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Group-specific, degenerate polymerase chain reaction primers for DNA-based detection of springtails (Hexapoda: Collembola) within predator gut contents have been developed for the first time. Primers were designed from 18S rDNA and amplified fragments of 272 bp and 177 bp from 17 springtail species collected in agricultural habitats. Specificity tests against 41 nontarget species revealed no cross-reactivity. Group-specific polymerase chain reaction is advantageous when working in species-rich habitats and these primers could facilitate studies of trophic links between springtails and generalist arthropod predators worldwide.

Gut content analysis is a useful tool when studying arthropod predator‐prey interactions. We used polymerase chain reaction (PCR) technique to examine how detection of prey DNA in the gut content of predators was influenced by digestion time and temperature. Such knowledge is critical before applying PCR‐based gut content analysis to field collected predators. Larvae of the two‐spotted ladybeetle (Adalia bipunctata L.) were fed with the bird cherry‐oat aphid (Rhopalosiphum padi L.) at either 21°C or 14°C. After consuming one aphid, the predators were allowed to digest the prey for a range of time periods up to 24 hours. The influence of temperature on A. bipunctata feeding behavior was also recorded. From the fed larvae, total DNA was extracted and PCR reactions with R. padi specific primers were run. The number of A. bipunctata that tested positive for R. padi DNA was negatively related to the length of digestion time. Temperature influenced larval feeding behavior but did not have a significant effect on R. padi DNA detection. After pooling the data from both temperature treatments we estimated the time point when R. padi DNA could be amplified from 50% of the fed A. bipunctata by PCR to be 4.87 hours. With such a rapid decrease in prey DNA detection success, positive PCR reactions will most likely be the result of predation events occurring shortly before capture. If a defined digestion temperature range has proven not to influence prey detection, PCR data obtained from predators collected within that particular range can be interpreted in the same way.

Generalist arthropod predators are potential drivers of population dynamics in a wide variety of ecosystems but their feeding habits are often difficult to reveal as they are small, mobile, and live among dense vegetation or in soils. DNA-based gut-content analysis is a powerful tool that enables studies on arthropod predator-prey interactions. We studied lycosid spiders (Pardosa spp.) in agroecosystems to see if they consumed cereal aphids (Rhopalosiphum padi) and Collembolans at random, i.e., in proportion to their abundance in the field. We also tested if consumption of the target prey items was affected by the presence of alternative food. Spiders were captured in farmers' fields and their gut-contents screened by PCR with R. padi and Collembola primers. On all sampling occasions, concurrent assessments of total prey availability were carried out. Spider predation rates on R. padi always exceeded 50 %. Spiders also tested positive for Collembola but to a lower and more varying degree. In general, Pardosa did not consume R. padi and Collembolans in relation to their abundance in the field. Aphid predation was much higher than expected whereas consumption of Collembolans was considerably lower. The presence of alternative prey influenced consumption of the aphid. It was concluded that prey consumption by Pardosa spiders generally cannot be assumed to simply mirror prey availability. The spatial distribution of the target prey needs to be considered as well as the abundance, composition, and nutritional content of potential alternative food items.