Prey Status Affects Paralysis Investment in the Ponerine Ant Harpegnathos venator

The paralysis behavior of some ponerine ants when foraging may be important for food storage and colony development. However, how workers invest in paralysis under different prey circumstances is often overlooked. Here, we report the prey-foraging behavior and paralysis behavior of Harpegnathos venator under different food supply conditions. Solitary hunting was the main foraging mode of H. venator, with occasional simple collective hunting. Nymphal cockroaches with high activity were the most attractive to H. venator. In the experiment, we found that the stings of H. venator completely paralyzed the cockroaches. The stinging time was significantly longer at a higher prey activity level and for larger cockroaches. In addition, there was no significant difference in the stinging time of H. venator for different prey densities. The results showed that the longer similar cockroaches were stung, the longer it took for them to revive and move. These results are helpful for further understanding the behavioral mechanism underlying the food storage of live prey by predatory insects.

Interneuron Control of C. elegans Developmental Decision-making

Animals integrate external stimuli to shape their physiological responses throughout development. In adverse environments, Caenorhabditis elegans larvae can enter a stress-resistant diapause state with arrested metabolism and reproductive physiology. Amphid sensory neurons feed into both rapid chemotactic and short-term foraging mode decisions, mediated by amphid and pre-motor interneurons, as well as the long-term diapause decision. We identify amphid interneurons that integrate pheromone cues and propagate this information via a neuropeptidergic pathways to influence larval developmental fate, bypassing the pre-motor system. AIA interneuron-derived FLP-2 neuropeptide signaling promotes reproductive growth and AIA activity is suppressed by pheromone. FLP-2 acts antagonistically to the insulin-like INS-1. FLP-2's growth promoting effects are inhibited by upstream metabotropic glutamatergic signaling and mediated by the broadly-expressed neuropeptide receptor NPR-30. Conversely, the AIB interneurons and their neuropeptide receptor NPR-9/GALR2 promote diapause entry. These neuropeptidergic outputs allow reuse of parts of a sensory system for a decision with a distinct timescale.

A partial skeleton of Septencoracias from the early Eocene London Clay reveals derived features of bee-eaters (Meropidae) in a putative stem group roller (Aves, Coracii)

A partial skeleton of the putative stem group roller Septencoracias is described from the early Eocene London Clay of Walton-on-the-Naze (Essex, UK). With an age of about 55 million years, the bones represent one of the earliest fossil records of a coraciiform bird. The new fossil reveals that the proximal pedal phalanges of the three anterior toes of Septencoracias exhibit markedly widened distal ends. This distinctive trait is not found in other representatives of the Coracii, but occurs in the Meropidae (bee-eaters). The quadrate likewise exhibit a derived characteristic of the Meropidae, and the beak is narrower than in rollers. These previously unnoticed features are of particular interest, because the Meropidae result as the sister taxon of the Coracii in sequence-based analyses. Calibrated molecular data suggest that the divergence between the Coracii and the Meropidae occurred at 55.6 Ma, with the new fossil being only slightly younger than this date. However, phylogenetic analyses recovered Septencoracias within the Coracii, so that the derived features shared with the Meropidae most likely are either plesiomorphic and were lost in the Coracii, or they represent parallelisms that evolved convergently in Septencoracias and the Meropidae. In any case, these traits suggest that Septencoracias differed from extant rollers in its ecological preferences and foraging mode.

Energy expenses on prey processing are comparable, but paid at a higher metabolic scope and for a longer time in ambush vs active predators: a multispecies study on snakes

Snakes are characterized by distinct foraging strategies, from ambush to active hunting, which can be predicted to substantially affect the energy budget as a result of differential activity rates and feeding frequencies. Intense foraging activity and continuously upregulated viscera as a result of frequent feeding leads to a higher standard metabolic rate (SMR) in active than in ambush predators. Conversely, the costs of digestion (Specific Dynamic Action—SDA) are expected to be higher in ambush predators following the substantial remodelling of the gut upon ingestion of a meal after a long fasting period. This prediction was tested on an interspecific scale using a large multispecies dataset (> 40 species) obtained from published sources. I found that the metabolic scope and duration of SDA tended to reach higher values in ambush than in active predators, which probably reflects the greater magnitude of postprandial physiological upregulation in the former. In contrast, the SDA energy expenditure appeared to be unrelated to the foraging mode. The costs of visceral activation conceivably are not negligible, but represent a minor part of the total costs of digestion, possibly not large enough to elicit a foraging-mode driven variation in SDA energy expenditure. Non-mutually exclusive is that the higher costs of structural upregulation in ambush predators are balanced by the improved, thus potentially less expensive, functional performance of the more efficient intestines. I finally suggest that ambush predators may be less susceptible than active predators to the metabolic ‘meltdown effect’ driven by climate change.

Adaptive foraging strategy of an insular snake (Lycodon semicarinatus, Colubridae) feeding on patchily distributed nests of sea turtles

Foraging tactics of predators generally include two major modes, active searching and ambushing. A colubrid snake, Lycodon semicarinatus, is a typical example of a predator, which uses both tactics to forage on sea turtles on islands of the Kerama Group in the Central Ryukyu Archipelago, Japan. To investigate factors that determine the foraging mode of this snake, we conducted a four-year field survey on its foraging behaviour on sea turtles on another island, Okinawa Island. We found that the snake performs only active searching at our study site. Snakes visited a small area exactly above the nest of sea turtles and attempted to burrow a tunnel to feed on eggs and hatchlings in the sand. Tunnels leading from the surface of the beach to the inside of the nest were formed only by large snakes. Many other snakes used the already made tunnels to capture eggs and hatchlings in the nest. When the snakes caught a hatchling, they brought the hatchling away into the nearby bush area without swallowing it above the nest (taking-away behaviour). When snakes failed to find food on a nest, they terminated the intensive search above the nest in approximately 5 minutes irrespective of snake body size, season, and the condition of the nest. Subsequently, they left the nest and resumed extensive searching for other nests. Our findings showed that L. semicarinatus has a different foraging strategy depending on populations. Two environmental traits, diversity of available prey animals other than sea turtles and characteristics of sand that beaches consist of, were considered as factors that might cause the difference in the foraging strategy. The fine sand of our study site enables snakes to form a sturdy tunnel in nests. We presume that such an environment facilitates the use of active searching by the snakes to find the nest with tunnels suitable for exploitation. The taking-away behaviour may be effective to reduce excessive contact with other conspecifics under the situation that the nest with tunnels attracts many visitors. Furthermore, the observation that the snake left the nest site after a consistent duration of unprofitable searching supports the giving-up time rule, which has been predicted by a theoretical model concerning the optimal time for predators to leave a patch.

Foraging modes and movements of Oncorhynchus mykiss as flow and invertebrate drift recede in a California stream

Salmonids frequently adapt their feeding and movement strategies to cope with seasonally fluctuating stream environments. Oncorhynchus mykiss tend to drift-forage in higher velocity habitat than other salmonids, yet their presence in streams with seasonally low velocity and drift suggests behavioral flexibility. We combined 3-D videogrammetry with measurements of invertebrate drift and stream hydraulics to investigate the drivers of O. mykiss foraging mode and movement during the seasonal recession in a California stream. From May to July (2016), foraging movement rate increased as prey concentration and velocity declined; however, movement decreased in August as pools became low and still. In May, 80% of O. mykiss were drift-foraging, while by July, over 70% used search or benthic-foraging modes. Velocity and riffle crest depth were significant predictors of foraging mode, while drift concentration was a poor univariate predictor. However top ranked additive models included both hydraulic variables and drift concentration. A drift-foraging bioenergetic model was a poor predictor of foraging mode. We suggest that infall and benthic prey, as well as risk aversion, may influence late-summer foraging decisions.

Using animal tracks to decipher the foraging mode of species capable of altering between the sit-and-wait and widely foraging modes: a case study of the sand viper Cerastes vipera

The sand viper Cerastes vipera can employ one of two distinct foraging modes, the widely foraging or sit-and-wait mode, depending on the interplay between external and internal factors. Here, I illustrate how tracking methods can be used to evaluate the relative usage of each of the two foraging modes by the sand viper. Foraging theory models generally refer to the time invested in foraging as the main indicator of the energy invested in foraging. I suggest that tracking and counting print marks on trails offer a more precise method of estimating foraging costs in the field. I model the benefits and costs of the viper employing each of the two foraging modes using tracking data, and discuss how it can be used to decipher its foraging mode. I present a measurement approach by which to assess the relative usage of different foraging modes. I contend that the proposed tracking methods and their analysis should prove to be equally applicable to other animals that leave print marks on sand or snow.