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Reduced plant fitness by pre-dispersal seed predation in the threatened plant species Cirsium decussatum

Published online by Cambridge University Press:  11 May 2018

Alina Stachurska-Swakoń ,
Beata Barabasz-Krasny ,
Anna Klasa  and
Andrzej Palaczyk
Alina Stachurska-Swakoń*
Affiliation:
Jagiellonian University, Institute of Botany, Gronostajowa 3, 30-387 Kraków, Poland
Beata Barabasz-Krasny
Affiliation:
Department of Botany, Institute of Biology, Pedagogical University Kraków, Podchorążych 2, 30-084 Kraków, Poland
Anna Klasa
Affiliation:
Ojców National Park, 32-047 Ojców 9, Poland
Andrzej Palaczyk
Affiliation:
Museum of the Institute of Systematics and Evolution of Animals PAS, św. Sebastiana 9, 31-049 Kraków, Poland
*
Author for correspondence: Alina Stachurska-Swakoń Email: [email protected]
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Abstract

Seed predation has been suggested to play a crucial role in plant population dynamics and could act as a strong selective force in the evolution of plant traits such as plant phenology, size and number of flowers. The loss of seeds could be particularly threatening for population maintenance of rare plant species. We investigated the influence of seed predators on plant fitness of the rare monocarpic thistle Cirsium decussatum. We tested the following hypotheses: (1) pre-dispersal seed predators reduce the number of dispersed propagules; (2) seed predators select larger inflorescences as oviposition sites; (3) the size of the capitulum is correlated with seed productivity; and (4) seed predators compete for the oviposition sites. We identified ten insect taxa from different taxonomic groups in the capitula of C. decussatum. Terellia longicauda larvae (Diptera: Tephritidae) were the most common. The presence of the flies’ larvae was positively correlated with the predation level in the capitula. Females of T. longicauda selected larger inflorescences for laying eggs that may increase offspring fitness as larger inflorescences promise more food resources. We could not prove the presence of competition between insect species inhabiting the capitula. Our data suggest, however, that T. longicauda, a specialized seminophagous dipteran, is one of the factors that negatively influence the fitness of threatened C. decussatum, lowering significantly the seed pool. Terellia longicauda potentially acts as a strong selective force in the evolution of C. decussatum inflorescence size.

Keywords

Cirsium decussatumco-evolutionendangered plantsfactors limiting plant distributionfruit fliesplant–animal interactionsseed predationseed productivity
Type
Research Paper
Information
Seed Science Research , Volume 28 , Issue 2 , June 2018 , pp. 123 - 130
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Copyright
Copyright © Cambridge University Press 2018 

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References

Aluja, M and Norrbom, AL (1999) Fruit Flies (Tephritidae): Phylogeny and Evolution of Behavior. Boca Raton, FL, USA. CRC Press.Google Scholar
Barabasz-Krasny, B and Sołtys-Lelek, A (2010) Plant communities containing thistle (Cirsium decussatum) Janka on Przemyśl Foothills. Fragmenta Agronomica 27, 20–33.Google Scholar
Batra, SWT et al. (1981) Insects and fungi associated with Carduus thistles (Compositae). Technical Bulletin 1616, US Department of Agriculture.Google Scholar
Briese, DT (2000) Impact of the Onopordum capitulum weevil Larinus latus on seed production by its host plant. Journal of Applied Ecology 37, 238–246.CrossRefGoogle Scholar
Campagna, G and Rapparini, G (2002) Sviluppo di mezzi biologici per il contenimiento delle malerbe. Informatore Agrario 58, 53–58.Google Scholar
Cariveau, D et al. (2004) Direct and indirect effects of pollinators and seed predators to selection on plant and floral traits. Oikos 104, 15–26.CrossRefGoogle Scholar
Celedon-Neghme, C, Gonzales, WL and Gianoli, E (2007) Cost and benefits of attractive floral traits in the annual species Madia sativa (Asteraceae). Evolutionary Ecology 21, 247–257.CrossRefGoogle Scholar
Combs, JK et al. (2011) Invasive competitor and native seed predators contribute to rarity of the narrow endemic Astragalus sinuatus Piper. Ecological Applications 21, 2498–2509.CrossRefGoogle ScholarPubMed
Combs, JK, Lambert, AM and Reichard, SH (2013) Predispersal seed predation is higher in a rare species than in its widespread sympatric congeners (Astragalus, Fabaceae). American Journal of Botany 100, 2149–2157.CrossRefGoogle Scholar
Dostal, J (1958) Klíč k úplené květeně ČSR. Nakladatelství Československé Akademie Věd. Věda Všem. Sekce bologická, p. 726. Praha.Google Scholar
Falińska, K (1997) Life history variation in Cirsium palustre and its consequences for the population demography in vegetation succession. Acta Societatis Botanicorum Poloniae 66, 207–220.CrossRefGoogle Scholar
Fenner, M et al. (2002) Relationship between capitulum size and pre-dispersal seed predation by insect larvae in common Asteraceae. Oecologia, 130, 72–77.CrossRefGoogle ScholarPubMed
Fenner, M and Thompson, K (2005) Ecology of Seeds. Cambridge: Cambridge University Press.CrossRefGoogle Scholar
Fröborg, H and Eriksson, O (2003) Predispersal seed predation and population dynamics in the perennial understorey herb Actaea spicata. Canadian Journal of Botany 81, 1058–1069.CrossRefGoogle Scholar
Goto, R et al. (2010) Selective flower abortion maintains moth cooperation in a newly discovered pollination mutualism. Ecology Letters 13, 321–329.CrossRefGoogle Scholar
Hegazy, AK and Eesa, NM (1991) On the ecology, insect seed-predation, and conservation of a rare endemic plant species, Ebenus armitagei (Leguminosae). Conservation Biology 5, 317–324.CrossRefGoogle Scholar
Holt, C and Zwölfer, H (2007) Life history and behavior of Terellia longicauda (Meigen), a highly specialised tephritid of the woolly thistle, Cirsium eriophorum. Studia Dipterologica 14, 335–344.Google Scholar
Honek, A and Martinkova, Z (2005) Pre-dispersal predation of Taraxacum officinale (dandelion) seed. Journal of Ecology 93, 335–344.CrossRefGoogle Scholar
Hulme, PE and Benkman, CW (2002) Granivory. Plant–Animal Interactions: An Evolutionary Approach, pp. 132–154 in Herrera, CM and Pellmyr, O (eds). Oxford, UK: Blackwell Science.Google Scholar
Ibanez, S et al. (2009) Plant chemical defense: a partner control mechanism stabilizing plant - seed-eating pollinator mutualisms. BMC Evolutionary Biology 9, 261–270.CrossRefGoogle ScholarPubMed
Janzen, DH (1971) Seed predation by animals. Annual Review of Ecology, Evolution, and Systematics 2, 465–492.CrossRefGoogle Scholar
Kaźmierczakowa, R et al. (2016) Polish red list of pteridophytes and flowering plants. Instytut Ochrony Przyrody Polskiej Akademii Nauk, KrakówGoogle Scholar
Klasa, A and Palaczyk, A (2004) Ocena zagrożenia ostrożenia siedmiogrodzkiego Cirsium decussatum Janka (Asteraceae) przez nasionnicę Terellia longicauda (Diptera; Tephritidae) i inne owady. Chrońmy Przyrodę Ojczystą 60, 13–24.Google Scholar
Kolb, A, Ehrlen, J and Eriksson, O (2007) Ecological and evolutionary consequences of spatial and temporal variation in pre-dispersal seed predation. Perspectives in Plant Ecology, Evolution and Systematics 9, 79–100.CrossRefGoogle Scholar
Koprdova, S et al. (2015) Does gall midge larvae cause pre-dispersal seed mortality and limit cornflower population growth? Acta Oecologica 69, 167–172.CrossRefGoogle Scholar
Kozyra, M and Skalicka-Woźniak, K (2014) Quantitative analysis of flavonoids and phenolic acids from inflorescences and aerial parts of selected Cirsium species using ASE method. Acta Poloniae Pharmaceutica 71, 877–881.Google ScholarPubMed
Kurkjian, E, Carothers, SK and Jules, ES (2017) Seed predation has the potential to drive a rare plant to extinction. Journal of Applied Ecology 54, 862–871.Google Scholar
Lavergne, S, Debussche, M and Thompson, JD (2005) Limitations on reproductive success in endemic Aquilegia viscosa (Ranunculaceae) relative to its widespread congener Aquilegia vulgaris: the interplay of herbivory and pollination. Oecologia 142, 212–220.CrossRefGoogle ScholarPubMed
Larson, BMH, Kevan, PG and Inouye, DW (2001) Flies and flowers: taxonomic diversity of anthophiles and pollinators. Canadian Entomologist 133, 439–465.CrossRefGoogle Scholar
Louda, SM and Potvin, MA (1995) Effect of inflorescence feeding insects on the demography and lifetime fitness of a native plant. Ecology 76, 229–245.CrossRefGoogle Scholar
Maron, JL, Combs, JK and Louda, SM (2002) Convergent demographic effects of insect attack on related thistles in coastal vs continental dunes. Ecology 83, 3382–3392.CrossRefGoogle Scholar
Maron, JL and Crone, E (2006) Herbivory: effects on plant abundance, distribution, and population growth. Proceedings of the Royal Society of London, Series B 273, 2575–2584.Google ScholarPubMed
Münzbergová, Z (2005) Determinants of species rarity: population growth rates of species sharing the same habitat. American Journal of Botany 92, 1987–1994.CrossRefGoogle ScholarPubMed
Piórecki, J and Zarzycki, K (2008) Ostrożeń siedmiogrodzki Cirsium decussatum Janka. pp. 364–365 in Mirek, Z and Piękoś-Mirkowa, H (eds), Czerwona Księga Karpat Polskich. Rośliny naczyniowe. Instytut Botaniki im. W. Szafera Polska Akademia Nauk, Kraków.Google Scholar
Piórecki, J and Zarzycki, K (2014) Cirsium decussatum Janka Ostrożeń siedmiogrodzki, pp. 386–388 in Kaźmierczakowa, R (ed), Polska czerwona księga roślin. Instytut Ochrony Przyrody PAN, Instytut Botaniki im. W. Szafera PAN, Kraków.Google Scholar
Rotheray, GE (2014) Development sites, feeding modes and early stages of seven European Palloptera species (Diptera, Pallopteridae). Zootaxa 3900, 50–76.CrossRefGoogle ScholarPubMed
Steiger, S and Stökl, J (2017). Pheromones involved in insect parental care and family life. Current Opinion in Insect Science 24, 89–95.CrossRefGoogle ScholarPubMed
Szafer, W, Kulczyński, S and Pawłowski, B (1986) Rośliny Polskie. 2. Polskie Wydawnictwo Naukowe, Warszawa.Google Scholar
Thomann, M et al. (2015) Contemporary evolution of plant reproductive strategies under global change is revealed by stored seeds. Journal of Evolutionary Biology 28, 766–778.CrossRefGoogle ScholarPubMed
Tofts, R (1999) Biological flora of British Islands. No 206: Cirsium eriophorum L. (Scop.) (Carduus eriophorus L., Cnicus eriophorus (L.) Roth). Journal of Ecology 87, 529–542.CrossRefGoogle Scholar
van der Meijden, E (1971) Senecio and Tyrio (Callimorpha) in a Dutch dune area. A study on an interaction between a monophagous consumer and its host plant, pp. 390–404 in den Boer, PJ and Gradwell, GR (eds), Dynamics of Numbers in Populations. Centre for Agricultural Publishing and Documentation.Google Scholar
Werner, K (1976) Cirsium Miller, pp. 232–242 in Tutin, TG, Heywood, VA, Burges, NA, Moore, DM, Valentine, DH, Walters, SM and Webb, DA (eds), Flora Europaea, vol, 4. Cambridge, UK: Cambridge University Press.Google Scholar
Zimmerman, TG and Reichard, SH (2005) Factors affecting persistence of Wenatchee Mountains checker-mallow: an exploratory look at a rare endemic. Northwest Science 79, 172–178.Google Scholar