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Brochuchusis a small crocodylid originally based on specimens from the early Miocene of Rusinga Island, Lake Victoria, Kenya. Here, we report occurrences ofBrochuchusfrom several early and middle Miocene sites. Some are from the Lake Victoria region, and others are in the Lake Turkana Basin. Specimens from the middle Miocene Maboko locality form the basis of a new species,Brochuchus parvidens, which has comparatively smaller maxillary alveoli. Because of the smaller alveoli, the teeth appear to be more widely spaced in the new species. We also provide a revised diagnosis forBrochuchusand its type species,B.pigotti. A phylogenetic analysis supports a close relationship betweenBrochuchusand tube-snoutedEuthecodon, but although relationships among crocodylids appear poorly resolved in the set of optimal trees, this is becauseBrochuchusandEuthecodon, along with early Miocene “Crocodylus”gariepensisfrom the early Miocene of Namibia, jointly adopt two distinct positions—either closely related to the living sharp-nosed crocodile (Mecistops) or to a group including the living dwarf crocodiles (Osteolaemus). Character support for a close relationship withMecistopsis problematic, and we suspect a closer relationship toOsteolaemuswill be recovered with improved sampling, but the results here are ambiguous. In either case,Brochuchusis more closely related to living groups not currently found in East Africa. This material helps constrain the timing of crocodylian faunal turnover in the East African Rift Valley System, with endemic lineages largely being replaced byCrocodylusin the middle or late Miocene possibly in response to regional xerification and the replacement of continuous rainforest cover with open grasslands and savannas.UUID:http://zoobank.org/e6f0b219-5f3e-44e5-bdb9-60a4fae8d126

The “death roll” is an iconic crocodylian behaviour, and yet it is documented in only a small number of species, all of which exhibit a generalist feeding ecology and skull ecomorphology. This has led to the interpretation that only generalist crocodylians can death roll, a pattern which has been used to inform studies of functional morphology and behaviour in the fossil record, especially regarding slender-snouted crocodylians and other taxa sharing this semi-aquatic ambush predator body plan. In order to test this hypothesis, we surveyed death roll behaviour across animals representing all extant crocodylian species. Animals were prompted to death roll using two methods of stimulation: a feeding cue and an escape cue. The feeding cue involved presenting each animal with a bait item, to which resistance would be applied during a biting event. The second cue involved capturing each animal with a rope or catch pole, a standard technique for capturing crocodylians, but one that also often prompts an attempt to escape. All species tested, except Paleosuchus palpebrosus, exhibited the behaviour in response to at least one of the stimuli. This included the following slender-snouted species: Gavialis gangeticus, Tomistoma schlegelii, Mecistops cataphractus, Mecistops leptorhynchus, Crocodylus johnstoni, and Crocodylus intermedius. The patterns of death roll behavior observed in this survey suggest that this behaviour is not novel to any one crocodylian clade, morphotype, or dietary niche. Also, the prevalence of death rolling behaviour across Crocodylia in response to perceived threats indicates that it is not solely, or maybe even primarily, a feeding behaviour, but is also utilised during inter- and intra-specific conflict as a means to escape or injure an opponent. The results of this case study highlight the importance of using multiple modern analogues when attempting to correlate form and function across diverse clades, both living and extinct.

Several data loggers deployed to monitor temperature and humidity of Crocodylus acutus (American crocodile) nests in South Florida could not be located after hatching. One badly damaged data logger was retrieved, providing insight into the possible fate of the others. Using a taphonomic approach, we identified numerous indentations, consistent with crocodylian bite marks, and inconsistent with potential mammalian or squamate bites. It seems most likely that the data logger was damaged by the nesting C. acutus rather than during attempted nest predation. Estimated bite forces for reproductive age, female C. acutus exceed the predicted material properties of the data logger’s housing, suggesting that the bites were exploratory in nature. We suggest that data loggers be removed prior to hatching or permit remote data storage.

Captive broad snouted crocodylians are generally thought to have wider, shorter rostra than their wild counterparts. Interpreted to reflect morphological change in response to the conditions of captivity, this qualitative pattern could affect the utility of these animals in a variety of fields of research. However, due to relative ease of access and availability of life history data, captive animals are often utilized in actualistic research. Thus, this issue should be addressed in more detail. Here we explore snout shape variation between captive and wild members of Alligator mississippiensis using two-dimensional (2D) morphometric techniques. Several landmark schemesare used to assess the utility of different aspects of morphology in distinguishing the groups. While statistical analyses consistently differentiated between the groups, the area of morphospace occupied by wild members of A. mississippiensis generally overlapped with the larger area encompassing the captive specimens. This indicates that the captive condition is not as uniform as previously thought and instead encompasses a large spectrum of morphologies, ranging from the stereotypical broad, shortened snouts to outlines that are indistinguishable from the wild morphotype. These results align well with the interpretation that this change reflects an extreme example of ecophenotypy, since ranched, farmed, or zoo organisms are held in an array of enclosures, ranging from indoor, climate controlled pens to outdoor, more natural areas. This variation in environments should be reflected in different reactions to the animals' surroundings, resulting in a broad spectrum of morphotypes. While wild specimens are still preferred, especially for fine scale analyses, these results indicate that not all captive members of A. mississippiensis exhibit the extreme morphological alterations often cited in the literature. Weighing the conditions in which the animals are held and exploring the possibility of morphological differences against the benefits of using captive specimens should be part of any actualistic study. J. Morphol. 277:866-878, 2016. © 2016 Wiley Periodicals, Inc.

Crocodylians are known to consume and modify bones, but actualistic observations of their bite marks have been limited to forensic case studies and surveys of two taxa: Crocodylus niloticus and Crocodylus porosus. To further explore patterns of crocodylian bite mark expression, we conducted a survey of traces left by Alligator mississippiensis. We compared the results to pre-existing crocodylian datasets regarding the potentially diagnostic traits of bisected marks, hook scores, and a lack of furrows. Mark type did not correlate with vital statistics of the sampled animals or collections protocol. Bisected marks were found in rates similar to those seen in one previous survey of C. niloticus, and rates of hook scoring and bone breakage were higher. These traces were all present in higher rates than those reported in C. porosus. Unlike results seen in Crocodylus, furrows were identified in the A. mississippiensis samples. Hook scores were also identified, but recent surveys of non-crocodylian taxa have sho...

Crocodyliforms serve as important taphonomic agents, accumulating and modifying vertebrate remains. Previousdiscussions of Mesozoic crocodyliform feeding in terrestrial and riverine ecosystems have often focused on larger taxa and their interactions with equally large dinosaurian prey. However, recent evidence suggests that the impact of smaller crocodyliforms on their environments should not be discounted. Here we present direct evidence of feeding by a small crocodyliform on juvenile specimens of a ‘hypsilophodontid’ dinosaur from the Upper Cretaceous (Campanian) Kaiparowits Formation of southern Utah. Diagnostic crocodyliform bite marks present on a left scapula and a right femur, as well as a partial probable crocodyliform tooth crown (ovoid in cross-section) preserved within a puncture on the right femur, comprise the bulk of the feeding evidence. Computed tomography scans of the femoral puncture reveal impact damage to the surrounding bone and that the distal tip of the embedded tooth was missing prior to the biting event. This is only the second reported incidence of a fossil crocodyliform tooth being found embedded directly into prey bone. These bite marks provide insight into the trophic interactions of the ecosystem preserved in the Kaiparowits Formation. The high diversity of crocodyliforms within this formation may have led to accentuated niche partitioning, which seems to have included juvenile dinosaurian prey.