Abstract
We investigated feeding and fecundity of the two-spotted spider mite, Tetranychus urticae (Acari: Tetranychidae), on leaves of cucumber (Cucumis sativus) seedlings that had been acclimatized to different light intensities. Based on these data, we analyzed the relationships between mite performance (feeding and fecundity) and leaf properties. The cucumber seedlings were grown in controlled-environment chambers under different light intensities at a photosynthetic photon flux density of 50, 100, 150, 300, or 450 µmol m− 2 s− 1 until the first true leaves had expanded. Adult females were released on the adaxial surfaces of excised leaf samples from the seedlings of each treatment group and held under standardized light intensity (200 µmol m− 2 s− 1). Fecundity and leaf damage area increased and decreased, respectively, as the acclimatization light intensity increased, indicating indirect effects of light intensity on feeding and fecundity through changes in the host leaf properties. Leaf mass per area (LMA) and photosynthetic capacity, which increased as the acclimatization light intensity increased, was positively related to the fecundity, but was negatively related to the leaf damage area. The higher LMA and photosynthetic capacity results in an increased amount of mesophyll per unit leaf area. This would allow the mites to feed efficiently from a limited area, which may explain the increased fecundity on these leaves.
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References
Albright LD, Both AJ, Chiu AJ (2000) Controlling greenhouse light to a consistent daily integral. Trans ASAE 43:421–431
Amini MY, Ullah MS, Kitagawa A, Kanazawa R, Takano Y, Suzuki T, Gotoh T (2016) Scotophase interruption with LEDs and OLEDs to inhibit photoperiodic induction of diapause in Tetranychus urticae and T. kanzawai (Acari: Tetranychidae). Syst Appl Acarol 21:1436–1446
Barcelo JA (1981) Photoeffects of visible and ultraviolet radiation on the two-spotted spider mite, Tetranychus urticae. Photochem Photobiol 33:703–706
Barczak-Brzyżek AK, Kiełkiewicz M, Gawroński P, Kot K, Filipecki M, Karpińska B (2017) Cross-talk between high light stress and plant defence to the two-spotted spider mite in Arabidopsis thaliana. Exp Appl Acarol 73:177–189
Bensoussan N, Santamaria ME, Zhurov V, Diaz I, Grbić M, Grbić V (2016) Plant-herbivore interaction: dissection of the cellular pattern of Tetranychus urticae feeding on the host plant. Front Plant Sci 7:1105
Bensoussan N, Zhurov V, Yamakawa S, O’Neil CH, Suzuki T, Grbić M, Grbić V (2018) The digestive system of the two-spotted spider mite, Tetranychus urticae Koch, in the context of the mite-plant interaction. Front Plant Sci 9:1206
Boardman NT (1977) Comparative photosynthesis of sun and shade plants. Annu Rev Plant Physiol 28:355–377
Chabot BF, Chabot JF (1977) Effects of light and temperature on leaf anatomy and photosynthesis in Fragaria vesca. Oecologia 26:363–377
Cronin G, Lodge DM (2003) Effects of light and nutrient availability on the growth, allocation, carbon/nitrogen balance, phenolic chemistry, and resistance to herbivory of two freshwater macrophytes. Oecologia 137:32–41
Enrique G, Olmo M, Poorter H, Ubera JL, Villar R (2016) Leaf mass per area (LMA) and its relationship with leaf structure and anatomy in 34 Mediterranean woody species along a water availability gradient. PLoS ONE 11:e0148788
Gerson U, Weintraub PG (2012) Mites (Acari) as a factor in greenhouse management. Annu Rev Entomol 57:229–247
Huffaker CB, van de Vrie M, McMurtry JA (1969) The ecology of tetranychid mites and their natural control. Annu Rev Entomol 14:125–174
Koveos DS, Suzuki T, Terzidou A, Kokkari A, Floros G, Damos P, Kouloussis NA (2017) Egg hatching response to a range of ultraviolet-B (UV-B) radiation doses for four predatory mites and the herbivorous spider mite Tetranychus urticae. Exp Appl Acarol 71:35–46
Lichtenthaler HK, Buschmann C, Döll M, Fietz HJ, Bach T, Kozel U, Meier D, Rahmsdorf U (1981) Photosynthetic activity, chloroplast ultrastructure, and leaf characteristics of high-light and low-light plants and of sun and shade leaves. Photosynth Res 2:115–141
Maeda T, Takabayashi J, Yano S, Takafuji A (2000) Effects of light on the tritrophic interaction between kidney bean plants, two-spotted spider mites and predatory mites, Amblyseius womersleyi (Acari: Phytoseiidae). Exp Appl Acarol 24:415–425
Mattson WJ Jr (1980) Herbivory in relation to plant nitrogen content. Annu Rev Ecol Evol Syst 11:119–161
Nickel JL (1960) Temperature and humidity relationships of Tetranychus desertorum banks with special reference to distribution. Hilgardia 30:41–100
Nihoul P (1993) Do light intensity, temperature and photoperiod affect the entrapment of mites on glandular hairs of cultivated tomatoes? Exp Appl Acarol 17:709–718
Nunes MV, Veerman A (1984) Light-break experiments and photoperiodic time measurement in the spider mite Tetranychus urticae. J Insect Physiol 30:891–897
Ohtsuka K, Osakabe M (2009) Deleterious effects of UV-B radiation on herbivorous spider mites: they can avoid it by remaining on lower leaf surfaces. Environ Entomol 38:920–929
Park YL, Lee JH (2002) Leaf cell and tissue damage of cucumber caused by twospotted spider mite (Acari: Tetranychidae). J Econ Entomol 95:952–957
Poorter H, Niinemets Ü, Poorter L, Wright IJ, Villar R (2009) Causes and consequences of variation in leaf mass per area (LMA): a meta-analysis. New Phytol 182:565–588
Pramuk LA, Runkle ES (2005) Modeling growth and development of Celosia and Impatiens in response to temperature and photosynthetic daily light integral. J Am Soc Hortic Sci 130:813–818
Reddall AA, Wilson LJ, Gregg PC, Sadras VO (2007) Photosynthetic response of cotton to spider mite damage: interaction with light and compensatory mechanisms. Crop Sci 47:2047–2057
Rodriguez JG, Singh P, Seay TN, Walling MV (1967) Ingestion in the two-spotted spider mite, Tetranychus urticae Koch, as influenced by wavelength of light. J Insect Physiol 13:925–932
Sharkey TD, Bernacchi CJ, Farquhar GD, Singsaas EL (2007) Fitting photosynthetic carbon dioxide response curves for C3 leaves. Plant Cell Environ 30:1035–1040
Shibuya T, Itagaki K, Ueyama S, Hirai N, Endo R (2016) Atmospheric humidity influences oviposition rate of Tetranychus urticae (Acari: Tetranychidae) through morphological responses of host Cucumis sativus leaves. J Econ Entomol 109:255–258
Suzuki T, Amano H, Goto E, Takeda M, Kozai T (2007) Effects of extending the light phase on diapause induction in a Japanese population of the two-spotted spider mite, Tetranychus urticae. Exp Appl Acarol 42:131–138
Suzuki T, Fukunaga Y, Amano H, Takeda M, Goto E (2008) Effects of light quality and intensity on diapause induction in the two-spotted spider mite, Tetranychus urticae. Appl Entomol Zool 43:213–218
Suzuki T, Watanabe M, Takeda M (2009) UV tolerance in the two-spotted spider mite, Tetranychus urticae. J Insect Physiol 55:649–654
Suzuki T, Kojima T, Takeda M, Sakuma M (2013) Photo-orientation regulates seasonal habitat selection in the two-spotted spider mite Tetranychus urticae. J Exp Biol 216:977–983
Suzuki T, Yoshioka Y, Tsarsitalidou O, Ntalia V, Ohno S, Ohyama K, Kitashima Y, Gotoh T, Takeda M, Koveos DS (2014) An LED-based UV-B irradiation system for tiny organisms: system description and demonstration experiment to determine the hatchability of eggs from four Tetranychus spider mite species from Okinawa. J Insect Physiol 62:1–10
Van de Vrie M, Murtry JA, Huffaker CB (1972) Ecology of tetranychid mites and their natural enemies: a review. III. Biology, ecology and pest status, and host-plant relations of tetranychids. Hilgardia 41:343–432
Veerman A, Nunes MV (1987) Analysis of the operation of the photoperiodic counter provides evidence for hourglass time measurement in the spider mite Tetranychus urticae. J Comp Physiol A 160:421–430
Von Caemmerer S, Farquhar GD (1981) Some relationships between the biochemistry of photosynthesis and the gas exchange of leaves. Planta 153:376–387
Walters MB, Reich PB (1999) Low-light carbon balance and shade tolerance in the seedlings of woody plants: do winter deciduous and broad-leaved evergreen species differ? New Phytol 143:143–154
Watson TF (1964) Influence of host plant condition on population increase of Tetranychus telarius (Linnaeus) (Acarina: Tetranychidae). Hilgardia 35:273–322
Wermelinger B, Oertli JJ, Baumgärtner J (1991) Environmental factors affecting the life-tables of Tetranychus urticae (Acari: Tetranychidae) III. Host-plant nutrition. Exp Appl Acarol 12:259–274
Wright IJ, Cannon K (2001) Relationships between leaf lifespan and structural defences in a low-nutrient, sclerophyll flora. Funct Ecol 15:351–359
Acknowledgements
This research was supported by Grants-in-Aid for Challenging Exploratory Research (KAKENHI 16K15014) from the Japan Society for the Promotion of Science. We are grateful to the associate editor Professor Arne Janssen and anonymous referees for their helpful comments and suggestions, and to Professor Yoshiaki Kitaya for valuable discussion.
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Shibuya, T., Iwahashi, Y., Suzuki, T. et al. Light intensity influences feeding and fecundity of Tetranychus urticae (Acari: Tetranychidae) through the responses of host Cucumis sativus leaves. Exp Appl Acarol 81, 163–172 (2020). https://doi.org/10.1007/s10493-020-00496-0
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DOI: https://doi.org/10.1007/s10493-020-00496-0