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Selective consumption of acorns by the Japanese wood mouse according to tannin content: a behavioral countermeasure against plant secondary metabolites

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Ecological Research

Abstract

We examined the presence of selective consumption against tannins in acorns as a pre-ingestive countermeasure to plant secondary metabolites by using the Japanese wood mouse (Apodemus speciosus) and acorns of Quercus serrata, which contained ca. 6.4% tannins on a dry weight basis. In addition, the presence of selective consumption against proteins was also examined. In the acorn-feeding experiment, 18 wood mice were allocated to two groups: the experienced group (N = 9), which had previous experience in feeding on acorns, and the inexperienced group (N = 9), which had no experience. Mice of both groups were fed only acorns for 3 nights. Selectivity against tannins (an index estimated from the tannin content in control, remaining, and ingested acorns) was significantly positive in the experienced group, indicating the presence of selective consumption against tannins. In contrast, mice in the inexperienced group did not show significant selectivity against tannins. Comparing the selectivity indices directly between two groups, however, they did not differ significantly. Selective consumption against proteins rather than that for proteins also occurred in the experienced group, but it was thought to be a byproduct resulted from the selectivity against tannins. Selective consumption against tannins can mitigate the negative effects of tannins by decreasing tannin intake.

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References

  • Barnett RJ (1977) The effect of burial by squirrels on germination and survival of oak and hickory nuts. Am Midl Nat 98:319–330

    Article  Google Scholar 

  • Barthelmess EL (2001) The effects of tannin and protein on food preference in eastern grey squirrels. Ethol Ecol Evol 13:115–132

    Article  Google Scholar 

  • Blytt HJ, Guscar TK, Butler LG (1988) Antinutritional effects and ecological significance of dietary condensed tannins may not be due to binding and inhibiting digestive enzymes. J Chem Ecol 14:1455–1465

    Article  CAS  Google Scholar 

  • Cañas RA, Torre F, Cánovas FM, Cantón FR (2006) High levels of asparagine synthetase in hypocotyls of pine seedlings suggest a role of the enzyme in re-allocation of seed-stored nitrogen. Planta 224:83–95

    Article  PubMed  CAS  Google Scholar 

  • Dixon MD, Johnson WC, Adkisson CS (1997) Effects of caching on acorn tannin levels and Blue Jay dietary performance. Condor 99:756–764

    Article  Google Scholar 

  • Eshelman BD, Jenkins SH (1989) Food selection by Belding’s ground squirrels in relation to plant nutritional features. J Mammal 70:846–852

    Article  Google Scholar 

  • Foley WJ, Moore BD (2005) Plant secondary metabolites and vertebrate herbivores—from physiological regulation to ecosystem function. Curr Opin Plant Biol 8:430–435

    Article  PubMed  CAS  Google Scholar 

  • Fowler ME, Richards WP (1965) Acorn poisoning in a cow and a sheep. J Am Vet Med Assoc 147:1215–1220

    PubMed  CAS  Google Scholar 

  • Hagerman AE (1987) Radial diffusion method for determining tannin in plant extracts. J Chem Ecol 13:437–449

    Article  CAS  Google Scholar 

  • Iida S (1996) Quantitative analysis of acorn transportation by rodents using magnetic locator. Vegetation 124:39–43

    Article  Google Scholar 

  • Kanazawa Y, Nishikata S (1976) Disappearance of acorns from the floor in Quercus crispula forests. J Jpn For Soc 58:52–56

    Google Scholar 

  • Kenward RE, Holm JL (1993) On the replacement of the red squirrels in Britain: a phytotoxic explanation. Proc R Soc Lond B 251:187–194

    Article  CAS  Google Scholar 

  • Kikuzawa K (1988) Dispersal of Quercus mongolica acorns in a broadleaved forest 1. Disappearance. For Ecol Manage 25:1–8

    Article  Google Scholar 

  • Koenig WD, Faeth SH (1998) Effects of storage on tannin and protein content of cached acorns. Southwest Nat 43:170–175

    Google Scholar 

  • Marquis RJ, Batzli GO (1989) Influence of chemical factors on palatability of forage to voles. J Mammal 70:503–511

    Article  Google Scholar 

  • McShea WJ, Healy WM (2002) Oaks and acorns as a foundation for ecosystem management. In: McShea WJ, Healy WM (eds) Oak forest ecosystems. Johns Hopkins University Press, Baltimore, pp 1–12

    Google Scholar 

  • Miguchi H (1994) Role of wood mice on the regeneration of cool temperate forest. Proceedings of NAFRO seminar on sustainable forestry and its biological environment. Japan Society of Forest Planning Press, Tokyo, pp 115–121

    Google Scholar 

  • Miyaki M, Kikuzawa K (1988) Dispersal of Quercus mongolica acorns in a broadleaved forest. 2. Scatterhoarding by mice. For Ecol Manage 25:9–16

    Article  Google Scholar 

  • Ministry of Education, Culture, Sports, Science and Technology (2005) Standard tables of food composition in Japan 5th revised and enlarged edition 2005. Kagawa Nutrition University Publishing Division, Tokyo

  • Ohta K, Abe H, Kobayashi T, Fujisaki Y, Higuchi S, Igarashi B, Kuwahata T, Maeda M, Ueda M, Takayasu T (1976) A synecological study of murid rodents. Res Bull Coll Ex For Hokkaido Univ 34:119–159 (in Japanese)

    Google Scholar 

  • Post DM (1993) Detection of differences in nutrient concentrations by eastern woodrats (Neotoma floridana). J Mammal 74:493–497

    Article  Google Scholar 

  • Pyare S, Kent JA, Noxon DL, Murphy MT (1993) Acorn preference and habitat use in eastern chipmunks. Am Midl Nat 130:173–183

    Article  Google Scholar 

  • R Development Core Team (2005) R: a language and environment for statistical computing. R Foundation for Statistical Computing, Vienna

    Google Scholar 

  • Robbins CT (1983) Wildlife feeding and nutrition. Academic Press, San Diego, pp 13–18

    Google Scholar 

  • Robbins CT, Hanley TA, Hagerman AE, Hjeljord O, Baker DL, Schwartz CC, Mautz WW (1987) Role of tannins in defending plants against ruminants—reduction in protein availability. Ecology 68:98–107

    Article  CAS  Google Scholar 

  • Shimada T (2001) Nutrient compositions of acorns and horse chestnuts in relation to seed-hoarding. Ecol Res 16:803–808

    Article  Google Scholar 

  • Shimada T, Saitoh T (2003) Negative effects of acorns on the wood mouse Apodemus speciosus. Popul Ecol 45:7–17

    Google Scholar 

  • Shimada T, Saitoh T (2006) Re-evaluation of the relationship between rodent populations and acorn masting: a review from the aspect of nutrients and defensive chemicals in acorns. Popul Ecol 48:341–352

    Article  Google Scholar 

  • Shimada T, Saitoh T, Sasaki E, Nishitani Y, Osawa R (2006) Role of tannin-binding salivary proteins and tannase-producing bacteria in the acclimation of the Japanese wood mouse to acorn tannins. J Chem Ecol 36:1165–1180

    Article  CAS  Google Scholar 

  • Smallwood PD, Peters WD (1986) Grey squirrel food preferences: the effects of tannin and fat concentration. Ecology 67:168–174

    Article  Google Scholar 

  • Sone K, Sekijima T, Okumura H (1986) Stomach contents of the wood mouse, Apodemus speciosus Temminck. Trans Mtg Chubu Br Jpn For Soc 97:467–468 (in Japanese)

    Google Scholar 

  • Sork VL, Stacey P, Averett JE (1983) Utilization of red oak acorns in non-bumper crop year. Oecologia 59:49–53

    Article  Google Scholar 

  • Sokal RR, Rohlf FJ (1995) Biometry, 3rd edn. W.H. Freeman and Company, New York

    Google Scholar 

  • Steele MA, Knowles T, Bridle K, Simms EL (1993) Tannins and partial consumption of acorns—implications for dispersal of oaks by seed predators. Am Midl Nat 130:229–238

    Article  Google Scholar 

  • Tatsukawa K, Murakami O (1976) On the food utilization of the Japanese wood mouse Apodemus speciosus (Mammalia: Muridae). Phys Ecol Jpn 17:133–144 (in Japanese)

    Google Scholar 

  • Vander Wall SB (2001) The evolutionary ecology of nut dispersal. Bot Rev 67:74–117

    Article  Google Scholar 

  • Wada N (1993) Dwarf bamboos affect the regeneration of zoochorous trees by providing habitats to acorn-feeding rodents. Oecologia 94:403–407

    Article  Google Scholar 

  • Wainio WW, Forbes EB (1941) The chemical composition of forest fruits and nuts from Pennsylvania. J Agric Res 62:627–635

    CAS  Google Scholar 

  • Waterman PG, Mole S (1994) Analysis of phenolic plant metabolites. Blackwell Scientific Publications, Oxford

    Google Scholar 

Download references

Acknowledgments

We are grateful to Y. Takahata for letting us use some experimental equipment, H. Furusawa for instructing the usage of the NC analyzer, H. Itoh for advice on comparison of the tannin content of the two cotyledons of an acorn, Y. Segawa for great help with keeping many mice, K. Ohsumi for information about acorn sampling sites, and R. Narita for advice about randomization on R. We also thank all members of the Laboratory of Forest Biology for their helpful discussion. This research was supported partly by Grants-in-Aid for Scientific Research, nos. 17570027 and 19380091, to T.S. from the Ministry of Education, Science, Sports, and Culture of Japan.

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Correspondence to Akiko Takahashi.

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Takahashi, A., Shimada, T. Selective consumption of acorns by the Japanese wood mouse according to tannin content: a behavioral countermeasure against plant secondary metabolites. Ecol Res 23, 1033–1038 (2008). https://doi.org/10.1007/s11284-008-0473-5

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  • DOI: https://doi.org/10.1007/s11284-008-0473-5

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