gene dataset
Supplementary material 3 from: Lobban CS, Ashworth MP, Camacho T, Lam DW, Theriot EC (2022) Revision of Ardissoneaceae (Bacillariophyta, Mediophyceae) from Micronesian populations, with descriptions of two new genera, Ardissoneopsis and Grunowago, and new species in Ardissonea, Synedrosphenia and Climacosphenia. PhytoKeys 208: 103-184. https://doi.org/10.3897/phytokeys.208.89913
Figure S1. Plastids in a living cell of Ardissonea formosa showing movement from dispersed (peristrophy) to concentrated around the nucleus (karyostrophy)
Supplementary material 5 from: Lobban CS, Ashworth MP, Camacho T, Lam DW, Theriot EC (2022) Revision of Ardissoneaceae (Bacillariophyta, Mediophyceae) from Micronesian populations, with descriptions of two new genera, Ardissoneopsis and Grunowago, and new species in Ardissonea, Synedrosphenia and Climacosphenia. PhytoKeys 208: 103-184. https://doi.org/10.3897/phytokeys.208.89913
Figure S3. Molecular phylogenetic tree illustrating the results of the RAxML Maximum Likelihood analysis of the 3-gene dataset
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