Abstract
A commercial strain of Neoseiulus californicus (Spical®) has a conspicuously long postoviposition period in comparison with other strains of N. californicus or other phytoseiid mites. In many insects and mites, life span is shorter for multiple-mated females than for single-mated females, and is shorter under poor prey conditions than under ample prey conditions. We previously showed that the postoviposition period of multiple-mated females was 40% shorter than that of single-mated females, but that it was never shorter than 30 days. Here we focused on the effect of prey abundance on the postoviposition period. We examined three groups of multiple-mated females: mites that were fed ample prey (group I), mites that were subjected to repeated cycles of 2 days of fasting followed by 2 days of ample prey (group II), and mites that were subjected to repeated cycles of 4 days of fasting followed by 2 days of ample prey (group III). The postoviposition periods of groups II and III were 90% shorter than that of group I. Also the total adult longevity was significantly shorter in groups II and III than in group I. Total egg production in group III was about half that in groups I and II, although the oviposition periods in groups II and III were significantly longer than that in group I. These results suggest that the prolonged postoviposition period in single-mated females of the Spical strain may only appear under laboratory conditions, without multiple mating or starvation.

Similar content being viewed by others
Explore related subjects
Discover the latest articles and news from researchers in related subjects, suggested using machine learning.References
Ali FS (1998) Life tables of Phytoseiulus macropilis (Banks) [Gamasida: Phytoseiidae] at different temperatures. Exp Appl Acarol 22:335–342. doi:10.1023/A:1024560924642
Amano H, Chant DA (1978) Some factors affecting reproduction and sex ratios in two species of predacious mites, Phytoseiulus persimilis Athias-Henriot and Amblyseius andersoni (Chant) (Acarina: Phytoseiidae). Can J Zool 56:1593–1607. doi:10.1139/z78-221
Begon M, Harper JL, Townsend CR (1990) Ecology, 2nd edn. Blackwell, Boston, p 945
Blommers LHM, van Arendonk RCM (1979) The profit of senescence in phytoseiid mites. Oecologia 44:87–90. doi:10.1007/BF00346403
Chapman T, Miyatake T, Smith HK, Partridge L (1998) Interactions of mating, egg production and death rates in females of the Mediterranean fruit fly, Ceratitis capitata. Proc R Soc Lond B Biol Sci 265:1879–1894. doi:10.1098/rspb.1998.0516
de Moraes GJ, McMurtry JA, Denmark HA, Campos CB (2004) A revised catalog of the mite family Phytoseiidae. Zootaxa 434:1–494
Friese DD, Gilstrap FE (1982) Influence of prey availability on reproduction and prey consumption of Phytoseiulus persimilis, Amblyseius californicus, and Metaseiulus occidentalis (Acarina: Phytoseiidae). Int J Acarol 8:85–89
Gotoh T, Tsuchiya A (2008) Effect of multiple mating on reproduction and longevity of the phytoseiid mite Neoseiulus californicus. Exp Appl Acarol 44:185–197. doi:10.1007/s10493-008-9143-0
Gotoh T, Yamaguchi K, Mori K (2004) Effect of temperature on life history of the predatory mite Amblyseius (Neoseiulus) californicus (Acari: Phytoseiidae). Exp Appl Acarol 32:15–30. doi:10.1023/B:APPA.0000018192.91930.49
Gotoh T, Akizawa T, Watanabe M, Tsuchiya A, Shimazaki S (2005) Cold hardiness of Neoseiulus californicus and N. womersleyi (Acari: Phytoseiidae). J Acarol Soc Jpn 14:93–103. doi:10.2300/acari.14.93
Gotoh T, Tsuchiya A, Kitashima Y (2006) Influence of prey on developmental performance, reproduction and prey consumption of Neoseiulus californicus (Acari: Phytoseiidae). Exp Appl Acarol 40:189–204. doi:10.1007/s10493-006-9032-3
Janssen A, Sabelis MW (1992) Phytoseiid life-histories, local predator–prey dynamics, and strategies for control of tetranychid mites. Exp Appl Acarol 14:233–250. doi:10.1007/BF01200566
Ma W-L, Laing JE (1973) Biology, potential of increase and prey consumption of Amblyseius chilenensis (Dosse) (Acarina: Phytoseiidae). Entomophaga 18:47–60. doi:10.1007/BF02373013
Momen FM (1994) Fertilization and starvation affecting reproduction in Amblyseius barkeri (Hughes) (Acari, Phytoseiidae). Anz Schadlingskde Pflanz Umwelt 67:130–132. doi:10.1007/BF01909034
Momen FM (1996) Effect of prey density on reproduction, prey consumption and sex-ratio of Amblyseius barkeri (Acari: Phytoseiidae). Acarologia 37:3–6
Moya-Larano J (2002) Senescence and food limitation in a slowly aging spider. Funct Ecol 16:734–741. doi:10.1046/j.1365-2435.2002.00685.x
Munger F (1957) Equipment and technique used in laboratory studies of the citrus red mite. USDA ARS-33-39:1–5
Partridge L, Harvey PH (1988) The ecological context of life history evolution. Science 241:1449–1455. doi:10.1126/science.241.4872.1449
Sabelis MW (1981) Biological control of two-spotted spider mites using phytoseiid predators—part I. Modelling the predator–prey interaction at the individual level. Ph.D. Thesis, Agricultural University, Wageningen, 242 pp
Sabelis MW (1985) Predation on spider mites. In: Helle W, Sabelis MW (eds) Spider mites—their biology, natural enemies and control—world crop pests, vol 1B. Elsevier Science, Amsterdam, pp 103–129
Sabelis MW, Janssen A (1994) Evolution of life-history patterns in the Phytoseiidae. In: Houck MA (ed) Mites. Chapman & Hall, New York, pp 70–98
Sanderson JP, McMurtry JA (1984) Life history studies of the predaceous mite Phytoseius hawaiiensis. Entomol Exp Appl 35:227–234. doi:10.1007/BF00369137
Sokal RR, Rohlf FJ (1995) Biometry, 3rd edn. W.H. Freeman, New York, p 887
SPSS (2002) SPSS 11.5J brief guide (in Japanese). SPSS Inc., Tokyo, p 160
Takahashi F, Chant DA (1994) Adaptive strategies in the genus Phytoseiulus Evans (Acari: Phytoseiidae). II. Survivorship and reproduction. Int J Acarol 20:87–97
Toyoshima S, Amano H (1998) Effect of prey density on sex ratio of two predacious mites, Phytoseiulus persimilis and Amblyseius womersleyi (Acari: Phytoseiidae). Exp Appl Acarol 22:709–723. doi:10.1023/A:1006093424452
Toyoshima S, Amano H (1999) Comparison of development and reproduction in offspring produced by females of Phytoseiulus persimilis Athias-Henriot (Acari: Phytoseiidae) under two prey conditions. Appl Entomol Zool (Jpn) 34:285–292
van Noordwijke AJ, de Jong G (1986) Acquisition and allocation of resources: their influence on variation in life history tactics. Am Nat 128:137–142. doi:10.1086/284547
Yamamura K (1999) Transformation using (x + 0.5) to stabilize the variance of populations. Res Popul Ecol (Kyoto) 41:229–234
Yanagi S, Miyatake T (2003) Costs of mating and egg production in female Callosobruchus chinensis. J Insect Physiol 49:823–827. doi:10.1016/S0022-1910(03)00119-7
Zera AJ, Harshman LG (2001) The physiology of life history trade-offs in animals. Annu Rev Ecol Syst 32:95–126. doi:10.1146/annurev.ecolsys.32.081501.114006
Acknowledgments
We thank J. Kamata for providing the Spical strain of N. californicus, S. Toyoshima for helpful suggestions concerning references and Y. Kitashima for his kind assistance. We also thank two anonymous reviewers for valuable suggestions.
Author information
Authors and Affiliations
Corresponding author
Rights and permissions
About this article
Cite this article
Gotoh, T., Tsuchiya, A. Food scarcity reduces female longevity of Neoseiulus californicus (Acari: Phytoseiidae). Exp Appl Acarol 47, 249–256 (2009). https://doi.org/10.1007/s10493-008-9215-1
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s10493-008-9215-1