Hediste diversicolor

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Hediste diversicolor
Nereis diversicolor 1.jpg
Scientific classification OOjs UI icon edit-ltr.svg
Domain: Eukaryota
Kingdom: Animalia
Phylum: Annelida
Clade: Pleistoannelida
Subclass: Errantia
Order: Phyllodocida
Family: Nereididae
Genus: Hediste
Species:
H. diversicolor
Binomial name
Hediste diversicolor
(O.F. Müller, 1776) [1]
Synonyms [1]
  • Neanthes diversicolor (Müller, 1776)
  • Nereis (Hediste) diversicolor O.F. Müller, 1776
  • Nereis brevimanus Johnston, 1840
  • Nereis depressa Frey & Leuckart, 1847
  • Nereis diversicolor (Müller, 1776)
  • Nereis sarsii Rathke, 1843
  • Nereis versicolor Müller
  • Nereis viridis Johnston, 1840

Hediste diversicolor, commonly known as a ragworm, is a polychaete worm in the family Nereididae. It lives in a burrow in the sand or mud of beaches and estuaries in intertidal zones in the north Atlantic. This species is used in research but its classification is in dispute and in the literature it is often classified as Nereis diversicolor (O.F. Müller, 1776). [2] Its specific name "diversicolor" refers to the fact that its colour changes from brown to green as the breeding season approaches.

Contents

Description

Hediste diversicolor can grow up to 10 cm (4 in) in length and may have from ninety to one hundred and twenty segments when mature. The head has a pair of palps, two pairs of antennae, four pairs of tentacles and four eyes. Each body segment has a pair of bristly appendages known as parapodia which are used for swimming. There is a prominent blood vessel running along the dorsal surface of the animal. This ragworm is pale brown but changes to green as the gonads mature and the breeding season approaches. [2] [3]

Distribution and habitat

Hediste diversicolor is native to the north-east Atlantic. Its range extends from the Baltic Sea and North Sea southwards to the Azores and Mediterranean Sea. It has been introduced to the north-west Atlantic in the areas of Cobscook Bay, the Gulf of Maine and the Gulf of St Lawrence. [4] It is plentiful on beaches of sand, muddy sand and mud, including areas of low salinity, where it lives in a semi-permanent J-shaped or U-shaped burrow and under adjoining stones in the intertidal zone. [2] [3]

Biology

Examination of the contents of the gut shows that Hediste diversicolor is a predator and generalist scavenger, able to adapt its diet to whatever is currently available. It spins a mucus net at the entrance of its burrow in which it traps phytoplankton, zooplankton, diatoms, bacteria and other small particles. It creates a water current through its tube by writhing about inside to draw particles through the net. Periodically it rolls the net up and swallows it before spinning another. When the availability of suitably-sized food particles is low it emerges from its burrow and hunts for small invertebrates, seizing them with its strong jaws. It also eats detritus and even animal faeces. [5] They also draw, otherwise not edible, cordgrass seeds into their burrows and let them sprout to produce high-quality food, one of the rare examples of “gardening” by animals. [6]

The sexes are separate in Hediste diversicolor, and females heavily outnumber the males. As the breeding season approaches, the males, which were previously indistinguishable from the females, turn bright green. At the same time, the females turn a duller dark green on the dorsal surface with their earlier orange-brown pigmentation still showing through. Eggs develop within the female's body cavity. Histolysis then occurs and the body wall becomes brittle and eventually bursts, liberating the eggs into the burrow. [2]

Synchronized spawning takes place in early spring, usually at the time of the new or full moon when the water has warmed up after the winter and attained a temperature above 6 °C (43 °F). The timing of this event varies throughout the worm's range and more southern populations mature at a year of age while more northerly ones may be three years old before they breed. The male seems to be attracted to a burrow occupied by a female by the release of a pheromone into the water. He crawls across the seabed and liberates sperm into the water just outside the entrance of the female's burrow. The sperm is drawn into the tube by the water current that the female creates by undulating her body. Here fertilisation takes place and the larvae are brooded for ten to fourteen days. Both males and females die after spawning. [2] [7]

Ecology

Hediste diversicolor is widespread and common and is eaten by many species of birds and fish. It is the main food item for the pied avocet (Recurvirostra avosetta), the grey plover (Pluvialis squatarola), the curlew sandpiper (Calidris ferruginea), the bar-tailed godwit (Limosa lapponica) and the curlew (Numenius arquata). [8] Several flatfish which live on intertidal mudflats feed on the ragworm. These include the common dab (Limanda limanda), the common sole (Solea solea), the European flounder (Platichthys flesus) and the European plaice (Pleuronectes platessa). [2]

Hediste diversicolor has been found to have a deleterious effect on the establishment of saltmarshes. When tests were undertaken in southern England on establishing the seagrass Zostera noltei , it was found that efforts were more successful when the ragworm was excluded from the area of transplanted material. In another planting trial, the pioneering cordgrass Spartina anglica , used to prevent coastal erosion, was similarly adversely affected. In the laboratory, ragworms were seen to pull leaves of the grasses into their burrows where they fed on them, and the disturbance to the substrate caused by their burrowing activities was also thought to contribute to the reduced establishment rates. [9]

Uses

Hediste diversicolor is used as a model laboratory animal for research. It has also been used to evaluate the quality of marine sediment because it bioaccumulates certain heavy metals such as lead, cadmium, chromium and arsenic. [10] [11] Anglers use it for bait when sea fishing, digging it out of the substrate with a large fork. It is also available commercially. [2]

Related Research Articles

<span class="mw-page-title-main">Polychaete</span> Class of annelid worms

Polychaeta is a paraphyletic class of generally marine annelid worms, commonly called bristle worms or polychaetes. Each body segment has a pair of fleshy protrusions called parapodia that bear many bristles, called chaetae, which are made of chitin. More than 10,000 species are described in this class. Common representatives include the lugworm and the sandworm or clam worm Alitta.

<i>Nereis</i> Genus of annelid worms

Nereis is a genus of polychaete worms in the family Nereididae. It comprises many species, most of which are marine. Nereis possess setae and parapodia for locomotion and gas exchange. They may have two types of setae, which are found on the parapodia. Acicular setae provide support. Locomotor setae are for crawling, and are the bristles that are visible on the exterior of the Polychaeta. They are cylindrical in shape, found not only in sandy areas, and they are adapted to burrow. They often cling to seagrass (posidonia) or other grass on rocks and sometimes gather in large groups.

<span class="mw-page-title-main">Bioturbation</span> Reworking of soils and sediments by organisms.

Bioturbation is defined as the reworking of soils and sediments by animals or plants. It includes burrowing, ingestion, and defecation of sediment grains. Bioturbating activities have a profound effect on the environment and are thought to be a primary driver of biodiversity. The formal study of bioturbation began in the 1800s by Charles Darwin experimenting in his garden. The disruption of aquatic sediments and terrestrial soils through bioturbating activities provides significant ecosystem services. These include the alteration of nutrients in aquatic sediment and overlying water, shelter to other species in the form of burrows in terrestrial and water ecosystems, and soil production on land.

<span class="mw-page-title-main">Clitellata</span> Class of annelid worms

The Clitellata are a class of annelid worms, characterized by having a clitellum – the 'collar' that forms a reproductive cocoon during part of their life cycles. The clitellates comprise around 8,000 species. Unlike the class of Polychaeta, they do not have parapodia and their heads are less developed.

<span class="mw-page-title-main">Epitoky</span> Sexual maturation process in marine worms

Epitoky is a process that occurs in many species of polychaete marine worms wherein a sexually immature worm is modified or transformed into a sexually mature worm. Epitokes are pelagic morphs capable of sexual reproduction. Unlike the immature form, which is typically benthic, epitokes are specialized for swimming as well as reproducing. The primary benefit to epitoky is increased chances of finding other members of the same species for reproduction.

<span class="mw-page-title-main">Nereididae</span> Family of annelid worms

Nereididae are a family of polychaete worms. It contains about 500 – mostly marine – species grouped into 42 genera. They may be commonly called ragworms or clam worms.

<span class="mw-page-title-main">Eunicidae</span> Family of annelids

Eunicidae is a family of marine polychaetes. The family comprises marine annelids distributed in diverse benthic habitats across Oceania, Europe, South America, North America, Asia and Africa. The Eunicid anatomy typically consists of a pair of appendages near the mouth (mandibles) and complex sets of muscular structures on the head (maxillae) in an eversible pharynx. One of the most conspicuous of the eunicids is the giant, dark-purple, iridescent "Bobbit worm", a bristle worm found at low tide under boulders on southern Australian shores. Its robust, muscular body can be as long as 2 m. Eunicidae jaws are known from as far back as Ordovician sediments. Cultural tradition surrounds Palola worm reproductive cycles in the South Pacific Islands. Eunicidae are economically valuable as bait in both recreational and commercial fishing. Commercial bait-farming of Eunicidae can have adverse ecological impacts. Bait-farming can deplete worm and associated fauna population numbers, damage local intertidal environments and introduce alien species to local aquatic ecosystems.

<i>Alitta virens</i> Species of annelid worm

Alitta virens is an annelid worm that burrows in wet sand and mud. They constuct burrows of different shapes They range from being very complex to very simple. Long term burrows are held together by mucus. Their burrows are not connected to each other; they are generally solitary creatures. The spacing between the burrows depends on how readily they can propagate water signals.

<i>Nereis vexillosa</i> Species of annelid worm

Nereis vexillosa belongs to the phylum Annelida, a group known as the segmented worms. It is generally iridescent green and can reach 30 cm in length. It can be distinguished by the size of the upper ligules on the notopodia of the posterior region of the body. The upper ligules are much larger than the lower ligules. It is also without a collar-like structure around the peristomium.

<i>Hesionidae</i> Family of annelids

Hesionidae are a family of phyllodocid "bristle worms". They are marine organisms. Most are found on the continental shelf; Hesiocaeca methanicola is found on methane ice, where it feeds on bacterial biofilms.

<i>Serpula</i> Genus of annelid worms

Serpula is a genus of sessile, marine annelid tube worms that belongs to the family Serpulidae. Serpulid worms are very similar to tube worms of the closely related sabellid family, except that the former possess a cartilaginous operculum that occludes the entrance to their protective tube after the animal has withdrawn into it. The most distinctive feature of worms of the genus Serpula is their colorful fan-shaped "crown". The crown, used by these animals for respiration and alimentation, is the structure that is most commonly seen by scuba divers and other casual observers.

<i>Alitta succinea</i> Common clam worm

Alitta succinea is a species of marine annelid in the family Nereididae. It has been recorded throughout the North West Atlantic, as well as in the Gulf of Maine and South Africa.

<span class="mw-page-title-main">Phyllodocida</span> Order of annelid worms

Phyllodocida is an order of polychaete worms in the subclass Aciculata. These worms are mostly marine, though some are found in brackish water. Most are active benthic creatures, moving over the surface or burrowing in sediments, or living in cracks and crevices in bedrock. A few construct tubes in which they live and some are pelagic, swimming through the water column. There are estimated to be more than 4,600 accepted species in the order.

<i>Platynereis dumerilii</i> Species of annelid worm

Platynereis dumerilii is a species of annelid polychaete worm. It was originally placed into the genus Nereis and later reassigned to the genus Platynereis. Platynereis dumerilii lives in coastal marine waters from temperate to tropical zones. It can be found in a wide range from the Azores, the Mediterranean, in the North Sea, the English Channel, and the Atlantic down to the Cape of Good Hope, in the Black Sea, the Red Sea, the Persian Gulf, the Sea of Japan, the Pacific, and the Kerguelen Islands. Platynereis dumerilii is today an important lab animal, it is considered as a living fossil, and it is used in many phylogenetic studies as a model organism.

<span class="mw-page-title-main">Annelid</span> Phylum of segmented worms

The annelids, also known as the segmented worms, are a large phylum, with over 22,000 extant species including ragworms, earthworms, and leeches. The species exist in and have adapted to various ecologies – some in marine environments as distinct as tidal zones and hydrothermal vents, others in fresh water, and yet others in moist terrestrial environments.

<i>Scolelepis squamata</i> Species of annelid worm

Scolelepis squamata is a species of polychaete worm in the family Spionidae. It occurs on the lower shore of coasts on either side of the Atlantic Ocean.

Dipolydora commensalis is a species of polychaete worm in the family Spionidae. It has a commensal relationship with a hermit crab and occurs on the lower shore of coasts on the western side of the Atlantic Ocean.

<i>Neanthes fucata</i> Species of annelid worm

Neanthes fucata is a species of marine polychaete worm in the family Nereididae. It lives in association with a hermit crab such as Pagurus bernhardus. It occurs in the northeastern Atlantic Ocean, the North Sea and the Mediterranean Sea.

<i>Tylorrhynchus heterochetus</i> Edible species of annelid worm

Tylorrhynchus heterochetus, also known as the Japanese palolo is a species of edible ragworm.

References

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  2. 1 2 3 4 5 6 7 Budd, Georgina (2008). "Ragworm: Hediste diversicolor". Marine Life Information Network . Retrieved 2013-05-18.
  3. 1 2 "Ragworm (Nereis diversicolor)". Science and Nature: Animals. BBC. Retrieved 2013-05-17.
  4. A. L. Einfeldt, J. R. Doucet, J. A. Addison (2014). "Phylogeography and cryptic introduction of the ragworm Hediste diversicolor (Annelida, Nereididae) in the Northwest Atlantic". Invertebrate Biology. 133 (3): 232–241. doi:10.1111/ivb.12060.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  5. Costa, Pedro Fidalgo E.; Oliveira, Rui F.; Cancela da Fonseca, Luis (2006). "Feeding Ecology of Nereis diversicolor (O.F. Müller) (Annelida, Polychaeta) on Estuarine and Lagoon Environments in the Southwest Coast of Portugal" (PDF). Pan-American Journal of Aquatic Sciences. 1 (2): 114–126.
  6. Zhu, Z., J. van Belzen, T. Hong, T. Kunihiro, T. Ysebaert, P. M. J. Herman, et al. (2016). Sprouting as a gardening strategy to obtain superior supplementary food: evidence from a seed-caching marine worm. Ecology. doi: 10.1002/ecy.1613
  7. Bartels-Hardege, H. D.; Zeeck, E. (1990). "Reproductive behaviour of Nereis diversicolor (Annelida: Polychaeta)". Marine Biology. 106 (3): 409–412. doi:10.1007/BF01344320. S2CID   86682968.
  8. Goss-Custard, J. D.; Jones, R. E.; Newberry, P. E. (1989). "The ecology of the Wash. 1. Distribution and diet of wading birds". Journal of Applied Ecology. 14 (3): 681–700. doi:10.2307/2402803. JSTOR   2402803.
  9. Emmerson, M. (2000). "Remedial habitat creation: does Nereis diversicolor play a confounding role in the colonisation and establishment of the pioneering saltmarsh plant, Spartina anglica?". Helgoland Marine Research. 54 (2–3): 110–116. doi: 10.1007/s101520050009 .
  10. Gaion A, Sartori D, Scuderi A, Fattorini D (2014). "Bioaccumulation and biotransformation of arsenic compounds in Hediste diversicolor (Muller 1776) after exposure to spiked sediments". Environmental Science and Pollution Research. 21 (9): 5952–5959. doi:10.1007/s11356-014-2538-z. PMID   24458939. S2CID   12568097.
  11. Septier, François; Dhainaut, Nicole (1992). Etude de la bioconcentration de métaux lourds chez une annélide polychète estuarienne endobenthique (Nereis diversicolor). Utilisation des plans factoriels pour une meilleure évaluation des risques écotoxicologiques liés aux interactions métalliques [Study of the uptake of heavy metal by a burrowing annelid polychete (Nereis diversicolor). Use of experimental designs for a better evaluation of the ecotoxicological risks related to metal interactions]. Doctoral thesis, Université de Lille 1, France.