Statocyst

Last updated
Drawing of the statocyst system Statocyst.jpg
Drawing of the statocyst system
Statocysts (ss) and statolith (sl) inside the head of sea snail Gigantopelta chessoia Gigantopelta chessoia statocysts.png
Statocysts (ss) and statolith (sl) inside the head of sea snail Gigantopelta chessoia

The statocyst is a balance sensory receptor present in some aquatic invertebrates, including bivalves, [1] cnidarians, [2] ctenophorans, [3] echinoderms, [4] cephalopods, [5] [6] crustaceans, [7] and gastropods, [8] A similar structure is also found in Xenoturbella . [9] The statocyst consists of a sac-like structure containing a mineralised mass (statolith) and numerous innervated sensory hairs (setae). The statolith's inertia causes it to push against the setae when the animal accelerates. Deflection of setae by the statolith in response to gravity activates neurons, providing feedback to the animal on change in orientation and allowing balance to be maintained.

Contents

In other words, the statolith shifts as the animal moves. Any movement large enough to throw the organism off balance causes the statolith to brush against tiny bristles which in turn send a message to the brain to correct its balance.

It may have been present in the common ancestor of cnidarians and bilaterians.[ citation needed ]

Hearing

In cephalopods like squids, statocysts provide a cochlea-like mechanism to hear. [10] [11] As a result, the longfin inshore squid for instance can hear low-frequency sounds between 30 and 500 Hz when the water temperature is above 8 °C (46 °F). [12]

See also

Related Research Articles

<span class="mw-page-title-main">Squid</span> Superorder of cephalopod molluscs

A squid is a mollusc with an elongated soft body, large eyes, eight arms, and two tentacles in the orders Myopsida, Oegopsida, and Bathyteuthida. Though many other molluscs within the broader Neocoleoidea are also called squid despite not strictly fitting these criteria. Like all other cephalopods, squid have a distinct head, bilateral symmetry, and a mantle. They are mainly soft-bodied, like octopuses, but have a small internal skeleton in the form of a rod-like gladius or pen, made of chitin.

<span class="mw-page-title-main">Cephalopod</span> Class of mollusks

A cephalopod is any member of the molluscan class Cephalopoda such as a squid, octopus, cuttlefish, or nautilus. These exclusively marine animals are characterized by bilateral body symmetry, a prominent head, and a set of arms or tentacles modified from the primitive molluscan foot. Fishers sometimes call cephalopods "inkfish", referring to their common ability to squirt ink. The study of cephalopods is a branch of malacology known as teuthology.

<span class="mw-page-title-main">Antenna (biology)</span> Paired appendages used for sensing in arthropods

Antennae, sometimes referred to as "feelers", are paired appendages used for sensing in arthropods.

<span class="mw-page-title-main">Vampire squid</span> Species of cephalopod

The vampire squid is a small cephalopod found throughout temperate and tropical oceans in extreme deep sea conditions. The vampire squid uses its bioluminescent organs and its unique oxygen metabolism to thrive in the parts of the ocean with the lowest concentrations of oxygen. It has two long retractile filaments, located between the first two pairs of arms on its dorsal side, which distinguish it from both octopuses and squids, and places it in its own order, Vampyromorphida, although its closest relatives are octopods. As a phylogenetic relict, it is the only known surviving member of its order.

<span class="mw-page-title-main">Tentacle</span> Varied organ found in many animals and used for palpation and manipulation

In zoology, a tentacle is a flexible, mobile, and elongated organ present in some species of animals, most of them invertebrates. In animal anatomy, tentacles usually occur in one or more pairs. Anatomically, the tentacles of animals work mainly like muscular hydrostats. Most forms of tentacles are used for grasping and feeding. Many are sensory organs, variously receptive to touch, vision, or to the smell or taste of particular foods or threats. Examples of such tentacles are the eyestalks of various kinds of snails. Some kinds of tentacles have both sensory and manipulatory functions.

<span class="mw-page-title-main">Rhopalium</span>

Rhopalia from Ancient Greek ῥόπαλον (rhópalon) 'club' are small sensory structures of certain Scyphozoan and Cubozoan species.

<span class="mw-page-title-main">Cephalization</span> Evolutionary trend of a head region developing

Cephalization is an evolutionary trend in animals that, over many generations, the special sense organs and nerve ganglia become concentrated towards the rostral end of the body where the mouth is located, often producing an enlarged head. This is associated with the animal's movement direction and bilateral symmetry, and cephalization of the nervous system led to the formation of a functional centralized brain in three groups of bilaterian animals, namely the arthropods, cephalopod molluscs, and vertebrates (craniates).

<span class="mw-page-title-main">Otolith</span> Inner-ear structure in vertebrates which detects acceleration

An otolith, also called statoconium, otoconium or statolith, is a calcium carbonate structure in the saccule or utricle of the inner ear, specifically in the vestibular system of vertebrates. The saccule and utricle, in turn, together make the otolith organs. These organs are what allows an organism, including humans, to perceive linear acceleration, both horizontally and vertically (gravity). They have been identified in both extinct and extant vertebrates.

<i>Cranchia scabra</i> Species of squid

Cranchia scabra is a species of glass squid. It is the only species in the genus, and is fairly small. They reside in the epipelagic zones of the tropical Atlantic. The genus also contains bioluminescent species. Cranchia scabra are named after John Cranch who first described this species.

<span class="mw-page-title-main">Marine invertebrates</span> Marine animals without a vertebral column

Marine invertebrates are the invertebrates that live in marine habitats. Invertebrate is a blanket term that includes all animals apart from the vertebrate members of the chordate phylum. Invertebrates lack a vertebral column, and some have evolved a shell or a hard exoskeleton. As on land and in the air, marine invertebrates have a large variety of body plans, and have been categorised into over 30 phyla. They make up most of the macroscopic life in the oceans.

<span class="mw-page-title-main">Deep-sea gigantism</span> Tendency for deep-sea species to be larger than their shallower-water relatives

In zoology, deep-sea gigantism or abyssal gigantism is the tendency for species of deep-sea dwelling animals to be larger than their shallower-water relatives across a large taxonomic range. Proposed explanations for this type of gigantism include necessary adaptation to colder temperature, food scarcity, reduced predation pressure and increased dissolved oxygen concentrations in the deep sea. The harsh conditions and inhospitality of the underwater environment in general, as well as the inaccessibility of the abyssal zone for most human-made underwater vehicles, have hindered the study of this topic.

The sensory organs of gastropods include olfactory organs, eyes, statocysts and mechanoreceptors. Gastropods have no sense of hearing.

A sense is a biological system used by an organism for sensation, the process of gathering information about the surroundings through the detection of stimuli. Although, in some cultures, five human senses were traditionally identified as such, many more are now recognized. Senses used by non-human organisms are even greater in variety and number. During sensation, sense organs collect various stimuli for transduction, meaning transformation into a form that can be understood by the brain. Sensation and perception are fundamental to nearly every aspect of an organism's cognition, behavior and thought.

<span class="mw-page-title-main">Pain in animals</span>

Pain negatively affects the health and welfare of animals. "Pain" is defined by the International Association for the Study of Pain as "an unpleasant sensory and emotional experience associated with actual or potential tissue damage, or described in terms of such damage." Only the animal experiencing the pain can know the pain's quality and intensity, and the degree of suffering. It is harder, if even possible, for an observer to know whether an emotional experience has occurred, especially if the sufferer cannot communicate. Therefore, this concept is often excluded in definitions of pain in animals, such as that provided by Zimmerman: "an aversive sensory experience caused by actual or potential injury that elicits protective motor and vegetative reactions, results in learned avoidance and may modify species-specific behaviour, including social behaviour." Nonhuman animals cannot report their feelings to language-using humans in the same manner as human communication, but observation of their behaviour provides a reasonable indication as to the extent of their pain. Just as with doctors and medics who sometimes share no common language with their patients, the indicators of pain can still be understood.

<span class="mw-page-title-main">Pain in crustaceans</span> Ethical debate

There is a scientific debate which questions whether crustaceans experience pain. It is a complex mental state, with a distinct perceptual quality but also associated with suffering, which is an emotional state. Because of this complexity, the presence of pain in an animal, or another human for that matter, cannot be determined unambiguously using observational methods, but the conclusion that animals experience pain is often inferred on the basis of likely presence of phenomenal consciousness which is deduced from comparative brain physiology as well as physical and behavioural reactions.

<span class="mw-page-title-main">Pain in invertebrates</span> Contentious issue

Pain in invertebrates is a contentious issue. Although there are numerous definitions of pain, almost all involve two key components. First, nociception is required. This is the ability to detect noxious stimuli which evokes a reflex response that moves the entire animal, or the affected part of its body, away from the source of the stimulus. The concept of nociception does not necessarily imply any adverse, subjective feeling; it is a reflex action. The second component is the experience of "pain" itself, or suffering—i.e., the internal, emotional interpretation of the nociceptive experience. Pain is therefore a private, emotional experience. Pain cannot be directly measured in other animals, including other humans; responses to putatively painful stimuli can be measured, but not the experience itself. To address this problem when assessing the capacity of other species to experience pain, argument-by-analogy is used. This is based on the principle that if a non-human animal's responses to stimuli are similar to those of humans, it is likely to have had an analogous experience. It has been argued that if a pin is stuck in a chimpanzee's finger and they rapidly withdraw their hand, then argument-by-analogy implies that like humans, they felt pain. It has been questioned why the inference does not then follow that a cockroach experiences pain when it writhes after being stuck with a pin. This argument-by-analogy approach to the concept of pain in invertebrates has been followed by others.

<span class="mw-page-title-main">Hydrodynamic reception</span> Ability of an organism to sense water movements

In animal physiology, hydrodynamic reception refers to the ability of some animals to sense water movements generated by biotic or abiotic sources. This form of mechanoreception is useful for orientation, hunting, predator avoidance, and schooling. Frequent encounters with conditions of low visibility can prevent vision from being a reliable information source for navigation and sensing objects or organisms in the environment. Sensing water movements is one resolution to this problem.

<span class="mw-page-title-main">Xenacoelomorpha</span> A deep-branching bilaterian clade of animals with a simple body plan

Xenacoelomorpha is a small phylum of bilaterian invertebrate animals, consisting of two sister groups: xenoturbellids and acoelomorphs. This new phylum was named in February 2011 and suggested based on morphological synapomorphies, which was then confirmed by phylogenomic analyses of molecular data.

<span class="mw-page-title-main">Pain in cephalopods</span> Contentious issue

Pain in cephalopods is a contentious issue. Pain is a complex mental state, with a distinct perceptual quality but also associated with suffering, which is an emotional state. Because of this complexity, the presence of pain in non-human animals, or another human for that matter, cannot be determined unambiguously using observational methods, but the conclusion that animals experience pain is often inferred on the basis of likely presence of phenomenal consciousness which is deduced from comparative brain physiology as well as physical and behavioural reactions.

<span class="mw-page-title-main">Communication in aquatic animals</span>

Communication occurs when an animal produces a signal and uses it to influences the behaviour of another animal. A signal can be any behavioural, structural or physiological trait that has evolved specifically to carry information about the sender and/or the external environment and to stimulate the sensory system of the receiver to change their behaviour. A signal is different from a cue in that cues are informational traits that have not been selected for communication purposes. For example, if an alerted bird gives a warning call to a predator and causes the predator to give up the hunt, the bird is using the sound as a signal to communicate its awareness to the predator. On the other hand, if a rat forages in the leaves and makes a sound that attracts a predator, the sound itself is a cue and the interaction is not considered a communication attempt.

References

  1. Morton, B. (2009). "Statocyst structure in the Anomalodesmata (Bivalvia)". Journal of Zoology. 206: 23–34. doi:10.1111/j.1469-7998.1985.tb05633.x.
  2. Spangenberg, D. B. (1986). "Statolith formation in Cnidaria: effects of cadmium on Aurelia statoliths". Scanning Electron Microscopy (4): 1609–1618. PMID   11539690.
  3. Lowe, B. (1997). "The role of Ca2+ in deflection-induced excitation of motile, mechanoresponsive balancer cilia in the ctenophore statocyst". Journal of Experimental Biology. 200 (Pt 11): 1593–1606. doi:10.1242/jeb.200.11.1593. PMID   9202448.
  4. Ehlers, U. (1997). "Ultrastructure of the statocysts in the apodous sea cucumber Leptosynapta inhaerens (Holothuroidea, Echinodermata)". Acta Zoologica. 78: 61–68. doi:10.1111/j.1463-6395.1997.tb01127.x.
  5. Clarke, M. R. (2009). "The cephalopod statolithan—introduction to its form". Journal of the Marine Biological Association of the United Kingdom. 58 (3): 701–712. doi:10.1017/S0025315400041345.
  6. Levi, R.; Varona, P.; Arshavsky, Y. I.; Rabinovich, M. I.; Selverston, A. I. (2004). "Dual Sensory-Motor Function for a Molluskan Statocyst Network". Journal of Neurophysiology. 91 (1): 336–345. doi:10.1152/jn.00753.2003. PMID   14507988.
  7. Cohen, M. J. (1960). "The response patterns of single receptors in the crustacean statocyst". Proceedings of the Royal Society B: Biological Sciences. 152 (946): 30–49. doi:10.1098/rspb.1960.0020. PMID   13849418. S2CID   29494854.
  8. Deliagina, Tatiana G.; Arshavsky, Yuri I.; Orlovsky, Grigori N. (1998). "Control of spatial orientation in a mollusc". Nature. 393 (6681): 172–175. doi:10.1038/30251. ISSN   0028-0836.
  9. Israelsson, O. (2007). "Ultrastructural aspects of the 'statocyst' of Xenoturbella (Deuterostomia) cast doubt on its function as a georeceptor". Tissue and Cell. 39 (3): 171–177. doi:10.1016/j.tice.2007.03.002. PMID   17434196.
  10. "Scientists Find that Squid Can Detect Sounds".
  11. "How Squid Hear: It's All in the Motion of the Ocean". 2 February 2011.
  12. "Squid shown to be able to hear".