The intimacy between sexual traits and Grime’s CSR strategies for orchids coexisting in semi-natural calcareous grassland at the Olive Lawn
Abstract The diversity of orchid species in semi-natural calcareous grassland is thought to depend on floral variability. However, differences in primary life-history strategy, or the overall suite of functional traits, could also affect coexistence. Both primary strategy (affecting day-to-day survi...
Ausführliche Beschreibung
Gespeichert in:
| Autor*in: |
Pierce, Simon [verfasserIn] Vagge, Ilda [verfasserIn] Brusa, Guido [verfasserIn] Cerabolini, Bruno E. L. [verfasserIn] |
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| Format: |
E-Artikel |
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| Sprache: |
Englisch |
| Erschienen: |
2014 |
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| Schlagwörter: |
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| Übergeordnetes Werk: |
Enthalten in: Plant ecology - Dordrecht [u.a.] : Springer Science + Business Media B.V, 1997, 215(2014), 5 vom: 12. März, Seite 495-505 |
|---|---|
| Übergeordnetes Werk: |
volume:215 ; year:2014 ; number:5 ; day:12 ; month:03 ; pages:495-505 |
| Links: |
|---|
| DOI / URN: |
10.1007/s11258-014-0318-y |
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| Katalog-ID: |
SPR01835906X |
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| 245 | 1 | 4 | |a The intimacy between sexual traits and Grime’s CSR strategies for orchids coexisting in semi-natural calcareous grassland at the Olive Lawn |
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| 520 | |a Abstract The diversity of orchid species in semi-natural calcareous grassland is thought to depend on floral variability. However, differences in primary life-history strategy, or the overall suite of functional traits, could also affect coexistence. Both primary strategy (affecting day-to-day survival) and reproductive traits (representing periodic events) have been hypothesized to contribute to a general mechanism regulating the local persistence and relative abundance of species. We recorded species identity at 8,000 points at the centimetre scale along sixteen 5-m long transects at the Olive Lawn, a xeric sand calcareous grassland near Lecco, Italy. Transects allowed the relative abundance and spatial aggregation of Grime’s competitor, stress-tolerator, ruderal (CSR) strategies to be quantified. Orchid flowering and fruiting phenology was recorded alongside the phenology of graminoid growth. Seven orchid species were present and exhibited a spectrum of strategies spanning two extremes, (1) small early-flowering ruderals (R/CR-selected), and (2) larger-leaved competitors (C/CR) flowering later as dominant graminoids attained maximum height. These orchids, and other subordinate species in the community, exhibited random spatial distributions amongst dominant graminoids that exhibited a high degree of spatial aggregation and similar, but non-identical, stress-tolerator (S) strategies. The reproductive phenology of meadow orchids is an intimate component of their CSR strategies, and appears to promote coexistence by allowing segregation between temporal niches and the exploitation of opportunities between clumps of dominant species. Only for closely related species with identical CSR strategies, such as Ophrys benacensis and Ophrys sphegodes, could specific floral differences alone explain coexistence. | ||
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| 700 | 1 | |a Brusa, Guido |e verfasserin |4 aut | |
| 700 | 1 | |a Cerabolini, Bruno E. L. |e verfasserin |4 aut | |
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10.1007/s11258-014-0318-y doi (DE-627)SPR01835906X (SPR)s11258-014-0318-y-e DE-627 ger DE-627 rakwb eng 580 ASE 42.44 bkl Pierce, Simon verfasserin aut The intimacy between sexual traits and Grime’s CSR strategies for orchids coexisting in semi-natural calcareous grassland at the Olive Lawn 2014 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract The diversity of orchid species in semi-natural calcareous grassland is thought to depend on floral variability. However, differences in primary life-history strategy, or the overall suite of functional traits, could also affect coexistence. Both primary strategy (affecting day-to-day survival) and reproductive traits (representing periodic events) have been hypothesized to contribute to a general mechanism regulating the local persistence and relative abundance of species. We recorded species identity at 8,000 points at the centimetre scale along sixteen 5-m long transects at the Olive Lawn, a xeric sand calcareous grassland near Lecco, Italy. Transects allowed the relative abundance and spatial aggregation of Grime’s competitor, stress-tolerator, ruderal (CSR) strategies to be quantified. Orchid flowering and fruiting phenology was recorded alongside the phenology of graminoid growth. Seven orchid species were present and exhibited a spectrum of strategies spanning two extremes, (1) small early-flowering ruderals (R/CR-selected), and (2) larger-leaved competitors (C/CR) flowering later as dominant graminoids attained maximum height. These orchids, and other subordinate species in the community, exhibited random spatial distributions amongst dominant graminoids that exhibited a high degree of spatial aggregation and similar, but non-identical, stress-tolerator (S) strategies. The reproductive phenology of meadow orchids is an intimate component of their CSR strategies, and appears to promote coexistence by allowing segregation between temporal niches and the exploitation of opportunities between clumps of dominant species. Only for closely related species with identical CSR strategies, such as Ophrys benacensis and Ophrys sphegodes, could specific floral differences alone explain coexistence. Biodiversity (dpeaa)DE-He213 Coexistence (dpeaa)DE-He213 Community assembly (dpeaa)DE-He213 Plant functional type (dpeaa)DE-He213 Species richness (dpeaa)DE-He213 Universal adaptive strategy theory (dpeaa)DE-He213 Vagge, Ilda verfasserin aut Brusa, Guido verfasserin aut Cerabolini, Bruno E. L. verfasserin aut Enthalten in Plant ecology Dordrecht [u.a.] : Springer Science + Business Media B.V, 1997 215(2014), 5 vom: 12. März, Seite 495-505 (DE-627)271177578 (DE-600)1479167-5 1573-5052 nnns volume:215 year:2014 number:5 day:12 month:03 pages:495-505 https://dx.doi.org/10.1007/s11258-014-0318-y lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA 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_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 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_374 GBV_ILN_602 GBV_ILN_636 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_2018 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_2939 GBV_ILN_2946 GBV_ILN_2949 GBV_ILN_2951 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_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4346 GBV_ILN_4393 GBV_ILN_4700 42.44 ASE AR 215 2014 5 12 03 495-505 |
| spelling |
10.1007/s11258-014-0318-y doi (DE-627)SPR01835906X (SPR)s11258-014-0318-y-e DE-627 ger DE-627 rakwb eng 580 ASE 42.44 bkl Pierce, Simon verfasserin aut The intimacy between sexual traits and Grime’s CSR strategies for orchids coexisting in semi-natural calcareous grassland at the Olive Lawn 2014 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract The diversity of orchid species in semi-natural calcareous grassland is thought to depend on floral variability. However, differences in primary life-history strategy, or the overall suite of functional traits, could also affect coexistence. Both primary strategy (affecting day-to-day survival) and reproductive traits (representing periodic events) have been hypothesized to contribute to a general mechanism regulating the local persistence and relative abundance of species. We recorded species identity at 8,000 points at the centimetre scale along sixteen 5-m long transects at the Olive Lawn, a xeric sand calcareous grassland near Lecco, Italy. Transects allowed the relative abundance and spatial aggregation of Grime’s competitor, stress-tolerator, ruderal (CSR) strategies to be quantified. Orchid flowering and fruiting phenology was recorded alongside the phenology of graminoid growth. Seven orchid species were present and exhibited a spectrum of strategies spanning two extremes, (1) small early-flowering ruderals (R/CR-selected), and (2) larger-leaved competitors (C/CR) flowering later as dominant graminoids attained maximum height. These orchids, and other subordinate species in the community, exhibited random spatial distributions amongst dominant graminoids that exhibited a high degree of spatial aggregation and similar, but non-identical, stress-tolerator (S) strategies. The reproductive phenology of meadow orchids is an intimate component of their CSR strategies, and appears to promote coexistence by allowing segregation between temporal niches and the exploitation of opportunities between clumps of dominant species. Only for closely related species with identical CSR strategies, such as Ophrys benacensis and Ophrys sphegodes, could specific floral differences alone explain coexistence. Biodiversity (dpeaa)DE-He213 Coexistence (dpeaa)DE-He213 Community assembly (dpeaa)DE-He213 Plant functional type (dpeaa)DE-He213 Species richness (dpeaa)DE-He213 Universal adaptive strategy theory (dpeaa)DE-He213 Vagge, Ilda verfasserin aut Brusa, Guido verfasserin aut Cerabolini, Bruno E. L. verfasserin aut Enthalten in Plant ecology Dordrecht [u.a.] : Springer Science + Business Media B.V, 1997 215(2014), 5 vom: 12. März, Seite 495-505 (DE-627)271177578 (DE-600)1479167-5 1573-5052 nnns volume:215 year:2014 number:5 day:12 month:03 pages:495-505 https://dx.doi.org/10.1007/s11258-014-0318-y lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA 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_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 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_374 GBV_ILN_602 GBV_ILN_636 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_2018 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_2939 GBV_ILN_2946 GBV_ILN_2949 GBV_ILN_2951 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_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4346 GBV_ILN_4393 GBV_ILN_4700 42.44 ASE AR 215 2014 5 12 03 495-505 |
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10.1007/s11258-014-0318-y doi (DE-627)SPR01835906X (SPR)s11258-014-0318-y-e DE-627 ger DE-627 rakwb eng 580 ASE 42.44 bkl Pierce, Simon verfasserin aut The intimacy between sexual traits and Grime’s CSR strategies for orchids coexisting in semi-natural calcareous grassland at the Olive Lawn 2014 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract The diversity of orchid species in semi-natural calcareous grassland is thought to depend on floral variability. However, differences in primary life-history strategy, or the overall suite of functional traits, could also affect coexistence. Both primary strategy (affecting day-to-day survival) and reproductive traits (representing periodic events) have been hypothesized to contribute to a general mechanism regulating the local persistence and relative abundance of species. We recorded species identity at 8,000 points at the centimetre scale along sixteen 5-m long transects at the Olive Lawn, a xeric sand calcareous grassland near Lecco, Italy. Transects allowed the relative abundance and spatial aggregation of Grime’s competitor, stress-tolerator, ruderal (CSR) strategies to be quantified. Orchid flowering and fruiting phenology was recorded alongside the phenology of graminoid growth. Seven orchid species were present and exhibited a spectrum of strategies spanning two extremes, (1) small early-flowering ruderals (R/CR-selected), and (2) larger-leaved competitors (C/CR) flowering later as dominant graminoids attained maximum height. These orchids, and other subordinate species in the community, exhibited random spatial distributions amongst dominant graminoids that exhibited a high degree of spatial aggregation and similar, but non-identical, stress-tolerator (S) strategies. The reproductive phenology of meadow orchids is an intimate component of their CSR strategies, and appears to promote coexistence by allowing segregation between temporal niches and the exploitation of opportunities between clumps of dominant species. Only for closely related species with identical CSR strategies, such as Ophrys benacensis and Ophrys sphegodes, could specific floral differences alone explain coexistence. Biodiversity (dpeaa)DE-He213 Coexistence (dpeaa)DE-He213 Community assembly (dpeaa)DE-He213 Plant functional type (dpeaa)DE-He213 Species richness (dpeaa)DE-He213 Universal adaptive strategy theory (dpeaa)DE-He213 Vagge, Ilda verfasserin aut Brusa, Guido verfasserin aut Cerabolini, Bruno E. L. verfasserin aut Enthalten in Plant ecology Dordrecht [u.a.] : Springer Science + Business Media B.V, 1997 215(2014), 5 vom: 12. März, Seite 495-505 (DE-627)271177578 (DE-600)1479167-5 1573-5052 nnns volume:215 year:2014 number:5 day:12 month:03 pages:495-505 https://dx.doi.org/10.1007/s11258-014-0318-y lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA 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_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 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_374 GBV_ILN_602 GBV_ILN_636 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_2018 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_2939 GBV_ILN_2946 GBV_ILN_2949 GBV_ILN_2951 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_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4346 GBV_ILN_4393 GBV_ILN_4700 42.44 ASE AR 215 2014 5 12 03 495-505 |
| allfieldsGer |
10.1007/s11258-014-0318-y doi (DE-627)SPR01835906X (SPR)s11258-014-0318-y-e DE-627 ger DE-627 rakwb eng 580 ASE 42.44 bkl Pierce, Simon verfasserin aut The intimacy between sexual traits and Grime’s CSR strategies for orchids coexisting in semi-natural calcareous grassland at the Olive Lawn 2014 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract The diversity of orchid species in semi-natural calcareous grassland is thought to depend on floral variability. However, differences in primary life-history strategy, or the overall suite of functional traits, could also affect coexistence. Both primary strategy (affecting day-to-day survival) and reproductive traits (representing periodic events) have been hypothesized to contribute to a general mechanism regulating the local persistence and relative abundance of species. We recorded species identity at 8,000 points at the centimetre scale along sixteen 5-m long transects at the Olive Lawn, a xeric sand calcareous grassland near Lecco, Italy. Transects allowed the relative abundance and spatial aggregation of Grime’s competitor, stress-tolerator, ruderal (CSR) strategies to be quantified. Orchid flowering and fruiting phenology was recorded alongside the phenology of graminoid growth. Seven orchid species were present and exhibited a spectrum of strategies spanning two extremes, (1) small early-flowering ruderals (R/CR-selected), and (2) larger-leaved competitors (C/CR) flowering later as dominant graminoids attained maximum height. These orchids, and other subordinate species in the community, exhibited random spatial distributions amongst dominant graminoids that exhibited a high degree of spatial aggregation and similar, but non-identical, stress-tolerator (S) strategies. The reproductive phenology of meadow orchids is an intimate component of their CSR strategies, and appears to promote coexistence by allowing segregation between temporal niches and the exploitation of opportunities between clumps of dominant species. Only for closely related species with identical CSR strategies, such as Ophrys benacensis and Ophrys sphegodes, could specific floral differences alone explain coexistence. Biodiversity (dpeaa)DE-He213 Coexistence (dpeaa)DE-He213 Community assembly (dpeaa)DE-He213 Plant functional type (dpeaa)DE-He213 Species richness (dpeaa)DE-He213 Universal adaptive strategy theory (dpeaa)DE-He213 Vagge, Ilda verfasserin aut Brusa, Guido verfasserin aut Cerabolini, Bruno E. L. verfasserin aut Enthalten in Plant ecology Dordrecht [u.a.] : Springer Science + Business Media B.V, 1997 215(2014), 5 vom: 12. März, Seite 495-505 (DE-627)271177578 (DE-600)1479167-5 1573-5052 nnns volume:215 year:2014 number:5 day:12 month:03 pages:495-505 https://dx.doi.org/10.1007/s11258-014-0318-y lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA 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_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 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_374 GBV_ILN_602 GBV_ILN_636 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_2018 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_2939 GBV_ILN_2946 GBV_ILN_2949 GBV_ILN_2951 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_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4346 GBV_ILN_4393 GBV_ILN_4700 42.44 ASE AR 215 2014 5 12 03 495-505 |
| allfieldsSound |
10.1007/s11258-014-0318-y doi (DE-627)SPR01835906X (SPR)s11258-014-0318-y-e DE-627 ger DE-627 rakwb eng 580 ASE 42.44 bkl Pierce, Simon verfasserin aut The intimacy between sexual traits and Grime’s CSR strategies for orchids coexisting in semi-natural calcareous grassland at the Olive Lawn 2014 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract The diversity of orchid species in semi-natural calcareous grassland is thought to depend on floral variability. However, differences in primary life-history strategy, or the overall suite of functional traits, could also affect coexistence. Both primary strategy (affecting day-to-day survival) and reproductive traits (representing periodic events) have been hypothesized to contribute to a general mechanism regulating the local persistence and relative abundance of species. We recorded species identity at 8,000 points at the centimetre scale along sixteen 5-m long transects at the Olive Lawn, a xeric sand calcareous grassland near Lecco, Italy. Transects allowed the relative abundance and spatial aggregation of Grime’s competitor, stress-tolerator, ruderal (CSR) strategies to be quantified. Orchid flowering and fruiting phenology was recorded alongside the phenology of graminoid growth. Seven orchid species were present and exhibited a spectrum of strategies spanning two extremes, (1) small early-flowering ruderals (R/CR-selected), and (2) larger-leaved competitors (C/CR) flowering later as dominant graminoids attained maximum height. These orchids, and other subordinate species in the community, exhibited random spatial distributions amongst dominant graminoids that exhibited a high degree of spatial aggregation and similar, but non-identical, stress-tolerator (S) strategies. The reproductive phenology of meadow orchids is an intimate component of their CSR strategies, and appears to promote coexistence by allowing segregation between temporal niches and the exploitation of opportunities between clumps of dominant species. Only for closely related species with identical CSR strategies, such as Ophrys benacensis and Ophrys sphegodes, could specific floral differences alone explain coexistence. Biodiversity (dpeaa)DE-He213 Coexistence (dpeaa)DE-He213 Community assembly (dpeaa)DE-He213 Plant functional type (dpeaa)DE-He213 Species richness (dpeaa)DE-He213 Universal adaptive strategy theory (dpeaa)DE-He213 Vagge, Ilda verfasserin aut Brusa, Guido verfasserin aut Cerabolini, Bruno E. L. verfasserin aut Enthalten in Plant ecology Dordrecht [u.a.] : Springer Science + Business Media B.V, 1997 215(2014), 5 vom: 12. März, Seite 495-505 (DE-627)271177578 (DE-600)1479167-5 1573-5052 nnns volume:215 year:2014 number:5 day:12 month:03 pages:495-505 https://dx.doi.org/10.1007/s11258-014-0318-y lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA 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_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 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_374 GBV_ILN_602 GBV_ILN_636 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_2018 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_2939 GBV_ILN_2946 GBV_ILN_2949 GBV_ILN_2951 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_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4346 GBV_ILN_4393 GBV_ILN_4700 42.44 ASE AR 215 2014 5 12 03 495-505 |
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English |
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Enthalten in Plant ecology 215(2014), 5 vom: 12. März, Seite 495-505 volume:215 year:2014 number:5 day:12 month:03 pages:495-505 |
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Enthalten in Plant ecology 215(2014), 5 vom: 12. März, Seite 495-505 volume:215 year:2014 number:5 day:12 month:03 pages:495-505 |
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Biodiversity Coexistence Community assembly Plant functional type Species richness Universal adaptive strategy theory |
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Plant ecology |
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Pierce, Simon @@aut@@ Vagge, Ilda @@aut@@ Brusa, Guido @@aut@@ Cerabolini, Bruno E. L. @@aut@@ |
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However, differences in primary life-history strategy, or the overall suite of functional traits, could also affect coexistence. Both primary strategy (affecting day-to-day survival) and reproductive traits (representing periodic events) have been hypothesized to contribute to a general mechanism regulating the local persistence and relative abundance of species. We recorded species identity at 8,000 points at the centimetre scale along sixteen 5-m long transects at the Olive Lawn, a xeric sand calcareous grassland near Lecco, Italy. Transects allowed the relative abundance and spatial aggregation of Grime’s competitor, stress-tolerator, ruderal (CSR) strategies to be quantified. Orchid flowering and fruiting phenology was recorded alongside the phenology of graminoid growth. Seven orchid species were present and exhibited a spectrum of strategies spanning two extremes, (1) small early-flowering ruderals (R/CR-selected), and (2) larger-leaved competitors (C/CR) flowering later as dominant graminoids attained maximum height. These orchids, and other subordinate species in the community, exhibited random spatial distributions amongst dominant graminoids that exhibited a high degree of spatial aggregation and similar, but non-identical, stress-tolerator (S) strategies. The reproductive phenology of meadow orchids is an intimate component of their CSR strategies, and appears to promote coexistence by allowing segregation between temporal niches and the exploitation of opportunities between clumps of dominant species. Only for closely related species with identical CSR strategies, such as Ophrys benacensis and Ophrys sphegodes, could specific floral differences alone explain coexistence.</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Biodiversity</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Coexistence</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Community assembly</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Plant functional type</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Species richness</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Universal adaptive strategy theory</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Vagge, Ilda</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Brusa, Guido</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Cerabolini, Bruno E. 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Pierce, Simon |
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Pierce, Simon ddc 580 bkl 42.44 misc Biodiversity misc Coexistence misc Community assembly misc Plant functional type misc Species richness misc Universal adaptive strategy theory The intimacy between sexual traits and Grime’s CSR strategies for orchids coexisting in semi-natural calcareous grassland at the Olive Lawn |
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580 ASE 42.44 bkl The intimacy between sexual traits and Grime’s CSR strategies for orchids coexisting in semi-natural calcareous grassland at the Olive Lawn Biodiversity (dpeaa)DE-He213 Coexistence (dpeaa)DE-He213 Community assembly (dpeaa)DE-He213 Plant functional type (dpeaa)DE-He213 Species richness (dpeaa)DE-He213 Universal adaptive strategy theory (dpeaa)DE-He213 |
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ddc 580 bkl 42.44 misc Biodiversity misc Coexistence misc Community assembly misc Plant functional type misc Species richness misc Universal adaptive strategy theory |
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The intimacy between sexual traits and Grime’s CSR strategies for orchids coexisting in semi-natural calcareous grassland at the Olive Lawn |
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| title_full |
The intimacy between sexual traits and Grime’s CSR strategies for orchids coexisting in semi-natural calcareous grassland at the Olive Lawn |
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Pierce, Simon |
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Plant ecology |
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Pierce, Simon Vagge, Ilda Brusa, Guido Cerabolini, Bruno E. L. |
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Pierce, Simon |
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10.1007/s11258-014-0318-y |
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intimacy between sexual traits and grime’s csr strategies for orchids coexisting in semi-natural calcareous grassland at the olive lawn |
| title_auth |
The intimacy between sexual traits and Grime’s CSR strategies for orchids coexisting in semi-natural calcareous grassland at the Olive Lawn |
| abstract |
Abstract The diversity of orchid species in semi-natural calcareous grassland is thought to depend on floral variability. However, differences in primary life-history strategy, or the overall suite of functional traits, could also affect coexistence. Both primary strategy (affecting day-to-day survival) and reproductive traits (representing periodic events) have been hypothesized to contribute to a general mechanism regulating the local persistence and relative abundance of species. We recorded species identity at 8,000 points at the centimetre scale along sixteen 5-m long transects at the Olive Lawn, a xeric sand calcareous grassland near Lecco, Italy. Transects allowed the relative abundance and spatial aggregation of Grime’s competitor, stress-tolerator, ruderal (CSR) strategies to be quantified. Orchid flowering and fruiting phenology was recorded alongside the phenology of graminoid growth. Seven orchid species were present and exhibited a spectrum of strategies spanning two extremes, (1) small early-flowering ruderals (R/CR-selected), and (2) larger-leaved competitors (C/CR) flowering later as dominant graminoids attained maximum height. These orchids, and other subordinate species in the community, exhibited random spatial distributions amongst dominant graminoids that exhibited a high degree of spatial aggregation and similar, but non-identical, stress-tolerator (S) strategies. The reproductive phenology of meadow orchids is an intimate component of their CSR strategies, and appears to promote coexistence by allowing segregation between temporal niches and the exploitation of opportunities between clumps of dominant species. Only for closely related species with identical CSR strategies, such as Ophrys benacensis and Ophrys sphegodes, could specific floral differences alone explain coexistence. |
| abstractGer |
Abstract The diversity of orchid species in semi-natural calcareous grassland is thought to depend on floral variability. However, differences in primary life-history strategy, or the overall suite of functional traits, could also affect coexistence. Both primary strategy (affecting day-to-day survival) and reproductive traits (representing periodic events) have been hypothesized to contribute to a general mechanism regulating the local persistence and relative abundance of species. We recorded species identity at 8,000 points at the centimetre scale along sixteen 5-m long transects at the Olive Lawn, a xeric sand calcareous grassland near Lecco, Italy. Transects allowed the relative abundance and spatial aggregation of Grime’s competitor, stress-tolerator, ruderal (CSR) strategies to be quantified. Orchid flowering and fruiting phenology was recorded alongside the phenology of graminoid growth. Seven orchid species were present and exhibited a spectrum of strategies spanning two extremes, (1) small early-flowering ruderals (R/CR-selected), and (2) larger-leaved competitors (C/CR) flowering later as dominant graminoids attained maximum height. These orchids, and other subordinate species in the community, exhibited random spatial distributions amongst dominant graminoids that exhibited a high degree of spatial aggregation and similar, but non-identical, stress-tolerator (S) strategies. The reproductive phenology of meadow orchids is an intimate component of their CSR strategies, and appears to promote coexistence by allowing segregation between temporal niches and the exploitation of opportunities between clumps of dominant species. Only for closely related species with identical CSR strategies, such as Ophrys benacensis and Ophrys sphegodes, could specific floral differences alone explain coexistence. |
| abstract_unstemmed |
Abstract The diversity of orchid species in semi-natural calcareous grassland is thought to depend on floral variability. However, differences in primary life-history strategy, or the overall suite of functional traits, could also affect coexistence. Both primary strategy (affecting day-to-day survival) and reproductive traits (representing periodic events) have been hypothesized to contribute to a general mechanism regulating the local persistence and relative abundance of species. We recorded species identity at 8,000 points at the centimetre scale along sixteen 5-m long transects at the Olive Lawn, a xeric sand calcareous grassland near Lecco, Italy. Transects allowed the relative abundance and spatial aggregation of Grime’s competitor, stress-tolerator, ruderal (CSR) strategies to be quantified. Orchid flowering and fruiting phenology was recorded alongside the phenology of graminoid growth. Seven orchid species were present and exhibited a spectrum of strategies spanning two extremes, (1) small early-flowering ruderals (R/CR-selected), and (2) larger-leaved competitors (C/CR) flowering later as dominant graminoids attained maximum height. These orchids, and other subordinate species in the community, exhibited random spatial distributions amongst dominant graminoids that exhibited a high degree of spatial aggregation and similar, but non-identical, stress-tolerator (S) strategies. The reproductive phenology of meadow orchids is an intimate component of their CSR strategies, and appears to promote coexistence by allowing segregation between temporal niches and the exploitation of opportunities between clumps of dominant species. Only for closely related species with identical CSR strategies, such as Ophrys benacensis and Ophrys sphegodes, could specific floral differences alone explain coexistence. |
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| title_short |
The intimacy between sexual traits and Grime’s CSR strategies for orchids coexisting in semi-natural calcareous grassland at the Olive Lawn |
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| score |
7.402261 |