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1

White, Philip J. "Confirming a conformist conformation: the topology of AtHKT1." Trends in Plant Science 6, no. 7 (July 2001): 293–94. http://dx.doi.org/10.1016/s1360-1385(01)02036-2.

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2

Rus, Ana, Byeong-ha Lee, Alicia Muñoz-Mayor, Altanbadralt Sharkhuu, Kenji Miura, Jian-Kang Zhu, Ray A. Bressan, and Paul M. Hasegawa. "AtHKT1 Facilitates Na+ Homeostasis and K+ Nutrition in Planta." Plant Physiology 136, no. 1 (September 2004): 2500–2511. http://dx.doi.org/10.1104/pp.104.042234.

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3

Horie, Tomoaki, Rie Horie, Wai-Yin Chan, Ho-Yin Leung, and Julian I. Schroeder. "Calcium Regulation of Sodium Hypersensitivities of sos3 and athkt1 Mutants." Plant and Cell Physiology 47, no. 5 (May 1, 2006): 622–33. http://dx.doi.org/10.1093/pcp/pcj029.

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4

Rus, A., S. Yokoi, A. Sharkhuu, M. Reddy, B. h. Lee, T. K. Matsumoto, H. Koiwa, J. K. Zhu, R. A. Bressan, and P. M. Hasegawa. "AtHKT1 is a salt tolerance determinant that controls Na+ entry into plant roots." Proceedings of the National Academy of Sciences 98, no. 24 (November 6, 2001): 14150–55. http://dx.doi.org/10.1073/pnas.241501798.

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5

Rus, Ana, Ivan Baxter, Balasubramaniam Muthukumar, Jeff Gustin, Brett Lahner, Elena Yakubova, and David E. Salt. "Natural Variants of AtHKT1 Enhance Na+ Accumulation in Two Wild Populations of Arabidopsis." PLoS Genetics 2, no. 12 (2006): e210. http://dx.doi.org/10.1371/journal.pgen.0020210.

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Rus, Ana, Ivan Baxter, Balasubramaniam Muthukumar, Jeff Gustin, Brett Lahner, Elena Yakubova, and David E. Salt. "Natural Variants of AtHKT1 Enhance Na+ Accumulation in Two Wild Populations of Arabidopsis." PLoS Genetics preprint, no. 2006 (2005): e210. http://dx.doi.org/10.1371/journal.pgen.0020210.eor.

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7

An, Dong, Jiu-Geng Chen, Yi-Qun Gao, Xiang Li, Zhen-Fei Chao, Zi-Ru Chen, Qian-Qian Li, et al. "AtHKT1 drives adaptation of Arabidopsis thaliana to salinity by reducing floral sodium content." PLOS Genetics 13, no. 10 (October 30, 2017): e1007086. http://dx.doi.org/10.1371/journal.pgen.1007086.

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8

KATO, Yasuhiro, Akihiro HAZAMA, Mutsumi YAMAGAMI, and Nobuyuki UOZUMI. "Addition of a Peptide Tag at the C Terminus of AtHKT1 Inhibits Its Na+Transport." Bioscience, Biotechnology, and Biochemistry 67, no. 10 (January 2003): 2291–93. http://dx.doi.org/10.1271/bbb.67.2291.

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9

Sunarpi, Tomoaki Horie, Jo Motoda, Masahiro Kubo, Hua Yang, Kinya Yoda, Rie Horie, et al. "Enhanced salt tolerance mediated by AtHKT1 transporter-induced Na+ unloading from xylem vessels to xylem parenchyma cells." Plant Journal 44, no. 6 (November 25, 2005): 928–38. http://dx.doi.org/10.1111/j.1365-313x.2005.02595.x.

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10

Berthomieu, P. "Functional analysis of AtHKT1 in Arabidopsis shows that Na+ recirculation by the phloem is crucial for salt tolerance." EMBO Journal 22, no. 9 (May 1, 2003): 2004–14. http://dx.doi.org/10.1093/emboj/cdg207.

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11

Mäser, Pascal, Brendan Eckelman, Rama Vaidyanathan, Tomoaki Horie, David J. Fairbairn, Masahiro Kubo, Mutsumi Yamagami, et al. "Altered shoot/root Na+ distribution and bifurcating salt sensitivity in Arabidopsis by genetic disruption of the Na+ transporter AtHKT1." FEBS Letters 531, no. 2 (October 9, 2002): 157–61. http://dx.doi.org/10.1016/s0014-5793(02)03488-9.

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12

Zhang, Huiming, Mi-Seong Kim, Yan Sun, Scot E. Dowd, Huazhong Shi, and Paul W. Paré. "Soil Bacteria Confer Plant Salt Tolerance by Tissue-Specific Regulation of the Sodium Transporter HKT1." Molecular Plant-Microbe Interactions® 21, no. 6 (June 2008): 737–44. http://dx.doi.org/10.1094/mpmi-21-6-0737.

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Elevated sodium (Na+) decreases plant growth and, thereby, agricultural productivity. The ion transporter high-affinity K+ transporter (HKT)1 controls Na+ import in roots, yet dysfunction or overexpression of HKT1 fails to increase salt tolerance, raising questions as to HKT1's role in regulating Na+ homeostasis. Here, we report that tissue-specific regulation of HKT1 by the soil bacterium Bacillus subtilis GB03 confers salt tolerance in Arabidopsis thaliana. Under salt stress (100 mM NaCl), GB03 concurrently down- and upregulates HKT1 expression in roots and shoots, respectively, resulting in lower Na+ accumulation throughout the plant compared with controls. Consistent with HKT1 participation in GB03-induced salt tolerance, GB03 fails to rescue salt-stressed athkt1 mutants from stunted foliar growth and elevated total Na+ whereas salt-stressed Na+ export mutants sos3 show GB03-induced salt tolerance with enhanced shoot and root growth as well as reduced total Na+. These results demonstrate that tissue-specific regulation of HKT1 is critical for managing Na+ homeostasis in salt-stressed plants, as well as underscore the breadth and sophistication of plant–microbe interactions.
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13

Nawaz, Ismat, Mazhar Iqbal, Henk W. J. Hakvoort, Albertus H. de Boer, and Henk Schat. "Analysis of Arabidopsis thaliana HKT1 and Eutrema salsugineum/botschantzevii HKT1;2 Promoters in Response to Salt Stress in Athkt1:1 Mutant." Molecular Biotechnology 61, no. 6 (April 12, 2019): 442–50. http://dx.doi.org/10.1007/s12033-019-00175-5.

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14

Baek, Dongwon, Jiafu Jiang, Jung-Sung Chung, Bangshing Wang, Junping Chen, Zhanguo Xin, and Huazhong Shi. "Regulated AtHKT1 Gene Expression by a Distal Enhancer Element and DNA Methylation in the Promoter Plays an Important Role in Salt Tolerance." Plant and Cell Physiology 52, no. 1 (November 18, 2010): 149–61. http://dx.doi.org/10.1093/pcp/pcq182.

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15

Kato, Y., M. Sakaguchi, Y. Mori, K. Saito, T. Nakamura, E. P. Bakker, Y. Sato, S. Goshima, and N. Uozumi. "Evidence in support of a four transmembrane-pore-transmembrane topology model for the Arabidopsis thaliana Na+/K+ translocating AtHKT1 protein, a member of the superfamily of K+ transporters." Proceedings of the National Academy of Sciences 98, no. 11 (May 8, 2001): 6488–93. http://dx.doi.org/10.1073/pnas.101556598.

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16

Pace, Roberto. "Introduzione alla conoscenza della sottofamiglia Aleocharinae della Guyana Francese: Parte III (Coleoptera, Staphylinidae)." Beiträge zur Entomologie = Contributions to Entomology 64, no. 1 (July 31, 2014): 93–110. http://dx.doi.org/10.21248/contrib.entomol.64.1.93-110.

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23 neue Arten der Tribus Athetini werden beschrieben: Ischnopoda pulchritudinis n. sp., Xyronarchusa amazonica n. gen., n. sp., Atheta (Acrotona) obscurepyga n. sp., Atheta (Acrotona) tanpokensis n. sp., Atheta (Acrotona) guyterminicornis n. sp., Atheta (Acrotona) subparcior n. sp., Atheta (Acrotona) guyminima n. sp., Atheta (Microdota) ungulifera n. sp., Atheta (Microdota) guyarufa n. sp., Atheta (Xestota) guyattenuata n. sp., Atheta (Datomicra) guymimetica n. sp., Atheta (Datomicra) guydivergens n. sp., Atheta (Datomicra) guyanelegans n. sp., Atheta (Datomicra) guydifferens n. sp., Atheta (Datomicra) caussadensis n. sp., Atheta (Datomicra) camopiensis n. sp., Atheta (Datomicra) struyvei n. sp., Atheta (Gyroatheta subg. n.) guyanicola n. sp., Lamprostiba pulchra n. sp., Parademosoma (Elixusa subg. n.) guyanensis n. sp., Dolerella cayennensis n. sp., Dinusella angularis n. sp., Dinusella pulchripennis n. sp. Für 7 Arten werden zusätzliche Daten aufgeführt. Zwei neue Gattungen, Xyronarchusa n. gen. und Dolerella n. gen. und zwei neue Untergattungen Gyroatheta subg. n. von Atheta und Elixusa subg. n. von Parademosoma werden beschrieben. Jede neue Art wird illustriert und mit ähnlichen Arten verglichen.SommarioDescrizione di 23 nuove specie della tribù Athetini: Ischnopoda pulchritudinis n. sp., Xyronarchusa amazonica n. gen., n. sp., Atheta (Acrotona) obscurepyga n. sp., Atheta (Acrotona) tanpokensis n. sp., Atheta (Acrotona) guyterminicornis n. sp., Atheta (Acrotona) subparcior n. sp., Atheta (Acrotona) guyminima n. sp., Atheta (Microdota) ungulifera n. sp., Atheta (Microdota) guyarufa n. sp., Atheta (Xestota) guyattenuata n. sp., Atheta (Datomicra) guymimetica n. sp., Atheta (Datomicra) guydivergens n. sp., Atheta (Datomicra) guyanelegans n. sp., Atheta (Datomicra) guydifferens n. sp., Atheta (Datomicra) caussadensis n. sp., Atheta (Datomicra) camopiensis n. sp., Atheta (Datomicra) struyvei n. sp., Atheta (Gyroatheta subg. n.) guyanicola n. sp., Lamprostiba pulchra n. sp., Parademosoma (Elixusa subg. n.) guyanensis n. sp., Dolerella cayennensis n. sp., Dinusella angularis n. sp., Dinusella pulchripennis n. sp. Sono riportati dati distributivi supplementari per 7 specie. Sono descritti due nuovi generi Xyronarchusa n. gen. e Dolerella n. gen. e due nuovi sottogeneri Gyroatheta subg. n. di Atheta ed Elixusa subg. n. di Parademosoma. Ogni specie nuova è illustrata e comparata con specie simili.StichwörterColeoptera, Staphylinidae, Aleocharinae, taxonomy, French Guiana.Nomenklatorische HandlungenDolerella Pace, 2014 (Aleocharinae), gen. n. Type species: Dolerella cayennensis Pace, 2014Xyronarchusa Pace, 2014 (Aleocharinae), gen. n. Type species: Xyronarchusa amazonica Pace, 2014Gyroatheta Pace, 2014 (Atheta), subgen. n. of Atheta Thomson, 1858; typical species: Atheta (Gyroatheta) guyanicola Pace, 2014guyminima Pace, 2014 (Atheta (Acrotona)), spec. n.guyterminicornis Pace, 2014 (Atheta (Acrotona)), spec. n.obscurepyga Pace, 2014 (Atheta (Acrotona)), spec. n.tanpokensis Pace, 2014 (Atheta (Acrotona)), spec. n.camopiensis Pace, 2014 (Atheta (Datomicra)), spec. n.caussadensis Pace, 2014 (Atheta (Datomicra)), spec. n.guyanelegans Pace, 2014 (Atheta (Datomicra)), spec. n.guydivergens Pace, 2014 (Atheta (Datomicra)), spec. n.guymimetica Pace, 2014 (Atheta (Datomicra)), spec. n.struyvei Pace, 2014 (Atheta (Datomicra)), spec. n.guyanicola Pace, 2014 (Atheta (Gyroatheta)), spec. n.guyarufa Pace, 2014 (Atheta (Microdota)), spec. n.ungulifera Pace, 2014 (Atheta (Microdota)), spec. n.guyattenuata Pace, 2014 (Atheta (Xestota)), spec. n.angularis Pace, 2014 (Dinusella), spec. n.pulchripennis Pace, 2014 (Dinusella), spec. n.cayennensis Pace, 2014 (Dolerella), spec. n.pulchritudinis Pace, 2014 (Ischnopoda), spec. n.pulchra Pace, 2014 (Lamprostiba), spec. n.Elixusa Pace, 2014 (Parademosoma), subgen. n. of Parademosoma Bernhauer, 1929; typical species: Parademosoma (Elixura) guyanensis Pace, 2014guyanensis Pace, 2014 (Parademosoma (Elixura)), spec. n.amazonica Pace, 2014 (Xyronarchusa), spec. n.
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17

Pace, Roberto. "Nuovi dati faunistici e tassonomici su Aleocharinae des Sudamerica delle tribu Deinopsini, Athetini e Thamiaraeini (Coleoptera, Staphylinidae)." Beiträge zur Entomologie = Contributions to Entomology 58, no. 2 (November 15, 2008): 399–439. http://dx.doi.org/10.21248/contrib.entomol.58.2.399-439.

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Für 185 Exemplare der Deinopsini, Athetini und Thamiaraeini aus dem Zoologischen Museum der Humboldt Universität zu Berlin, aus dem Naturhistorischen Museum in Wien, aus dem Deutschen Entomologischen Institut in Müncheberg, aus dem Städtischen Museum der Naturgeschichte in Genua und aus der Sammlung Herbert Franz werden taxonomische und faunistische Angaben präsentiert. Das Material wird 7 Gattungen (Adinopsis, Amischa, Atheta, Leptonia, Dinusella, Heterostiba und Leptoglossula), einer neuen Untergattung und 56 Arten zugeordnet. Weiterhin werden 29 neue Arten und die neue Untergattung Dysanomota für Atheta cinctella (Erichson) beschrieben, illustriert und mit ähnlichen Taxa verglichen.SommarioSono forniti dati tassonomici e faunistici di 185 esemplari di Deinopsini, Athetini e Thamiaraeini del Museo Zoologico dell’Università Humboldt di Berlino, del Deutsches Entomologisches Institut di Müncheberg, del Museo civico di Storia naturale di Genova e della collezione di Herbert Franz al Naturhistorisches Museum di Vienna. Sono riconosciuti 7 generi (Adinopsis, Amischa, Atheta, Leptonia, Dinusella, Heterostiba e Leptoglossula) e 56 specie. Sono descritti e illustrati 29 nuove specie e il nuovo sottogenere Dysanomota per Atheta cinctella (Erichson). Le nuove specie e il nuovo sottogenere sono confrontati con taxa affini.StichwörterColeoptera, Staphylinidae, Aleocharinae, taxonomy, South America.Nomenklatorische Handlungenfranzi Pace, 2008 (Amischa), spec. n.Dysanomota Pace, 2008 (Atheta), sgen. n.alegrensis Pace, 2008 (Atheta (Acrotona)), spec. n.aracauriarum Pace, 2008 (Atheta (Acrotona)), spec. n.bernardina Pace, 2008 (Atheta (Acrotona)), spec. n.iguazuensis Pace, 2008 (Atheta (Acrotona)), spec. n.paraparcior Pace, 2008 (Atheta (Acrotona)), spec. n.plaumanni Pace, 2008 (Atheta (Acrotona)), spec. n.botocudorum Pace, 2008 (Atheta (Chaetida)), spec. n.colonorum Pace, 2008 (Atheta (Datomicra)), spec. n.condei Pace, 2008 (Atheta (Datomicra)), spec. n.guaranorum Pace, 2008 (Atheta (Datomicra)), spec. n.montesensis Pace, 2008 (Atheta (Datomicra)), spec. n.piauiensis Pace, 2008 (Atheta (Datomicra)), spec. n.sublongula Pace, 2008 (Atheta (Datomicra)), spec. n.tupiorum Pace, 2008 (Atheta (Datomicra)), spec. n.waageni Pace, 2008 (Atheta (Datomicra)), spec. n.bogotana Pace, 2008 (Atheta (Dimetrota)), spec. n.caecilia Pace, 2008 (Atheta (Dimetrota)), spec. n.cyanocompsae Pace, 2008 (Atheta (Dimetrota)), spec. n.nigricauda Pace, 2008 (Atheta (Dimetrota)), spec. n.paramorum Pace, 2008 (Atheta (Dimetrota)), spec. n.cinctella (Erichson, 1839) (Atheta (Dysanomota)), Lectotype; comb. n. hitherto Homalota cinctellacaneparii Pace, 2008 (Atheta (Microdota)), spec. n.obidosensis Pace, 2008 (Atheta (Microdota)), spec. n.amazonica Pace, 2008 (Atheta (Pseudobessobia)), spec. n.macropana Pace, 2008 (Atheta (Pseudobessobia)), spec. n.tucumanensis Pace, 2008 (Atheta (Pseudobessobia)), spec. n.parva Pace, 2008 (Heterostiba), spec. n.venezuelensis Pace, 2008 (Heterostiba), spec. n.sanctaecrucis Pace, 2008 (Leptonia), spec. n.
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18

Pace, Roberto. "Biodiversità delle Aleocharinae della Cina: Genere Atheta Thomson (Coleoptera, Staphylinidae)." Beiträge zur Entomologie = Contributions to Entomology 61, no. 2 (November 10, 2011): 285–355. http://dx.doi.org/10.21248/contrib.entomol.61.2.285-355.

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Es werden Daten zur Taxonomie von 109 Arten der Gattung Atheta gebracht, die in die folgenden Untergattungen gehören: Chaetida, Sipalatheta, Philhygra, Oxypodera, Acrotona, Sinodota, Microdota, Bessobia, Dimetrota, Datomicra, Dalotia, Poromicrodota, Oreostiba, Atheta und Ekkliatheta. Für 52 Arten werden neue Daten mitgeteilt. 57 Arten werden neu beschrieben und illustriert: A. (Sipalatheta) fuscoterminalis n. sp., A. (S.) nitidearmata n. sp., A. (Philhygra) longefalciferoides n. sp., A. (P.) tibetapicalis n. sp., A. (P.) sinobifalcifera n. sp., A. (P.) taibaimontis n. sp., A. (Oxypodera) sinorelicta n. sp., A. (Acrotona) yongshengensis n. sp., A. (A.) magnalanima n. sp., A. (A.) qinlingicola n. sp., A. (Sinodota) sinobulbosa n. sp., A. (Microdota) sinobscura n. sp., A. (M.) sphaerae n. sp., A. (M.) megatheca n. sp., A. (M.) acrotonotheca n. sp., A. (M.) guanxianensis n. sp., A. (M.) neatang n. sp., A. (M.) cavazzutii n. sp., A. (M.) caudata n. sp., A. (M.) sinocolorata n. sp., A. (M.) colortang n. sp., A. (M.) pseudonana n. sp., A. (M.) perindistincta n. sp., A. (M.) ogivalis n. sp., A. (M.) daxuepraticola n. sp., A. (M.) pseudoplacita n. sp., A. (M.) sinosulcata n. sp., A. (M.) naniensis n. sp., A. (Bessobia) foedemarginata n. sp., A. (B.) forcipis n. sp., A. (B.) luojimontis n. sp., A. (B.) mimosibirica n. sp., A. (B.) sinonigra n. sp., A. (B.) extabescens n. sp., A. (B.) sinopusilla n. sp., A. (Dimetrota) qinlingensis n. sp., A. (D.) shaluliopaca n. sp., A. (D.) suburumqiensis n. sp., A. (D.) leshanensis n. sp., A. (D.) daxuecoprobia n. sp., A. (D.) gigarcuata n. sp., A. (D.) daxuefurtiva n. sp., A. (D.) huamontis n. sp., A. (D.) granulotibetana n. sp., A. (D.) hailougouicola n. sp., A. (D.) robustina n. sp., A. (D.) sinodenticulata n. sp., A. (D.) zanettii n. sp., A. (D.) dalibaiensis n. sp., A. (D.) sinorufipennis n. sp., A. (D.) sinolucida n. sp., A. (D.) aesculapii n. sp., A. (Datomicra) contractionis n. sp., A. (D.) shalulifalcifera n. sp., A. (D.) tibetana n. sp., A. (D.) semicircularis n. sp., A. (D.) mugecuensis n. sp. Die neue Untergattung Sinodota ist ähnlich Microdota. Eine neue Kombination wird vorgeschlagen.SommarioE’ presentato uno studio tassonomico di 109 specie di Atheta dei sottogeneri Chaetida, Sipalatheta, Philhygra, Oxypodera, Acrotona, Sinodota, Microdota, Bessobia, Dimetrota, Datomicra, Dalotia, Poromicrodota, Oreostiba, Atheta, Ekkliatheta. Sono riferiti nuovi dati per 52 specie e sono descritte e illustrate 57 nuove specie: A. (Sipalatheta) fuscoterminalis n. sp., A. (S.) nitidearmata n. sp., A. (Philhygra) longefalciferoides n. sp., A. (P.) tibetapicalis n. sp., A. (P.) sinobifalcifera n. sp., A. (P.) taibaimontis n. sp., A. (Oxypodera) sinorelicta n. sp., A. (Acrotona) yongshengensis n. sp., A. (A.) magnalanima n. sp., A. (A.) qinlingicola n. sp., A. (Sinodota) sinobulbosa n. sp., A. (Microdota) sinobscura n. sp., A. (M.) sphaerae n. sp., A. (M.) megatheca n. sp., A. (M.) acrotonotheca n. sp., A. (M.) guanxianensis n. sp., A. (M.) neatang n. sp., A. (M.) cavazzutii n. sp., A. (M.) caudata n. sp., A. (M.) sinocolorata n. sp., A. (M.) colortang n. sp., A. (M.) pseudonana n. sp., A. (M.) perindistincta n. sp., A. (M.) ogivalis n. sp., A. (M.) daxuepraticola n. sp., A. (M.) pseudoplacita n. sp., A. (M.) sinosulcata n. sp., A. (M.) naniensis n. sp., A. (Bessobia) foedemarginata n. sp., A. (B.) forcipis n. sp., A. (B.) luojimontis n. sp., A. (B.) mimosibirica n. sp., A. (B.) sinonigra n. sp., A. (B.) extabescens n. sp., A. (B.) sinopusilla n. sp., A. (Dimetrota) qinlingensis n. sp., A. (D.) shaluliopaca n. sp., A. (D.) suburumqiensis n. sp., A. (D.) leshanensis n. sp., A. (D.) daxuecoprobia n. sp., A. (D.) gigarcuata n. sp., A. (D.) daxuefurtiva n. sp., A. (D.) huamontis n. sp., A. (D.) granulotibetana n. sp., A. (D.) hailougouicola n. sp., A. (D.) robustina n. sp., A. (D.) sinodenticulata n. sp., A. (D.) zanettii n. sp., A. (D.) dalibaiensis n. sp., A. (D.) sinorufipennis n. sp., A. (D.) sinolucida n. sp., A. (D.) aesculapii n. sp., A. (Datomicra) contractionis n. sp., A. (D.) shalulifalcifera n. sp., A. (D.) tibetana n. sp., A. (D.) semicircularis n. sp., A. (D.) mugecuensis n. sp. Il nuovo sottogenere Sinodota è affine a Microdota. E’ proposta una nuova combinazione.StichwörterColeoptera, Staphylinidae, Aleocharinae, taxonomy, China.Nomenklatorische Handlungenmagnalanima Pace, 2011 (Atheta (Acrotona)), spec.nov. misspelling, recte: "magnalamina" (see Etimologia)qinlingicola Pace, 2011 (Atheta (Acrotona)), spec.nov.yongshengensis Pace, 2011 (Atheta (Acrotona)), spec.nov.extabescens Pace, 2011 (Atheta (Bessobia)), spec.nov.foedemarginata Pace, 2011 (Atheta (Bessobia)), spec.nov.forcipis Pace, 2011 (Atheta (Bessobia)), spec.nov.luojimontis Pace, 2011 (Atheta (Bessobia)), spec.nov.mimosibirica Pace, 2011 (Atheta (Bessobia)), spec.nov.sinonigra Pace, 2011 (Atheta (Bessobia)), spec.nov.sinopusilla Pace, 2011 (Atheta (Bessobia)), spec.nov.contractionis Pace, 2011 (Atheta (Datomicra)), spec.nov.mugecuensis Pace, 2011 (Atheta (Datomicra)), spec.nov.semicircularis Pace, 2011 (Atheta (Datomicra)), spec.nov.shalulifalcifera Pace, 2011 (Atheta (Datomicra)), spec.nov.tibetana Pace, 2011 (Atheta (Datomicra)), spec.nov.aesculapii Pace, 2011 (Atheta (Dimetrota)), spec.nov.dalibaiensis Pace, 2011 (Atheta (Dimetrota)), spec.nov.daxuecoprobia Pace, 2011 (Atheta (Dimetrota)), spec.nov.daxuefurtiva Pace, 2011 (Atheta (Dimetrota)), spec.nov.gigarcuata Pace, 2011 (Atheta (Dimetrota)), spec.nov.gonggana (Pace, 1998) (Atheta (Dimetrota)), comb.nov. hitherto Liogluta gonggana Pace, 1998granulotibetana Pace, 2011 (Atheta (Dimetrota)), spec.nov.hailougouicola Pace, 2011 (Atheta (Dimetrota)), spec.nov.huamontis Pace, 2011 (Atheta (Dimetrota)), spec.nov.leshanensis Pace, 2011 (Atheta (Dimetrota)), spec.nov.qinlingensis Pace, 2011 (Atheta (Dimetrota)), spec.nov.robustina Pace, 2011 (Atheta (Dimetrota)), spec.nov.shaluliopaca Pace, 2011 (Atheta (Dimetrota)), spec.nov.sinodenticulata Pace, 2011 (Atheta (Dimetrota)), spec.nov.sinolucida Pace, 2011 (Atheta (Dimetrota)), spec.nov.sinorufipennis Pace, 2011 (Atheta (Dimetrota)), spec.nov.suburumqiensis Pace, 2011 (Atheta (Dimetrota)), spec.nov.zanettii Pace, 2011 (Atheta (Dimetrota)), spec.nov.acrotonotheca Pace, 2011 (Atheta (Microdota)), spec.nov.caudata Pace, 2011 (Atheta (Microdota)), spec.nov.cavazzutii Pace, 2011 (Atheta (Microdota)), spec.nov.colortang Pace, 2011 (Atheta (Microdota)), spec.nov.daxuepraticola Pace, 2011 (Atheta (Microdota)), spec.nov.guanxianensis Pace, 2011 (Atheta (Microdota)), spec.nov.megatheca Pace, 2011 (Atheta (Microdota)), spec.nov.naniensis Pace, 2011 (Atheta (Microdota)), spec.nov.neatang Pace, 2011 (Atheta (Microdota)), spec.nov.ogivalis Pace, 2011 (Atheta (Microdota)), spec.nov.perindistincta Pace, 2011 (Atheta (Microdota)), spec.nov.pseudonana Pace, 2011 (Atheta (Microdota)), spec.nov.pseudoplacita Pace, 2011 (Atheta (Microdota)), spec.nov.sinobscura Pace, 2011 (Atheta (Microdota)), spec.nov.sinocolorata Pace, 2011 (Atheta (Microdota)), spec.nov.sinosulcata Pace, 2011 (Atheta (Microdota)), spec.nov.sphaerae Pace, 2011 (Atheta (Microdota)), spec.nov.sinorelicta Pace, 2011 (Atheta (Oxypodera)), spec.nov.longefalciferoides Pace, 2011 (Atheta (Philhygra)), spec.nov.sinobifalcifera Pace, 2011 (Atheta (Philhygra)), spec.nov.taibaimontis Pace, 2011 (Atheta (Philhygra)), spec.nov.tibetapicalis Pace, 2011 (Atheta (Philhygra)), spec.nov.sinobulbosa Pace, 2011 (Atheta (Sinodota)), spec.nov.fuscoterminalis Pace, 2011 (Atheta (Sipalatheta)), spec.nov.nitidearmata Pace, 2011 (Atheta (Sipalatheta)), spec.nov.
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Ejmal, Mahjoub A., David J. Holland, Robin M. MacDiarmid, and Michael N. Pearson. "The Effect of Aspergillus Thermomutatus Chrysovirus 1 on the Biology of Three Aspergillus Species." Viruses 10, no. 10 (October 2, 2018): 539. http://dx.doi.org/10.3390/v10100539.

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This study determined the effects of Aspergillus thermomutatus chrysovirus 1 (AthCV1), isolated from Aspergillus thermomutatus, on A. fumigatus, A. nidulans and A. niger. Protoplasts of virus-free isolates of A. fumigatus, A. nidulans and A. niger were transfected with purified AthCV1 particles and the phenotype, growth and sporulation of the isogenic AthCV1-free and AthCV1-infected lines assessed at 20 °C and 37 °C and gene expression data collected at 37 °C. AthCV1-free and AthCV1-infected A. fumigatus produced only conidia at both temperatures but more than ten-fold reduced compared to the AthCV1-infected line. Conidiation was also significantly reduced in infected lines of A. nidulans and A. niger at 37 °C. AthCV1-infected lines of A. thermomutatus and A. nidulans produced large numbers of ascospores at both temperatures, whereas the AthCV1-free line of the former did not produce ascospores. AthCV1-infected lines of all species developed sectoring phenotypes with sclerotia produced in aconidial sectors of A. niger at 37 °C. AthCV1 was detected in 18% of sclerotia produced by AthCV1-infected A. niger and 31% of ascospores from AthCV1-infected A. nidulans. Transcriptome analysis of the naturally AthCV1-infected A. thermomutatus and the three AthCV1-transfected Aspergillus species showed altered gene expression as a result of AthCV1-infection. The results demonstrate that AthCV1 can infect a range of Aspergillus species resulting in reduced sporulation, a potentially useful attribute for a biological control agent.
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Ádám, László. "Remarks on some European Aleocharinae, with description of a new Rhopaletes species from Croatia (Coleoptera: Staphylinidae)." Travaux du Muséum National d'Histoire Naturelle "Grigore Antipa" 53, no. 1 (December 1, 2010): 191–215. http://dx.doi.org/10.2478/v10191-010-0015-6.

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Remarks on some European Aleocharinae, with description of a new Rhopaletes species from Croatia (Coleoptera: Staphylinidae) Based on an examination of type and non-type material, ten species-group names are synonymised: Atheta mediterranea G. Benick, 1941, Aloconota carpathica Jeannel et Jarrige, 1949 and Atheta carpatensis Tichomirova, 1973 with Aloconota mihoki (Bernhauer, 1913); Amischa jugorum Scheerpeltz, 1956 with Amischa analis (Gravenhorst, 1802); Amischa strupii Scheerpeltz, 1967 with Amischa bifoveolata (Mannerheim, 1830); Atheta tricholomatobia V. B. Semenov, 2002 with Atheta boehmei Linke, 1934; Atheta palatina G. Benick, 1974 and Atheta palatina G. Benick, 1975 with Atheta dilaticornis (Kraatz, 1856); Atheta degenerata G. Benick, 1974 and Atheta degenerata G. Benick, 1975 with Atheta testaceipes (Heer, 1839). A new name, Atheta velebitica nom. nov. is proposed for Atheta serotina Ádám, 2008, a junior primary homonym of Atheta serotina Blackwelder, 1944. A revised key for the Central European species of the Aloconota sulcifrons group is provided. Comments on the separation of the males of Amischa bifoveolata and A. analis are given. A key for the identification of Amischa species occurring in Hungary and its close surroundings is presented. Remarks are presented about the relationships of Alevonota Thomson, 1858 and Enalodroma Thomson, 1859. The taxonomic status of Oxypodera Bernhauer, 1915 and Mycetota Ádám, 1987 is discussed. The specific status of Pella hampei (Kraatz, 1862) is debated. Remarks are presented about the relationships of Alevonota Thomson, 1858, as well as Mycetota Ádám, 1987, Oxypodera Bernhauer, 1915 and Rhopaletes Cameron, 1939. The publication date of several Atheta species described by G. Benick is discussed. Aloconota mihoki, Amischa forcipata, A. filum and Atheta boehmei are reported from Hungary, Croatia and Romania, respectively, for the first time. A new species, Rhopaletes slavoniae sp. n. is described from Croatia.
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Bhagat, Prakash Kumar, Deepanjali Verma, Kirti Singh, Raghuram Badmi, Deepika Sharma, and Alok Krishna Sinha. "Dynamic Phosphorylation of miRNA Biogenesis Factor HYL1 by MPK3 Involving Nuclear–Cytoplasmic Shuttling and Protein Stability in Arabidopsis." International Journal of Molecular Sciences 23, no. 7 (March 30, 2022): 3787. http://dx.doi.org/10.3390/ijms23073787.

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MicroRNAs (miRNAs) are one of the prime regulators of gene expression. The recruitment of hyponastic leaves 1 (HYL1), a double-stranded RNA binding protein also termed as DRB1, to the microprocessor complex is crucial for accurate primary-miRNA (pri-miRNA) processing and the accumulation of mature miRNA in Arabidopsis thaliana. In the present study, we investigated the role of the MAP kinase-mediated phosphorylation of AtHYL1 and its sub-cellular activity. AtMPK3 specifically phosphorylates AtHYL1 at the evolutionarily conserved serine-42 present at the N-terminal regions and plays an important role in its nuclear–cytosolic shuttling. Additionally, we identified that AtHYL1 is cleaved by trypsin-like proteases into an N-terminal fragment, which renders its subcellular activities. We, for the first time, report that the dimerization of AtHYL1 not only takes place in the nucleus, but also in the cytosol, and the C-terminal of AtHYL1 has a role in regulating its stability, as well as its subcellular localization. AtHYL1 is hyper-phosphorylated in mpk3 mutants, leading to higher stability and reduced degradation. Our data show that AtMPK3 is a negative regulator of AtHYL1 protein stability and that the AtMPK3-induced phosphorylation of AtHYL1 leads to its protein degradation.
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Pace, Roberto. "Aleocharinae dell'Africa meridionale al Naturkundemuseum di Erfurt (Coleoptera, Staphylinidae)." Beiträge zur Entomologie = Contributions to Entomology 56, no. 1 (August 15, 2006): 161–88. http://dx.doi.org/10.21248/contrib.entomol.56.1.161-188.

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In dieser Arbeit werden neun Triben (Hypocyphtini, Leucocraspedini, Homalotini, Autaliini, Falagriini, Athetini, Lomechusini, Thamiaraeini und Aleocharini), vierzehn Gattungen (Oligota, Leucocraspedum, Placusa, Autalia, Cordalia, Falagria, Amischa, Aloconota, Parapodoxya, Atheta, Pelioptera, Zyras, Akronusa und Aleochara) und 32 Arten anerkannt. Eine Gattung, Akronusa, von den Thamiaraeini, wird als neu für die Wissenschaft beschrieben. Siebzehn Arten werden als neu für die Wissenschaft beschrieben: zwei in der Gattung Oligota (O. namibiensis, O. klimaszewskii), eine in der Gattung Leucocraspedum (L. zuluense), eine in der Gattung Amischa (A. sudafricana), eine in der Gattung Aloconota (A. capensis), eine in der Gattung Parapodoxya (P. elephantium), acht in der Gattung Atheta (A. cerdarmontis, A. klimaszewskii, A. biflagellifera, A. arndti, A. addensis, A. afrocaviphila, A. topiaria und A. tsitsikammensis), eine in der Gattung Pelioptera (P. natalensis) eine in der Gattung Akronusa (A. sudafricana) und eine in der Gattung Aleochara (A. zulu). Leucocraspedum cameroni ist ein neuer Name für Leucocraspedum africanum Cameron, 1948 ein jüngeres Homonym von Leucocraspedum africanum Bernhauer, 1943. Eine Art wird neu kombiniert. Alle neue Arten und die neue Gattung werden abgebildet und die neuen Arten mit ähnlichen Arten verglichen. Acrotona und Oxypodera werden als jüngere Synonyme (als Untergattungen) von Atheta abgehandelt.StichwörterColeoptera, Staphylinidae, Aleocharinae, taxonomy, new genus, new species, Southern Africa.Nomenklatorische Handlungensudafricana Pace, 2006 (Akronusa), spec. n.zulu Pace, 2006 (Aleochara (Coprochala)), spec. n.capensis Pace, 2006 (Aloconota), spec. n.sudafricana Pace, 2006 (Amischa (Amischa)), spec. n.addensis Pace, 2006 (Atheta (Acrotona)), spec. n.arndti Pace, 2006 (Atheta (Acrotona)), spec. n.biflagellifera Pace, 2006 (Atheta (Acrotona)), spec. n.cerdarmontis Pace, 2006 (Atheta (Acrotona)), spec. n.klimaszewskii Pace, 2006 (Atheta (Acrotona)), spec. n.afrocaviphila Pace, 2006 (Atheta (Alomacrotona)), spec. n.topiaria Pace, 2006 (Atheta (Oxypodera)), spec. n.tsitsikammensis Pace, 2006 (Atheta (Oxypodera)), spec. n.cameroni Pace, 2006 (Leucocraspedum), nom. n. pro Leucocraspedum africanum Cameron, 1948, nec Bernhauer, 1943zuluense Pace, 2006 (Leucocraspedum), spec. n.klimaszewskii Pace, 2006 (Oligota (Holobus)), spec. n.namibiensis Pace, 2006 (Oligota (Holobus)), spec. n.elephantium Pace, 2006 (Parapodoxya), spec. n.natalensis Pace, 2006 (Pelioptera), spec. n.Akronusa Pace, 2006 (Staphylinidae), gen. n.
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Pace, Roberto. "Nota correttiva." Beiträge zur Entomologie = Contributions to Entomology 62, no. 1 (May 15, 2012): 164. http://dx.doi.org/10.21248/contrib.entomol.62.1.164.

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24

Sun, Guanghua, Luhao Yang, Weimin Zhan, Shizhan Chen, Meifang Song, Lijian Wang, Liangliang Jiang, et al. "HFR1, a bHLH Transcriptional Regulator from Arabidopsis thaliana, Improves Grain Yield, Shade and Osmotic Stress Tolerances in Common Wheat." International Journal of Molecular Sciences 23, no. 19 (October 10, 2022): 12057. http://dx.doi.org/10.3390/ijms231912057.

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Common wheat, Triticum aestivum, is the most widely grown staple crop worldwide. To catch up with the increasing global population and cope with the changing climate, it is valuable to breed wheat cultivars that are tolerant to abiotic or shade stresses for density farming. Arabidopsis LONG HYPOCOTYL IN FAR-RED 1 (AtHFR1), a photomorphogenesis-promoting factor, is involved in multiple light-related signaling pathways and inhibits seedling etiolation and shade avoidance. We report that overexpression of AtHFR1 in wheat inhibits etiolation phenotypes under various light and shade conditions, leading to shortened plant height and increased spike number relative to non-transgenic plants in the field. Ectopic expression of AtHFR1 in wheat increases the transcript levels of TaCAB and TaCHS as observed previously in Arabidopsis, indicating that the AtHFR1 transgene can activate the light signal transduction pathway in wheat. AtHFR1 transgenic seedlings significantly exhibit tolerance to osmotic stress during seed germination compared to non-transgenic wheat. The AtHFR1 transgene represses transcription of TaFT1, TaCO1, and TaCO2, delaying development of the shoot apex and heading in wheat. Furthermore, the AtHFR1 transgene in wheat inhibits transcript levels of PHYTOCHROME-INTERACTING FACTOR 3-LIKEs (TaPIL13, TaPIL15-1B, and TaPIL15-1D), downregulating the target gene STAYGREEN (TaSGR), and thus delaying dark-induced leaf senescence. In the field, grain yields of three AtHFR1 transgenic lines were 18.2–48.1% higher than those of non-transgenic wheat. In summary, genetic modification of light signaling pathways using a photomorphogenesis-promoting factor has positive effects on grain yield due to changes in plant architecture and resource allocation and enhances tolerances to osmotic stress and shade avoidance response.
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LEE, SEUNG-GYU, and KEE-JEONG AHN. "A taxonomic review of Korean Atheta Thomson subgenus Atheta Thomson (Coleoptera, Staphylinidae, Aleocharinae), with descriptions of two new species." Zootaxa 4613, no. 2 (June 5, 2019): 305. http://dx.doi.org/10.11646/zootaxa.4613.2.5.

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A taxonomic review of Atheta Thomson subgenus Atheta Thomson in the Korean Peninsula is presented. The subgenus is represented in Korea by eight species including two new species, A. (A.) prolixa Lee & Ahn, sp. nov. and A. (A.) vegrandis Lee & Ahn, sp. nov. Atheta (A.) sauteri Bernhauer is reported for the first time in South Korea. A key, descriptions, habitus photographs and illustrations of the diagnostic characters are provided.
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Glotov, S., K. Hushtan, H. Hushtan, N. Koval, and V. Diedus. "The Genus Atheta (Coleoptera, Staphylinidae, Aleocharinae) in the Ukrainian Carpathians." zoodiversity 56, no. 2 (2022): 91–110. http://dx.doi.org/10.15407/zoo2022.02.091.

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The Carpathian species of the genus Atheta Thomson, 1858 are reviewed. The list contains 65 species, of which 8 species: Atheta kochi Roubal, 1937, A. intermedia (Thomson, 1852), A. setigera (Sharp, 1869), A. foveicollis (Kraatz, 1856), A. luctuosa (Mulsant & Rey, 1853), A. cribrata (Kraatz, 1856), A. mortuorum Thomson, 1867, A. picipes (Thomson, 1856), are recorded for Ukraine for the first time. Species composition, data on bionomics and distribution genus Atheta in the studied region are discussed.
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Tian, Lu, Jianlin Wang, M. Paulus Fong, Meng Chen, Hongbin Cao, Stanton B. Gelvin, and Z. Jeffrey Chen. "Genetic Control of Developmental Changes Induced by Disruption of Arabidopsis Histone Deacetylase 1 (AtHD1) Expression." Genetics 165, no. 1 (September 1, 2003): 399–409. http://dx.doi.org/10.1093/genetics/165.1.399.

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Abstract Little is known about the role of genetic and epigenetic control in the spatial and temporal regulation of plant development. Overexpressing antisense Arabidopsis thaliana HD1 (AtHD1) encoding a putative major histone deacetylase induces pleiotropic effects on plant growth and development. It is unclear whether the developmental abnormalities are caused by a defective AtHD1 or related homologs and are heritable in selfing progeny. We isolated a stable antisense AtHD1 (CASH) transgenic line and a T-DNA insertion line in exon 2 of AtHD1, resulting in a null allele (athd1-t1). Both athd1-t1 and CASH lines display increased levels of histone acetylation and similar developmental abnormalities, which are heritable in the presence of antisense AtHD1 or in the progeny of homozygous (athd1-t1/athd1-t1) plants. Furthermore, when the athd1-t1/athd1-t1 plants are crossed to wild-type plants, the pleiotropic developmental abnormalities are immediately restored in the F1 hybrids, which correlates with AtHD1 expression and reduction of histone H4 Lys12 acetylation. Unlike the situation with the stable code of DNA and histone methylation, developmental changes induced by histone deacetylase defects are immediately reversible, probably through the restoration of a reversible histone acetylation code needed for the normal control of gene regulation and development.
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28

Weeramantry, J. Romesh. "Eritrea’s Damages Claims (Eritrea v. Ethiopia), Final Award. Ethiopia’s Damages Claims (Ethiopia v. Eritrea), Final Award." American Journal of International Law 104, no. 3 (July 2010): 480–88. http://dx.doi.org/10.5305/amerjintelaw.104.3.0480.

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ERITREA'S DAMAGES CLAIMS (ERITREA V. ETHIOPIA), FINAL AWARD. Athttp://www.pca-cpa.org.Eritrea Ethiopia Claims Commission, August 17, 2009.ETHIOPIA'S DAMAGES CLAIMS (ETHIOPIA V. ERITREA), FINAL AWARD. Athttp://www.pca-cpa.org.Eritrea Ethiopia Claims Commission, August 17, 2009.
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GUSAROV, VLADIMIR I. "A revision of Nearctic species of the genera Adota Casey, 1910 and Psammostiba Yosii & Sawada, 1976 (Coleoptera: Staphylinidae: Aleocharinae)." Zootaxa 185, no. 1 (April 24, 2003): 1. http://dx.doi.org/10.11646/zootaxa.185.1.1.

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Holarctic genera Psammostiba Yosii & Sawada, 1976 (new to North America) and Adota Casey, 1910 are redescribed. Halostiba Yosii & Sawada, 1976 is placed in synonymy with Adota Casey, 1910. Keys to Nearctic species of Adota and Psammostiba are provided. Adota colpophila Gusarov, sp. n. from Mexico and Psammostiba kenaii Gusarov, sp. n. from Alaska, British Columbia and California are described. Atheta setositarsis Casey, 1910, At. subintima Casey, 1910, At. scortea Casey, 1911, At. scolopacina Casey, 1911 and At. insons Casey, 1911 are placed in synonymy with Adota maritima (Mannerheim, 1843). Three Palaearctic species, Atheta ushio (Sawada, 1971), At. magnipennis Bernhauer, 1943 and At. madida Bernhauer, 1907 are transferred to Adota. Lectotypes are designated for Atheta massettensis Casey, 1910, At. subintima Casey, 1910, At. scortea Casey, 1911, At. scolopacina Casey, 1911 and At. insons Casey, 1911. Atheta finita Moore & Legner, 1975 (replacement name for At. definita Casey, 1911), At. pavidula Casey, 1911 and At. irrita Casey, 1911 described by Casey in Atheta (Adota) do not belong to Adota. Psammostiba Yosii & Sawada, 1976 is raised to generic rank and Adota comparabilis (Mäklin in Mannerheim, 1853) is transferred to Psammostiba
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Oka Silantari, I. Gusti Ayu, and I. Ketut Mardika. "Penerapan Athiti Krama Dalam Peningkatan Mutu Pendidikan Agama Hindu Pada Pasraman Dharma Bhakti Gianyar." Jurnal Penjaminan Mutu 4, no. 2 (August 31, 2018): 163. http://dx.doi.org/10.25078/jpm.v4i2.570.

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<p><em>In human nature, apart from being individual beings as well as social beings who have their own culture. Culture arises in humans due to reason and thought in the human being itself. Humans will be able to live perfectly when they live together with other humans, in relation to other humans, certain norms or rules are needed. In the regulation, one of them was written about the procedure for honoring guests called Athiti Krama. Athiti Krama gives motivation in human life because through this human being can foster good relations between humans one with other human beings in harmony. The implementation of Athiti Krama can be found in societies everywhere in the world, both in the advanced society and the people who are still modest in their civilization.<br /> In social life, everyone should behave well so as to create happiness for themselves and the community, because in the teachings of Hinduism, Athiti Krama teachings are basically contained which can bring people to achieve harmony in social order in society. The basis of Athiti Krama's teachings is the ethics or morality that many of the Vedic scriptures have mentioned, one of which is Tri Kaya Parisudha. Considering the importance of Athiti Krama as a social guide in people's lives. So it should be known to be applied in the learning process in Pasraman Dharma Bhakti.</em><strong><em></em></strong></p>
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Tada, Yuichi. "The HKT Transporter Gene from Arabidopsis, AtHKT1;1, Is Dominantly Expressed in Shoot Vascular Tissue and Root Tips and Is Mild Salt Stress-Responsive." Plants 8, no. 7 (July 4, 2019): 204. http://dx.doi.org/10.3390/plants8070204.

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The Arabidopsis high-affinity K+ transporter (AtHKT1;1) plays roles in salt tolerance by unloading Na+ from the root xylem to the xylem parenchyma cells and/or uploading Na+ from the shoot/leaf xylem to the xylem parenchyma cells. To use this promoter for the molecular breeding of salt-tolerant plants, I evaluated the expression profile of the AtHKT1;1 promoter in detail. Approximately 1.1 kbp of sequence upstream from the start codon of AtHKT1;1 was polymerase chain reaction (PCR)-amplified, fused to the β-glucuronidase (GUS) gene, and introduced into Arabidopsis. The resultant transformants were evaluated under nonstressed and salt-stress conditions at the seedling and reproductive stages. Histochemical analysis showed that GUS activity was detected in vascular bundle tissue in roots, hypocotyls, petioles, leaves, and petals, and in root tips. GUS enzyme activity in shoots tended to be higher than that in roots at both stages. After treatment with 50 mM NaCl for 24 h, GUS transcription levels and GUS enzyme activity were enhanced in transgenic lines. These results indicate that the AtHKT1;1 promoter isolated in this study could be useful in expressing transgenes specifically in vascular tissue and root tips, and in a mild salt-stress-responsive manner. The data provide novel insights into the functions of AtHKT1;1.
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GUSAROV, VLADIMIR I. "A revision of the Nearctic species of the genus Halobrecta Thomson, 1858 (Coleoptera: Staphylinidae: Aleocharinae) with notes on some Palaearctic species of the genus." Zootaxa 746, no. 1 (December 1, 2004): 1. http://dx.doi.org/10.11646/zootaxa.746.1.1.

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The marine littoral genus Halobrecta Thomson, 1858 is redescribed. Descriptions and a key to species known from the Nearctic Region (Ha. algophila (Fenyes, 1909) and Ha. flavipes Thomson, 1861) are provided. Atheta barbarae Casey, 1910 and At. importuna Casey, 1911 are placed in synonymy with Halobrecta algophila (Fenyes, 1909). Atheta pocahontas Casey, 1910, At. vaticina Casey, 1910 and Aloconota incertula Casey, 1910 are synonymized with Halobrecta flavipes Thomson, 1861. Lectotypes are designated for Homalota puncticeps Thomson, 1852, Halobrecta flavipes Thomson, 1861, Atheta algophila Fenyes, 1909, At. pocahontas Casey, 1910, At. vaticina Casey, 1910, Aloconota incertula Casey, 1910 and At. importuna Casey, 1911.
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Wang, Qian, Chao Guan, Pei Wang, Qing Ma, Ai-Ke Bao, Jin-Lin Zhang, and Suo-Min Wang. "The Effect of AtHKT1;1 or AtSOS1 Mutation on the Expressions of Na+ or K+ Transporter Genes and Ion Homeostasis in Arabidopsis thaliana under Salt Stress." International Journal of Molecular Sciences 20, no. 5 (March 2, 2019): 1085. http://dx.doi.org/10.3390/ijms20051085.

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HKT1 and SOS1 are two key Na+ transporters that modulate salt tolerance in plants. Although much is known about the respective functions of HKT1 and SOS1 under salt conditions, few studies have examined the effects of HKT1 and SOS1 mutations on the expression of other important Na+ and K+ transporter genes. This study investigated the physiological parameters and expression profiles of AtHKT1;1, AtSOS1, AtHAK5, AtAKT1, AtSKOR, AtNHX1, and AtAVP1 in wild-type (WT) and athkt1;1 and atsos1 mutants of Arabidopsis thaliana under 25 mM NaCl. We found that AtSOS1 mutation induced a significant decrease in transcripts of AtHKT1;1 (by 56–62% at 6–24 h), AtSKOR (by 36–78% at 6–24 h), and AtAKT1 (by 31–53% at 6–24 h) in the roots compared with WT. This led to an increase in Na+ accumulation in the roots, a decrease in K+ uptake and transportation, and finally resulted in suppression of plant growth. AtHKT1;1 loss induced a 39–76% (6–24 h) decrease and a 27–32% (6–24 h) increase in transcripts of AtSKOR and AtHAK5, respectively, in the roots compared with WT. At the same time, 25 mM NaCl decreased the net selective transport capacity for K+ over Na+ by 92% in the athkt1;1 roots compared with the WT roots. Consequently, Na+ was loaded into the xylem and delivered to the shoots, whereas K+ transport was restricted. The results indicate that AtHKT1;1 and AtSOS1 not only mediate Na+ transport but also control ion uptake and the spatial distribution of Na+ and K+ by cooperatively regulating the expression levels of relevant Na+ and K+ transporter genes, ultimately regulating plant growth under salt stress.
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Miguel, Virginia N., Pablo A. Manavella, Raquel L. Chan, and Mat�as Capella. "The AtHB1 Transcription Factor Controls the miR164-CUC2 Regulatory Node to Modulate Leaf Development." Plant and Cell Physiology 61, no. 3 (December 23, 2019): 659–70. http://dx.doi.org/10.1093/pcp/pcz233.

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Abstract The presence of small tooth-like indentations, or serrations, characterizes leaf margins of Arabidopsis thaliana plants. The NAC family member CUP-SHAPED COTYLEDON 2 (CUC2), which undergoes post-transcriptional gene silencing by three micro-RNA genes (MIR164A, B and C), controls the extension of leaf serration. Here, we analyzed the role of AtHB1, a transcription factor (TF) belonging to the homeodomain-leucine zipper subfamily I, in shaping leaf margins. Using mutants with an impaired silencing pathway as background, we obtained transgenic plants expressing AtHB1 over 100 times compared to controls. These plants presented an atypical developmental phenotype characterized by leaves with deep serration. Transcript measurements revealed that CUC2 expression was induced in plants overexpressing AtHB1 and repressed in athb1 mutants, indicating a positive regulation exerted by this TF. Moreover, molecular analyses of AtHB1 overexpressing and mutant plants revealed that AtHB1 represses MIR164 transcription. We found that overexpression of MIR164B was able to reverse the serration phenotype of plants overexpressing AtHB1. Finally, chromatin immunoprecipitation assays revealed that AtHB1 was able to bind in vivo the promoter regions of all three MIR164 encoding loci. Altogether, our results indicate that AtHB1 directly represses MIR164 expression to enhance leaf serration by increasing CUC2 levels.
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GUSAROV, VLADIMIR I. "A revision of Nearctic species of the genus Earota Mulsant & Rey, 1874 (Coleoptera: Staphylinidae: Aleocharinae)." Zootaxa 92, no. 1 (November 5, 2002): 1. http://dx.doi.org/10.11646/zootaxa.92.1.1.

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Nearctic species of the genus Earota Mulsant & Rey, 1874a are revised. Synonymy of generic names Earota and Macroterma Casey, 1906 is confirmed. Earota dentata (Bernhauer, 1906) (= E. alutacea (Casey, 1906) = E. borealis (Casey, 1906) = E. iowensis (Casey, 1910a)) is recognized as the only valid Nearctic species of the genus. Redescription and illustrations are provided for distinguishing Earota from other aleocharine genera. Atheta sulcata Blatchley, 1910 is placed in synonymy with A. klimschi Bernhauer, 1909 and transferred from Earota to Atheta Thomson, 1858. Lectotypes for Atheta dentata Bernhauer, 1906, Macroterma alutacea Casey, 1906, M. borealis Casey, 1906, A. klimschi Bernhauer, 1909, A. iowensis Casey, 1910a and A. sulcata Blatchley, 1910 are designated.
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36

Pace, Roberto. "Due nuove Aleocharinae orofile e microttere della Cina (Coleoptera: Staphylinidae)." Beiträge zur Entomologie = Contributions to Entomology 49, no. 2 (September 13, 1999): 377–81. http://dx.doi.org/10.21248/contrib.entomol.49.2.377-381.

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Eine neue Gattung und zwei neue Arten der Tribus Athetini (Aleocharinae) werden beschrieben und abgebildet: Oroekklina g. n., daxuensis sp. n. aus Sichuan sowie Atheta (Microdota) puetzi sp. n. aus Shaanxi. Die außergewöhnliche neue Gattung wird kurz erörtert.StichwörterColeoptera, Staphylinidae, Aleocharinae, Taxonomy, New genus, New species, China.Nomenklatorische Handlungenpuetzi Pace, 1999 (Atheta (Microdota)), spec. n.daxuensis Pace, 1999 (Oroekklina), spec. n.Oroekklina Pace, 1999 (Staphylinidae), gen. n.
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Lee, Seung-Gyu, and Kee-Jeong Ahn. "Atheta gangwonensis Lee and Ahn, a New Name for Atheta prolixa Lee and Ahn (Coleoptera: Staphylinidae)." Coleopterists Bulletin 74, no. 1 (March 25, 2020): 76. http://dx.doi.org/10.1649/0010-065x-74.1.76.

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38

GUSAROV, VLADIMIR I. "A revision of the Nearctic species of the genus Stethusa Casey, 1910 (Coleoptera: Staphylinidae: Aleocharinae)." Zootaxa 239, no. 1 (July 16, 2003): 1. http://dx.doi.org/10.11646/zootaxa.239.1.1.

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The Nearctic and Neotropical genus Stethusa Casey, 1910 is redescribed. Descriptions and a key to the three valid Nearctic species of Stethusa (S. dichroa (Gravenhorst, 1802), S. klimschi (Bernhauer, 1909), and S. spuriella (Casey, 1910)) are provided. Atheta affluens Casey, 1910, At. irvingi Casey, 1910, At. galvestonica Casey, 1910, At. canonica Casey, 1910, At. sagax Casey, 1910, At. sororella Casey, 1910, At. clarescans Casey, 1911a, At. videns Casey, 1911a, At. cynica Casey, 1911a, At. cernens Casey, 1911a, At. officiosa Casey, 1911a, At. tuta Casey, 1911a, Dimetrota novella Casey, 1910 and D. sentiens Casey, 1910 are placed in synonymy with Stethusa dichroa. Atheta unigranosa Bernhauer, 1909 (nec 1908), At. subdebilis Casey, 1910, At. duplicata Fenyes, 1920 and At. macrops Notman, 1920 are synonymized with S. spuriella (Casey, 1910). Neotropical At. lurida (Erichson, 1839) and At. luederwaldti Bernhauer, 1908 are transferred to Stethusa. Atheta texana Casey, 1910, At. crenuliventris Bernhauer, 1907 and At. iheringi Bernhauer, 1908 do not belong to Stethusa. Atheta mendosa Casey, 1910 is placed in synonymy with At. texana Casey, 1910. Dimetrota bradorensis Lohse, 1990 is synonymized with At. crenuliventris Bernhauer, 1907. Lectotypes are designated for Aleochara dichroa Gravenhorst, 1802, Atheta crenuliventris Bernhauer, 1907, At. luederwaldti Bernhauer, 1908, At. iheringi Bernhauer, 1908, At. unigranosa Bernhauer, 1909, At. affluens Casey, 1910, At. irvingi Casey, 1910, At. galvestonica Casey, 1910, At. canonica Casey, 1910, At. sagax Casey, 1910, At. sororella Casey, 1910, At. spuriella Casey, 1910, At. subdebilis Casey, 1910, At. texana Casey, 1910, At. clarescans Casey, 1911a, At. cynica Casey, 1911a, At. cernens Casey, 1911a, At. officiosa Casey, 1911a, Dimetrota novella Casey, 1910 and D. sentiens Casey, 1910.
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39

ASHE, JAMES S., and VLADIMIR I. GUSAROV. "Review of the genus Sableta Casey, 1910 (Coleoptera: Staphylinidae: Aleocharinae: Athetini)." Zootaxa 745, no. 1 (December 1, 2004): 1. http://dx.doi.org/10.11646/zootaxa.745.1.1.

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The status of the athetine aleocharine genus Sableta Casey, 1910, and its previously included species, is reviewed. Sableta and Sa. infulata Casey, 1910, the single species remaining in the genus after others are reassigned, are described and illustrations of habitus, structural and genitalic features are provided. All species previously placed in Sableta are assigned to appropriate taxonomic categories. Sableta curata Casey, 1910 is transferred to Acrotona Thomson, 1859; Silusida nanella Casey, 1906, Sableta flaviventris Casey, 1910, Sa. longiclava Casey, 1910, Sa. immunis Casey, 1910 and Sa. remissa Casey, 1910 are transferred to Atheta Thomson, 1858. Homalota flaveola Melsheimer, 1844 is placed in synonymy with Hoplandria lateralis (Melsheimer, 1844) (Hoplandriini) and Sableta ornator Casey, 1910 is placed in synonymy with Atheta nanella (Casey, 1906). Synonymy of Sableta beatula Casey, 1910 and Atheta nanella (Casey, 1906) is confirmed.
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40

Pace, Roberto. "New distribution data, new species and two new genera of Aleocharinae from Tropical Africa (Coleoptera, Staphylinidae)." Beiträge zur Entomologie = Contributions to Entomology 63, no. 1 (June 14, 2013): 129–47. http://dx.doi.org/10.21248/contrib.entomol.63.1.129-147.

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Im bearbeiteten Material aus dem tropischen Afrika werden 9 Tribus (Pronomaeini, Pygostenini, Gyrophaenini, Diestotini, Falagriini, Athetini, Lomechusini, Thamiaraeini, Aleocharini), 15 Gattungen (Nopromaea, Typhloponemys, Brachida, Diestota, Falagria, Ischnopoda, Atheta, Brachycraspedusa, Catarractodes, Brachysipalia, Diplopleurus, Zyras, Paramyrmoecia, Spaniodmoinusa, Aleochara) und 26 Arten determiniert. In zwei neuen Gattungen, Brachycraspedusa n. gen. der Tribus Athetini und Spaniodmoinusa n. gen. der Tribus Thamiaraeini werden 19 Arten neu beschrieben: Nopromaea nakuruensis n. sp., Nopromaea cornelli n. sp., Brachida burkinensis n. sp., Diestota doulaensis n. sp., Falagria bartolozzii n. sp., Ischnopoda riftensis n. sp., Atheta senecicola n. sp., Atheta willersi n. sp., Brachycraspedusa naivashaensis n. sp., Catarractodes cristatus n. sp., Brachysipalia melanica n. sp., Diplopleurus maculipennis n. sp., Diplopleurus intermedius n. sp., Zyras paraopticus n. sp., Zyras taitaorum n. sp., Zyras trinus n. sp., Zyras digorum n. sp., Zyras triumbonatus n. sp., und Spaniodmoinusa cornelli n. sp. Sämtliche neue Arten und Gattungen werden mit verwandten Arten oder Gattungen verglichen und sind illustriert.StichwörterInsecta, Coleoptera, Staphylinidae, Aleocharinae, taxonomy, new genera, new species, Kenya, Burkina Faso, Cameroon, Zambia.Nomenklatorische HandlungenBrachycraspedusa Pace, 2013 (Aleocharinae), gen. nov.Spaniodmoinusa Pace, 2013 (Aleocharinae), gen. nov.senecicola Pace, 2013 (Atheta (Oxypodera)), spec. nov.willersi Pace, 2013 (Atheta (Oxypodera)), spec. nov.burkinensis Pace, 2013 (Brachida), spec. nov.naivashaensis Pace, 2013 (Brachycraspedusa), spec. nov.melanica Pace, 2013 (Brachysipalia), spec. nov.cristatus Pace, 2013 (Catarractodes), spec. nov.doualensis Pace, 2013 (Diestota), spec. nov.intermedius Pace, 2013 (Diplopleurus), spec. nov.maculipennis Pace, 2013 (Diplopleurus), spec. nov.bartolozzi Pace, 2013 (Falagria (Leptagria)), spec. nov.riftensis Pace, 2013 (Ischnopoda), spec. nov.cornelli Pace, 2013 (Nopromaea), spec. nov.nakuruensis Pace, 2013 (Nopromaea), spec. nov.cornelli Pace, 2013 (Spaniodmoinusa), spec. nov.triumbunatus Pace, 2013 (Zyras (Androdonia)), spec. nov.digorum Pace, 2013 (Zyras (Camonia)), spec. nov.paraopticus Pace, 2013 (Zyras (Camonia)), spec. nov.taitaorum Pace, 2013 (Zyras (Camonia)), spec. nov.trinus Pace, 2013 (Zyras (Camonia)), spec. nov.
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41

Klimaszewski, Jan, and Christopher G. Majka. "Two new Atheta species (Coleoptera: Staphylinidae: Aleocharinae) from eastern Canada: taxonomy, bionomics, and distribution." Canadian Entomologist 139, no. 1 (February 2007): 45–53. http://dx.doi.org/10.4039/n05-089.

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AbstractTwo new athetine beetles from eastern Canada are described and illustrated: Atheta (Metadimetrota) savardae Klimaszewski and Majka, sp. nov. (Nova Scotia, Quebec) and Atheta (Datomicra) acadiensis Klimaszewski and Majka, sp. nov. (Nova Scotia, New Brunswick, Prince Edward Island, and Quebec). Their relationships to other closely related species are discussed, and new data on bionomics and distribution are provided. The new species are presented with a short diagnosis, description, colour habitus images, and black-and-white genital images.
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42

Pace, Roberto. "New genera and new species of Aleocharinae from Australia (Coleoptera, Staphylinidae)." Beiträge zur Entomologie = Contributions to Entomology 65, no. 2 (December 21, 2015): 327–39. http://dx.doi.org/10.21248/contrib.entomol.65.2.327-339.

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Die vorliegende Studie behandelt 18 Arten, die zu 6 Tribus gehören (Gyrophaenini, Homalotini, Bolitocharini, Athetini, Thamiaraeini, Aleocharini). Die für die Wissenschaft neuen Gattungen sind: Austraepiskia gen. nov. und Austracoenonica gen. nov., der Homalotini, und Tryphopsichara gen. nov. der Bolitocharini. Die 17 neuen Arten sind Brachida linsaymontis spec. nov., Sternotropa linsaymontis spec. nov., Sternotropa tambourinensis spec. nov., Sternotropa brisbanensis spec. nov., Austraepiskia barrinensis spec. nov., Austracoenonica laminaris spec. nov., Tryphopsichara australiana spec. nov., Leptostiba tambourinensis spec. nov., Atheta (Acrotona) wachteli spec. nov., Atheta (Traumoecia) tambourinensis spec. nov., Gastropaga brisbanensis spec. nov., Gastropaga barrinensis spec. nov., Pelioptera barrinensis spec. nov., Mimacrotona bowravillensis spec. nov., Apimela carnavonensis spec. nov., Apimela queenslandica spec. nov., Pseudoplandria bowravillensis spec. nov. Alle neuen Gattungen und neuen Arten werden illustriert und mit ähnlichen Taxa verglichen.StichwörterInsecta, Coleoptera, Staphylinidae, Aleocharinae, Taxonomy, New Genera, New Spe­cies, Australia.Nomenklatorische Handlungencarnavonensis Pace, 2015 (Apimela), spec. n.queenslandica Pace, 2015 (Apimela), spec. n.wachteli Pace, 2015 (Atheta (Acrotona)), spec. n.tambourinensis Pace, 2015 (Atheta (Traumoecia)), spec. n.laminaris Pace, 2015 (Austracoenonica), spec. n.barrinensis Pace, 2015 (Austraepiskia), spec. n.Tryphopsichara Pace, 2015 (Bolitocharini), gen. n.linsaymontis Pace, 2015 (Brachida), spec. n.barrinensis Pace, 2015 (Gastropaga), spec. n.brisbanensis Pace, 2015 (Gastropaga), spec. n.Austracoenonica Pace, 2015 (Homalotini), gen. n.Austraepiskia Pace, 2015 (Homalotini), gen. n.tambourinensis Pace, 2015 (Leptostiba), spec. n.bowravillensis Pace, 2015 (Mimacrotona), spec. n.barrinensis Pace, 2015 (Pelioptera), spec. n.bowravillensis Pace, 2015 (Pseudoplandria), spec. n.brisbanensis Pace, 2015 (Sternotropa), spec. n.linsaymontis Pace, 2015 (Sternotropa), spec. n.tambourinensis Pace, 2015 (Sternotropa), spec. n.australiana Pace, 2015 (Tryphopsichara), spec. n.tambourinensis Pace, 2015 (Tryphopsichara), spec. n.
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43

Lv, Xueqin, Yanping Jing, Jianwei Xiao, Yongdeng Zhang, Yingfang Zhu, Russell Julian, and Jinxing Lin. "Membrane microdomains and the cytoskeleton constrain AtHIR1 dynamics and facilitate the formation of an AtHIR1-associated immune complex." Plant Journal 90, no. 1 (March 20, 2017): 3–16. http://dx.doi.org/10.1111/tpj.13480.

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44

LEE, SEUNG-GYU, and KEE-JEONG AHN. "Korean species of the Atheta Thomson subgenus Dimetrota Mulsant &amp; Rey (Coleoptera: Staphylinidae: Aleocharinae) with a description of new species." Zootaxa 5138, no. 4 (May 19, 2022): 401–16. http://dx.doi.org/10.11646/zootaxa.5138.4.3.

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A taxonomic review of the Atheta Thomson subgenus Dimetrota Mulsant & Rey in the Korean Peninsula is presented. The subgenus is represented in Korea by 11 species including a new species, A. (D.) ovata Lee & Ahn, sp. nov. and a new synonym [A. (Badura) tokiokai Sawada = A. (D.) chagangensis Paśnik syn. nov.]. Atheta (D.) yamamotoi Sawada is reported for the first time in the Korean Peninsula and A. (D.) machonryongica in South Korea. A key to Korean species and descriptions with illustrations of habitus photographs and diagnostic characters of three species new to Korea are provided.
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45

LEE, SEUNG-GYU, and KEE-JEONG AHN. "A taxonomic review of the Korean species of the subgenus Datomicra Mulsant & Rey of the genus Atheta Thomson, with description of a new species (Coleoptera, Staphylinidae, Aleocharinae)." Zootaxa 4268, no. 4 (May 18, 2017): 508. http://dx.doi.org/10.11646/zootaxa.4268.4.3.

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A taxonomic review of the subgenus Datomicra Mulsant & Rey of the genus Atheta Thomson in Korea is presented. A new synonym is proposed: Datomicra Mulsant & Rey, 1874 = Datostiba Sawada, 1976, syn. nov. The subgenus is represented in Korea by eight species including a new species, Atheta (Datomicra) semidentiventris Lee & Ahn, sp. nov. Two species [A. (D.) dadopora Thomson and A. (D.) dentiventris Bernhauer] are new to the Korean Peninsula and one [A. (D.) celata (Erichson)] to South Korea. A key, descriptions, habitus photographs and illustrations of the diagnostic characters of the new species and two newly recorded species are provided.
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46

Heydarnezhad, Fatemeh, Mehran Hoodaji, Mahdi Shahriarinour, and Arezoo Tahmourespour. "TOLUENE DEGRADATION BY FREE STAPHYLOCOCCUS GALLINARUM AND IMMOBILIZED ON MULTI-WALLED CARBON NANOTUBES." Fronteiras: Journal of Social, Technological and Environmental Science 10, no. 1 (March 3, 2021): 61–73. http://dx.doi.org/10.21664/2238-8869.2021v10i1.p61-73.

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Hydrocarbons pollution is a most important environmental and healthanxiety . Using free and immobilized bacteria could be a suitable attitude to find a proper bioaugmentation agent. A toluene degrading bacterium was isolated from oil-contaminated environs (located in Bandar-Anzali, Guilan, Iran). The strain was molecularly identified as Staphylococcus gallinarum ATHH41 (Accession number: KX344723) by partial sequencing of 16SrDNA gene. The response surface methodology (RSM) was expended for biodegradation of the toluene by ATHH41. The central composite design (CCD) was utilized to optimize pH, temperature, and toluene concentration by ATHH41. In accordance with the optimization purpose of the Design-Expert software, the optimum circumstances of toluene degradation were obtained when pH, temperature and toluene concentration were adjusted to 7.68, 31.73°C and 630.04 mg.l-1, respectively. Multi-walled carbon nanotubes (MWCNTs) were used to immobilize the strain. Infrared spectroscopy and scanning electron microscopy showed that the cells adhered to the MWCNT surface and developed a biofilm. Results reveal that free cells were able to degrade 68.01% of the toluene as the sole carbon and energy source within 24 h under optimized conditions. The immobilized cells reached 95.68%.
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47

Groessl, Joan M., and Christine L. Vandenhouten. "Examining Students’ Attitudes and Readiness for Interprofessional Education and Practice." Education Research International 2019 (January 2, 2019): 1–7. http://dx.doi.org/10.1155/2019/2153292.

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This study examined RN-to-BSN and Master of Social Work students’ attitudes and readiness for interprofessional (IP) practice and educational experiences. The Attitudes toward Health Care Teams Scale (ATHCTS) developed by Heinemann et al. measures attitudes toward health care teams including the quality of care/process and physician centrality. Students’ readiness for IP education was measured by the Readiness for Interprofessional Learning Scale (RIPLS) developed by Parsell and Bligh. Discussion of an interprofessional activity including student reactions is provided. Statistically significant differences were found in the mean scores for the Patient-Centeredness subscale of the RIPLS and in overall ATHCTS scores as well as the Physician Centrality subscale scores. Overall, participants demonstrated readiness and benefits of IP education.
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48

Sanobar, Neda, Pin-Chun Lin, Zhao-Jun Pan, Ru-Ying Fang, Veny Tjita, Fang-Fang Chen, Hao-Ching Wang, et al. "Investigating the Viral Suppressor HC-Pro Inhibiting Small RNA Methylation through Functional Comparison of HEN1 in Angiosperm and Bryophyte." Viruses 13, no. 9 (September 15, 2021): 1837. http://dx.doi.org/10.3390/v13091837.

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In plants, HEN1-facilitated methylation at 3′ end ribose is a critical step of small-RNA (sRNA) biogenesis. A mutant of well-studied Arabidopsis HEN1 (AtHEN1), hen1-1, showed a defective developmental phenotype, indicating the importance of sRNA methylation. Moreover, Marchantia polymorpha has been identified to have a HEN1 ortholog gene (MpHEN1); however, its function remained unfathomed. Our in vivo and in vitro data have shown MpHEN1 activity being comparable with AtHEN1, and their substrate specificity towards duplex microRNA (miRNA) remained consistent. Furthermore, the phylogenetic tree and multiple alignment highlighted the conserved molecular evolution of the HEN1 family in plants. The P1/HC-Pro of the turnip mosaic virus (TuMV) is a known RNA silencing suppressor and inhibits HEN1 methylation of sRNAs. Here, we report that the HC-Pro physically binds with AtHEN1 through FRNK motif, inhibiting HEN1’s methylation activity. Moreover, the in vitro EMSA data indicates GST-HC-Pro of TuMV lacks sRNA duplex-binding ability. Surprisingly, the HC-Pro also inhibits MpHEN1 activity in a dosage-dependent manner, suggesting the possibility of interaction between HC-Pro and MpHEN1 as well. Further investigations on understanding interaction mechanisms of HEN1 and various HC-Pros can advance the knowledge of viral suppressors.
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49

Jandricic, S., C. D. Scott-Dupree, A. B. Broadbent, C. R. Harris, and G. Murphy. "Compatibility of Atheta coriaria with other biological control agents and reduced-risk insecticides used in greenhouse floriculture integrated pest management programs for fungus gnats." Canadian Entomologist 138, no. 5 (October 2006): 712–22. http://dx.doi.org/10.4039/n05-106.

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AbstractFungus gnats (FG) (Diptera: Sciaridae: Bradysia spp.) are economically important pests of greenhouse flowers. Larvae feed on root tissue and transmit a variety of phytopathogens. Atheta coriaria (Kraatz) (Coleoptera: Staphylinidae) is a new biological control agent (BCA) for FG. To support its successful use by the greenhouse industry, its compatibility with current integrated pest management (IPM) programs used in floriculture was assessed. This included investigations of prey preference, possible detrimental interactions with other soil-dwelling BCAs, and the toxicity to A. coriaria of registered and novel insecticides. Atheta coriaria showed little preference among eggs of different pest species or between pest eggs and eggs of the intraguild predator Hypoaspis aculeifer (Canestrini) (Acari: Mesostigmata: Laelapidae). It preferred FG 1st-instar larvae to larvae and pupae of other soil-dwelling pests. The entomopathogenic nematode Steinernema feltiae (Filipjev) (Rhabditida: Steinernematidae) was compatible with A. coriaria, but H. aculeifer mites fed on A. coriaria larvae. Insect growth regulators with limited contact activity (e.g., diflubenzuron) were compatible with adult A. coriaria and had minimal effects on larvae compared with other insecticides. Atheta coriaria can be incorporated into an IPM program for FG if harsh insecticides are avoided, but interactions with predatory mites, as well as its effectiveness against other greenhouse pests when FG are present, require further investigation.
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50

Klimaszewski, Jan. "Aleocharinae rove beetles (Coleoptera: Staphylinidae) of the ancient Sitka spruce forest on Vancouver Island, British Columbia, Canada: new synonymy and generic considerations." Canadian Entomologist 135, no. 6 (December 2003): 867–68. http://dx.doi.org/10.4039/n03-020.

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AbstractAtheta vancouveri Klimaszewski, 2002, described from Vancouver Island, is a junior synonym of Pseudota nescia Casey, 1910, described from the Queen Charlotte Islands. The combination Atheta (Pseudota) nescia (Casey, 1910) is proposed.
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