Melibe leonina

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Hooded nudibranch
Melibe leonina.jpg
Melibe leonina
Scientific classification
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M. leonina
Synonyms
  • Chioraera dalliHeath, 1917
  • Chioraera leoninaGould, 1852
  • Melibe pellucidaBergh, 1904

Melibe leonina, commonly referred to as the hooded nudibranch, lion nudibranch, or lion's mane nudibranch, is a species of predatory nudibranch in the family Tethydidae.

Contents

Description

Melibe leonina from Santa Cruz, California. Melibe leonina from Santa Cruz, California.jpg
Melibe leonina from Santa Cruz, California.

The body of M. leonina is translucent and is usually colorless to pale yellow or green. [1] [2] The average body dimensions are 102mm long and 25mm wide. [2] It has a large expandable oral hood, fringed with two rows of cirri. [2] [3] The oral hood is typically over 51mm wide. [2] This species of Melibe lacks jaws or a radula. [1]

There are a single pair of rhinophores on the hood that contain four to six lamellae. [1] Two rows containing three to six pairs of flat, paddle-shaped cerata run along the body. [1] The cerata range in size, with the front most cerata being the largest. [1] Cerata are capable of autotomy. [4] There are unique granule filled cells at the base of the cerata that are found no where else in the animal that seem to be involved in breaking down connective tissue, as well as two special muscular sphincters. It is thought that after the connective tissue is broken down, these sphincters contract to cut the cerata and then close the wound. [5] The anus and nephroproct are positioned before the second ceras. [1] All other members of the genus Melibe contain chitinous plates in the stomach, however, they are absent in M. leonina. [1]

Distribution

This species occurs in the eastern Pacific Ocean from Alaska to Baja California. [1] [2] [3] M. leonina is the only member of the genus Melibe found on the Pacific coast of North America. [3]

Ecology

Habitat

Melibe leonina in kelp forest. Melibe leonina, Big Sur 2.jpg
Melibe leonina in kelp forest.

M. leonina are common on seagrass and blades of Macrocystis kelp within their range, [3] from the lower intertidal to approximately 37m. [6]

Reproduction

M. leonina is a simultaneous hermaphrodite, with its female and male reproductive organs located on the right side of the body. [3] Fertilization occurs internally, and individuals can lay up to 30,000 eggs at a time. [7] Both females and males lay eggs in protective ribbons that are secreted from the mucus gland. Ribbons contain egg capsules with 15 - 25 eggs. The eggs will turn into larva after about 10 days and then hatch and become veligers. They are born with shells initially but lose them after they hatch. [8] Mating has only been observed during the day. [3]

Feeding habits

Melibe leonina in aquaria. Melibe leonina feeding.jpg
Melibe leonina in aquaria.

While most nudibranchs are predators of sessile benthic organisms, M. leonina feeds on planktonic invertebrates. [3] M. leonina is carnivorous and has been observed eating several types of planktonic crustaceans, including amphipods, copepods, ostracods, and various types of larvae. [1] [3] [9] M. leonina lack any features associated with chewing, so prey are swallowed whole. [9] M. leonina have been observed displaying feeding behavior even in the complete absence of food. [3]

Adults and juveniles display different feeding behaviors, however, they both feed by first attaching their foot firmly to its substratum. Adults feed by pulling back their oral hood until it is almost perpendicular to the body, and then thrust it forward until contact is made with a prey organism. Once prey has been contacted, the hood closes and the rows of cirri interlock to prevent escape. [3] The hood is compressed further, pushing excess water out and forcing the prey towards the mouth. [3] Closing the oral hood takes approximately 4 seconds. [9] In aquarium settings, M. leonina have been observed exhibiting different feeding strategies, including surface floating and bottom grazing. [9]

Juveniles start with their hood nearly parallel to their substratum. As they move their body forward, they bring their hood down until it makes contact with the substratum. Water is pushed from the hood once contact has been made with the substratum, and prey is forced towards the mouth. [3] Researchers believe that the differences in feeding behaviors indicate that adults feed from the water and juveniles feed directly from the substratum. [3] Juveniles feed during the day or night, while adults feed exclusively at night. [3]

Predators

There have been very few observations of predation on M. leonina; the few known observations of predation have mostly involved the crab Pugettia producta [3] and the main defense against predation is thought to be its ability to produce an odorous secretion called a terpenoid that is repellent to other organisms. [3] The gland that produces these secretions are known as repugnatorial glands. [10] Some sources have described the secretion as a watermelon-like smell. [7] Because M.leonina prey are not known to produce secondary metabolites it is thought that they biosynthesis their own terpenoids. [11]

Locomotion

M. leonina are capable swimmers, however, they have rarely been observed leaving their substratum. [3] M. leonina swim through a behavior known as lateral bending. [10] Individuals swim by first closing their oral hood and releasing themselves from their substrate. [10] Next, they curl their foot and extend their cerrata. [10] They then flatten their body laterally, to create more surface area. [10] To propel themselves forward they bend their body from side to side, forming a "C" shape. [10] [12] M. leonina are capable of trapping air in their hood for buoyancy. [12]

Studies have shown that M. leonina individuals regularly move to other kelp blades, but have rarely been observed swimming during the day in nature. [3] [10] This has led researchers to speculate that M. leonina swim mostly at night. [3] Experiments in a laboratory setting have supported this theory; showing that on average M. leonina swim 20 times more often at night. [10]

Related Research Articles

Nudibranch Order of gastropods

Nudibranchs are a group of soft-bodied, marine gastropod molluscs which shed their shells after their larval stage. They are noted for their often extraordinary colours and striking forms, and they have been given colourful nicknames to match, such as "clown," "marigold," "splendid," "dancer," "dragon," or "sea rabbit." Currently, about 3,000 valid species of nudibranchs are known.

Veliger

A veliger is the planktonic larva of many kinds of sea snails and freshwater snails, as well as most bivalve molluscs (clams) and tusk shells.

<i>Glaucus atlanticus</i> Species of mollusc

Glaucus atlanticus is a species of small, blue sea slug, a pelagic aeolid nudibranch, a shell-less gastropod mollusk in the family Glaucidae.

<i>Paralabrax clathratus</i> Species of fish

Paralabrax clathratus, the kelp bass, bull bass or calico bass, is a species of marine ray-finned fish, a sea bass from the subfamily Serraninae, classified as part of the family Serranidae which includes the groupers and anthias. It is found in the eastern North Pacific Ocean where it is an important species for both recreational and commercial fisheries.

<i>Fiona pinnata</i> Species of gastropod

Fiona pinnata, common name Fiona, is a species of small pelagic nudibranch, a marine gastropod mollusk in the superfamily Fionoidea. This nudibranch species lives worldwide on floating objects on seas, and feeds mainly on barnacles, specifically goose barnacles in the genus Lepas.

<i>Aeolidia papillosa</i> Species of gastropod

Aeolidia papillosa, known as the common grey sea slug, is a species of nudibranch in the family Aeolidiidae.

<i>Nembrotha lineolata</i> Species of gastropod

Nembrotha lineolata is a species of nudibranch, a sea slug, a marine gastropod mollusk in the family Polyceridae. It is found in shallow water in the Indo-Pacific. It was first described in 1905 by the Danish malacologist Rudolph Bergh. The type locality is Selayar Island, Indonesia.

<i>Melibe</i> Genus of gastropods

Melibe is a genus of sea slugs, nudibranchs, marine gastropod mollusks in the family Tethydidae.

<i>Tritonicula hamnerorum</i> Species of gastropod

Tritonicula hamnerorum is a species of dendronotid nudibranch. It is a marine gastropod mollusc in the family Tritoniidae. A number of Caribbean species of Tritonia were moved to a new genus Tritonicula in 2020 as a result of an integrative taxonomic study of the family Tritoniidae.

<i>Tethys fimbria</i> Species of gastropod

Tethys fimbria is a species of predatory sea slug, a nudibranch, a marine gastropod mollusk in the family Tethydidae.

<i>Ziminella salmonacea</i> Species of gastropod

Ziminella salmonacea, common name the salmon aeolis, is a species of sea slug, an aeolid nudibranch, a marine gastropod mollusc in the family Paracoryphellidae.

<i>Berghia</i> Genus of gastropods

Berghia is a genus of sea slugs, aeolid nudibranchs. They are shell-less marine gastropod molluscs in the family Aeolidiidae. They are covered in cerata which give them their unique tentacle look and color. Berghia are commonly found in shallow waters and their diet consists of strictly Aiptasia Anemone. This genus is now commonly used commercially to fight off Anemone populations in fish tanks.

<i>Coryphella verrucosa</i> Species of gastropod

Coryphella verrucosa, is a species of sea slug, an aeolid nudibranch, a marine gastropod mollusc in the family Flabellinidae. It is found on either side of the northern part of the Atlantic Ocean.

<i>Coryphellina rubrolineata</i> Species of gastropod

Coryphellina rubrolineata is a species of sea slug, an aeolid nudibranch, a marine heterobranch mollusc in the family Flabellinidae.

<i>Kelletia kelletii</i> Species of gastropod

Kelletia kelletii, common name Kellet's whelk, is a species of large sea snail, a whelk, a marine gastropod mollusc in the family Buccinidae, the true whelks.

<i>Berghia stephanieae</i> Species of gastropod

Berghia stephanieae is a species of sea slug, an aeolid nudibranch. It is a marine gastropod mollusc in the family Aeolidiidae. It was previously known as Aeolidiella stephanieae.

<i>Aeolidiella alderi</i> Species of gastropod

Aeolidiella alderi is a species of sea slug, an aeolid nudibranch in the family Aeolidiidae. It is native to northwestern Europe where it occurs in the intertidal zone. It is a predator and feeds on sea anemones.

<i>Gorgonorhynchus repens</i> Species of ribbon worm

Gorgonorhynchus repens is a species of the proboscis worm in the subclass Heteronemertea and of the family Gorgonorhynchidae. It is to be found on the seabed in shallow water in the Pacific Ocean.

<i>Octopus bimaculatus</i> Species of octopus

Octopus bimaculatus, commonly referred to as Verill's two-spot octopus, is a similar species to the Octopus bimaculoides, a species it is often mistaken for. The two can be distinguished by the difference in the blue and black chain-like pattern of the ocelli. O. bimaculatus hunt and feed on a diverse number of benthic organisms that also reside off the coast of Southern California. Once the octopus reaches sexual maturity, it shortly dies after mating, which is approximately 12–18 months after hatching. Embryonic development tends to be rapid due to this short lifespan of these organisms.

Janolus flavoanulatus is a sea slug species. The specific name is derived from Latin words flavus (“yellow”) and anulatus (“ringed”). These soft-bodied mollusks are known for their extraordinary colors and prominent forms. The first description of this species was reported by researcher Terry Gosliner, a leading researcher in the evolutionary history of nudibranchs. Upon his conducted research in the Philippines, Gosliner named Janolus flavoanulatus for its yellow ring around its cerata.

References

  1. 1 2 3 4 5 6 7 8 9 Gosliner, Terrence (1987). "Review of the Nudibranch Genus Melibe (Opisthobranchia: Dendronotacea) with Descriptions of Two New Species". The Veliger. 29 (4): 400–414.
  2. 1 2 3 4 5 Meinkoth, Norman (1981). The Audubon Society Field Guide to North American Seashore Creatures. New York: Alfred A. Knopf, Inc. pp. 531–532.
  3. 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 Ajeska, Richard; Nybakken, James (1976). "Contributions to the Biology of Melibe leonina". The Veliger. 19: 19–26.
  4. Bickell-Page, L. R (1989). "Autotomy of Cerata by the Nudibranch Melibe leonina (Mollusca): Ultrastructure of the Autotomy Plane and Neural Correlate of the Behaviour". Philosophical Transactions of the Royal Society B: Biological Sciences. 324 (1222): 149–172. Bibcode:1989RSPTB.324..149B. doi: 10.1098/rstb.1989.0042 .
  5. Bickell-Page, Louise (1989). "Autotomy of Cerata by the Nudibranch Melibe Leonina (Mollusca): Ultrastructure of the Autotomy Plane and Neural Correlate of the Behaviour". Philosophical Transactions of the Royal Society of London. 324 (1222): 149–172. Bibcode:1989RSPTB.324..149B. doi:10.1098/rstb.1989.0042. JSTOR   2990175 via Astor.
  6. Cowles, Dave. "Melibe leonina". inverts.wallawalla.edu. Retrieved 2018-01-15.
  7. 1 2 "Melibe, Kelp Forest, Invertebrates, Melibe leonina at the Monterey Bay Aquarium". www.montereybayaquarium.org. Retrieved 2018-01-15.
  8. H. P. Von W. Kjerschow-Agersborg (May–June 1921). "Contribution to the Knowledge of the Nudibranchiate Mollusk, Melibe Leonina". The American Naturalist. 55: 222–253. doi:10.1086/279809. JSTOR   2456514. S2CID   84256920 via Astor.
  9. 1 2 3 4 Watson, Winsor H; Trimarchi, James (1992). "A quantitative description of Melibe feeding behavior and its modification by prey density". Marine Behaviour and Physiology. 19 (3): 183–194. doi:10.1080/10236249209378807.
  10. 1 2 3 4 5 6 7 8 Watson, Winsor H; Lawrence, Kaddee A; Newcomb, James M (2001). "Neuroethology of Melibe leonina Swimming Behavior". American Zoologist. 41 (4): 1026–1035. doi: 10.1093/icb/41.4.1026 .
  11. Barbsy (2019). "De Novo terpenoid biosynthesis by the dendronotid nudibranch Melibe leonina ". Chemoecology. 12 (4): 199–202. doi:10.1007/PL00012669. S2CID   35384332.
  12. 1 2 Kozloff, Eugene N (1983). Seashore life of the northern Pacific coast : an illustrated guide to northern California, Oregon, Washington, and British Columbia. Seattle: University of Washington Press. ISBN   978-0295960302. OCLC   9196536.[ page needed ]