Zooarchaeological collections from shell mounds in Rio de Janeiro (2,470-4,632 cal BP) contain a high prevalence of swollen fish bones belonging to the Atlantic spadefish (Chaetodipterus faber), crevalle jack (Caranx hippos) and fat snook (Centropomus parallelus). Given the lack of knowledge of the bone degenerative process in senile fishes, this study analysed hyperostotic bone in zooarchaeological and modern specimens to obtain high-resolution morphology and microstructure reconstruction. We used microCT as well as X-ray diffraction to characterize the crystallographic changes associated with fish senility. Our results showed that trabecular microstructures in hyperostotic bones were consistent with estimated values of the per cent bone volume-to-total volume ratio (BV/TV) and were greater than 60% in cortical bone. Hyperostotic bones indicated a high radiograph density, and X-ray diffractograms showed a decrease in hydroxyapatite [Ca (PO ) (OH) ] and calcite (CaCO ) neocrystallization. These crystalline and density changes revealed an advanced stage of fish senile and indicate the vulnerability of ageing fish populations.
Ancient and modern stromatolites are potentially a challenge for petrophysicists when characterizing biosediments of microbial origin. Because of the heterogeneity, sometimes very cemented and lacking porosity, sometimes highly porous, these widely differing states can be used to develop techniques that can have wider application to addressing the representative elementary volume (REV -single or multiple REVs) challenge in microbial carbonates. Effective media properties -like porosity -need to be defined on REV scales and the challenge is that this scale is often close to or significantly larger than the traditional core plugs on which properties are traditionally measured. A combination of outcrop images, image analysis techniques, micro-computed tomography (CT) and modelling have been used to capture the porosity (or in some cases, precursor porosity) architecture and provide a framework for estimating petrophysical property sensitivities in a range of situations that can be subjected to further calibration by measurements in relevant microbial reservoir rocks. This work will help guide the sampling approach along with the interpretation and use of petrophysical measurements from microbial carbonates. The bioarchitectural component, when controlling porosity in microbial carbonates, presents a significant challenge as the REV scale is often much larger than core plugs, requiring careful screening of existing data and measurement and additional geostatistical model-based approaches (with further calibration).
Fossil Diodontidae in Tropical America consist mostly of isolated and fused beak-like jawbones, and tooth plate batteries. These durophagous fishes are powerful shell-crushing predators on shallow water invertebrate faunas from Neogene tropical carbonate bottom, rocky reefs and surrounding flats. We use an ontogenetic series of high-resolution micro CT of fossil and extant species to recognize external and internal morphologic characters of jaws and tooth plate batteries. We compare similar sizes of jaws and/or tooth-plates from both extant and extinct species. Here, we describe three new fossil species including †Chilomycterus exspectatus n. sp. and †Chilomycterus tyleri n. sp. from the late Miocene Gatun Formation in Panama, and †Diodon serratus n. sp. from the middle Miocene Socorro Formation in Venezuela. Fossil Diodontidae review included specimens from the Neogene Basins of the Proto-Caribbean (Brazil: Pirabas Formation; Colombia: Jimol Formation, Panama: Gatun and Tuira formations; Venezuela: Socorro and Cantaure formations). Diodon is present in both the Atlantic and Pacific oceans, whereas the distribution of Chilomycterus is highly asymmetrical with only one species in the Pacific. It seems that Diodon was as abundant in the Caribbean/Western Atlantic during the Miocene as it is there today. We analyze the paleogeographic distribution of the porcupinefishes group in Tropical America, after the complete exhumation of the Panamanian isthmus during the Pliocene.
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