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Higher productivity environments are predicted to destabilize consumer–resource dynamics. Conversely, greater heterogeneity in resource productivity is expected to contribute to stability. Yet the importance of these two factors for the dynamics of arthropod communities has been largely overlooked. I manipulated nutrient availability for strawberry plants in a multi-patch experiment, and measured effects of overall plant quality and heterogeneity in plant quality on the stability of interactions between the phytophagous mite Tetranychus urticae and its predator Phytoseiulus persimilis. Plant size, leaf N content and T. urticae population growth increased monotonically with increasing soil nitrogen availability. This gradient in plant quality affected two correlates of mite population stability, population variability over time (i.e., coefficient of variation) and population persistence (i.e., proportion of plant patches colonized). However, the highest level of plant quality did not produce the least stable dynamics, which is inconsistent with the “paradox of enrichment”. Heterogeneity in plant productivity had modest effects on stability, with the only significant difference being less variable T. urticae densities in the heterogeneous compared to the corresponding homogeneous treatment. These results are generally congruent with metapopulation theory and other models for spatially segregated populations, which predict that stability should be governed largely by relative movement rates of predators and prey—rather than patch quality.",{"EN":229},"Host plant quality, spatial heterogeneity, and the stability of mite predator–prey dynamics",{"VOID":231},"[\"11327848162479441645\"]",{"VOID":233},"Banks J (1998) The scale of landscape fragmentation affects herbivore response to vegetation heterogeneity. Oecologia 117:239–246\nConnell JH, Sousa WP (1983) On the evidence needed to judge ecological stability or persistence. Ecology 121:789–824\nCrawley M (2009) The R book. Wiley, West Sussex\nDaane KM, Williams LE (2003) Manipulating vineyard irrigation amounts to reduce insect pest damage. Ecol Appl 13:1650–1666\nDayton PK, Currie V, Gerrodette T, Keller BD, Rosenthal R, Ven Tresca D (1984) Patch dynamics and stability of some California kelp communities. Ecol Monogr 54:253–289\nDenyer JL, Hartley SE, John EA (2010) Both bottom-up and top-down processes contribute to plant diversity maintenance in an edaphically heterogeneous ecosystem. J Ecol 98:498–508\nEllner SP, McCauley E, Kendall B, Briggs CJ, Hosseini PR, Wood SN, Janssen A, Sabelis MW, Turchin P, Nisbet RM, Murdoch WW (2001) Habitat structure and population persistence in an experimental community. Nature 412:538–543\nElton CS (1924) Periodic fluctuations in the numbers of animals: their causes and effects. Brit J Exp Biol 2:119–163\nFussmann GF, Ellner SP, Shertzer KW, Hairston NG (2000) Crossing the Hopf bifurcation in a live predator–prey system. Science 290:1358–1360\nGlasby TM, Underwood AJ (1996) Sampling to differentiate between pulse and press perturbations. Environ Monit Assess 42:241–252\nHarmsen R, Sabelis MW (1992) Of mites and models: an introduction to the symposium proceedings. Exp Appl Acarol 14:179–184\nHassell MP (1978) The dynamics of arthropod predator–prey systems. Princeton University Press, Princeton\nHelms SE, Hunter MD (2005) Variation in plant quality and the population dynamics of Herbivores: there is nothing average about Aphids. Oecologia 145:197–204\nHolt RD, Hassell MP (1993) Environmental heterogeneity and the stability of host-parasitoid interactions. J Anim Ecol 62:89–100\nHolyoak M (2000) Effects of nutrient enrichment on predator-prey metapopulation dynamics. J Anim Ecol 69:985–997\nHuffaker CB, Shea KP, Herman SG (1963) Experimental studies on predation: complex dispersion and levels of food in an acarine predator–prey interaction. Hilgardia 34:305–330\nHuffaker CB, van de Vrie M, McMurtry JA (1969) The ecology of Tetranychid mites and their natural control. Annu Rev Entomol 14:125–174\nJansen VAA (1995) Regulation of predator–prey systems through spatial interactions: a possible solution to the paradox of enrichment. Oikos 74:384–390\nJanssen A, van Gool E, Lingeman R, Jacas J, van de Klashorst G (1997) Metapopulation dynamics of a persisting predator–prey system in the laboratory: time series analysis. Exp Appl Acarol 21:415–430\nJenkins B, Kitching RL, Pimm SL (1992) Productivity, disturbance and food web structure at a local spatial scale in experimental container habitats. Oikos 65:249–255\nKarban R, English-Loeb GM (1990) A “vaccination” of Willamette spider mites (Acari: Tetranychidae) to prevent large populations of Pacific spider mites on grapevines. J Econ Entomol 83:2252–2257\nMcCauley E, Murdoch WW (1990) Predator–prey dynamics in environments rich and poor in nutrients. Nature 343:455–457\nMcCauley E, Murdoch WW, Watson S (1988) Simple models and the variation in plankton densities among lakes. Am Nat 132:383–403\nMcCauley E, Kendall B, Janssen A, Wood S, Murdoch W, Hosseini P, Briggs C, Ellner S, Nisbet R, Sabelis M, Turchin P (2000) Inferring colonization processes from population dynamics in spatially-structured predator–prey systems. Ecology 81:3350–3361\nMcLaughlin JF, Roughgarden J (1992) Pattern and stability in predator–prey communities: how diffusion in spatially variable environments affects the Lotka-Volterra model. Theor Popul Biol 40:148–172\nMitsunaga T, Fujii K (1997) The effects of spatial and temporal environmental heterogeneities on persistence in a laboratory experimental community. Res Popul Ecol 39:249–260\nMueller LD, Joshi A (2000) Stability in model populations. Princeton University Press, Princeton\nNachman G, Zemek R (2003) Interactions in a tritrophic acarine predator–prey metapopulation system V: within-plant dynamics of Phytoseiulus persimilis and Tetranychus urticae (Acarina: Tetranychidae, Phytoseiidae). Exp Appl Acarol 29:35–68\nPels B, Sabelis MW (1999) Local dynamics, overexploitation and predator dispersal in an acarine predator–prey system. Oikos 86:573–583\nPfeiffer DG, Burts EC (1983) Effect of tree fertilization on numbers and development of pear psylla (Homoptera: Psyllidae) and on fruit damage. Environ Entomol 12:895–901\nPrice PW, Bouton CE, Gross P, McPheron BA, Thompson JN, Weis AE (1980) Interactions among three trophic levels: influence of plants on interactions between insect herbivores and natural enemies. Ann Rev Ecol Syst 11:41–65\nRosenzweig ML (1971) Paradox of enrichment: destabilization of exploitation ecosystems in ecological time. Science 171:385–387\nRoss CW (1974) Plant physiology laboratory manual. Wadsworth, Belmont\nSabelis MW, Diekmann O, Jansen VAA (1991) Metapopulation persistence despite local extinction: predator–prey patch models of the Lotka-Volterra type. Biol J Linn Soc 42:267–283\nSabelis MW, Janssen A, Diekmann O, Jansen VAA, van Gool E, van Baalen M (2005) Global persistence despite local extinction in acarine predator–prey systems: lessons from experimental and mathematical exercises. Adv Ecol Res 37:183–220\nUnderwood N (2007) Variation in and correlation between intrinsic rate of increase and carrying capacity. Am Nat 169:136–141\nUnderwood N (2009) Effect of genetic variance in plant quality on the population dynamics of a herbivorous insect. J Anim Ecol 78:839–847\nUtsumi S, Nakamura M, Ohgushi T (2009) Community consequences of herbivore-induced bottom-up trophic cascades: the importance of resource heterogeneity. J Anim Ecol 78:953–963\nvan de Klashorst G, Readshaw JL, Sabelis MW, Lingeman R (1992) A demonstration of asynchronous local cycles in an acarine predator–prey system. Exp Appl Acarol 14:185–199\nWalde SJ (1995) How quality of host plant affects a predator–prey interaction in biological control. Ecology 76:1206–1219\nZemek R, Nachman G (1998) Interactions in a tritrophic acarine predator–prey metapopulation system: effects of Tetranychus urticae on the dispersal rates of Phytoseiulus persimilis (Acarina: Tetranychidae, Phytoseiidae). Exp Appl Acarol 22:259–278",{"VOID":235},"10.1007\u002Fs10493-010-9410-8","PUBLICATION","VERIFIED","2024-06-26T21:17:50.872+00:00","Auto Verify","https:\u002F\u002Flink.springer.com\u002Farticle\u002F10.1007\u002Fs10493-010-9410-8",[242],{"id":243,"sortIndex":100,"researcher":24,"roles":244,"affiliations":246,"properties":268,"displayName":270,"givenName":24,"familyName":24},"bf30a5a2-e8b3-4a44-9021-f961fa1da8ce",[245],"AUTHOR",[247,258],{"id":248,"sortIndex":100,"affiliation":249,"properties":255},"c0b75281-cc6d-4911-81a8-56ce5b9ee6b8",{"id":248,"createTime":24,"updateTime":24,"relativeEntities":250,"slug":24,"properties":251,"entityType":24,"verifyStatus":24,"verifyTime":24,"verifyNote":24,"languages":24,"translateLanguages":24,"viewCount":24,"url":24,"parentIds":254,"statistic":24},[],{"title":252},{"VI":253},"Department of Integrative Biology, University of California, Berkeley, United States",[],{"title":256},{"VI":257},"Department of Integrative Biology, University of California, Berkeley, USA",{"id":259,"sortIndex":260,"affiliation":261,"properties":267},"16a6ef51-d583-4cb2-8167-766c7509b244",1,{"id":259,"createTime":24,"updateTime":24,"relativeEntities":262,"slug":24,"properties":263,"entityType":24,"verifyStatus":24,"verifyTime":24,"verifyNote":24,"languages":24,"translateLanguages":24,"viewCount":24,"url":24,"parentIds":266,"statistic":24},[],{"title":264},{"VI":265},"Department of Entomology, University of California, Riverside, USA",[],{},{"title":269},{"VI":270},"Matthew P. 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were commenced to study the potential use of the fungi, Beauveria bassiana, Metarhizium anisopliae, and the attraction-aggregation-attachment pheromone (AAAP) for the control of Ambloyomma variegatum as an environmentally friendly technology. The objective of the study was to develop and test a device, which could be used for pheromone and carbon dioxide delivery and infection of ticks with the fungi in an attempt to control the tick populations in the vegetation. Using a pheromone-baited device treated with the fungi mixture, 79% of the ticks released were attracted and exposed to the fungi and of these, 78% died during incubation in the laboratory. In another set of experiments, of the released ticks that were similarly exposed to fungi using the pheromone-baited device and left in the vegetation, 33.8% were recovered compared to recoveries of between 76 and 84% in the controls. These results were significantly different at the 5% level, an indication that the pheromone\u002Ffungi mixtures had significant effect in reducing the tick population in the field.",{"EN":347},"Performance of a Prototype Baited-trap in Attracting and Infecting the Tick Amblyomma variegatum (Acari: Ixodidae) in Field Experiments",{"VOID":349},"[\"9924433673180303065\"]",{"VOID":351},"N. Barré G.I. Garris O. Lorvelec (1997) ArticleTitleField sampling of the tick Amblyomma variegatum (Acari: Ixodidae) on pastures in Guadeloupe; attraction of CO2 and\u002For tick pheromone and conditions of use Exp. Appl. Acarol. 21 95–108 Occurrence Handle9080680\nH.D. Burgess N.W. Hussey (1971) Microbial Control of Insects and Mites Academic press New York\u002FLondon\nW.J. Gladney S.E. Ernst R.R. Grabbe (1974) ArticleTitleThe aggregation response of the Gulf Coast ticks on cattle Ann. Entomol. Soc. Am. 67 750–752\nE. Hess J.J. DeCastro (1986) ArticleTitleField tests of the response of female Amblyomma variegatum (Acari: Ixodidae) to the synthetic aggregation-attachment pheromone and its components Exp. Appl. Acarol. 2 249–255 Occurrence Handle10.1007\u002FBF01193957 Occurrence Handle1:CAS:528:DyaL28XmtVCks78%3D Occurrence Handle3451866\nG.P. Kaaya (1989) ArticleTitle Glossina morsitans morsitans. Mortalities caused in adults by experimental infection with entomopathogenic fungi Acta Trop. 46 107–114 Occurrence Handle1:STN:280:BiaB3crit1Y%3D Occurrence Handle2565071\nG.P. Kaaya K.V. Seshu-Reddy E.D. Kokwaro D.M. Munyinyi (1993) ArticleTitlePathogenicity of Beauveria bassiana, Metarhizium anisopliae and Serrata marcescens to the banana weevil, Cosmopolites sordidus Biocon. Sci. Technol. 3 177–187\nG.P. Kaaya E.N. Mwangi E.A. Ouna (1996) ArticleTitleProspects for biological control of livestock ticks, Rhipicephalus appendiculatus and Amblyomma variegatumusing entomogenous fungi Beauveria bassiana and Metarhizum anisopliae J. Invert. Pathol. 67 15–20 Occurrence Handle10.1006\u002Fjipa.1996.0003 Occurrence Handle1:STN:280:BymH3M7osVw%3D\nG.P. Kaaya S.M. Hassan (2000) ArticleTitleEntomogenous fungi as promising bio-pesticides for tick control Exp. Appl. Acarol. 24 913–923 Occurrence Handle10.1023\u002FA:1010722914299\nR.O. Maranga A. Hassanali G.P. Kaaya J.M. Mueke (2003) ArticleTitleAttraction of Amblyomma variegatum (ticks) to the attraction-aggregation-attachment pheromone with or without carbon dioxide Exp. Appl. Acarol. 29 121–130 Occurrence Handle10.1023\u002FA:1024265529030 Occurrence Handle1:CAS:528:DC%2BD3sXks1Oksro%3D Occurrence Handle14580064\nR.O. Maranga G.P. Kaaya J.M. Mueke A. Hassanali (2005) ArticleTitleEffects of combining the fungi Beauvetia bassiana and Metarhizium anisopliae on the mortality of the tick Amblyomma variegatum (Ixodidae) in relation to seasonal changes Mycopathologia 159 IssueID4 527–532 Occurrence Handle10.1007\u002Fs11046-005-3374-y Occurrence Handle1:STN:280:DC%2BD2Mzjt1Gqtg%3D%3D Occurrence Handle15983739\nR.A.I. Norval C.E. Yunker J.F. Butler (1987) ArticleTitleField sampling of unfed adults of Amblyomma hebraeum Koch Exp. Appl. Acarol. 3 213–217 Occurrence Handle10.1007\u002FBF01270457 Occurrence Handle1:STN:280:BieB1czjt1I%3D Occurrence Handle3135161\nR.A.I. Norval J.F. Butler C.E. Yunker (1989a) ArticleTitleUse of carbon dioxide and natural or synthetic aggregation-attachment pheromone of the bont tick, Amblyomma hebraeum to attract and trap unfed adults in the field Exp. Appl. Acarol. 7 171–180 Occurrence Handle10.1007\u002FBF01194058\nR.A.I. Norval H.R. Andrew C.E. Yunker (1989b) ArticleTitlePheromone mediation of host selection in bont tick, Amblyomma hebraeum (Koch) Science 243 364–365 Occurrence Handle1:STN:280:BiaC3c%2Fisl0%3D\nR.A.I. Norval C.E. Yunker I.M. Duncan T. Peter (1991) ArticleTitlePheromone\u002Facaricide mixtures in the control of the tick Amblyomma hebraeum: effects of acaricides on attraction and attachment Exp. Appl. Acarol. 11 233–240 Occurrence Handle10.1007\u002FBF01246095 Occurrence Handle1:CAS:528:DyaK3MXltlSjsrc%3D Occurrence Handle1893800\nNorval R.A.I., Sonenshine D.E., Meltzer M.I. and Burridge M.J. 1994. Attractant Decoy for Controlling Bont Ticks. US Patent OfficeWashington, D.C. United States patent number 5,296,227.\nR.A.I. Norval D.E. Sonenshine S.A. Allan M.J. Burridge (1996) ArticleTitleEfficacy of pheromone-acaricide impregnated tail-tag decoys for controlling the bont tick, Amblyomma hebraeum (Acari: Ixodidae), on cattle in Zimbabwe Exp. Appl. Acarol. 20 31–46 Occurrence Handle10.1007\u002FBF00052810 Occurrence Handle1:CAS:528:DyaK28Xhs1yrs7w%3D Occurrence Handle8746132\nY. Rechav G.B. Whitehead (1978) ArticleTitleField trials with pheromone-acaricide mixtures for Amblyomma hebraeum (Acarina:Ixodidae) J. Econ. Entomol. 71 150–151\nInstitutionalAuthorNameSAS Institute Inc. (1988) SAS\u002FSTAT User’s GuideRelease 60.3 Edition SAS Institute Inc Cary, NC\nR. Schöni E. Hess W. Blum K. Ramstein (1984) ArticleTitleThe aggregation-attachment pheromone of the tropical boat tick Amblyomma variegatumFabricius (Acari: Ixodoidea): isolation, identification and action of its components J. Insect. Physiol. 30 613–618",{"VOID":353},"10.1007\u002Fs10493-006-0002-6","2024-06-23T11:09:39.260+00:00","https:\u002F\u002Flink.springer.com\u002Farticle\u002F10.1007\u002Fs10493-006-0002-6",[357,372,387,405],{"id":358,"sortIndex":100,"researcher":24,"roles":359,"affiliations":360,"properties":369,"displayName":371,"givenName":24,"familyName":24},"799316aa-d791-4a72-b31f-7af51239db9b",[245],[361],{"id":362,"sortIndex":100,"affiliation":363,"properties":24},"0272ae28-e4f4-4521-a972-6eabf011d0eb",{"id":362,"createTime":24,"updateTime":24,"relativeEntities":364,"slug":24,"properties":365,"entityType":24,"verifyStatus":24,"verifyTime":24,"verifyNote":24,"languages":24,"translateLanguages":24,"viewCount":24,"url":24,"parentIds":368,"statistic":24},[],{"title":366},{"VI":367},"Department of Zoology, Jomo Kenyatta University of Agriculture and Technology, Nairobi, Kenya",[],{"title":370},{"VI":371},"R. O. Maranga",{"id":373,"sortIndex":260,"researcher":24,"roles":374,"affiliations":375,"properties":384,"displayName":386,"givenName":24,"familyName":24},"0cdae8d8-823a-45b2-992c-089d2d22ff5a",[245],[376],{"id":377,"sortIndex":100,"affiliation":378,"properties":24},"996e330c-7c55-462d-ad47-66e45e639cf2",{"id":377,"createTime":24,"updateTime":24,"relativeEntities":379,"slug":24,"properties":380,"entityType":24,"verifyStatus":24,"verifyTime":24,"verifyNote":24,"languages":24,"translateLanguages":24,"viewCount":24,"url":24,"parentIds":383,"statistic":24},[],{"title":381},{"VI":382},"The International Centre of Insect Physiology and Ecology (ICIPE), Nairobi, Kenya",[],{"title":385},{"VI":386},"A. Hassanali",{"id":388,"sortIndex":389,"researcher":24,"roles":390,"affiliations":391,"properties":400,"displayName":402,"givenName":24,"familyName":24},"a5d2bd63-f640-4d4a-bfcc-67e4cb3cd1bb",2,[245],[392],{"id":393,"sortIndex":100,"affiliation":394,"properties":24},"e9eb0d2f-60f1-494c-a5e9-60f8b1d39437",{"id":393,"createTime":24,"updateTime":24,"relativeEntities":395,"slug":24,"properties":396,"entityType":24,"verifyStatus":24,"verifyTime":24,"verifyNote":24,"languages":24,"translateLanguages":24,"viewCount":24,"url":24,"parentIds":399,"statistic":24},[],{"title":397},{"VI":398},"Department of Biology, University of Namibia, Windhoek, Namibia",[],{"title":401,"gsAuthor":403},{"VI":402},"G. P. Kaaya",{"VOID":404},"[\"Qcyoks4AAAAJ\"]",{"id":406,"sortIndex":198,"researcher":24,"roles":407,"affiliations":408,"properties":417,"displayName":419,"givenName":24,"familyName":24},"7d535281-a2dc-448f-bdbc-06f34b7e05c8",[245],[409],{"id":410,"sortIndex":100,"affiliation":411,"properties":24},"27c99c91-1894-490d-a436-85929a9b9b2b",{"id":410,"createTime":24,"updateTime":24,"relativeEntities":412,"slug":24,"properties":413,"entityType":24,"verifyStatus":24,"verifyTime":24,"verifyNote":24,"languages":24,"translateLanguages":24,"viewCount":24,"url":24,"parentIds":416,"statistic":24},[],{"title":414},{"EN":415},"Department of Biological Sciences, Kenyatta University, Nairobi, Kenya",[],{"title":418},{"VI":419},"J. M. Mueke",{"url":355,"publisher":421,"properties":472},{"id":6,"createTime":7,"updateTime":8,"relativeEntities":422,"slug":10,"properties":423,"entityType":22,"verifyStatus":23,"verifyTime":24,"verifyNote":24,"languages":24,"translateLanguages":24,"viewCount":25,"subjectFields":428,"manageAffiliations":441,"indexDatabases":452,"url":98,"thumbnailPath":24,"statistic":467,"gsStatistic":24,"type":24,"analyzePriority":24},[],{"country":424,"eissn":425,"issn":426,"title":427},{"VOID":13},{"VOID":15},{"VOID":17},{"EN":19},[429,433,437],{"id":28,"createTime":24,"updateTime":24,"relativeEntities":430,"label":431,"description":432,"parentId":24,"standard":24,"scholarHubFieldId":24},[],{"EN":31},{},{"id":34,"createTime":24,"updateTime":24,"relativeEntities":434,"label":435,"description":436,"parentId":24,"standard":24,"scholarHubFieldId":24},[],{"EN":37},{},{"id":40,"createTime":24,"updateTime":24,"relativeEntities":438,"label":439,"description":440,"parentId":24,"standard":24,"scholarHubFieldId":24},[],{"EN":43},{},[442,447],{"id":47,"createTime":24,"updateTime":24,"relativeEntities":443,"slug":24,"properties":444,"entityType":24,"verifyStatus":24,"verifyTime":24,"verifyNote":24,"languages":24,"translateLanguages":24,"viewCount":24,"url":24,"parentIds":446,"statistic":24},[],{"title":445},{"EN":51},[],{"id":54,"createTime":24,"updateTime":24,"relativeEntities":448,"slug":24,"properties":449,"entityType":24,"verifyStatus":24,"verifyTime":24,"verifyNote":24,"languages":24,"translateLanguages":24,"viewCount":24,"url":24,"parentIds":451,"statistic":24},[],{"title":450},{"EN":58},[60],[453,460],{"id":63,"indexDatabase":454,"url":74,"indexYears":75,"academicFieldIds":459,"indexDatabaseRanking":80},{"id":65,"createTime":24,"updateTime":24,"relativeEntities":455,"label":456,"description":457,"key":71,"publicationTags":458,"standard":24},[],{"EN":68,"VI":68},{"EN":68,"VI":70},[73],[77,78,79],{"id":82,"indexDatabase":461,"url":95,"indexYears":24,"academicFieldIds":466,"indexDatabaseRanking":24},{"id":84,"createTime":24,"updateTime":24,"relativeEntities":462,"label":463,"description":464,"key":91,"publicationTags":465,"standard":24},[],{"EN":87,"VI":87},{"EN":89,"VI":90},[93,94],[97],{"impactFactor":100,"impactFactorByYear":468,"i10Index":114,"i10IndexLast5Year":115,"totalPublication":116,"totalPublicationByYear":469,"totalCitation":148,"totalCitationByYear":470,"totalCitationPerPublication":181,"totalCitationPerPublicationByYear":471,"hindexLast5Year":127,"hindex":127},{"1993":102,"2012":103,"2013":104,"2014":105,"2015":106,"2016":107,"2017":108,"2018":109,"2019":110,"2020":111,"2021":112,"2022":107,"2023":113},{"1985":118,"1986":119,"1987":120,"1988":121,"1989":122,"1990":123,"1991":124,"1992":125,"1993":126,"1994":127,"1995":128,"1996":129,"1997":127,"1998":130,"1999":131,"2000":132,"2001":133,"2002":134,"2003":133,"2004":135,"2005":136,"2006":137,"2007":124,"2008":134,"2009":138,"2010":139,"2011":126,"2012":140,"2013":141,"2014":142,"2015":143,"2016":139,"2017":144,"2018":144,"2019":145,"2020":141,"2021":144,"2022":146,"2023":147,"2024":118},{"1985":150,"1986":151,"1987":152,"1988":153,"1989":154,"1990":155,"1991":156,"1992":157,"1993":158,"1994":159,"1995":160,"1996":114,"1997":161,"2002":162,"2003":163,"2004":164,"2005":165,"2006":166,"2007":167,"2008":168,"2009":169,"2010":170,"2011":171,"2012":172,"2013":156,"2014":173,"2015":174,"2016":175,"2017":176,"2018":177,"2019":178,"2020":150,"2021":179,"2022":180,"2023":25},{"1985":183,"1986":184,"1987":185,"1988":186,"1989":187,"1990":188,"1991":189,"1992":190,"1993":191,"1994":192,"1995":193,"1996":194,"1997":195,"2002":196,"2003":197,"2004":198,"2005":199,"2006":200,"2007":201,"2008":202,"2009":181,"2010":203,"2011":204,"2012":203,"2013":205,"2014":206,"2015":207,"2016":193,"2017":208,"2018":209,"2019":210,"2020":211,"2021":212,"2022":213,"2023":214},{"pages":473,"volume":475},{"VOID":474},"211-218",{"VOID":476},"38",39,{"total":477,"publishYear":479,"statisticByYear":480},2006,{"2006":260,"2007":389,"2008":481,"2009":198,"2010":482,"2011":260,"2012":389,"2013":389,"2015":260,"2016":198,"2017":389,"2019":260,"2020":389,"2022":389,"2023":260,"2024":198,"2025":198},4,6,"2006-02-01","DONE_ANALYZE_CITATION",[80,93],{"id":487,"createTime":488,"updateTime":489,"relativeEntities":490,"slug":491,"properties":492,"entityType":236,"verifyStatus":237,"verifyTime":503,"verifyNote":239,"languages":24,"translateLanguages":24,"viewCount":100,"primaryUrl":504,"fullTextUrl":24,"authors":505,"publicationType":271,"publisherRelationship":534,"citationCount":100,"citationInfo":591,"publishDate":594,"publishYear":592,"citationAnalyzeStatus":333,"lastCitationAnalyze":595,"indexDatabases":596,"openAccess":24,"references":24,"isForceReanalyzing":336},"2593dd59-296e-4441-811c-063ad7983e7b","2024-01-03T08:18:59.387+00:00","2026-07-29T11:19:03.751+00:00",[],"Observations-onColeoscirus-simplex-Acarina-Prostigmata-a-predatory-mite-that-colonizes-greenhouse-cultures-of-rootknot-nematode-Meloidogyne-spp-and-a-review-of-feeding-behavior-in-the-Cunaxidae",{"abstract":493,"title":495,"gsPaper":497,"references":499,"doi":501},{"EN":494},"\nColeoscirus simplex (Ewing) · (Cunaxidae: Coleoscirinae) colonizes greenhouse pot cultures of rootknot nematodes (Meloidogyne spp.) in Orlando, Florida, where it preys on vermiform nematodes and soil arthropods. This is the first report of nematophagy in a cunaxid mite. Mating was required for oviposition inC. simplex. An average of 4.4 eggs were laid per day, and mean generation time was 14.3 days at 28°C. A silken web was spun around the mite and the end of each active instar.Coleoscirus simplex fed near the top of the food web that colonized rootknot nematode cultures, but feeding relationships were complex. Size, degree of sclerotization, speed, and availability of alternative prey influenced predatory success. Cannibalism was common, including attacks on quiescent immatures in the molting web.Coleoscirus simplex did not feed on the eggs of either rootknot nematodes or arthropods. \nNeoscirula sp. (Coleoscirinae) andPulaeus sp. (Cunaxoidinae) also fed on both arthropods and nematodes, but three species in the Cunaxinae,Dactyloscirus inermis (Tragardh),Dactyloscirus sp., andCunaxa sp., fed only on arthropods.",{"EN":496},"Observations onColeoscirus simplex (Acarina: Prostigmata), a predatory mite that colonizes greenhouse cultures of rootknot nematode (Meloidogyne spp.), and a review of feeding behavior in the Cunaxidae",{"VOID":498},"[\"10094881553606114160\"]",{"VOID":500},"Barron, G.L., 1977. The Nematode Destroying Fungi. Topics in Mycobiology, Volume 1. Canadian Biological Publications, Guelph, Ontario.\nDen Heyer, J., 1981. Systematics of the family Cunaxidae Thor, 1902 (Actinedida: Acarida). Univ. North, Pietersburg, S. Afr., Publ. Ser. A24.\nDen Heyer, J. and Ryke, P.A.J., 1970. The mite complex and associated insects on citrus trees at Zebediela. Wet. Bydr. P.U. C.H.O. Reeks B: Natuurwet., 32: 1–23.\nHuettel, R.N., 1985. Carrot disc culture. In: N.M., Zuckerman, W.F. Mai and M.B. Harrison (Editors), Plant Nematology Laboratory Manual. Univ. of Massachusetts, Amherst, pp. 153–154.\nHuey, R.B. and Pianka, E.R., 1981. Ecological consequences of foraging mode. Ecology, 62: 991–999.\nHussey, R.S. and Barker, K.R., 1973. A comparison of methods of collecting inocula ofMeloidogyne spp., including a new technique. Plant Dis. Rep., 57: 1025–1028.\nKoenning, S.R. and Barker, K.R., 1985. Gnotobiotic techniques for plant-parasitic nematodes. In: K.R. Barker, C.C. Carter and J.N. Sasser, (Editors), An Advanced Treatise onMeloidogyne. Volume II: Methodology. North Carolina State University, Raleigh, pp. 49–66.\nO'Brien, W.J., Browman, H.I. and Evans, B.I., 1990. Search strategies of foraging animals. Am. Sci., 78: 152–160.\nPolis, G.A., Myers, C.A. and Holt, R.D., 1989. The ecology and evolution of intraguild predation: Potential competitors that each each other. Annu. Rev. Ecol. Syst., 20: 297–330.\nPugh, P.J.A. and King, P.E., 1985. Feeding in intertidal Acari. J. Exp. Mar. Biol. Ecol., 94:269–280.\nRosen, D. and Huffaker, C.B., 1983. An overview of desired attributes of effective biological control agents, with particular emphasis on mites. In: M.A. Hoy, G.L. Cunningham and L. Knutson (Editors), Biological Control of Pests by Mites. Univ. of Calif., Berkeley, Spec. Publ., 3304: 2–11.\nSasser, J.N. and Carter, C.C., 1985. An advanced treatise onMeloidogyne. Volume I: Biology and control. North Carolina State University, Raleigh.\nSchruft, G., 1971.Haleupalus olivveri nov. spec., eine Dornpalpenmilbe an Reben (Vitis spec.). Dtsch. Entomol. Z., 18: 377–382.\nSmiley, R.L., 1975. A generic revision of the mites of the family Cunaxidae (Acarina). Ann. Entomol. Soc. Am., 68: 227–244.\nSnetsinger, R., 1956. Biology ofBdella depressa, a predaceous mite. J. Econ. Entomol., 49: 745–746.\nSorensen, J.T., Kinn, D.N. and Doutt, R.L., 1983. Biological observations onBdella longicornis: A predatory mite in California vineyards (Acari: Bdellidae). Entomogrpahy, 2: 297–305.\nWalter, D.E., 1988. Nematophagy by soil arthropods from the shortgrass steppe, Chihuahuan desert, and Rocky mountains of the central United States. Agric. Ecosyst. Environ. 24: 307–316.\nWalter, D.E. and Ikonen, E.K., 1989. Species, guilds and functional groups: Taxonomy and behavior in nematophagous arthropods. J. Nematol., 21: 315–327.\nWalter, D.E., Kethley, J. and Moore, J.C., 1987. A heptane flotation method for recovering microarthropods from semiarid soils, with comparison to the Merchant-Crossley hrgh-gradient extraction method and estimates of microarthropod biomass. Pedobiologia, 30: 221–232.\nWalter, D.E., Hunt, H.W. and Elliot, E.T., 1988. Guilds or functional groups? An analysis of predatory arthropods from a shortgrass prairie soil. Pedobiologia, 31: 247–260.\nZaher, M.A., Soliman, Z.R. and El-Bishlawy, S.M., 1975. Feeding habits of the predaceous mite,Cunaxa capreolus [Acarina: Cunaxidae]. Entomophaga, 20: 209–212.",{"VOID":502},"10.1007\u002FBF01204399","2024-06-23T10:59:33.938+00:00","https:\u002F\u002Flink.springer.com\u002Farticle\u002F10.1007\u002FBF01204399",[506,521],{"id":507,"sortIndex":100,"researcher":24,"roles":508,"affiliations":509,"properties":518,"displayName":520,"givenName":24,"familyName":24},"e4bf816c-a1aa-4450-bfcd-607da9ba4ea7",[245],[510],{"id":511,"sortIndex":100,"affiliation":512,"properties":24},"355723a1-19b3-4b9f-a810-128f59b08c84",{"id":511,"createTime":24,"updateTime":24,"relativeEntities":513,"slug":24,"properties":514,"entityType":24,"verifyStatus":24,"verifyTime":24,"verifyNote":24,"languages":24,"translateLanguages":24,"viewCount":24,"url":24,"parentIds":517,"statistic":24},[],{"title":515},{"VI":516},"Agricultural Research Service, U.S. Horticultural Research Laboratory, U.S. Department of Agriculture, Orlando, USA",[],{"title":519},{"VI":520},"David Evans Walter",{"id":522,"sortIndex":260,"researcher":24,"roles":523,"affiliations":524,"properties":531,"displayName":533,"givenName":24,"familyName":24},"7ab11872-5b05-49e2-bc5e-93366575fa5b",[245],[525],{"id":511,"sortIndex":100,"affiliation":526,"properties":24},{"id":511,"createTime":24,"updateTime":24,"relativeEntities":527,"slug":24,"properties":528,"entityType":24,"verifyStatus":24,"verifyTime":24,"verifyNote":24,"languages":24,"translateLanguages":24,"viewCount":24,"url":24,"parentIds":530,"statistic":24},[],{"title":529},{"VI":516},[],{"title":532},{"VI":533},"David T. Kaplan",{"url":504,"publisher":535,"properties":586},{"id":6,"createTime":7,"updateTime":8,"relativeEntities":536,"slug":10,"properties":537,"entityType":22,"verifyStatus":23,"verifyTime":24,"verifyNote":24,"languages":24,"translateLanguages":24,"viewCount":25,"subjectFields":542,"manageAffiliations":555,"indexDatabases":566,"url":98,"thumbnailPath":24,"statistic":581,"gsStatistic":24,"type":24,"analyzePriority":24},[],{"country":538,"eissn":539,"issn":540,"title":541},{"VOID":13},{"VOID":15},{"VOID":17},{"EN":19},[543,547,551],{"id":28,"createTime":24,"updateTime":24,"relativeEntities":544,"label":545,"description":546,"parentId":24,"standard":24,"scholarHubFieldId":24},[],{"EN":31},{},{"id":34,"createTime":24,"updateTime":24,"relativeEntities":548,"label":549,"description":550,"parentId":24,"standard":24,"scholarHubFieldId":24},[],{"EN":37},{},{"id":40,"createTime":24,"updateTime":24,"relativeEntities":552,"label":553,"description":554,"parentId":24,"standard":24,"scholarHubFieldId":24},[],{"EN":43},{},[556,561],{"id":47,"createTime":24,"updateTime":24,"relativeEntities":557,"slug":24,"properties":558,"entityType":24,"verifyStatus":24,"verifyTime":24,"verifyNote":24,"languages":24,"translateLanguages":24,"viewCount":24,"url":24,"parentIds":560,"statistic":24},[],{"title":559},{"EN":51},[],{"id":54,"createTime":24,"updateTime":24,"relativeEntities":562,"slug":24,"properties":563,"entityType":24,"verifyStatus":24,"verifyTime":24,"verifyNote":24,"languages":24,"translateLanguages":24,"viewCount":24,"url":24,"parentIds":565,"statistic":24},[],{"title":564},{"EN":58},[60],[567,574],{"id":63,"indexDatabase":568,"url":74,"indexYears":75,"academicFieldIds":573,"indexDatabaseRanking":80},{"id":65,"createTime":24,"updateTime":24,"relativeEntities":569,"label":570,"description":571,"key":71,"publicationTags":572,"standard":24},[],{"EN":68,"VI":68},{"EN":68,"VI":70},[73],[77,78,79],{"id":82,"indexDatabase":575,"url":95,"indexYears":24,"academicFieldIds":580,"indexDatabaseRanking":24},{"id":84,"createTime":24,"updateTime":24,"relativeEntities":576,"label":577,"description":578,"key":91,"publicationTags":579,"standard":24},[],{"EN":87,"VI":87},{"EN":89,"VI":90},[93,94],[97],{"impactFactor":100,"impactFactorByYear":582,"i10Index":114,"i10IndexLast5Year":115,"totalPublication":116,"totalPublicationByYear":583,"totalCitation":148,"totalCitationByYear":584,"totalCitationPerPublication":181,"totalCitationPerPublicationByYear":585,"hindexLast5Year":127,"hindex":127},{"1993":102,"2012":103,"2013":104,"2014":105,"2015":106,"2016":107,"2017":108,"2018":109,"2019":110,"2020":111,"2021":112,"2022":107,"2023":113},{"1985":118,"1986":119,"1987":120,"1988":121,"1989":122,"1990":123,"1991":124,"1992":125,"1993":126,"1994":127,"1995":128,"1996":129,"1997":127,"1998":130,"1999":131,"2000":132,"2001":133,"2002":134,"2003":133,"2004":135,"2005":136,"2006":137,"2007":124,"2008":134,"2009":138,"2010":139,"2011":126,"2012":140,"2013":141,"2014":142,"2015":143,"2016":139,"2017":144,"2018":144,"2019":145,"2020":141,"2021":144,"2022":146,"2023":147,"2024":118},{"1985":150,"1986":151,"1987":152,"1988":153,"1989":154,"1990":155,"1991":156,"1992":157,"1993":158,"1994":159,"1995":160,"1996":114,"1997":161,"2002":162,"2003":163,"2004":164,"2005":165,"2006":166,"2007":167,"2008":168,"2009":169,"2010":170,"2011":171,"2012":172,"2013":156,"2014":173,"2015":174,"2016":175,"2017":176,"2018":177,"2019":178,"2020":150,"2021":179,"2022":180,"2023":25},{"1985":183,"1986":184,"1987":185,"1988":186,"1989":187,"1990":188,"1991":189,"1992":190,"1993":191,"1994":192,"1995":193,"1996":194,"1997":195,"2002":196,"2003":197,"2004":198,"2005":199,"2006":200,"2007":201,"2008":202,"2009":181,"2010":203,"2011":204,"2012":203,"2013":205,"2014":206,"2015":207,"2016":193,"2017":208,"2018":209,"2019":210,"2020":211,"2021":212,"2022":213,"2023":214},{"pages":587,"volume":589},{"VOID":588},"47-59",{"VOID":590},"12",{"total":100,"publishYear":592,"statisticByYear":593},1991,{},"1991-09-01","2026-07-29T11:19:03.747+00:00",[80,93],{"id":598,"createTime":599,"updateTime":600,"relativeEntities":601,"slug":602,"properties":603,"entityType":236,"verifyStatus":237,"verifyTime":614,"verifyNote":239,"languages":24,"translateLanguages":24,"viewCount":100,"primaryUrl":615,"fullTextUrl":24,"authors":616,"publicationType":271,"publisherRelationship":647,"citationCount":704,"citationInfo":705,"publishDate":709,"publishYear":706,"citationAnalyzeStatus":333,"lastCitationAnalyze":710,"indexDatabases":711,"openAccess":24,"references":24,"isForceReanalyzing":336},"a6edc04e-c533-4c8b-80bc-f667bb5394e3","2023-12-11T12:11:14.758+00:00","2026-07-27T23:58:46.552+00:00",[],"Tick-infestation-risk-and-Borrelia-burgdorferi-s-l-infection-induced-increase-in-host-finding-efficacy-of-female-Ixodes-ricinus-under-natural-conditions",{"abstract":604,"title":606,"gsPaper":608,"references":610,"doi":612},{"EN":605},"An investigation of the risk of human tick infestation, together with the prevalence of Borrelia burgdorferi s.l. infection, was conducted in a sylvatic habitat in western Germany to provide data needed for future risk-benefit evaluations of acaricides used for clothing impregnation. Additionally, data were collected on behavioural changes in Borrelia burgdorferi s.l.-infected adult female I. ricinus ticks and the possible impact of such changes on host-finding efficacy. The risk of I. ricinus-infestation was determined by collecting from the protective clothing of volunteers and by dragging in known tick-infested sites in the Kühkopf Mountain area, Koblenz, Germany, from June through October 2006. The overall tick infestation rate per person per hour was 7.4 ± 5.5, with the following sex- and stage-specific differences: males 0.32 ± 0.37, females 1.1 ± 1.2, nymphs 3.6 ± 4.4, larvae 2.4 ± 3.5. Concurrent dragging revealed an average 19.4 ± 16.2 times higher infestation rate as well as a markedly lower infection rate with borreliae in adult I. ricinus ticks when compared to ticks collected from exposed human volunteers. Although the difference in infection rates was statistically significant (P \u003C 0.023) only in adult female ticks, our data indicate that B. burgdorferi s.l. infection may increase host-finding efficacy in adult I. ricinus. The overall exposure risk was 1.0 B. burgdorferi s.l.-infected ticks per person per hour of exposure, or 0.25 ticks per 100 m walking distance in the study area.",{"EN":607},"Tick infestation risk and Borrelia burgdorferi s.l. infection-induced increase in host-finding efficacy of female Ixodes ricinus under natural conditions",{"VOID":609},"[\"12717649656623989257\"]",{"VOID":611},"Alekseev AN, Dubinina HV (2000) Abiotic parameters and diel and seasonal activity of Borrelia-infected and uninfected Ixodes persulcatus (Acarina: Ixodidae). J Med Entomol 37:9–15\nAlekseev AN, Jensen PM, Dubinina HV, Smirnova LA, Makrouchina NA, Zharkov SD (2000) Peculiarities of behaviour of taiga (Ixodes persulcatus) and sheep (Ixodes ricinus) ticks (Acarina: Ixodidae) determined by different methods. Folia Parasitol 47:147–153\nBellet-Edimo OR (1997) Importance de la transmission transstadiale et de la transmission transovarienne du spirochète Borrelia burgdorferi (Spirochaetales: Spirochaetaceae) chez la tique Ixodes ricinus (Acari: Ixodidae) dans l`épidemiologie de la borréliose de Lyme. PhD thesis, University of Neuchâtel, Neuchâtel, Switzerland\nCarroll JF, Kramer M (2001) Different activities and footwear influence exposure to host-seeking nymphs of Ixodes scapularis and Amblyomma americanum (Acari: Ixodidae). J Med Entomol 38:596–600\nChavasse DC, Yap HH (1997) Chemical methods for the control of vectors and pests of public health importance. WHO\u002FCTD\u002FWHOPES\u002F97.2. World Health Organization Distribution and Sales, Geneva\nFaulde M, Uedelhoven W (2006) A new clothing impregnation method for personal protection against ticks and biting insects. Int J Med Microbiol 296(Suppl 1):225–229\nFaulde MK, Uedelhoven WM, Malerius M, Robbins RG (2006) Factory-based permethrin impregnation of uniforms: residual activity against Aedes aegypti and Ixodes ricinus in battle dress uniforms worn under field conditions, and cross contamination during the laundering and storage process. Mil Med 171:472–477\nFerquel E, Garnier M, Marie J, Bernede-Bauduin C, Baranton G, Perez-Eid C, Postic D (2006) Prevalence of Borrelia burgdorferi sensu lato and Anaplasmataceae members in Ixodes ricinus ticks in Alsace, a focus of lyme borreliosis endemicity in France. Appl Environ Microbiol 72:3074–3078\nGern L, Humair P-F (2002) Ecology of Borrelia burgdorferi sensu lato in Europe. In: Gray JS, Kahl O, Lane RS, Stanek G (eds) Lyme borreliosis—biology, epidemiology and control. CABI International, pp 149–174\nGinsberg HS, Faulde MK Ticks. In: Urban pests and health. WHO, European Centre for Environment and Health, Bonn Office, Bonn, Germany (in press)\nKipp S, Dorn W, Wilske B, Fingerle V (2006) Heterogeneity in prevalence and genetic diversity of Borrelia burgdorferi sensu lato in Ixodes ricinus ticks collected in different localities in Thuringia, Germany. Int J Med Microbiol 296(Suppl 1):119–121\nLane RS, Steinlein DB, Mun J (2004) Human behaviors elevating exposure to Ixodes pacificus (Acari: Ixodidae) nymphs and their associated bacterial zoonotic agents in a hardwood forest. J Med Entomol 41:239–248\nLieboldt T (2007) Anwendung der Biostoffverordnung bei Borrelienexposition: Auswirkungen auf den Dienstbetrieb der Bundeswehr. Wehrmed Wehrpharm 31:66–69\nMencke N (2006) Acaricidal and repellent properties of permethrin, its role in reducing transmission of vector-borne pathogens. Parassitologia 48:130–140\nRauter C, Oehme R, Diterich I, Engele M, Hartung T (2002) Distribution of clinically relevant Borrelia genospecies in ticks assessed by a novel, single-run, Real-Time PCR. J Clin Microbiol 40:36–43\nRey JL (1998) Moyen actuel de protection contre les maladies transmises par les tiques. Med Mal Infect 28:393–395\nRossbach B, Scharnbacher J, Heinrich K, Mross KG, Letzel S, Egerer E (2005) Influence of permethrin impregnated uniforms to the internal pyrethroid exposure of soldiers during deployment. Arbeitsmed Sozialmed Praeventivmed 3:127\nRothmaler W (1984) Exkursionsflora, vol 2. Volk und Wissen Volkseigener Verlag, Berlin, pp 44–54\nSchreck CE, Mount GA, Carlson DA (1982) Pressurized sprays of permethrin on clothing for personal protection against the lone star tick (Acari: Ixodidae). J Econ Entomol 75:1059–1061\nSnodgrass HL (1992) Permethrin transfer from treated cloth to the skin surface: potential for exposure to humans. J Toxicol Environ Health 35:91–105\nSüss J, Schrader C (2004) Durch Zecken übertragene humanpathogene und bisher als apathogen geltende Mikroorganismen in Europa. Teil I: Zecken und Viren. Bundesgesundheitsbl Gesundheitsforsch Gesundheitsschutz 47:392–404\nSüss J, Fingerle V, Hunfeld K-P, Schrader C, Wilske B (2004) Durch Zecken übertragene humanpathogene und bisher als apathogen geltende Mikroorganismen in Europa. Teil II: Bakterien, Parasiten und Mischinfektionen. Bundesgesundheitsbl Gesundheitsforsch Gesundheitsschutz 47:470–486\nWHO (2001a) Vectors of diseases: hazards and risks for travellers—Part I. WER 25:189–194\nWHO (2001b) Vectors of diseases: hazards and risks for travellers—Part II. WER 26:201–203\nYoung D, Evans S (1998) Safety and efficacy of DEET and permethrin in the prevention of arthropod attack. Mil Med 163:1–7",{"VOID":613},"10.1007\u002Fs10493-008-9131-4","2024-05-13T07:09:51.688+00:00","http:\u002F\u002Flink.springer.com\u002F10.1007\u002Fs10493-008-9131-4",[617,632],{"id":618,"sortIndex":100,"researcher":24,"roles":619,"affiliations":620,"properties":629,"displayName":631,"givenName":24,"familyName":24},"d71bc59d-7007-47a2-b992-f5c358dab12c",[245],[621],{"id":622,"sortIndex":100,"affiliation":623,"properties":24},"537fa1a9-dddb-4c40-a9cc-cf2c49e6ef37",{"id":622,"createTime":24,"updateTime":24,"relativeEntities":624,"slug":24,"properties":625,"entityType":24,"verifyStatus":24,"verifyTime":24,"verifyNote":24,"languages":24,"translateLanguages":24,"viewCount":24,"url":24,"parentIds":628,"statistic":24},[],{"title":626},{"VI":627},"Department of Medical Entomology\u002FZoology, Central Institute of the Federal Armed Forces Medical Service, Koblenz, Germany",[],{"title":630},{"VI":631},"Michael K. Faulde",{"id":633,"sortIndex":260,"researcher":24,"roles":634,"affiliations":635,"properties":644,"displayName":646,"givenName":24,"familyName":24},"81e129ba-0609-4589-91ce-4faf42ad8bee",[245],[636],{"id":637,"sortIndex":100,"affiliation":638,"properties":24},"4f711a00-05e7-47a9-944b-f43cbf560bd2",{"id":637,"createTime":24,"updateTime":24,"relativeEntities":639,"slug":24,"properties":640,"entityType":24,"verifyStatus":24,"verifyTime":24,"verifyNote":24,"languages":24,"translateLanguages":24,"viewCount":24,"url":24,"parentIds":643,"statistic":24},[],{"title":641},{"VI":642},"Defense Pest Management Information Analysis Center, Armed Forces Pest Management Board, Walter Reed Army Medical Center, Washington, USA",[],{"title":645},{"VI":646},"Richard G. Robbins",{"url":615,"publisher":648,"properties":699},{"id":6,"createTime":7,"updateTime":8,"relativeEntities":649,"slug":10,"properties":650,"entityType":22,"verifyStatus":23,"verifyTime":24,"verifyNote":24,"languages":24,"translateLanguages":24,"viewCount":25,"subjectFields":655,"manageAffiliations":668,"indexDatabases":679,"url":98,"thumbnailPath":24,"statistic":694,"gsStatistic":24,"type":24,"analyzePriority":24},[],{"country":651,"eissn":652,"issn":653,"title":654},{"VOID":13},{"VOID":15},{"VOID":17},{"EN":19},[656,660,664],{"id":28,"createTime":24,"updateTime":24,"relativeEntities":657,"label":658,"description":659,"parentId":24,"standard":24,"scholarHubFieldId":24},[],{"EN":31},{},{"id":34,"createTime":24,"updateTime":24,"relativeEntities":661,"label":662,"description":663,"parentId":24,"standard":24,"scholarHubFieldId":24},[],{"EN":37},{},{"id":40,"createTime":24,"updateTime":24,"relativeEntities":665,"label":666,"description":667,"parentId":24,"standard":24,"scholarHubFieldId":24},[],{"EN":43},{},[669,674],{"id":47,"createTime":24,"updateTime":24,"relativeEntities":670,"slug":24,"properties":671,"entityType":24,"verifyStatus":24,"verifyTime":24,"verifyNote":24,"languages":24,"translateLanguages":24,"viewCount":24,"url":24,"parentIds":673,"statistic":24},[],{"title":672},{"EN":51},[],{"id":54,"createTime":24,"updateTime":24,"relativeEntities":675,"slug":24,"properties":676,"entityType":24,"verifyStatus":24,"verifyTime":24,"verifyNote":24,"languages":24,"translateLanguages":24,"viewCount":24,"url":24,"parentIds":678,"statistic":24},[],{"title":677},{"EN":58},[60],[680,687],{"id":63,"indexDatabase":681,"url":74,"indexYears":75,"academicFieldIds":686,"indexDatabaseRanking":80},{"id":65,"createTime":24,"updateTime":24,"relativeEntities":682,"label":683,"description":684,"key":71,"publicationTags":685,"standard":24},[],{"EN":68,"VI":68},{"EN":68,"VI":70},[73],[77,78,79],{"id":82,"indexDatabase":688,"url":95,"indexYears":24,"academicFieldIds":693,"indexDatabaseRanking":24},{"id":84,"createTime":24,"updateTime":24,"relativeEntities":689,"label":690,"description":691,"key":91,"publicationTags":692,"standard":24},[],{"EN":87,"VI":87},{"EN":89,"VI":90},[93,94],[97],{"impactFactor":100,"impactFactorByYear":695,"i10Index":114,"i10IndexLast5Year":115,"totalPublication":116,"totalPublicationByYear":696,"totalCitation":148,"totalCitationByYear":697,"totalCitationPerPublication":181,"totalCitationPerPublicationByYear":698,"hindexLast5Year":127,"hindex":127},{"1993":102,"2012":103,"2013":104,"2014":105,"2015":106,"2016":107,"2017":108,"2018":109,"2019":110,"2020":111,"2021":112,"2022":107,"2023":113},{"1985":118,"1986":119,"1987":120,"1988":121,"1989":122,"1990":123,"1991":124,"1992":125,"1993":126,"1994":127,"1995":128,"1996":129,"1997":127,"1998":130,"1999":131,"2000":132,"2001":133,"2002":134,"2003":133,"2004":135,"2005":136,"2006":137,"2007":124,"2008":134,"2009":138,"2010":139,"2011":126,"2012":140,"2013":141,"2014":142,"2015":143,"2016":139,"2017":144,"2018":144,"2019":145,"2020":141,"2021":144,"2022":146,"2023":147,"2024":118},{"1985":150,"1986":151,"1987":152,"1988":153,"1989":154,"1990":155,"1991":156,"1992":157,"1993":158,"1994":159,"1995":160,"1996":114,"1997":161,"2002":162,"2003":163,"2004":164,"2005":165,"2006":166,"2007":167,"2008":168,"2009":169,"2010":170,"2011":171,"2012":172,"2013":156,"2014":173,"2015":174,"2016":175,"2017":176,"2018":177,"2019":178,"2020":150,"2021":179,"2022":180,"2023":25},{"1985":183,"1986":184,"1987":185,"1988":186,"1989":187,"1990":188,"1991":189,"1992":190,"1993":191,"1994":192,"1995":193,"1996":194,"1997":195,"2002":196,"2003":197,"2004":198,"2005":199,"2006":200,"2007":201,"2008":202,"2009":181,"2010":203,"2011":204,"2012":203,"2013":205,"2014":206,"2015":207,"2016":193,"2017":208,"2018":209,"2019":210,"2020":211,"2021":212,"2022":213,"2023":214},{"pages":700,"volume":702},{"VOID":701},"137-145",{"VOID":703},"44",58,{"total":704,"publishYear":706,"statisticByYear":707},2008,{"2008":260,"2009":198,"2010":708,"2011":389,"2012":260,"2013":482,"2014":260,"2015":708,"2016":481,"2017":708,"2019":260,"2020":260,"2021":260,"2022":708,"2023":389,"2024":198,"2025":260},5,"2008-02-14","2026-07-27T23:58:46.551+00:00",[80,93],{"id":713,"createTime":714,"updateTime":715,"relativeEntities":716,"slug":717,"properties":718,"entityType":236,"verifyStatus":237,"verifyTime":729,"verifyNote":239,"languages":24,"translateLanguages":24,"viewCount":100,"primaryUrl":730,"fullTextUrl":24,"authors":731,"publicationType":271,"publisherRelationship":807,"citationCount":100,"citationInfo":864,"publishDate":867,"publishYear":865,"citationAnalyzeStatus":333,"lastCitationAnalyze":868,"indexDatabases":869,"openAccess":24,"references":24,"isForceReanalyzing":336},"607a1088-accf-4283-813c-28ab16ffcf4b","2024-01-18T21:08:54.693+00:00","2026-07-25T09:13:07.294+00:00",[],"Host-plant-effects-on-the-behaviour-and-performance-of-Amblyseius-swirskii-Acari-Phytoseiidae-",{"abstract":719,"title":721,"gsPaper":723,"references":725,"doi":727},{"EN":720},"Biological control in ornamental crops is challenging due to the wide diversity of crops and cultivars. In this study, we tested the hypothesis that trichome density on different host plants influences the behavior and performance of the predatory mite Amblyseius swirskii Athias-Henriot (Acari: Phytoseiidae). Behavioural observations of this predator in the presence or absence of prey (western flower thrips, Frankliniella occidentalis Pergande) (Thysanoptera: Thripidae) were done on leaf squares of ornamental plant species differing in trichome density (rose, chrysanthemum and gerbera) and compared to a smooth surface (plastic). Tomato leaves were used to observe the influence of glandular trichomes. The performance of A. swirskii was assessed by measuring predation and oviposition rate. Behaviour of A. swirskii was influenced by plant species. Up to a certain density of trichomes, trichome number had a negative effect on walking speed. It was highest on plastic, followed by rose. No differences were found among chrysanthemum, gerbera and tomato. Walking speed was slightly higher on disks without prey. Proportion of time spent walking was the same on leaf disks of all plant species, with and without prey. No effect of glandular trichomes on tomato leaves was seen. Most thrips were killed and consumed on gerbera, and least on rose. Predation rates on chrysanthemum and plastic were intermediate. In contrast, no differences in oviposition rate were found among plant species. The results of this study indicate that trichome density can explain some of the variability in efficacy of A. swirskii on different crops. Release rates of A. swirskii may need to be adjusted depending on the crop in which it is used.",{"EN":722},"Host plant effects on the behaviour and performance of Amblyseius swirskii (Acari: Phytoseiidae)",{"VOID":724},"[\"17875937995956445942\"]",{"VOID":726},"Bell WJ (1990) Searching behavior patterns in insects. Annu Rev Entomol 35:447–467\nBroufas GD, Koveos DS (2000) Effect of different pollens on development, survivorship and reproduction of Euseius finlandicus (Acari: Phytoseiidae). Environ Entomol 29:743–749\nCédola CV, Sánchez NE, Liljesthröm GG (2002) Effect of tomato leaf hairiness on functional and numerical response of Neoseiulus californicus (Acari: Phytoseiidae). Exp Appl Acarol 25:819–831\nCortesero AM, Stapel JO, Lewis WJ (2000) Understanding and manipulating plant attributes to enhance biological control. Biol Control 17:35–47\nde Almeida AA, Janssen A (2013) Juvenile prey induce antipredator behaviour in adult predators. Exp Appl Acarol 59:275–282\nde Clercq P, Mohaghegh J, Tirry L (2000) Effect of host plant on the functional response of the predator Podisus nigrispinus (Heteroptera: Pentatomidae). Biol Control 18:65–70\nEl-Laithy AYM, Fouly AH (1992) Life table parameters of the two phytoseiid predators Amblyseius scutalis (Athias-Henriot) and A. swirskii A.-H. (Acari, Phytoseiidae) in Egypt. J Appl Entomol 113:8–12\nFaraji F, Janssen A, Sabelis MW (2002) Oviposition patterns in a predatory mite reduce the risk of egg predation caused by prey. Ecol Entomol 27(6):660–664\nGnanvossou D, Hanna R, Dicke M (2003) Infochemical-mediated intraguild interactions among three predatory mites on cassava plants. Oecologia 135(1):84–90\nHeinz KM, Parrella MP (1994) Poinsettia (Euphorbia pulcherrima Willd. ex Koltz) cultivar-mediated differences in performance of five natural enemies of Bemisia argentifolii Bellows and Perring, n. sp. (Homoptera: Aleyrodidae). Biol Control 4:305–318\nJanssen A, Willemse E, Van der Hammen T (2003) Poor host plant quality causes omnivore to consume predator eggs. J Anim Ecol 72:478–483\nKrips OE, Kleijn PW, Willems PEL, Gols GJZ, Dicke M (1999) Leaf hairs influence searching efficiency and predation rate of the predatory mite Phytoseiulus persimilis (Acari: Phytoseiidae). Exp Appl Acarol 23:119–131\nLoomans AJM, van Lenteren JC, Tommasini MG, Maini S, Riudavets J (1995) Biological control of thrips pests. Wageningen Agricultural University papers 95-1. Veenman, Wageningen\nLoughner R, Goldman K, Loeb G, Nyrop J (2008) Influence of leaf trichomes on predatory mite (Typhlodromus pyri) abundance in grape varieties. Exp Appl Acarol 45:111–122\nLoughner R, Wentworth K, Loeb G, Nyrop J (2010a) Influence of leaf trichomes on predatory mite density and distribution in plant assemblages and implications for biological control. Biol Control 54:255–262\nLoughner R, Wentworth K, Loeb G, Nyrop J (2010b) Leaf trichomes influence predatory mite densities through dispersal behavior. Entomol Exp Appl 134:78–88\nLoughner R, Nyrop J, Wentworth K, Sanderson J (2011) Effects of supplemental pollen and fibers on canopy abundance of Amblyseius swirskii. IOBC Bull 68:105–109\nMadadi H, Enkegaard A, Brodsgaard HF, Kharrazi-Pakdel A, Mohaghegh J, Ashouri A (2007) Host plant effects on the functional response of Neoseiulus cucumeris to onion thrips larvae. J Appl Entomol 313:728–733\nMesselink GJ, Van Steenpaal SEF, Ramakers PMJ (2006) Evaluation of phytoseiid predators for control of western flower thrips on greenhouse cucumber. Biocontrol 51:753–768\nNomikou M, Janssen A, Schraag R, Sabelis MW (2001) Phytoseiid predators as potential biological control agents for Bemisia tabaci. Exp Appl Acarol 25:271–291\nO’Dowd DJ, Wilson MF (1991) Associations between mites and leaf domatia. Trends Ecol Evol 6:179–182\nOttoni EB (2000) EthoLog 2.2: a tool for the transcription and timing of behavior observation sessions. Behav Res Methods Instrum Comput 32:446–449\nOvermeer WPJ (1985) Rearing and handling. In: Helle W, Sabelis MW (eds) Spider mites: their biology, natural enemies and control. Elsevier, Amsterdam, pp 161–170\nPark HH, Shipp JL, Buitenhuis R (2010) Predation, development, and oviposition by the predatory mite Amblyseius swirkii (Acari: Phytoseiidae) on tomato russet mite (Acari: Eriophyidae). J Econ Entomol 103:563–569\nPrice PW, Bouton CE, Gross P, McPheron BA, Thompson JN, Weis AE (1980) Interactions among three trophic levels: influence of plants on interactions between insect herbivores and natural enemies. Annu Rev Ecol Syst 11:41–65\nRobb KL (1989) Analysis of Frankliniella occidentalis (Pergande) as a pest of floricultural crops in California. University of California, Riverside\nRoda A, Nyrop J, Dicke M, English-Loeb G (2000) Trichomes and spider-mite webbing protect predatory mite eggs from intraguild predation. Oecologia 125:428–435\nRott AS, Ponsonby DJ (2001) Control of two-spotted spider mite Tetranychus urticae Kock (Acari: Tetranychidae) on edible crops in glasshouses using two interacting species of predatory mite. In: Halliday RB, Walter DE, Proctor HC, Norton RA, Colloff MJ (eds) Acarology: proceedings of the 10th international congress. CSIRO Publishing, Melbourne, pp 387–391\nSabelis MW, van Baalen M, Bakker FM, Bruin J, Drukker B, Egas M, Janssen ARM, Lesna IK, Pels B, Van Rijn PCJ, Scutareanu P (1999) The evolution of direct and indirect plant defence against herbivorous arthropods. In: Olff H, Brown VK, Drent RH (eds) Herbivores: between plants and predators. Blackwell Science Ltd., Oxford, pp 109–166\nSAS Institute Inc. (2005) SAS\u002FSTAT user’s guide. SAS Institute, Cary, NC\nScott Brown AS, Simmonds MS, Blaney WM (1999) Influence of species of host plants on the predation of thrips by Neoseiulus cucumeris, Iphiseius degenerans and Orius laevigatus. Entomol Exp Appl 92:283–288\nShipp JL, Boland GJ, Shaw LA (1991) Integrated pest management of disease and arthropod pests of greenhouse vegetable crops in Ontario: current status and future possibilities. Can J Plant Sci 71:887–914\nSkirvin DJ, Fenlon JS (2001) Plant species modifies the functional response of Phytoseiulus persimilis (Acari: Phytoseiidae) to Tetranychus urticae (Acari: Tetranychidae) implications for biological control. Bull Entomol Res 91:61–67\nSouthwood TRE (1986) Plant surfaces and insects—an overview. In: Juniper B, Southwood TRE (eds) Insects and the plant surface. Edward Arnold, London, pp 1–22\nStavrinides MC, Skirvin DJ (2003) The effect of chrysanthemum leaf trichome density and prey spatial distribution on predation of Tetranychus urticae (Acari: Tetranychidae) by Phytoseiulus persimilis (Acari: Phytoseiidae). Bull Entomol Res 93:343–350\nSütterlin S, Van Lenteren JC (1997) Influence of hairiness of Gerbera jamesonii leaves on the searching efficiency of the parasitoid Encarsia formosa. Biol Control 9:157–165\nvan Haren RJF, Steenhuis MM, Sabelis MW, de Ponti OMB (1987) Tomato stem trichomes and dispersal success of Phytoseiulus persimilis relative to its prey Tetranychus urticae. Exp Appl Acarol 3:115–121\nVan Maanen R, Vila E, Sabelis MW, Janssen A (2010) Biological control of broad mites (Polyphagotarsonemus latus) with the generalist predator Amblyseius swirskii. Exp Appl Acarol 52:29–34\nXu X, Enkegaard A (2010) Prey preference of the predatory mite, Amblyseius swirskii between first instar western flower thrips Frankliniella occidentalis and nymphs of the twospotted spider mite Tetranychus urticae. 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influence of plant species on the population dynamics of the spider mite pest, Tetranychus urticae, and its predator, Phytoseiulus persimilis, was examined as a prerequisite to effective biological control on ornamental nursery stock. Experiments have been done to investigate how the development, fecundity and movement of T. urticae, and the movement of P. persimilis were affected by plant species. A novel experimental method, which incorporates plant structure, was used to investigate the functional response of P. persimilis. Development times for T. urticae were consistent with published data and did not differ with plant species in a biologically meaningful way. Plant species was shown to have a major influence on fecundity (P \u003C 0.001) and movement of the pest mite (P \u003C 0.01), but no influence on the movement of the predator. The movement of both pest and predator was shown to be related to the density of the adult pest mites on the plant (P \u003C 0.001). Plant structure affected the functional response, particularly in relation to the ability of the predator to locate prey at low densities. The impact of these findings on the effective use of biological control on ornamental nursery stock is discussed.",{"EN":880},"Differential Effects of Plant Species on a Mite Pest (Tetranychus Urticae) and its Predator (Phytoseiulus Persimilis): Implications for Biological Control",{"VOID":882},"[\"8509022288850055753\"]",{"EN":884},"",{"VOID":886},"10.1023\u002FA:1006150521031","2024-05-02T22:09:32.227+00:00",[889],"EN","https:\u002F\u002Flink.springer.com\u002Farticle\u002F10.1023\u002FA:1006150521031",[892,909],{"id":893,"sortIndex":100,"researcher":24,"roles":894,"affiliations":895,"properties":904,"displayName":908,"givenName":24,"familyName":24},"9237e5bd-6cea-433c-8fd3-97367b840b99",[],[896],{"id":897,"sortIndex":100,"affiliation":898,"properties":24},"d79e6227-79ad-47cf-8e3e-05adf6eb076b",{"id":897,"createTime":24,"updateTime":24,"relativeEntities":899,"slug":24,"properties":900,"entityType":24,"verifyStatus":24,"verifyTime":24,"verifyNote":24,"languages":24,"translateLanguages":24,"viewCount":24,"url":24,"parentIds":903,"statistic":24},[],{"title":901},{"EN":902},"Horticulture Research International, Wellesbourne, Warwick, UK. 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Ecol 46: 249–262.",{"id":24,"text":992,"url":24,"identifiers":24},"Hislop, R.G. and Prokopy, R.J. 1981. Mite predator responses to prey and predator-emitted stimuli. J. Chem. Ecol. 7(5): 895–904.",{"id":24,"text":994,"url":24,"identifiers":24},"Holling, C.S. 1959. Some characteristics of simple types of predation and parasitism. Can. Entomol. 91(7): 385–398.",{"id":24,"text":996,"url":24,"identifiers":24},"Hussey, N.W. and Scopes, N.E.A. 1985. Greenhouse vegetables (Britain). In: Spider Mites — their biology, natural enemies and control, W. Helle and M.W. Sabelis (eds), Vol. 1B, pp. 285–298. Elsevier.",{"id":24,"text":998,"url":24,"identifiers":24},"Hussey, N.W., Parr, W.J. and Gould, H.J. 1965. Observations on the control of Tetranychus urticae Koch on cucumbers by the predatory mite Phytoseiulus riegeli Dosse. Entomol. Exp. Appl. 8: 271–281.",{"id":24,"text":1000,"url":24,"identifiers":24},"Kropczynska, D. and Tomczyk, A. 1996. Development of Tetranychus urticae Koch and Tetranychus cinnabirinus Boisd. populations on sweet pepper and Phytoseiulus persimilis (A-H.) effectiveness in their control. IOBC WPRS Bulletin 19(1): 71–74.",{"id":24,"text":1002,"url":24,"identifiers":24},"McCullagh, P. and Nelder, J.A. 1989. Generalized Linear Models, 2nd edn. Chapman & Hall.",{"id":24,"text":1004,"url":24,"identifiers":24},"Nachman, G. 1981. Temporal and spatial dynamics of an acarine predator-prey system. J. Anim. Ecol. 50: 435–451.",{"id":24,"text":1006,"url":24,"identifiers":24},"Overmeer, W.P.J. 1985. Rearing and handling. In: Spider Mites — their biology, natural enemies and control, W. Helle and M.W. Sabelis (eds), Vol.1B, pp. 161–170. Elsevier.",{"id":24,"text":1008,"url":24,"identifiers":24},"Rabbinge, R. and Hoy, M.A. 1980. A population model for two-spotted spider mite Tetranychus urticae and its predator Metaseiulus occidentalis. Entomol. Exp. Appl. 28: 64–81.",{"id":24,"text":1010,"url":24,"identifiers":24},"Ryoo, M.I. 1986. Studies on the basic components of the predation of Phytoseiulus persimilis Athias-Henriot (Acarina: Phytoseiidae). Res. Popul. Ecol. 28: 17–26.",{"id":24,"text":1012,"url":24,"identifiers":24},"Sabelis, M.W. 1981. Biological control of two-spotted spider mites using phytoseiid predators Part I. Agricultural Research Reports 910. Pudoc, Wageningen.",{"id":24,"text":1014,"url":24,"identifiers":24},"Sabelis M.W. 1985. Predation on spider mites. In: Spider Mites — their biology, natural enemies and control, W. Helle and M.W. Sabelis (eds), Vol.1B, pp. 103–130. Elsevier.",{"id":24,"text":1016,"url":24,"identifiers":24},"Sabelis, M.W. and Van de Baan, H.E. 1983. Location of distant spider mite colonies by phytoseiid predators: demonstration of specific kairomones emitted by Tetranychus urticae and Panonychus ulmi. Entomol. Exp. and Appl. 33: 303–314.",{"id":24,"text":1018,"url":24,"identifiers":24},"Sabelis, M.W. and van der Weel, J.J. 1993. Anemotactic responses of the predatory mite Phytoseiulus persimilis Athias-Henriot, and their role in prey finding. Exp. Appl. Acarol. 17: 521–529.",{"id":24,"text":1020,"url":24,"identifiers":24},"Sabelis, M.W., Vermaat, J.E. and Groeneveld, A. 1984. Arrestment responses of the predatory mite, Phytoseiulus persimilis, to steep odour gradients of a kairomone. Physiol. Entomol. 9: 437–446.",{"id":24,"text":1022,"url":24,"identifiers":24},"Takafuji, A. and Chant, D.A. 1976. Comparative studies of two species of predacious phytoseiid mites (Acarina: Phytoseiidae), with special reference to their responses to the density of their prey. Res. Popul. Ecol. 17: 255–310.",{"id":24,"text":1024,"url":24,"identifiers":24},"Van de Vrie, M. 1985. Greenhouse ornamentals. In: Spider Mites — their biology, natural enemies and control, W. Helle and M.W. 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The aims of this study were to determine whether certain crops constitute overwintering sites for the Argentine strain of the predator Neoseiulus californicus and whether females underwent reproductive diapause in winter. Neoseiulus californicus was recorded monthly on the vegetables tomato, sweet pepper, eggplant, and artichoke, and on strawberry, among other crops in Buenos Aires province, Argentina. This mite was found at a lower percentage of crops in the winter than in the other seasons. Since the predator was quite frequent on artichoke, this crop could constitute a refuge during adverse environmental conditions. The mite’s frequency on several crops in other seasons and potential association with a strawberry pest is discussed. In the laboratory, individuals exposed to winter conditions throughout the life cycle exhibited a long pre-oviposition period and low oviposition rate, but did not diapause. After being kept under winter conditions from larva to adult, when individuals were transferred to the optimal spring temperatures and lighting, the pre-oviposition period was shorter and the fecundity higher than under winter conditions. When individuals remained under spring conditions from larva to adult and were then transferred to the winter parameters during the first 15 days of adulthood, the pre-oviposition period was long and the oviposition rate low. Once the optimal conditions were restored, the daily fecundity became similar to that of the individuals remaining under optimal conditions throughout the life cycle. 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J Acarol Soc Jpn 14:93–103",{"doi":1245},{"id":1265,"text":1266,"url":1267,"identifiers":1268},"963810c2-487e-41ab-a58f-a46024700dfc","Greco N, Liljesthröm G, Sánchez N (1999) Spatial distribution and coincidence of Neoseiulus californicus and Tetranychus urticae (Acari: Phytoseiidae, Tetranychidae) on strawberry. Exp Appl Acarol 23:567–580","https:\u002F\u002Flink.springer.com\u002Farticle\u002F10.1023\u002FA:1006125103981",{"doi":1269},"10.1023\u002FA:1006125103981",{"id":1241,"text":1271,"url":1243,"identifiers":1272},"Greco NM, Sánchez NE, Liljesthröm GG (2005) Neoseiulus californicus (Acari: Phytoseiidae) as a potential control agent of Tetranychus urticae (Acari: Tetranychidae): effect of pest\u002Fpredator ratio on the pest abundance on strawberry. 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Zootaxa 1884:1–35",{"doi":1245},{"id":1241,"text":1283,"url":1243,"identifiers":1284},"Gugole Ottaviano MF (2012) Manejo Integrado de la plaga Tetranychus urticae (Acari: Tetranychidae) en cultivos de frutilla del Cinturón Hortícola Platense. Ph.D. thesis, Universidad Nacional de La Plata, p 198",{"doi":1245},{"id":1241,"text":1286,"url":1243,"identifiers":1287},"Gugole Ottaviano MF, Cédola CV, Sánchez NE, Greco NM (2015) Conservation biological control in strawberry: effect of different pollen on development, survival, and reproduction of Neoseiulus californicus (Acari: Phytoseiidae). Exp Appl Acarol 67:507–521",{"doi":1245},{"id":1289,"text":1290,"url":1291,"identifiers":1292},"a6fd395a-1347-4ac1-8bc7-3f104f226c21","Hart AJ, Bale JS, Tullett AG, Worland MR, Walter K (2002) Effects of temperature on the establishment potential of the predatory mite Amblyseius californicus McGregor (Acari: Phytoseiidae) in the UK. J Insect Physiol 48:593–599","https:\u002F\u002Fwww.sciencedirect.com\u002Fscience\u002Farticle\u002Fpii\u002FS0022191002000872",{"doi":1293},"10.1016\u002Fs0022-1910(02)00087-2",{"id":24,"text":1295,"url":24,"identifiers":1296},"Jolly R (2001) The status of the predatory mite Neoseiulus californicus (McGregor) (Acari: Phytoseiidae) in the UK, and its potential as a biocontrol agent of Panonychus ulmi (Koch) (Acari: Tetranychidae). Ph.D. thesis. University of Birmingham, p 173",{},{"id":1241,"text":1298,"url":1243,"identifiers":1299},"Jung C, Croft BA (2000) Survival and plant-prey finding by Neoseiulus fallacis (Acari: Phytoseiidae) on soil substrates after aerial dispersal. Exp Appl Acarol 24:579–596",{"doi":1245},{"id":1241,"text":1301,"url":1243,"identifiers":1302},"Kawashima M, Jung C (2010) Overwintering sites of the predacious mite Neoseiulus californicus (McGregor) (Acari: Phytoseiidae) in satsuma mandarin orchards on Jeju Island, Korea. 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Annu Rev Entomol 45:175–201",{"doi":1245},{"id":24,"text":1316,"url":24,"identifiers":1317},"McMurtry JA, Flaherty DL (1977) An ecological study of phytoseiid and tetranychid mites on walnut in Tulare County, California. Environ Entomol 6:287–292",{},{"id":1241,"text":1319,"url":1243,"identifiers":1320},"McMurtry JA, Mahr DL, Johnson HG (1976) Geographic races in the predaceous mite, Amblyseius potentillae (Acari: Phytoseiidae). Int J Acarol 2:23–48",{"doi":1245},{"id":1241,"text":1322,"url":1243,"identifiers":1323},"Morewood W (1993) Diapause and cold hardiness of phytoseiid mites (Acarina: Phytoseiidae). Eur J Entomol 90:3–10",{"doi":1245},{"id":1241,"text":1325,"url":1243,"identifiers":1326},"Mori H, Saito Y (1979) Biological control of Tetranychus urticae Koch (Acarina: Tetranychidae) populations by the three species of phytoseiid mites (Acarina: Phytoseiidae). J Fac Agric Hokkaido Univ 59:303–311",{"doi":1245},{"id":1241,"text":1328,"url":1243,"identifiers":1329},"Nyrop JP, Minns JC, Herring CP (1994) Influence of ground cover on dynamics of Amblyseius fallacis Garman (Acarina; Phytoseiidae) in New York apple orchards. Agric Ecosyst Environ 50:61–72",{"doi":1245},{"id":24,"text":1331,"url":24,"identifiers":1332},"Overmeer WPJ (1985) Diapause. In: Helle W, Sabelis MW (eds) Spider mites, their biology, natural enemies and control, vol B. Elsevier, Amsterdam, pp 95–102",{},{"id":1241,"text":1334,"url":1243,"identifiers":1335},"Pielou EC (1984) The interpretation of ecological data. A primer on classification and ordination. Wiley, Hoboken",{"doi":1245},{"id":1241,"text":1337,"url":1243,"identifiers":1338},"Putman WL (1959) Hibernation sites of phytoseiids (Acarina: Phytoseiidae) in Ontario peach orchards. 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J Comp Physiol A 167:201–209",{"doi":1245},{"id":1349,"text":1350,"url":1351,"identifiers":1352},"0ebc9277-b483-4b20-870c-6bb60dbae6a7","van Lenteren JC (2012) The state of commercial augmentative biological control: plenty of natural enemies, but a frustrating lack of uptake. Biocontrol 57:1–20","http:\u002F\u002Flink.springer.com\u002F10.1007\u002Fs10526-011-9395-1",{"doi":1353},"10.1007\u002Fs10526-011-9395-1",{"id":1355,"text":1356,"url":1357,"identifiers":1358},"0c423514-49c2-46e5-806f-c67fc3c6d6f2","Veerman A (1992) Diapause in phytoseiid mites: a review. Exp Appl Acarol 14:1–60","https:\u002F\u002Flink.springer.com\u002Farticle\u002F10.1007\u002FBF01205351",{"doi":1359},"10.1007\u002FBF01205351",{"id":24,"text":1361,"url":24,"identifiers":1362},"Wysoki M, Swirski E (1971) Studies on overwintering of predacious mites of the genera Seiulus Berlese and Phytoseius Ribaga in Israel (Acarina, Phytoseiidae). Israel J Entomol 6:55–70",{},{"id":1241,"text":1364,"url":1243,"identifiers":1365},"Zar HJ (1996) Biostatistical analysis. Prentice-Hall, New Jersey",{"doi":1245},{"id":1367,"createTime":1368,"updateTime":1369,"relativeEntities":1370,"slug":1371,"properties":1372,"entityType":236,"verifyStatus":237,"verifyTime":1383,"verifyNote":239,"languages":24,"translateLanguages":24,"viewCount":100,"primaryUrl":1384,"fullTextUrl":24,"authors":1385,"publicationType":271,"publisherRelationship":1487,"citationCount":24,"citationInfo":24,"publishDate":1544,"publishYear":1545,"citationAnalyzeStatus":23,"lastCitationAnalyze":1546,"indexDatabases":1547,"openAccess":24,"references":24,"isForceReanalyzing":336},"7cb985e2-66bd-440e-8163-edc53850c3e0","2024-01-05T19:02:23.325+00:00","2026-07-22T16:07:34.559+00:00",[],"Effect-of-Tagetes-minuta-essential-oil-on-the-central-nervous-system-of-unfed-Rhipicephalus-sanguineus-sensu-lato-tropical-lineage-ticks",{"abstract":1373,"title":1375,"gsPaper":1377,"references":1379,"doi":1381},{"EN":1374},"Rhipicephalus sanguineus sensu lato ‘tropical lineage’ (Acari: Ixodidae) is considered a sanitary concern due to its role as a disease vector. Tick strains resistant to synthetic acaricides have caused difficulties in their control, besides synthetic acaricides are harmful to the environment and to the health of non-target animals. The research of plants with acaricidal and repellent properties has proved to be an efficient alternative in tick control. The genus Tagetes spp. excels for its use as traditional pest control in households and plantations and also for its potential as an acaricide against R. sanguineus under laboratory conditions. The first aim of the present study was to evaluate the effect of different doses of Tagetes minuta essential oil (TMEO) on the central nervous system (synganglion) in unfed R. sanguineus adults. The histological analysis of synganglion exposed to the different concentrations of TMEO and amitraz 12.5% (50% of the recommended dose in the package insert) showed a significant effect with signs of cell damage including volume increase, loss of shape, and vacuolization, in addition to chromatin alterations such as condensation, margination, and fragmentation. TMEO were analyzed by gas chromatography coupled with mass spectrometry showing the presence of 21 compounds that according to their chemical structure are classified as terpenoids. Among them (Z)-β-ocimene, ocimene, (Z)-tagetone, and verbenone were found in major quantities.",{"EN":1376},"Effect of Tagetes minuta essential oil on the central nervous system of unfed Rhipicephalus sanguineus sensu lato ‘tropical lineage’ ticks",{"VOID":1378},"[\"4902055372067914774\"]",{"VOID":1380},"Adenubi OT, Fasina FO, Mcgaw LJ, Eloff JN, Naidoo V (2016) Plant extracts to control ticks of veterinary and medical importance: a review. South Afr J Bot 105:178–193. https:\u002F\u002Fdoi.org\u002F10.1016\u002Fj.sajb.2016.03.010\nAki T, Nara A, Uemura K (2012) Cytoplasmic vacuolization during exposure to drugs and other substances. Cell Biol Toxicol 28(3):125–131. https:\u002F\u002Fdoi.org\u002F10.1007\u002Fs10565-012-9212-3\nAmbiental Madre Monte. Colombia, Popayán. Available in: https:\u002F\u002Fdigitalrepository.unm.edu\u002Fabya_yala\u002F430\u002F\nAndreotti R, Garcia. MV, Cunha RC, Barros JC (2013) Protective action of Tagetes minuta (Asteraceae) essential oil in the control of Rhipicephalus Microplus (Canestrini, 1887) (Acari: Ixodidae) in a cattle Pen Trial. Vet Parasitol 197(1–2):341–345. https:\u002F\u002Fdoi.org\u002F10.1016\u002Fj.vetpar.2013.04.045\nAraujo AM (2012) Alterações histológicas no intestino de fêmeas de carrapatos Rhipicephalus sanguineus (Latreille, 1806) (Acari: Ixodidae) expostas a diferentes concentrações de selamectina. 70 F. Dissertação - (Mestrado) - Universidade Estadual Paulista, Instituto De Biociências De Rio Claro. http:\u002F\u002Fhdl.handle.net\u002F11449\u002F87702\nAyoub A, Fatima K, Sanaa C, Meriem E, Laila B, Et Al (2018) Chemical composition and anti-insecticidal activity of the essential oils of thymus of Morocco: Thymus capitates, Thymus bleicherianus and Thymus satureioides. Org Med Chem Ij. https:\u002F\u002Fdoi.org\u002F10.19080\u002FOMCIJ.2018.06.555687\nBaldeón XR (2011) Actividad insecticida de los aceites esenciales de Tagetes minuta, Tagetes terniflora y Tagetes zipaquirensis Sobre Premnotrypes vorax. Tesis de grado para optar el titulo de bioquímico farmacéutico. Escuela Superior Politécnica De Chimborazo; Facultad De Ciencias, Escuela De Bioquímica Y Farmacia. Ecuador, Riobamba. 131 P. http:\u002F\u002Fdspace.espoch.edu.ec\u002Fhandle\u002F123456789\u002F1608\nBechara GH (2013) Introdução. In: Camargo-Mathias MI (2013) Guia básico de morfologia de carrapatos Ixodídeos. São Paulo: Editora UNESP. 9–24. 2013\nBenelli G, pavela R, Canale A, Mehlhorn H (2016) Tick repellents and acaricides of botanical origin: a green roadmap to control tick-borne Diseases? Parasitol Res 115(7):2545–2560. https:\u002F\u002Fdoi.org\u002F10.1007\u002Fs00436-016-5095-1\nBicalho KA, Ferreira F, Borges LMF, Ribeiro MFB (2001) In vitro evaluation of the effects of some acaricides on life stages of Rhipicephalus sanguineus (acari: ixodidae). Arq. Bras. Med. Vet. Zootec., belo Horizonte, v. 53, n. 5, p. 548–552, oct. https:\u002F\u002Fdoi.org\u002F10.1590\u002FS0102-09352001000500006\nBinnington KC (1982) Physiology of ticks. Structure and function of the circulatory, nervous, and neuroendocrine systems of ticks. 351–398. https:\u002F\u002Fdoi.org\u002F10.1016\u002FB978-0-08-024937-7.50015-9\nBlenau W, Rademacher E, Baumann A (2012) Plant essential oils and formamidines as insecticides\u002Facaricides: what are the molecular targets? vol 43. 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The female reproductive system. In: Sonenshine, D.E. (Ed.). Biology of ticks. New York: Oxford University Press\nVale L, de Paula LGF, Vieira MS, Alves SDGA, Junior NRDM, Gomes MDF, Teixeira WFP, Rizzo PV, Freitas FMC, Ferreira LL, Lopes WDZ, Monteiro C (2021) Hide details. Binary combinations of thymol, carvacrol and eugenol for Amblyomma sculptum control: Evaluation of in vitro synergism and effectiveness under semi-field conditions. Ticks and Tick-borne Diseases, Volume 12, Issue 6, November. https:\u002F\u002Fdoi.org\u002F10.1016\u002Fj.ttbdis.2021.101816\nWalker JB, Keirans JE, Horak IG (2000) The genus Rhipicephalus (Acari, Ixodidae): A guide to the brown ticks of the world. Cambridge University Press. Pag 384. https:\u002F\u002Fdoi.org\u002F10.1017\u002FCBO9780511661754\nYou CX, Guo SS, Zhang WJ, Yang K, Wang CF, Geng ZF, Du SS, Deng ZW, Wang YY (2015) Chemical constituents and activity of Murraya microphylla essential oil against Lasioderma serricorne. 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zhonghuajia Yu, Zhang and He is a newly discovered native ectoparasitic mite that efficiently controls stem borers in China. To provide a steady and sufficient supply, extend adult lifespan and synchronize field augmentative releases of P. zhonghuajia, we determined the optimal cold storage temperature and duration by storing 1-day-old mated females at 8, 10 and 12 °C for 10–90 days with a 10-day interval in the laboratory. We then recorded mite survival during storage and monitored the post-storage reproductive performance of mites at a control temperature of 25 °C. We found that all mites survived at 10 and 12 °C for different durations, but mortality occurred when mites were stored at 8 °C for ≥ 30 days with more than 70% of mites dead when the storage duration prolonged up to 50 days. The proportion of reproductive females was higher at 10 °C but decreased with the prolonged storage duration at all test temperatures. Storage temperature had no significant effect on the pre-reproductive period and offspring sex ratio, whereas prolonged storage induced longer pre-reproductive period and lower proportion of female offspring. The reproductive period increased with increasing storage temperature and with prolonged storage up to 50 and 60 days; however, the longer reproductive period did not directly translate into greater reproductive output. We found that compared with the control, mites stored at 10 °C for up to 30 days did not significantly reduce their survival, proportion of reproductive success and number and sex ratio of offspring, suggesting that 10 °C and ≤ 30 days were the optimal cold storage temperature and duration, respectively, for post-mass production storage before the field augmentative release of P. zhonghuajia.",{"EN":1558},"Optimizing cold storage of the ectoparasitic mite Pyemotes zhonghuajia (Acari: Pyemotidae), an efficient biological control agent of stem borers",{"VOID":1560},"[\"2286004369696379128\"]",{"EN":884},{"VOID":1563},"Abdel-Salam AH, Abdel-Baky NF (2000) Possible storage of Coccinella undecimpunctata (Coleoptera: Coccinellidae) under low temperature and its effect on some biological characteristics. 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Bol Comis Parasitol Agric 1:245–261\nRathee M, Ram P (2018) Impact of cold storage on the performance of entomophagous insects: an overview. Phytoparasitica 46:421–449. https:\u002F\u002Fdoi.org\u002F10.1007\u002Fs12600-018-0683-5\nRenault D, Hance T, Vannier G, Vernon P (2003) Is body size an influential parameter in determining the duration of survival at low temperatures in Alphitobius diaperinus Panzer (Coleoptera: Tenebrionidae)? J Zool 259:381–388. https:\u002F\u002Fdoi.org\u002F10.1017\u002Fs0952836902003382\nRiddick EW (2001) Effect of cold storage on emergence, longevity, fertility, and survival of Cotesia marginiventris (Hymenoptera: Braconidae). J Entomol Sci 36:366–379. https:\u002F\u002Fdoi.org\u002F10.18474\u002F0749-8004-36.4.366\nRiddick EW, Wu Z (2010) Potential long-term storage of the predatory mite Phytoseiulus persimilis. Biocontrol 55:639–644. https:\u002F\u002Fdoi.org\u002F10.1007\u002Fs10526-010-9297-7\nŞenal D, Demirözer O, Karaca İ (2017) Investigation on the storage possibilities of Rhyzobius lophantae Blaisdell (Coleoptera: Coccinellidae) at different temperatures and periods. Phytoparasitica 45:175–182. https:\u002F\u002Fdoi.org\u002F10.1007\u002Fs12600-017-0581-2\nSmith KGV (1973) Insects and other arthropods of medical importance. British Museum, London\nTahriri S, Talebi AA, Fathipour Y, Zamani AA (2007) Host stage preference, functional response and mutual interference of Aphidius matricariae (Hym.: Braconidae: Aphidiinae) on Aphis fabae (Hom.: Aphididae). Entomol Sci 10:323–331. https:\u002F\u002Fdoi.org\u002F10.1111\u002Fj.1479-8298.2007.00234.x\nThorvilson HG Jr, Phillips SA, Ann Sorensen A, Trostle MR (1987) The straw itch mite, Pyemotes Tritici (Acari: Pyemotidae), as a biological control agent of red imported fire ants, Solenopsis Invicta (Hymenoptera: Formicidae). Fla Entomol 70:439–444. https:\u002F\u002Fdoi.org\u002F10.2307\u002F3494785\nTollarová-Borovanská M, Lalouette L, Koštál V (2009) Insect cold tolerance and repair of chill-injury at fluctuating thermal regimes: role of 70 kDa heat shock protein expression. CryoLetters 30:312–319\nTomalski MD, Bruce WA, Travis J, Blum MS (1988) Preliminary characterization of toxins from the straw itch mite, Pyemotes tritici, which induce paralysis in the larvae of a moth. Toxicon 26:127–132. https:\u002F\u002Fdoi.org\u002F10.1016\u002F0041-0101(88)90164-x\nVan Lenteren J, Tommasini M (2002) Mass production, storage, shipment and quality control of natural enemies. In: Albajes R, Gullino ML, Van Lenteren JC, Elad Y (eds) Mass production, storage, shipment and quality control of natural enemies, integrated pest and disease management in greenhouse crops. Springer, Dordrecht, pp 276–294. https:\u002F\u002Fdoi.org\u002F10.1007\u002F0-306-47585-5_20\nVenkatesan T, Singh SP, Jalali SK (2000) Effect of cold storage on cocoons of Goniozus nephantidis Muesebeck (Hymenoptera: Bethylidae) stored for varying periods at different temperature regimes. J Entomol Res 24:43–47\nVilela EF (1986) Status of leaf-cutting ant control in forest plantations in Brazil. In: Lofgren CS, Vander Meer RK (eds) Fire ants and leaf-cutting ants: biology and management. Westview, Boulder, pp 399–408\nWebster FM (1910) A predaceous and supposedly beneficial mite, Pediculoides, becomes noxious to man. Ann Entomol Soc Am 3:15–39. https:\u002F\u002Fdoi.org\u002F10.1093\u002Faesa\u002F3.1.15\nWeiser J, Hrdy I (1962) Pyemotes-mites as parasites of termites. Z Angew Entomol 51:94–97. https:\u002F\u002Fdoi.org\u002F10.1111\u002Fj.1439-0418.1962.tb04062.x\nWeiser J, Slama K (1964) Effects of the toxin of Pyemotes (Acarina: Pyemotidae) on the insect prey, with special reference to respiration. Ann Entomol Soc Am 57:479–482. https:\u002F\u002Fdoi.org\u002F10.1093\u002Faesa\u002F57.4.479\nWrensch DL, Bruce WA (1991) Sex ratio, fitness and capacity for population increase in Pyemotes tritici (L.-F. & M.) (Pyemotidae). In: Schuster R, Murphy PW (eds) The Acari, reproduction, development and life history strategies. Chapman & Hall, London, pp 209–421. https:\u002F\u002Fdoi.org\u002F10.1007\u002F978-94-011-3102-5_13\nYan Z, Yue JJ, Bai C, Peng ZQ, Zhang CH (2017) Effects of cold storage on the biological characteristics of Microplitis prodeniae (Hymenoptera: Braconidae). Bull Entomol Res 107:506–512. https:\u002F\u002Fdoi.org\u002F10.1017\u002Fs0007485317000037\nYu L, He L, Xu C (2000) General biology of a Pyemotes sp. and its development and reproduction affected by temperature. In: Proc Entomol Soc China Ann Acad Conf, pp 1031–1032\nYu L, Zhang ZQ, He L (2010) Two new species of Pyemotes closely related to P. tritici (Acari: Pyemotidae). Zootaxa 2723:1–40\nZhang ZS, Xiong DP, Cheng W (2004) To control trunk insect pest Semanotus bifasciatus with its natural enemy Pyemotes sp. Chin Landsc Archit 20(2):75–77. https:\u002F\u002Fdoi.org\u002F10.3969\u002Fj.issn.1000-6664.2004.02.024\nZhang ZS, Xiong DP, Cheng W (2008) Control of stem borers by a parasitoid, Pyemotes tritici Lagreze-Fossot and Montane. Chin J Biol Control 24:1–6. https:\u002F\u002Fdoi.org\u002F10.16409\u002Fj.cnki.2095-039x.2008.01.002",{"VOID":1565},"10.1007\u002Fs10493-019-00386-0","2024-05-01T03:22:07.490+00:00","https:\u002F\u002Flink.springer.com\u002Farticle\u002F10.1007\u002Fs10493-019-00386-0",[1569,1586,1599,1612,1629,1642,1655,1668],{"id":1570,"sortIndex":100,"researcher":24,"roles":1571,"affiliations":1572,"properties":1581,"displayName":1583,"givenName":24,"familyName":24},"d7ba1392-f24c-4cd1-9926-e1f21cf1ff05",[245],[1573],{"id":1574,"sortIndex":100,"affiliation":1575,"properties":24},"dd17acc1-6ee1-41d2-9e70-e00f5c025b21",{"id":1574,"createTime":24,"updateTime":24,"relativeEntities":1576,"slug":24,"properties":1577,"entityType":24,"verifyStatus":24,"verifyTime":24,"verifyNote":24,"languages":24,"translateLanguages":24,"viewCount":24,"url":24,"parentIds":1580,"statistic":24},[],{"title":1578},{"VI":1579},"Changli Institute of Pomology, Hebei Academy of Agriculture and Forestry Sciences, Changli, China",[],{"title":1582,"gsAuthor":1584},{"VI":1583},"Limin He",{"VOID":1585},"[\"vvVcW0wAAAAJ\"]",{"id":1587,"sortIndex":260,"researcher":24,"roles":1588,"affiliations":1589,"properties":1596,"displayName":1598,"givenName":24,"familyName":24},"941818eb-efad-4232-9173-2af1a15cecf1",[245],[1590],{"id":1574,"sortIndex":100,"affiliation":1591,"properties":24},{"id":1574,"createTime":24,"updateTime":24,"relativeEntities":1592,"slug":24,"properties":1593,"entityType":24,"verifyStatus":24,"verifyTime":24,"verifyNote":24,"languages":24,"translateLanguages":24,"viewCount":24,"url":24,"parentIds":1595,"statistic":24},[],{"title":1594},{"VI":1579},[],{"title":1597},{"VI":1598},"Litao Li",{"id":1600,"sortIndex":389,"researcher":24,"roles":1601,"affiliations":1602,"properties":1609,"displayName":1611,"givenName":24,"familyName":24},"47aa907f-0b09-43ff-b396-0f0f372e4e3e",[245],[1603],{"id":1574,"sortIndex":100,"affiliation":1604,"properties":24},{"id":1574,"createTime":24,"updateTime":24,"relativeEntities":1605,"slug":24,"properties":1606,"entityType":24,"verifyStatus":24,"verifyTime":24,"verifyNote":24,"languages":24,"translateLanguages":24,"viewCount":24,"url":24,"parentIds":1608,"statistic":24},[],{"title":1607},{"VI":1579},[],{"title":1610},{"VI":1611},"Lichen Yu",{"id":1613,"sortIndex":198,"researcher":24,"roles":1614,"affiliations":1615,"properties":1624,"displayName":1626,"givenName":24,"familyName":24},"3fa6206e-389b-48ea-9f97-4c72e025ade6",[245],[1616],{"id":1617,"sortIndex":100,"affiliation":1618,"properties":24},"80d375b9-aaba-44bb-bb94-996838799c93",{"id":1617,"createTime":24,"updateTime":24,"relativeEntities":1619,"slug":24,"properties":1620,"entityType":24,"verifyStatus":24,"verifyTime":24,"verifyNote":24,"languages":24,"translateLanguages":24,"viewCount":24,"url":24,"parentIds":1623,"statistic":24},[],{"title":1621},{"VI":1622},"School of Agriculture and Environment, Massey University, Palmerston North, New Zealand",[],{"title":1625,"gsAuthor":1627},{"VI":1626},"Xiong Z. 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phytoseiids are best known as predators of phytophagous mites and other small arthropods, several species can also feed and reproduce on pollen. In laboratory assays, we assessed the profitability of two types of dietary supplements (three pollen species—cattail, maize and apple—and eggs of the Mediterranean flour moth, Ephestia kuehniella) for the two species of predatory mites most commonly used as biocontrol agents in horticulture in Canada, Neoseiulus cucumeris and Amblyseius swirskii. We measured the effects of each diet on phytoseiid fitness parameters (survival, development, sex ratio, fecundity) and, as a means of comparison, when fed larvae of the common targeted pest species, western flower thrips Frankliniella occidentalis. A soluble protein assay was also performed on the alternative food sources as protein content is often linked to high nutritive value according to the literature. All food sources tested were suitable for N. cucumeris and A. swirskii, both species being able to develop from egg to adult. The dietary supplements had a beneficial impact on biological parameters, mostly resulting in shorter development times and higher survival rates when compared to thrips larvae. Amblyseius swirskii exhibited a wider dietary range than N. cucumeris. Overall, flour moth eggs, cattail pollen and apple pollen are food sources of equal quality for A. swirskii, whereas apple and cattail pollen are better when it comes to N. cucumeris. In contrast, maize pollen is a less suitable food source for N. cucumeris and A. swirskii. Soluble protein content results did not match the prediction under which the most beneficial food source would contain the highest concentration in protein.",{"EN":1750},"Evaluation of various types of supplemental food for two species of predatory mites, Amblyseius swirskii and Neoseiulus cucumeris (Acari: Phytoseiidae)",{"VOID":1752},"[\"684552607301184952\"]",{"VOID":1754},"Arthurs S, Mckenzie CL, Chen J, Dogramaci M, Brennan M, Houben K, Osborne L (2009) Evaluation of Neoseiulus cucumeris and Amblyseius swirskii (Acari: Phytoseiidae) as biological control agents of chilli thrips, Scirtothrips dorsalis (Thysanoptera: Thripidae) on pepper. Biol Control 49:91–96\nBakker FM, Sabelis MW (1989) How larvae of Thrips tabaci reduce the attack success of Phytoseiid predators. Entomol Exp Appl 50:47–51\nBarrette M, Wu GM, Brodeur J, Giraldeau LA, Boivin G (2008) Testing competing measures of profitability for mobile resources. Oecologia 158:757–764\nBonte M, De Clercq P (2008) Development and reproductive fitness of Orius laevigatus (Hemiptera: Anthocoridae) reared on factitious and artificial diets. J Econ Entomol 101:1127–1133\nBuitenhuis R, Shipp L, Scott-Dupree C (2010) Intra-guild versus extra-guild prey: effect on predator fitness and preference of Amblyseius swirskii (Athias-Henriot) and Neoseiulus cucumeris (Oudemans) (Acari: Phytoseiidae). Bull Entomol Res 100:167–173\nChant DA (1959) Phytoseiid mites (Acarina: Phytoseiidae). Part I. Bionomics of seven species in southeastern England. Part II. A taxonomic review of the Phytoseiidae, with description of 38 new species. Mem Entomol Soc Canada 91:1–166\nCloutier C, Johnson GS (1993) Interaction between life stages in a phytoseiid predator: western flower thrips prey killed by adults as food for protonymphs of Amblyseius cucumeris. Exp Appl Acarol 17:441–449\nCohen AC, Smith LK (1998) A new concept in artificial diets for Chrysoperla rufilabris: the efficacy of solid diets. Biol Control 13:49–54\nColl M, Guershon M (2002) Omnivory in terrestrial arthropods: mixing plant and prey diets. Annu Rev Entomol 47:267–297\nde Almeida AA, Janssen A (2013) Juvenile prey induce antipredator behaviour in adult predators. Exp Appl Acarol 59:275–282\nDe Clercq P, Bonte M, Van Speybroeck K, Bolckmans K, Deforce K (2005) Development and reproduction of Adalia bipunctata (Coleoptera: Coccinellidae) on eggs of Ephestia kuehniella (Lepidoptera: Phycitidae) and pollen. Pest Manag Sci 61:1129–1132\nFaraji F, Janssen A, Sabelis MW (2001) Predatory mites avoid ovipositing near counterattacking prey. Exp Appl Acarol 25:613–623\nFlechtmann CHW, McMurtry JA (1992) Studies of cheliceral and deutosternal morphology of some Phytoseiidae (Acari: Mesostigmata) by scanning electron microscopy. 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