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S., 1998, Weak trophic interactions and the balance of nature, Nature, 395, 455, 10.1038\u002F27427",{"doi":454},"10.1038\u002F27427",{"id":23,"text":456,"url":23,"identifiers":457},"10.1073\u002Fpnas.111055298",{"doi":456},{"id":23,"text":459,"url":23,"identifiers":460},"10.1038\u002F416084a",{"doi":459},{"id":23,"text":462,"url":23,"identifiers":463},"Primack R, 2008, A primer of conservation biology",{},{"id":23,"text":465,"url":23,"identifiers":466},"10.1139\u002Ff90-227",{"doi":465},{"id":23,"text":468,"url":23,"identifiers":469},"10.1016\u002FB978-0-12-381363-3.00003-4",{"doi":468},{"id":23,"text":471,"url":23,"identifiers":472},"10.1016\u002Fj.baae.2011.09.006",{"doi":471},{"id":23,"text":474,"url":23,"identifiers":475},"10.1890\u002F03-5353",{"doi":474},{"id":23,"text":477,"url":23,"identifiers":478},"10.1371\u002Fjournal.pone.0010378",{"doi":477},{"id":23,"text":480,"url":23,"identifiers":481},"10.1016\u002Fj.tree.2011.09.001",{"doi":480},{"id":23,"text":483,"url":23,"identifiers":484},"10.1139\u002Ff01-213",{"doi":483},{"id":23,"text":486,"url":23,"identifiers":487},"10.1073\u002Fpnas.1014353108",{"doi":486},{"id":23,"text":489,"url":23,"identifiers":490},"10.1111\u002Fj.1461-0248.2010.01535.x",{"doi":489},{"id":23,"text":492,"url":23,"identifiers":493},"Walker C. H., 2001, Principles of ecotoxicology",{},{"id":23,"text":495,"url":23,"identifiers":496},"10.1038\u002F35004572",{"doi":495},{"id":23,"text":498,"url":23,"identifiers":499},"Williams R. J., 2004, Stabilization of chaotic and non‐permanent food web dynamics, Eur. Phys. J. B, 38, 297, 10.1140\u002Fepjb\u002Fe2004-00122-1",{"doi":500},"10.1140\u002Fepjb\u002Fe2004-00122-1",{"id":23,"text":502,"url":23,"identifiers":503},"10.1111\u002Fj.1365-2656.2008.01362.x",{"doi":502},{"id":23,"text":505,"url":23,"identifiers":506},"10.1086\u002F285380",{"doi":505},{"id":23,"text":508,"url":23,"identifiers":509},"10.1111\u002Fj.0030-1299.2006.14220.x",{"doi":508},{"id":511,"createTime":512,"updateTime":512,"relativeEntities":513,"slug":514,"properties":515,"entityType":138,"verifyStatus":22,"verifyTime":512,"verifyNote":526,"languages":527,"translateLanguages":23,"viewCount":24,"primaryUrl":528,"fullTextUrl":23,"authors":529,"publicationType":166,"publisherRelationship":559,"citationCount":610,"citationInfo":611,"publishDate":616,"publishYear":612,"citationAnalyzeStatus":22,"lastCitationAnalyze":23,"indexDatabases":617,"openAccess":23,"references":618,"isForceReanalyzing":225},"d3b3004f-b749-4118-87e4-b5ece2372872","2025-02-10T01:42:33.228+00:00",[],"Stable-isotope-analyses-document-intraguild-predation-in-wolf-spiders-Araneae-Lycosidae-and-underline-beneficial-effects-of-alternative-prey-and-microhabitat-structure-on-intraguild-prey-survival",{"openalex":516,"mag":518,"abstract":520,"title":522,"doi":524},{"VOID":517},"W2040934860",{"VOID":519},"2040934860",{"EN":521},"\u003Cjats:p>Intraguild predation (IGP) is common among generalist predators and an important issue in food web theory, because IGP may destabilise communities by increasing extinction of species. Also, IGP may interfere with the effectiveness of generalist predators as biological control agents. In general, occurrence of IGP in laboratory or field studies is inferred from abundance data or direct observations only. We investigated if tracing stable isotopes allows distinction between different types of predation and confirmation of IGP. Wolf spiders were chosen as model organisms for generalist predators; IGP of third instar\u003Cjats:italic>A. cuneata\u003C\u002Fjats:italic>on second instar\u003Cjats:italic>P. palustris\u003C\u002Fjats:italic>was investigated in a laboratory experiment. The availability of alternative prey and the complexity of the microhabitat were manipulated, since both factors are thought to facilitate coexistence of predators.\u003C\u002Fjats:p>\u003Cjats:p>Stable isotope analysis documented predation of\u003Cjats:italic>A. cuneata\u003C\u002Fjats:italic>on\u003Cjats:italic>P. palustris\u003C\u002Fjats:italic>and predation on alternative prey by both juveniles. Both the presence of alternative prey and the availability of shelter reduced mortality of juvenile\u003Cjats:italic>P. palustris\u003C\u002Fjats:italic>during the first week. During the second week mortality increased in complex structure without alternative prey presumably due to enhanced activity and cannibalism among starving\u003Cjats:italic>P. palustris\u003C\u002Fjats:italic>. Thus, microhabitat complexity and prey abundance may foster coexistence of wolf spiders in the field.\u003C\u002Fjats:p>\u003Cjats:p>In conclusion, stable isotope analysis was proven a powerful tool to investigate animal behaviour without direct observation. The method allowed disentangling predator feeding behaviour when more than one type of prey was present.\u003C\u002Fjats:p>",{"EN":523},"Stable isotope analyses document intraguild predation in wolf spiders (Araneae: Lycosidae) and underline beneficial effects of alternative prey and microhabitat structure on intraguild prey survival",{"VOID":525},"10.1111\u002Fj.2006.0030-1299.14421.x","Author affiliation is blank",[142],"https:\u002F\u002Fonlinelibrary.wiley.com\u002Fdoi\u002F10.1111\u002Fj.2006.0030-1299.14421.x",[530,539,548],{"id":531,"sortIndex":24,"researcher":23,"roles":532,"affiliations":533,"properties":534,"displayName":536,"givenName":23,"familyName":23},"30de9ab0-7eb4-4692-9991-89cec5d7a820",[],[],{"title":535,"openalex":537},{"EN":536},"Silke 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Q., 1992, Cannibalism: ecology and evolution among diverse taxa, 13, 10.1093\u002Foso\u002F9780198546504.003.0002",{"doi":649},"10.1093\u002Foso\u002F9780198546504.003.0002",{"id":23,"text":651,"url":23,"identifiers":652},"10.1007\u002F978-3-642-74001-5",{"doi":651},{"id":23,"text":654,"url":23,"identifiers":655},"10.1890\u002F0012-9658(2002)083[0643:IPDICS]2.0.CO;2",{"doi":654},{"id":23,"text":657,"url":23,"identifiers":658},"Hodge M. A., 1999, The implications of intraguild predation for the role of spiders in biological control, J. Arachnol., 27, 351",{},{"id":23,"text":660,"url":23,"identifiers":661},"10.1139\u002Ff95-116",{"doi":660},{"id":23,"text":663,"url":23,"identifiers":664},"10.1086\u002F286018",{"doi":663},{"id":23,"text":666,"url":23,"identifiers":667},"10.1016\u002Fj.biocontrol.2004.10.002",{"doi":666},{"id":23,"text":669,"url":23,"identifiers":670},"10.1007\u002Fs00442-004-1497-3",{"doi":669},{"id":23,"text":672,"url":23,"identifiers":673},"10.1111\u002Fj.0307-6946.2004.00601.x",{"doi":672},{"id":23,"text":675,"url":23,"identifiers":676},"10.1034\u002Fj.1600-0706.2002.960113.x",{"doi":675},{"id":23,"text":678,"url":23,"identifiers":679},"10.1890\u002F0012-9658(1998)079[1084:IPAAPC]2.0.CO;2",{"doi":678},{"id":23,"text":681,"url":23,"identifiers":682},"Marshall S. D., 1999, Spider competition in structurally simple ecosystems, J. Arachnol., 27, 343",{},{"id":23,"text":684,"url":23,"identifiers":685},"10.1890\u002F03-0629",{"doi":684},{"id":23,"text":687,"url":23,"identifiers":688},"10.1098\u002Frspb.1997.0172",{"doi":687},{"id":23,"text":690,"url":23,"identifiers":691},"10.1111\u002Fj.0030-1299.2006.13990.x",{"doi":690},{"id":23,"text":693,"url":23,"identifiers":694},"10.1078\u002F0031-4056-00087",{"doi":693},{"id":23,"text":696,"url":23,"identifiers":697},"10.1046\u002Fj.1570-7458.2000.00722.x",{"doi":696},{"id":23,"text":699,"url":23,"identifiers":700},"10.1890\u002F0012-9658(1997)078[1266:RFLRSO]2.0.CO;2",{"doi":699},{"id":23,"text":702,"url":23,"identifiers":703},"10.1078\u002F1439-1791-00094",{"doi":702},{"id":23,"text":705,"url":23,"identifiers":706},"10.1007\u002Fs004420100813",{"doi":705},{"id":23,"text":708,"url":23,"identifiers":709},"10.1007\u002FBF00377328",{"doi":708},{"id":23,"text":711,"url":23,"identifiers":712},"10.1890\u002F0012-9658(2000)081[0852:WCSINA]2.0.CO;2",{"doi":711},{"id":23,"text":714,"url":23,"identifiers":715},"10.1890\u002F0012-9658(2002)083[0703:USITET]2.0.CO;2",{"doi":714},{"id":23,"text":717,"url":23,"identifiers":718},"10.1146\u002Fannurev.es.18.110187.001453",{"doi":717},{"id":23,"text":720,"url":23,"identifiers":721},"Reineking A. Langel R. and Schikowski J. 1993.15N 13C‐online‐measurements with an elemental analyser (Carlo Erba NA 1500) a modified trapping box and a gas isotope mass spectrometer (Finnigan MAT251). – Isotopenpraxis Environ. Health Stud. 29: 169–174.",{"doi":722},"10.1080\u002F10256019308046151",{"id":23,"text":724,"url":23,"identifiers":725},"10.1016\u002Fj.baae.2005.02.007",{"doi":724},{"id":23,"text":727,"url":23,"identifiers":728},"Rickers S. Langel R. and Scheu S. 2006. Dieatary routing of nutrients from prey to offspring in a generalist predator: effects of prey quality. – Funct. Ecol. 20: 124–131.",{"doi":729},"10.1111\u002Fj.1365-2435.2006.01077.x",{"id":23,"text":731,"url":23,"identifiers":732},"Riechert S. E., 1999, The hows and whys of successful pest suppression by spiders: insights from case studies, J. Arachnol., 27, 387",{},{"id":23,"text":734,"url":23,"identifiers":735},"Roberts M. J., 1995, Collins field guide: spiders, Britain and northern Europe",{},{"id":23,"text":737,"url":23,"identifiers":738},"10.1007\u002Fs002650050570",{"doi":737},{"id":23,"text":740,"url":23,"identifiers":741},"Scheu S. and Folger M. 2004. Single and mixed diets in Collembola: effects on reproduction and stable isotope fractioning. – Funct. Ecol. 18: 94–102.",{"doi":742},"10.1046\u002Fj.0269-8463.2004.00807.x",{"id":23,"text":744,"url":23,"identifiers":745},"Snyder W. E. and Hurd L. E. 1995. Egg. hatched phenology and intraguild predation between two mantid species. – Oecologia 104: 496–500.",{"doi":746},"10.1007\u002FBF00341347",{"id":23,"text":748,"url":23,"identifiers":749},"10.1006\u002Fbcon.1999.0723",{"doi":748},{"id":23,"text":751,"url":23,"identifiers":752},"Sokal R. R., 2001, Biometry",{},{"id":23,"text":754,"url":23,"identifiers":755},"10.1007\u002FBF01875456",{"doi":754},{"id":23,"text":757,"url":23,"identifiers":758},"10.1146\u002Fannurev.ento.47.091201.145240",{"doi":757},{"id":23,"text":760,"url":23,"identifiers":761},"Toft S., 1999, Prey choice and spider fitness, J. Arachnol., 27, 301",{},{"id":23,"text":763,"url":23,"identifiers":764},"10.1007\u002Fs004420050776",{"doi":763},{"id":23,"text":766,"url":23,"identifiers":767},"Uetz G. W., 1992, Survivorship of wolf spiders (Lycosidae) reared on different diets, J. Arachnol., 20, 207",{},{"id":23,"text":769,"url":23,"identifiers":770},"10.1007\u002Fs00442-003-1270-z",{"doi":769},{"id":23,"text":772,"url":23,"identifiers":773},"10.2307\u002F2265637",{"doi":772},{"id":23,"text":775,"url":23,"identifiers":776},"10.1007\u002Fs004420050107",{"doi":775},{"id":23,"text":778,"url":23,"identifiers":779},"10.1006\u002Fanbe.1999.1180",{"doi":778},{"id":23,"text":781,"url":23,"identifiers":782},"Walker S. E., 2003, The relationship between offspring size and performance in the wolf spider Hogna helluo (Araneae: Lycosidae), Evol. Ecol. Res., 5, 19",{},{"id":23,"text":784,"url":23,"identifiers":785},"10.1111\u002Fj.1570-7458.1992.tb01636.x",{"doi":784},{"id":23,"text":787,"url":23,"identifiers":788},"10.1007\u002Fs004420050914",{"doi":787},{"id":23,"text":790,"url":23,"identifiers":791},"10.2307\u002F1940688",{"doi":790},{"id":23,"text":793,"url":23,"identifiers":794},"10.1046\u002Fj.1365-2656.2002.00669.x",{"doi":793},{"id":796,"createTime":797,"updateTime":797,"relativeEntities":798,"slug":799,"properties":800,"entityType":138,"verifyStatus":139,"verifyTime":797,"verifyNote":140,"languages":811,"translateLanguages":23,"viewCount":24,"primaryUrl":812,"fullTextUrl":23,"authors":813,"publicationType":166,"publisherRelationship":893,"citationCount":944,"citationInfo":945,"publishDate":951,"publishYear":946,"citationAnalyzeStatus":22,"lastCitationAnalyze":23,"indexDatabases":952,"openAccess":23,"references":953,"isForceReanalyzing":225},"44d9f7df-291c-4f0a-9896-747b35884b1f","2025-02-08T13:25:23.900+00:00",[],"Forest-dynamics-following-eastern-hemlock-mortality-in-the-southern-Appalachians",{"openalex":801,"mag":803,"abstract":805,"title":807,"doi":809},{"VOID":802},"W2158503093",{"VOID":804},"2158503093",{"EN":806},"\u003Cjats:p>Understanding changes in community composition caused by invasive species is critical for predicting effects on ecosystem function, particularly when the invasive threatens a foundation species. Here we focus on dynamics of forest structure, composition and microclimate, and how these interact in southern Appalachian riparian forests following invasion by hemlock woolly adelgid, HWA, \u003Cjats:italic>Adelges tsugae\u003C\u002Fjats:italic>. We measured and quantified changes in microclimate; canopy mortality; canopy and shrub growth; understory species composition; and the cover and diversity in riparian forests dominated by eastern hemlock \u003Cjats:italic>Tsuga canadensis\u003C\u002Fjats:italic> over a period of seven years. Treatments manipulated hemlock mortality either through invasion (HWA infested stands) or girdling (GDL) hemlock trees.\u003C\u002Fjats:p>\u003Cjats:p>Mortality was rapid, with 50% hemlock tree mortality occurring after six years of invasion, in contrast to more than 50% mortality in two years following girdling. Although 50% of hemlock trees were still alive five years after infestation, leaf area lost was similar to that of girdled trees. As such, overall responses over time (changes in light transmittance, growth, soil moisture) were identical to girdled stands with 100% mortality. Our results showed different growth responses of the canopy species, shrubs and ground layer, with the latter being substantially influenced by presence of the evergreen shrub, rhododendron \u003Cjats:italic>Rhododendron maximum\u003C\u002Fjats:italic>. Although ground layer richness in the infested and girdled stands increased by threefold, they did not approach levels recorded in hardwood forests without rhododendron. Increased growth of co‐occurring canopy trees occurred in the first few years following hemlock decline, with similar responses in both treatments. In contrast, growth of rhododendron continued to increase over time. By the end of the study it had a 2.6‐fold higher growth rate than expected, likely taking advantage of increased light available during leaf‐off periods of the deciduous species. Increased growth and dominance of rhododendron may be a major determinant of future responses in southern Appalachian ecosystems; however, our results suggest hemlock will be replaced by a mix of \u003Cjats:italic>Acer\u003C\u002Fjats:italic>, \u003Cjats:italic>Betula\u003C\u002Fjats:italic>, \u003Cjats:italic>Fagus\u003C\u002Fjats:italic> and \u003Cjats:italic>Quercus\u003C\u002Fjats:italic> canopy genera where establishment is not limited by rhododendron.\u003C\u002Fjats:p>",{"EN":808},"Forest dynamics following eastern hemlock mortality in the southern Appalachians",{"VOID":810},"10.1111\u002Fj.1600-0706.2011.19622.x",[142],"https:\u002F\u002Fonlinelibrary.wiley.com\u002Fdoi\u002F10.1111\u002Fj.1600-0706.2011.19622.x",[814,831,846,861,876],{"id":815,"sortIndex":24,"researcher":23,"roles":816,"affiliations":817,"properties":826,"displayName":828,"givenName":23,"familyName":23},"bfdb7174-0a6c-4e08-bb63-6398f8b5b45d",[],[818],{"id":819,"sortIndex":24,"affiliation":820,"properties":23},"37863c17-817a-4c29-970f-635bb42cbed9",{"id":819,"createTime":23,"updateTime":23,"relativeEntities":821,"slug":23,"properties":822,"entityType":23,"verifyStatus":23,"verifyTime":23,"verifyNote":23,"languages":23,"translateLanguages":23,"viewCount":23,"url":23,"parentIds":825,"statistic":23},[],{"title":823},{"VI":824},"USDA Forest Service, Southern Research Station, Coweeta Hydrologic Laboratory, Otto, NC 28763, USA",[],{"title":827,"openalex":829},{"EN":828},"Chelcy R. 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Since birch aphids actively seek the first yellowing leaves for breeding in autumn, it is obvious that autumn colour of foliage does not repel migrating aphids. We suggest that aphids use bright colours as a cue to detect individual trees and leaves that are good sources of nitrogen in the form of amino acids in autumn. The active formation of bright‐coloured pigments in leaves is needed to protect them from photo inhibition during energy consuming nutrient retranslocation under cold autumn conditions. During nutrient export from leaves, nitrogen is in the form of amino acids in the sieve elements and easily available for aphids. Therefore, bright colours may act as a signal of easily available high‐quality food for viviparous aphid migrants that are selecting suitable trees for their sexual offspring reproduction. The females of sexual generation grown on the better quality food probably can oviposit the over‐wintering eggs to the twigs in higher numbers, which may have an adaptive advantage in competition with conspecific females.\u003C\u002Fjats:p>",{"EN":1194},"Bright autumn colours of deciduous trees attract aphids: nutrient retranslocation hypothesis",{"VOID":1196},"10.1034\u002Fj.1600-0706.2002.990119.x",[142],"https:\u002F\u002Fonlinelibrary.wiley.com\u002Fdoi\u002F10.1034\u002Fj.1600-0706.2002.990119.x",[1200,1219],{"id":1201,"sortIndex":24,"researcher":23,"roles":1202,"affiliations":1203,"properties":1212,"displayName":1216,"givenName":23,"familyName":23},"6a39b31a-7611-45b0-8220-fff5c957c42c",[],[1204],{"id":1205,"sortIndex":24,"affiliation":1206,"properties":23},"33cfe988-13e7-4877-8abd-78e3eb504001",{"id":1205,"createTime":23,"updateTime":23,"relativeEntities":1207,"slug":23,"properties":1208,"entityType":23,"verifyStatus":23,"verifyTime":23,"verifyNote":23,"languages":23,"translateLanguages":23,"viewCount":23,"url":23,"parentIds":1211,"statistic":23},[],{"title":1209},{"EN":1210},"Dept of Ecology and Environmental Science, Univ. of Kuopio, P.O. 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Despite growing evidence for the widespread occurrence HFA effects, what drives HFA is not understood as its strength appears highly variable and context‐dependent. Our work advances current knowledge about HFA effects by testing under what conditions HFA is most important. Using published data on mass loss from 125 reciprocal litter transplants from 35 studies, we evaluated if HFA effects were modulated by macroclimate, litter quality traits, and the dissimilarity between ‘home’ and ‘away’ of both the quality of reciprocally exchanged litters and plant community type. Our results confirmed the occurrence of an overall, worldwide, HFA effect on decomposition with on average 7.5% faster decomposition at home. However, there was considerable variation in the strength and direction (sometimes opposite to expectations) of these effects. While macroclimate and average litter quality had weak or no impact on HFA effects, home‐field effects became stronger (regardless of the direction) when the quality of ‘home’ and ‘away’ litters became more dissimilar (e.g. had a greater dissimilarity in N:P ratio; F\u003Cjats:sub>1,42\u003C\u002Fjats:sub>= 6.39, p = 0.015). Further, home‐field effects were determined by the degree of difference between the types of dominant plant species in the ‘home’ versus ‘away’ communities (F\u003Cjats:sub>2,105\u003C\u002Fjats:sub>= 4.03, p = 0.021). We conclude that home‐field advantage is not restricted to particular litter types or climate zones, and that the dissimilarity in plant communities and litter quality between the ‘home’ and ‘away’ locations, are the most significant drivers of home‐field effects.\u003C\u002Fjats:p>",{"EN":1389},"Litter quality and environmental controls of home‐field advantage effects on litter decomposition",{"VOID":1391},"10.1111\u002Foik.01374","2025-02-04T05:51:38.959+00:00",[142],"https:\u002F\u002Fonlinelibrary.wiley.com\u002Fdoi\u002F10.1111\u002Foik.01374",[1396,1423,1450,1469],{"id":1397,"sortIndex":24,"researcher":23,"roles":1398,"affiliations":1399,"properties":1416,"displayName":1420,"givenName":23,"familyName":23},"34c06df5-b173-42f6-bded-c2e6a69da69e",[],[1400,1408],{"id":1401,"sortIndex":24,"affiliation":1402,"properties":23},"930d813a-8d01-4c3c-bad3-4a62206afe56",{"id":1401,"createTime":23,"updateTime":23,"relativeEntities":1403,"slug":23,"properties":1404,"entityType":23,"verifyStatus":23,"verifyTime":23,"verifyNote":23,"languages":23,"translateLanguages":23,"viewCount":23,"url":23,"parentIds":1407,"statistic":23},[],{"title":1405},{"EN":1406},"Dept of Terrestrial Ecology Netherlands Inst. of Ecology PO Box 50, NL‐6700 AB Wageningen the Netherlands",[],{"id":1409,"sortIndex":87,"affiliation":1410,"properties":23},"aa5d3daa-6867-49b7-823c-357c588e12a4",{"id":1409,"createTime":23,"updateTime":23,"relativeEntities":1411,"slug":23,"properties":1412,"entityType":23,"verifyStatus":23,"verifyTime":23,"verifyNote":23,"languages":23,"translateLanguages":23,"viewCount":23,"url":23,"parentIds":1415,"statistic":23},[],{"title":1413},{"EN":1414},"Dept of Terrestrial Ecology, Netherlands Inst. of Ecology, PO Box 50, NL-6700 AB Wageningen, the Netherlands",[],{"orcid":1417,"title":1419,"openalex":1421},{"VOID":1418},"https:\u002F\u002Forcid.org\u002F0000-0001-7736-9998",{"EN":1420},"G. 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In the second year of the experiment, community biomass, CE and SE increased compared to the first year. The contribution of SE to this positive effect was greater than that of CE. The increased contribution of SE was associated with root traits: SE increased most in communities with high abundance of species with deep, thick and dense roots. In contrast, changes in CE were not related to trait diversity or CWM trait values. Together, these results suggest that increased positive effects of species richness on community biomass in a dry year were mainly driven by increased dominance of deep‐rooting species, supporting the insurance hypothesis of biodiversity. 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