Source: CORNELL UNIVERSITY submitted to
PEST RESPONSES TO PREDATION RISK: MAXIMIZING BIOLOGICAL CONTROL OF THE COLORADO POTATO BEETLE
Sponsoring Institution
National Institute of Food and Agriculture
Project Status
TERMINATED
Funding Source
Reporting Frequency
Annual
Accession No.
1002357
Grant No.
2014-67013-21785
Project No.
NYC-139563
Proposal No.
2013-02649
Multistate No.
(N/A)
Program Code
A1111
Project Start Date
Mar 1, 2014
Project End Date
Feb 28, 2018
Grant Year
2014
Project Director
Thaler, J.
Recipient Organization
CORNELL UNIVERSITY
(N/A)
ITHACA,NY 14853
Performing Department
Entomology
Non Technical Summary
A central goal for modern agriculture is to increase the success of insect biological control. A profound result of the last 20 years is that over 50% of the effect of predators on prey is through changes in prey behavior and development (not consumption!) in response to predation risk. In the course of studying non-consumptive effects of a native stink bug predator we discovered that its prey dramatically reduces feeding to avoid predation, but is able to maintain growth. This finding presents an important question and a challenge: The question, from the herbivore's perspective, is under what conditions can the herbivore compensate for reductions in feeding and what are the costs of this compensation? The challenge however, is: How can we manipulate conditions to reduce prey compensatory ability and maximize the costs of predator exposure to maximize both the consumptive and non-consumptive effect of predators?Studying Colorado potato beetles, a major pest of potatoes, we will measure how plant resistance affects the non-consumptive and total effect of the stink bug predator on the beetle life time fitness and plant damage including effects on the next generation that is not exposed to predation. We will measure physiological, behavioral and developmental mechanisms by which beetle larvae compensate for responses to predation risk and how these contribute to fitness in the presence of additional stresses.
Animal Health Component
0%
Research Effort Categories
Basic
100%
Applied
(N/A)
Developmental
(N/A)
Classification

Knowledge Area (KA)Subject of Investigation (SOI)Field of Science (FOS)Percent
21113101070100%
Knowledge Area
211 - Insects, Mites, and Other Arthropods Affecting Plants;

Subject Of Investigation
1310 - Potato;

Field Of Science
1070 - Ecology;
Goals / Objectives
Objective 1: Determine how plant resistance influences the strength of non-consumptive effects on pests.Objective 2: Determine behavioral, physiological, and developmental mechanisms by which prey compensate for responses to predation risk in different environmental conditions.Objective 3: Determine the trans-generational consequences of predation risk.
Project Methods
Objective 1: Determine how plant resistance influences the strength of non-consumptive effects on pests. We will test the hypothesis that high plant resistance, manipulated by induction of the jasmonate plant defense pathway and Bacillus thuringiensis toxin, enhances the total effect of the predator on prey fitness through enhancement of the non-consumptive pathway. This hypothesis will be tested in a benign environment and when the prey are challenged by additional stresses.Treatments: We will manipulate plant resistance and predation risk in field mesocosms. We will establish 3 predator levels (control, lethal predator, predation risk), 3 plant resistance levels (control, jasmonate induced, Bacillus treated)(details below), and 20 replicates per treatment (3x3x20= 180 total replicate cages). Each 1 m3 mesocosm (amber fabric, Lumite, Inc, Gainesville, GA) will be placed in a plowed field and 10 4-week old potato plants of the appropriate resistance level planted. Thirty 1st instar CPB larva from a single mother (sibship) will added to all cages. The lethal cages will receive one adult female stink bug, the predation risk cages will receive one sham stink bug, the control cages will not have a predator.We will use three plant resistance levels. The susceptible cultivar, Yukon Gold will be the low resistance control. Our second treatment will be Yukon Gold plants treated with the plant hormone jasmonic acid to induce plant defenses (Li et al. 2004, Kaplan and Thaler 2010). The jasmonate response is a biochemical pathway induced by herbivory and hormonal application that confers resistance to a wide range of herbivores including CPB (Orozco-Cardenas et al. 1993, Thaler et al. 2001, Li et al. 2002). In potato plants, jasmonic acid induces many defenses, including cysteine proteinase inhibitors, which provide increased resistance to CPB (Rivard et al. 2004). The third treatment will be Yukon Gold plants treated with Bacillus thuringiensis tenebrionis toxin which contains δ-endotoxins (cryIIIA and cryIIIBb) that are highly active and specific to beetles interfering with their digestion. Inducing the jasmonic acid pathway changes many resistance traits (toxins, trichomes, defensive proteins), whereas using the Bt treatment adds only specific toxins. CPB larvae are sensitive to Bt, which can kill larvae at high doses or slow their growth at lower doses (Cloutier and Jean 1998). Foliage will be treated with 0.5 mM jasmonic acid or a sub-lethal dose of B. thuringiensis toxin (to slow the growth but not kill all the larvae the Bt will be applied at 10% of manufacturers recommended dose of trade name Foil (Costa et al. 2000)) one day prior to beginning the experiment and once per week until the experiment ends (Thaler et al. 1996).Once per week, we will count surviving larvae, record their instar, weigh the group and replace them into their cage. We will estimate the percent of the plant consumed and check for stink bug survival, replacing any dead individuals.Statistical analysis: We will use MANOVA to determine whether any of the response variables measured several times during the experiment were affected by the treatments followed by ANOVA to compare fitness measures across treatments. From the survival and egg production data, we will generate a cohort life-table.Objective 2: Determine behavioral, physiological, and developmental mechanisms by which prey compensate for responses to predation risk in different environmental conditions.We will establish replicates with single CPB larvae in greenhouse cages and study the mechanisms of how the CPB larvae respond to the predator. CPB pupae will be sexed and upon emergence individual females will be put in cages with a single male, and mated. Eggs from these singly mated females (called sibships) will be used in experiments. Sibships vary in their response to predation risk; preliminary experiments showed that 9/14 sibships reduced feeding in the predation risk treatment and 5/14 sibships increased assimilation efficiency in the predation risk treatment compared to controls. This variation in responsiveness of the sibships will allow us to correlate particular responses with fitness.Individual plants (replicates) will be caged in spun polyester mesh transmitting 90% of ambient light (Agrifabrics, Pro 17 material). Each plant will have one CPB larva and the chosen plant resistance, predation treatment. Within each treatment, we will use 20 sibships of prey (20 sibships, 8 replicates per sibship = 160 replicates per treatment). We need high replication per treatment to allow for destructive collections during the experiment. We will identify where in the life-cycle the behavioral, physiological or developmental changes in responses to predation risk and plant resistance treatments occur, and how these translate into net impacts on fitness using a statistical approach. We will calculate CPB fitness in the same way as described in Objective 1. Here, however, we will be able to compare sibships that vary in their expression of particular responses and so we will extrapolate the fitness consequences of particular strategies or combinations of strategies. We will use MANOVA and non-linear mixed effect models to determine whether any of the response variables measured several times during the experiment (e.g., instar, assimilation efficiency, mandible size, and plant resistance traits) are affected by treatment. We will use ANOVA to analyze the effects of predation risk (fixed effect), plant resistance (fixed effect), prey sibship (random effect) and their interactions on r as well as specific attributes of fitness (pupal mass, # eggs).Objective 3: Determine the transgenerational consequences of predation risk.We will test the hypothesis that effects of predation risk in the first generation may translate into large impacts on subsequent generations, especially when coupled with other control methods. It is likely that prey will come into contact with predators for a portion of their larval period, and this may have consequences long after the predator is gone. Because such delayed effects are especially important for "populations" of insects and have been relatively poorly described in agricultural pests, we have propose to 1) describe the responses in offspring of threatened and unthreatened adults, 2) test their consequences for growth in unstressed conditions, and 3) test for the impact of additional stresses (feeding on a resistant host plant, challenged by a lethal stink bug, and challenged by the pathogen Beauveria).Starting in the first instar, CPB larvae will be exposed to predation risk or control treatment until they pupate. Each replicate will consist of a single plant (Yukon Gold) with either the sham predator or control treatment (120 replicates per treatment). CPB will be reared until pupating. Pupa will be collected and females will be mated with a male from the same treatment (if the male dies, it will be replaced with another male from the same treatment, if the female dies the replicate is ended). Adult oviposition (number of eggs and date laid) will be measured until the female beetle dies.Eggs from each female will be hatched and the growth and survival of young larvae measured under several conditions; unstressed control, lethal stink bug predator, resistant host plant, pathogen Beauveria. Larvae will be challenged with these stresses as outlined in Obj 1.

Progress 03/01/14 to 02/28/18

Outputs
Target Audience:We presented this research to the general public at the annual Insectapalooza open house which is attended by several thousand people in Upstate New York annually. The PD presented the research at talks at the University of Montana, Missoula, Montana, the University of Kentucky, Lexington, Kentucky as the Student Invited Speaker, University of Colorado, Boulder, Colorado, at the Gordon Research Conference on Predator-Prey Interactions, the Gordon Research Conference on Plant-Herbivore Interactions, and at the Entomological Society of America Annual meeting in a symposium on Agricultural Applications of non-consumptive effects. One of the postdocs working on the project, Natasha Tigreros, gave a presentation about this research at the Ecological Society of America meeting in August 2015. And a graduate student Nick Afflito presented a poster at the Predator-Prey Gordon Conference: Temporal patterns in predator-prey interactions We present the highlights of our findings in a factsheet for vegetable growers that was published on the New York Integrated Pest Management website. (https://ecommons.cornell.edu/handle/1813/45068) I presented our research to Cornell undergraduates who I teach and they conducted independent research projects building on our findings. Changes/Problems: Nothing Reported What opportunities for training and professional development has the project provided?The six undergraduates working on the project this period received one on one mentoring from me and the postdoc associated with the project, Natasha Tigreros. Two of the students on the project also conducted independent research and earned authorship on three published manuscripts. The postdoc and one of the undergraduates also attended a two-day professional development retreat run yearly for the lab members. Three of the undergraduate students and the postdoc received constructive feedback on their research at our weekly lab meetings, in the Plant Insect Interactions seminar course, and two of the undergraduates attended the Ecological Society of America Annual meeting. How have the results been disseminated to communities of interest?We have presented this research to the general public at the annual Insectapalooza open house and it has contributed to undergraduate teaching in Insect Ecology and Chemical Ecology courses at Cornell. What do you plan to do during the next reporting period to accomplish the goals? Nothing Reported

Impacts
What was accomplished under these goals? Objective 1: Determine how plant resistance influences the strength of non-consumptive effects on pests. The first work on this objective, led by a graduate student, showed that predation risk reduces oviposition and feeding damage by adult beetles in the field (Hermann and Thaler 2014). Next, we evaluated the theoretical expectations for when prey should optimally respond to predators (Orrock et al. 2015). We ended with an experiment showing that plant resistance strongly affects how young larvae respond to predation risk and that in spite of many prey compensatory processes, early predator exposure affects life-time fitness measured as oviposition and offspring quality. These results are important because they show long-term consequences of predator exposure on fitness and magnification of the costs for prey on high-resistance plants (Thaler, Nelson, Nelson, and Nyrop, in review). Objective 2: Determine behavioral, physiological, and developmental mechanisms by which prey compensate for responses to predation risk in different environmental conditions. We started this Objective by writing a synthesis paper discussing the behavioral and physiological intersections between prey responses to predation risk and plant resistance (Wetzel and Thaler 2016). Then, a postdoc and undergraduate research student conducted an experiment investigating behavioral and physiological mechanisms of prey responses to predation risk (Tigreros et al., Functional Ecology 2018). These experiments showed that beetles balance behavioral feeding responses and physiological changes in metabolic rate and nutrient storage to reduce the negative effects of predator exposure. There is substantial family-level variation in responses to predation risk and larval nutritional condition, in part mediated by cannibalistic behavior, which underlies these responses. Cannibalistic beetles have stronger feeding responses to predators and compensate for reductions in feeding by reducing their metabolic rate and storing more nutrients as lipids for future use. This research helps us understand under what conditions prey will have strong, potentially costly, responses to predation risk. Objective 3: Determine the trans-generational consequences of predation risk. Our first research showed strong trans-generational effects of adult predator exposure that affected offspring cannibalism, growth and survival when attacked by predators (Tigreros et al, Ecology Letters in 2017). This showed that predator exposure has the potential to have long-lasting effects on prey and prey populations. To see how general the predator-induced increase in cannibalism and prey responsiveness was, we investigated the consequences of predator exposure during the larval stage for investment in offspring. We found that larval exposure also increases parental investment in offspring, but instead of through cannibalism as found when adults were exposed, through increased provisioning of eggs. This manuscript is authored by a postdoc and an undergraduate Honor's student and is currently in review (Tigreros, Norris, and Thaler). In addition, we conducted a quantitative genetics experiment to determine the genetic and environmental contributions to parental effects of exposure to predation risk; this manuscript is currently in review (Tigreros, Agrawal, Thaler). In combination, these experiments are yielding new insights into how prey avoid the negative effects of predation and suggest that using biological control agents that differentially target adults and their offspring may result in more successful control.

Publications

  • Type: Journal Articles Status: Published Year Published: 2018 Citation: Tigreros, N., E. Wang and J.S. Thaler. 2018. Prey nutritional state drives divergent behavioural and physiological responses to predation risk. Functional Ecology. 10.1111/1365-2435.13046
  • Type: Journal Articles Status: Published Year Published: 2017 Citation: Kersch-Becker, M.F., Kessler, A, and J.S. Thaler. 2017. Plant defenses limit herbivore population growth by changing predator-prey interactions. Proceedings of the Royal Society B. DOI: 10.1098/rspb.2017.1120
  • Type: Journal Articles Status: Submitted Year Published: 2019 Citation: Tigreros, N, Agrawal, A, J.S. Thaler. Parental genetic effects contribute to variation in anti-predator plasticity
  • Type: Journal Articles Status: Submitted Year Published: 2019 Citation: Jennifer S. Thaler, Scott Nelson, Rebecca Loughner, Jan Nyrop. Interactive effects of predation risk and host plant resistance over prey life-time.
  • Type: Journal Articles Status: Under Review Year Published: 2019 Citation: Tigreros, N., R. Norris, J.S. Thaler. Prey reproductive allocation decisions in the presence of predators: Do moms always sacrifice offspring quantity for quality


Progress 03/01/16 to 02/28/17

Outputs
Target Audience:Our target audience includes the grower community reached through a factsheet where we present the highlights of our findings in a factsheet for vegetable growers that was published on the New York Integrated Pest Management website. (https://ecommons.cornell.edu/handle/1813/45068) We have presented this research to the general public at the annual Insectapalooza open house which is attended by several thousand people in Upstate New York. I presented results from this research to the scientific community at the Gordon Research Conference on Predator-Prey Interactions. I presented our research to Cornell undergraduates who I teach and they conducted independent research projects building on our findings. Changes/Problems: Nothing Reported What opportunities for training and professional development has the project provided?Two postdoctoral researchers, including one Hispanic women, seven undergraduates including 4 women and 3 men, and one technician received training in the scientific method through working on this project. These students have also attended lab meetings, scientific conferences, and University seminars and attended several professional development workshops to further their training. How have the results been disseminated to communities of interest?Our target audience includes the grower community reached through a factsheet where we present the highlights of our findings in a factsheet for vegetable growers that was published on the New York Integrated Pest Management website. (https://ecommons.cornell.edu/handle/1813/45068) We have presented this research to the general public at the annual Insectapalooza open house which is attended by several thousand people in Upstate New York. I presented results from this research to the scientific community at the Gordon Research Conference on Predator-Prey Interactions. I presented our research to Cornell undergraduates who I teach and they conducted independent research projects building on our findings. What do you plan to do during the next reporting period to accomplish the goals?Objective 1: The part of the study on the interaction between plant resistance and responses to predation risk will be submitted to the journal Ecology and the results on sibling variation in responses will be submitted to Oecologia. Objective 2: We have collected the data for this project and are in the process of writing for publication in Functional Ecology. To complete Objective 3, we need to finish data collection, finish analyzing the data, and write the second manuscript.

Impacts
What was accomplished under these goals? Objective 1: Determine how plant resistance influences the strength of non-consumptive effects on pests. We have completed the experiments for Objective 1 and are currently writing the results for publication. Our results show that plant resistance strongly affects how young larvae respond to a predator. On low-resistance plants, first instar larvae reduced feeding and had lower mass in the predation risk treatment. However, on high-resistance plants, beetle sibships had divergent responses to predation risk early in life, some increasing and others decreasing feeding. Older larvae consistently reduced feeding and mass in the presence of the predator on both low- and high-resistance plants. In spite of reduced feeding through most of larval development, larvae on both low- and high- resistance plants appeared to compensate for responses to predation risk by the time they reached pupation as life-time feeding and pupal mass did not differ between treatments. This compensation was due to increased assimilation efficiency early in life and compensatory feeding and delayed development later in life. In spite of apparent compensation in terms of pupal mass, larval plant resistance and predation-risk treatments had effects on the adult stage and the offspring. Adult beetles that had been exposed to predation stress as larvae, but not as adults, had lower fecundity. These results demonstrate an effect of predator exposure that lasts over the life-time of the individual prey. These data are collected and are currently being written for publication. The part of the study on the interaction between plant resistance and responses to predation risk will be submitted to the journal Ecology and the results on sibling variation in responses will be submitted to Oecologia. Objective 2: Determine behavioral, physiological, and developmental mechanisms by which prey compensate for responses to predation risk in different environmental conditions. Our experiments show that beetles use behavioral, physiological and developmental mechanisms to reduce the negative effects of predator exposure. There is substantial family-level variation in responses to predation risk and larval nutritional condition seems to underlie these responses. Beetles in good condition and rapidly growing employ more behavioral responses to predators (reduced feeding) and increase their assimilation efficiency to compensate for reductions in feeding. Beetles in poor condition either don't change how much they feed or even increase their feeding in response to predators. Two environmental conditions influence this outcome. First, beetles grow more slowly on highly-resistant plants and this makes them less responsive to predators. Second, if their parents were exposed to predators, beetles are more likely to cannibalize siblings (see Objective 3). Being a cannibal increases larval nutrition which increases their behavioral responses to predators. Cannibalistic beetles compensate for reductions in feeding by reduce their metabolic rate and storing more nutrients as lipids for future use. Nutritional status of the beetle influences how it responds to predators and the physiological compensatory mechanisms that it uses. We have collected the data for this project and are in the process of writing for publication in Functional Ecology. Objective 3: Determine the trans-generational consequences of predation risk. We have shown there are strong trans-generational effects of predator exposure on Colorado Potato Beetles that affect beetle survival when attacked by predators. When female Colorado potato beetles are exposed to predation risk, their offspring are more likely to cannibalize a sibling compared to offspring whose parents were not exposed to predators. This is an active response of the mothers who produce a higher proportion of unviable eggs which are then consumed by their viable offspring. Egg feeding reduces larval vulnerability to predation by shortening larval development time and improving larval anti-predator responses. This study is accepted pending minor revisions to Ecology Letters. In addition, we are completing experiments investigating when in the parental life-cycle predator exposure affects cannibalism in offspring. In combination, these experiments are yielding new insights into how prey avoid the negative effects of predation. Adults exposed to predators lay fewer eggs (Objective 1), but their larvae are more defended against predators. Using biological control agents that differentially target adults and their offspring may result in more successful control. To complete this Objective, we need to finish data collection, finish analyzing the data, and write the second manuscript.

Publications

  • Type: Journal Articles Status: Published Year Published: 2017 Citation: Tigreros, N, R. Norris, E. Wang, J. S. Thaler. 2017. Maternally induced intraclutch cannibalism: an adaptive response to predation risk? Ecology Letters, in press.
  • Type: Journal Articles Status: Published Year Published: 2016 Citation: Wetzel, W. C. and J.S. Thaler. 2016. Does plant trait diversity reduce the ability of herbivores to defend against predators? The plant variability-gut acclimation hypothesis. Current Opinion in Insect Science 14:25-31.


Progress 03/01/15 to 02/29/16

Outputs
Target Audience:We have presented this research to the general public at the annual Insectapalooza open house which is attended by several thousand people in Upstate New York. One of the postdocs, Natasha Tigreros, working on the project gave a presentation about this research at the Ecological Society of America meeting in August 2015. I presented results from this research at the Entomological Society of America Annual meeting in a symposium on Agricultural Applications of non-consumptive effects. Changes/Problems: Nothing Reported What opportunities for training and professional development has the project provided?The six undergraduates working on the project received one on one mentoring from and the two postdocs associated with the project, Natasha Tigreros and Will Wetzel. Two of the students on the project also conducted independent research. Both of the postdocs and one of the undergraduates also attended a two-day professional development retreat. Three of the undergraduate students and the two postdocs received constructive feedback on their research at our weekly lab meetings, in the Plant Insect Interactions seminar course, and the postdocs attended the Ecological Society of America Annual meeting. In addition, the two postdocs attended a biweekly writing workshop run by the lab group aimed at improving their writing. How have the results been disseminated to communities of interest?We have presented this research to the general public at the annual Insectapalooza open house, the Ecological Society of America meeting in August 2015 and the Entomological Society of America Annual meeting in a symposium on Agricultural Applications of non-consumptive effects. What do you plan to do during the next reporting period to accomplish the goals?This coming year we will be writing up our results from Objectives 1 and 3, continuing experiments targeted at different aspects of Objectives 1 and 2, and beginning in earnest our efforts on the physiological mechanisms in Objective 2.

Impacts
What was accomplished under these goals? We have made substantial progress on Objective 1 and 3. Plant resistance strongly affected how young larvae responded to the predator. On low-resistance plants, first instar larvae reduced feeding and had lower mass in the predation risk treatment. However, on high-resistance plants beetle sibships had divergent responses to predation risk early in life, some increasing and others decreasing feeding. Older larvae consistently reduced feeding and mass in the presence of the predator on both low- and high-resistance plants. In spite of reduced feeding through most of larval development, larvae on both low- and high- resistance plants compensated for predation risk by the time they reached pupation as life-time feeding and pupal mass did not differ between treatments. This compensation was due to increased assimilation efficiency early in life and compensatory feeding and delayed development later in life. In spite of apparent compensation in terms of pupal mass, larval plant resistance and predation-risk treatments had effects on the adult stage and the offspring. Adult beetles that had been exposed to predation stress as larvae, but not as adults, had lower fecundity. There was substantial family-level variation in the behavioral (feeding reduction) and physiological (assimilation efficiency increase) responses to predation risk and these responses were positively correlated with each other. There are both maternal and genetic components to this variation. The offspring of beetles exposed to predators as larvae showed reduced growth and feeding in spite of similarity in egg mass. The variation in feeding responses of the different sibships resulted in different fitness costs; the greater the reduction in feeding in the predation risk treatment the greater the reduction in fitness on high-resistance plants, although they were not correlated on low resistance plants.

Publications

  • Type: Journal Articles Status: Published Year Published: 2015 Citation: Claflin, S., J.S. Thaler, A. Power. 2015. Predators, host abundance, and host spatial distribution affect the movement of wingless non-colonizing vector Rhopalosiphum padi (L.) and PVY prevalence in an oat/potato system. Arthropod-Plant Interactions 9:301-309. 10.1007/s11829-015-9370-3
  • Type: Journal Articles Status: Published Year Published: 2015 Citation: Orrock, J.L., A. Sih, M.C.O Ferrari, R. Karban, E.L. Preisser, M.J. Sheriff, and J.S. Thaler. 2015. Error management in plant allocation to herbivore defense. Trends in Ecology and Evolution 8:441-445. http://dx.doi.org/10.1016/j.tree.2015.06.005


Progress 03/01/14 to 02/28/15

Outputs
Target Audience: This year, the results of our research were presented to ecologists at the Ecological Society of America Annual meeting, entomologists at the Entomological Society of America meeting and chemical ecologists at the Symposium for Insect Plant Interactions. Changes/Problems: Nothing Reported What opportunities for training and professional development has the project provided? The four undergraduates received one on one mentoring from the Project Director and the postdoctoral researchers (Natasha Tigreros and Will Wetzel) working on the project. The graduate student, Sara Hermann,got experiencebypresenting her research at several international conferences including the Symposium on Insect Plant Interactions and at the International Society for Chemical Ecology Annual meeting. The postdoc, Natash Tigreros, participated in a two-day professional development retreat. The two postdocs also got experience and constructivefeedback presenting their research findings and future plans at the Plant Insect Interactions seminar course. How have the results been disseminated to communities of interest? We have presented our research for the general public at the annual Insectapalooza Open house which is attended by several thousand people from Upstate New York. A graduate student involved in the project has presented these research concepts to elementary school children in the Ithaca area as part of a program to interest young children in science. What do you plan to do during the next reporting period to accomplish the goals? Nothing Reported

Impacts
What was accomplished under these goals? We made significant progress on Objective 1: Determine how plant resistance influences the strength of non-consumptive effects on pests. We compared the consumptive and non-consumptive effect of the predator on prey and plant damage in three species: tobacco hornworm caterpillars (Manduca sexta), Colorado potato beetle larvae (Leptinotarsa decemlineata) and cabbage looper (Trichoplusia ni) and have found that the non-consumptive effect accounts for at least 50% of the effect of the predator on plant damage in all three species. All three species respond to the presence of the predator by greatly reducing their feeding but varied in how they offset the detrimental effects of reduced food intake. Our research with aphids shows that risk of predation by ladybugs increases aphid wing production, dispersal of wingless aphids and aphid fecundity and that these effects are greater on plants with low levels of resistance compared to high levels of resistance. We have started working on Objective 2: Determine behavioral, physiological, and developmental mechanisms by which prey compensate for responses to predation risk in different environmental conditions. Our results to date show that prey condition, influenced by both plant quality and larval cannibalism greatly influence behavioral responses of prey to predation risk. We find that small prey are less likely to reduce feeding in the presence of the predator and we are currently investigating how physiological and developmental mechanisms change in low and high condition individuals. We are currently developing methods for measuring metablic and hormonal responses to predation risk. We will begin work on Objective 3 in the upcoming year.

Publications

  • Type: Journal Articles Status: Published Year Published: 2015 Citation: Thaler, J.S., E.L. Olsen, I. Kaplan. 2015. Jasmonate-induced plant defenses and prey availability impact the preference and performance of an omnivorous stink bug, Podisus maculiventris. Arthropod-Plant Interactions, in press. DOI: 10.1007/s11829-015-9357-0
  • Type: Journal Articles Status: Awaiting Publication Year Published: 2015 Citation: Kersch-Becker, M and J.S. Thaler. 2015. Plant resistance reduces the strength of consumptive and non-consumptive effects of predators on aphids. Journal of Animal Ecology, in press.
  • Type: Journal Articles Status: Published Year Published: 2014 Citation: Kaplan, I., S.H. McArt, Thaler, J.S. 2014. Plant defenses and predation risk differentially shape patterns of consumption, growth, and digestive efficiency in a guild of leaf-chewing insects. Plos One: 9(4) e93714
  • Type: Journal Articles Status: Published Year Published: 2014 Citation: Hermann, S.L. and J.S. Thaler. 2014. Prey Perception of Predation Risk: volatile chemical cues mediate non-consumptive effects of a predator on a herbivorous insect. Oecologia 176:669-676. DOI 10.1007/s00442-014-3069-5