Abstract
Drought associated with climate change is undoubtedly one of the most prodigious challenges facing agricultural production and human food security throughout the world. Regarding the increasing incidence and potency of drought under ongoing global warming, determining the potential impacts of water-deficit tension on insect demographic attributes is a key element in success of any management program. By subjecting the western flower thrips (WFT), Frankliniella occidentalis, to well-watered and water-stressed cherry tomato plants, the impacts of this stressor on thrips performance were assessed. The key life-history parameters of WFT on fully-irrigated plants (FIT), 80% and 60% FIT were compared. WFT performed worse on drought-stress plants. Thrips specimens developed faster on 60% FIT and the female individuals were less fecund. When reared on plants grown under 60% full irrigation treatment (FIT), WFT displayed lower net reproductive rates and intrinsic and finite rates of increase compared to those reared on stress-free plants. Moreover, with increasing water stress intensity, the sex ratio became more male-biased which might in turn cause mate shortages and consequently a reduction in population growth. Our analysis showed that activities of the enzymes CAT and POD are elevated under WS conditions, and this might be correlated with reduced WFT fitness. In total, 60% FIT drought stress could have the capacity to lessen the abundance and upsurge risk of this destructive pest species under future climate change scenarios. The knowledge gained in this study will aid tomato producers understand how drought stress impact WFT demographic traits, and to foresee if pesticide treatments will be required to manage this infamous pest.
Similar content being viewed by others
References
Aebi H (1984) Catalase in Vitro. In: Packer L (ed) Methods in Enzymology. Academic Press, San Diego, pp 121–126
Akköprü EP, Atlıhan R, Okut H, Chi H (2015) Demographic assessment of plant cultivar resistance to insect pests: a case study of the dusky-veined walnut aphid (Hemiptera: Callaphididae) on five walnut cultivars. J Econ Entomol 108(2):378–387. https://doi.org/10.1093/jee/tov011
Al Hassan M, Fuertes MM, Sánchez FJR, Vicente O, Boscaiu M (2015) Effects of salt and water stress on plant growth and on accumulation of osmolytes and antioxidant compounds in cherry tomato. Not Bot Horti Agrobot Cluj Napoca 43(1):1–11. https://doi.org/10.15835/nbha4319793
Aleosfoor M, Zahediannezhad M, Minaei K, Fekrat L, Razi H (2022) Effects of drought stress and plant cultivar type on demographic characteristics of the rose-grain aphid, Metopolophium dirhodum (Hemiptera: Aphididae). Bull Entomol Res. https://doi.org/10.1017/S0007485322000463
Beetge L, Krüger K (2019) Drought and heat waves associated with climate change affect performance of the potato aphid Macrosiphum euphorbiae. Sci Rep 9(1):1–9. https://doi.org/10.1038/s41598-018-37493-8
Broadbent AB, Rhainds M, Shipp L, Murphy G, Wainman L (2003) Pupation behavior of western flower thrips (Thysanoptera: Thripidae) on potted chrysanthemum. Canadian Entomol 135:741–744. https://doi.org/10.4039/n03-007
Buitenhuis R, Shipp JL (2008) Influence of plant species and plant growth stage on Frankliniella occidentalis pupation behavior in greenhouse ornamentals. J Appl Entomol 132:86–88. https://doi.org/10.1111/j.1439-0418.2007.01250.x
Chaves MM, Pereira JS, Maroco J, Rodrigues ML, Ricardo CP, Osório ML, Carvalho I, Faria T, Pinheiro C (2002) How plants cope with water stress in the field? Photosynthesis and Growth Ann Bot 89(7):907–916. https://doi.org/10.1093/aob/mcf105
Chi H (1988) Life-table analysis incorporating both sexes and variable development rates among individuals. Environ Entomol 17(1):26–34. https://doi.org/10.1093/ee/17.1.26
Chi H, Su H-Y (2006) Age-stage, two-sex life tables of Aphidius gifuensis (Ashmead) (Hymenoptera: Braconidae) and its host Myzus persicae (Sulzer) (Homoptera: Aphididae) with mathematical proof of the relationship between female fecundity and the net reproductive rate. Environ Entomol 35(1):10–21. https://doi.org/10.1603/0046-225X-35.1.10
Chi H (2022a) TWOSEX-MSChart: A computer program for the age-stage, two-sex life table analysis. http://140.120.197.173/ecology/Download/TWOSEX-MSChart.rar. Accessed 25 Oct 2022a
Chi H (2022b) TIMING–MSChart: a computer program for the population projection based on age-stage, two-sex life table. Retrieved from http://140.120.197.173/ecology/Download/TIMING-MSChart.rar. Accessed 27 Dec 2022b
Copolovici L, Kännaste A, Remmel T, Niinemets Ü (2014) Volatile organic compound emissions from Alnus glutinosa under interacting drought and herbivory stresses. Environ Exp Bot 100:55–63
Cornelissen T, Fernandes GW, Vasconcellos-Neto J (2008) Size does matter: Variation in herbivory between and within plants and the plant vigor hypothesis. Oikos 117:1121–1130. https://doi.org/10.1111/j.0030-1299.2008.16588.x
Gely C, Laurance SGW, Stork NE (2020) How do herbivorous insects respond to drought stress in trees? Biol Rev 95:434–448. https://doi.org/10.1111/brv.12571
Han P, Desneux N, Michel T, Le Bot J, Seassau A, Wajnberg E, Amiens-Desneux E, Lavoir A-V (2016) Does plant cultivar difference modify the bottom-up effects of resource limitation on plant-insect herbivore interactions? J Chem Ecol 42(12):1293–1303. https://doi.org/10.1007/s10886-016-0795-7
Hansen EA, Funderburk JE, Reitz SR, Ramachandran S, Eger JE, McAuslane H (2003) Within-plant distribution of Frankliniella species (Thysanoptera: Thripidae) and Orius insidiosus (Heteroptera: Anthocoridae) in field pepper. Environ Entomol 32(5):1035–1044
Harvey JA, Tougeron K, Gols R, Heinen R, Abarca M, Abram PK, Basset Y, Berg M, Boggs C, Brodeur J, Cardoso P, de Boer JG, De Snoo GR, Deacon C, Dell JE, Desneux N, Dillon ME, Duffy GA, Dyer LA, Ellers J, Espíndola A, Fordyce J, Forister ML, Fukushima C, Gage MJG, García-Robledo C, Gely C, Gobbi M, Hallmann C, Hance T, Harte J, Hochkirch A, Hof C, Hoffmann AA, Kingsolver JG, Lamarre GPA, Laurance WF, Lavandero B, Leather SR, Lehmann P, Le Lann C, López-Uribe MM, Ma C-S, Ma G, Moiroux J, Monticelli L, Nice C, Ode PJ, Pincebourde S, Ripple WJ, Rowe M, Samways MJ, Sentis A, Shah AA, Stork N, Terblanche JS, Thakur MP, Thomas MB, Tylianakis JM, Van Baaren J, Van de Pol M, Van der Putten WH, Van Dyck H, Verberk WCEP, Wagner DL, Weisser WW, Wetzel WC, Woods HA, Wyckhuys KAG, Chown SL (2023) Scientists’ warning on climate change and insects. Ecol Monogr 93:e1553. https://doi.org/10.1002/ecm.1553
He Z, Guo JF, Reitz SR, Lei ZR, Wu SY (2020) A global invasion by the thrip, Frankliniella occidentalis: current virus vector status and its management. Insect Sci 27(4):626–645. https://doi.org/10.1111/1744-7917.12721
Huberty AF, Denno RF (2004) Plant water stress and its consequences for herbivorous insects: a new synthesis. Ecology 85(5):1383–1398. https://doi.org/10.1890/03-0352
Jactel H, Koricheva J, Castagneyrol B (2019) Responses of forest insect pests to climate change: not so simple. Curr Opin Insect Sci 35:103–108. https://doi.org/10.1016/j.cois.2019.07.010
Jamali B, Eshghi S (2015) Salicylic acid–induced salinity redressal in hydroponically grown strawberry. Commun Soil Sci Plant Anal 46:1482–1493
Kansman J, Nalam V, Nachappa P, Finke D (2020) Plant water stress intensity mediates aphid host choice and feeding behavior. Ecol Entomol 45:1437–1444. https://doi.org/10.1111/een.12928
Kansman J, Basu S, Casteel CL, Crowder D, Lee BW, Nihranz CT, Finke DL (2022) Plant water stress reduces aphid performance: Exploring mechanisms driven by water stress intensity. Front Ecol Evol. https://doi.org/10.3389/fevo.2022.846908
Krauska JJ (2019) Influence of drought stress on interactions of cotton (Gossypium hirsutum), twospotted spider mites (Tetranychus urticae), and western flower thrips (Frankliniella occidentalis). Master of Science), Kansas State University, Kansas
Lewis T (1973) Thrips: Their biology, ecology and economic importance. Academic Press, London
Leybourne DJ, Preedy KF, Valentine TA, Bos JIB, Karley AJ (2021) Drought has negative consequences on aphid fitness and plant vigor: insights from a meta-analysis. Ecol and Evol 11(17):11915–11929. https://doi.org/10.1002/ece3.7957
Lin P-A, Paudel S, Afzal A, Shedd NL, Felton GW (2021) Changes in tolerance and resistance of a plant to insect herbivores under variable water availability. Environ Exp Bot 183:104334. https://doi.org/10.1016/j.envexpbot.2020.104334
Liu D, Dai P, Li S, Ahmed SS, Shang Z, Shi X (2018) Life-history responses of insects to water-deficit stress: a case study with the aphid Sitobion avenae. BMC Ecol 18(1):1–15. https://doi.org/10.1186/s12898-018-0173-0
Liu J, Liao J, Li C (2022) Bottom-up effects of drought on the growth and development of potato, Leptinotarsa decemlineata Say and Arma chinensis Fallou. Pest Manag Sci 78(10):4353–4360. https://doi.org/10.1002/ps.7054
Lopez-Reyes K, Armstrong KF, Teulon DA, Butler RC, van Dooremalen C, Roher M, van Tol RW (2022) Color response in western flower thrips varies intraspecifically. Insects 13(6):538. https://doi.org/10.3390/insects13060538
Ma G, Tian B-L, Zhao F, Wei G-S, Hoffmann AA, Ma C-S (2017) Soil moisture conditions determine phenology and success of larval escape in the peach fruit moth, Carposina sasakii (Lepidoptera, Carposinidae): Implications for predicting drought effects on a diapausing insect. Appl Soil Ecol 110:65–72. https://doi.org/10.1016/j.apsoil.2016.10.013
Masson-Delmotte V, Zhai P, Pörtner H-O, Roberts D, Skea J, Shukla PR (2022) GlobalWarming of 1.5 C: IPCC special report on impacts of global warming of 1.5 C above pre-industrial levels in context of strengthening response to climate change, sustainable development, and efforts to eradicate poverty: Cambridge University Press
Mody K, Eichenberger D, Dorn S (2009) Stress magnitude matters: different intensities of pulsed water stress produce non-monotonic resistance responses of host plants to insect herbivores. Ecol Entomol 34:133–143. https://doi.org/10.1111/j.1365-2311.2008.01053.x
Mokarram M, Pourghasemi HR, Hu M, Zhang H (2021) Determining and forecasting drought susceptibility in southwestern Iran using multi-criteria decision-making (MCDM) coupled with CA-Markov model. Sci Total Environ 781:146703. https://doi.org/10.1016/j.scitotenv.2021.146703
Omena-Garcia RP, Martins AO, Medeiros DB, Vallarino JG, Ribeiro DM, Fernie AR, Araújo WL, Nunes-Nesi A (2019) Growth and metabolic adjustments in response to gibberellin deficiency in drought stressed tomato plants. Environ Exp Bot 159:95–107. https://doi.org/10.1016/j.envexpbot.2018.12.011
Osswaldi WF, Kraus R, Hippeli S, Benz B, Volpert R, Elstner EF (1992) Comparison of the enzymatic activities of dehydroascorbic acid reductase, glutathione reductase, catalase, peroxidase and superoxide dismutase of healthy and damaged spruce needles (Picea abies (L.) Karst.). J Plant Physiol 139(6):742–748. https://doi.org/10.1016/S0176-1617(11)81721-9
Ozden M, Demirel U, Kahraman A (2009) Effects of proline on antioxidant system in leaves of grapevine (Vitis vinifera L.) exposed to oxidative stress by H2O2. Sci Horti 119:163–168. https://doi.org/10.1016/j.scienta.2008.07.031
Patanè C, Cosentino SL, Romano D, Toscano S (2022) Relative water content, proline, and antioxidant enzymes in leaves of long shelf-life tomatoes under drought stress and rewatering. Plants 11:3045. https://doi.org/10.3390/plants11223045
Raderschall CA, Vico G, Lundin O, Taylor AR, Bommarco R (2021) Water stress and insect herbivory interactively reduce crop yield while the insect pollination benefit is conserved. Glob Change Biol 27(1):71–83
Rahbe Y, Febvay G (1993) Protein toxicity to aphids: an in vitro test on Acyrthosiphon pisum. Entomol Exp Appl 67(2):149–160. https://doi.org/10.1007/BF02386520
Reitz SR (2002) Seasonal and within plant distribution of Frankliniella thrips (Thysanoptera: Thripidae) in north Florida tomatoes. Florida Entomol 85:431–439. https://doi.org/10.1653/0015-4040(2002)085[0431:SAWPDO]2.0.CO;2
Sconiers WB, Rowland DL, Eubanks MD (2020) Pulsed drought: the effects of varying water stress on plant physiology and predicting herbivore response. Crop Sci 60(5):2543–2561. https://doi.org/10.1002/csc2.20235
Shehzad M, Gulzar A, Staley JT, Tariq M (2021) The effects of drought stress and type of fertiliser on generalist and specialist herbivores and their natural enemies. Ann App Biol 178(2):377–386. https://doi.org/10.1111/aab.12654
Shipp J, Gillespie T (1993) Influence of temperature and water vapor pressure deficit on survival of Frankliniella occidentalis (Thysanoptera: Thripidae). Environ Entomol 22(4):726–732. https://doi.org/10.1093/ee/22.4.726
Staley JT, Mortimer SR, Masters GJ, Morecroft MD, Brown VK, Taylor ME (2006) Drought stress differentially affects leaf-mining species. Ecol Entomol 31(5):460–469
Szyp-Borowska I, Ukalska J, Niemczyk M, Wojda T, Thomas BR (2022) Effects of water deficit stress on growth parameters of Robinia pseudoacacia L. selected clones under in vitro conditions. Forests 13:1979. https://doi.org/10.3390/f13121979
Tao M, Wan Y, Zheng X, Qian K, Merchant A, Xu B, Zhang Y, Zhou X, Wu Q (2022) Tomato spotted wilt orthotospovirus shifts sex ratio toward males in the western flower thrips, Frankliniella occidentalis, by down-regulating a FSCB-like gene. Pest Manag Sci 78(11):5014–5023. https://doi.org/10.1002/ps.7125
Terry LI, Kelly CK (1993) Patterns of change in secondary and tertiary sex ratios of the Terebrantian thrips, Frankliniella occidentalis. Entomol Exp Appl 66(3):213–225. https://doi.org/10.1111/j.1570-7458.1993.tb00712.x
Verdugo J, Sauge MH, Lacroze JP, Francis F, Ramirez C (2015) Drought-stress and plant resistance affect herbivore performance and proteome: the case of the green peach aphid Myzus persicae (Hemiptera: Aphididae). Physiol Entomol 40:265–276. https://doi.org/10.1111/phen.12111
Walter J (2018) Effects of changes in soil moisture and precipitation patterns on plant-mediated biotic interactions in terrestrial ecosystems. Plant Ecol 219(12):1449–1462. https://doi.org/10.1007/s11258-018-0893-4
War AR, Paulraj MG, Ignacimuthu S, Sharma HC (2013) Defensive responses in groundnut against chewing and sap-sucking insects. J Plant Growth Reg 32:259–272
Wei M, Chi H, Guo Y, Li X, Zhao L, Ma R (2020) Demography of Cacopsylla chinensis (Hemiptera: Psyllidae) reared on four cultivars of Pyrus bretschneideri (Rosales: Rosaceae) and P. communis pears with estimations of confidence intervals of specific life table statistics. J Econ Entomol 113(5):2343–2353. https://doi.org/10.1093/jee/toaa149
White TCR (1984) The abundance of invertebrate herbivores in relation to the availability of nitrogen in stressed food plants. Oecologia 63:90–105. https://doi.org/10.1007/BF00379790
Xie H, Shi J, Shi F, Xu H, He K, Wang Z (2020) Aphid fecundity and defenses in wheat exposed to a combination of heat and drought stress. J Exp Bot 71(9):2713–2722. https://doi.org/10.1093/jxb/eraa017
Ximénez-Embún MG, Glas JJ, Ortego F, Alba JM, Castañera P, Kant MR (2017) Drought stress promotes the colonization success of a herbivorous mite that manipulates plant defenses. Exp Appl Acarol 73(3):297–315. https://doi.org/10.1007/s10493-017-0200-4
Yu L-Y, Chen Z-Z, Zheng F-Q, Shi A-J, Guo T-T, Yeh B-H, Chi H, Xu Y-Y (2013) Demographic analysis, a comparison of the jackknife and bootstrap methods, and predation projection: a case study of Chrysopa pallens (Neuroptera: Chrysopidae). J Econ Entomol 106(1):1–9. https://doi.org/10.1603/EC12200
Zeng G, Zhi J, Ye M, Yue W, Song J (2020) Inductive effects of exogenous calcium on the defense of kidney bean plants against Frankliniella occidentalis (Thysanoptera: Thripidae). Arthropod-Plant Interact 14(4):473–480. https://doi.org/10.1007/s11829-020-09753-w
Zeng G, Zhi J-R, Ye M, Xie W, Zhang T, Li D-Y, Liu L, Wu X-B, Cao Y (2021) Life table and preference choice of Frankliniella occidentalis (Thysanoptera: Thripidae) for kidney bean plants treated by exogenous calcium. Insects 12(9):838. https://doi.org/10.3390/insects12090838
Zhang T, Reitz SR, Wang H, Lei Z (2015) Sublethal effects of Beauveria bassiana (Ascomycota: Hypocreales) on life table parameters of Frankliniella occidentalis (Thysanoptera: Thripidae). J Econ Entomol 108(3):975–985. https://doi.org/10.1093/jee/tov091
Zhao H, Sun X, Xue M, Zhang X, Li Q (2016) Antioxidant enzyme responses induced by whiteflies in tobacco plants in defense against aphids: catalase may play a dominant role. PLoS One 11(10):e0165454
Acknowledgements
This research was supported by a grant from Iranian Vice-Presidency for Science and Technology Project No. “99017268” and Vice Chancellor for Research and Technology of Shiraz University.
Funding
Iran National Science Foundation, Science deputy of presidency, Grant number: 99017268, Maryam Aleosfoor.
Author information
Authors and Affiliations
Contributions
All authors contributed to the study’s conception and design. MA conceived research, MA and FR conducted experiments, MA, LF and KM analyzed data and conducted statistical analyses, LF and MA wrote the first draft of the manuscript. KM edited the manuscript and provided additional information. All authors read and approved the manuscript.
Corresponding author
Ethics declarations
Conflict of interest
All authors declare that they have no conflict of interest.
Ethical approval
This article does not contain any studies with humans or animals performed by any of the authors.
Additional information
Handling Editor: Sylvain Pincebourde.
Publisher's Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Rights and permissions
Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.
About this article
Cite this article
Rad, F., Aleosfoor, M., Fekrat, L. et al. Water stress decreases the demographic performance of western flower thrips, Frankliniella occidentalis (Thysanoptera: Thripidae), on tomato. Arthropod-Plant Interactions 18, 105–116 (2024). https://doi.org/10.1007/s11829-023-09989-2
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s11829-023-09989-2