Search results for "GIA"
showing 10 items of 33231 documents
Growth patterns and life-history strategies in Placodontia (Diapsida: Sauropterygia)
2015
Placodontia is a clade of durophagous, near shore marine reptiles from Triassic sediments of modern-day Europe, Middle East and China. Although much is known about their primary anatomy and palaeoecology, relatively little has been published regarding their life history, i.e. ageing, maturation and growth. Here, growth records derived from long bone histological data of placodont individuals are described and modelled to assess placodont growth and life-history strategies. Growth modelling methods are used to confirm traits documented in the growth record (age at onset of sexual maturity, age when asymptotic length was achieved, age at death, maximum longevity) and also to estimate undocum…
New Bovid Remains from the Early Pleistocene of Umbria (Italy) and a Reappraisal of Leptobos merlai
2017
The extinct bovid Leptobos is one of the most characteristic elements of Eurasian faunal assemblages during most of the Villafranchian Land Mammal Age (i.e., from the late Pliocene to most of the early Pleistocene). Several species of this genus have been established since the end of XIX Century, but their taxonomic status and phylogenetic relationships remain unclear due to the fact that most of them are described on the basis of scanty material. European species are divided into two groups or lineages. The first includes L. stenometopon, L. merlai, and the poorly known L. furtivus, the second L. etruscus and L. vallisarni. While the last two species are well documented in the Italian earl…
The evolution of gigantism in active marine predators
2017
A novel hypothesis to better understand the evolution of gigantism in active marine predators and the diversity of body sizes, feeding strategies and thermophysiologies of extinct and living aquatic vertebrates is proposed. Recent works suggest that some aspects of animal energetics can act as constraining factors for body size. Given that mass-specific metabolic rate decreases with body mass, the body size of active predators should be limited by the high metabolic demand of this feeding strategy. In this context, we propose that shifts towards higher metabolic levels can enable the same activity and feeding strategy to be maintained at bigger body sizes, offering a satisfactory explanatio…
Biomechanical insights into the dentition of megatooth sharks (Lamniformes: Otodontidae)
2021
AbstractThe evolution of gigantism in extinct otodontid sharks was paralleled by a series of drastic modifications in their dentition including widening of the crowns, loss of lateral cusplets, and acquisition of serrated cutting edges. These traits have generally been interpreted as key functional features that enabled the transition from piscivory to more energetic diets based on marine mammals, ultimately leading to the evolution of titanic body sizes in the most recent forms (including the emblematic Otodus megalodon). To investigate this hypothesis, we evaluate the biomechanics of the anterior, lateral, and posterior teeth of five otodontid species under different loading conditions by…
Patterns of ecological diversification in thelodonts
2018
Here we explore the spatial, temporal and phylogenetic patterns of ecological diversification for the entire clade of thelodonts, one of the earliest groups of vertebrates and longest lasting of the Palaeozoic agnathans in the fossil record. Parsimony and maximum-likelihood methods are used to reconstruct ancestral states of their geographical distributions, habitats and lifestyles. Our results support the concept that thelodonts originated during the Middle?-Late Ordovician probably in marine open waters of Laurasia, with a demersal lifestyle on hard substrates being the ancestral condition for the whole clade. Later, thelodonts underwent a complex ecological diversification and palaeobiog…
Categorical versus geometric morphometric approaches to characterizing the evolution of morphological disparity in Osteostraci (Vertebrata, stem Gnat…
2020
Morphological variation (disparity) tends to be evaluated through two non-mutually exclusive approaches: (i) quantitatively, through geometric morphometrics, and (ii) in terms of discrete, ‘cladistic’, or categorical characters. Uncertainty over the comparability of these approaches diminishes the potential to obtain nomothetic insights into the evolution of morphological disparity, and the few benchmarking studies conducted so far show contrasting results. Here, we apply both approaches to characterising morphology in the stem-gnathostome vertebrate clade Osteostraci, in order to assess congruence between these alternative methods as well as to explore the evolutionary patterns of the grou…
Assessing metabolic constraints on the maximum body size of actinopterygians: locomotion energetics of Leedsichthys problematicus (Actinopterygii, Pa…
2018
Maximum sizes attained by living actinopterygians are much smaller than those reached by chondrichthyans. Several factors, including the high metabolic requirements of bony fishes, have been proposed as possible body‐size constraints but no empirical approaches exist. Remarkably, fossil evidence has rarely been considered despite some extinct actinopterygians reaching sizes comparable to those of the largest living sharks. Here, we have assessed the locomotion energetics of Leedsichthys problematicus, an extinct gigantic suspension‐feeder and the largest actinopterygian ever known, shedding light on the metabolic limits of body size in actinopterygians and the possible underlying factors th…
Use of nursery areas by the extinct megatooth shark Otodus megalodon (Chondrichthyes: Lamniformes)
2020
Nursery areas are fundamental for the success of many marine species, particularly for large, slow-growing taxa with low fecundity and high age of maturity. Here, we examine the population size-class structure of the extinct gigantic shark Otodus megalodon in a newly described middle Miocene locality from Northeastern Spain, as well as in eight previously known formations (Temblor, Calvert, Pisco, Gatún, Chucunaque, Bahía Inglesa, Yorktown and Bone Valley). In all cases, body lengths of all individuals were inferred from dental parameters and the size-class structure was estimated from kernel probability density functions and Gaussian mixture models. Our analyses support the presence of fi…
Evidence of endothermy in the extinct macropredatory osteichthyan Xiphactinus audax (Teleostei, Ichthyodectiformes)
2020
Xiphactinus audax is the largest macropredatory osteichthyan ever known (Everhart et al., 2010). Some of the largest specimens exceed 5 m in total length, although the discovery of a few large, isolated teeth suggests that this teleost could reach even larger body sizes (Vavrek et al., 2016, and references therein). Fossil remains of this species have only been reported from the Upper Cretaceous of North America, across the Western Interior Basin (Schwimmer et al., 1997; Vavrek et al., 2016). The discovery of several virtually complete individuals in this area has provided valuable information about the anatomy, the dimensions, and the ecology of this species (Cope, 1872; Bardack, 1965). Xi…
Nomenclatural revision concerning some genera of the Order Trigoniida (Bivalvia)
2018
The authors have become aware of a couple of nomenclatural conflicts involving Mesozoic trigoniid genera, which are in need of clarification and proposal of replacement names: The case of Protrigonia. The subgenus Trigonia (Protrigonia) Guo, 1985 (p. 204, 269; type species Trigonia (Protrigonia) yunnanensis Guo, 1985), was proposed to encompass those species referred to the genus Trigonia which, according to that author, have small and nearly smooth shells and relatively weak teeth. Guo (1985) also included other Triassic species: Trigonia gaytani (von Klipstein, 1843) and Trigonia zlambachiensis Haas, 1909. According to Fang et al. (2009, p. 55) there was a wrong translation from the Chine…