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Variation in Predispersal Losses in Reproductive Potential in Rowan (Sorbus aucuparia L. Rosaceae) in the NW Iberian Peninsula

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Abstract

We identified the principal factors causing losses in reproductive potential (i.e. quantity of potentially dispersable seeds) over the predispersal period of the reproductive cycle of Sorbus aucuparia L. (Rosaceae) in various populations in the NW Iberian Peninsula. Over the period 1999–2002 we examined the magnitude and variability of losses observed in each stage from bud production to seed production (i.e. bud to flower, flower to initiated fruit, initiated to full-size fruit, and full-size to mature fruit). We also investigated spatial and temporal variation in these losses. Reproductive potential showed very significant losses over the predispersal period in all 4 years: in no case did the number of mature fruits available for dispersal exceed 20% of the initial number of flower buds. In all 4 years of study, we detected statistically significant variation among populations in total losses. The principal cause of loss of reproductive potential over the predispersal period in our Sorbus aucuparia populations was non-initiation of fruit. The plant’s interactions with predispersal predators of buds and seeds show high spatial and temporal variability. Also, the proportions of loss due to the different components did not show within-individual consistency over time. It thus seems unlikely that the different factors contributing to predispersal losses in rowan are currently generating significant selective pressures in our study populations.

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References

  • Agassiz DJL (1996) Yponomeutidae. In: Maintland Emmet A (ed) The moths and butterflies of Great Britain and Ireland, vol 3. Harley Books

  • Aldasoro JJ (1998) Sorbus aucuparia L. Rosaceae. In: Muñoz-Garmendia F, Navarro-Real C (eds) Flora Iberica, vol 4. Jardín Botánico de Madrid, CSIC

    Google Scholar 

  • Baker AM, Barret SCH, Thompson JD (2000) Variation of pollen limitation in the early flowering Mediterranean geophyte Narcissus assoanus (Amaryllidaceae). Oecologia 124:529–535

    Article  Google Scholar 

  • Bermejo T, Guitián J (1996) Consumo de frutos y dispersión de semillas de serbal (Sorbus aucuparia L.) por zorros y martas en la Cordillera Cantábrica occidental. Doñana Acta Vertebrata 233: 215–229

  • Brody AK (1997) Effects of pollinators, herbivores and seed predators on flowering phenology. Ecology 78:1624–1631

    Google Scholar 

  • Burd M (1994) Bateman’s principle and plant reproduction: the role of pollen limitation on fruit and seed set. Bot Rev 60:83–139

    Google Scholar 

  • Crawley MJ (1992) Seed predators and plant population dynamics. In: Fenner M (ed) Seeds, the ecology of regeneration in plant communities. CAB International, Wallingford, pp 157–191

    Google Scholar 

  • Crawley MJ, Long CR (1995) Alternate bearing, predator satiation and seedling recruitment in Quercus robur L. J Ecol 83:683–696

    Article  Google Scholar 

  • Dudash MR, Fenster CB (1997) Multiyear study of pollen limitation and cost of reproduction in the iteroparous Silene virginica. Ecology 78:484–493

    Google Scholar 

  • Ehrlén J (1992) Proximate limits to seed production in a herbaceous perennial legume, Lathyrus vernus. Ecology 73:1820–1831

    Article  Google Scholar 

  • Ehrlén J (1995) Demography of the perennial herb Lathyrus vernus. II. Herbivory and population dynamics. J Ecol 83:297–308

    Article  Google Scholar 

  • Ehrlén J, Käck S, Ågren J (2002). Pollen limitation, seed predation, and scape length in Primula farinosa. Oikos 97:45–51

    Article  Google Scholar 

  • Gómez JM, Zamora R (2000) Spatial variation in the selective scenarios of Hormatophylla spinosa (Cruciferaceae). Am Nat 155:657–668

    Article  PubMed  Google Scholar 

  • Griffin SR, Barret SCH (2002) Factors affecting low seed: ovule ratios in a spring woodland herb, Trillium grandiflorum (Melanthiaceae). Int J Plant Sci 163:581–590

    Article  Google Scholar 

  • Guitián J (1994) Selective fruit abortion in Prunus mahaleb (Rosaceae). Am J Bot 81:1555–1558

    Article  Google Scholar 

  • Guitián J, Guitián P, Munilla I, Guitián J, Bermejo T, Larrinaga A., Navarro L, López B (2000) Zorzales, espinos y serbales Un estudio sobre el consumo de frutos silvestres de las aves migratorias en la costa occidental europea. Universidade de Santiago de Compostela

  • Haig D, Westoby M (1988) On limits to seed production. Am Nat 131:757–759

    Article  Google Scholar 

  • Hainsworth FR, Wolf LL, Mercier T (1984) Pollination and pre-dispersal seed predation: net effects on reproduction and inflorescence characteristics in Ipomopsis aggregata. Oecologia 63:405–409

    Article  Google Scholar 

  • Heithaus ER, Stashko E, Anderson PK (1982) Cumulative effects of plant–animal interactions on seed production by Bauhinia ungulata, a neotropical legume. Ecology 63:1294–1302

    Article  Google Scholar 

  • Herrera CM (1991) Dissecting factors responsible for individual variation in plant fecundity. Ecology 72:1436–1448

    Article  Google Scholar 

  • Herrera CM (2000a) Measuring the effects of pollinators and herbivores: evidence for non-additivity in a perennial herb. Ecology 81:2170–2176

    Google Scholar 

  • Herrera CM (2000b) Flower-to-seedling consequences of different pollination regimes in an insect-pollinated shrub. Ecology 81:15–29

    Google Scholar 

  • Herrera CM (2000c) Individual differences in progeny viability in Lavandula latifolia: a long-term field study. Ecology 81:3036–3047

    Google Scholar 

  • Herrera CM, Pellmyr O (2002) Plant–animal interactions. An evolutionary approach. Blackwell Science, Oxford, UK

    Google Scholar 

  • Herrera CM, Jordano P, Guitián J, Traveset A (1998) Annual variability in seed production by Woody Plants and the Masting Concept: reassessment of principles and relationship to pollination and seed dispersal. Am Nat 152:576–594

    Article  CAS  PubMed  Google Scholar 

  • Herrera CM, Medrano M, Rey PJ, Sánchez-Lafuente AM, García MB, Guitián J, Manzaneda AJ (2002) Interaction of pollinators and herbivores on plant fitness suggest a pathway for correlated evolution of mutualism- and antagonism-related traits. PNAS 99:16823–16828

    Article  PubMed  CAS  Google Scholar 

  • Hulme PE, Benkman CW (2002) Granivory. In: Herrera CM, Pellmyr O (eds) Plant–animal interactions. An␣evolutionary approach. Blackwell Publishing, pp 132–155

  • Isagi K, Sugimura A, Sumida A, Ito H (1997) How does masting happen and synchronize? J Theor Biol 187:231–239

    Article  Google Scholar 

  • Janzen DH (1971) Seed predation by animals. Annu Rev Ecol Syst 1:465–492

    Article  Google Scholar 

  • Jordano P (1989) Pre-dispersal biology of Pistacia lentiscus (Anacardiaceae): cumulative effects on seed removal by birds. Oikos 55:375–386

    Article  Google Scholar 

  • Kaye TN (1999) From flowering to dispersal: reproductive ecology of an endemic plant, Astragalus australis var. olympicus (Fabaceae). Am J Bot 86:1248–1256

    Article  PubMed  Google Scholar 

  • Kelly D (1994) The evolutionary ecology of mast seeding. Trends Ecol Evol 9:465–470

    Article  Google Scholar 

  • Kelly D, Sork VL (2002) Mast seeding in perennial plants: why, how, here? Annu Rev Ecol Syst 33:427–447

    Article  Google Scholar 

  • Kobro S, Søreide L, Djønne TR, Jaastad G, Witzgall P (2003) Masting of rowan Sorbus aucuparia L. and consequences for the apple fruit moth Argyresthia conjugella Zeller. Popul Ecol 45:25–30

    Google Scholar 

  • Larson BMH, Barret SCH (2000) A comparative analysis of pollen limitation in flowering plants. Biol J Linn Soc 69:503–520

    Article  Google Scholar 

  • Littell RC, Milliken GA, Stroup WW, Wolfinger RD (1996) SAS system for mixed models. SAS Institute, Cary, North Carolina, USA

    Google Scholar 

  • Nilsson SG, Wästljung U (1987) Seed predation and cross-pollination in mast-seeding beech (Fagus sylvatica) patches. Ecology 68:260–265

    Article  Google Scholar 

  • Pías B, Guitián P (2006) Breeding system and pollen limitation in the masting tree Sorbus aucuparia L. (Rosaceae). Acta Oecol 29:97–103

    Article  Google Scholar 

  • Raspé O, Findlay C, Jacquemart AL (2000) Sorbus aucuparia L. J Ecol 88:910–930

    Article  Google Scholar 

  • Rees M, Kelly D, BjØrnstad ON (2002) Snow tussocks, chaos, and the evolution of mast seeding. Am Nat 160:44–59

    Article  PubMed  Google Scholar 

  • Rey PJ, Herrera CM, Guitián J, Cerdá X, Sánchez-Lafuente AM, Medrano M, Garrido JL (2006) The geographical mosaic in pre-dispersal interactions and selection on Helleborus foetidus (Ranunculaceae). J Evol Biol 19: 21–34

    Google Scholar 

  • SAS Institute Inc. (1999) SAS/STAT Software Institute. Cary, NC

  • Schemske DW, Horvitz CC (1988) Plant–animal interactions and fruit production in a neotropical herb: a path analysis. Ecology 69:1128–1137

    Article  Google Scholar 

  • Shuterland S (1986) Floral sex ratios, fruit set, and resource allocation in plants. Ecology 67:991–1001

    Article  Google Scholar 

  • Sperens U (1996) Is fruit and seed production in Sorbus aucuparia L. (Rosaceae) pollen limited? Ecoscience 3:325–329

    Google Scholar 

  • Sperens U (1997a) Fruit production in Sorbus aucuparia L. (Rosaceae) and predispersal seed predation by the apple fruit moth (Argyresthia conjugella Zell.). Oecologia 110:368–373

    Article  Google Scholar 

  • Sperens U (1997b) Long-term variation in, and effects of fertiliser addition on, flower, fruit and seed production in the tree Sorbus aucuparia (Rosaceae). Ecography 20:521–534

    Article  Google Scholar 

  • Sperens U (1998) Reproductive strategies in the hermaphroditic tree Sorbus aucuparia L. (Rosaceae). Ph.D. Thesis, University of Umea, Sweden

  • Stephenson AG (1981) Flower and fruit abortion: proximate causes and ultimate functions. Annu Rev Ecol Syst 12:253–279

    Article  Google Scholar 

  • Stephenson AG (1984) The regulation of maternal investment in an indeterminate flowering plant (Lotus corniculatus). Ecology 65:113–121

    Article  Google Scholar 

  • Stephenson AG (1992) The regulation of maternal investment in plants. In: Marshall C, Grace J (eds) Fruit and seed production. Cambridge, pp 151–171

  • Strauss SY (1997) Floral characters link herbivores, pollinators and plant fitness. Ecology 78:1640–1645

    Google Scholar 

  • Thompson JN, Cunningham BM (2002) Geographic structure and dynamics of coevolutionary selection. Nature 417:735–738

    Article  PubMed  CAS  Google Scholar 

  • Totland Ø (2001) Environment-dependent pollen limitation and selection on floral traits in an Alpine species. Ecology 82:2233–2244

    Article  Google Scholar 

  • Traveset A (1994) Cumulative effects on the reproductive output of Pistacia terebinthus (Anacardiaceae). Oikos 71:152–162

    Article  Google Scholar 

  • Traveset A (1995) Spatio-temporal variation in pre-dispersal reproductive losses of a Mediterranean shrub, Euphorbia dendroides L. Oecologia 103:118–126

    Article  Google Scholar 

  • Verbeke G, Molenberghs G (1997) Linear mixed models in practice. A SAS-oriented approach. Lecture Notes in Statistics 126. New York, Springer

  • Wilcock CC, Neiland MRM (2002) Pollination failure in plants: why it happens and when it matters. Trends Plant Sci 7:270–277

    Article  PubMed  CAS  Google Scholar 

Download references

Acknowledgements

Carlos Herrera, José Guitián and Anna Traveset made useful comments on previous versions of the manuscript. Adrián Escudero helped with the statistical analysis. Two anonymous referees made useful comments to a previous version of the paper. During most of this work, B. Pías and M. Salvande were supported by predoctoral grant (FP98-78789092 to BP and AP97-33299901 to MS) by the Spanish Ministerio de Educación y Ciencia. All the investigations described here are included in projects PB97-0516 (1999–2001) by Spanish Ministerio de Educación y Ciencia and BOS2001-3267 (2002–2004) by Spanish Ministerio de Ciencia y Tecnología. We thank Guy Norman for English translation.

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Pías, B., Salvande, M. & Guitián, P. Variation in Predispersal Losses in Reproductive Potential in Rowan (Sorbus aucuparia L. Rosaceae) in the NW Iberian Peninsula. Plant Ecol 188, 191–203 (2007). https://doi.org/10.1007/s11258-006-9156-x

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