Parasitism cost of living in a high quality habitat in the bog fritillary butterfly
Abstract Habitat quality and the impact of natural enemies might profoundly affect metapopulation dynamics and viability. However, their relative impact has usually been considered independently. Here we address the question of how caterpillar habitat quality and parasitism prevalence interact to sh...
Ausführliche Beschreibung
Gespeichert in:
| Autor*in: |
Choutt, Julie [verfasserIn] Turlure, Camille [verfasserIn] Baguette, Michel [verfasserIn] Schtickzelle, Nicolas [verfasserIn] |
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| Format: |
E-Artikel |
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| Sprache: |
Englisch |
| Erschienen: |
2011 |
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| Schlagwörter: |
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| Übergeordnetes Werk: |
Enthalten in: Biodiversity and conservation - Dordrecht : Springer Netherlands, 1992, 20(2011), 13 vom: 13. Sept., Seite 3117-3131 |
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| Übergeordnetes Werk: |
volume:20 ; year:2011 ; number:13 ; day:13 ; month:09 ; pages:3117-3131 |
| Links: |
|---|
| DOI / URN: |
10.1007/s10531-011-0151-8 |
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| Katalog-ID: |
SPR010916199 |
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| 245 | 1 | 0 | |a Parasitism cost of living in a high quality habitat in the bog fritillary butterfly |
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| 520 | |a Abstract Habitat quality and the impact of natural enemies might profoundly affect metapopulation dynamics and viability. However, their relative impact has usually been considered independently. Here we address the question of how caterpillar habitat quality and parasitism prevalence interact to shape habitat selection in the bog fritillary butterfly Boloria eunomia, parasitized at the caterpillar stage by a specialist wasp, Cotesiaeunomiae. We first classified habitat quality by relating caterpillar density to descriptors of different microhabitat types. Second, we investigated parasitism prevalence in those different microhabitats. Our results show that caterpillars and parasitoids mapped onto the same microhabitats, mainly zones with high abundance of the host plant. Accordingly, we suggest that both egg-laying females and parasitoids use the same cues for habitat selection. As a consequence, there should be a fitness cost for B. eunomia females to lay their eggs in places where parasitism prevalence is high. We indeed detected that B. eunomia females frequently laid eggs in habitat types that presented suboptimal microhabitat conditions for caterpillars. This suggests that the lower parasitism prevalence in these suboptimal habitat types counterbalances lower caterpillar survival, leading to an overall similar survival in optimal and suboptimal habitat types. Spreading eggs in different habitat types is thus expected to be a safe strategy to mitigate the adverse possible effects of environmental stochasticity and parasitism prevalence on offspring survival unequal among microhabitat types. From a conservation viewpoint, the preservation of habitat heterogeneity, including optimal but also suboptimal habitat areas, is crucial to ensure persistence of both the host and its parasitoid. | ||
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| 700 | 1 | |a Turlure, Camille |e verfasserin |4 aut | |
| 700 | 1 | |a Baguette, Michel |e verfasserin |4 aut | |
| 700 | 1 | |a Schtickzelle, Nicolas |e verfasserin |4 aut | |
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10.1007/s10531-011-0151-8 doi (DE-627)SPR010916199 (SPR)s10531-011-0151-8-e DE-627 ger DE-627 rakwb eng 570 ASE 42.90 bkl 43.31 bkl Choutt, Julie verfasserin aut Parasitism cost of living in a high quality habitat in the bog fritillary butterfly 2011 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Habitat quality and the impact of natural enemies might profoundly affect metapopulation dynamics and viability. However, their relative impact has usually been considered independently. Here we address the question of how caterpillar habitat quality and parasitism prevalence interact to shape habitat selection in the bog fritillary butterfly Boloria eunomia, parasitized at the caterpillar stage by a specialist wasp, Cotesiaeunomiae. We first classified habitat quality by relating caterpillar density to descriptors of different microhabitat types. Second, we investigated parasitism prevalence in those different microhabitats. Our results show that caterpillars and parasitoids mapped onto the same microhabitats, mainly zones with high abundance of the host plant. Accordingly, we suggest that both egg-laying females and parasitoids use the same cues for habitat selection. As a consequence, there should be a fitness cost for B. eunomia females to lay their eggs in places where parasitism prevalence is high. We indeed detected that B. eunomia females frequently laid eggs in habitat types that presented suboptimal microhabitat conditions for caterpillars. This suggests that the lower parasitism prevalence in these suboptimal habitat types counterbalances lower caterpillar survival, leading to an overall similar survival in optimal and suboptimal habitat types. Spreading eggs in different habitat types is thus expected to be a safe strategy to mitigate the adverse possible effects of environmental stochasticity and parasitism prevalence on offspring survival unequal among microhabitat types. From a conservation viewpoint, the preservation of habitat heterogeneity, including optimal but also suboptimal habitat areas, is crucial to ensure persistence of both the host and its parasitoid. Habitat heterogeneity (dpeaa)DE-He213 Larval parasitoid (dpeaa)DE-He213 Peat bog (dpeaa)DE-He213 Turlure, Camille verfasserin aut Baguette, Michel verfasserin aut Schtickzelle, Nicolas verfasserin aut Enthalten in Biodiversity and conservation Dordrecht : Springer Netherlands, 1992 20(2011), 13 vom: 13. Sept., Seite 3117-3131 (DE-627)31751055X (DE-600)2000787-5 1572-9710 nnns volume:20 year:2011 number:13 day:13 month:09 pages:3117-3131 https://dx.doi.org/10.1007/s10531-011-0151-8 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA SSG-OPC-GGO SSG-OPC-ASE GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_381 GBV_ILN_602 GBV_ILN_636 GBV_ILN_647 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2360 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 42.90 ASE 43.31 ASE AR 20 2011 13 13 09 3117-3131 |
| spelling |
10.1007/s10531-011-0151-8 doi (DE-627)SPR010916199 (SPR)s10531-011-0151-8-e DE-627 ger DE-627 rakwb eng 570 ASE 42.90 bkl 43.31 bkl Choutt, Julie verfasserin aut Parasitism cost of living in a high quality habitat in the bog fritillary butterfly 2011 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Habitat quality and the impact of natural enemies might profoundly affect metapopulation dynamics and viability. However, their relative impact has usually been considered independently. Here we address the question of how caterpillar habitat quality and parasitism prevalence interact to shape habitat selection in the bog fritillary butterfly Boloria eunomia, parasitized at the caterpillar stage by a specialist wasp, Cotesiaeunomiae. We first classified habitat quality by relating caterpillar density to descriptors of different microhabitat types. Second, we investigated parasitism prevalence in those different microhabitats. Our results show that caterpillars and parasitoids mapped onto the same microhabitats, mainly zones with high abundance of the host plant. Accordingly, we suggest that both egg-laying females and parasitoids use the same cues for habitat selection. As a consequence, there should be a fitness cost for B. eunomia females to lay their eggs in places where parasitism prevalence is high. We indeed detected that B. eunomia females frequently laid eggs in habitat types that presented suboptimal microhabitat conditions for caterpillars. This suggests that the lower parasitism prevalence in these suboptimal habitat types counterbalances lower caterpillar survival, leading to an overall similar survival in optimal and suboptimal habitat types. Spreading eggs in different habitat types is thus expected to be a safe strategy to mitigate the adverse possible effects of environmental stochasticity and parasitism prevalence on offspring survival unequal among microhabitat types. From a conservation viewpoint, the preservation of habitat heterogeneity, including optimal but also suboptimal habitat areas, is crucial to ensure persistence of both the host and its parasitoid. Habitat heterogeneity (dpeaa)DE-He213 Larval parasitoid (dpeaa)DE-He213 Peat bog (dpeaa)DE-He213 Turlure, Camille verfasserin aut Baguette, Michel verfasserin aut Schtickzelle, Nicolas verfasserin aut Enthalten in Biodiversity and conservation Dordrecht : Springer Netherlands, 1992 20(2011), 13 vom: 13. Sept., Seite 3117-3131 (DE-627)31751055X (DE-600)2000787-5 1572-9710 nnns volume:20 year:2011 number:13 day:13 month:09 pages:3117-3131 https://dx.doi.org/10.1007/s10531-011-0151-8 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA SSG-OPC-GGO SSG-OPC-ASE GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_381 GBV_ILN_602 GBV_ILN_636 GBV_ILN_647 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2360 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 42.90 ASE 43.31 ASE AR 20 2011 13 13 09 3117-3131 |
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10.1007/s10531-011-0151-8 doi (DE-627)SPR010916199 (SPR)s10531-011-0151-8-e DE-627 ger DE-627 rakwb eng 570 ASE 42.90 bkl 43.31 bkl Choutt, Julie verfasserin aut Parasitism cost of living in a high quality habitat in the bog fritillary butterfly 2011 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Habitat quality and the impact of natural enemies might profoundly affect metapopulation dynamics and viability. However, their relative impact has usually been considered independently. Here we address the question of how caterpillar habitat quality and parasitism prevalence interact to shape habitat selection in the bog fritillary butterfly Boloria eunomia, parasitized at the caterpillar stage by a specialist wasp, Cotesiaeunomiae. We first classified habitat quality by relating caterpillar density to descriptors of different microhabitat types. Second, we investigated parasitism prevalence in those different microhabitats. Our results show that caterpillars and parasitoids mapped onto the same microhabitats, mainly zones with high abundance of the host plant. Accordingly, we suggest that both egg-laying females and parasitoids use the same cues for habitat selection. As a consequence, there should be a fitness cost for B. eunomia females to lay their eggs in places where parasitism prevalence is high. We indeed detected that B. eunomia females frequently laid eggs in habitat types that presented suboptimal microhabitat conditions for caterpillars. This suggests that the lower parasitism prevalence in these suboptimal habitat types counterbalances lower caterpillar survival, leading to an overall similar survival in optimal and suboptimal habitat types. Spreading eggs in different habitat types is thus expected to be a safe strategy to mitigate the adverse possible effects of environmental stochasticity and parasitism prevalence on offspring survival unequal among microhabitat types. From a conservation viewpoint, the preservation of habitat heterogeneity, including optimal but also suboptimal habitat areas, is crucial to ensure persistence of both the host and its parasitoid. Habitat heterogeneity (dpeaa)DE-He213 Larval parasitoid (dpeaa)DE-He213 Peat bog (dpeaa)DE-He213 Turlure, Camille verfasserin aut Baguette, Michel verfasserin aut Schtickzelle, Nicolas verfasserin aut Enthalten in Biodiversity and conservation Dordrecht : Springer Netherlands, 1992 20(2011), 13 vom: 13. Sept., Seite 3117-3131 (DE-627)31751055X (DE-600)2000787-5 1572-9710 nnns volume:20 year:2011 number:13 day:13 month:09 pages:3117-3131 https://dx.doi.org/10.1007/s10531-011-0151-8 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA SSG-OPC-GGO SSG-OPC-ASE GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_381 GBV_ILN_602 GBV_ILN_636 GBV_ILN_647 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2360 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 42.90 ASE 43.31 ASE AR 20 2011 13 13 09 3117-3131 |
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10.1007/s10531-011-0151-8 doi (DE-627)SPR010916199 (SPR)s10531-011-0151-8-e DE-627 ger DE-627 rakwb eng 570 ASE 42.90 bkl 43.31 bkl Choutt, Julie verfasserin aut Parasitism cost of living in a high quality habitat in the bog fritillary butterfly 2011 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Habitat quality and the impact of natural enemies might profoundly affect metapopulation dynamics and viability. However, their relative impact has usually been considered independently. Here we address the question of how caterpillar habitat quality and parasitism prevalence interact to shape habitat selection in the bog fritillary butterfly Boloria eunomia, parasitized at the caterpillar stage by a specialist wasp, Cotesiaeunomiae. We first classified habitat quality by relating caterpillar density to descriptors of different microhabitat types. Second, we investigated parasitism prevalence in those different microhabitats. Our results show that caterpillars and parasitoids mapped onto the same microhabitats, mainly zones with high abundance of the host plant. Accordingly, we suggest that both egg-laying females and parasitoids use the same cues for habitat selection. As a consequence, there should be a fitness cost for B. eunomia females to lay their eggs in places where parasitism prevalence is high. We indeed detected that B. eunomia females frequently laid eggs in habitat types that presented suboptimal microhabitat conditions for caterpillars. This suggests that the lower parasitism prevalence in these suboptimal habitat types counterbalances lower caterpillar survival, leading to an overall similar survival in optimal and suboptimal habitat types. Spreading eggs in different habitat types is thus expected to be a safe strategy to mitigate the adverse possible effects of environmental stochasticity and parasitism prevalence on offspring survival unequal among microhabitat types. From a conservation viewpoint, the preservation of habitat heterogeneity, including optimal but also suboptimal habitat areas, is crucial to ensure persistence of both the host and its parasitoid. Habitat heterogeneity (dpeaa)DE-He213 Larval parasitoid (dpeaa)DE-He213 Peat bog (dpeaa)DE-He213 Turlure, Camille verfasserin aut Baguette, Michel verfasserin aut Schtickzelle, Nicolas verfasserin aut Enthalten in Biodiversity and conservation Dordrecht : Springer Netherlands, 1992 20(2011), 13 vom: 13. Sept., Seite 3117-3131 (DE-627)31751055X (DE-600)2000787-5 1572-9710 nnns volume:20 year:2011 number:13 day:13 month:09 pages:3117-3131 https://dx.doi.org/10.1007/s10531-011-0151-8 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA SSG-OPC-GGO SSG-OPC-ASE GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_381 GBV_ILN_602 GBV_ILN_636 GBV_ILN_647 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2360 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 42.90 ASE 43.31 ASE AR 20 2011 13 13 09 3117-3131 |
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10.1007/s10531-011-0151-8 doi (DE-627)SPR010916199 (SPR)s10531-011-0151-8-e DE-627 ger DE-627 rakwb eng 570 ASE 42.90 bkl 43.31 bkl Choutt, Julie verfasserin aut Parasitism cost of living in a high quality habitat in the bog fritillary butterfly 2011 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Habitat quality and the impact of natural enemies might profoundly affect metapopulation dynamics and viability. However, their relative impact has usually been considered independently. Here we address the question of how caterpillar habitat quality and parasitism prevalence interact to shape habitat selection in the bog fritillary butterfly Boloria eunomia, parasitized at the caterpillar stage by a specialist wasp, Cotesiaeunomiae. We first classified habitat quality by relating caterpillar density to descriptors of different microhabitat types. Second, we investigated parasitism prevalence in those different microhabitats. Our results show that caterpillars and parasitoids mapped onto the same microhabitats, mainly zones with high abundance of the host plant. Accordingly, we suggest that both egg-laying females and parasitoids use the same cues for habitat selection. As a consequence, there should be a fitness cost for B. eunomia females to lay their eggs in places where parasitism prevalence is high. We indeed detected that B. eunomia females frequently laid eggs in habitat types that presented suboptimal microhabitat conditions for caterpillars. This suggests that the lower parasitism prevalence in these suboptimal habitat types counterbalances lower caterpillar survival, leading to an overall similar survival in optimal and suboptimal habitat types. Spreading eggs in different habitat types is thus expected to be a safe strategy to mitigate the adverse possible effects of environmental stochasticity and parasitism prevalence on offspring survival unequal among microhabitat types. From a conservation viewpoint, the preservation of habitat heterogeneity, including optimal but also suboptimal habitat areas, is crucial to ensure persistence of both the host and its parasitoid. Habitat heterogeneity (dpeaa)DE-He213 Larval parasitoid (dpeaa)DE-He213 Peat bog (dpeaa)DE-He213 Turlure, Camille verfasserin aut Baguette, Michel verfasserin aut Schtickzelle, Nicolas verfasserin aut Enthalten in Biodiversity and conservation Dordrecht : Springer Netherlands, 1992 20(2011), 13 vom: 13. Sept., Seite 3117-3131 (DE-627)31751055X (DE-600)2000787-5 1572-9710 nnns volume:20 year:2011 number:13 day:13 month:09 pages:3117-3131 https://dx.doi.org/10.1007/s10531-011-0151-8 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA SSG-OPC-GGO SSG-OPC-ASE GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_381 GBV_ILN_602 GBV_ILN_636 GBV_ILN_647 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2360 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 42.90 ASE 43.31 ASE AR 20 2011 13 13 09 3117-3131 |
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English |
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Enthalten in Biodiversity and conservation 20(2011), 13 vom: 13. Sept., Seite 3117-3131 volume:20 year:2011 number:13 day:13 month:09 pages:3117-3131 |
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Enthalten in Biodiversity and conservation 20(2011), 13 vom: 13. Sept., Seite 3117-3131 volume:20 year:2011 number:13 day:13 month:09 pages:3117-3131 |
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Habitat heterogeneity Larval parasitoid Peat bog |
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Biodiversity and conservation |
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Choutt, Julie @@aut@@ Turlure, Camille @@aut@@ Baguette, Michel @@aut@@ Schtickzelle, Nicolas @@aut@@ |
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2011-09-13T00:00:00Z |
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However, their relative impact has usually been considered independently. Here we address the question of how caterpillar habitat quality and parasitism prevalence interact to shape habitat selection in the bog fritillary butterfly Boloria eunomia, parasitized at the caterpillar stage by a specialist wasp, Cotesiaeunomiae. We first classified habitat quality by relating caterpillar density to descriptors of different microhabitat types. Second, we investigated parasitism prevalence in those different microhabitats. Our results show that caterpillars and parasitoids mapped onto the same microhabitats, mainly zones with high abundance of the host plant. Accordingly, we suggest that both egg-laying females and parasitoids use the same cues for habitat selection. As a consequence, there should be a fitness cost for B. eunomia females to lay their eggs in places where parasitism prevalence is high. We indeed detected that B. eunomia females frequently laid eggs in habitat types that presented suboptimal microhabitat conditions for caterpillars. This suggests that the lower parasitism prevalence in these suboptimal habitat types counterbalances lower caterpillar survival, leading to an overall similar survival in optimal and suboptimal habitat types. Spreading eggs in different habitat types is thus expected to be a safe strategy to mitigate the adverse possible effects of environmental stochasticity and parasitism prevalence on offspring survival unequal among microhabitat types. 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Choutt, Julie |
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Choutt, Julie ddc 570 bkl 42.90 bkl 43.31 misc Habitat heterogeneity misc Larval parasitoid misc Peat bog Parasitism cost of living in a high quality habitat in the bog fritillary butterfly |
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570 ASE 42.90 bkl 43.31 bkl Parasitism cost of living in a high quality habitat in the bog fritillary butterfly Habitat heterogeneity (dpeaa)DE-He213 Larval parasitoid (dpeaa)DE-He213 Peat bog (dpeaa)DE-He213 |
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| title_sort |
parasitism cost of living in a high quality habitat in the bog fritillary butterfly |
| title_auth |
Parasitism cost of living in a high quality habitat in the bog fritillary butterfly |
| abstract |
Abstract Habitat quality and the impact of natural enemies might profoundly affect metapopulation dynamics and viability. However, their relative impact has usually been considered independently. Here we address the question of how caterpillar habitat quality and parasitism prevalence interact to shape habitat selection in the bog fritillary butterfly Boloria eunomia, parasitized at the caterpillar stage by a specialist wasp, Cotesiaeunomiae. We first classified habitat quality by relating caterpillar density to descriptors of different microhabitat types. Second, we investigated parasitism prevalence in those different microhabitats. Our results show that caterpillars and parasitoids mapped onto the same microhabitats, mainly zones with high abundance of the host plant. Accordingly, we suggest that both egg-laying females and parasitoids use the same cues for habitat selection. As a consequence, there should be a fitness cost for B. eunomia females to lay their eggs in places where parasitism prevalence is high. We indeed detected that B. eunomia females frequently laid eggs in habitat types that presented suboptimal microhabitat conditions for caterpillars. This suggests that the lower parasitism prevalence in these suboptimal habitat types counterbalances lower caterpillar survival, leading to an overall similar survival in optimal and suboptimal habitat types. Spreading eggs in different habitat types is thus expected to be a safe strategy to mitigate the adverse possible effects of environmental stochasticity and parasitism prevalence on offspring survival unequal among microhabitat types. From a conservation viewpoint, the preservation of habitat heterogeneity, including optimal but also suboptimal habitat areas, is crucial to ensure persistence of both the host and its parasitoid. |
| abstractGer |
Abstract Habitat quality and the impact of natural enemies might profoundly affect metapopulation dynamics and viability. However, their relative impact has usually been considered independently. Here we address the question of how caterpillar habitat quality and parasitism prevalence interact to shape habitat selection in the bog fritillary butterfly Boloria eunomia, parasitized at the caterpillar stage by a specialist wasp, Cotesiaeunomiae. We first classified habitat quality by relating caterpillar density to descriptors of different microhabitat types. Second, we investigated parasitism prevalence in those different microhabitats. Our results show that caterpillars and parasitoids mapped onto the same microhabitats, mainly zones with high abundance of the host plant. Accordingly, we suggest that both egg-laying females and parasitoids use the same cues for habitat selection. As a consequence, there should be a fitness cost for B. eunomia females to lay their eggs in places where parasitism prevalence is high. We indeed detected that B. eunomia females frequently laid eggs in habitat types that presented suboptimal microhabitat conditions for caterpillars. This suggests that the lower parasitism prevalence in these suboptimal habitat types counterbalances lower caterpillar survival, leading to an overall similar survival in optimal and suboptimal habitat types. Spreading eggs in different habitat types is thus expected to be a safe strategy to mitigate the adverse possible effects of environmental stochasticity and parasitism prevalence on offspring survival unequal among microhabitat types. From a conservation viewpoint, the preservation of habitat heterogeneity, including optimal but also suboptimal habitat areas, is crucial to ensure persistence of both the host and its parasitoid. |
| abstract_unstemmed |
Abstract Habitat quality and the impact of natural enemies might profoundly affect metapopulation dynamics and viability. However, their relative impact has usually been considered independently. Here we address the question of how caterpillar habitat quality and parasitism prevalence interact to shape habitat selection in the bog fritillary butterfly Boloria eunomia, parasitized at the caterpillar stage by a specialist wasp, Cotesiaeunomiae. We first classified habitat quality by relating caterpillar density to descriptors of different microhabitat types. Second, we investigated parasitism prevalence in those different microhabitats. Our results show that caterpillars and parasitoids mapped onto the same microhabitats, mainly zones with high abundance of the host plant. Accordingly, we suggest that both egg-laying females and parasitoids use the same cues for habitat selection. As a consequence, there should be a fitness cost for B. eunomia females to lay their eggs in places where parasitism prevalence is high. We indeed detected that B. eunomia females frequently laid eggs in habitat types that presented suboptimal microhabitat conditions for caterpillars. This suggests that the lower parasitism prevalence in these suboptimal habitat types counterbalances lower caterpillar survival, leading to an overall similar survival in optimal and suboptimal habitat types. Spreading eggs in different habitat types is thus expected to be a safe strategy to mitigate the adverse possible effects of environmental stochasticity and parasitism prevalence on offspring survival unequal among microhabitat types. From a conservation viewpoint, the preservation of habitat heterogeneity, including optimal but also suboptimal habitat areas, is crucial to ensure persistence of both the host and its parasitoid. |
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Parasitism cost of living in a high quality habitat in the bog fritillary butterfly |
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Turlure, Camille Baguette, Michel Schtickzelle, Nicolas |
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2024-07-03T19:09:56.704Z |
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| score |
7.4002924 |