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dismutases (SODs) are a group of important antioxidant defense enzymes. In this study, a putative extracellular Cu\u002FZn superoxide dismutase (ecCuZnSOD) complementary DNA was cloned and characterized from the whitefly, \u003Cjats:italic>Bemisia tabaci\u003C\u002Fjats:italic>. Quantitative polymerase chain reaction analysis showed that the expression level of Bt‐ecCuZnSOD was more than 10‐fold higher in the invasive Middle East Asia Minor 1 (MEAM1) than in the native Asia II 3 species of the \u003Cjats:italic>B. tabaci\u003C\u002Fjats:italic> species complex. After exposure to low temperature (4 °C), the expression of Bt‐ecCuZnSOD gene was significantly up‐regulated in MEAM1 but not in Asia II 3. Furthermore, the expression level of \u003Cjats:italic>B. tabaci\u003C\u002Fjats:italic> intracellular CuZnSOD (Bt‐icCuZnSOD), Bt‐ecCuZnSOD and mitochondrial MnSOD (Bt‐mMnSOD) was compared after transferring MEAM1 and Asia II 3 whiteflies from favorable (cotton) to unfavorable host plants (tobacco). On cotton, both CuZnSOD genes were expressed at a higher level in MEAM1 compared with Asia II 3. Interestingly, after transferring onto tobacco, the expression of Bt‐ecCuZnSOD was significantly induced in Asia II 3 but not in MEAM1. On the other hand, while Bt‐mMnSOD was expressed equally in both species on cotton, Bt‐mMnSOD messenger RNA was up‐regulated in MEAM1 on tobacco. Consistently, enzymatic activity assays of CuZnSOD and MnSOD demonstrated that CuZnSOD might play an important protective role against oxidative stress in Asia II 3, whereas MnSOD activation was critical for MEAM1 whiteflies during host adaptation. Taken together, our results suggest that the successful invasion of MEAM1 is correlated with its constitutive high activity of CuZnSOD and inducible expression of MnSOD under stress conditions.\u003C\u002Fjats:p>",{"EN":464},"Cloning of a putative extracellular Cu\u002FZn superoxide dismutase and functional differences of superoxide dismutases in invasive and indigenous 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Aleyrodidae)",{},{"id":24,"text":780,"url":24,"identifiers":781},"10.1016\u002FS0742-8413(98)10121-4",{"doi":780},{"id":24,"text":783,"url":24,"identifiers":784},"10.1016\u002Fj.fsi.2011.08.023",{"doi":783},{"id":24,"text":786,"url":24,"identifiers":787},"Tang Q.Y., 2007, DPS Data Processing System",{},{"id":24,"text":789,"url":24,"identifiers":790},"Tong L.(2007)Preliminary investigation on the physiological mechanisms of the interactions betweenBemisia babaci begomoviruses and their host plants. Master Thesis. Zhejiang University Hangzhou China.",{},{"id":24,"text":792,"url":24,"identifiers":793},"10.1007\u002Fs11427-008-0135-4",{"doi":792},{"id":24,"text":795,"url":24,"identifiers":796},"10.1186\u002F1471-2164-12-458",{"doi":795},{"id":24,"text":798,"url":24,"identifiers":799},"10.1186\u002F1471-2164-13-529",{"doi":798},{"id":24,"text":801,"url":24,"identifiers":802},"10.1371\u002Fjournal.pone.0062176",{"doi":801},{"id":24,"text":804,"url":24,"identifiers":805},"Xu J.(2009)Studies on the invasion by alienBemisia tabaciin Zhejiang and comparison of biological characteristics between biotypes of the whitefly.PhD thesis. Zhejiang University Hangzhou China.",{},{"id":24,"text":807,"url":24,"identifiers":808},"10.1111\u002Fj.1570-8703.2006.00482.x",{"doi":807},{"id":24,"text":810,"url":24,"identifiers":811},"10.1016\u002FS0891-5849(02)00905-X",{"doi":810},{"id":813,"createTime":814,"updateTime":814,"relativeEntities":815,"slug":816,"properties":817,"entityType":171,"verifyStatus":241,"verifyTime":829,"verifyNote":242,"syncStatus":23,"languages":830,"translateLanguages":24,"viewCount":25,"primaryUrl":831,"fullTextUrl":24,"authors":832,"publicationType":177,"publisherRelationship":969,"citationCount":142,"citationInfo":1006,"publishDate":1008,"publishYear":1009,"citationAnalyzeStatus":23,"lastCitationAnalyze":24,"indexDatabases":24,"openAccess":24,"references":1010,"isForceReanalyzing":221},"e79173a1-0510-4391-b272-847bda5cb203","2024-10-13T10:51:36.786+00:00",[],"Testing-the-rate-isomorphy-hypothesis-using-five-statistical-methods",{"mag":818,"keywords":820,"openalex":821,"abstract":823,"title":825,"doi":827},{"VOID":819},"2171587277",{},{"VOID":822},"W2171587277",{"EN":824},"\u003Cjats:p>\u003Cjats:bold>Abstract \u003C\u002Fjats:bold> Organisms are said to be in developmental rate isomorphy when the proportions of developmental stage durations are unaffected by temperature. Comprehensive stage‐specific developmental data were generated on the cabbage beetle, \u003Cjats:italic>Colaphellus bowringi\u003C\u002Fjats:italic> Baly (Coleoptera: Chrysomelidae), at eight temperatures ranging from 16°C to 30°C (in 2°C increments) and five analytical methods were used to test the rate isomorphy hypothesis, including: (i) direct comparison of lower developmental thresholds with standard errors based on the traditional linear equation describing developmental rate as the linear function of temperature; (ii) analysis of covariance to compare the lower developmental thresholds of different stages based on the Ikemoto‐Takai linear equation; (iii) testing the significance of the slope item in the regression line of \u003Cjats:inline-graphic xmlns:xlink=\"http:\u002F\u002Fwww.w3.org\u002F1999\u002Fxlink\" xlink:href=\"graphic\u002FINS_1428_mu1.gif\" xlink:title=\"inline image\" \u002F> versus temperature, where \u003Cjats:italic>p\u003C\u002Fjats:italic> is the ratio of the developmental duration of a particular developmental stage to the entire pre‐imaginal developmental duration for one insect or mite species; (iv) analysis of variance to test for significant differences between the ratios of developmental stage durations to that of pre‐imaginal development; and (v) checking whether there is an element less than a given level of significance in the \u003Cjats:italic>p\u003C\u002Fjats:italic>‐value matrix of rotating regression line. The results revealed no significant difference among the lower developmental thresholds or among the aforementioned ratios, and thus convincingly confirmed the rate isomorphy hypothesis.\u003C\u002Fjats:p>",{"EN":826},"Testing the rate isomorphy hypothesis using five statistical methods",{"VOID":828},"10.1111\u002Fj.1744-7917.2011.01428.x","2024-10-13T10:51:36.785+00:00",[174],"https:\u002F\u002Fonlinelibrary.wiley.com\u002Fdoi\u002F10.1111\u002Fj.1744-7917.2011.01428.x",[833,863,890,907,952],{"id":834,"sortIndex":25,"researcher":24,"roles":835,"affiliations":836,"properties":858},"1bc96f0b-3dc0-4c23-8cf3-047bfeec86ad",[],[837,847],{"id":838,"sortIndex":131,"affiliation":839,"properties":24},"534a28a5-55a1-4b85-b0d7-d7b12adf66ea",{"id":840,"createTime":841,"updateTime":841,"relativeEntities":842,"slug":843,"properties":844,"entityType":68,"verifyStatus":23,"verifyTime":24,"verifyNote":24,"syncStatus":23,"languages":24,"translateLanguages":24,"viewCount":25},"6b608946-366c-40e1-9b03-609d1419bc2f","2024-10-13T10:51:36.810+00:00",[],"These-three-authors-contributed-equally-to-the-work-",{"title":845},{"EN":846},"These three authors contributed equally to the work.",{"id":848,"sortIndex":25,"affiliation":849,"properties":24},"d179505d-aa39-4a8d-933a-948e4d5fbed1",{"id":850,"createTime":851,"updateTime":852,"relativeEntities":853,"slug":854,"properties":855,"entityType":68,"verifyStatus":23,"verifyTime":24,"verifyNote":24,"syncStatus":23,"languages":24,"translateLanguages":24,"viewCount":25},"83c868c3-3518-418d-9c07-69f8c88fce92","2024-01-03T13:42:13.274+00:00","2024-10-13T10:51:36.808+00:00",[],"Institute-of-Entomology-Jiangxi-Agricultural-University-Nanchang-China",{"title":856},{"VI":857},"Institute of Entomology, Jiangxi Agricultural University, Nanchang, China",{"openalex":859,"title":861},{"VOID":860},"A5037929540",{"EN":862},"Xian‐Ju Kuang",{"id":864,"sortIndex":131,"researcher":24,"roles":865,"affiliations":866,"properties":883},"9ef02966-93f6-4d85-ac65-4d8e3129703c",[],[867,877],{"id":868,"sortIndex":25,"affiliation":869,"properties":24},"9bb62096-ae3e-4bb8-a50c-2d380564a3a4",{"id":870,"createTime":871,"updateTime":871,"relativeEntities":872,"slug":873,"properties":874,"entityType":68,"verifyStatus":23,"verifyTime":24,"verifyNote":24,"syncStatus":23,"languages":24,"translateLanguages":24,"viewCount":25},"14bc85e6-b39c-404e-bb07-8ecff62ea5e2","2024-10-13T10:51:36.823+00:00",[],"Texas-A-M-AgriLife-Research-and-Extension-Center-Lubbock-Texas-USA",{"title":875},{"EN":876},"Texas A&M AgriLife Research and Extension Center, Lubbock, Texas, USA",{"id":878,"sortIndex":131,"affiliation":879,"properties":24},"e22c1930-da14-4945-ac6f-2d8ac8afcae1",{"id":840,"createTime":841,"updateTime":841,"relativeEntities":880,"slug":843,"properties":881,"entityType":68,"verifyStatus":23,"verifyTime":24,"verifyNote":24,"syncStatus":23,"languages":24,"translateLanguages":24,"viewCount":25},[],{"title":882},{"EN":846},{"openalex":884,"orcid":886,"title":888},{"VOID":885},"A5015935124",{"VOID":887},"https:\u002F\u002Forcid.org\u002F0000-0002-1804-2845",{"EN":889},"Megha N. 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Although exogenous treatment of plants with jasmonic acid (JA) may result in induced responses similar to plant defences induced by herbivory, few studies have compared the details of insect herbivory and JA‐mimicked responses. We compared volatiles of two crucifer species, \u003Cjats:italic>Cardamine impatiens\u003C\u002Fjats:italic> and \u003Cjats:italic>Lepidium virginicum\u003C\u002Fjats:italic>, in response to \u003Cjats:italic>Plutella xylostella\u003C\u002Fjats:italic> larval feeding and exogenous application of JA, over the entire period of time when induced changes were detectable. Significant differences in the composition and timing of volatiles occurred between herbivory and JA treatments in both plants. The quantity of nitrile and isothiocyanate released in response to herbivory was significantly larger than that upon JA treatment. In each of the two plant species, most volatile components were emitted immediately upon larval feeding and their quantity dropped rapidly once feeding ceased. In contrast, the emission of volatiles in response to JA treatment lasted for a longer period of time, and the maximum emission rate was recorded 2 and 3 days after JA treatment in \u003Cjats:italic>L. virginicum\u003C\u002Fjats:italic> and \u003Cjats:italic>C. impatiens\u003C\u002Fjats:italic> respectively. These findings are discussed in the context of signal‐transduction pathways and mechanisms involved in induced emissions of plant volatiles, as well as induced defences mediated by plant volatiles.\u003C\u002Fjats:p>",{"EN":1070},"Different headspace profiles in wild crucifer species in response to \u003Ci>Plutella xylostella\u003C\u002Fi> herbivory and exogenous jasmonic acid 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In this study, we characterize the bacterial endosymbionts of\u003Cjats:italic>A. gossypii\u003C\u002Fjats:italic>collected in Karaj, Iran and their role in the performance of the aphid. Our results indicated that beside\u003Cjats:italic>Buchnera aphidicola\u003C\u002Fjats:italic>,\u003Cjats:italic>A. gossypii\u003C\u002Fjats:italic>, also harbors both\u003Cjats:italic>Hamiltonella defensa\u003C\u002Fjats:italic>and\u003Cjats:italic>Arsenophonus\u003C\u002Fjats:italic>sp. Quantitative PCR (qPCR) results revealed that the populations of the endosymbionts increased throughout nymphal development up to adult emergence; thereafter, populations of\u003Cjats:italic>Buchnera\u003C\u002Fjats:italic>and\u003Cjats:italic>Arsenophonus\u003C\u002Fjats:italic>were diminished while the density of\u003Cjats:italic>H. defensa\u003C\u002Fjats:italic>constantly increased.\u003Cjats:italic>Buchnera\u003C\u002Fjats:italic>reduction caused prolonged development and no progeny production. Furthermore, secondary symbiont reduction led to reduction of the total life span and intrinsic rate of natural increase as well as appearance of the deformed dead offspring in comparison with the control insects. Reduction of the secondary symbionts did not affect parasitism rate of the aphid by the parasitic wasp\u003Cjats:italic>Aphidius matricariae\u003C\u002Fjats:italic>. Together these findings showed that\u003Cjats:italic>H. defensa\u003C\u002Fjats:italic>and\u003Cjats:italic>Arsenophonus\u003C\u002Fjats:italic>contributed to the fitness of\u003Cjats:italic>A. gossypii\u003C\u002Fjats:italic>by enhancing its performance, but not through parasitoid resistance.\u003C\u002Fjats:p>","\u003Cjats:title>Trừu tượng\u003C\u002Fjats:title>\u003Cjats:p>Các vi khuẩn đồng sinh đóng vai trò quan trọng trong các đặc điểm sinh thái của bọ aphid. Trong nghiên cứu này, chúng tôi đã phân tích các vi khuẩn đồng sinh của \u003Cjats:italic>A. gossypii\u003C\u002Fjats:italic> được thu thập ở Karaj, Iran và vai trò của chúng trong hiệu suất của bọ aphid. Kết quả của chúng tôi cho thấy ngoài \u003Cjats:italic>Buchnera aphidicola\u003C\u002Fjats:italic>, \u003Cjats:italic>A. gossypii\u003C\u002Fjats:italic> cũng chứa cả hai loài \u003Cjats:italic>Hamiltonella defensa\u003C\u002Fjats:italic> và \u003Cjats:italic>Arsenophonus\u003C\u002Fjats:italic> sp. Kết quả PCR định lượng (qPCR) cho thấy rằng dân số của các vi khuẩn đồng sinh tăng lên trong suốt quá trình phát triển của ấu trùng cho tới khi bọ trưởng thành xuất hiện; sau đó, dân số của \u003Cjats:italic>Buchnera\u003C\u002Fjats:italic> và \u003Cjats:italic>Arsenophonus\u003C\u002Fjats:italic> giảm, trong khi mật độ của \u003Cjats:italic>H. defensa\u003C\u002Fjats:italic> liên tục tăng. Việc giảm \u003Cjats:italic>Buchnera\u003C\u002Fjats:italic> dẫn đến thời gian phát triển kéo dài và không sản xuất con non. Hơn nữa, việc giảm các vi khuẩn đồng sinh thứ cấp dẫn đến giảm tuổi thọ tổng cộng và tỷ lệ tăng trưởng tự nhiên nội tại cũng như sự xuất hiện của các con non bị deformed và chết so với côn trùng đối chứng. Việc giảm các vi khuẩn đồng sinh thứ cấp không ảnh hưởng đến tỷ lệ ký sinh của bọ aphid bởi ong ký sinh \u003Cjats:italic>Aphidius matricariae\u003C\u002Fjats:italic>. Tổng hợp các phát hiện này cho thấy \u003Cjats:italic>H. defensa\u003C\u002Fjats:italic> và \u003Cjats:italic>Arsenophonus\u003C\u002Fjats:italic> đóng góp vào sự sung mãn của \u003Cjats:italic>A. gossypii\u003C\u002Fjats:italic> bằng cách tăng cường hiệu suất của nó, nhưng không thông qua khả năng kháng ký sinh.",{"EN":1814,"VI":1815},"Coinfection of the secondary symbionts,\u003Ci>Hamiltonella defensa\u003C\u002Fi>and\u003Ci>Arsenophonus\u003C\u002Fi>sp. contribute to the performance of the major aphid pest,\u003Ci>Aphis gossypii\u003C\u002Fi>(Hemiptera: Aphididae)","Sự đồng nhiễm của các vi khuẩn đồng sinh thứ cấp, \u003Ci>Hamiltonella defensa\u003C\u002Fi> và \u003Ci>Arsenophonus\u003C\u002Fi> sp. góp phần vào hiệu suất của dịch hại chính \u003Ci>Aphis gossypii\u003C\u002Fi> (Hemiptera: Aphididae)",{"VOID":1817},"29749703",{"VOID":1819},"10.1111\u002F1744-7917.12603",[174],[1822],"VI","https:\u002F\u002Fonlinelibrary.wiley.com\u002Fdoi\u002F10.1111\u002F1744-7917.12603",[1825,1845,1862,1879],{"id":1826,"sortIndex":25,"researcher":24,"roles":1827,"affiliations":1828,"properties":1840},"7e98094e-8a2e-4284-971f-d12625309af9",[],[1829],{"id":1830,"sortIndex":25,"affiliation":1831,"properties":24},"bb4770dc-be54-4b88-8ca0-f47556015b96",{"id":1832,"createTime":1833,"updateTime":1834,"relativeEntities":1835,"slug":1836,"properties":1837,"entityType":68,"verifyStatus":23,"verifyTime":24,"verifyNote":24,"syncStatus":23,"languages":24,"translateLanguages":24,"viewCount":25},"03e7b711-703e-459d-ad4f-bfe6d9404cb9","2024-04-18T00:43:42.831+00:00","2025-06-11T17:12:50.575+00:00",[],"Faculty-of-Agriculture-Department-of-Entomology-Tarbiat-Modares-University-Tehran-Iran",{"title":1838},{"EN":1839},"Faculty of Agriculture, Department of Entomology, Tarbiat Modares University, Tehran, Iran",{"openalex":1841,"title":1843},{"VOID":1842},"A5072326451",{"EN":1844},"Aida Ayoubi",{"id":1846,"sortIndex":126,"researcher":24,"roles":1847,"affiliations":1848,"properties":1855},"2839586a-30a4-4a69-9744-40058536a6a9",[],[1849],{"id":1850,"sortIndex":25,"affiliation":1851,"properties":24},"dd1b9f37-5fec-40fd-9264-a5b511778f6d",{"id":1832,"createTime":1833,"updateTime":1834,"relativeEntities":1852,"slug":1836,"properties":1853,"entityType":68,"verifyStatus":23,"verifyTime":24,"verifyNote":24,"syncStatus":23,"languages":24,"translateLanguages":24,"viewCount":25},[],{"title":1854},{"EN":1839},{"openalex":1856,"orcid":1858,"title":1860},{"VOID":1857},"A5076781847",{"VOID":1859},"https:\u002F\u002Forcid.org\u002F0000-0003-2981-7308",{"EN":1861},"Mohammad 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P., 1958, Eine neue Form der Endosymbiose bei Aphiden, Zoologischer Anzeiger, 160, 222",{},{"id":24,"text":1958,"url":24,"identifiers":1959},"Carey J.R., 1993, Applied Demography for Biologists, with Special Emphasis on Insects, 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M.(1980)Studies on the life cycle and polymorphism ofAphis gossypiiGlover (Homptera Aphididae).Special Bulletin of the College of Agriculture Utsunomiya 132.",{},{"id":24,"text":2022,"url":24,"identifiers":2023},"10.1098\u002Frspb.2003.2537",{"doi":2022},{"id":24,"text":2025,"url":24,"identifiers":2026},"10.1111\u002Fj.1574-6941.2007.00284.x",{"doi":2025},{"id":24,"text":2028,"url":24,"identifiers":2029},"Liu X.D. Xu T.T.andLei H.X.(2017)Refuge and host shift pathways of host‐specialized aphidsAphis gossypii.Scientific Reports 7 2008.",{"doi":2030},"10.1038\u002Fs41598-017-02248-4",{"id":24,"text":2032,"url":24,"identifiers":2033},"10.1006\u002Fmeth.2001.1262",{"doi":2032},{"id":24,"text":2035,"url":24,"identifiers":2036},"10.1111\u002Fele.12031",{"doi":2035},{"id":24,"text":2038,"url":24,"identifiers":2039},"10.1111\u002Fmec.12550",{"doi":2038},{"id":24,"text":2041,"url":24,"identifiers":2042},"10.1098\u002Frspb.2015.0977",{"doi":2041},{"id":24,"text":2044,"url":24,"identifiers":2045},"10.1016\u002Fj.micron.2011.11.008",{"doi":2044},{"id":24,"text":2047,"url":24,"identifiers":2048},"10.1046\u002Fj.1365-2311.2002.00393.x",{"doi":2047},{"id":24,"text":2050,"url":24,"identifiers":2051},"10.1128\u002FAEM.71.6.3302-3310.2005",{"doi":2050},{"id":24,"text":2053,"url":24,"identifiers":2054},"10.1016\u002Fj.jinsphys.2009.01.001",{"doi":2053},{"id":24,"text":2056,"url":24,"identifiers":2057},"10.1111\u002Fj.1570-7458.2010.01021.x",{"doi":2056},{"id":24,"text":2059,"url":24,"identifiers":2060},"10.1098\u002Frspb.2007.1192",{"doi":2059},{"id":24,"text":2062,"url":24,"identifiers":2063},"10.1146\u002Fannurev-ento-112408-085305",{"doi":2062},{"id":24,"text":2065,"url":24,"identifiers":2066},"Oliver K.M., 2005, Variation in resistance to parasitism in aphids is due to symbionts not host genotype, Proceedings of the Royal Society B: Biological Sciences, 102, 12795",{},{"id":24,"text":2068,"url":24,"identifiers":2069},"10.1098\u002Frspb.2005.3436",{"doi":2068},{"id":24,"text":2071,"url":24,"identifiers":2072},"10.1073\u002Fpnas.0335320100",{"doi":2071},{"id":24,"text":2074,"url":24,"identifiers":2075},"10.1128\u002FAEM.03193-12",{"doi":2074},{"id":24,"text":2077,"url":24,"identifiers":2078},"10.1603\u002F0013-8746(2006)99[577:VTOAPC]2.0.CO;2",{"doi":2077},{"id":24,"text":2080,"url":24,"identifiers":2081},"10.1007\u002Fs13199-013-0256-9",{"doi":2080},{"id":24,"text":2083,"url":24,"identifiers":2084},"Souri M.K, 2009, Split daily application of ammonium can not ammeliorate ammonium toxicity in tomato plants, Horticulture Environment and Biotechnology, 50, 384",{},{"id":24,"text":2086,"url":24,"identifiers":2087},"10.1111\u002Fmec.12211",{"doi":2086},{"id":24,"text":2089,"url":24,"identifiers":2090},"10.1098\u002Frspb.2005.3348",{"doi":2089},{"id":24,"text":2092,"url":24,"identifiers":2093},"10.1128\u002FAEM.71.7.4069-4075.2005",{"doi":2092},{"id":24,"text":2095,"url":24,"identifiers":2096},"10.1046\u002Fj.1365-294X.2001.01189.x",{"doi":2095},{"id":24,"text":2098,"url":24,"identifiers":2099},"SAS, 2003, GLM: A Guide to Statistical and Data 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Journal of International Society for Microbial Ecology, 6, 384",{},{"id":24,"text":2125,"url":24,"identifiers":2126},"10.1303\u002Faez.2006.129",{"doi":2125},{"id":24,"text":2128,"url":24,"identifiers":2129},"10.1046\u002Fj.1365-294X.2002.01606.x",{"doi":2128},{"id":24,"text":2131,"url":24,"identifiers":2132},"10.1126\u002Fscience.1195463",{"doi":2131},{"id":24,"text":2134,"url":24,"identifiers":2135},"10.1016\u002Fj.cub.2014.07.065",{"doi":2134},{"id":24,"text":2137,"url":24,"identifiers":2138},"10.1111\u002Fj.1558-5646.2009.00660.x",{"doi":2137},{"id":24,"text":2140,"url":24,"identifiers":2141},"10.14411\u002Feje.2009.007",{"doi":2140},{"id":24,"text":2143,"url":24,"identifiers":2144},"10.1111\u002Fj.1365-2583.2009.00942.x",{"doi":2143},{"id":24,"text":2146,"url":24,"identifiers":2147},"10.1371\u002Fjournal.pbio.0040188",{"doi":2146},{"id":24,"text":2149,"url":24,"identifiers":2150},"10.1371\u002Fjournal.pone.0062145",{"doi":2149},{"id":24,"text":2152,"url":24,"identifiers":2153},"10.1038\u002Fsrep22958",{"doi":2152},{"id":2155,"createTime":2156,"updateTime":2157,"relativeEntities":2158,"slug":2159,"properties":2160,"entityType":171,"verifyStatus":241,"verifyTime":2176,"verifyNote":242,"syncStatus":23,"languages":2177,"translateLanguages":2178,"viewCount":25,"primaryUrl":2179,"fullTextUrl":24,"authors":2180,"publicationType":177,"publisherRelationship":2241,"citationCount":143,"citationInfo":2279,"publishDate":2282,"publishYear":2283,"citationAnalyzeStatus":23,"lastCitationAnalyze":24,"indexDatabases":24,"openAccess":24,"references":2284,"isForceReanalyzing":221},"20774db8-621d-48ad-b053-154d304247b3","2024-10-13T10:52:00.383+00:00","2025-02-06T04:21:21.512+00:00",[],"Confidence-interval-of-intrinsic-optimum-temperature-estimated-using-thermodynamic-SSI-model",{"mag":2161,"keywords":2163,"openalex":2164,"abstract":2166,"title":2169,"pm":2172,"doi":2174},{"VOID":2162},"1535229665",{"VI":1807},{"VOID":2165},"W1535229665",{"EN":2167,"VI":2168},"\u003Cjats:title>Abstract\u003C\u002Fjats:title>\u003Cjats:p>The intrinsic optimum temperature for the development of ectotherms is one of the most important factors not only for their physiological processes but also for ecological and evolutional processes. The Sharpe–Schoolfield–Ikemoto (SSI) model succeeded in defining the temperature that can thermodynamically meet the condition that at a particular temperature the probability of an active enzyme reaching its maximum activity is realized. Previously, an algorithm was developed by Ikemoto (Tropical malaria does not mean hot environments. \u003Cjats:italic>Journal of Medical Entomology\u003C\u002Fjats:italic>, 45, 963–969) to estimate model parameters, but that program was computationally very time consuming. Now, investigators can use the SSI model more easily because a full automatic computer program was designed by Shi \u003Cjats:italic>et al\u003C\u002Fjats:italic>. (A modified program for estimating the parameters of the SSI model. \u003Cjats:italic>Environmental Entomology\u003C\u002Fjats:italic>, 40, 462–469). However, the statistical significance of the point estimate of the intrinsic optimum temperature for each ectotherm has not yet been determined. Here, we provided a new method for calculating the confidence interval of the estimated intrinsic optimum temperature by modifying the approximate bootstrap confidence intervals method. For this purpose, it was necessary to develop a new program for a faster estimation of the parameters in the SSI model, which we have also done.\u003C\u002Fjats:p>","\u003Cjats:title>Tóm tắt\u003C\u002Fjats:title>\u003Cjats:p>Nhiệt độ tối ưu nội sinh cho sự phát triển của động vật biến nhiệt là một trong những yếu tố quan trọng nhất không chỉ đối với các quá trình sinh lý mà còn đối với các quá trình sinh thái và tiến hóa. Mô hình Sharpe–Schoolfield–Ikemoto (SSI) đã thành công trong việc xác định nhiệt độ mà tại đó, về mặt nhiệt động lực học, xác suất một enzyme hoạt động đạt được mức độ hoạt động tối đa có thể xảy ra. Trước đây, một thuật toán đã được phát triển bởi Ikemoto (Sốt rét nhiệt đới không có nghĩa là môi trường nóng. \u003Cjats:italic>Tạp chí Côn trùng Y học\u003C\u002Fjats:italic>, 45, 963–969) để ước lượng các tham số mô hình, nhưng chương trình đó rất tốn thời gian tính toán. Hiện nay, các nhà nghiên cứu có thể sử dụng mô hình SSI dễ dàng hơn vì đã có một chương trình máy tính tự động hoàn chỉnh được thiết kế bởi Shi \u003Cjats:italic>et al\u003C\u002Fjats:italic>. (Chương trình sửa đổi để ước lượng các tham số của mô hình SSI. \u003Cjats:italic>Côn trùng Môi trường\u003C\u002Fjats:italic>, 40, 462–469). Tuy nhiên, ý nghĩa thống kê của ước tính điểm nhiệt độ tối ưu nội sinh cho mỗi động vật biến nhiệt vẫn chưa được xác định. Tại đây, chúng tôi cung cấp một phương pháp mới để tính khoảng tin cậy của nhiệt độ tối ưu nội sinh ước lượng bằng cách điều chỉnh phương pháp khoảng tin cậy bootstrap gần đúng. Để mục đích này, cần phát triển một chương trình mới để ước tính nhanh hơn các tham số trong mô hình SSI, điều mà chúng tôi cũng đã thực hiện.",{"EN":2170,"VI":2171},"Confidence interval of intrinsic optimum temperature estimated using thermodynamic SSI model","Khoảng tin cậy của nhiệt độ tối ưu nội sinh được ước lượng bằng mô hình SSI nhiệt động lực học",{"VOID":2173},"23955893",{"VOID":2175},"10.1111\u002Fj.1744-7917.2012.01525.x","2024-10-13T10:52:00.382+00:00",[174],[1822],"https:\u002F\u002Fonlinelibrary.wiley.com\u002Fdoi\u002F10.1111\u002Fj.1744-7917.2012.01525.x",[2181,2202,2221],{"id":2182,"sortIndex":25,"researcher":24,"roles":2183,"affiliations":2184,"properties":2195},"9092b64d-ec51-41cb-ac0d-1c393956cc51",[],[2185],{"id":2186,"sortIndex":25,"affiliation":2187,"properties":24},"85907726-e71b-40a3-84a1-1421829608e1",{"id":2188,"createTime":2189,"updateTime":2189,"relativeEntities":2190,"slug":2191,"properties":2192,"entityType":68,"verifyStatus":23,"verifyTime":24,"verifyNote":24,"syncStatus":23,"languages":24,"translateLanguages":24,"viewCount":25},"bfc489ac-b9b8-42bc-8063-0b2c20352960","2024-10-13T10:52:00.405+00:00",[],"Department-of-Microbiology-Teikyo-University-School-of-Medicine",{"title":2193},{"EN":2194},"Department of Microbiology Teikyo University School of Medicine",{"openalex":2196,"orcid":2198,"title":2200},{"VOID":2197},"A5006644093",{"VOID":2199},"https:\u002F\u002Forcid.org\u002F0009-0000-4623-8522",{"EN":2201},"Takaya IKEMOTO",{"id":2203,"sortIndex":132,"researcher":24,"roles":2204,"affiliations":2205,"properties":2217},"98d9fb3e-0905-4251-959c-714e455a2e31",[],[2206],{"id":2207,"sortIndex":25,"affiliation":2208,"properties":24},"ebe87b3a-8208-4763-ac2e-4bb11f9582a2",{"id":2209,"createTime":2210,"updateTime":2211,"relativeEntities":2212,"slug":2213,"properties":2214,"entityType":68,"verifyStatus":23,"verifyTime":24,"verifyNote":24,"syncStatus":23,"languages":24,"translateLanguages":24,"viewCount":25},"64551cf8-de18-4941-883d-f0d331bb0584","2023-12-13T19:06:03.996+00:00","2024-10-13T10:52:00.427+00:00",[],"State-Key-Laboratory-of-Integrated-Management-of-Pest-Insects-and-Rodents-Institute-of-Zoology-Chinese-Academy-of-Sciences-Beijing-China",{"title":2215},{"VI":2216},"State Key Laboratory of Integrated Management of Pest Insects and Rodents, Institute of Zoology, Chinese Academy of Sciences, Beijing, China",{"openalex":2218,"orcid":2219,"title":2220},{"VOID":947},{"VOID":949},{"EN":951},{"id":2222,"sortIndex":131,"researcher":24,"roles":2223,"affiliations":2224,"properties":2236},"6dd5bbb5-756c-4c08-b8fd-e98d5e7f9d1d",[],[2225],{"id":2226,"sortIndex":25,"affiliation":2227,"properties":24},"08d321f9-9e54-4c98-b02e-edd5549d19b3",{"id":2228,"createTime":2229,"updateTime":2230,"relativeEntities":2231,"slug":2232,"properties":2233,"entityType":68,"verifyStatus":23,"verifyTime":24,"verifyNote":24,"syncStatus":23,"languages":24,"translateLanguages":24,"viewCount":25},"eb979c36-d506-4166-80be-4c12297e0b24","2023-12-25T08:03:33.862+00:00","2024-10-13T10:52:00.417+00:00",[],"Department-of-Planning-Information-and-Management-The-University-of-Tokyo-Hospital-Tokyo-Japan",{"title":2234},{"VI":2235},"Department of Planning Information and Management, The University of Tokyo Hospital, Tokyo, Japan",{"openalex":2237,"title":2239},{"VOID":2238},"A5004845953",{"EN":2240},"Issei Kurahashi",{"url":24,"publisher":2242,"properties":2272},{"id":6,"createTime":7,"updateTime":8,"relativeEntities":2243,"slug":10,"properties":2244,"entityType":22,"verifyStatus":23,"verifyTime":24,"verifyNote":24,"syncStatus":23,"languages":24,"translateLanguages":24,"viewCount":25,"subjectFields":2250,"manageAffiliations":2251,"indexDatabases":2252,"url":123,"thumbnailPath":24,"statistic":2267,"gsStatistic":24,"type":24,"analyzePriority":24},[],{"country":2245,"issn":2246,"introduce":2247,"eissn":2248,"title":2249},{"VOID":13},{"VOID":15},{"EN":17},{"VOID":19},{"EN":21},[],[],[2253,2260],{"id":102,"indexDatabase":2254,"url":115,"indexYears":116,"academicFieldIds":2259,"indexDatabaseRanking":122},{"id":104,"createTime":105,"updateTime":106,"relativeEntities":2255,"label":2256,"description":2257,"key":112,"publicationTags":2258,"standard":24},[],{"EN":109,"VI":109},{"EN":109,"VI":111},[114],[118,119,120,121],{"id":83,"indexDatabase":2261,"url":98,"indexYears":24,"academicFieldIds":2266,"indexDatabaseRanking":24},{"id":85,"createTime":86,"updateTime":87,"relativeEntities":2262,"label":2263,"description":2264,"key":94,"publicationTags":2265,"standard":24},[],{"EN":90,"VI":90},{"VI":92,"EN":93},[96,97],[100],{"impactFactor":25,"impactFactorByYear":2268,"i10Index":134,"i10IndexLast5Year":131,"totalPublication":134,"totalPublicationByYear":2269,"totalCitation":136,"totalCitationByYear":2270,"totalCitationPerPublication":146,"totalCitationPerPublicationByYear":2271,"hindexLast5Year":150,"hindex":150},{"2013":126,"2014":127,"2015":128,"2016":129,"2017":130,"2018":131,"2019":132,"2021":133,"2022":127},{"2005":131,"2006":131,"2008":131,"2009":132,"2012":131,"2013":131,"2014":131,"2015":132,"2017":131,"2020":131},{"2005":138,"2006":139,"2008":140,"2009":141,"2012":142,"2013":143,"2014":144,"2015":145,"2017":134,"2020":139},{"2005":138,"2006":139,"2008":140,"2009":148,"2012":142,"2013":143,"2014":144,"2015":149,"2017":134,"2020":139},{"volume":2273,"pages":2275,"issue":2277},{"VOID":2274},"20",{"VOID":2276},"420-428",{"VOID":2278},"3",{"total":143,"publishYear":24,"statisticByYear":2280},{"2012":131,"2013":79,"2014":126,"2015":2281,"2016":131,"2017":127,"2018":1935,"2019":79,"2020":131,"2021":132,"2022":127,"2023":132},7,"2013-06-01",2013,[2285,2288,2291,2294,2297,2300,2303,2306,2310,2313,2316,2319,2322,2324,2327,2330,2333,2337,2340,2343,2346,2349],{"id":24,"text":2286,"url":24,"identifiers":2287},"10.1201\u002F9781420074468",{"doi":2286},{"id":24,"text":2289,"url":24,"identifiers":2290},"10.1079\u002FBER2003259",{"doi":2289},{"id":24,"text":2292,"url":24,"identifiers":2293},"10.1603\u002F0046-225X(2007)36[657:DSAROT]2.0.CO;2",{"doi":2292},{"id":24,"text":2295,"url":24,"identifiers":2296},"10.1146\u002Fannurev.en.05.010160.001131",{"doi":2295},{"id":24,"text":2298,"url":24,"identifiers":2299},"10.1093\u002Fbiomet\u002F79.2.231",{"doi":2298},{"id":24,"text":2301,"url":24,"identifiers":2302},"10.1214\u002Fss\u002F1032280214",{"doi":2301},{"id":24,"text":2304,"url":24,"identifiers":2305},"10.1214\u002Fss\u002F1063994968",{"doi":2304},{"id":24,"text":2307,"url":24,"identifiers":2308},"Efron B., 1994, An Introduction to the Bootstrap, 436, 10.1201\u002F9780429246593",{"doi":2309},"10.1201\u002F9780429246593",{"id":24,"text":2311,"url":24,"identifiers":2312},"Gilpin M.E., 1979, Systems analysis of the yellow fever mosquito Aedes aegypti, Fortschritte der Zoologie, 25, 355",{},{"id":24,"text":2314,"url":24,"identifiers":2315},"10.1303\u002Faez.2003.487",{"doi":2314},{"id":24,"text":2317,"url":24,"identifiers":2318},"10.1603\u002F0046-225X-34.6.1377",{"doi":2317},{"id":24,"text":2320,"url":24,"identifiers":2321},"10.1093\u002Fjmedent\u002F45.6.963",{"doi":2320},{"id":24,"text":1027,"url":24,"identifiers":2323},{"doi":1027},{"id":24,"text":2325,"url":24,"identifiers":2326},"10.1303\u002Faez.2006.171",{"doi":2325},{"id":24,"text":2328,"url":24,"identifiers":2329},"10.1093\u002Faesa\u002F51.2.109",{"doi":2328},{"id":24,"text":2331,"url":24,"identifiers":2332},"10.1093\u002Fcomjnl\u002F7.4.308",{"doi":2331},{"id":24,"text":2334,"url":24,"identifiers":2335},"Ogwan'g R.A., 1993, Factors affecting exflagelation of invitro‐cultivated Plasmodium falciparum gametocytes, American Journal of Tropical Medicine and Hygiene, 49, 25, 10.4269\u002Fajtmh.1993.49.25",{"doi":2336},"10.4269\u002Fajtmh.1993.49.25",{"id":24,"text":2338,"url":24,"identifiers":2339},"10.1016\u002F0022-5193(81)90246-0",{"doi":2338},{"id":24,"text":2341,"url":24,"identifiers":2342},"10.1016\u002F0022-5193(77)90265-X",{"doi":2341},{"id":24,"text":2344,"url":24,"identifiers":2345},"10.1603\u002FEN10265",{"doi":2344},{"id":24,"text":2347,"url":24,"identifiers":2348},"10.1303\u002Faez.2001.409",{"doi":2347},{"id":24,"text":2350,"url":24,"identifiers":2351},"10.1093\u002Fee\u002F1.5.537",{"doi":2350},{"id":2353,"createTime":2354,"updateTime":2355,"relativeEntities":2356,"slug":2357,"properties":2358,"entityType":171,"verifyStatus":241,"verifyTime":2372,"verifyNote":242,"syncStatus":23,"languages":2373,"translateLanguages":2374,"viewCount":25,"primaryUrl":2375,"fullTextUrl":24,"authors":2376,"publicationType":177,"publisherRelationship":2398,"citationCount":2435,"citationInfo":2436,"publishDate":2438,"publishYear":2439,"citationAnalyzeStatus":23,"lastCitationAnalyze":24,"indexDatabases":24,"openAccess":24,"references":2440,"isForceReanalyzing":221},"d50dbefb-8348-4456-a6f3-11971b71dc91","2024-10-02T18:22:19.653+00:00","2025-02-06T04:20:24.735+00:00",[],"High-nickel-insects-and-nickel-hyperaccumulator-plants-A-review",{"mag":2359,"keywords":2361,"openalex":2362,"abstract":2364,"title":2367,"doi":2370},{"VOID":2360},"2110943901",{"VI":1807},{"VOID":2363},"W2110943901",{"EN":2365,"VI":2366},"\u003Cjats:title>Abstract\u003C\u002Fjats:title>\u003Cjats:p>Insects can vary greatly in whole‐body elemental concentrations. Recent investigations of insects associated with Ni hyperaccumulator plants have identified insects with relatively elevated whole‐body Ni levels. Evaluation of the limited data available indicates that a whole‐body Ni concentration of 500 μg Ni\u002Fg is exceptional: I propose that an insect species with a mean value of 500 μg Ni\u002Fg or greater, in either larval\u002Fnymphal or adult stages, be considered a “high‐Ni insect”. Using the 500 μg Ni\u002Fg criterion, 15 species of high‐Ni insects have been identified to date from studies in Mpumalanga (South Africa), New Caledonia and California (USA). The highest mean Ni concentration reported is 3 500 μg Ni\u002Fg for nymphs of a South African \u003Cjats:italic>Stenoscepa\u003C\u002Fjats:italic> species (Orthoptera: Pyrgomorphidae). The majority of high‐Ni insects (66%) are heteropteran herbivores. Studies of high‐Ni insect host preference indicate they are monophagous (or nearly so) on a particular Ni hyperaccumulator plant species. Much of the Ni in bodies of these insects is in their guts (up to 66%–75%), but elevated levels have also been found in Malpighian tubules, suggesting efficient elimination as one strategy for dealing with a high‐Ni diet. Tissue levels of Ni are generally much lower than gut concentrations, but up to 1200 μg Ni\u002Fg has been reported from exuviae, suggesting that molting may be another pathway of Ni elimination. One ecological function of the high Ni concentration of these insects may be to defend them against natural enemies, but to date only one experimental test has supported this “elemental defense” hypothesis. Community‐level studies indicate that high‐Ni insects mobilize Ni into food webs but that bioaccumulation of Ni does not occur at either plant‐herbivore or herbivore‐predator steps. Unsurprisingly, Ni bioaccumulation indices are greater for high‐Ni insects compared to other insect species that feed on Ni hyperaccumulator plants. There is some evidence of Ni mobilization into food webs by insect visitors to flowers of Ni hyperaccumulator plants, but no high‐Ni insect floral visitors have been reported.\u003C\u002Fjats:p>","\u003Cjats:title>Tóm tắt\u003C\u002Fjats:title>\u003Cjats:p>Côn trùng có thể có sự khác biệt lớn về nồng độ nguyên tố trong toàn bộ cơ thể. Các cuộc điều tra gần đây về côn trùng liên quan đến các loại cây tích lũy nickel cao đã xác định được những loại côn trùng có nồng độ nickel trong cơ thể tương đối cao. Đánh giá dữ liệu hạn chế có sẵn cho thấy nồng độ nickel trong toàn bộ cơ thể là 500 μg Ni\u002Fg là điều đặc biệt: Tôi đề xuất rằng một loài côn trùng có giá trị trung bình là 500 μg Ni\u002Fg hoặc cao hơn, ở giai đoạn ấu trùng\u002Fnymph hoặc trưởng thành, được coi là \"côn trùng chứa nickel cao\". Sử dụng tiêu chí 500 μg Ni\u002Fg, 15 loài côn trùng chứa nickel cao đã được xác định cho đến nay từ các nghiên cứu ở Mpumalanga (Nam Phi), New Caledonia và California (Mỹ). Nồng độ nickel trung bình cao nhất được báo cáo là 3 500 μg Ni\u002Fg cho nymph của một loài \u003Cjats:italic>Stenoscepa\u003C\u002Fjats:italic> ở Nam Phi (Orthoptera: Pyrgomorphidae). Phần lớn côn trùng chứa nickel cao (66%) là côn trùng ăn cỏ thuộc nhóm Heteroptera. Các nghiên cứu về sở thích ký sinh của côn trùng chứa nickel cao cho thấy chúng thường ăn một loài cây tích lũy nickel cao cụ thể (hoặc gần như vậy). Một phần lớn nickel trong cơ thể của những côn trùng này nằm ở ruột (lên đến 66%–75%), nhưng nồng độ cao cũng được tìm thấy trong các ống Malpighian, cho thấy việc loại bỏ hiệu quả có thể là một chiến lược để đối phó với chế độ ăn giàu nickel. Mức độ nickel trong mô thường thấp hơn nhiều so với nồng độ trong ruột, nhưng đã có báo cáo lên đến 1200 μg Ni\u002Fg từ xác, cho thấy rằng việc lột xác có thể là một con đường khác để loại bỏ nickel. Một chức năng sinh thái của nồng độ nickel cao ở những côn trùng này có thể là để bảo vệ chúng khỏi kẻ thù tự nhiên, nhưng cho đến nay chỉ có một thử nghiệm thực nghiệm hỗ trợ giả thuyết \"phòng thủ nguyên tố\" này. Các nghiên cứu ở cấp độ cộng đồng cho thấy côn trùng chứa nickel cao chuyển động nickel vào chuỗi thực phẩm nhưng sự tích lũy nickel không xảy ra ở các bước giữa thực vật - côn trùng ăn cỏ hoặc côn trùng ăn cỏ - kẻ ăn thịt. Không có gì ngạc nhiên khi chỉ số tích lũy nickel cao hơn cho côn trùng chứa nickel cao so với các loài côn trùng khác ăn các loại cây tích lũy nickel cao. Có một số bằng chứng về việc di chuyển nickel vào chuỗi thực phẩm bởi các côn trùng thăm hoa của các loại cây tích lũy nickel cao, nhưng chưa báo cáo về sự thăm hoa của côn trùng chứa nickel cao.",{"EN":2368,"VI":2369},"High‐nickel insects and nickel hyperaccumulator plants: A review","Côn trùng chứa nickel cao và thực vật tích lũy nickel cao: Một tổng quan",{"VOID":2371},"10.1111\u002Fj.1744-7917.2009.00250.x","2024-10-02T18:22:19.652+00:00",[174],[1822],"https:\u002F\u002Fonlinelibrary.wiley.com\u002Fdoi\u002F10.1111\u002Fj.1744-7917.2009.00250.x",[2377],{"id":2378,"sortIndex":25,"researcher":24,"roles":2379,"affiliations":2380,"properties":2391},"b21b6d46-a819-4154-9be9-967b77057bbd",[],[2381],{"id":2382,"sortIndex":25,"affiliation":2383,"properties":24},"4bdbb276-9b70-4925-b243-2a36a948001b",{"id":2384,"createTime":2385,"updateTime":2385,"relativeEntities":2386,"slug":2387,"properties":2388,"entityType":68,"verifyStatus":23,"verifyTime":24,"verifyNote":24,"syncStatus":23,"languages":24,"translateLanguages":24,"viewCount":25},"ebb8415a-db02-43d3-b1a6-39d595940058","2024-10-02T18:22:19.671+00:00",[],"Department-of-Biological-Sciences-101-Life-Sciences-Building-Auburn-University-Alabama-36849-5407-USA",{"title":2389},{"EN":2390},"Department of Biological Sciences, 101 Life Sciences Building, Auburn University, Alabama 36849–5407, USA",{"openalex":2392,"orcid":2394,"title":2396},{"VOID":2393},"A5011861850",{"VOID":2395},"https:\u002F\u002Forcid.org\u002F0000-0003-3941-1205",{"EN":2397},"Robert S. Boyd",{"url":24,"publisher":2399,"properties":2429},{"id":6,"createTime":7,"updateTime":8,"relativeEntities":2400,"slug":10,"properties":2401,"entityType":22,"verifyStatus":23,"verifyTime":24,"verifyNote":24,"syncStatus":23,"languages":24,"translateLanguages":24,"viewCount":25,"subjectFields":2407,"manageAffiliations":2408,"indexDatabases":2409,"url":123,"thumbnailPath":24,"statistic":2424,"gsStatistic":24,"type":24,"analyzePriority":24},[],{"country":2402,"issn":2403,"introduce":2404,"eissn":2405,"title":2406},{"VOID":13},{"VOID":15},{"EN":17},{"VOID":19},{"EN":21},[],[],[2410,2417],{"id":102,"indexDatabase":2411,"url":115,"indexYears":116,"academicFieldIds":2416,"indexDatabaseRanking":122},{"id":104,"createTime":105,"updateTime":106,"relativeEntities":2412,"label":2413,"description":2414,"key":112,"publicationTags":2415,"standard":24},[],{"EN":109,"VI":109},{"EN":109,"VI":111},[114],[118,119,120,121],{"id":83,"indexDatabase":2418,"url":98,"indexYears":24,"academicFieldIds":2423,"indexDatabaseRanking":24},{"id":85,"createTime":86,"updateTime":87,"relativeEntities":2419,"label":2420,"description":2421,"key":94,"publicationTags":2422,"standard":24},[],{"EN":90,"VI":90},{"VI":92,"EN":93},[96,97],[100],{"impactFactor":25,"impactFactorByYear":2425,"i10Index":134,"i10IndexLast5Year":131,"totalPublication":134,"totalPublicationByYear":2426,"totalCitation":136,"totalCitationByYear":2427,"totalCitationPerPublication":146,"totalCitationPerPublicationByYear":2428,"hindexLast5Year":150,"hindex":150},{"2013":126,"2014":127,"2015":128,"2016":129,"2017":130,"2018":131,"2019":132,"2021":133,"2022":127},{"2005":131,"2006":131,"2008":131,"2009":132,"2012":131,"2013":131,"2014":131,"2015":132,"2017":131,"2020":131},{"2005":138,"2006":139,"2008":140,"2009":141,"2012":142,"2013":143,"2014":144,"2015":145,"2017":134,"2020":139},{"2005":138,"2006":139,"2008":140,"2009":148,"2012":142,"2013":143,"2014":144,"2015":149,"2017":134,"2020":139},{"volume":2430,"pages":2432,"issue":2434},{"VOID":2431},"16",{"VOID":2433},"19-31",{"VOID":215},83,{"total":2435,"publishYear":24,"statisticByYear":2437},{"2012":69,"2013":79,"2014":127,"2015":2281,"2016":131,"2017":79,"2018":127,"2019":79,"2020":150,"2021":126,"2022":1935,"2023":127,"2024":131},"2009-02-01",2009,[2441,2445,2448,2451,2454,2457,2460,2463,2466,2469,2472,2475,2478,2481,2484,2487,2490,2493,2497,2500,2503,2506,2509,2512,2515,2518,2521,2524,2527,2530,2533,2536,2539,2542,2545,2548,2551,2554,2557,2560,2563,2566,2569,2572,2575,2578,2581,2584,2587,2590,2593,2596,2599,2602,2605,2608,2611,2614],{"id":24,"text":2442,"url":24,"identifiers":2443},"Alexander E.B., 2007, Serpentine Geoecology of Western North America., 10.1093\u002Foso\u002F9780195165081.001.0001",{"doi":2444},"10.1093\u002Foso\u002F9780195165081.001.0001",{"id":24,"text":2446,"url":24,"identifiers":2447},"10.1016\u002FS0375-6742(99)00055-2",{"doi":2446},{"id":24,"text":2449,"url":24,"identifiers":2450},"Anderson T.R., 1997, Studies on the nickel hyperaccumulator, Berkheya coddii. The Ecology of Ultramafic and Metalliferous Areas, 261",{},{"id":24,"text":2452,"url":24,"identifiers":2453},"Augustyniak M., 2002, Food relations between Chrysolina pardalina and Berkheya coddii, a nickel hyperaccumulator from South African ultramafic outcrops, Fresenius Environmental Bulletin, 11, 85",{},{"id":24,"text":2455,"url":24,"identifiers":2456},"10.1002\u002Fxrs.1037",{"doi":2455},{"id":24,"text":2458,"url":24,"identifiers":2459},"Babaoglu M., 2004, Gypsophila spaerocephala Fenzl ex Tchihat.: A boron hyperaccumulator plant species that may phytoremediate soils with toxic B levels, Turkish Journal of Botany, 28, 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Approach.",{},{"id":24,"text":2501,"url":24,"identifiers":2502},"10.1016\u002F0375-6742(77)90074-7",{"doi":2501},{"id":24,"text":2504,"url":24,"identifiers":2505},"10.1111\u002Fj.1469-8137.2007.02285.x",{"doi":2504},{"id":24,"text":2507,"url":24,"identifiers":2508},"10.1038\u002Fnature06877",{"doi":2507},{"id":24,"text":2510,"url":24,"identifiers":2511},"10.1016\u002FS0269-7491(00)00179-2",{"doi":2510},{"id":24,"text":2513,"url":24,"identifiers":2514},"Hickman J.C., 1993, The Jepson Manual: Higher Plants of California.",{},{"id":24,"text":2516,"url":24,"identifiers":2517},"10.1663\u002F0006-8101(2002)068[0235:AHIAAR]2.0.CO;2",{"doi":2516},{"id":24,"text":2519,"url":24,"identifiers":2520},"10.1111\u002Fj.1469-8137.2005.01504.x",{"doi":2519},{"id":24,"text":2522,"url":24,"identifiers":2523},"Kruckeberg A.R., 1984, California Serpentines: Flora, Vegetation, Geology, Soils, and Management Problems.",{},{"id":24,"text":2525,"url":24,"identifiers":2526},"10.2307\u002F3545083",{"doi":2525},{"id":24,"text":2528,"url":24,"identifiers":2529},"10.1038\u002F35054664",{"doi":2528},{"id":24,"text":2531,"url":24,"identifiers":2532},"10.1016\u002FS0065-2296(05)40002-6",{"doi":2531},{"id":24,"text":2534,"url":24,"identifiers":2535},"10.1007\u002FBF00324227",{"doi":2534},{"id":24,"text":2537,"url":24,"identifiers":2538},"Mesjasz‐Przybylowicz J., 2001, Phytophagous insects associated with the Ni‐hyperaccumulating plant Berkheya coddii (Asteraceae) in Mpumalanga, South Africa, South African Journal of Science, 97, 596",{},{"id":24,"text":2540,"url":24,"identifiers":2541},"10.1016\u002FS0168-583X(01)01127-2",{"doi":2540},{"id":24,"text":2543,"url":24,"identifiers":2544},"10.1007\u002Fs11104-007-9231-7",{"doi":2543},{"id":24,"text":2546,"url":24,"identifiers":2547},"10.1007\u002Fs00049-003-0234-4",{"doi":2546},{"id":24,"text":2549,"url":24,"identifiers":2550},"10.1146\u002Fannurev.arplant.56.032604.144214",{"doi":2549},{"id":24,"text":2552,"url":24,"identifiers":2553},"10.1890\u002F1540-9295(2006)004[0203:ECUPBA]2.0.CO;2",{"doi":2552},{"id":24,"text":2555,"url":24,"identifiers":2556},"10.1046\u002Fj.1469-8137.2000.00651.x",{"doi":2555},{"id":24,"text":2558,"url":24,"identifiers":2559},"10.1080\u002F0735-260291044359",{"doi":2558},{"id":24,"text":2561,"url":24,"identifiers":2562},"Posthuma L., 1993, Heavy‐metal adaptation in terrestrial invertebrates: A review of occurrence, genetics, physiology and ecological consequences, Comparative Biochemistry and Physiology, 106, 11",{},{"id":24,"text":2564,"url":24,"identifiers":2565},"10.1016\u002FS0169-5347(99)01698-5",{"doi":2564},{"id":24,"text":2567,"url":24,"identifiers":2568},"10.1016\u002Fj.nimb.2004.01.028",{"doi":2567},{"id":24,"text":2570,"url":24,"identifiers":2571},"10.1016\u002FS0168-583X(03)01029-2",{"doi":2570},{"id":24,"text":2573,"url":24,"identifiers":2574},"10.1002\u002Fieam.5630030317",{"doi":2573},{"id":24,"text":2576,"url":24,"identifiers":2577},"Reeves R.D., 1992, The Vegetation of Ultramafic (Serpentine) Soils, 252",{},{"id":24,"text":2579,"url":24,"identifiers":2580},"10.1007\u002Fs11104-007-9192-x",{"doi":2579},{"id":24,"text":2582,"url":24,"identifiers":2583},"Reeves R.D., 2000, Phytoremediation of Toxic Metals: Using Plants to Clean Up the Environment, 193",{},{"id":24,"text":2585,"url":24,"identifiers":2586},"10.1002\u002Fj.1537-2197.1981.tb12403.x",{"doi":2585},{"id":24,"text":2588,"url":24,"identifiers":2589},"10.1111\u002Fj.1469-8137.2004.01264.x",{"doi":2588},{"id":24,"text":2591,"url":24,"identifiers":2592},"10.1104\u002Fpp.104.047753",{"doi":2591},{"id":24,"text":2594,"url":24,"identifiers":2595},"Schwartz M.D., 2001, Melanotrichus boydi, a new species of plant bug (Heteroptera: Miridae: Orthotylini) restricted to the nickel hyperaccumulator Streptanthus polygaloides (Brassicaceae), Pan-Pacific Entomologist, 77, 39",{},{"id":24,"text":2597,"url":24,"identifiers":2598},"10.1111\u002Fj.1744-7917.2009.00256.x",{"doi":2597},{"id":24,"text":2600,"url":24,"identifiers":2601},"10.1007\u002Fs004420100666",{"doi":2600},{"id":24,"text":2603,"url":24,"identifiers":2604},"10.1023\u002FB:ECTX.0000003036.81351.31",{"doi":2603},{"id":24,"text":2606,"url":24,"identifiers":2607},"Wall M.A.(1999)Nickel accumulation in serpentine arthropods with emphasis on a species ofMelanotrichus(Heteroptera: Miridae).M.S. thesis Auburn University Auburn Alabama .",{},{"id":24,"text":2609,"url":24,"identifiers":2610},"10.1894\u002F0038-4909(2006)51[481:MBHMIA]2.0.CO;2",{"doi":2609},{"id":24,"text":2612,"url":24,"identifiers":2613},"Wall M.A., 2002, Nickel accumulation in serpentine arthropods from the Red Hills, California, Pan-Pacific Entomologist, 78, 168",{},{"id":24,"text":2615,"url":24,"identifiers":2616},"10.1111\u002Fj.1744-7917.2009.00252.x",{"doi":2615},{"id":2618,"createTime":2619,"updateTime":2620,"relativeEntities":2621,"slug":2622,"properties":2623,"entityType":171,"verifyStatus":241,"verifyTime":2619,"verifyNote":242,"syncStatus":23,"languages":2641,"translateLanguages":2642,"viewCount":25,"primaryUrl":2643,"fullTextUrl":24,"authors":2644,"publicationType":177,"publisherRelationship":2709,"citationCount":2745,"citationInfo":2746,"publishDate":2752,"publishYear":657,"citationAnalyzeStatus":23,"lastCitationAnalyze":24,"indexDatabases":24,"openAccess":24,"references":2753,"isForceReanalyzing":221},"85cb9a33-2cde-47e6-b3f7-4c7361e31928","2024-10-01T03:05:36.739+00:00","2025-02-06T04:19:26.264+00:00",[],"MAPK-signaling-A-key-element-in-plant-defense-response-to-insects",{"mag":2624,"keywords":2626,"pmc":2627,"openalex":2629,"abstract":2631,"title":2634,"pm":2637,"doi":2639},{"VOID":2625},"1950321052",{"VI":1807},{"VOID":2628},"5295641",{"VOID":2630},"W1950321052",{"EN":2632,"VI":2633},"\u003Cjats:title>Abstract\u003C\u002Fjats:title>\u003Cjats:p>Insects have long been the most abundant herbivores, and plants have evolved sophisticated mechanisms to defend against their attack. In particular, plants can perceive specific patterns of tissue damage associated with insect herbivory. Some plant species can perceive certain elicitors in insect oral secretions (OS) that enter wounds during feeding, and rapidly activate a series of intertwined signaling pathways to orchestrate the biosynthesis of various defensive metabolites. Mitogen‐activated protein kinases (MAPKs), common to all eukaryotes, are involved in the orchestration of many cellular processes, including development and stress responses. In plants, at least two MAPKs, salicylic acid‐induced protein kinase (SIPK) and wound‐induced protein kinase (WIPK), are rapidly activated by wounding or insect OS; importantly, genetic studies using transgenic or mutant plants impaired in MAPK signaling indicated that MAPKs play critical roles in regulating the herbivory‐induced dynamics of phytohormones, such as jasmonic acid, ethylene and salicylic acid, and MAPKs are also required for transcriptional activation of herbivore defense‐related genes and accumulation of defensive metabolites. In this review, we summarize recent developments in understanding the functions of MAPKs in plant resistance to insect herbivores.\u003C\u002Fjats:p>","\u003Cjats:title>Tóm tắt\u003C\u002Fjats:title>\u003Cjats:p>Côn trùng từ lâu đã là nhóm động vật ăn cỏ phong phú nhất, và thực vật đã tiến hóa các cơ chế tinh vi để phòng thủ trước sự tấn công của chúng. Đặc biệt, thực vật có khả năng nhận biết các mô hình tổn thương tế bào cụ thể liên quan đến sự ăn cỏ của côn trùng. Một số loài thực vật có thể nhận diện một số chất kích thích nhất định có trong tiết nước bọt của côn trùng (OS) mà đi vào vết thương trong quá trình ăn, từ đó nhanh chóng kích hoạt một loạt các con đường tín hiệu liên kết để điều phối quá trình tổng hợp các hợp chất phòng thủ khác nhau. Các kinase protein hoạt hóa bởi mitogen (MAPK), phổ biến ở tất cả các eukaryote, tham gia vào việc điều phối nhiều quá trình tế bào, bao gồm cả phát triển và phản ứng với căng thẳng. Ở thực vật, ít nhất hai loại MAPK, kinase protein kích thích bởi axit salicylic (SIPK) và kinase protein kích thích bởi tổn thương (WIPK), được kích hoạt nhanh chóng bởi sự tổn thương hoặc tiết dịch từ côn trùng; điều quan trọng là, các nghiên cứu di truyền bằng cách sử dụng thực vật chuyển gen hoặc thực vật đột biến bị khuyết tật trong tín hiệu MAPK cho thấy rằng MAPK đóng vai trò quan trọng trong việc điều chỉnh động lực học của phytohormone kích thích do sự ăn cỏ, như axit jasmonic, etylen và axit salicylic, và MAPK cũng cần thiết cho việc kích hoạt phiên mã các gen liên quan đến phòng thủ chống côn trùng và tích lũy các hợp chất phòng thủ. Trong bài tổng quan này, chúng tôi tóm tắt những phát triển gần đây trong việc hiểu biết về chức năng của MAPK trong khả năng kháng côn trùng của thực vật.\u003C\u002Fjats:p>",{"EN":2635,"VI":2636},"MAPK signaling: A key element in plant defense response to insects","Tín hiệu MAPK: Một yếu tố then chốt trong phản ứng phòng thủ của cây đối với côn trùng",{"VOID":2638},"24753304",{"VOID":2640},"10.1111\u002F1744-7917.12128",[174],[1822],"https:\u002F\u002Fonlinelibrary.wiley.com\u002Fdoi\u002F10.1111\u002F1744-7917.12128",[2645,2677,2692],{"id":2646,"sortIndex":132,"researcher":24,"roles":2647,"affiliations":2648,"properties":2670},"6d544972-45e0-4151-9f8c-c1501086f001",[],[2649,2660],{"id":2650,"sortIndex":131,"affiliation":2651,"properties":24},"157d83a8-e5b3-4fd3-b677-32908a074cf0",{"id":2652,"createTime":2653,"updateTime":2654,"relativeEntities":2655,"slug":2656,"properties":2657,"entityType":68,"verifyStatus":23,"verifyTime":24,"verifyNote":24,"syncStatus":23,"languages":24,"translateLanguages":24,"viewCount":25},"6012a1c2-100a-4c1b-8a91-436190d76a07","2024-01-10T17:50:41.978+00:00","2024-10-01T03:05:36.749+00:00",[],"Kunming-Institute-of-Botany-Chinese-Academy-of-Sciences-Kunming-China",{"title":2658},{"VI":2659},"Kunming Institute of Botany, Chinese Academy of Sciences, Kunming, China",{"id":2661,"sortIndex":25,"affiliation":2662,"properties":24},"ea7912e9-4846-4b7e-910f-67b6ab5e6aba",{"id":2663,"createTime":2664,"updateTime":2664,"relativeEntities":2665,"slug":2666,"properties":2667,"entityType":68,"verifyStatus":23,"verifyTime":24,"verifyNote":24,"syncStatus":23,"languages":24,"translateLanguages":24,"viewCount":25},"d3122a90-418f-4476-ae71-f963c0d35495","2024-10-01T03:05:36.755+00:00",[],"Department-of-Molecular-Ecology-Prof-I-T-Baldwin-MPI-for-Chemical-Ecology-Max-Planck-Society",{"title":2668},{"EN":2669},"Department of Molecular Ecology, Prof. I. 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