Heterogeneity of free and occluded bitumen in a natural maturity sequence from Oligocene Lake Enspel

Sedimentation in Oligocene Lake Enspel was rapidly terminated by a basaltic lava flow. This introduced a preservational barrier while imparting a ‘natural flash pyrolysis’, during which the organic matter in underlying stratigraphic units was subjected to rapid thermal maturation resulting in hydrocarbon generation. Samples from these strata exhibit a steep maturity gradient (0.25–1.07% optical vitrinite reflectance, or RO) over uniform organofacies. This offers the opportunity to investigate bitumen generation during rapid thermal maturation mechanistically, in particular the nature of Bitumen 2—occluded bitumen, which is only recoverable after the digestion of the mineral matrix and was frequently dismissed as an artifact of incomplete extraction. Elaborate sequential extraction of the contact metamorphic sequence of oil shales at Enspel revealed systematic changes in bitumen composition. These trend progressively towards those of occluded bitumen, which exhibits a systematically elevated thermal maturity, a higher degree of catalytic biomarker-rearrangement and the conspicuous absence of molecular signatures from vascular plants that are present in the free bitumen. One plausible explanation involves a contribution of allochthonous clay-adsorbed organic matter to Bitumen 2. This could represent a mixture of older reworked bitumen and an early-diagenetic snapshot of clay adsorbed organic matter. Alternatively, a close association of early-generated bitumen with clay minerals may have led to enhanced isomerization and catalytically influenced ‘uniformization’ of alkane signatures. Deviations from the expected relationships between various thermal maturity parameters suggest variable dependence on the time-pressure-temperature pathway (i.e. metamorphic facies). The maturation of organic matter likely behaves differently under a contact metamorphic regime or during rapid subsidence and exhumation, as compared to slow maturation during regional subsidence. Our data also suggest that geologically brief shallow intrusive or extrusive magmatism might not be as destructive to the sedimentary hydrocarbon inventory as hitherto thought. This study draws attention to the small-scale compositional heterogeneity of bitumen that can be studied using sequential extraction methods. More importantly, it suggests that occluded bitumen could potentially harbor information on organic matter that pre-dates in situ primary productivity and may be derived from allochthonous biomass and detrital input

Increasing flood risk awareness and warning readiness by participation – But who understands what under ‘participation’?

Participation is an often-demanded process in disaster risk reduction (DRR). However, it is often unclear who understands what under this term. International organizations such as the United Nations have promoted participation in their DRR strategies since the 1980s, but further research is needed on its opportunities and limitations. Here we highlight what is understood by participation according to different actors and various international contexts. This study was motivated by a workshop where flood-risk and resilience experts from 14 countries perceived the nature of participation and the lack of its implementation differently. To unravel the multitude of these perspectives, 27 expert interviews were conducted in seven countries: Belgium, Germany, Indonesia, Iran, Nepal, Pakistan and Peru between March and August 2020. Results show that constraints on the conduction of participation are not only related to the specific country context but differ even within countries. Limitations such as capacities and willingness to participate as well as the role and importance of participation are common issues across the investigated contexts and countries

Clay - leachate interaction: a first insight

peer reviewe

Differentiation of Opioid Drug Effects by Hierarchical Multi-Site Phosphorylation

Differences in the ability of opioid drugs to promote regulated endocytosis of μ-opioid receptors are related to their tendency to produce drug tolerance and dependence. Here we show that drug-specific differences in receptor internalization are determined by a conserved, 10-residue sequence in the receptor’s carboxyl-terminal cytoplasmic tail. Diverse opioids induce receptor phosphorylation at serine (S)375, present in the middle of this sequence, but opioids differ markedly in their ability to drive higher-order phosphorylation on flanking residues [threonine (T)370, T376, and T379]. Multi-phosphorylation is required for the endocytosis-promoting activity of this sequence and occurs both sequentially and hierarchically, with S375 representing the initiating site. Higher-order phosphorylation involving T370, T376, and T379 specifically requires GRK2/3 isoforms, and the same sequence controls opioid receptor internalization in neurons. These results reveal a biochemical mechanism differentiating the endocytic activity of opioid drugs

Differentiation of Opioid Drug Effects by Hierarchical Multi-Site Phosphorylation

Differences in the ability of opioid drugs to promote regulated endocytosis of μ-opioid receptors are related to their tendency to produce drug tolerance and dependence. Here we show that drug-specific differences in receptor internalization are determined by a conserved, 10-residue sequence in the receptor's carboxyl-terminal cytoplasmic tail. Diverse opioids induce receptor phosphorylation at serine (S)375, present in the middle of this sequence, but opioids differ markedly in their ability to drive higher-order phosphorylation on flanking residues [threonine (T)370, T376, and T379]. Multi-phosphorylation is required for the endocytosis-promoting activity of this sequence and occurs both sequentially and hierarchically, with S375 representing the initiating site. Higher-order phosphorylation involving T370, T376, and T379 specifically requires GRK2/3 isoforms, and the same sequence controls opioid receptor internalization in neurons. These results reveal a biochemical mechanism differentiating the endocytic activity of opioid drugs