BACKGROUND INFORMATION  

Since the discovery of the first hydrothermal vent in 1977 (Corliss et al., 1979), one of the most important findings in Ocean Sciences of the XXth century, vent research has been mainly of descriptive nature. Quantitative approach was hindered by the specific technical, financial, infrastructural and human resource constraints associated with deep-sea research. However, now that the importance of hydrothermal vent circulation within the global oceans is being increasingly realized, an international co-operation is growing to overcome technological and scientific challenges for exploring, observing and monitoring these extreme deep-sea ecosystems. The newly discovered hydrothermal vents, in the vicinity of the Azores islands have brought the Portuguese archipelago and its reputable marine research institutes in the confluence of these international scientific goals.
 
Although hydrothermal vents are hostile (Sarradin et al., 1999), they are crowded with life (Fowler and Tunnicliffe, 1997) the main features of the ecosystem being strong biological endemisms and high productivity. Additionally, while anatomy and physiology of vent species is extensively investigated the mechanisms that are responsible for surviving under complete darkness, closed to the hot vent discharge, in the presence of heavy metals and other toxic compounds, and the remarkable water pressure are not yet elucidated.
 
Mussels (Bathymodiolus azoricus) from the MAR dominate the vent community due to their flexible feeding strategy (Fisher et al., 1989): they are filter feeders that simultaneously rely on a dual symbiosis (Kadar et al., 2005; Fiala-Medioni et al., 1986). The constant discharge of toxic metals at hydrothermal vents (over 4000 ppm Fe, 500 ppm Cu and Zn, 12 ppm Hg, etc) (Kadar et al., 2005a) provides a useful analogue of contaminated marine environments, with the notable difference that the time scale of contamination here is geological, thus having deep-seated evolutionary implications of the detoxification mechanisms.
Shell formation of hydrothermal bivalves per se, and its involvement in detoxification lacked attention of vent scientists. Shell morphology and ultra-structure reflects many aspects of growth related processes such as potential seasonal effects, the rate of shell dissolution vs growth etc, all unresolved processes in vent mussels. As the basic mechanism of skeleton crystallization is common among living organisms, using bivalves as a model, is a very practical way to widen our general knowledge of crystallization laws relative to the influencing phisico-chemical factors. Application of the theoretical concepts resulting from this research would contribute to our understanding biomineralisation of calcareous deposits with prospective medical applications (osteoporosis research).
 
Deposition of heavy metals into the shell has been previously reported as a detoxification mechanism in shore bivalves from anthropogenically-polluted areas (Schein et al., 1991) and thus it is important that this process be investigated in vent species that are naturally exposed to various toxic metals.
Because bacteria, the primary producers of these ecosystems derive energy by mediating thermodynamically favorable chemical reactions, it is axiomatic that the chemical and physical environment will have a direct impact on the type of organisms that can exist there. Investigation of the organism habitat interaction is therefore the key to understand these geologically and biologically unique features on Earth, and may light the way to the development of new drugs, industrial processes, and other products useful to us all.
 
 

Bibliography

  • 1. Corliss, J.B., et al. (1979) Submarine thermal spings on the Galapagos Rift. Science, 203:1073-1083
  • 2. Fialamedioni, A., et al. (1986). Ultrastructure of the Gill of the Hydrothermal-Vent Mytilid Bathymodiolus Sp. Marine Biology 92, 65-72.
  • 3. Fisher, C. R., et al. (1989). Microhabitat Requirements of the Hydrothermal Vent Mussel, Bathymodiolus-Thermophilus. American Zoologist 29, A81-A81.
  • 4. Fowler, C. M. R. and Tunnicliffe, V., 1997. Hydrothermal vent communities and plate tectonics. Endeavour 214: 164-168.
  • 5. Gustafson, R. G., et al. (1998). A new genus and five new species of mussels (Bivalvia, Mytilidae) from deep-sea sulphide/hydrocarbon seeps in the Gulf of Mexico. Malacologia 40, 63-112.
  • 6. Kádár E, Bettencourt R, Costa V, Santos Rs, Lobo-Da-Cunha A, Dando P, (2005b) Experimentally induced endosymbiont loss and re-acquirement in the hydrothermal vent bivalve Bathymodiolus azoricus Journal of Experimental Marine Biology and Ecology 318: 99-110.
  • 7. Kádár E, Costa V, Martins I, Santos RS, Powell JJ (2005a) Enrichment in trace metals of macro-invertebrate habitats at hydrothermal vents along the Mid Atlantic Ridge. Hydrobiologia 548: 191-205.
  • 8. Sarradin, P. M., et al. 1999. Chemical environment of the hydrothermal mussel communities in the Lucky Strike and Menez Gwen vent fields, Mid Atlantic ridge. Cahiers De Biologie Marine 40 (1): 93-104.
  • 9. Schein E, et al. (1991)Ecological parameters recorded by bivalve shell - pluridisciplinary approach. Bulletin De La Societe Geologique De France 162 (4): 687-698.
 
     
   
   
         
 
 
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