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MARNAUT
Spatial distribution and charaterization of seep faunal assemblages in Marmara Sea
12 May - 11 June 2007 Atalante / Nautile
Chief scientists: P. Henry, C. Sengor
Localisation
Indicators of cold seep areas
during the Marmarascarps cruise (2002)
28°0’0’’E 29°0’0’’E
41°0’0’’N
40°45’0’’N
40°30’0’’N
Scientific objectives
• To establish community structure with faunal quantitative samples Assessment of diversity, density, biomass
• To characterize trophic relationships between dominant megafaunal species using stable isotope analysis
• To compare the structure of cold seeps at different spatial scales (local and regional)
• To assess links between faunal distribution and in situ environmental factors (in collaboration with CNRS, …)
Observed organisms BIONIL (2006)
Habitat Fauna Sampling device
Tubeworms, pteropods Blade corer
Carbonate crusts Actinians, serpulids, gastropodes, bivalves, tubeworms
ROV claw
Sediments with biogenic mounds
Stomatopods (Crustacea, Eucarids)
Gravity corer
Fissures Siboglinids, sea urchins, galathae
ROV claw, sampling net
Soft sediments
© Marum/University of Bremen
Pre-selected microhabitats frompictures of Marmarascarps
Black patches of reduced sediments
Polychaetes, bivalves…
Bacterial mats and chimneys
Polychaetes, bivalves…
Carbonate crusts
Siboglinids, bivalves, echinoderms…
Sampling strategy
1. Site and habitat pre-selection
2. Habitat imagery
3. Faunal quantitative sampling : 3 replicates per habitatwith Nautile lasers visible on video capture/photo Soft sediments with: (2 hours)
suction sampler (epifauna) blade cores (endofauna)
Carbonate crusts with: (3-4 hours) suction sampler(epifauna)
Nautile claw (crusts) blade corer (endofauna underneath crust)
Carbonate chimneys: (3-4 hours) suction sampler(epifauna)
Nautile claw (crusts) suction sampler (attached small fauna)
On board tasks
• Recover faunal samples in wet lab
• Slice sediment cores in sections of different thickness
• Sieve faunal samples through a column of sieves
• Observe and determine taxa with binocular magnifier
• Fix samples with alcohol, formalin or freezing (-80°C)