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Fish otolith stable isotope paleothermometry in the early Paleogene: limitations and future directions
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The climate of the early Paleogene is characterized by short-scale temperature variations which are superimposed on a general trend of rising temperatures culminating during the late early Eocene (early Eocene climatic optimum, EECO). These include several transient periods of abrupt climate warming or ‘hyperthermals’, such as the PETM (~55 Ma). Profound proxy development is needed to successfully extract shorter-scale variability from suitable records and unravel its underlying mechanisms. This study assesses and extends the use of fossil fish otolith O and C stable isotopes as a paleotemperature and seasonality proxy for early Paleogene marginal marine sedimentary environments. Well-known limitations include the lack of accurate estimates for the oxygen isotope composition of ambient water, and potential bias when applying paleotemperature equations. Moreover, taxon inconsistencies for both O and C were observed, complicating data interpretation (Vanhove et al., 2011). A single locality test case in the southern North Sea Basin has been performed to address this observation (Egem, Belgium, coastal sands). In each of four fossiliferous levels sampled, the same three demersal otolith species were analyzed (Platycephalus janeti, Paraconger papointi and “genus Neobythitinorum” subregularis). Cross-plots of δ18O and δ13C isotopes show three statistically different data clouds, corresponding to the three taxa. Several processes can cause such discrepancies. The most likely option is the influence of freshwater influx. According to this interpretation, Paraconger sp. and Platycephalus janeti lived in coastal areas prone to freshwater influx, while “genus Neobythitinorum” subregularis inhabited more distal realms. This is confirmed by similar analyses on Callista sp. and Venericardia sp. bivalves of the same locality, because these were deposited relatively in situ compared with otoliths, which predominantly arrive in the sediment after post-mortem predation-related transport. Taxon-sensitive differential diagenesis is disproved by SEM, cold cathodoluminescence and X-ray diffraction investigations, revealing the presence of pristine aragonite in all cases. Bias resulting from variability in the amount of summer or winter carbonate deposition is contradicted by visual inspection of growth ring thicknesses, and cyclical incremental stable isotope patterns of individual growth bands. Taxon inconsistencies were not described previously by authors working on the same taxa and in the same area, hence the paleoecological interpretation of this data could indicate enhanced runoff and freshwater influx during the EECO relative to later time intervals, or the presence of a large river mound close the investigated location. Temperature calculations based on “genus Neobythitinorum” subregularis reveal mean annual temperatures around 27.5 °C and a seasonality of 9 °C for the EECO interval. Given the mentioned assumptions, future directions should include other quantitative, preferably salinity-independent paleotemperature proxies to test these data interpretations. VANHOVE D., STASSEN P., SPEIJER R. P. and STEURBAUT E., 2011. Assessing paleotemperature and seasonality during the early Eocene climatic optimum (EECO) in the Belgian Basin by means of fish otolith stable O and C isotopes. Geologica Belgica, 14(3-4): 143-158.
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Variable benthic foraminiferal ecosystems responses to the PETM in shelf environments
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The Paleocene-Eocene thermal maximum (PETM) is characterized by a worldwide 5-8 °C warming of Earth’s surface as well as the deep oceans, major global faunal and floral turnovers and large changes in ocean chemistry. In order to establish clear biogeographic patterns of how shallow benthic foraminiferal communities responded to these climate changes, we compare shallow marine ecosystems in three separated regions and provide a synthesis of the short-term biotic responses. These regions are located in Tunisia (Northern and Gafsa Basin), Egypt (Nile Basin) and the North Atlantic Coastal Plain (Salisbury Embayment, United States). In Egypt, widespread anoxia during PETM peak warming led to the collapse of Paleocene deep shelf communities and a basin-wide downslope migration of pioneering shallow water taxa (A. aegyptiacus) during the initial recovery phase. In the shallower Tunisian settings, the PETM is marked by dysoxia, increased water depth and an elevated sedimentation rate. This resulted in the migration of deeper-dwelling species (lagenid and buliminid fauna) at the onset of the PETM, replacing the former shallow water community. At the onset of the PETM in the North Atlantic Coastal Plain, deposition occurred in a basin-wide mud belt, inhabited by opportunistic deep shelf taxa. Increased eutrophication, high sedimentation rates and widespread hypoxia are linked to the establishment of a river-dominated shelf during the PETM. As a result, in shallow and deep shelf settings, diverse Paleocene assemblages were replaced by characteristic river-outflow assemblages (P. prima, A. acutus, T. selmensis), either by upslope migration or increased abundances of these background taxa. Due to the magnitude and tempo of global warming, the PETM exerted worldwide environmental stress on benthic foraminiferal communities, triggering prominent transient changes in population structure and biodiversity, yet the evolutionary impact was minor compared to the deep-sea extinction event. This implies the existence of refugia on the shelves. In general, stable latest Paleocene benthic foraminiferal assemblages were abruptly replaced by more stress-tolerant faunas, reflecting stressed dysoxic to anoxic eutrophic environments, due to higher nutrient delivery (increased runoff and upwelling) and stratification. These hypoxic conditions occurred in the early stages of the PETM continually or with high frequencies and evolved towards periodic (seasonal?) oxygen depletion during the latter stages of peak warming or initial recovery. The final recovery phase reflects a reoxygenation of the sea floor and a distinctive buliminid bloom (B. callahani) occurred at both sides of the Atlantic Ocean. These eutrophic conditions remained stable and continued in the aftermath of the PETM, yet the oxygenation of bottom waters became restored. The PETM sequences thus document a progression of environmental regimes that is somewhat similar in all studied settings, indicating a widespread mutual response to the massive injection of carbon dioxide at the onset of the PETM.
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The onset of the negative Carbon Isotope Excursion on dispersed organic matter as criterion of the Paleocene-Eocene boundary: uses, biases and limits
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The primary criterion ratified by the International Subcommission on Paleogene Stratigraphy (ISPS) to define the Paleocene-Eocene (P/E) boundary, and the beginning of the Paleocene-Eocene Thermal Maximum (PETM), is the onset of a prominent negative Carbon Isotope Excursion (CIE; Aubry et al., 2007), located in the lower to middle part of Chron C24r, in calcareous nannofossil Zone NP9 and at the base of planktonic foraminiferal Zone E1 of Berggren & Pearson, 2005 (see also Wade et al., 2011), also termed Zone P5 in Aubry et al. (2007). Based on cyclostratigraphy, the CIE is estimated to have spanned 150 ± 20 kyr and would reflect a major perturbation of the global carbon cycle. Organic matter (OM) may be judged as a (very) reliable material for isotopic chemostratigraphy, in both marine and terrestrial settings. Here we show several examples of successions (Belgium, Egypt, France, Spain, Tunisia, USA-Wyoming) where: isotopic analyses on OM are necessary to define the P-E boundary (lack of carbonates and/or diagenetic 1. alteration of the isotopic signal on carbonates, including calcitic shells, bulk rocks and pedogenic nodules), organics are probably not the best material to precise the P-E boundary,2. geological processes, such as hiatuses, and potential reworking of OM in channels and turbidites, may per3. turb the reliability of the carbon isotope results (on both organics and carbonates). Aubry, M.P. et al., 2007. Episodes, 30, 271-286. Berggren, W. A., and Pearson, P. M., 2005, J. of Foraminiferal Research, 35/4, 279–298. Wade, B.S. et al. 2011, Earth Science Reviews 104, 111-142.
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Biotic and lithologic expressions of lower Paleogene hyperthermals in the Nile Basin, Egypt.
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Molecular and morphological evidence for several species within the cosmopolitan eurybathic deep-sea lysianassoid amphipod Eurythenes gryllus sensu lato
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Identification of forensically important Sarcophaga species (Diptera: Sarcophagidae) using the mitochondrial COI gene
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Towards a molecular reference database for the identification of forensically important Sarcophaga species (Diptera: Sarcophagidae)
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Towards a molecular database for the identification of forensically important Diptera in Belgium
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Molecular data elucidate species limits and some relationships of Ploceus weavers
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Using DNA barcodes for assessing diversity of dance flies (Diptera: Empidoidea) and as a basis for phylogenetic research
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