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Senior Scholars Day

Apr 28th, 12:00 AM - 12:00 AM

Socially-Facilitated Antipredator Responses in the Wolf milvina

Kaitlyn Herron

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Part of the Behavioral Neurobiology Commons

Herron, Kaitlyn, "Socially-Facilitated Antipredator Responses in the " (2020). Senior Scholars Day. 12. https://scholarlycommons.susqu.edu/ssd/2020/posters/12

This Event is brought to you for free and open access by Scholarly Commons. It has been accepted for inclusion in Senior Scholars Day by an authorized administrator of Scholarly Commons. For more information, please contact [email protected]. Socially-facilitated antipredator responses in the wolf spider Pardosa milvina ! Kaitlyn A. Herron and Matthew H. Persons ! ! Neuroscience Program, Susquehanna University, Selinsgrove, PA 17870 !

ABSTRACT Conspecifics with No Predator Conspecifics with Predator Conspecifics with No Predator METHODS cues, Subject with Predator cues, Subject without cues, Subject without Predator use diverse sources of information to assess predation risk. Many may use direct A cues (CNPSP) Female Pardosa test Predator (CPSNP) Female cues (CNPSNP) Female Pardosa test B D subject (center) has access to cues from Pardosa test subject (center) has no silk subject (center) has no access to silk cues information such as visual or odor cues associated with a predator. Additionally, social its larger predatory wolf spider, while cues from Tigrosa while two other female from Tigrosa while two other female Pardosa two other female Pardosa (outside ring) do Pardosa (outside ring) do have access to (outside ring) also have no access to predator species may use indirect sources of information such as observing antipredator responses of not have access to predator cues. predator cues. cues. nearby conspecifics even when they themselves have no direct information about risk. The relative value and interaction of direct predator cues and indirect social information about predation risk is unclear, particularly when these sources provide conflicting information. The wolf spider, Pardosa milvina, displays effective antipredator behavior (freezing) when detecting silk from adults of another co-occurring wolf spider, . Pardosa also C occurs at high densities in agricultural fields where encounters with Tigrosa vary spatially and Figure 1. Female Pardosa temporally. We tested how Pardosa antipredator responses varied when detecting Tigrosa milvina (A) and predator silk cues directly compared to social cues from conspecifics with or without access to Tigrosa helluo (B) were Conspecifics with Predator predator silk. Using an automated digital tracking system, we measured activity of Pardosa No Conspecifics, Subject No Conspecifics, Subject collected from ground litter cues, Subject without Predator with Predator cues (NCSP) without Predator cues (NCSNP) under six different social and predator cue conditions including variations of when the subject cues (CPSP) Female Pardosa test Female Pardosa milvina test subject Female Pardosa milvina test subject (center) around fields and mowed lawns subject (center) has no access to silk cues (center) has access to silk cues from has no access to silk cues from Tigrosa and does or does not have access to predator cues directly, and/or is able to observe conspecifics from Tigrosa while two other female Pardosa Tigrosa but there are no conspecific there are no conspecifics present. (C). Pardosa were assigned to (outside ring) can detect predator cues. present. with or without access to these same predator cues. We found spiders walked significantly one of six treatments (D) (see E F Figure 2 less in the presence of direct predator cues independent of social cues, however mean speed Figure 2) and their activity was (right).The six of movement and freezing responses were both significantly influenced by both direct recorded (E) and measured for social and predator cues and social cues. When nearby conspecifics had access to predator silk but the predator cue subject did not, the subject increased antipredator responses. When the subject had direct one hour with the automated treatments used in exposure to predator silk cues but nearby subjects did not, the subject reduced antipredator video-tracking system, responses. Although Pardosa mediate some defensive behavior based on social cues, direct Ethovision (F). our experiment information about a predator generally had a stronger effect on antipredator behavior. Our (N=123, n=18-21)) results suggest that behaviors of nearby conspecifics can influence the intensity and prevalence of antipredator behaviors of this spider in complex ways. RESULTS INTRODUCTION SUMMARY & CONCLUSIONS Animals use a variety of information to assess predation risk. They may use information gathered directly Resting Both direct predator cues and indirect social cues such as as odor or visual cues associated with a predator or they may use indirect social information from 3000 others to assess risk. This may include eavesdropping on predator alarm calls made by conspecifics or C C mediate antipredator responses of Pardosa. heterospecifics, detecting heightened vigilance of others in the area, or watching antipredator behaviors of BC AB Figure 5: Mean time (±SE) others nearby (reviewed in Magrath et al. 2014; Lilly et al. 2019). The extent to which animals value predator 2500 We found significant differences in activity level across all treatments information acquired directly compared to indirectly through social cues of others remains unclear. A spent resting and engaged A for all three measured antipredator responses: time spent resting, 2000 The wolf spider Pardosa milvina is an excellent model to compare the relative importance of direct versus in non-forward movements freezing, and speed. The presence of conspecifics without predator socially-mediated information on inducing antipredator behaviors. Pardosa can detect silk and excreta cues (One-way ANOVA, cues showed the same activity patterns as the subject alone without from the larger predatory wolf spider, Tigrosa helluo, and deploy effective antipredator responses that 1500 increase their survival in the presence of a live predator (Persons et al. 2001, 2002). When detecting silk and F5,117=6.06; p<0.0001). predator cues. This indicates that it wasn’t simply the presence of excreta cues from these predators, Pardosa exhibits a freeze response with long periods of no movement Different letters above bars conspecifics mediating activity. Activity level was significantly lower for and when they do move, it is reduced saltatory locomotion at lower speeds. This shift in locomotion allows 1000 them to evade detection by Tigrosa helluo (Persons et al. 2001). Not only can Pardosa detect the presence of indicate statistically test subjects when either conspecifics, the subject, or both had access the predator from these silk cues alone, but they grade their freeze response proportional to the perceived (sec) resting spent Time significant differences to predator cues. When nearby spiders showed freeze responses, risk with elevated defensive responses. For example using only information from predator silk, Pardosa can 500 estimate predator size (Persons & Rypstra 2001), sex (Lehmann et al. 2004), the diet of the predator between groups (N=123). subjects significantly mirrored these responses even when they had (Persons et al. 2001), when it ate last (Bell et al. 2006). and how recently it was in the area (Barnes et al. 0 no additional information about predators. This same pattern was also 2002). CNPSNP CNPSP CPSNP CPSP NCSNP NCSP observed for average speed, but not resting behavior. When the Pardosa milvina occur at high densities of 16 individuals/m2 in agricultural fields. Encounters with Tigrosa subject had access to predator cues and the conspecifics did not, the helluo are frequent but detection of predator silk may be spatially and temporally variable (Marshall and Freezing subject did not significantly reduce antipredator responses. Rypstra 1999). Given the high conspecific density, Pardosa may benefit not just by detecting Tigrosa silk 10000 Collectively this indicates that although indirect social cues can directly but also using the behavior of nearby Pardosa behavior to assess predation risk and modify their B Figure 6: Mean number 9000 B BC mediate and contribute to antipredator responses, direct cues about behavior based on these social cues. We tested the extent to which Pardosa will show antipredator response AB (±SE) of observations when in direct contact with predator cues. We predicted that Pardosa will show a heightened antipredator 8000 between samples without predator risk can override information from conspecific behavior. response when in direct contact with predator cues but will also show elevated antipredator responses when 7000 A nearby conspecifics are exhibiting antipredator behavior even when the spider has no direct information about AC 6000 any spider movement the presence of a predator. We also predicted that antipredator responses of nearby conspecifics will increase defensive responses when combined with direct cues and dampen or reduce antipredator responses 5000 (One-way ANOVA, when social cues conflict with direct information about a predator. Finally, we predicted that direct cues from 4000 F5,117=4.28; p<0.0013). a predator will elicit stronger responses than social cues. 3000 Different letters above 2000 bars indicate statistically 1000 0 significant differences QUESTIONS movement without Observations CNPSNP CNPSP CPSNP CPSP NCSNP NCSP between groups (N=123).

Do Pardosa modulate their antipredator Adult female Tigrosa helluo eating a Pardosa Adult female Pardosa milvina wolf spider Velocity milvina wolf spider responses based on combinations of 2.25 A Figure 6: Mean spider 2 AC References indirect social cues and direct chemical speed (±SE) during time BC B Bell, R. Rypstra, A.L., & Persons, M.H. 2006. The effect of predator hunger on chemically-mediated antipredator responses and survival in the wolf spider 1.75 B B Pardosa milvina. Ethology, 112:903-910. cues from predators? spent in forward Lehmann, L. Walker, S.E., & Persons, M.H. 2004. The influence of predator sex on chemically-mediated antipredator response in the wolf spider Pardosa milvina (Araneae: Lycosidae. Ethology. 110:1-17. 1.5 locomotion (One-way Barnes, M.C., Persons, M.H., & A.L. Rypstra. 2002. The effect of predator chemical cue age on chemically-mediated antipredator behavior in the wolf • Do social cues about predators and direct spider Pardosa milvina (Araneae: Lycosidae). Journal of Behavior, 15:269-281. 1.25 ANOVA, F =3.722; Lilly, M.V., Lucore, E.C., & Tarvin, K.A. 2019. Eavesdropping grey squirrels infer safety from chatter. PLoS 14:e0221279. 5,117 Magrath, R.D. Haff, T.M., Fallow, P.M. & Radford, A.N. 2014. Eavesdropping on heterospecific alarm calls: from mechanism to consequences. Biological Reviews. 90:560-586. predator cues modulate different reductions 1 p<0.0037). Different Marshall, S., & Rypstra, A.L. 1999. Patterns in the distribution of two wolf spiders (Araneae: Lycosidae) in two soybean agroecosystems. Environmental Entomology, 28:1052-1059. .75 letters above bars indicate Persons, M.H. & Rypstra, A.L. 2000. Wolf spiders show graded antipredator behavior in the presence of chemical cues from different sized predators. in activity (i.e. freezing, reduced walking, Journal of Chemical Ecology, 27:2493-2504. Centimeters/sec statistically significant Persons, M.H., Walker, S.E., Rypstra, A.L., & S.D. Marshall. 2001. Wolf spider predator avoidance tactics and survival in the presence of diet-associated .5 predator cues (Araneae:Lycosidae). Behavior, 61:43-51. reduced speed)? differences between Persons, M.H., Walker, S.E., & Rypstra, A.L. 2002. Fitness costs and benefits of chemotactile-mediated antipredator behavior in the wolf spider Pardosa .25 milvina. Behavioral Ecology, 13:386-392. groups (N=123). • Are direct predator cues more important 0 CNPSNP CNPSP CPSNP CPSP NCSNP NCSP than social cues from conspecific spiders?