Regions below the
epipelagic are divided into further zones, beginning with the
bathyal zone (also considered the
continental slope) which spans from below sea level and is essentially transitional, containing elements from both the shelf above and the abyss below. Below this zone, the deep sea consists of the
abyssal zone (ocean depth between ) and the
hadal zone (). Food consists of falling organic matter known as '
marine snow' and carcasses derived from the productive zone above, and is scarce both in terms of spatial and temporal distribution. Instead of relying on gas for their buoyancy, many deep-sea
species have jelly-like flesh consisting mostly of
glycosaminoglycans, which provides them with very low density. It is also common among deep water
squid to combine the gelatinous tissue with a flotation chamber filled with a
coelomic fluid made up of the metabolic waste product
ammonium chloride, which is lighter than the surrounding water. The midwater fish have special adaptations to cope with these conditions—they are small, usually being under ; they have slow
metabolisms and unspecialized diets, preferring to sit and wait for food rather than waste energy searching for it. They have elongated bodies with weak, watery
muscles and
skeletal structures. They often have extendable, hinged jaws with recurved teeth. Because of the sparse distribution and lack of light, finding a partner with which to breed is difficult, and many organisms are
hermaphroditic. Because light is so scarce, fish often have larger than normal, tubular eyes with only
rod cells. Their upward field of vision allows them to seek out the silhouette of possible prey.
Prey fish however also have adaptations to cope with
predation. These adaptations are mainly concerned with reduction of silhouettes, a form of
camouflage. The two main methods by which this is achieved are reduction in the area of their shadow by lateral compression of the body, and counter illumination via
bioluminescence.
Flashlight fish have this plus
photophores, which combination they use to detect
eyeshine in other fish (see
tapetum lucidum). Organisms in the deep sea are almost entirely reliant upon sinking living and dead organic matter which falls at approximately 100 meters per day. In addition, only about 1 to 3% of the production from the surface reaches the seabed, mostly in the form of marine snow. This ends up accumulating on the benthic floor, around 1 cm every 1,000 years. Larger food falls, such as
whale carcasses, also occur and studies have shown that these may happen more often than currently believed. There are many
scavengers that feed primarily or entirely upon large food falls and the distance between whale carcasses is estimated to only be 8 kilometers. In addition, there are a number of filter feeders that feed upon organic particles using tentacles, such as
Freyella elegans.
Marine bacteriophages play an important role in cycling nutrients in deep sea sediments. They are extremely abundant (between 5×1012 and 1×1013 phages per square meter) in sediments around the world. Despite being so isolated, deep sea organisms have still been harmed by human interaction with the oceans. The
London Convention aims to protect the marine environment from dumping of wastes such as
sewage sludge and
radioactive waste. A study found that at one region there had been a decrease in deep sea coral from 2007 to 2011, with the decrease being attributed to global warming and
ocean acidification, and biodiversity estimated as being at the lowest levels in 58 years. Ocean acidification is particularly harmful to deep sea corals because they are made of aragonite, an easily soluble carbonate, and because they are particularly slow growing and will take years to recover. Deep sea trawling is also harming the biodiversity by destroying deep sea habitats which can take years to form. Another human activity that has altered deep sea biology is mining. One study found that at one mining site fish populations had decreased at six months and at three years, and that after twenty six years populations had returned to the same levels as prior to the disturbance.
Chemosynthesis There are a number of species that do not primarily rely upon dissolved organic matter for their food. These species and communities are found at
hydrothermal vents at sea-floor spreading zones. One example is the symbiotic relationship between the tube worm
Riftia and chemosynthetic bacteria. It is this
chemosynthesis that supports the complex communities that can be found around hydrothermal vents. These complex communities are one of the few
ecosystems on the planet that do not rely upon
sunlight for their supply of energy.
Adaptation to hydrostatic pressure Deep-sea fish have different adaptations in their proteins, anatomical structures, and metabolic systems to survive in the Deep sea, where the inhabitants have to withstand great amount of hydrostatic pressure. While other factors like food availability and predator avoidance are important, the deep-sea organisms must have the ability to maintain well-regulated metabolic system in the face of high pressures. In order to adjust for the extreme environment, these organisms have developed unique characteristics. Proteins are affected greatly by the elevated hydrostatic pressure, as they undergo changes in water organization during hydration and dehydration reactions of the binding events. This is due to the fact that most enzyme-ligand interactions form through charged or polar non-charge interactions. Because hydrostatic pressure affects both protein folding and assembly and enzymatic activity, the deep sea species must undergo physiological and structural adaptations to preserve protein functionality against pressure. Actin is a protein that is essential for different cellular functions. The α-actin serves as a main component for muscle fiber, and it is highly conserved across numerous different species. Some Deep-sea fish developed pressure tolerance through the change in mechanism of their α-actin. In some species that live in depths greater than ,
C.armatus and
C.yaquinae have specific substitutions on the active sites of α-Actin, which serves as the main component of muscle fiber. These specific substitutions, Q137K and V54A from
C.armatus or I67P from
C.yaquinae are predicted to have importance in pressure tolerance. It was found that deep sea fish have more salt bridges in their actins compared to fish inhabiting the upper zones of the sea. Due to the ability of TMAO being able to protect proteins from high hydrostatic pressure destabilizing proteins, the osmolyte adjustment serves are an important adaptation for deep sea fish to withstand high hydrostatic pressure. Deep-sea organisms possess molecular adaptations to survive and thrive in the deep oceans.
Mariana hadal snailfish developed modification in the
Osteocalcin(
burlap) gene, where premature termination of the gene was found. Osteocalcin gene regulates bone development and tissue mineralization, and the frameshift mutation seems to have resulted in the open skull and cartilage-based bone formation. Due to high hydrostatic pressure in the deep sea, closed skulls that organisms living on the surface develop cannot withstand the enforcing stress. Similarly, common bone developments seen in surface vertebrates cannot maintain their structural integrity under constant high pressure. == Exploration ==