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Lineus longissimus
Lineus longissimus
Lineus longissimus
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Bootlace worm
Scientific classification Edit this classification
Kingdom: Animalia
Phylum: Nemertea
Class: Pilidiophora
Order: Heteronemertea
Family: Lineidae
Genus: Lineus
Species:
L. longissimus
Binomial name
Lineus longissimus
(Gunnerus, 1770)
Synonyms

Nemertes borlasii Cuvier, 1817

The bootlace worm (Lineus longissimus) is a species of ribbon worm and one of the longest known animals, with specimens typically measuring 5–15 m (16–49 ft), and individuals known to measure up to 30 m (98 ft) long.[1] There exist reports claiming lengths of up to 55 m (180 ft), although it is possible that these are reporting individuals that have been stretched beyond their usual length.[2][3] Its mucus is highly toxic.[4]

Taxonomy

[edit]

The bootlace worm is in the phylum Nemertea or ribbon worms. It is the most common nemertean found along the coasts of Britain.[5]

Description

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Bootlace worms may grow very long but are usually only 5 to 10 millimetres (0.20 to 0.39 in) in width. The body is brown with lighter (longitudinal) stripes.[6] Its mucus contains a relatively strong neurotoxin which it uses as a defense against predators.[7] When handled, it produces large amounts of thick mucus with a faint pungent smell, reminiscent of iron or sewage.[8] This toxic mucus has been shown to kill crabs and cockroaches, and could have applications as an agricultural insecticide.[9] Tests on this toxin have shown low toxicity in humans cells, as well as low bactericidal and bacteriostatic properties.[10]

In 1864, William M'Intosh described a specimen that had washed ashore in the aftermath of a severe storm by St Andrews, Scotland, which was more than 55 m (180 ft) long,[11] longer than the longest known lion's mane jellyfish, the animal which is often considered to be the longest in the world. However, records of extreme length should be taken with caution, because the bodies of nemerteans are flexible and can easily stretch to much more than their usual length.[12]

Like other nemerteans, Lineus longissimus feeds using its eversible proboscis. As it is in the class Anopla, its proboscis is not armed with a barbed stylet. Instead, it has a cluster of sticky filaments at the end of its proboscis that it uses to immobilize prey.[citation needed]

Habitat

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Lineus longissimus can be found on Norway's and Britain's coasts, on the Danish east coast and also on Sweden's west coast. [citation needed]

References

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[edit]
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Lineus longissimus

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from Grokipedia
Lineus longissimus, commonly known as the bootlace worm, is a species of ribbon worm belonging to the phylum , distinguished as one of the longest animals on , with specimens typically measuring 5–15 meters in length and exceptional individuals reported to reach up to 55 meters (though some sources indicate up to 30 meters) when fully extended. This unsegmented, elongated marine invertebrate features a slender body, 5–10 mm wide, that ranges from dark olive brown in juveniles to blackish brown in adults, often displaying a purplish due to epidermal cilia. It possesses a rectangular head with a pale tip and 10–20 reddish-brown eyes on each side, along with pale longitudinal streaks on the anterior dorsal surface. Native to the , L. longissimus inhabits intertidal and shallow subtidal zones, commonly found coiled beneath boulders, in rock pools among holdfasts, or burrowed in muddy, sandy, stony, or shelly substrata from the lower shore to depths of at least 10 meters. Its distribution spans the coasts of Britain and , including western and northern regions with possible scarcity in eastern and , , the North Atlantic, , and regions, including areas like the west coast of and . As a predatory nemertean, it employs an eversible muscular to capture small prey such as crustaceans, and it secretes a thick, pungent containing potent neurotoxins—such as nemertides α-1, α-2, and β-1—that target voltage-gated sodium channels, inducing and in organisms like green crabs and at doses as low as 1 µg/kg. These toxins, structured with inhibitor cystine motifs, render the worm highly defended against predators and highlight its potential applications in bioinsecticides and biomedical research. In 2021, its genome was sequenced, further advancing research into these toxins. Behaviorally, L. longissimus often forms intricate knots when resting and exhibits remarkable elasticity, able to contract to short lengths when resting or disturbed and extend to several meters when active. Classified within the order Heteronemertea and genus Lineus, this contributes to the of over 1,300 known nemerteans, underscoring the ecological role of ribbon worms in marine benthic communities.

Taxonomy and classification

Taxonomic history

Lineus longissimus was first formally described by Johan Ernst Gunnerus in 1770 as Ascaris longissima, placing it within the nematode genus Ascaris under the early Linnaean system of classification for worms (Vermes). This description appeared in Gunnerus's work Nogle smaa rare og meestendeelen nye Norske Soedyr, published in the proceedings of the Royal Norwegian Society of Sciences and Letters, where he documented the species based on specimens from Norwegian waters. In 1806, James Sowerby established the Lineus and transferred the species to it as Lineus longissimus, marking a shift toward recognizing its distinct ribbon-like morphology separate from nematodes; this renaming was detailed in Sowerby's The British Miscellany, including an illustration of the worm. Earlier, in 1817, had synonymized it under Nemertes borlasii within his newly proposed Nemertes, which later gave rise to the name , reflecting initial confusions with flatworm-like forms. Other historical synonyms include Borlasia longissimus and Heterolineus longissimus, stemming from 19th-century reassignments as nemertean evolved beyond broad groupings. Throughout the 19th and early 20th centuries, classifications refined with the establishment of the family Lineidae by Carmichael McIntosh in , which encompassed Lineus and related heteronemertean genera based on anatomical features like rhynchocoel structure. Modern revisions, such as those in the , affirm Lineus longissimus (Gunnerus, 1770) as the valid name, prioritizing the while resolving junior synonyms through nomenclatural priority.

Phylogenetic position

Lineus longissimus is classified within the phylum , class Pilidiophora, order Heteronemertea, family Lineidae, and genus Lineus. In older taxonomic systems, it was assigned to the class Anopla, a grouping now subsumed under Pilidiophora alongside former Enopla taxa. Its position in Heteronemertea is bolstered by distinctive morphological features, notably an eversible that lacks a stylet, setting it apart from Hoplonemertea where a stylet is typically present for prey capture. This unarmed structure aligns with the broader characteristics of pilidiophoran nemerteans, emphasizing their evolutionary adaptations for predation without armature. Molecular phylogenies, including those based on 18S rRNA and subunit I (COI) genes, affirm its close affinity to other Lineus species and basal nemerteans. For instance, multi-gene analyses incorporating COI, 16S rRNA, 18S rRNA, 28S rRNA, and sequences position Lineus longissimus within a monophyletic Lineus in the family Lineidae, supporting its placement among crown-group heteronemerteans. These studies also reinforce Nemertea's location as sister to or Annelida in the eutrochozoan of . As one of the longest recorded animals and the first nemertean with a chromosome-level assembly, Lineus longissimus provides a valuable model for exploring ribbon worm diversification, particularly in marine habitats where nemertean lineages have radiated.

Physical description

Morphology and size

Lineus longissimus is an unsegmented, elongated ribbon worm characterized by a flattened, ribbon-like body that lacks any segmentation. Typical specimens measure 5–15 meters in length and 5–10 mm in width, though individuals can extend beyond 30 meters under certain conditions. The body exhibits a rectangular head with deep lateral slits, a pale tip, and 10–20 reddish-brown eyes on each side, and the entire surface is ciliated, contributing to its mobility across substrates. The worm's coloration varies by age and condition, with young individuals displaying dark olive brown to chocolate brown hues, while adults are blackish brown to black. A uniform brown base is often accented by iridescent longitudinal pale stripes, particularly along the anterior dorsal surface and venter, giving the body a subtle purplish sheen in life. These markings may fade upon preservation. Specimens elongate considerably during active periods or maturity and can contract to approximately one-sixth of their extended length when disturbed, allowing them to coil tightly into crevices. No sexual dimorphism in size has been observed, consistent with the rarity of such traits in nemerteans. A length of 55 meters has been reported for a specimen washed ashore near St. Andrews, Scotland, in 1864 following a severe storm, though this is based on an unverified historical account. As the longest known nemertean, L. longissimus surpasses the typical dimensions of most ribbon worms, which rarely exceed a few meters.

Anatomical features

Lineus longissimus, like other heteronemerteans, possesses a distinctive apparatus that is a defining feature of the phylum . The is an eversible, muscular tube housed within a fluid-filled cavity called the rhynchocoel, which extends most of the body length and allows for rapid protrusion through a rhynchodeal pore anterior to the . As a member of the class Anopla, its is unarmed, lacking a stylet, and instead features glandular cells that secrete sticky filaments and adhesive substances to entangle and capture prey. The apparatus includes layered musculature—outer longitudinal, circular, and inner longitudinal—with reinforcing muscle crosses that enable controlled eversion and retraction. The of L. longissimus is closed, consisting of paired lateral vessels connected anteriorly by a cephalic loop and posteriorly by a tail loop, along with a dorsal median vessel running between the rhynchocoel and the gut. circulation is facilitated by peristaltic contractions of the vessels, and the often contains a hemoglobin-like that imparts a or hue, particularly noticeable in the neural tissues. This system supports oxygen transport in the worm's elongated body, which can vary dramatically in length from a few centimeters to over 30 meters. The is centralized, featuring a composed of four cerebral ganglia arranged in two pairs—dorsal and ventral—encased in fibrous neurilemma and connected by commissures. Paired ventral cords extend posteriorly from the ventral ganglia, fusing at intervals and often accompanied by a thinner dorsal cord; additional cephalic nerves innervate sensory structures like the cerebral organs, which are paired sacs aiding in chemoreception. This organization allows for coordinated movement and sensory processing along the worm's ribbon-like body. The digestive tract is complete, beginning with a located ventrally behind the and leading to an eversible that can protrude to ingest . The foregut transitions into a intestine with a dorsal and paired lateral diverticula for nutrient absorption, followed by a short that terminates in a opening via a subterminal . Glandular epithelia line the tract, secreting enzymes to break down ingested material. L. longissimus, like other nemerteans, exhibits remarkable regenerative abilities, capable of and regenerating a complete individual from small body fragments via formation at the cut ends, rebuilding a head and tail within 1–2 weeks, though success diminishes if fragments are shorter than their width or taken too near the posterior end. This capacity underscores the worm's resilience, enabling recovery from predation or environmental damage.

Distribution and habitat

Geographic range

Lineus longissimus is primarily distributed along the temperate coasts of the North Atlantic, mainly in the northern regions from approximately 50°N to 70°N, with longitudinal extent from 23°W in the west to 10°E in the east. This range encompasses the northeastern , including areas from eastward to the Atlantic, , and Baltic coasts of . Key regions within this distribution include the coasts of Britain, particularly , as well as Denmark's east coast and Sweden's west coast, where the species is commonly reported in intertidal and subtidal zones extending to depths of at least 35 m. Records confirm presence around most British coasts, including eastern and , based on recent surveys. It is also present in the and more broadly. The species was first described in 1770 from specimens collected in by Johan Ernst Gunnerus, marking the initial historical record of its presence in the northern extent of its range. Recent observations continue to confirm its occurrence across these areas, supplemented by contributions on platforms like , which document sightings primarily in northern European coastal sites. No evidence of invasive spread beyond its established temperate North Atlantic range has been reported, though monitoring for potential climate-driven distributional shifts is advisable given ongoing environmental changes in marine ecosystems. Within its range, it inhabits a variety of coastal marine environments, from rocky shores to subtidal sediments.

Environmental preferences

Lineus longissimus inhabits intertidal and subtidal zones, primarily on the lower shore where it coils in dense, writhing knots beneath boulders, within rockpools amid holdfasts, or in rock fissures, and extends into sublittoral areas on muddy, sandy, stony, or shelly substrata. This benthic lifestyle keeps the worm in close association with the , favoring sheltered microhabitats that provide protection from physical disturbance. The occurs in fully marine conditions typical of temperate northeastern Atlantic waters, with salinities around 34–35 ppt and temperatures from 5°C in winter to 14°C in summer. It avoids high-energy wave-exposed zones, instead occupying substrates like muddy sand that buffer against strong currents and abrasion. Adaptations such as copious enable to substrates and offer protection in dynamic intertidal environments, where the worm's produces a thick, pungent layer upon disturbance. This likely aids in maintaining position amid tidal fluctuations and shifts.

Biology and behavior

Feeding mechanisms

Lineus longissimus employs an predation strategy, remaining coiled or stretched along the substrate in intertidal and shallow subtidal zones to intercept passing prey. Upon detecting movement, the worm rapidly everts its to ensnare targets from a distance. This eversion is powered by hydrostatic pressure from the rhynchocoel, allowing the proboscis to strike swiftly and coil around prey. The of L. longissimus, characteristic of the class Anopla, lacks a stylet for mechanical piercing and instead relies on secreted by frontal glands to immobilize victims. This , often laced with toxins from specialized glands, entangles small , preventing escape while the worm approaches. Prey is then drawn toward the without tearing, preserving the body for . The diet of L. longissimus consists primarily of annelids, small mollusks, and crustaceans, with opportunistic scavenging of carrion supplementing active hunting. worms and amphipods form common targets, reflecting the worm's benthic lifestyle and ability to exploit diverse zoobenthic resources. Following capture, digestion begins with secretions from the proboscis that aid in prey breakdown via contact with the . The partially digested material is then swallowed whole through the expandable mouth and , entering the for further breakdown by gastrodermal cells. This process enables efficient nutrient absorption in the long, tubular digestive tract, adapted to the worm's elongated morphology.

Reproduction and life cycle

Lineus longissimus is dioecious, with distinct male and female individuals engaging in sexual reproduction through external fertilization in the water column. Mature females release oocytes via gonoducts or directly into the surrounding seawater, where contact with the medium induces germinal vesicle breakdown and meiotic resumption within 20–40 minutes. Males similarly spawn sperm, facilitating broadcast fertilization; this process likely follows an annual cycle, with females capable of producing over 40,000 oocytes across numerous gonads, indicating potential for mass spawning events. Fertilized eggs develop into planktotrophic pilidium larvae, which are free-swimming and hat-shaped, featuring an aboral apical organ, ciliated lophophore-like bands for locomotion, and a functional gut for feeding on . This larval stage persists for several weeks in the , allowing dispersal before into the juvenile worm. During , the juvenile form develops internally within the pilidium, eventually resorbing and consuming the larval tissues in a process known as catastrophic . The overall life cycle from hatching to sexual maturity remains poorly documented, with precise timelines unavailable. Asexual reproduction via transverse fragmentation is known in some nemerteans but remains unconfirmed for L. longissimus, with genetic analyses indicating that predominates in natural populations. The species' notable regenerative abilities, stemming from its diffuse and muscle organization, may facilitate recovery from any incidental fragmentation.

General behavior

Lineus longissimus often forms intricate knots when resting, which may serve to deter predators or conserve moisture in intertidal zones. The worm exhibits elastic body properties, capable of contracting significantly when active or disturbed, from extended lengths of up to 55 meters to as little as 1 meter.

Ecology and interactions

Predatory role

Lineus longissimus functions as an apex micro-predator within intertidal communities, exerting control over populations of annelids and molluscs through targeted predation. As a secondary in marine food webs, it preys primarily on worms such as those in the genus Amphitrite, which it invades within their tubes, as well as small crustaceans and molluscs. This predatory activity influences prey and contributes to sediment turnover, as the worm's burrowing targets disrupt the engineering roles of tube-dwelling polychaetes in muddy substrata. By regulating herbivorous or detritivorous prey populations, L. longissimus indirectly affects biodiversity in soft-sediment environments, promoting community stability through top-down control. Surveys indicate that it is commonly the most abundant nemertean under low-shore rocks in optimal intertidal sites, with higher abundances observed in shallow, sheltered areas.

Toxicity and defenses

_Lineus longissimus employs a mechanism through its epidermal , which contains a suite of neurotoxic peptides known as nemertides, including α-nemertide-1 and α-nemertide-2. These cysteine-rich peptides target voltage-gated sodium channels in , leading to and death upon contact. The is secreted copiously when the worm is stressed or handled, serving to deter predators by creating a toxic barrier that inhibits feeding attempts. The toxins in the mucus demonstrate potent effects against crustaceans and insects; for instance, sub-nanomolar concentrations of α-nemertide-1 can paralyze and kill green crabs () within minutes. Similarly, exposure to the mucus has been shown to immobilize and eliminate , highlighting its selective toxicity toward arthropods with minimal impact on vertebrates. This paralytic action occurs rapidly on contact, providing an effective passive defense against potential threats in the marine environment. Research into these nemertides has revealed their potential applications beyond , particularly as natural insecticides due to their efficacy against pest species like and invasive crabs. As part of the 2021 Darwin Tree of Life project, genomic sequencing of L. longissimus has facilitated the identification of novel bioactive compounds in its , with ongoing studies exploring their use in antihelminthic drugs and marine-derived pharmaceuticals. These efforts emphasize the worm's as a source of invertebrate-specific neurotoxins for biotechnological development.

References

  1. https://www.marlin.ac.uk/species/detail/2075
  2. https://www.guinnessworldrecords.com/world-records/longest-animal
  3. https://www.nature.com/articles/s41598-018-22305-w
  4. https://pmc.ncbi.nlm.nih.gov/articles/PMC8593623/
  5. https://www.marinespecies.org/aphia.php?p=sourcedetails&id=90278
  6. https://repository.naturalis.nl/pub/261764/ZM82-07_GittenbergerA.pdf
  7. https://www.marinespecies.org/aphia.php?p=sourcedetails&id=8260
  8. https://www.marinespecies.org/aphia.php?p=taxdetails&id=122528
  9. http://www.marinespecies.org/aphia.php?p=taxdetails&id=122314
  10. https://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&id=88925
  11. https://biodiversity.no/Pages/196727/Heteronemertea
  12. https://www.researchgate.net/publication/354810461_An_updated_classification_of_the_phylum_Nemertea
  13. https://pubmed.ncbi.nlm.nih.gov/40184201/
  14. https://www.mdpi.com/2073-4441/15/4/809
  15. https://animaldiversity.org/accounts/Nemertea/
  16. https://www.researchgate.net/publication/289317274_Phylum_Nemertea
  17. https://pmc.ncbi.nlm.nih.gov/articles/PMC6410017/
  18. https://pdfs.semanticscholar.org/f26b/d92d9f0a091a558a90f9d2b11def29243d10.pdf
  19. https://www.researchgate.net/publication/229819660_Regeneration_in_Nemerteans
  20. https://species.nbnatlas.org/species/NBNSYS0000176159
  21. https://www.inaturalist.org/taxa/467341-Lineus-longissimus
  22. https://data.jncc.gov.uk/data/a8574bd9-38fc-4e1a-8cf5-20589ee8d169/jncc-mncr-sector-5-part-3.pdf
  23. https://www.sealifebase.ca/Reproduction/ReproSummary.php?id=57093
  24. https://repository.si.edu/bitstream/handle/10088/11149/iz_stricker_etal2001_text.pdf
  25. https://pmc.ncbi.nlm.nih.gov/articles/PMC4584431/
  26. https://livrepository.liverpool.ac.uk/3175082/1/386867.pdf
  27. https://pmc.ncbi.nlm.nih.gov/articles/PMC6617912/
  28. https://pmc.ncbi.nlm.nih.gov/articles/PMC9132205/
  29. https://www.researchgate.net/publication/282664686_Nemerteans_in_an_Irish_marine_reserve_Synopsis_of_current_and_historical_records
  30. https://www.uu.se/en/news/2018/2018-03-22-insect-toxin-detected-in-worlds-longest-animal
  31. https://pubs.acs.org/doi/10.1021/acs.jnatprod.1c00104
  32. https://www.darwintreeoflife.org/news_item/lineus-longissimus-marine-medicines-from-the-ribbon-worm/
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