Cartography and the others – aspects of a complicated relationship

ABSTRACT

Cartographic visualizations have been known for thousands of years and have brought forth a wealth of different map projections and cartographic products. Yet, cartography as an independent science has been established only about 100 years ago and sometimes its position among the spatial disciplines is challenged by the scientific community. In this respect it is a young science based on a very long tradition of map making, globe production, and the development of map projections. Maps and map related visualizations play an important and indispensable role in many other spatial disciplines such as geography and geodesy. Cartography has many overlaps with these traditional disciplines as well as with the more recent ones of photogrammetry and remote sensing. This paper reviews fundamental aspects of the conception of space and time throughout human history, the historic development of cartography from a technique of map making to a spatial science, highlighting major milestones in the history of the discipline. As a young science and confronted with major technological developments in the late 20^th century cartography underwent several crises as to what exactly is cartography and how it relates to other spatial sciences, in particular to geographic information systems. Major pitfalls and misconceptions are discussed and the three major scientific pillars of cartography are identified. The relationships of cartography with neighboring disciplines are discussed and the position of cartography vis a vis the others is delineated. Finally, desirable future developments of scientific cartography are discussed.     

Extension of the Paraná Basin to offshore Brazil: Implications for coalbed methane evaluation

Coalbed methane (CBM) is a worldwide exploration target of the petroleum industry. In Brazil, the most important coal-bearing succession is associated with the Permian Rio Bonito Formation of the Paraná Basin. The gas-prone areas are located at the southeastern margin of the Paraná Basin and possibly in the offshore region of the northern part of the Pelotas Basin. Coalfields end abruptly at the present day shoreline, a result of rifting of Gondwana and the evolution of the South Atlantic Ocean. All geologic indicators suggest that in pre-rift times the coal seams extended further eastwards, probably now lying deeply buried below the sedimentary succession of the Pelotas Basin. The present paper discusses structural, stratigraphic, seismic and aeromagenetic data that support the preservation of continental crust beneath ocean sediment. If the coal beds had similar lateral extent to known onshore coals, and coal beds extended across the projected extension of the Parana basin, and there was a conservative 5 m of cumulative coal thickness, then a potential methane volume can be estimated for this newly inferred resource. Average onshore coal gas content is 32 scf/ton (1.00 m³/ton). If this is similar in the offshore coal deposits, then the hypothetical methane volume in the offshore area could be in excess of 1.9 × 10¹² scf (56 × 10⁹ m³). Metamorphism from dikes associated with rifting are potential complicating factors in these deposits, and since no borehole reaching the deep-lying strata in the offshore area are available, this is a hypothetical gas resource with a certain level of uncertainty which should be tested in the future by drilling a deep borehole.     

Geophysiology and Parahistology of the Interactions of Organisms with the Environment*

Abstract. Ecology and Global Ecology (GE) are terms by which the relations between the organism (or living matter as a whole) and the environment (or Earth as a whole) have been treated for almost a century. Geophysiology and Parahistology (PH) are terms slowly replacing older scientific thoughts jointly with an increasing number of modifications and alterations of the Darwinian Evolution (DE) concept. Somehow Geophysiology and Parahistology seem to describe evolution in a non-Darwinian domain. According to V.I. Vernadsky (1929,1930,1988) - the great Russian naturalist and biogeochemist - the biogeochemical processes on Earth are controlled by the force of living matter rather than by species associations developing in and with individual ecosystems as expressed by darwinian evolutionary terms. He also claimed that Goethe was incorrectly regarded as a predecessor of DE by some authors (including Darwin) and that “Natur” (nature) and “Lebendige Natur” (the totality of creatures) are two very different things for Goethe. Detailed analyses of microbial mat systems in the German Wadden Sea and in artificial hypersaline WInogradsky columns have shown that the totality of creatures and matter around them i.e., the “lebendige Natur”sensu Goethe or “living matter”sensu Vernadsky of such environments control to a considerable extent the structure, stability. and (geo-)morphology of sediments and thereby the geological structure of the living Earth. These structures do not follow the rules of sedimentation formulated by the laws of Stokes They represent growth structures (Aufwuchs), whose physics and dynamics are controlled by complex fractal systems. The factors controlling the ultimate shape and stabilisation potential of the eventually resulting rocks and fossils are comparable to tissue development in macroorganisms. Also, certain microbial associations in the sub-recent and in the fossil record may be compared to metazoan tissues. Chemical gradients in the sedimentary column, regulated by the interplay of living matter and sluggish (slow-reactive to non-reactive) compounds, combine to create a pattern of porosity and structure of the resulting deposits that clearly indicates microbial influences and especially those of extracellular polymeric substances on the morphology and texture. The combined effects of microbiota or living matter on the sedimentary record are described as parahistology of sediments in analogy of the histology of tissue on a geological scale. This conceptual living tissue made up of microbially generated rocks and ore deposits cycled through metabolic processes and forced into tissue-like structures by microbial biofilms and mats may extend down to the upper mantle of Earth and far up into the stratosphere when Earth is regarded as a living entity over geological periods. We may have to conceive Earth as a living specimen, which is breathing at a frequency of thousands of years instead of the normal physiological breathing rate of man or an insect. Macroorganisms in all terrestrial systems represent the transport and logistic media, which, however, utterly depend on myriads of intra-, inter-, and extracellular microbial symbiotic partners.     

Diet of Haplognathia ruberrima (Gnathostomulida) in a Caribbean marine mangrove

Haplognathia ruberrima is a cosmopolitan gnathostomulid species found in sulfur bacterial mats in mangroves in Guadeloupe (French West Indies). Haplognathia ruberrima presents a δ¹³C value lower than all measured meiofaunal grazers and lower than the available measured food sources of this environment. This low δ¹³C value can not be due to specific ingestion of ¹³C‐depleted methanogenic bacteria because abundances of those bacteria are reduced in surficial and deep sediments as revealed by δ¹³C of bacterial fatty acid. According to scanning electron microscope observations, no bacterial ectosymbionts were observed at the surface of the gnathostomulids, and transmission electron microscope views revealed the absence of bacterial endosymbionts. Energy‐dispersive X‐ray spectroscopy analysis detected low levels of sulfur (0.32%±0.8) in biological tissues of H. ruberrima, confirming the absence of thioautotrophic bacterial symbionts in these animals. Consequently, the low δ¹³C value of H. ruberrima can not be due to the presence of sulfur‐oxidizing symbionts but more probably to the selective and exclusive consumption of free‐living, sulfur‐oxidizing bacteria.     

Atlantic Water flow through the Barents and Kara Seas

The pathway and transformation of water from the Norwegian Sea across the Barents Sea and through the St. Anna Trough are documented from hydrographic and current measurements of the 1990s. The transport through an array of moorings in the north-eastern Barents Sea was between 0.6 Sv in summer and 2.6 Sv in winter towards the Kara Sea and between zero and 0.3 Sv towards the Barents Sea with a record mean net flow of 1.5 Sv. The westward flow originates in the Fram Strait branch of Atlantic Water at the Eurasian continental slope, while the eastward flow constitutes the Barents Sea branch, continuing from the western Barents Sea opening.About 75% of the eastward flow was colder than 0°C. The flow was strongly sheared, with the highest velocities close to the bottom. A deep layer with almost constant temperature of about −0.5°C throughout the year formed about 50% of the flow to the Kara Sea. This water was a mixture between warm saline Atlantic Water and cold, brine-enriched water generated through freezing and convection in polynyas west of Novaya Zemlya, and possibly also at the Central Bank. Its salinity is lower than that of the Atlantic Water at its entrance to the Barents Sea, because the ice formation occurs in a low salinity surface layer. The released brine increases the salinity and density of the surface layer sufficiently for it to convect, but not necessarily above the salinity of the Atlantic Water. The freshwater west of Novaya Zemlya primarily stems from continental runoff and at the Central Bank probably from ice melt. The amount of fresh water compares to about 22% of the terrestrial freshwater supply to the western Barents Sea. The deep layer continues to the Kara Sea without further change and enters the Nansen Basin at or below the core depth of the warm, saline Fram Strait branch. Because it is colder than 0°C it will not be addressed as Atlantic Water in the Arctic Ocean.In earlier decades, the Atlantic Water advected from Fram Strait was colder by almost 2 K as compared to the 1990s, while the dense Barents Sea water was colder by up to 1 K only in a thin layer at the bottom and the salinity varied significantly. However, also with the resulting higher densities, deep Eurasian Basin water properties were met only in the 1970s. The very low salinities of the Great Salinity Anomaly in 1980 were not discovered in the outflow data. We conclude that the thermal variability of inflowing Atlantic water is damped in the Barents Sea, while the salinity variation is strongly modified through the freshwater conditions and ice growth in the convective area off Novaya Zemlya.     

Bathymetry of Molloy Deep: Fram Strait between Svalbard and Greenland

The sea floor of Fram Strait, the over 2500 m deep passage between the Arctic Ocean and the Norwegian-Greenland Sea, is part of a complex transform zone between the Knipovich mid-oceanic ridge of the Norwegian-Greenland Sea and the Nansen-Gakkel Ridge of the Arctic Ocean. Because linear magnetic anomalies formed by sea-floor spreading have not been found, the precise location of the boundary between the Eurasian and the North American plate is unknown in this region. Systematic surveying of Fram Strait with SEABEAM and high resolution seismic profiling began in 1984 and continued in 1985 and 1987, providing detailed morphology of the Fram Strait sea floor and permitting better definition of its morphotectonics. The 1984 survey presented in this paper provided a complete set of bathymetric data from the southernmost section of the Svalbard Transform, including the Molloy Fracture Zone, connecting the Knipovich Ridge to the Molloy Ridge; and the Molloy Deep, a nodal basin formed at the intersection of the Molloy Transform Fault and the Molloy Ridge. This nodal basin has a revised maximum depth of 5607 m water depth at 79°8.5N and 2°47E.     

Geomorphic evolution of the Tongue of the Ocean and the Providence Channels,Bahamas

During their early history the Tongue of the Ocean and the Providence Channels were broad, relatively shallow basins flanked by growing carbonate banks. As the Blake-Bahama platform subsided, sedimentation kept pace with subsidence on the banks, but not in these flat-bottomed troughs, thus increasing the relief. At the outer end of the troughs the Blake-Bahama escarpment, bounding the platform on the east, dropped steeply to the abyssal plain. Sediment gravity flows coursing down this escarpment began to erode a valley headward into the flat-bottom ancestral Northeast Providence Channel. As the relief between the banks and the troughs increased, the flows increased in vigor, and some of them were able to move down the troughs and into the headwardly eroding central valley. The rate of headward erosion thus increased, with the result that still more flows found their way into the valley. The head of this valley is now off central Andros Island, about 225 km from its point of origin, and headward erosion is continuing.Study of bathymetric charts, observations made during sixteen dives in the Tongue of the Ocean using the submersible DSRV “Alvin”, and analogies with subaerial geomorphic processes and their products contributed to the development of this model. The model is consistent with available stratigraphic information.It is emphasized that the morphology of the Tongue of the Ocean and the Providence Channels cannot be explained as the result of a single unidirectional process, such as upbuilding alone or erosion alone. Both have occurred and both are still occurring. Upbuilding predominated early in the history of the Bahamas; it is responsible for the high walls. Erosion began later and has been accelerating through time. It is responsible for the central valley.     

Coral Recruitment and Regeneration on a Maldivian Reef 21 Months after the Coral Bleaching Event of 1998

Abstract. This paper describes the quantitative inventory of stony corals on a Maldivian reef after the bleaching event of 1998. The detailed data, collected in March 1999 and March 2000, comprise survival, new recruitment and regenerates. They were obtained in 6 transects laid out randomly on the reef flat, on 22 Acropora tables on 6 sites at the reef edge and on 39 Porites lobata blocks and 1 Diploastrea heliopora colony. The present cover of living zooxanthellate corals is reduced to ca. 2 – 5 % of its previous state. Acroporidae and Pocilloporidae were practically wiped out, while Poritidae survived partly and Agariciidae (esp. Pavona) are now the dominant group. New settlements on dead Acropora tables were mainly Agariciidae, followed by Acroporidae and Pocilloporidae. Regenerates on Porites were pronounced and the apparent yearly increase in mass was about threefold that of Diploastrea, which is 3 – 4 mm per year. The influence on reef ecology in terms of coral substrate and species, possible sources of larvae, change of guilds in reef builders, other species and the prospect for further development of the reef, with respect to growth versus erosion, is discussed.     

The impact of salt water inflows on the distribution of polycyclic aromatic hydrocarbons in the deep water of the Baltic Sea

Salt-water inflows into the Baltic Sea are important events for renewing the deep and bottom waters of the deep basins of the Baltic Sea. These events occur only at irregular intervals. The last strong event was in January 1993 followed by minor inflows in winter 1993/1994. As a result of these inflows, the deep water of the central Baltic basins was completely renewed.Based on extensive observations of polycyclic aromatic hydrocarbons (PAHs) in water, fluffy layer material and surface sediments between 1992 and 1998, the transformation of PAHs and the modification of their distribution in the Baltic deep water is discussed in connection with the spreading of the inflowing highly saline and oxygen-rich water along its pathway from the sills into the central basins. In the course of the inflows in 1993/1994, the PAH concentration in the deep water of the different basins increased significantly. The concentrations were elevated, at least by a factor of 2 and as much as seven to eight times (for the four-ring PAHs) compared to the previous and the following years. Two hypotheses for the causes were discussed: the inflowing salt water may have entrained more highly polluted surface water in the western Baltic Sea, or it may have entrained contaminated fluffy layer material or sediment particles along the route of transport.