Foraging and scavenging behaviour of the prairie rattlesnake (Crotalus viridis): no evidence that envenomation cues facilitate kleptoparasitism of struck prey

Most viperids are ambush predators that primarily use venom to subdue prey, employing a strike-release-trail hunting strategy whereby snakes follow the unique scent of envenomated prey to locate carcasses they have bitten and released. In addition to killing prey, rattlesnakes (like most carnivores) will also opportunistically scavenge carrion. This scavenging strategy likely includes the occasional consumption of carcasses killed by other snakes (i.e., kleptoparasitism). In areas with high densities of other pitvipers, utilizing the unique scent of animals envenomated by other snakes might be a viable alternative foraging strategy. We evaluated this possibility experimentally using a series of captive behavioural trials on prairie rattlesnakes (Crotalus viridis) to determine whether conspecific or heterospecific (C. scutulatus, C. ornatus) envenomation cues might increase the likelihood of kleptoparasitism. Rattlesnakes did not prefer envenomated prey over nonenvenomated prey, nor did they prefer venom cues of one species over another. Although they did frequently scavenge carcasses, in the absence of striking, snakes generally located carcasses using random searching movements instead of scent trails. Additionally, the amount of time rattlesnakes spent investigating carcass trails did not differ significantly among treatments, suggesting that striking, and the resultant formation of a chemical search image of prey, is more crucial to trailing behaviour than venom cues. Moreover, a high degree of behavioural variation among individuals was observed, suggesting that scavenging and kleptoparasitism in rattlesnakes is more complex than previously realized, and making generalizations about these behaviours is challenging.

Variable crab camouflage patterns defeat search image formation

Understanding what maintains the broad spectrum of variation in animal phenotypes and how this influences survival is a key question in biology. Frequency dependent selection – where predators temporarily focus on one morph at the expense of others by forming a “search image” – can help explain this phenomenon. However, past work has never tested real prey colour patterns, and rarely considered the role of different types of camouflage. Using a novel citizen science computer experiment that presented crab “prey” to humans against natural backgrounds in specific sequences, we were able to test a range of key hypotheses concerning the interactions between predator learning, camouflage and morph. As predicted, switching between morphs did hinder detection, and this effect was most pronounced when crabs had “disruptive” markings that were more effective at destroying the body outline. To our knowledge, this is the first evidence for variability in natural colour patterns hindering search image formation in predators, and as such presents a mechanism that facilitates phenotypic diversity in nature.

Baby tyrannosaurid bones and teeth from the Late Cretaceous of western North America

Tyrannosaurids were the apex predators of Late Cretaceous Laurasia and their status as dominant carnivores has garnered considerable interest since their discovery, both in the popular and scientific realms. As a result, they are well studied and much is known of their anatomy, diversity, growth, and evolution. In contrast, little is known of the earliest stages of tyrannosaurid development. Tyrannosaurid eggs and embryos remain elusive, and juvenile specimens — although known — are rare. Perinatal tyrannosaurid bones and teeth from the Campanian–Maastrichtian of western North America provide the first window into this critical period of the life of a tyrannosaurid. An embryonic dentary (cf. Daspletosaurus) from the Two Medicine Formation of Montana, measuring just 3 cm long, already exhibits distinctive tyrannosaurine characters like a “chin” and a deep Meckelian groove, and reveals the earliest stages of tooth development. When considered together with a remarkably large embryonic ungual from the Horseshoe Canyon Formation of Alberta, minimum hatchling size of tyrannosaurids can be roughly estimated. A perinatal premaxillary tooth from the Horseshoe Canyon Formation likely pertains to Albertosaurus sarcophagus and it shows small denticles on the carinae. This tooth shows that the hallmark characters that distinguish tyrannosaurids from other theropods were present early in life and raises questions about the ontogenetic variability of serrations in premaxillary teeth. Sedimentary and taphonomic similarities in the sites that produced the embryonic bones provide clues to the nesting habits of tyrannosaurids and may help to refine the prospecting search image in the continued quest to discover baby tyrannosaurids.

Robust A*-Search Image Segmentation Algorithm for Mine-like Objects Segmentation in SONAR Images

This paper addresses a sonar image segmentation method employing a Robust A*-Search Image Segmentation (RASIS) algorithm. RASIS is applied on Mine-Like Objects (MLO) in sonar images, where an object is defined by highlight and shadow regions, i.e. regions of high and low pixel intensities in a side-scan sonar image. RASIS uses a modified A*-Search method, which is usually used in mobile robotics for finding the shortest path where the environment map is predefined, and the start/goal locations are known. RASIS algorithm represents the image segmentation problem as a path-finding problem. Main modification concerning the original A*-Search is in the cost function that takes pixel intensities and contour curvature in order to navigate the 2D segmentation contour. The proposed method is implemented in Matlab and tested on real MLO images. MLO image dataset consist of 70 MLO images with manta mine present, and 70 MLO images with cylinder mine present. Segmentation success rate is obtained by comparing the ground truth data given by the human technician who is detecting MLOs. Measured overall success rate (highlight and shadow regions) is 91% for manta mines and 81% for cylinder mines.