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Why should we bother to study deep-sea biology?

Find out why studying deep-sea biology is crucial as we delve into the mysterious and diverse ecosystem of the ocean's bottom. Discover the unique conditions, adaptations, and fascinating organisms that inhabit this largely unexplored realm.

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Why should we bother to study deep-sea biology?

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  1. Why should we bother to study deep-sea biology? “..we know more about the moon’s behind than the ocean’s bottom…” Dr. Cindy Lee Van Dover New Yorker classic

  2. Most of “biology” (~80%) takes place in the deep sea:The deep sea is the most common habitat in the biosphere! Average depth = 3,800 m

  3. Deep Sea • Life strongly influenced by environmental conditions • Conditions • Temperature • Cold – Typically -1 to 4 oC • Exceptions • Deep Mediterranean is ca. 13 oC • Red Sea can be 21.5 oC @ 2000 m depth • Weddell Sea can be -1.9 oC • Hydrothermal vent effluent can approach 400 oC • Pressure • Increases predictably by 1 atmosphere (14.7 psi) every 10 m • Mean depth of oceans – 3800 m = 5600 psi • Affects biological molecules – Membranes, enzymes • Light • Decreases with depth • Sunlight present in mesopelagic zone; absent below 1000 m • Affects development of eyes

  4. Deep Sea • Conditions • Dissolved Oxygen • Near saturation and not limiting in most of the deep sea • Exceptions: OMZ and certain enclosed basins (Santa Barbara Basin, Cariaco Basin, Black Sea) • OMZ and anoxic basins may act as barriers • Substrate • Exposed hard rock is uncommon • Biogenic hard substrate may be important • Sediment is common • Continental margins – coarse terrigenous material • Deep-sea floor – biogenic oozes, terrigenous clays • Deep-sea sediments typically very low in organic carbon – 0.5% beneath productive areas and <0.1% beneath oligotrophic waters

  5. Oxygen Minimum Zone (OMZ)

  6. Oxygen Minimum Zone (OMZ) • How do OMZ species adapt to low levels of oxygen? • Metabolic rate (O2 consumption) declines • Gill ventilation rates increase • Hemoglobin binds oxygen at lower saturation • Gene expression: enzyme isoforms for anaerobiosis • Some may be food-deprived

  7. Oxygen Minimum Zone (OMZ)

  8. Deep Sea • Conditions • Dissolved Oxygen • Near saturation and not limiting in most of the deep sea • Exceptions: OMZ and certain enclosed basins (Santa Barbara Basin, Cariaco Basin, Black Sea) • OMZ and anoxic basins may act as barriers • Substrate • Most of deep sea floor covered by sediments • Margins – Coarse terrigenous sediments • Basins – Biogenic oozes (>30% biogenic skeletal material) and terrigenous clays (depth related) • Siliceous oozes – Diatoms (high latitudes) or radiolarians (tropics) • Calcareous oozes – Foraminiferans (productive areas) • Low organic content (typically <1%) • Exposed hard substrate uncommon • Rocks, manganese nodules, biogenic

  9. Deep Sea • Conditions • Currents • Generally slow – Mean speeds typically <5 cm s-1, with peaks less than 20 cm s-1 in most areas • Periodically, certain areas experience benthic storms • Typically last days to weeks • Tidal currents • Source of temporal and spatial variability • Food Supply • Variable in time and space • Seasonal variation • Seasonality in productivity, migration patterns, storms, etc. • May produce seasonal patterns in biological processes (Ex:behavior, feeding, metabolism, reproduction, recruitment) • Episodic large inputs may introduce variability on other time and space scales • Trends • Gigantism – Ex: Xenophyophores, Amphipods, Isopods • Miniaturization – Ex: Ostracods, Tanaids, Harpacticoid Copepods

  10. Philippine Trench Hirondellea gigas – Scavenging Amphipods

  11. Deep Sea • Conditions • Currents • Generally slow – Mean speeds typically <5 cm s-1, with peaks less than 20 cm s-1 in most areas • Periodically, certain areas experience benthic storms • Typically last days to weeks • Tidal currents • Source of temporal and spatial variability • Food Supply • Variable in time and space • Seasonal variation • Seasonality in productivity, migration patterns, storms, etc. • May produce seasonal patterns in biological processes (Ex:behavior, feeding, metabolism, reproduction, recruitment) • Episodic large inputs may introduce variability on other time and space scales • Trends • Gigantism – Ex: Xenophyophores, Amphipods, Isopods • Miniaturization – Ex: Ostracods, Tanaids, Harpacticoid Copepods

  12. Deep Sea • Fauna • Most animal phyla present • Total faunal abundance decreases sharply with depth • Pelagic community biomass at 4000 m ca. 1% of surface values • Sinking food accumulates at interfaces (e.g. sediment surface) • Pelagic biomass 10 mab double that at 200 mab (Wishner) • Changes in relative abundance of faunal taxa with depth • Kurile-Kamchatka Trench - Sponges dominant component of benthic macro-/megafauna to 2000 m • Holothuroids important below 2000 m and dominant below 8000 m • Asteroids important to 7000 m and absent below that

  13. Deep Sea • Fauna • Trophic modes • Detritivores and scavengers dominant • Good chemosensory capabilities • Distensible guts • Predators relatively uncommon • Opportunistic feeding strategies especially useful • Why?

  14. Scavengers converge on a food fall 2000m deep off coast of Mexico http://news.bbc.co.uk/1/hi/sci/tech Dec 11 2006

  15. Deep Sea • Fauna • Fishes relatively scarce and modified to various degrees, compared to shallow living relatives • Typically have reduced or large eyes, watery tissues, low muscle protein content, reduced skeletons, oil-filled swim bladders, body forms not designed for rapid swimming • Most important mobile scavengers in deep sea, along with amphipods & isopods • Many apparently find food using olfaction • Some sit-and-wait predators (e.g.Bathypterois) • Some nomadic foragers (e.g.Coryphaenoides)

  16. Coryphaenoides Bathypterois Lycodes

  17. Whale skull • Deep Sea • Fauna • Sessile organisms may be attached to hard substrate of many types • Exposed rock • Manganese nodules or bits of geological material • Biogenic hard substrate (sponges, shells, wood, bone) • Occurrence limited by • Available substrate • Flux of POM (food)

  18. Crinoids Gorgonians Barnacle Antipatharians

  19. Brachiopods Bryozoan Stalked tunicate

  20. Deep Sea • Diversity • Through 1960s, deep sea perceived as highly uniform and consistent over time/space • Prevailing ecological theory predicted that spatial and temporal uniformity plus sparse, low-grade food resources should lead to an equilibrium condition with a few competitively dominant species • Mid-1960s: epibenthic sled developed and deployed by Howard Sanders and Bob Hessler (WHOI) • Covered much smaller area than conventional deep-sea bottom trawl but sampled upper few cm of sediments and retained organisms in a fine-meshed sampling bag • Samples effectively ended notion of low diversity in deep sea

  21. Deep Sea • Diversity • Number of spp. within many taxa (e.g. bivalves, gastropods, polychaetes) tends to increase from surface to mid-slope depths (ca. 2000 m) then decrease with increasing depth

  22. Deep Sea • Diversity • Trend suggests low species diversity in deep sea • Pattern could be artifact of reduced sampling effort with increasing depth • How do we know if we’ve sampled enough area and organisms to generate a meaningful picture of the actual diversity of the deep-sea benthic community?

  23. Deep Sea • Diversity • Rarefaction curves for most deep-sea habitats never approach an asymptote • Largest quantitative data set to date for deep-sea macro- and meiofauna was obtained during early 1980s from Atlantic slope off US • 554 box cores (30 x 30 cm) from depths to 3000 m • Over 1600 species identified • Factoring out depth, 233 cores taken at 2100 m depth along 176-km long transect • Samples: 798 species from 14 invertebrate phyla

  24. Deep Sea • Diversity • Rarefaction curves for most deep-sea habitats never approach an asymptote • Expected number of species increasing at about 25 m-2 • Prediction: 5-10 million species in deep sea!! • No single species >8% of community • Similar to other deep-sea sites (except HEBBLE, where single species may be 50-64% of community)

  25. Deep Sea • Diversity • Patterns • Deep-sea species diversity differs among ocean basins • Differences may be related to oxygen content, nutritional input, geological history, etc. • High species diversity may be due to • Processes that establish diversity (speciation) • Process that maintain diversity (extinction)

  26. Deep Sea • Diversity • Maintenance • Equilibrium processes • Ex: Resource partitioning, habitat partitioning • Species that are well-adapted to a particular set of conditions co-exist at densities near carrying capacity of environment • Disequilibrium processes • Ex: Local disturbance • Patchy habitat supports many populations at early growth stages, hence at relatively low densities (not near carrying capacity), reducing competitive exclusion as an important structuring mechanism • Connell (1978) suggested that highest diversity maintained at intermediate levels of disturbance

  27. Hydrothermal Vents

  28. Hydrothermal Vent fluids: Acidic (pH 2.8), Hydrogen Sulfide >1mM Temperature up to 400°C

  29. Chemosynthetic Food Web: Sulfide Oxidizing Bacteria Riftia pachyptila (2 m tall)

  30. Fine-scale adaptation to thermal niches Distribution patterns at the vents. Black Smoker Warm vent Alvinella pompejana & A. caudata Bythograea thermydron Riftia pachyptila Cool vent Cool vent Deep Sea- Vent H2S 0->1mM Temp 2-400°C pH 8 -2.8 Bathymodiolus thermophilus Calyptogena magnifica

  31. Vents are short-lived.

  32. Seamounts have higher biomass and different communities

  33. Seamount Food Webs • Vertical migrators move to regions with more food • Swept over seamounts by currents • Trapped on top at dawn • Abundance of predators high, musculature robust, but SLOW growth

  34. What types of adaptations are needed to support life at depth? • Tolerance Adaptations: adapt to perturbation from abiotic conditions, e.g., hydrostatic pressure and temperature • Capacity Adaptations: adjust rates of life in accord with the abiotic and biotic conditions

  35. ‘Rate of living’ falls for visual predators, but notfor gelatinous ‘float and wait’ predators. For review, see: Childress, J.J. (1995). Trends Ecol. Evol. 10: 30-36

  36. “Float-and-wait” feeding may become more important than intense predation with reduced visual predation

  37. Capacity Adaptations: conclusions • Reduced intensity of locomotory activity less reliance on visual predation = lower metabolic capacity. • Reduced muscle protein levels = lower costs of maintenance metabolism & growth • Lower O2 consumption • Reduced/Absent swim bladders; reduced calcification • Migrators and Non-Migrators differ

  38. Tolerance Adaptations:Pressure & Temperature • Adaptive Solutions: a cooperative venture between macro- and ‘micro’molecules. • Proteins: amino acid substitutions • Enhance flexibility • Conserve Km (substrate binding) at habitat pressure • Osmolytes: protein-stabilizing solutes • Lipids & membranes: fluidity-effects • Homeoviscous adaptation • More unsaturated acyl phospholipid chains

  39. Gas-filled spaces—obvious problemsV = nRT/P

  40. PRESSURE EFFECTS IN THE LIQUID PHASE— • PROTEIN conformational changes a problem! • Movement during substrate binding/release • Subunit polymerization Lactate Dehydrogenase (LDH) Pyruvate + NADH + H+ lactate + NAD+

  41. Pressure inhibits membrane-spanning proteins:resistance to conformational change. Membrane-spanning protein Conformational change Low resistance—high activity High resistance--inhibition

  42. Homeoviscous Adaptation Shifts in acyl chain ‘saturation’ (double-bond content: =) saturated mono-unsaturated poly-unsaturated Viscous Fluid

  43. Homeoviscous adaptation Change lipid composition (saturation of fatty acid side chains, cholesterol) Maintain stable fluidity at habitat conditions Preserve membrane permeability and membrane enzyme function C B A Viscosity A B C Temperature (°C) Pressure (atms)

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