Showing posts with label lateral line. Show all posts
Showing posts with label lateral line. Show all posts

Tuesday, May 11, 2010

Senses of the Deep Sea


The most abundant life on this planet is found deep beneath the waves at depths that sunlight hardly penetrates. Species that live at these depths are impossible to capture for behavioural studies where questions can then be asked about how fish at these depths 'see' the world. Thus, deep sea scientists are restricted to undertaking morphological analysis on these organisms and interpreting the results. One of the long held beliefs is that vision becomes less important for fish the deeper you go, and this is obvious when you look at eye size. Generally, after a certain point, when sunlight can no longer penetrate, the size of fish eyes becomes increasingly smaller and the non-visual senses become elaborate and highly specialised. In this post I discuss two papers that investigate what senses are utilised by mesopelagic and abyssal demersal fish species. For those of you who do not know mesopelagic fish are those that swim in the water column at depths of 500 and 1500m while abyssal demersal fish are those found near the bottom of the sea floor at depths of 2000-6000m.

What the author did was capture fish during deep water trawls in the Atlantic and Pacific oceans, and investigate their brain morphology. He described the brains with special reference to the differentiation of the sensory centres - olfactory bulb (smell), optic tectum (vision), octavolateral region (water motion via lateral line), and gustatory lobes (taste). For those who do not know what the lateral line is it is a hair cell based sensory system that detects local water movements surrounding the fish. Such as the wake of a passing prey. By comparing the size of each brain region for a specific species, with the overall average across all species, the author was able to determine whether the fish was a specialist for that particular sensory system.

Some species were 'specialised' in one particular sensory system (mesopelagic fishes 36%; abyssal demersal fishes 40%). Other species 'dominated' in two sensory systems (mesopelagic fishes 49%; abyssal demersal fishes 46%), while the remaining species were generalists and specialised in three senses (mesopelagic fishes 15%; abyssal demersal fishes 14%). No fish therefore were not specialised in any sense.

For mesopelagic fishes that were specialists 92% were masters of vision. This pattern, although not as strong, continues to hold true when you take into account 'dominated' and 'generalist' species. Sixty one percent of fish had above average volumes of the optic tectum. This would suggest that vision is the most important sense in the mesopelagic environment. This pattern is not as strong for abyssal demersal fish with fish specialising in vision in only 50% of cases both for specialists and when dominated and generalist species are accounted for. Vision therefore seems to play a lesser role in the deeper abyss.

The use of the lateral line shows the reverse trend becoming more important the deeper you go. Mesopelagic fish that specialised in the lateral line (25%) were less than those found in the abyss (49%). However, in both environments the lateral line was the second most important sensory system. This pattern of increasing importance of non-visual senses in deeper waters continues to hold for the other senses also. When shifting from the mesopelagic to the abyss, species with above average gustation areas (taste) increased from 10% to 34% , and from 3% to 37% for olfaction.

This pattern shows that the sensory environment of the abyss is markedly different than the open waters of the deep sea. Vision was clearly dominant in the mesopelagic waters, and this may be due to the abundant sources of bioluminescence found in this environment. This is quite evident when comparing the species between the two depth categories. Bioluminescent species were common in the mesopelagic, but not a single bioluminescent species was found in the abyss. With a lack of any visual cues for feeding or mating it is not surprising that non-visual senses begin to become more dominant at greater depth.

Wagner, H. (2001). Sensory Brain Areas in Mesopelagic Fishes Brain, Behavior and Evolution, 57 (3), 117-133 DOI: 10.1159/000047231
Wagner, H. (2001). Brain Areas in Abyssal Demersal Fishes Brain, Behavior and Evolution, 57 (6), 301-316 DOI: 10.1159/000047249
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Tuesday, February 23, 2010

Tracking the wakes of prey

Image: http://www.flower-horn.de

I received a comment yesterday asking about the mechanosensory lateral line. So I thought I would write a post today about one of the really cool behaviours that is mediated by this sensory system. I know this is not a well known sensory system but it is a very important one for fish and aquatic amphibians. The lateral line is a hair cell based sensory system that detects the water movement surrounding the fish. Normally this is to within one or two body lengths. However a recent study has shown that in the European catfish (see picture above) it is involved in the detection of wakes left by potential prey.

Here is the abstract:

Swimming fish leave wakes containing hydrodynamic and chemical traces. These traces mark their swim paths and could guide predators. We now show that nocturnal European catfish (Silurus glanis) locate a piscine prey (guppy, Poecilia reticulata) by accurately tracking its three-dimensional swim path before an attack in the absence of visible light. Wakes that were up to 10 s old were followed over distances up to 55 prey-body lengths in our setup. These results demonstrate that prey wakes remain sufficiently identifiable to guide predators, and to extend considerably the area in which prey is detectable. Moreover, wakes elicit rear attacks, which may be more difficult to detect by prey. Wake tracking may be a common strategy among aquatic predators.

In a later paper the lateral line was ablated and once this was done the fish could no longer track the prey. Thus the lateral line was essential in the tracking behaviour. Although this would have limited functional value in coastal water ecosystems where there is a large degree of water motion, and thus background noise breaking up the wake, this may become more important in still water environments. The catfish in this study is obviously a case in point inhabiting slow flowing or still waters such as lakes.

Image: http://oceanexplorer.noaa.gov

This predation strategy may be even more important in deep sea fish where below 1000m, when vision becomes useless, the lateral line is likely to be the dominant sensory system. In such a hydrodynamically 'noiseless' environment many deep sea fish would be capable of detecting the wakes of prey for up to three minutes since they had passed by. Although this next idea is purely conjecture this may also explain why so many deep sea fishes have rat tails (see pic above). Such a tail would likely result in a much reduced wake!

Hanke W, Brucker C, & Bleckmann H (2000). The ageing of the low-frequency water disturbances caused by swimming goldfish and its possible relevance to prey detection. Journal of Experimental Biology 203(7), 1193-1200
Pohlmann K, Grasso FW, & Breithaupt T (2001). Tracking wakes: the nocturnal predatory strategy of piscivorous catfish. Proceedings of the National Academy of Sciences of the United States of America, 98 (13), 7371-4 PMID: 11390962
Pohlmann K, Atema J, & Breithaupt T (2004). The importance of the lateral line in nocturnal predation of piscivorous catfish. The Journal of Experimental Biology 207, 2971-2978

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