Skip to main content

Advertisement

Log in

Carbon and nitrogen transfer from a desert stream to riparian predators

  • Ecosystems Ecology
  • Published:
Oecologia Aims and scope Submit manuscript

Abstract

Adult aquatic insects emerging from streams may be a significant source of energy for terrestrial predators inhabiting riparian zones. In this study, we use natural abundance δ13C and δ15N values and an isotopic 15N tracer addition to quantify the flow of carbon and nitrogen from aquatic to terrestrial food webs via emerging aquatic insects. We continuously dripped labeled 15N-NH4 for 6 weeks into Sycamore Creek, a Sonoran desert stream in the Tonto National Forest (central Arizona) and traced the flow of tracer 15N from the stream into spiders living in the riparian zone. After correcting for natural abundance δ15N, we used isotopic mixing models to calculate the proportion of 15N from emerging aquatic insects incorporated into spider biomass. Natural abundance δ13C values indicate that orb-web weaving spiders inhabiting riparian vegetation along the stream channel obtain almost 100% of their carbon from instream sources, whereas ground-dwelling hunting spiders obtain on average 68% of their carbon from instream sources. During the 6-week period of the 15N tracer addition, orb-web weaving spiders obtained on average 39% of their nitrogen from emerging aquatic insects, whereas spider species hunting on the ground obtained on average 25% of their nitrogen from emerging aquatic insects. To determine if stream subsidies might be influencing the spatial distribution of terrestrial predators, we measured the biomass, abundance and diversity of spiders along a gradient from the active stream channel to a distance of 50 m into the upland using pitfall traps and timed sweep net samples. Spider abundance, biomass and richness were highest within the active stream channel but decreased more than three-fold 25 m from the wetted stream margin. Changes in structural complexity of vegetation, ground cover or terrestrial prey abundance could not account for patterns in spider distributions, however nutrient and energy subsidies from the stream could explain elevated spider numbers and richness within the active stream channel and riparian zone of Sycamore Creek.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1.
Fig. 2.
Fig. 3.
Fig. 4.
Fig. 5a--c.
Fig. 6a, b.
Fig. 7.

Similar content being viewed by others

References

  • Anderson JF (1974) Responses to starvation in the spiders Lycosa lenta Hentz and Filistata hibernalis (Hentz). Ecology 55:576–585

    Google Scholar 

  • Bastow JL, Sabo JL, Finlay JC, Power ME (2002) A basal aquatic- terrestrial trophic link in rivers: algal subsidies via shore-dwelling grasshoppers. Oecologia (in press)

    Google Scholar 

  • Busch DE, Fisher SG (1981) Metabolism of a desert stream. Freshwater Biol 11:301–307

    CAS  Google Scholar 

  • Cabana G, Rasmussen JB (1994) Modeling food chain structure and contaminant bioaccumulation using stable nitrogen isotopes. Nature 372: 255–257

    CAS  Google Scholar 

  • Cadenasso ML, Pickett STA (2000) Linking forest edge structure to edge function: mediation of herbivore damage. J Ecol 88:31–44

    Article  Google Scholar 

  • Coddington JA, Young LH, Coyle FA (1996) Estimating spider species richness in southern Appalachian cove hardwood forest. J Arachnol 24:11–28

    Google Scholar 

  • DeNiro MJ, Epstein S (1978) Influence of diet on the distribution of carbon isotopes in animals. Geochim Cosmochim Acta 42:495–506

    CAS  Google Scholar 

  • Doucett RR, Power G, Barton DR, Drimmie RJ, Cunjak RA (1996) Stable isotope analysis of nutrient pathways leading to Atlantic salmon. Can J Fish Aquat Sci 53:2058–2066

    Article  Google Scholar 

  • Fagan WF, Cantrell RS, Cosner C (1999) How habitat edges change species interactions. Am Nat 153:165–182

    Article  Google Scholar 

  • Ferguson SH (2000) Predator size and distance to edge: is bigger better? Can J Zool 78:713–720

    Article  Google Scholar 

  • Finlay JC, Power ME, Cabana G (1999) Effects of water velocity on algal carbon isotope ratios: Implications for river food web studies Limnol Oceanogr 44:1198–1203

    Google Scholar 

  • Fisher SG, Gray LJ (1983) Secondary production and organic matter processing by collector macroinvertebrates in a desert stream. Ecology 64:1217–1224

    Google Scholar 

  • Foelix RF (1996) Biology of spiders, 2nd edn. Oxford University Press, Oxford

  • Gillespie RG (1987) The mechanism of habitat selection in the long-jawed orb-weaving spider Tetragnatha elongata (Araneae, Tetragnathidae). J Arachnol 15:81–90

    Google Scholar 

  • Gray LJ (1981) Species composition and life histories of aquatic insects in a lowland Sonoran desert stream. Am Midl Nat 106:229–242

    Google Scholar 

  • Gray LJ (1989) Emergence production and export of aquatic insects from a tallgrass prairie stream. Southwest Nat 34:313–318

    Google Scholar 

  • Gray LJ (1993) Response of insectivorous birds to emerging aquatic insects in riparian habitats of a tallgrass prairie stream. Am Midl Nat 129:288–300

    Google Scholar 

  • Greenstone MH (1984) Determinants of web spider species diversity: vegetation structural diversity vs prey availability. Oecologia 62:299–304

    Google Scholar 

  • Greenwood MT, Bickerton MA, Petts GE (1995) Spatial distribution of spiders on the floodplain of the River Trent, UK- the role of hydrologic setting. Regul Rivers Res Manage 10:303–313

    Google Scholar 

  • Grimm NB (1987) Nitrogen dynamics during succession in a desert stream. Ecology:1157–1170

  • Grimm NB (1988) Role of macroinvertebrates in nitrogen dynamics of a desert stream. Ecology 69:1884–1893

    Google Scholar 

  • Hall RO Jr, Peterson BJ, Meyer JL (1998) Testing a nitrogen-cycling model for a forest stream by using a nitrogen-15 tracer addition. Ecosystems 1:283–298

    Article  CAS  Google Scholar 

  • Hansson L (1994) Vertebrate distributions relative to clear-cut edges in a boreal forest landscape. Landscape Ecol 9:105–115

    Google Scholar 

  • Heiling A (1999) Why do nocturnal orb-web spiders (Araneidae) search for light? Behav Ecol Sociobiol 46:43–49

    Article  Google Scholar 

  • Henschel JR, Stumpf H, Mahsberg D (1996) Increase of arachnid abundance and biomass at water shores. Rev Suisse Zool, pp 265–268

  • Henschel J, Mahsberg D, Stumpf H (2002) Stream subsidies: the influence of river insects on spider predation of terrestrial insects. In: Polis GA, Power ME, Huxel GR (eds) Food webs at the landscape level. University of Chicago Press, Chicago (in press)

  • Herrera LG (1998) Trophic relationships in a neotropical bat community: a preliminary study using carbon and nitrogen isotopic signatures. Trop Ecol 39:23–29

    Google Scholar 

  • Hershey AE, Pastor J, Peterson BJ, Kling GW (1993) Stable isotopes resolve the drift paradox for Baetis mayflies in an arctic river. Ecology 74:2315–2325

    Google Scholar 

  • Jackson JK (1984) Aquatic insect emergence from a desert stream. Thesis. Arizona State University, Tempe, Arizona, USA

  • Jackson JK, Fisher SG (1986) Secondary production, emergence and export of aquatic insects of a Sonoran Desert Stream. Ecology 67:629–638

    Google Scholar 

  • JMP (1995) Statistical discovery software. SAS Institute, Cary, N.C.

  • Jordan MJ, Nadelhoffer KJ, Fry B (1997) Nitrogen cycling in forest and grass ecosystems irrigated with 15N enriched wastewater. Ecol Appl 7:864–881

    Google Scholar 

  • Junger M, Planas D (1994) Quantitative use of stable carbon isotope analysis to determine the trophic base of invertebrate communities in a boreal forest lotic system. Can J Fish Aquat Sci 51:52–61

    Google Scholar 

  • Kareiva P (1987) Habitat fragmentation and the stability of predator-prey interactions. Nature 326:388–390

    Google Scholar 

  • Kaston BJ (1978) How to know the spiders, 3rd edn. Brown, Dubuque, Iowa

  • Kelly JF (2000) Stable isotopes of carbon and nitrogen in the study of avian and mammalian trophic ecology. Can J Zool 78:1–27

    Article  Google Scholar 

  • Koba K, Takahashi K, Kohzu A (1999) A review of stable isotope studies of nitrogen dynamics in soil-plant systems in forest ecosystems. Jpn J Ecol 49:47–51

    Google Scholar 

  • Leopold A (1941) Lakes in relation to terrestrial life patterns. In: The University of Wisconsin symposium volume on hydrology. Madison, Wis., pp 17–22

  • Likens GE, Bormann FH (1974) Linkages between terrestrial and aquatic ecosystems. BioScience 24:447–456

    Google Scholar 

  • Malt S (1995) Epigeic spiders as an indicator system to evaluate biotope quality of riversides and floodplain grasslands on the River Ilm (Thuringia). In: Ruzicka V (ed) Proceedings of the 15th European Colloquium of Arachnology, Ceske Budejovice, Czech Republic, pp 136–146

  • Martí E, Fisher SG, Schade JD, Grimm NB (2000) Flood frequency and stream-riparian linkages in arid lands. In: Jones JB Mulholland PJ (eds) Stream and groundwaters. Academic Press, New York, pp 111–136

  • Mulholland PJ, Tank JL, Sanzone DM, Wollheim WM, Peterson BJ, Webster JR, Meyer JL (2000a) Nitrogen cycling in a deciduous forest stream determined from a tracer 15N addition experiment in Walker Branch, Tennessee. Ecol Monogr 70:471–493

    Google Scholar 

  • Mulholland PJ, Tank JL, Sanzone DM, Wollheim WM, Peterson BJ, Webster JR, Meyer JL (2000b) Food resources of stream macroinvertebrates determined by natural- abundance stable C and N isotopes and a 15N addition. J N Am Benthol Soc 19:145–157

    Google Scholar 

  • Nakano S, Murakami M (2001) Reciprocal subsidies: dynamic interdependence between terrestrial and aquatic food webs. Proc Natl Acad Sci USA 98:166–170

    CAS  PubMed  Google Scholar 

  • Nyffeler M, Sterling WL, Dean DA (1994) How spiders make a living. Environ Entomol 23:1357–1367

    Google Scholar 

  • Orians GH, Wittenberger JF (1991) Spatial and temporal scales in habitat selection. Am Nat 137:S29–S49

    Article  Google Scholar 

  • Peterson BJ, Fry B (1987) Stable isotopes in ecosystem studies. Annu Rev Ecol Syst 18:293–320

    Article  Google Scholar 

  • Polis GA, Hurd SD (1996) Linking marine and terrestrial food webs: allochthonous input from the ocean supports high secondary production in small islands and coastal land communities. Am Nat 147:396–417

    Article  Google Scholar 

  • Ponsard S, Arditi R (2000) What can stable isotopes (δ15N and δ13C) tell about the food web of soil macroinvertebrates? Ecology 81:852–864

    Google Scholar 

  • Power ME, Rainey WE (2000) Food webs and resource sheds: towards spatially delimiting trophic interactions. In: Hutchings MJ, John EA, Stewart AJA (eds) The ecological consequences of environmental heterogeneity. Blackwell, Oxford, pp 291–314

  • Power ME, Rainey WE, Parker MS, Sabo JL, Smyth A, Khandwala S, Finlay JC, McNeely FC, Marsee K, Anderson C (2002) River to watershed subsidies in old-growth conifer forests. In: Polis GA, Power ME, Huxel GR (eds) Food webs at the landscape level. University of Chicago Press, Chicago (in press)

  • Rainey WE, Pierson ED, Coberg M, Barclay JH (1992) Bats in hollow redwoods: seasonal use and role in nutrient transfer into old growth communities. Bat Res News 33:71

    Google Scholar 

  • Sabo JL, Power ME (2002) River-watershed exchange: effects of riverine subsidies on riparian lizards and their terrestrial prey. Ecology (in press)

    Google Scholar 

  • Sanzone DM (2001) Linking communities across ecosystem boundaries: the influence of aquatic subsidies on terrestrial predators. Doctoral thesis, University of Georgia, Athens, Ga.

    Google Scholar 

  • Sanzone DM, Draney ML (1996) Effect of woody debris on spider assemblages. In: Crossley DA Jr (ed) Arthropod diversity and coarse woody debris in southern forests, report 232. USFS, Washington, D.C.

  • SAS (1996) SAS version 6.12. SAS Institute, Cary, N.C.

  • Schade JD, Fisher SG (1997) Leaf litter in a Sonoran Desert stream ecosystem. J N Am Benthol Soc 16:612–626

    Google Scholar 

  • Shapiro SS, Wilk MB (1965) An analysis of variance test for normality (complete samples). Biometrika 52:591–611

    Google Scholar 

  • Sokal RR, Rohlf F (1995) Biometry, 3rd edn. Freeman, San Francisco

  • Southwood TRE, Brown VK, Reader PM (1979) The relationship of plant and insect diversities in succession. Biol J Linn Soc 12:327–348

    Google Scholar 

  • Stamp NE (1978) Breeding birds of a riparian woodland in south-central Arizona. Condor 80:64–71

    Google Scholar 

  • Stamp NE, Ohmart RD (1979) Rodents of desert shrub and riparian woodland habitats in the Sonoran Desert. Southwest Nat 24:279–289

    Google Scholar 

  • Summerhayes VS, Elton CS (1923) Contributions to the ecology of Spitsbergen and Bear Island. J Ecol 11:214–286

    Google Scholar 

  • Tank JL, Meyer JL, Sanzone DM, Mulhollland PJ, Webster JR, Peterson BJ (2000) Analysis of nitrogen cycling in a forest stream during autumn using a 15N-tracer addition. Limnol Oceanogr 45:1013–1029

    CAS  Google Scholar 

  • Webster JR, Ehrman TP (1996) Solute dynamics. In: Hauer FR Lamberti GA (eds) Methods in stream ecology. Academic Press, New York, pp 145–160

  • Williams DD, Ambrose LG, Browning LN (1995) Trophic dynamics of two sympatric species of riparian spider (Araneae: Tetragnathidae). Can J Zool 73:1545–1553

    Google Scholar 

  • Williams B, Silcock D, Young M (1999) Seasonal dynamics of N in two Sphagnum moss species and the underlying peat treated with 15NH415NO3. Biogeochemistry 45:285–302

    Article  Google Scholar 

  • Winning MA, Connolly RM, Loneragan NR, Bunn SE (1999) 15N enrichment as a method of separating the isotopic signatures of seagrass and its epiphytes for food web analysis. Mar Ecol Prog Ser 189:289–294

    CAS  Google Scholar 

  • Wise DH (1993) Spiders in ecological webs. Cambridge University Press, Cambridge

Download references

Acknowledgements

The authors thank Bruce Peterson and Wil Wolheim for helping us think through the isotopic mixing model calculations. Stephanie Eden and Norm Leonard assisted in the laboratory. Kris Tholke and Tom Maddox performed mass spectrometry at the Ecosystems Center (MBL) and University of Georgia Analytical Chemistry Laboratories. John Sabo, Jim Elser and one anonymous reviewer provided valuable comments on the manuscript that greatly improved its content. This research was supported by grants from the National Science Foundation to J.R. Webster, P.J. Mulholland, J.L. Meyer and B.J. Peterson (DEB-9628860) and the Coweeta LTER program (DEB- 9632854).

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to D. M. Sanzone.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Sanzone, D.M., Meyer, J.L., Marti, E. et al. Carbon and nitrogen transfer from a desert stream to riparian predators. Oecologia 134, 238–250 (2003). https://doi.org/10.1007/s00442-002-1113-3

Download citation

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00442-002-1113-3

Keywords

Navigation