ALBERT

Description: We mapped, sampled, and quantified gas emissions at the continental margin west of Svalbard during R/V Heincke cruise He-387 in late summer 2012. Hydroacoustic mapping revealed that gas emissions were not limited to a zone just above 396 m below sea level (m b.s.l.). Flares from this depth gained significant attention in the scientific community in recent years because they may be caused by bottom water-warming induced hydrate dissolution in the course of global warming and/or by recurring seasonal hydrate formation and decay. We found that gas emissions occurred widespread between about 80 and 415 m b.s.l. which indicates that hydrate dissolution might only be one of several triggers for active hydrocarbon seepage in that area. Gas emissions were remarkably intensive at the main ridge of the forlandet moraine complex in 80 to 90 m water depths, and may be related to thawing permafrost. Focused seafloor investigations were performed with the remotely operated vehicle (ROV) "Cherokee". Geochemical analyses of gas bubbles sampled at about 240 m b.s.l. as well as at the 396 m gas emission sites revealed that the vent gas is primarily composed of methane (〉 99.70%) of microbial origin (average d13C = -55.7 per mil V-PDB). Estimates of the regional gas bubble flux from the seafloor to the water column in the area of possible hydrate decomposition were achieved by combining flare mapping using multibeam and single beam echosounder data, bubble stream mapping using a ROV-mounted horizontally-looking sonar, and quantification of individual bubble streams using ROV imagery and bubble counting. We estimated that about 53 × 10**6 mol methane were annually emitted at the two areas and allow a large range of uncertainty due to our method (9 to 118 × 10**6 mol yr**-1). These amounts, first, show that gas emissions at the continental margin west of Svalbard were in the same order of magnitude as bubble emissions at other geological settings, and second, may be used to calibrate models predicting hydrate dissolution at present and in the future, third, may serve as baseline (year 2012) estimate of the bubble flux that will potentially increase in future due to ever-increasing global-warming induced bottom water-warming and hydrate dissolution.

Description: We compared particle data from a moored video camera system with sediment trap derived fluxes at ~1100 m depth in the highly dynamic coastal upwelling system off Cape Blanc, Mauritania. Between spring 2008 and winter 2010 the trap collected settling particles in 9-day intervals, while the camera recorded in-situ particle abundance and size-distribution every third day. Particle fluxes were highly variable (40-1200 mg m**-2 d**-1) and followed distinct seasonal patterns with peaks during spring, summer and fall. The particle flux patterns from the sediment traps correlated to the total particle volume captured by the video camera, which ranged from1 to 22 mm**3 l**-1. The measured increase in total particle volume during periods of high mass flux appeared to be better related to increases in the particle concentrations, rather than to increased average particle size. We observed events that had similar particle fluxes, but showed clear differences in particle abundance and size-distribution, and vice versa. Such observations can only be explained by shifts in the composition of the settling material, with changes both in particle density and chemical composition. For example, the input of wind-blown dust from the Sahara during September 2009 led to the formation of high numbers of comparably small particles in the water column. This suggests that, besides seasonal changes, the composition of marine particles in one region underlies episodical changes. The time between the appearance of high dust concentrations in the atmosphere and the increase lithogenic flux in the 1100 m deep trap suggested an average settling rate of 200 m d**-1, indicating a close and fast coupling between dust input and sedimentation of the material.