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Composition of speciose leaf litter alters stream detritivore growth, feeding activity and leaf breakdown

  • Plant Animal Interactions
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Abstract

Leaf litter derived from riparian trees can control secondary production of detritivores in forested streams. Species-rich assemblages of leaf litter reflect riparian plant species richness and represent a heterogeneous resource for stream consumers. Such variation in resource quality may alter consumer growth and thus the feedback on leaf breakdown rate via changes in feeding activity. To assess the consequences of this type of resource heterogeneity on both consumer growth and subsequent litter breakdown, we performed a laboratory experiment where we offered a leaf-shredding stream detritivore (the stonefly Tallaperla maria, Peltoperlidae) ten treatments of either single- or mixed-species leaf litter. We measured consumer growth rate, breakdown rate and feeding activity both with and without consumers for each treatment and showed that all three variables responded to speciose leaf litter. However, the number of leaf species was not responsible for these results, but leaf species composition explained the apparent non-additive effects. T. maria growth responded both positively and negatively to litter composition, and growth on mixed-litter could not always be predicted by averaging estimates of growth in single-species treatments. Furthermore, breakdown and feeding rates in mixed litter treatments could not always be predicted from estimates of single-species rates. Given that species richness and composition of senesced leaves in streams reflects riparian plant species richness, in-stream secondary production of detritivores and organic matter dynamics may be related to species loss of trees in the riparian zone. Loss of key species may be more critical to maintaining such processes than species richness per se.

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References

  • Anderson NH, Cummins KW (1979) Influences of diet on the life histories of aquatic insects. J Fish Res Board Can 36:335–342

    Google Scholar 

  • Anderson WB, Polis GA (1998) Marine subsidies of island communities in the Gulf of California: evidence from stable carbon and nitrogen isotopes. Oikos 81:75–80

    Article  Google Scholar 

  • Bärlocher F (1985) The role of fungi in the nutrition of stream invertebrates. Bot J Linn Soc 91:83–94

    Article  Google Scholar 

  • Bärlocher F, Kendrick B (1975) Leaf-conditioning by microorganisms. Oecologia 20:359–362

    Article  Google Scholar 

  • Bernays EA, Bright KL, Gonzalez N, Angel J (1994) Dietary mixing in a generalist herbivore: tests of two hypotheses. Ecology 75:1997–2006

    Article  Google Scholar 

  • Blair JM, Parmelee RW, Beare MH (1990) Decay rates, nitrogen fluxes, and decomposer communities of single- and mixed-species foliar litter. Ecology 71:1976–1985

    Article  Google Scholar 

  • Campbell IC, Fuchshuber L (1995) Polyphenols, condensed tannins, and processing rates of tropical and temperate leaves in an Australian stream. J North Amer Benthol Soc 14:174–182

    Article  Google Scholar 

  • Crowl TA, McDowell WH, Covich AP, Johnson SL (2001) Freshwater shrimp effects on detrital processing and nutrients in a tropical headwater stream. Ecology 82:775–783

    Google Scholar 

  • Cummins KW, Klug MJ (1979) Feeding ecology of stream invertebrates. Annu Rev Ecol Syst 10:147–172

    Article  Google Scholar 

  • Cummins KW, Wilzbach MA, Gates DM, Perry JB, Taliaferro WB (1989) Shredders and riparian vegetation. BioScience 39:24–30

    Article  Google Scholar 

  • Fisher SG, Likens GE (1973) Energy flow in Bear Brook, New Hampshire: an integrative approach to stream ecosystem metabolism. Ecol Monogr 43:421–439

    Article  Google Scholar 

  • Findlay S, Meyer JL, Smith PG (1986) Incorporation of microbial biomass by Peltoperla sp. (Plecoptera) and Tipula sp. (Diptera). J North Am Benthol Soc 5:306–310

    Article  Google Scholar 

  • Findlay S, Carreiro M, Jones CG. 1991. Ozone stress and mite damage to cottonwood plants alter subsequent litter decomposition: the afterlife effect. Bull Ecol Soc Am 72(Suppl):113

    Google Scholar 

  • Findlay S, Carriero M, Krischik V, Jones CG (1996) Effects of damage to living plants on leaf litter quality. Ecol Appl 6: 269–275

    Article  Google Scholar 

  • Freeland WH, Janzen (1974) Strategies in herbivory by mammals: the role of plant secondary compounds. Am Nat 108:269–289

    Article  CAS  Google Scholar 

  • Fox LR, Macauley BJ (1977) Insect grazing in Eucalyptus in response to variation in leaf tannins and nitrogen. Oecologia 29:145–162

    Google Scholar 

  • Gende SM, Willson MF (2001) Passerine densities in riparian forests of southeast Alaska: Potential effects of anadromous spawning salmon. Condor 103:624–629

    Article  Google Scholar 

  • Golladay SW, Webster JR, Benfield EF (1983) Factors affecting food utilization by a leaf shredding aquatic insect: leaf species and conditioning time. Holarctic Ecol 6:157–162

    Google Scholar 

  • Haapala A, Muotka T, Markkola A (2001) Breakdown and macroinvertebrate and fungal colonization of alder, birch, and willow leaves in a boreal forest stream. J North Am Benthol Soc 20:395–407

    Article  Google Scholar 

  • Hall RO, Likens GE, Malcom HM (2001) Trophic basis of invertebrate production in 2 streams at the Hubbard Brook Experimental Forest. J North Am Benthol Soc 20:432–447

    Article  Google Scholar 

  • Hanski I (1981) Coexistence of competitors in patchy environments with and without predators. Oikos 37:306–312

    Article  Google Scholar 

  • Herbst GN (1982) Effects of leaf type on the consumption rates of aquatic detritivores. Hydrobiologia 89:77–87

    Article  Google Scholar 

  • Hilborn R (1975) The effect of spatial heterogeneity on the persistence of predator-prey interactions. Theor Popul Biol 8:346–355

    Article  PubMed  CAS  Google Scholar 

  • Huxel GR, McCann K (1998) Food web stability: the influence of trophic flows across habitats. Am Nat 152:460–469

    Article  CAS  PubMed  Google Scholar 

  • Hynes HBN (1970) The ecology of running waters. University of Toronto Press, Toronto

    Google Scholar 

  • Irons JG, Oswood MW, Bryant JP (1988) Consumption of leaf detritus by a stream shredder: Influence of tree species and nutrient status. Hydrobiologia 160:53–61

    CAS  Google Scholar 

  • Iversen TM (1974) Ingestion and growth in Sericosoma personatum (Trichoptera) in relation to the nitrogen content of ingested leaves. Oikos 25:278–282

    Article  Google Scholar 

  • Johnson BR, Wallace JB (2005) Bottom-up limitation of a stream salamander in a detritus-based food web. Can J Fish Aquat Sci 62:301–311

    Article  Google Scholar 

  • Kaneko N, Salamanca EF (1999) Mixed leaf litter effects on decomposition rates and soil microarthropod communities in an oak-pine stand in Japan. Ecol Res 14:131–138

    Article  Google Scholar 

  • Kenward MG, Roger JH (1997) Small sample inference for fixed effects from restricted maximum likelihood. Biometrics 53:983–997

    Article  PubMed  CAS  Google Scholar 

  • Leff LG, McArthur JV (1989) The effect of leaf pack composition on processing: a comparison of mixed and single species packs. Hydrobiologia 182:219–224

    Google Scholar 

  • Lindroth RL, Kinney KK, Platz CL (1993) Responses of deciduous trees to elevated atmospheric CO2: productivity, phytochemistry, and insect performance. Ecology 74:763–777

    Article  CAS  Google Scholar 

  • Melillo JM, Aber JD, Muratore JF (1982) Nitrogen and lignin control of hardwood leaf litter decomposition dynamics. Ecology 63:621–626

    Article  CAS  Google Scholar 

  • Motomori K, Mitsuhashi H, Nakano S (2001) Influence of leaf litter quality on the colonization and consumption of stream invertebrate shredders. Ecol Res 16:173–182

    Article  Google Scholar 

  • Murakami M., Nakano S (2002) Indirect effect of aquatic insect emergence on a terrestrial insect population through predation by birds. Ecol Lett 5:333–337

    Article  Google Scholar 

  • Naeem S, Colwell RK (1991) Ecological consequences of heterogeneity of consumable resources. In: Kolasa J, Pickett STA (eds) Ecological heterogeneity. Springer, Berlin Heidelberg New York, pp 224–254

    Google Scholar 

  • Ostrofsky ML (1993) Effect of tannins on leaf processing and conditioning rates in aquatic ecosystems: an empirical approach. Can J Fish Aquat Sci 50:1176–1180

    Article  CAS  Google Scholar 

  • Ostrofsky ML (1997) Relationship between chemical characteristics of autumn-shed leaves and aquatic processing rates. J North Am Benthol Soc 16:750–759

    Article  Google Scholar 

  • Pacala SW, Roughgarden J (1982) Spatial heterogeneity and interspecific competition. Theor Popul Biol 121:92–113

    Article  Google Scholar 

  • Pennings SC, Masatomo TN, Paul VJ (1993) Selectivity and growth of the generalist herbivore Dolabella auricularia feeding upon complimentary resources. Ecology 74:879–890

    Article  Google Scholar 

  • Petersen RC, Cummins KW (1974) Leaf processing in a woodland stream. Fresh Biol 4:343–368

    Article  Google Scholar 

  • Polis GA, Hurd SD (1996) Allochthonous input across habitats, subsidized consumers, and apparent trophic cascades: examples from the ocean-land interface. In: Polis GA, Winemiller KO (eds) Food Webs: integration of patterns and dynamics. Chapman and Hall, New York, pp 275–285

    Google Scholar 

  • Polis GA, Anderson WB, Holt RD (1997) Towards an integration of landscape and food web ecology: the dynamics of spatially subsidized food webs. Ann Rev Ecol Syst 28:289–316

    Article  Google Scholar 

  • Power ME (2001) Prey exchange between a stream and its forested watershed elevates predator densities in both habitats. Proc Nat Acad Sci USA 98:14–15

    Google Scholar 

  • Richardson JS (1991) Seasonal food limitation of detritivores in a montane stream: an experimental test. Ecology 72:873–887

    Article  Google Scholar 

  • Schindler DE, Scheuerell MD (2002) Habitat coupling in lake ecosystems. Oikos 98:177–189

    Article  Google Scholar 

  • Short RA, Maslin PE (1977) Processing of leaf litter by a stream detritivore: effect of nutrient availability to collectors. Ecology 58:935–938

    Article  Google Scholar 

  • Simpson SJ, Simpson CL (1990) The mechanisms of nutritional compensation by phytophagus insects. In: Bernays EA (ed) Insect--plant interactions, vol 2. CRC Press, Boca Raton, pp 111–160

  • Smock LA, MacGregor CM (1988) Impact of the American chestnut blight on aquatic shredding macroinvertebrates. J North Am Benthol Soc 7:212–221

    Article  Google Scholar 

  • Snyder CD, Young JA, Lemarié DP, Smith DR (2002) Influence of eastern hemlock (Tsuga canadensis) forests on aquatic invertebrate assemblages in headwater streams. Can J Fish Aquat Sci 59:232–275

    Google Scholar 

  • Sokal RR, Rohlf FJ (1981) Biometry. 2nd edn. W.H. Freeman and Company, New York

    Google Scholar 

  • Sponseller RA, Benfield EF (2001) Influences of land-use on leaf breakdown in southern Appalachian headwater streams: a multiple-scale analysis. J North Am Benthol Soc 20:44–59

    Article  Google Scholar 

  • Stewart KW, Harper PP (1996) Plecoptera. In: Merritt RW, Cummins KW (eds) An introduction to the aquatic insects of North America. 3rd edn. Kendall/Hunt Publishing Company, Dubuqeue, pp 217–266

    Google Scholar 

  • Strong DR (1992) Are trophic cascades all wet? Differentiation and donor-control in speciose ecosystems. Ecology 73:747–754

    Article  Google Scholar 

  • Swan CM, Palmer MA (2004) Leaf diversity alters litter breakdown in a Piedmont stream. J North Am Benthol Soc 23:15–28

    Article  Google Scholar 

  • Swan CM, Palmer MA (2005) Leaf litter diversity leads to non-additivity in stream detritivore colonization dynamics. Oceanol Hydrobiol Stud 34:19–38

    Google Scholar 

  • Sweeney BW (1993) Effects of streamside vegetation on macroinvertebrate communities of White Clay Creek in eastern North America. Proc Acad Nat Sci USA 144:291–340

    Google Scholar 

  • Takimoto G, Iwata T, Murakami M (2002) Seasonal subsidy stabilizes food web dynamics: Balance in a heterogeneous landscape. Ecol Res 17:433–439

    Article  Google Scholar 

  • Taylor BR, Parsons WFJ, Parkinson D (1989a) Decomposition of Populus tremuloides leaf litter accelerated by addition of Alnus crispa litter. Can J For Res 19:674–707

    Article  Google Scholar 

  • Taylor BR, Parkinson D, Parsons WFJ (1989b) Nitrogen and lignin content as predictors of litter decay rates: a microcosm test. Ecology 70:97–104

    Article  Google Scholar 

  • Wallace JB, Eggert SL, Meyer JL, Webster JR (1997) Multiple trophic levels of a forest stream linked to terrestrial litter inputs. Science 277:102–104

    Article  CAS  Google Scholar 

  • Wallace JB, Eggert SL, Meyer JL, Webster JR (1999) Effects of resource limitation on a detrital-based ecosystem. Ecol Monogr 69:409–442

    Article  Google Scholar 

  • Webster JR, Benfield EF (1986) Vascular plant breakdown in freshwater ecosystems. Ann Rev Ecol Syst 17:567–594

    Article  Google Scholar 

  • Westfall PH, Tobias RD, Rom D, Wolfinger RD, Hochberg Y (1999) Concepts and basic methods for multiple comparisons and tests. In: Multiple comparisons and multiple tests using the SAS system, SAS Institute, Inc., Cary, pp 13–40

  • Wold EN, Marquis RJ (1997) Induced defense in white oak: effects on herbivores and consequences for the plant. Ecology 78:1356–1369

    Google Scholar 

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Acknowledgements

We thank Emily Bernhardt, Laura Craig, Holly Menninger, Aaron Moore, Dave Richardson and Bob Smith for their scientific input, comments and editing. Comments by two anonymous reviewers greatly improved the text. This research was supported by grants awarded to CMS from the Chesapeake Bay Fund (University of Maryland) and to MAP from the National Science Foundation (DEB-9981376).

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Correspondence to Christopher M. Swan.

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Communicated by David Post

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Swan, C.M., Palmer, M.A. Composition of speciose leaf litter alters stream detritivore growth, feeding activity and leaf breakdown. Oecologia 147, 469–478 (2006). https://doi.org/10.1007/s00442-005-0297-8

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