Search results

Raman spectroscopy is an interesting tool to assess the thermal maturity of solid organic matter. For carbonaceous material with moderate to high maturities, several studies have found good correlations between Raman spectral parameters and thermal maturity, expressed as vitrinite reflectance (VR) or bitumen reflectance (BR). However, at low maturities a large part of the Raman peaks is lost under an intense background radiation, caused by fluorescence. This fluorescence problem mainly occurs at 0.4-1.0% VR (the oil window), and makes it difficult to recognize the original spectrum. In this study, Raman parameters that have been put forward in literature were tested on a low maturity, solid bitumen sample of approximately 0.61% BR. The investigated parameters include the peak’s full width at half maximum FWHM, peak position W, peak area A, area ratio AD/AG and intensity ratio ID/IG. Fluorescence in this sample is very high and covers Raman peaks. It was found that during consecutive measurements at a single location (i.e. irradiation with the Raman laser), fluorescence decreases with time and Raman peaks appear. This is in line with Quirico et al. (2005), who observed the same effect at coal measurements. An interesting observation is the behaviour of Raman parameters during ongoing irradiation. The full widths at half maximum do not change at all for every investigated peak in our spectra. Also peak positions remain the same. The peak areas do change with irradiation, and show a decrease with decreasing fluorescence. Comparison of areas under individual peaks and total spectrum area however suggests that A and fluorescence decrease at equal speeds. This is the case for most important Raman peaks at 1370 (D-band), 1600 (G-band) and 3200 cm-1, with correlation coefficients of 0.66, 0.97 and 0.92 respectively. Lastly, the area ratio AD/AG and intensity ratio ID/IG(approximation) show no trend with fluorescence, indicating that the shape of the spectrum remains the same with irradiation. This is a promising result, because it suggests that fluorescence can be controlled without changing spectral parameters. Although not all peak parameters in this study (FWHM and AD/AG) correspond to parameters from literature regarding maturity, the behaviour of the Raman peak parameters in combination with the decreasing fluorescence is an exciting outcome. If further research proves that the original parameters are not altered by irradiation, this will provide an answer to the problem of fluorescence at low maturity samples.

1) SUMMARY a) Context The improvement of our understanding of ecological processes and the role of biodiversity in the Southern Ocean ecosystems remains a high priority on the research agenda in today’s changing world and is inextricably linked to sustainable development policies on a global scale. Global environmental changes influence species distributions and consequently the structure of communities and ecosystems. Only advances in our knowledge of the Southern Ocean biodiversity and processes important for ecosystem functioning can allow us to address complex evolutionary and ecological questions and enable estimations of the expected change of the biota distribution and composition. Polar regions experience greater rates of global change than any other region in the world. Their biota are highly adapted to the extreme environment they are living in and appear vulnerable to shifts in environmental conditions. Antarctic marine species are especially more sensitive to temperature variation as their physiology is set to a narrow range of temperatures. Also changes in food quality and quantity, together with other environmental shifts such as in pH of the seawater, are likely to impact densities, biomass and community composition but also functional aspects of the Antarctic biota. Because of the key-role of the Southern Ocean for the global ocean system and the growing impact of global environmental change, it is crucial to establish comprehensive baseline information on Antarctic marine biodiversity as a sound benchmark against which future change can be assessed reliably. It is equally important to understand better the ability of taxa to cope with changes in environmental parameters (temperature, pH, ice cover, food quantity and quality) linked to global change, and this from the individual to the community level. Imperative in this approach is to assess how structural and functional characteristics of the biota may be affected by a changing climate. Finally, advanced integrative spatial modelling of the distribution of key species in relation to environmental conditions is needed to predict the future of the marine ecosystems related to climate change. These aspects are addressed in the Bianzo II project by focusing on benthic organisms and communities, specifically representatives from three different size classes of the zoobenthos: Nematoda (meiobenthos), Amphipoda (macrobenthos) and Echinoidea (megabenthos). These three groups are characterised by a high diversity and many of the well over 4000 Antarctic benthic species described so far (Clarke & Johnston, 2003) belong to these taxa. These three selected benthic taxa are also ecologically important in terms of biomass, their role in biogeochemical cycles (C and N) and the trophic role they fulfil in the benthic ecosystem. Furthermore, they are characterised by different biogeographical and diversity patterns, speciation mechanisms, and reproductive and dispersal strategies. Because of these differences and the intrinsic ecological variability between these taxa, it is difficult to assess the extent to which global change will affect the Antarctic benthos in general. Rarely do biodiversity and ecological studies focus on multiple benthic groups. Yet, combining putative size groups in ecological/biodiversity research is imperative to understand the benthic ecosystem as a complex and interactive unity. b) Objectives Climate change and its complex and interactive chain of associated effects will affect the physiology, distribution, phenology, and ontogeny of many Antarctic benthic organisms, but the resulting changes from the species to the community level remain poorly quantified and understood. Individual species may appear vulnerable to environmental shifts or regime changes, but community and ecosystem responses may not act accordingly. Therefore we investigated the biodiversity and responses of the three representative groups of benthic organisms to climate change effects from individual species, over populations, up to the community level During its first phase (2007-2008), BIANZO II aimed at investigating (1) biodiversity patterns of the Antarctic zoobenthos and their causal processes by focussing on the three selected benthic groups (Work package 1: NOWBIO); Furthermore (2) trophodynamic aspects of each of the benthic groups, and their ability to cope with temperature and temperature-related changes (i.e. food composition and availability) but also the effect of pH of the seawater were on the benthos (Work package 2: DYNABIO). In the second phase (2009-2010) of the project, a joint review paper dealing with the effects of global climate change on the Antarctic zoobenthos is being written, based on the results of experiments, field results and literature data. Information collected in previous studies and in the first two work packages of this project was also used to develop a habitat suitability model in order to identify the drivers of benthic distribution patterns and forecast possible changes of benthic communities related to global change (Work package 3: FOREBIO). c) Conclusions i) NOWBIO (1) Benthic biodiversity in new ice free habitats Due to large-scale ice-shelf disintegration events, the Antarctic Larsen A and B areas along the Eastern Antarctic Peninsula recently became ice-free. Our study is the first one to investigate benthic communities and their response to the collapse of ice shelves in this area. At the time of sampling, meiofauna community structure at the inner stations, most remote from the original ice margin, was not or only slightly influenced by colonization, and might be structured by local environmental conditions. Communities living close to the former ice-shelf edge are believed to be at an intermediate or late stage of succession. Densities and diversity here were comparable to those at other more northern Antarctic stations in the Weddell Sea, whereas they were considerably lower at the inner stations. The three echinoid species collected in Larsen A&B areas are good candidates as pioneering species in a changing marine environment. They are known as indirect developers (or at least non-brooders), consistent with high dispersal capabilities. Moreover, this is congruent with the wide Antarctic distribution of these species. These examples stand in contrast to other Antarctic echinoids which are known as direct developers that brood their young and, accordingly, are supposed to present low dispersal capacities. The three Larsen species also display a ‘generalist’ feeding behaviour which can also be considered a characteristic of pioneering species. Furthermore, the symbiotic communities of echinoids in the Larsen area showed a low diversity and a strong similarity with epibionts present on stones, something which has not been observed in other regions so far. These results suggest that ectosymbioses linked to cidaroids could contribute to benthic colonization of the seafloor in these new ice free areas. The Larsen ice-shelf disintegration also led to the discovery of a low-activity methane seep. The observation of elevated densities, subsurface maxima and high dominance of one nematode species was similar to other cold-seep ecosystems world-wide and suggested a dependence on a chemosynthetic food source. However, stable 13C isotopic signals were indicative of phytoplankton-based feeding. This implied that the community was in transition from a chemosynthetic community to a classic phytodetritus feeding community, a temporary ecotone as it were. The characteristic parthenogenetic reproduction of the dominant species is rather unusual for marine nematodes and may be responsible for the successful colonisation by this single species.

The International Council for the Exploration of the Sea (ICES; French: Conseil International pour l'Exploration de la Mer, CIEM) is an intergovernmental marine science organization that brings together the efforts and knowledge of 20 Member States, bordering the North Atlantic and the Arctic Circumpolar Zone, on physical oceanography, marine ecosystems and fisheries management. Nowadays, more than 80 Belgian scientists are directly involved in the work of the 150 bodies and expert groups of ICES, which gather the expertise of more than 1500 scientists yearly, totalling up to 5000 scientists from over 700 marine institutes and organizations over the years. This important and often voluntary dedication of Belgian scientists to the work of ICES deserves more visibility among the Belgian scientific community itself and to policy makers.This is, among others, why the BICEpS initiative was launched in 2018. BICEpS general aim is to offer a platform to the Belgian ICES community to get to know each other, to improve collaboration and share information, and to promote ICES to the wider scientific community in Belgium. BICEpS Annual report 2019 presents the second year of activity of this initiative created to reinforce Belgian ICES people. The report targets marine scientists, marine managers and policy makers. It presents the results of the initiative so far. The report contains the list of Belgian ICES members in 2019 with their membership to the different ICES working groups, and the results of the second BICEpS Colloquium organised on 2 December 2019 and hosted by ILVO in Ghent (Summary of the sessions, abstracts of communications presented and list of participants). The abstracts of the colloquium are supplemented by a separate annex published online which assembles the PowerPoint presentations of the colloquium accessible at http://ices.dk/community/groups/Documents/BICEPS/BICEpS19-PPT-presentations.pdf This report is accessible on the ICES website at http://ices.dk/community/groups/Pages/BICEpS.aspx