In December 2002, large numbers of dead jellyfish, Crambionella orsini, were observed on the seabed over a wide area of the Arabian Sea off the coast of Oman at depths between 300 m and 3,300 m. Moribund jellyfish were seen tumbling down the continental slope. Large aggregations of dead jellyfish were evident within canyons and on the continental rise. At the deepest stations, patches of rotting, coagulated jellyfish occurred. The patches were several meters in diameter, at least 7-cm thick, and covered about 17% of the sediment surface. At other locations on the continental rise the seafloor was covered in a thin, almost continuous, layer of jelly ''slime'' a few millimeters thick or was littered with individual jellyfish corpses. Photographic transects were used to estimate the amount of carbon associated with the jelly detritus. The standing stock of carbon (C) varied between 1.5 g C m 22 and 78 g C m 22 , the higher figure exceeding the annual downward flux of organic carbon, as measured by sediment traps, by more than an order of magnitude. The episodic nature of jellyfish blooms, which may be modulated by global change phenomena, provides a hitherto unknown mechanism for large-scale spatial and temporal patchiness in deep-sea benthic ecosystems.

No abstract

Abstract. The morphology and structure of the submarine flanks of the Canary Islands were mapped using the GLORIA long-range side-scan sonar system, bathymetric multibeam systems, and sediment echosounders. Twelve young (<2 Ma) giant landslides have been identified on the submarine flanks of the Canary Islands up to now. Older landslide events are long buried under a thick sediment cover due to high sedimentation rates around the Canary Islands. Most slides were found on the flanks of the youngest and most active islands of La Palma, E1 Hierro, and Tenerife, but young giant landslides were also identified on the flanks of the older (15-20 Ma) but still active eastern islands. Large-scale mass wasting is an important process during all periods of major magmatic activity. The long-lived volcanic constructive history of the islands of the Canary Archipelago is balanced by a co•rrespondingly long history of destruction, resulting in a higher landslide frequency for the Canary Islands compared to the Hawaiian Islands, where giant landslides only occur late in the period of active shield growth. The lower stability of the flanks of the Canaries is probably due to the much steeper slopes of the islands, a result of the abundance of highly evolved intrusive and extrusive rocks. Another reason for the enhanced slope instability is the abundance of pyroclastic deposits on Canary Islands resulting from frequent explosive eruptions due to the elevated volatile contents in the highly alkalic magmas. Dike-induced rifting is most likely the main trigger mechanism for destabilization of the flanks. Flank collapses are a major geological hazard for the Canary Islands due to the sector collapses themselves as well as triggering of tsunamis. In at least one case, a giant lateral blast occurred when an active magmatic or hydrothermal system became unroofed during flank collapse.

In 2009 the NW and SE flanks of Anton Dohrn Seamount were surveyed using multibeam echosounder and video ground-truthing to characterise megabenthic biological assemblages (biotopes) and assess those which clearly adhere to the definition of Vulnerable Marine Ecosystems, for use in habitat mapping. A combination of multivariate analysis of still imagery and video ground-truthing defined 13 comprehensive descriptions of biotopes that function as mapping units in an applied context. The data reveals that the NW and SE sides of Anton Dohrn Seamount (ADS) are topographically complex and harbour diverse biological assemblages, some of which agree with current definitions of ‘listed’ habitats of conservation concern. Ten of these biotopes could easily be considered Vulnerable Marine Ecosystems; three coral gardens, four cold-water coral reefs, two xenophyophore communities and one sponge dominated community, with remaining biotopes requiring more detailed assessment. Coral gardens were only found on positive geomorphic features, namely parasitic cones and radial ridges, found both sides of the seamount over a depth of 1311–1740 m. Two cold-water coral reefs (equivalent to summit reef) were mapped on the NW side of the seamount; Lophelia pertusa reef associated with the cliff top mounds at a depth of 747–791 m and Solenosmilia variabilis reef on a radial ridge at a depth of 1318-1351 m. Xenophyophore communities were mapped from both sides of the seamount at a depth of 1099–1770 m and were either associated with geomorphic features or were in close proximity (< 100 m) to them. The sponge dominated community was found on the steep escarpment either side of the seamount over at a depth of 854-1345 m. Multivariate diversity revealed the xenophyophore biotopes to be the least diverse, and a hard substratum biotope characterised by serpulids and the sessile holothurian, Psolus squamatus, as the most diverse.

No abstract