Chlorophyll and true-color maps of sediments from the intertidal zones in Winyah Bay, South Carolina, USA and List, Sylt, Germany

We used hyperspectral imaging to study short-term effects of bioturbation by lugworms (Arenicola marina) on the surficial biomass of microphytobenthos (MPB) in permeable marine sediments. Within days to weeks after the addition of a lugworm to a homogenized and recomposed sediment, the average surficial MPB biomass and its spatial heterogeneity were, respectively, 150 - 250% and 280% higher than in sediments without lugworms. The surficial sediment area impacted by a single medium-sized lugworm (~4 g wet weight) over this time-scale was at least 340 cm**2. While sediment reworking was the primary cause of the increased spatial heterogeneity, experiments with lugworm-mimics together with modeling showed that bioadvective porewater transport from depth to the sediment surface, as induced by the lugworm ventilating its burrow, was the main cause of the increased surficial MPB biomass. Although direct measurements of nutrient fluxes are lacking, our present data show that enhanced advective supply of nutrients from deeper sediment layers induced by faunal ventilation is an important mechanism that fuels high primary productivity at the surface of permeable sediments even though these systems are generally characterized by low standing stocks of nutrients and organic material.

Global Homogeneous Response Units

The concept of homogenous response units (HRU) was designed as a general concept for the delineation of basic spatial units. Only those characteristics of landscape, which are relatively stable over time (even under climate change) and largely unsusceptible to anthropogenic influence, were selected. The HRU can be seen as a basic spatial framework for the implementation of climate change and land management alternative scenarios into global modeling and therefore is a basic input for delineation of landscape units. HRUs are defined based on classifications of altitude (five classes: 1 (0 - 300m), 2 (300 - 600m), 3 (600 - 1100m), 4 (1100 - 2500m), 5 (> 2500m)), slope (seven classes(degrees): 1 (0 - 3), 2 (3 - 6), 3 (6 - 10), 4 (10 - 15), 5 (15 - 30), 6 (30 - 50), 7 (> 50)) and soil composition (five classes: 1 (sandy), 2 (loamy), 3 (clay), 4 (stony), 5 (peat)). e.g. HRU111 refers to Altitude class 1: 0-300m; Slope class 1: 0-3 degrees; and Soil class 1: sandy. Areas of non-soil are assigned 88. HRUs have a spatial resolution of approximately 10 km**2.

(Table 2) Correlation of Mi zones with hiatuses in ODP Site 181-1124

Results from Ocean Drilling Program sites 1121-1124 show the Eastern New Zealand Oceanic Sedimentary System (ENZOSS) evolved in response to: (1) the inception of the circum-Antarctic circulation, (2) orbital and nonorbital regulation of the global thermohaline flow, and (3) development of the New Zealand plate boundary. ENZOSS began in the early Oligocene following opening of the Tasmanian gateway and inception of the ancestral Antarctic Circumpolar Current (ACC) and SW Pacific Deep Western Boundary Current (DWBC). Widespread erosion, marked by the Marshall Paraconformity, was followed by extensive drift formation in the late Oligocene- early Miocene. Alternating nannofossil chalk and nannofossil-rich mud deposited in response to 41-kyr orbital regulation of the abyssal circulation, with the mudstones representing times of increased inflow of corrosive southernsource waters. Drift deposition at the deepest sites was interrupted by bouts of erosion coincident with Mi 1-5 isotopic events signifying expansions of the East Antarctic Ice Sheet and enhanced bottom water formation. By late Miocene times, the basic ENZOSS was established. South of Bounty Trough, the energetic ACC instigated an erosional/low depositional regime. To the north, where the DWBC prevailed, orbitally regulated drift deposition continued. Increased convergence at the New Zealand plate boundary enhanced the terrigenous supply, but little of this sediment reached the deep ENZOSS as the three main sediment conduits - Solander, Bounty and Hikurangi channels - had not fully developed. The Plio-Pleistocene heralded a change from a carbonate- to terrigenous-dominant supply caused by interception of the DWBC by the three channels (~1.6 Ma for Bounty and Hikurangi, time of Solander interception unknown). The Solander and Bounty fans, and Hikurangi Fan-drift systems formed, and drifts downstream of those systems, received terrigenous detritus. Supply increased with accelerating uplift along the plate boundary, but delivery to the DWBC was regulated by eustatic fluctuations of sea level. Times of maximum supply to all three channels was during glacial lowstands whereas the supply either ceased (Bounty, Solander), or reduced (Hikurangi) in highstands. In glacial times, sediment was entrained by a DWBC invigorated by an increased input of Antarctic bottom water. The ACC also accelerated under strengthened glacial winds. Thus, glacials were times of optimum sediment supply to ENZOSS depocentres where depositional rates were 2-3 times more than interglacial rates.

Response of three krill species to hypoxia and warming: An experimental approach to oxygen minimum zones expansion in coastal ecosystems

To understand the adaptation of euphausiid (krill) species to oxygen minimum zones (OMZ), respiratory response and stress experiments combining hypoxia/reoxygenation exposure with warming were conducted. Experimental krill species were obtained from the Antarctic (South Georgia area), the Humboldt Current system (HCS, Chilean coast), and the Northern California Current system (NCCS, Oregon). Euphausia mucronata from the HCS shows oxyconforming or oxygen partial pressure (pO2)-dependent respiration below 80% air saturation (18 kPa). Normoxic subsurface oxygenation in winter posed a "high oxygen stress" for this species. The NCCS krill, Euphausia pacifica, and the Antarctic krill, Euphausia superba maintain respiration rates constant down to low critical pO2 values of 6 kPa (30% air saturation) and 11 kPa (55% air saturation), respectively. Antarctic krill had the lowest antioxidant enzyme activities, but the highest concentrations of the molecular antioxidant glutathione (GSH) and was not affected by 6 h exposure to moderate hypoxia. Temperate krill species had higher SOD (superoxide dismutase) values in winter than in summer, which relate to higher winter metabolic rate (E. pacifica). In all species, antioxidant enzyme activities remained constant during hypoxic exposure at habitat temperature. Warming by 7°C above habitat temperature in summer increased SOD activities and GSH levels in E. mucronata (HCS), but no oxidative damage occurred. In winter, when the NCCS is well mixed and the OMZ is deeper, +4°C of warming combined with hypoxia represents a lethal condition for E. pacifica. In summer, when the OMZ expands upwards (100 m subsurface), antioxidant defences counteracted hypoxia and reoxygenation effects in E. pacifica, but only at mildly elevated temperature (+2°C). In this season, experimental warming by +4°C reduced antioxidant activities and the hypoxia combination again caused mortality of exposed specimens. We conclude that a climate change scenario combining warming and hypoxia represents a serious threat to E. pacifica and, as a consequence, NCCS food webs.