The Acorn Connections – Complex Interaction Webs in Oak Forests
Clive G. Jones
Cary Institute of Ecosystem Studies
Gypsy Moth defoliation and Lyme disease are major problems in eastern US oak forests. Using a combination of long-term studies and large-scale experiments, our collaborative research has shown that acorns initiate a complex series of ecological chain reactions. These interactions can ultimately determine whether or not Gypsy Moth outbreaks will occur, and can determine Lyme disease risk to people. Acorns are a key food for white-footed mice. The mice are key predators on Gypsy Moth pupae. When there are many acorns the mouse population increases, which keeps the moth population low. However if there are no acorns, the mouse population collapses allowing the moth population to increase. Acorns also attract white-tailed deer into oak forests to feed on acorns. The deer carry adult ticks that drop off and spend the winter in the oak forests. The next year the female ticks lay eggs that hatch into larval ticks. The larval ticks are not infected with the bacteria that cause Lyme disease, but become infected when they feed on the mice that have increased because of acorns. This means that the risk of Lyme disease can be higher in oak forests two years after a large acorn crop.
Acorns initiate other chain reactions among species (e.g., mice, chipmunks, and songbirds; see R. Ostfeld and K. Schmidt), and Gypsy Moth defoliation has many effects on the forest, including influences on nutrient cycling (see G. Lovett). Because moth defoliation reduces acorn production, understanding how moths are able to persist in the forest amidst intense predation pressure by mice has also been a recent focus of our work. This has led us to study the roles of local dispersal of moths relative to local spatial variation in mouse predation as the primary determinants of moth persistence (see B. Goodwin, E. Schauber). Recent research has shown that there are mouse hot and cold spots in the forest of varying persistence. We are now investigating how these hot and cold spots affect moths, Lyme risk and songbird nesting success.
Overall, our research is trying to understand how the complexity of interactions among species – including how they vary in space and time – affects the functioning of oak forest ecosystems with important implications for understanding forest ecosystem health, human health and biodiversity.
Fig. 1. Interactions in eastern deciduous forests influencing forest dynamics, Lyme-disease risk (“pathogens”), nesting success of some ground-nesting songbirds, and gypsy moth dynamics. Arrows indicate the direction of the effect of one taxon on another. Solid lines indicate positive effects (e.g., mast production on mice), and dashed arrows indicate negative effects (e.g., gypsy moths on oak trees). From Ostfeld & Jones, In Press.
Acorn Connections Links
AAAS Science Netlinks Lessons
College Board, Advanced Placement environmental science exam question
NOVA Population Explosion
Nova Population Explosion Teacher's Guide
Overcoming Ecological Misconceptions, Binghamton University
Prentice-Hall Online Textbook for Distance Learning (go to Case Studies then Complex Indirect effects)
Science-Art.com
Teaching issues and experiments in ecology (TIEE)
Acorn Connections Publications
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Ostfeld, R. S. and C. G. Jones.
2010.
The ecology of place in oak forests: Progressive integration of pairwise interactions into webs. In: I. A. Billick and M. V. Price (eds). The Ecology of Place: Contributions of Place-based Research to Ecological Understanding.
University of Chicago Press, Chicago and London. 464 pp.
pp. 207-228. For reprint contact jonesc@caryinstitute.org.
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Schauber, E. M., M. J. Connors, B. J. Goodwin, C. G. Jones and R. S. Ostfeld
2009.
Quantifying a dynamic risk landscape: Heterogeneous predator activity and implications for prey persistence.
Ecology
90: 240–251.
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Schauber, E. M., B. J. Goodwin, C. G. Jones, and R. S. Ostfeld.
2007.
Spatial selection and inheritance: Applying evolutionary concepts to population dynamics in heterogeneous space.
Ecology
88(5):1112-1118.
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Schauber, E. M., and C. G. Jones.
2006.
Comparative predation on naturally occurring Gypsy Moth (Lepidoptera: Lymantriidae) pupae and deployed freeze-dried pupae.
Environ. Entomol.
35(2):293-294.
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Connors, M. J., E. M. Schauber, A. Forbes, C. G. Jones, B. J. Goodwin, and R. S. Ostfeld.
2005.
Use of track plates to quantify predation risk at small spatial scales.
J. Mammal.
86(5):991-996.
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Goodwin, B. J., C. G. Jones, E. M. Schauber, and R. S. Ostfeld.
2005.
Limited dispersal and heterogeneous predation risk synergistically enhance persistence of rare prey.
Ecology
86(12):3139–3148.
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Schauber, E. M., R. S. Ostfeld, and C. G. Jones.
2004.
Type 3 functional response of mice to gypsy moth pupae: Is it stabilizing?
Oikos
107(3):592-602.
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Jones, C. G.
2003.
Fungi, mice control tree menace.
Poughkeepsie Journal.
16 November, Sect B:7-8.
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Lovett, G. M., L. M. Christenson, P. M. Groffman, C. G. Jones, J. E. Hart, and M. J. Mitchell.
2002.
Insect defoliation and nitrogen cycling in forests.
BioScience
52:335-341.
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Ostfeld, R. S., E. M. Schauber, C. D. Canham, F. Keesing, C. G. Jones, and J. O. Wolff.
2001.
Effects of acorn production and mouse abundance on abundance and Borrelia burgdorferi-infection prevalence of nymphal Ixodes scapularis ticks.
Vector-Borne and Zoonotic Diseases
1:55-63.
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Ostfeld, R. S., and C. G. Jones.
1999.
Peril in the understory.
Audubon Magazine
101(4):74-82.
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Jones, C. G., R. S. Ostfeld, M. P. Richard, E. M. Schauber, and J. O. Wolff.
1998.
Chain reactions linking acorns to gypsy moth outbreaks and Lyme disease risk.
Science
279:1023-1026.
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Jones, C. G., R. S. Ostfeld, M. P. Richard, E. M. Schauber, and J. O. Wolff.
1998.
Mast seeding and Lyme disease.
Trends Ecol. Evol.
13:506.
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Lovett, G. M., J. E. Hart, L. M. Christenson, and C. G. Jones.
1998.
Caterpillar guts and ammonia volatilization: retention of nitrogen by gypsy moth larvae consuming oak foliage.
Oecologia
117:513-516.
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Ostfeld, R. S., C. G. Jones, M. P. Richard, E. M. Schauber, and J. O. Wolff.
1998.
Tick population trends and forest type [Response to Ginsberg et al.]
Science
281:350-351.
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Ostfeld, R. S., F. Keesing, C. G. Jones, C. D. Canham, and G. M. Lovett.
1998.
Integrative ecology and the dynamics of species in oak forests.
Integr. Biol.
1:178-186.
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Ostfeld, R. S., C. G. Jones, and J. O. Wolff.
1996.
Of mice and mast: ecological connections in eastern deciduous forests.
BioScience
46:323-330.
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Moore, K. E. B., and C. G. Jones.
1992.
Estimating field hatch and parasitism of the gypsy moth (Lepidoptera: Lymantriidae).
Environ. Entomol.
21:276-280.
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Jones, C. G., M. K. Steininger, P. Luciano, and K. E. B. Moore.
1990.
Estimating gypsy moth fecundity in the field: a comparison between data from North America and Sardinia (Italy).
Environ. Entomol.
19:108-110.
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Wallner, W. E., C. G. Jones, J. S. Elkinton, and B. L. Parker.
1990.
Sampling low-density gypsy moth populations.
USDAFS-NEFES. Gen. Tech. Rep.
NE-146:40-44.
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Moore, K. E. B., and C. G. Jones.
1987.
Field estimation of fecundity of the gypsy moth (Lepidoptera: Lymantriidae).
Environ. Entomol.
16(1):165-167.
- Karnosky, D. F. and Jones, C. G. 1981. Living with the gypsy moth. Garden 5:8-13.
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