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Biocontrol 63:505–518",{"doi":539},"10.1007\u002Fs10526-018-9866-8",{"id":20,"text":541,"url":20,"identifiers":542},"Bosco L, Moraglio ST, Tavella L (2018) Halyomorpha halys, a serious threat for hazelnut in newly invaded areas. J Pest Sci 91(2):661–670",{"doi":543},"10.1007\u002Fs10340-017-0937-x",{"id":20,"text":545,"url":20,"identifiers":546},"Cesari M, Maistrello L, Piemontese L, Bonini R, Dioli P, Lee W, Park CG, Partsinevelos GK, Rebecchi L, Guidetti R (2018) Genetic diversity of the brown marmorated stink bug Halyomorpha halys in the invaded territories of Europe and its patterns of diffusion in Italy. Biol Invasions 20:1073–1092",{"doi":547},"10.1007\u002Fs10530-017-1611-1",{"id":20,"text":549,"url":20,"identifiers":550},"Costi E (2018) Biologia e monitoraggio in campo della cimice invasiva Halyomorpha halys in Italia e indagini su potenziali antagonisti naturali autoctoni. PhD thesis. Università Emilia Romagna",{},{"id":20,"text":552,"url":20,"identifiers":553},"Dieckhoff C, Tatman KM, Hoelmer KA (2017) Natural biological control of Halyomorpha halys by native egg parasitoids: a multi-year survey in northern Delaware. J Pest Sci 90(4):1143–1158",{"doi":554},"10.1007\u002Fs10340-017-0868-6",{"id":20,"text":556,"url":20,"identifiers":557},"Folmer O, Black M, Hoeh W, Lutz R, Vrijenhoek R (1994) DNA primers for amplification of mitochondrial cytochrome c oxidase subunit I from diverse metazoan invertebrates. Mol Mar Biol Biotechnol 3:294–299",{},{"id":20,"text":559,"url":20,"identifiers":560},"Ganjisaffar F, Talamas EJ, Bon MC, Gonzalez L, Brown BV, Perring TM (2018) Trissolcus hyalinipennis Rajmohana & Narendran (Hymenoptera, Scelionidae), a parasitoid of Bagrada hilaris (Burmeister) (Hemiptera, Pentatomidae) emerges in North America. J Hymenopt Res 65:111–130",{"doi":561},"10.3897\u002Fjhr.65.25620",{"id":20,"text":563,"url":20,"identifiers":564},"Gariepy TD, Haye T, Zhang J (2014) A molecular diagnostic tool for the preliminary assessment of host–parasitoid associations in biological control programmes for a new invasive pest. Mol Ecol 23:3912–3924",{"doi":565},"10.1111\u002Fmec.12515",{"id":20,"text":567,"url":20,"identifiers":568},"Gariepy TD, Bruin A, Haye T, Milonas P, Vétek G (2015) Occurrence and genetic diversity of new populations of Halyomorpha halys in Europe. J Pest Sci 88:451–460",{"doi":569},"10.1007\u002Fs10340-015-0672-0",{"id":20,"text":571,"url":20,"identifiers":572},"Giantsis I, Chaskopoulou A, Bon MC (2015) Mild-vectolysis: a non-destructive DNA extraction method for vouchering sand flies and mosquitoes. J Med Entomol 53:692–695",{"doi":573},"10.1093\u002Fjme\u002Ftjv236",{"id":20,"text":575,"url":20,"identifiers":576},"Haye T, Fischer S, Zhang J, Gariepy T (2015) Can native egg parasitoids adopt the invasive brown marmorated stink bug, Halyomorpha halys (Heteroptera: Pentatomidae), in Europe? J Pest Sci 88:693–705",{"doi":577},"10.1007\u002Fs10340-015-0671-1",{"id":20,"text":579,"url":20,"identifiers":580},"Hedstrom C, Lowenstein D, Andrews H, Bai B, Wiman N (2017) Pentatomid host suitability and the discovery of introduced populations of Trissolcus japonicus in Oregon. J Pest Sci 90:1169–1179",{"doi":581},"10.1007\u002Fs10340-017-0892-6",{"id":20,"text":583,"url":20,"identifiers":584},"Hoebeke ER, Carter ME (2003) Halyomorpha halys (Stǻl) (Heteroptera: Pentatomidae): a polyphagous plant pest from Asia newly detected in North America. 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Environ Entomol 42:627–641",{"doi":598},"10.1603\u002FEN13006",{"id":20,"text":600,"url":20,"identifiers":601},"Leigh JW, Bryant D (2015) POPART: full-feature software for haplotype network construction. Methods Ecol Evol 6:1110–1116",{"doi":602},"10.1111\u002F2041-210X.12410",{"id":20,"text":604,"url":20,"identifiers":605},"Leskey TC, Nielsen AL (2018) Impact of the invasive brown marmorated stink bug in North America and Europe: history, biology, ecology, and management. Annu Rev Entomol 63:599–618",{"doi":606},"10.1146\u002Fannurev-ento-020117-043226",{"id":20,"text":608,"url":20,"identifiers":609},"Maistrello L, Vaccari G, Caruso S et al (2017) Monitoring of the invasive Halyomorpha halys, a new key pest of fruit orchards in northern Italy. J Pest Sci 90:1231–1244",{"doi":610},"10.1007\u002Fs10340-017-0896-2",{"id":20,"text":612,"url":20,"identifiers":613},"Matsuo K, Hirose Y, Johnson NF (2014) A taxonomic issue of two species of Trissolcus (Hymenoptera: Platygastridae) parasitic on eggs of the brown-winged green bug, Plautia stali (Hemiptera: Pentatomidae): resurrection of T. plautiae, a cryptic species of T. japonicus revealed by morphology, reproductive isolation and molecular evidence. Appl Entomol Zool 49:385–394",{"doi":614},"10.1007\u002Fs13355-014-0260-4",{"id":20,"text":616,"url":20,"identifiers":617},"Matsuo K, Honda T, Itoyama K, Toyama M, Hirose Y (2016) Discovery of three egg parasitoid species attacking the shield bug Glaucias subpunctatus (Hemiptera: Pentatomidae). Jpn J Appl Entomol Zool 60:43–45",{"doi":618},"10.1303\u002Fjjaez.2016.43",{"id":20,"text":620,"url":20,"identifiers":621},"Milnes JM, Wiman NG, Talamas EJ, Brunner JF, Hoelmer KA, Buffington ML, Beers EH (2016) Discovery of an exotic egg parasitoid of the brown marmorated stink bug, Halyomorpha halys (Stål) in the Pacific Northwest. Proc Entomol Soc Wash 118:466–470",{"doi":622},"10.4289\u002F0013-8797.118.3.466",{"id":20,"text":624,"url":20,"identifiers":625},"Morrison WR III, Mathews CR, Leskey TC (2016) Frequency, efficiency, and physical characteristics of predation by generalist predators of brown marmorated stink bug (Hemiptera: Pentatomidae) eggs. Biol Control 97:120–130",{"doi":626},"10.1016\u002Fj.biocontrol.2016.03.008",{"id":20,"text":628,"url":20,"identifiers":629},"Morrison WR III, Blaauw BR, Nielsen AL, Talamas E, Leskey TC (2018) Predation and parasitism by native and exotic natural enemies of Halyomorpha halys (Stål) (Hemiptera: Pentatomidae) eggs augmented with semiochemicals and differing host stimuli. Biol Control 121:140–150",{"doi":630},"10.1016\u002Fj.biocontrol.2018.02.016",{"id":20,"text":632,"url":20,"identifiers":633},"Qiu LF, Yang ZQ, Tao WQ (2007) Biology and population dynamics of Trissolcus halyomorphae. Sci Silvae Sin 43:62–65",{},{"id":20,"text":635,"url":20,"identifiers":636},"Rice KB, Bergh CJ, Bergmann EJ, Biddinger DJ, Dieckhoff C, Dively G, Fraser H, Gariepy T, Hamilton G, Haye T, Herbert A (2014) Biology, ecology, and management of brown marmorated stink bug (Hemiptera: Pentatomidae). J Integr Pest Manag 5:A1–A13",{"doi":637},"10.1603\u002FIPM14002",{"id":20,"text":639,"url":20,"identifiers":640},"Roversi PF, Marianelli L, Costi E, Maistrello L, Sabbatini PG (2016) Searching for native egg-parasitoids of the invasive alien species Halyomorpha halys Stål (Heteroptera Pentatomidae) in Southern Europe. Redia 99:63–70",{},{"id":20,"text":642,"url":20,"identifiers":643},"Ryu J, Hirashima Y (1984) Taxonomic studies on the genus Trissolcus Ashmead of Japan and Korea (Hymenoptera, Scelionidae). J Fac Agric Kyushu Univ 29:35–58",{"doi":644},"10.5109\u002F23793",{"id":20,"text":646,"url":20,"identifiers":647},"Schlaepfer MA, Sherman PW, Blossey B, Runge MC (2005) Introduced species as evolutionary traps. Ecol Lett 8(3):241–246",{"doi":648},"10.1111\u002Fj.1461-0248.2005.00730.x",{"id":20,"text":650,"url":20,"identifiers":651},"Servick K (2018) Control freaks. Science 361:542–545",{"doi":652},"10.1126\u002Fscience.361.6402.542",{"id":20,"text":654,"url":20,"identifiers":655},"Stahl J, Babendreier D, Haye T (2018) Using the egg parasitoid Anastatus bifasciatus against the invasive brown marmorated stink bug in Europe—can non-target effects be ruled out? J Pest Sci 91:1005–1017",{"doi":656},"10.1007\u002Fs10340-018-0969-x",{"id":20,"text":658,"url":20,"identifiers":659},"Talamas EJ, Herlihy MV, Dieckhoff C, Hoelmer KA, Buffington M, Bon MC, Weber DC (2015) Trissolcus japonicus (Ashmead) (Hymenoptera, Scelionidae) emerges in North America. J Hymenopt Res 43:119",{"doi":660},"10.3897\u002FJHR.43.4661",{"id":20,"text":662,"url":20,"identifiers":663},"Talamas EJ, Buffington ML, Hoelmer K (2017) Revision of Palearctic Trissolcus Ashmead (Hymenoptera, Scelionidae). In: Talamas EJ, Buffington ML (Eds) Advances in the systematics of Platygastroidea. J Hymenopt Res 56:3–185",{"doi":664},"10.3897\u002Fjhr.56.10158",{"id":20,"text":666,"url":20,"identifiers":667},"United States Apple Association (2010) Asian pest inflicting substantial losses, raising alarm in eastern apple orchards. Apple News 41:488",{},{"id":20,"text":669,"url":20,"identifiers":670},"World Bank (2018) Data retrieved October 15, 2018, from World Integrated Trade Solution. UNSD Commodity Trade (COMTRADE) database",{},{"id":20,"text":672,"url":20,"identifiers":673},"Yang Z-Q, Yao Y-X, Qiu L-F, Li Z-X (2009) A new species of Trissolcus (Hymenoptera: Scelionidae) parasitizing eggs of Halyomorpha halys (Heteroptera: Pentatomidae) in China with comments on its biology. Ann Entomol Soc Am 102:39–47",{"doi":674},"10.1603\u002F008.102.0104",{"id":20,"text":676,"url":20,"identifiers":677},"Zhang J, Zhang F, Gariepy T, Mason P, Gillespie D, Talamas E, Haye T (2017) Seasonal parasitism and host specificity of Trissolcus japonicus in northern China. 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Ggplot2. https:\u002F\u002Fdoi.org\u002F10.1007\u002F978-0-387-98141-3",{"doi":1234},"10.1007\u002F978-0-387-98141-3",{"id":1236,"createTime":1237,"updateTime":1238,"relativeEntities":1239,"slug":1240,"properties":1241,"entityType":297,"verifyStatus":298,"verifyTime":1252,"verifyNote":300,"languages":20,"translateLanguages":20,"viewCount":21,"primaryUrl":1253,"fullTextUrl":20,"authors":1254,"publicationType":449,"publisherRelationship":1344,"citationCount":21,"citationInfo":1408,"publishDate":1411,"publishYear":1409,"citationAnalyzeStatus":19,"lastCitationAnalyze":1412,"indexDatabases":1413,"openAccess":20,"references":20,"isForceReanalyzing":679},"e4a65060-c7e2-4ea9-80c6-abb52ebe99a4","2023-11-27T10:12:42.508+00:00","2026-07-23T11:49:18.052+00:00",[],"Insecticide-resistance-and-its-management-in-Bemisia-tabaci-species",{"abstract":1242,"title":1244,"gsPaper":1246,"references":1248,"doi":1250},{"EN":1243},"The sweet potato (cotton) whitefly Bemisia tabaci is a major agricultural pest in various fields and vegetable crops worldwide. It causes extensive damage by direct feeding on plants, reducing quality, secreting honeydew and transmitting plant viruses. B. tabaci is known for its genetic diversity and considered a complex of biotypes or, as suggested, a complex of distinct cryptic species. Management of whiteflies relies mainly on the use of insecticides; however, its ability to develop resistance to major insecticide classes creates a serious challenge to farmers and pest control specialists. Among the cryptic species of B. tabaci, MED is considered more resistant than the MEAM1 to insecticides such as pyriproxyfen and neonicotinoids; however, in recent years there are other species of B. tabaci including MEAM1, Asia I and Asia II-1 that have developed high resistance to various groups of insecticides. Advanced methods based on molecular and gene sequence data obtained from resistant and susceptible field-collected B. tabaci populations resulted in a better understanding of resistance mechanisms in this pest. Several components of IPM-IRM (Integrated Pest Management-Insecticide Resistance Management) programs such as selective and biorational insecticides, insecticide rotation with different modes of action and nonchemical control methods are among the countermeasures of insecticide resistance management for this pest. In the current review, we concentrate on insecticide resistance and resistance management of B. tabaci, focusing on reports published mainly over the past 10 years.",{"EN":1245},"Insecticide resistance and its management in Bemisia tabaci species",{"VOID":1247},"[\"12657847237308354631\"]",{"VOID":1249},"Ahmad M, Khan RA (2017) Field-evolved resistance of Bemisia tabaci (Hemiptera: Aleyrodidae) to carbodiimide and neonicotinoids in Pakistan. J Econ Entomol 110:1235–1242\nAhmad M, Arif MI, Naveed M (2010) Dynamics of resistance to organophosphate and carbamate insecticides in the cotton whitefly Bemisia tabaci (Hemiptera: Aleyrodidae) from Pakistan. 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most severe outcome of the widespread interspecific competition that occurs between invasive organisms and their local congeners is species displacement. The western flower thrips, Frankliniella occidentalis (Pergande), which originated from western North America, has invaded much of the agricultural world since the 1970s, and in so doing, has become a dominant thrips species in many of the areas it has invaded. Its invasion success and the extent of its distribution in the regions it has invaded can be largely attributed to its superiority in interspecific competition. In some instances, however, F. occidentalis has been less successful in its invasion attempts and has not become dominant in its new environment. Thrips species displacements often arise from interactions of different mechanisms that are mediated by numerous biotic and abiotic factors. In this review, we summarize competitive interaction events that have been documented between F. occidentalis and several species of other locally present thrips, their interaction mechanisms and mediating factors. This review will help to better understand displacement events of thrips species in some areas and to develop management strategies for thrips species with high invasion potential.",{"EN":1424},"Competitive interaction between Frankliniella occidentalis and locally present thrips species: a global review",{"VOID":1426},"[]",{"VOID":1428},"Alim MA, Song J, Seo HJ, Choi JJ (2018) Monitoring thrips species with yellow sticky traps in astringent persimmon orchards in Korea. Appl Entomol Zool 53(1):75–84\nArthurs SP, Kok-Yokomi ML, Smith H (2015) Florida flower thrips: Frankliniella bispinosa Morgan. Featured Creatures, IFAS Extension, University of Florida. https:\u002F\u002Fentnemdept.ufl.edu\u002Fcreatures\u002FVEG\u002FTHRIPS\u002FFrankliniella_bispinosa.htm. Accessed Oct 2015\nAtakan E, Uygur S (2005) Winter and spring abundance of Frankliniella spp. and Thrips tabaci Lindeman (Thysan., Thripidae) on weed host plants in Turkey. J Appl Entomol 129(1):17–26\nBeaudoin ALP, Kennedy GG (2012) Management of Winter Weeds Affects Frankliniella fusca (Thysanoptera: Thripidae) dispersal. Environ Entomol 41(2):362–369\nBerndt O, Meyhöfer R, Poehling HM (2004) The edaphic phase in the ontogenesis of Frankliniella occidentalis and comparison of Hypoaspis miles and Hypoaspis aculeifer as predators of soil dwelling thrips stage. Biol Control 30:17–24\nBielza P (2008) Insecticide resistance management strategies against the western flower thrips, Frankliniella occidentalis. Pest Manag Sci 64:1131–1138\nBorbón CM, Gracia O, Piccolo R (2006) Relationships between tospovirus incidence and thrips populations on tomato in Mendoza. Argentina J Phytopathol 154(2):93–99\nCannon RJC, Matthews L, Collins DW (2007) A review of the pest status and control options for Thrips palmi. Crop Prot 26(8):1089–1098\nCao Y, Zhi JR, Zhang RZ, Li C, Liu Y, Lv ZY, Gao YL (2018) Different population performances of Frankliniella occidentalis and Thrips hawaiiensis on flowers of two horticultural plants. J Pest Sci 91(1):79–91\nCarter E, Gillett-Kaufman JL (2015) Tobacco thrips: Frankliniella fusca (Hinds). Featured Creatures, IFAS Extension, University of Florida. https:\u002F\u002Fentnemdept.ufl.edu\u002Fcreatures\u002FVEG\u002FTHRIPS\u002FFrankliniella_fusca.htm. Accessed Sept 2015\nChitturi A, Riley DG, Joost PH (2006) Effect of pine pollen on settling behavior of Frankliniella occidentalis and Frankliniella fusca (Thysanoptera: Thripidae) on tomato and peanut. Environ Entomol 35(5):1396–1403\nCloyd RA (2009) Western flower thrips (Frankliniella occidentalis) management on ornamental crops grown in greenhouses: have we reached an impasse? 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Insecticide resistance is a common issue in pest management. The interactions between insecticide resistance in insect vector and the transmission of plant pathogen, however, are largely unknown. In this study, we assessed the effects of spinosad resistance on TSWV transmission using a pair of near-isogenic lines of susceptible (Ivf03) and resistant (NIL-R) F. occidentalis. NIL-R had a prolonged pre-adult stage, but a shorter adult life span than Ivf03. More importantly, the pupation rate and sex ratio (female\u002Fmale) in NIL-R were significantly reduced in comparison with Ivf03. When given a shorter acquisition access period (AAP) of 6 h, virus propagation and transmission efficiency in NIL-R were significantly higher than Ivf03. In contrast, a longer AAP of 96 h led to a similar virus acquisition and transmission efficiency for both strains, although TSWV replication was greater in NIL-R. 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Environ Entomol 47(3):623–628\nBielza P, Quinto V, Fernández E, Gravalos C, Contreras J (2007) Genetics of spinosad resistance in Frankliniella occidentalis (Thysanoptera: Thripidae). J Econ Entomol 100:916–920\nChi H (1988) Life-table analysis incorporating both sexes and variable development rates among individuals. Environ Entomol 17:26–34\nChi H (2012) TWOSEX-MSChart: computer program for age stage, two-sex life table analysis. https:\u002F\u002F140.120.197.173\u002Fecology\u002F\nChi H, Liu H (1985) Two new methods for the study of insect population ecology. Bull Inst Zool Acad Sin 24:225–240\nCulbreath AK, Srinivasan R (2011) Epidemiology of spotted wilt disease of peanut caused by Tomato spotted wilt virus in the southeastern U.S. Virus Res 159:101–109\nGoldbach R, Peters D (1994) Possible causes of the emergence of Tospovirus diseases. 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Biol Rev 90:89–111",{"doi":3223},"10.1111\u002Fbrv.12098",{"id":3225,"createTime":3226,"updateTime":3227,"relativeEntities":3228,"slug":3229,"properties":3230,"entityType":297,"verifyStatus":298,"verifyTime":3241,"verifyNote":300,"languages":20,"translateLanguages":20,"viewCount":21,"primaryUrl":3242,"fullTextUrl":20,"authors":3243,"publicationType":449,"publisherRelationship":3327,"citationCount":21,"citationInfo":3390,"publishDate":3392,"publishYear":517,"citationAnalyzeStatus":982,"lastCitationAnalyze":3393,"indexDatabases":3394,"openAccess":20,"references":20,"isForceReanalyzing":679},"a641ea1f-c56b-4e90-810f-5a6d4e2722c2","2024-01-10T22:07:01.351+00:00","2026-07-11T10:43:02.023+00:00",[],"Natural-habitat-increases-natural-pest-control-in-olive-groves-economic-implications",{"abstract":3231,"title":3233,"gsPaper":3235,"references":3237,"doi":3239},{"EN":3232},"Natural habitat at the landscape scale can promote biological control of crop pests, but farmers often regard natural habitat as a cost or a lost economic opportunity. Evaluating the benefits of promoting natural habitats in economic terms should make different management alternatives easier to compare. However, it is important to understand the mechanisms underlying the connection between natural habitat and natural pest control. In this study, we link measurements of natural habitat and ground cover with abundances of multiple natural enemy groups and biological control of the olive pest Prays oleae to describe spatial patterns in biocontrol and the economic value associated. Natural habitat increased biocontrol and crop yields by an average of 186.36 €\u002Fha. This could be attributable to the entire community of predatory natural enemies present in the olive regardless of natural habitat. One predator species of this community, Anthocoris nemoralis, whose abundance was influenced by natural habitat, was strongly associated with elevated biocontrol. We hypothesize that this predator species could be the link between natural habitat and the biological control. Our results suggest that olive growers could stand to gain from conserving natural habitat. Moreover, our evidence suggests that minimizing the use of chopped pruning remains may result in increased biocontrol by bolstering the abundance of A. nemoralis. More generally, our study indicates that diversifying olive orchards and surrounding landscapes may improve olive yields.",{"EN":3234},"Natural habitat increases natural pest control in olive groves: economic implications",{"VOID":3236},"[\"1269600326321450044\"]",{"VOID":3238},"Albedis H, Ávila de la Calle A, Matas P, Vargas-Osuna E (2004) Evaluación de los daños causados por la polilla del olivo, Prays oleae Bern., en distintas variedades y condiciones de cultivo. Boletín de Sanidad Vegetal Plagas 30:640–658\nBates D, Maechler M, Bolker B, Walker S (2015) Fitting linear mixed-effects models using lme4. 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Springer, Berlin",{"VOID":3240},"10.1007\u002Fs10340-019-01104-w","2024-06-24T14:06:49.347+00:00","https:\u002F\u002Flink.springer.com\u002Farticle\u002F10.1007\u002Fs10340-019-01104-w",[3244,3269,3286,3301,3314],{"id":3245,"sortIndex":21,"researcher":20,"roles":3246,"affiliations":3247,"properties":3264,"displayName":3266,"givenName":20,"familyName":20},"42ca119a-1881-40e9-ba7a-91f81c0127d7",[703],[3248,3256],{"id":3249,"sortIndex":21,"affiliation":3250,"properties":20},"cd329996-e21d-4eb5-9da6-c6bb839b767c",{"id":3249,"createTime":20,"updateTime":20,"relativeEntities":3251,"slug":20,"properties":3252,"entityType":20,"verifyStatus":20,"verifyTime":20,"verifyNote":20,"languages":20,"translateLanguages":20,"viewCount":20,"url":20,"parentIds":3255,"statistic":20},[],{"title":3253},{"VI":3254},"Environmental Protection Department, Estación Experimental del Zaidín, Spanish Council of Research (CSIC), Granada, Spain",[],{"id":3257,"sortIndex":162,"affiliation":3258,"properties":20},"eb4a0ceb-c978-426f-8ec9-b63e5fb3b2c8",{"id":3257,"createTime":20,"updateTime":20,"relativeEntities":3259,"slug":20,"properties":3260,"entityType":20,"verifyStatus":20,"verifyTime":20,"verifyNote":20,"languages":20,"translateLanguages":20,"viewCount":20,"url":20,"parentIds":3263,"statistic":20},[],{"title":3261},{"VI":3262},"Natural Capital Project, Stanford University, Stanford, USA",[],{"title":3265,"gsAuthor":3267},{"VI":3266},"Daniel Paredes",{"VOID":3268},"[\"hqovUogAAAAJ\"]",{"id":3270,"sortIndex":162,"researcher":20,"roles":3271,"affiliations":3272,"properties":3281,"displayName":3283,"givenName":20,"familyName":20},"6e2bf7bb-85ff-47e4-b130-adda613bc5b3",[703],[3273],{"id":3274,"sortIndex":21,"affiliation":3275,"properties":20},"7ce06b70-0268-4d6b-8833-af81f57eb81b",{"id":3274,"createTime":20,"updateTime":20,"relativeEntities":3276,"slug":20,"properties":3277,"entityType":20,"verifyStatus":20,"verifyTime":20,"verifyNote":20,"languages":20,"translateLanguages":20,"viewCount":20,"url":20,"parentIds":3280,"statistic":20},[],{"title":3278},{"VI":3279},"Department of Wildlife, Fish and Conservation Biology, University of California, Davis, USA",[],{"title":3282,"gsAuthor":3284},{"VI":3283},"Daniel S. Karp",{"VOID":3285},"[\"_5PRunQAAAAJ\"]",{"id":3287,"sortIndex":178,"researcher":20,"roles":3288,"affiliations":3289,"properties":3296,"displayName":3298,"givenName":20,"familyName":20},"cd411627-bfdb-425a-a082-8d94ea0166bf",[703],[3290],{"id":3257,"sortIndex":21,"affiliation":3291,"properties":20},{"id":3257,"createTime":20,"updateTime":20,"relativeEntities":3292,"slug":20,"properties":3293,"entityType":20,"verifyStatus":20,"verifyTime":20,"verifyNote":20,"languages":20,"translateLanguages":20,"viewCount":20,"url":20,"parentIds":3295,"statistic":20},[],{"title":3294},{"VI":3262},[],{"title":3297,"gsAuthor":3299},{"VI":3298},"Rebecca 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