ALBERT

Description: Tropical South America is one of the three main centres of the global, zonal overturning circulation of the equatorial atmosphere (generally termed the 'Walker' circulation1). Although this area plays a key role in global climate cycles, little is known about South American climate history. Here we describe sediment cores and down-hole logging results of deep drilling in the Salar de Uyuni, on the Bolivian Altiplano, located in the tropical Andes. We demonstrate that during the past 50,000 years the Altiplano underwent important changes in effective moisture at both orbital (20,000-year) and millennial timescales. Long-duration wet periods, such as the Last Glacial Maximum—marked in the drill core by continuous deposition of lacustrine sediments—appear to have occurred in phase with summer insolation maxima produced by the Earth's precessional cycle. Short-duration, millennial events correlate well with North Atlantic cold events, including Heinrich events 1 and 2, as well as the Younger Dryas episode. At both millennial and orbital timescales, cold sea surface temperatures in the high-latitude North Atlantic were coeval with wet conditions in tropical South America, suggesting a common forcing.

Description: Modern competition research started with G.E. Hutchinson’s, Homage to Santa Rosalia, and his now-famous question “why are there so many species?” (Hutchinson 1959,1961). This confronted observed species richness with the competitive exclusion principle, a principle that had been derived from theory and from highly artificial experiments. It would always have been easy to point at the “artificial” character of the competitive exclusion principle. Indeed many researchers have refused to deal with Hutchinson’s question because they considered it a pseudo-problem, which arose from a contradiction between overly simplified theory and complicated reality. However, those who took Hutchinson’s challenge seriously have gained fundamental insights into how competition plays out in nature, how species coexist, and how communities function. In this final chapter we attempt to synthesize these insights as they have been presented in this book. We focus on six key topics: - Identification of major trade-off axes (Sect. 8.1) - Confirmation of the “intermediate disturbance hypothesis”, and detection of interactions among competition, resource supply, predation and disturbance in field experiments (Sect. 8.2) - The interplay of space colonization, dispersal and neighborhood competition in sessile communities (Sect. 8.3) - Potential for chaotic, self-generated heterogeneity in communities (Sect. 8.4) - Role of exclusive resources in competition among mobile animals (Sect. 8.5) - Coexistence by slow exclusion (Sect. 8.6)

Description: According to small subunit ribosomal RNA (ss rRNA) sequence comparisons all known Archaea belong to the phyla Crenarchaeota, Euryarchaeota, and—indicated only by environmental DNA sequences—to the 'Korarchaeota'1, 2. Here we report the cultivation of a new nanosized hyperthermophilic archaeon from a submarine hot vent. This archaeon cannot be attached to one of these groups and therefore must represent an unknown phylum which we name 'Nanoarchaeota' and species, which we name 'Nanoarchaeum equitans'. Cells of 'N. equitans' are spherical, and only about 400 nm in diameter. They grow attached to the surface of a specific archaeal host, a new member of the genus Ignicoccus3. The distribution of the 'Nanoarchaeota' is so far unknown. Owing to their unusual ss rRNA sequence, members remained undetectable by commonly used ecological studies based on the polymerase chain reaction4. 'N. equitans' harbours the smallest archaeal genome; it is only 0.5 megabases in size. This organism will provide insight into the evolution of thermophily, of tiny genomes and of interspecies communication.

Description: One concept of evolutionary ecology holds that a living fossil is the result of past evolutionary events, and is adapted to recent selective forces only if they are similar to the selective forces in the past. We describe the present environment of the living coelacanth Latimeria chalumnae Smith, 1939 at Grande Comore, western Indian Ocean and report depth-dependent cave distribution, temperature, salinity and oxygen values which are compared to the fish's distribution and its physiological demands. We studied the activity pattern, feeding behaviour, prey abundance and hunting success to evaluate possible links between environmental conditions, feeding ecology and evolutionary success of this ancient fish. Transmitter tracking experiments indicate nocturnal activity of the piscivorous predator which hunts between approximately 200 m below the surface to 500 m depth. Fish and prey density were measured between 200 and 400 m, both increase with depth. Feeding tracks and feeding strikes of the coelacanth at various depths were simulated with the help of video and laser techniques. Along a 9447 m video transect a total of 31 potential feeding strikes occurred. Assuming 100% hunting success, medium-sized individuals would obtain 122 g and large females 299 g of prey. Estimates of metabolic rates revealed for females 3.7 ml O2 kg−1 h−1 and for males 4.5 ml O2 kg−1 h−1. Today coelacanths are considered to be a specialist deep-water form and to inhabit, with their ancient morphology, a contemporary environment where they compete with advanced, modern fish.

Description: Sediment transport processes in the northern North Atlantic have been investigated on the basis of various numerical models. A general circulation model has been used to investigate large-scale particle transport, a reduced gravity plume model has been used to investigate particle transport by cascading from the shelves into the deep basins, an ocean slice model has been used to investigate particle exchange processes between a bottom current and the ambient water mass, and a Bottom Boundary Layer model has been used to investigate particle interactions influencing the settling behavior of suspended particles. In this paper, the various processes investigated in these models are described (i) schematically, (ii) on the basis of field data, if available, and (iii) by employing results from numerical simulations. In a first attempt the northern North Atlantic will be divided into separate process defined areas, which can be used in carbon budgeting, for example.

Description: Denitrification was investigated in the Baltic proper at two stations with different conditions in the deep water. The Gotland Deep was examined as an example of a basin with anoxic, H2S‐containing deep water and station T was taken as an example of low‐oxygen (〈0.2 ml liter−1), sulfide‐free deep water. Denitrification was measured by the acetylene blockage method; in addition, N2O reduction was followed in samples without acetylene. To shed light on the factors limiting denitrification, we compared in situ rates to denitrification after adding nitrate or electron donors. Denitrification was restricted to the layer of the oxic‐anoxic interface in the Gotland Deep and to the water layer near the sediment of station T. For both stations it could be shown that denitrification was not limited by nitrate availability. A lack of available organic C seemed to limit denitrification rates and growth of denitrifiers. As a result of C limitation in the water column, denitrification was restricted to energy‐rich interfaces. In the low‐oxygen water away from energy‐rich interfaces, the less C‐demanding nitrification‐denitrification coupling (NH4+ → N2O → N2) seemed to be favored. Denitrification in the water of the central Baltic seems to be subjected to strong variability due to changing C supply during the course of the year. However, limitation by C availability can be assumed for most of the year and should be taken into account in calculating the N budget of the Baltic.

Description: The onset of the Palaeocene/Eocene thermal maximum (about 55 Myr ago) was marked by global surface temperatures warming by 5–7 °C over approximately 30,000 yr (ref. 1), probably because of enhanced mantle outgassing2, 3 and the pulsed release of approx1,500 gigatonnes of methane carbon from decomposing gas-hydrate reservoirs4, 5, 6, 7. The aftermath of this rapid, intense and global warming event may be the best example in the geological record of the response of the Earth to high atmospheric carbon dioxide concentrations and high temperatures. This response has been suggested to include an intensified flux of organic carbon from the ocean surface to the deep ocean and its subsequent burial through biogeochemical feedback mechanisms8. Here we present firm evidence for this view from two ocean drilling cores, which record the largest accumulation rates of biogenic barium—indicative of export palaeoproductivity—at times of maximum global temperatures and peak excursion values of delta13C. The unusually rapid return of delta13C to values similar to those before the methane release7 and the apparent coupling of the accumulation rates of biogenic barium to temperature, suggests that the enhanced deposition of organic matter to the deep sea may have efficiently cooled this greenhouse climate by the rapid removal of excess carbon dioxide from the atmosphere.

Description: Living coelacanths (Latimeria chalumnae) are normally found only in the western Indian Ocean, where they inhabit submarine caves in the Comores Islands. Two specimens have since been caught off the island of Manado Tua, north Sulawesi, Indonesia, some 10,000 kilometres away. We sought to determine the ecological and geographic distribution of Indonesian coelacanth populations with a view to drawing up conservation measures for this extremely rare fish. During our explorations, we discovered two living Indonesian coelacanths 360 km southwest of Manado Tua.

Description: Acoustic telemetry was used to examine patterns of activity and space utilisation of coelacanths, nocturnal predators which spend the day in submarine caves. Nine coelacanths (Latimeria chalumnae) were tracked, each for a period of 1 to 16 nights at Grande Comore, West Indian Ocean. Activities lasted on average 9 h, usually starting shortly after sunset and ending before sunrise. Vertically, coelacanths moved up and down at and below cave level by following the bottom contour, mainly between 180 and 400 m depth. The deepest record was 698 m, the shallowest 133 m. Most time was spent between 200 and 300 m depth. Large individuals performed deep excursions to depths below 400 m, usually once per night. The fish spent most time in water temperatures of 15 to 19 °C; they rarely ventured into waters warmer than 22 °C measured at depths shallower than 160 m depth. Horizontally, coelacanths stayed in narrow areas ranging from 〈1 to 10 km of coastline. Coelacanths are extremely slow drift-hunters with an estimated average swimming speed of 3.2 m min−1, often travelling not more than 3 km per night. They probably take advantage of local upwelling and downwelling and slow currents occurring parallel to the steep slopes. This study shows that coelacanths are inhabitants of the subphotic zone, where they are active mainly below the depth of their daytime refuges.