The other three extant (living) species in the family Limulidae are also called horseshoe crabs, but they are restricted to Asia.[5] Despite the name, horseshoe crabs are more closely related to arachnids like spiders and scorpions than they are to crabs or other crustaceans.[6]
Names and classification
Atlantic horseshoe crab with attached Crepidula shells on the Delaware Bay beach in Villas, New Jersey.Underside view of a living male crab, showing the mouth, gills and legs
This group of animals is also known as horsefoot, or saucepan. Some people call the horseshoe crab a "helmet crab", but this common name is more frequently applied to a true crab, a malacostracan, of the species Telmessus cheiragonus. The term "king crab" is sometimes used for horseshoe crabs, but it is more usually applied to a group of decapod crustaceans.
Limulus means "askew"[7] and polyphemus refers to Polyphemus, a giant in Greek mythology.[7] It is based on the misconception that the animal had a single eye.
Former scientific names include Limulus cyclops, Xiphosura americana, and Polyphemus occidentalis.
It is the tail that earns this order its name Xiphosura, which derives from the Greek for "sword tail".
Studies of microsatellite DNA have revealed several distinct geographic groups in the Atlantic horseshoe crab. While there is extensive mixing between neighbouring populations, primarily due to movements by males, there is little or no mixing between the US and isolated Yucatán Peninsula horseshoe crabs, leading some to suggest that a taxonomic review is necessary.[4][8]
Anatomy and physiology
Underside view: The mouth opening is between the legs, and the gills are visible below.Underside of a female showing the legs and book gills.Underside of a male, showing the first leg modified for grasping the female during copulation.
Horseshoe crabs have three main parts to the body: the head region, known as the "prosoma", the abdominal region or "opisthosoma", and the spine-like tail or "telson". The smooth shell or carapace is shaped like a horseshoe, and is greenish grey to dark brown in colour. The sexes are similar in appearance, but females are typically 25 to 30% larger than the male in length and width, and can reach more than twice the weight.[9][10] Females can grow up to 60cm (24in) in length, including tail,[11] and 4.8kg (11lb) in weight.[10] There are also geographic differences: In the United States, there is a north–south cline in the size. Central animals, between Georgia and Cape Cod, are the largest. North of Cape Cod and south of Georgia they gradually become smaller.[12][13] In Delaware Bay, females and males have an average carapace width of about 25.5cm (10.0in) and 20cm (7.9in), respectively. In Florida, females average about 21.5cm (8.5in) and males 16cm (6.3in).[4] However, this north-south pattern does not exist in the Yucatán Peninsula, the southernmost population of the species, where some subpopulations are intermediate between the Delaware Bay and Florida horseshoe crabs, and others are smaller, averaging about 3⁄4 the size of Florida horseshoe crabs.[4]
A wide range of marine species become attached to the carapace, including algae, flat worms, mollusks, barnacles, and bryozoans, and horseshoe crabs have been described as 'walking museums' due to the number of organisms they can support.[15] In areas where Limulus is common, the shells, exoskeletons or exuviae (molted shells) of horseshoe crabs frequently wash up on beaches, either as whole shells, or as disarticulated pieces.
The brain and the heart are located in the prosoma. On the underside of the prosoma, six pairs of appendages occur, the first of which (the small pincers or chelicerae) are used to pass food into the mouth, which is located in the middle of the underside of the cephalothorax, between the chelicerae. Although most arthropods have mandibles, the horseshoe crab is jawless.
The second pair of appendages, the pedipalps, are used as walking legs; in males they are tipped with 'claspers', which are used during mating to hold onto the female's carapace. The remaining four pairs of appendages are the 'pusher legs', also used in locomotion. The first four pairs of legs have claws, the last pair has a leaf-like structure used for pushing.[16]
The opisthosoma bears a further six pairs of appendages; the first pair houses the genital pores, while the remaining five pairs are modified into flattened plates, known as book gills, that allow them to breathe underwater, and can also allow them to breathe on land for short periods of time, provided the gills remain moist.
The telson (i.e., tail or caudal spine) is used to steer in the water and also to flip itself over if stuck upside down.
Among other senses, they have a small chemoreceptor organ that senses smells on the triangular area formed by the exoskeleton beneath the body near the ventral eyes.[17]
Vision
Limulus has been extensively used in research into the physiology of vision.[citation needed] The Nobel Prize in Medicine was awarded in 1967 in part for research performed on the horseshoe crab eye.
A large compound eye with monochromatic vision is found on each side of the prosoma;[note 1][18] it has five simple eyes on the carapace, and two simple eyes on the underside, just in front of the mouth,[18] making a total of nine eyes. The simple eyes are probably important during the embryonic or larval stages of the organism,[18] and even unhatched embryos seem to be able to sense light levels from within their buried eggs.[19] The less sensitive compound eyes, and the median ocelli, become the dominant sight organs during adulthood.[18]
In addition, the tail bears a series of light-sensing organs along its length.
Each compound eye is composed of about 1000 receptors called ommatidia,[16] complex structures consisting of upwards of 300 cells.[19] The ommatidia are somewhat messily arranged, not falling into the ordered hexagonal pattern seen in more derived arthropods.[18] Each ommatidium feeds into a single nerve fiber. Furthermore, the nerves are large and relatively accessible. This made it possible for electrophysiologists to record the nervous response to light stimulation easily, and to observe visual phenomena such as lateral inhibition working at the cellular level. More recently, behavioral experiments have investigated the functions of visual perception in Limulus. Habituation and classical conditioning to light stimuli have been demonstrated, as has the use of brightness and shape information by males when recognizing potential mates.
The retinula (literally, "small retina") cells of the ommatidium of the compound eye contain areas from which membranous organelles of conceivable size (rhabdomeres) extend. Rhabdomeres have tiny microvilli (tiny tubes extending out of the retinula) that interlock with neighboring retinular cells. This forms the rhabdom, which contains the dendrite of the eccentric cell, and may also contribute some microvilli. The only other species with an eccentric cell is the silkworm moth. Microvilli are composed of a double layer, 7nm each and with 3.5nm space of two electron-deficient boundaries in between. Where the microvilli meet, these outer borders fuse and yield five membranes about 15nm thick. In all arthropods, there is always a rhabdom below a crystalline cone, on or near the center of the ommatidium, and always aligned with the path of light. At right angles to the length of the rhabdome are the length of the microvilli, which are in line with each other. The microvilli are about 40–150nm in diameter.[20]
Blood
The blood of horseshoe crabs (as well as that of most mollusks, including cephalopods and gastropods) contains the copper-containing proteinhemocyanin at concentrations of about 50 g per liter.[21] These creatures do not have hemoglobin (iron-containing protein), which is the basis of oxygen transport in vertebrates. Hemocyanin is colorless when deoxygenated and dark blue when oxygenated. The blood in the circulation of these creatures, which generally live in cold environments with low oxygen tensions, is grey-white to pale yellow,[21] and it turns dark blue when exposed to the oxygen in the air, as seen when they bleed.[21] Hemocyanin carries oxygen in extracellular fluid, which is in contrast to the intracellular oxygen transport in vertebrates by hemoglobin in red blood cells.[21]
The blood of horseshoe crabs contains one type of blood cell, the amebocytes. These play an important role in the defense against pathogens. Amebocytes contain granules with a clotting factor known as coagulogen; this is released outside the cell when bacterial endotoxin is encountered.[22] The resulting coagulation is thought to contain bacterial infections in the animal's semiclosed circulatory system.[23]
Distribution and habitat
Atlantic horseshoe crabs in Mexico, such as this pair at Holbox Island, mostly breed in lagoons with mangrove and seagrass
The Atlantic horseshoe crab is the only extant (living) species of horseshoe crab native to the Americas, although there are other extinct species only known from fossil remains from this region. The other living species of horseshoe crab are restricted to Asia, but all are quite similar in form and behavior. The Asian species are Tachypleus tridentatus, Tachypleus gigas and Carcinoscorpius rotundicauda.[5][24]
Atlantic horseshoe crabs range from shallow coastal habitats such as lagoons, estuaries and mangrove to depths of more than 200m (660ft) up to 56km (35mi) offshore.[1] There are indications that they prefer depths shallower than 30m (98ft).[25] The temperature preference varies depending on the population, with the northernmost being the most cold-resistant: in the Great Bay in New Hampshire they show increased activity above 10.5°C (51°F) and in Delaware Bay they are active above 15°C (59°F).[1] In contrast, these northern populations do not tolerate as warm temperatures as southern populations of the species.[13] Atlantic horseshoe crabs can be seen in waters that range from brackish (almost fresh water) to hypersaline (almost twice the salinity of sea water), but their optimum growth is at salinities around or slightly below sea water (20–40‰).[1][26][27]
A 2022 study of ancient (Early Pleistocene, 2 million years ago) environmental DNA from the Kap Kobenhavn Formation of northern Greenland identified preserved DNA fragments of horseshoe crabs, assigned to L. polyphemus. This suggests that horseshoe crabs ranged and spawned as far north as Greenland during these warmer conditions. Around this time, the sea surface temperature would have been 8 °C warmer than the present. These are among the oldest DNA fragments ever sequenced.[28][29]
The crab feeds on mollusks, annelid worms, other benthic invertebrates, and bits of fish. Lacking jaws, it grinds up the food with bristles on its legs and a gizzard that contains sand and gravel.[9]
Spawning tends to occur in the intertidal zone and to be correlated with spring tides (the highest tides of the month).[1] The breeding season varies. Northern populations (all in the United States, except those in southern Florida) generally breed from the spring to the autumn, while southern populations (southern Florida and Yucatán Peninsula) breed year-round.[1] In the north, breeding is triggered by a temperature increase, but this is reversed in the Yucatán Peninsula, the southernmost population, where decreasing temperatures stimulate breeding.[1] In Massachusetts, horseshoe crabs spend the winters on the continental shelf and emerge at the shoreline in late spring to spawn, with the males arriving first. The smaller male grabs on to the back of a female with a "boxing glove" like structure on his front claws, often holding on for months at a time. Often several males will hold on to a single female.[30] Females reach the beach at high tide.[30] After the female has laid a batch of eggs in a nest at a depth of 15–20cm (6–8in) in the sand, the male or males fertilize them with their sperm.[30] Egg quantity is dependent on the female's body size, and ranges from 15,000 to 64,000 eggs per female.[31]
Development begins when the first egg cover splits and new membrane, secreted by the embryo, forms a transparent spherical capsule.[32] The larvae form and then swim for about five to seven days. After swimming, they settle, and begin the first molt. This occurs about 20 days after the formation of the egg capsule. As young horseshoe crabs grow, they move to deeper waters, where molting continues. Before becoming sexually mature around age 9, they have to shed their shells some 17 times.[9] In the first 2–3 years of their life, the juveniles stay in shallow coastal waters near the breeding beaches.[4]Longevity is difficult to assess, but the average lifespan is thought to be 20–40 years.[33]
Research from the University of New Hampshire gives insight into the circadian rhythm of Atlantic horseshoe crabs. For example, several studies have looked into the effect of a circa tidal rhythm on the locomotion of this species. While it has been known for a while that a circadian clock system controls eye sensitivity, scientists discovered a separate clock system for locomotion.[34] When a sample of Atlantic horseshoe crabs were exposed to artificial tidal cycles in the lab, circa tidal rhythms were observed. The study found that light and dark cycles influence locomotion, but not as much as tidal activity.[35]
Evolution
Horseshoe crabs were traditionally grouped with the extinct eurypterids (sea scorpions) as the Merostomata. However, recent studies suggest a relationship between the eurypterids and the arachnids, leaving Xiphosura in the cladeProsomapoda.[36] They may have evolved in the shallow seas of the Paleozoic Era (541–252 million years ago) with other primitive arthropods like the trilobites. The four species of horseshoe crab are the only remaining members of the Xiphosura, one of the oldest classes of marine arthropods.
The oldest known horseshoe crab, Lunataspis aurora, 4 centimetres (1.6in) from head to tail-tip, has been identified in 445-million-year-old Ordovician strata in Manitoba.[37]
Horseshoe crabs are often referred to as living fossils, as they have changed little in the last 445 million years.[9] Forms almost identical to this species were present during the Triassic period 230 million years ago, and similar species were present in the Devonian, 400 million years ago. However, horseshoe crab preservation in the fossil record is extremely rare[38] and the Atlantic horseshoe crab itself has no fossil record at all. Until recently it was thought that the genus Limulus "ranges back only some 20 million years, not 200 million".[39]
The oldest member of the subfamily Limulinae are known from the Late Jurassic (Tithonian), belonging to the species Crenatolimulus darwini from Poland. The oldest and currently only other known species in the genus Limulus is Limulus coffini from the Late Cretaceous (Maastrichtian) of the United States.[40]
Medical uses
Horseshoe crabs are valuable as a species to the medical research community, and in medical testing. An extract of blood cells (amoebocytes) from Limulus polyphemus is a critical component in the widely used Limulus amebocyte lysate (LAL) test to detect and quantify bacterial endotoxins in pharmaceuticals and to test for several bacterial diseases.[7] A protein from horseshoe crab blood is also under investigation as a novel antibiotic.[30]
Procuring the raw materials for LAL testing involves collecting and bleeding horseshoe crabs from wild populations. Horseshoe crabs are returned to the ocean after bleeding, however, there is a level of mortality and sub-lethal impact involved. It is estimated that between 10 and 30 percent of horseshoe crabs die after bleeding.[41][42]
Studies show the blood volume returns to normal in about a week, though blood cell count can take two to three months to fully rebound.[43] Animals that survive the process may be more lethargic when released and less likely to mate – which has prompted concerns about the longer-term impacts of harvesting horseshoe crabs.[44]
The LAL test is a major source of animal product dependence in the biomedical industry, and a challenge to the Three Rs of science in relation to the use of animals in testing.[45] There are efforts to reduce the dependence on horseshoe crabs, refine the process of collecting blood from the animals (including through aquaculture),[46] and even replace the use of animal-derived assays utilizing synthetic approaches, such as the recombinant factor C (rFC) assay.[47]
Conservation and management
Overall the Atlantic horseshoe crab is recognized as vulnerable by the IUCN due primarily to overharvesting and habitat loss. There are, however, significant geographic differences with some populations increasing, some stable and some declining.[1]
United States
Horseshoe crab harvest, Delaware, circa 1926. Millions of crabs were harvested for fertilizer around Delaware Bay. Some were fed to hogs.The loggerhead sea turtle has suffered from the reduction in numbers of Atlantic horseshoe crabs
Early in the 20th century and possibly before, there was the mistaken belief in some areas that horseshoe crabs were destructive to fisheries, folklore held that they used their long spines to drill into some shellfish. Because of this mistaken belief and folklore, bounties were sometimes offered by authorities for them. On Cape Cod in the early 20th century five cents was offered for every dead horseshoe crab turned in.
The Atlantic horseshoe crab is not presently endangered, but harvesting and habitat destruction have reduced its numbers at some locations and caused some concern for this animal's future. Since the 1970s, the horseshoe crab population has been decreasing in some areas, due to several factors, including the use of the crab as bait in eel, whelk and conch trapping. According to the Horseshoe Crab Benchmark Stock Assessment Peer Review Report published by the Atlantic States Marine Fisheries Commission (ASMFC), the population continues to remain stable where biomedical is present in the Northeast and thrive and grow in the Southeast due to protection efforts – a trend spanning decades.[49]
Red knots feeding on horseshoe crab eggs in Delaware
Conservationists have also voiced concerns about the declining population of shorebirds, such as red knots, which rely heavily on the horseshoe crabs' eggs for food during their spring migration. Precipitous declines in the population of the red knots have been observed in recent years. Predators of horseshoe crabs, such as the currently threatened Atlantic loggerhead turtle, have also suffered as crab populations diminish.[50]
In 1991, the species was provided legislated protection from bait fishing in South Carolina by calling on the management and regulation of the horseshoe crab fisheries, allowing only hand-collecting for biomedical applications and marine biological research.[51] Without the need for LAL in biomedical use, the legal protection of the horseshoe crab is not guaranteed in the future, and they would again fall prey to overfishing and use as bait. In 1995, the nonprofit Ecological Research and Development Group (ERDG) was founded with the aim of preserving the four remaining species of horseshoe crab.[52] Since its inception, the ERDG has made significant contributions to horseshoe crab conservation. ERDG founder Glenn Gauvry designed a mesh bag for whelk/conch traps, to prevent other species from removing the bait. This has led to a decrease in the amount of bait needed by approximately 50%. In the state of Virginia, these mesh bags are mandatory in whelk/conch fishery. The Atlantic States Marine Fisheries Commission in 2006 considered several conservation options, among them being a two-year ban on harvesting the animals, affecting both Delaware and New Jersey shores of Delaware Bay.[53] In June 2007, Delaware Superior Court Judge Richard Stokes has allowed limited harvesting of 100,000 males. He ruled that while the crab population was seriously depleted by overharvesting through 1998, it has since stabilized, and that this limited take of males will not adversely affect either horseshoe crab or red knot populations. In opposition, Delaware environmental secretary John Hughes concluded that a decline in the red knot bird population was so significant that extreme measures were needed to ensure a supply of crab eggs when the birds arrived.[54][55] Harvesting of the crabs was banned in New Jersey on March 25, 2008.[56]
Every year, about 10% of the horseshoe crab breeding population dies when rough surf flips the creatures onto their backs, a position from which they often cannot right themselves. In response, the ERDG launched a "Just Flip 'Em" campaign, in the hopes that beachgoers will simply turn the crabs back over.[57] New Jersey beaches campaign "ReTURN the Favor", trains volunteers to rescue impinged and overturned horseshoe crabs while collecting data on natural and man-made hazards.[58]
A large-scale project to tag and count horseshoe crabs along the North American coast was started in 2008, termed Project Limulus.[9] Due to the lack of information and knowledge regarding horseshoe crab populations, the management policies lack any abundance of rules and regulations. To implement management policies for the species, more population information needs to be obtained.[59]
Mexico
Since 1994, the populations in the Yucatán Peninsula have been recognized as endangered under Mexican law. They have declined since the 1960s and remaining significant Yucatán populations are mostly within protected areas.[4]
The subphylum Chelicerata constitutes one of the major subdivisions of the phylum Arthropoda. Chelicerates include the sea spiders, horseshoe crabs, and arachnids, as well as a number of extinct lineages, such as the eurypterids and chasmataspidids.
Amplexus is a type of mating behavior exhibited by some externally fertilizing species in which a male grasps a female with his front legs as part of the mating process, and at the same time or with some time delay, he fertilizes the eggs, as they are released from the female's body. In amphibians, females may be grasped by the head, waist, or armpits, and the type of amplexus is characteristic of some taxonomic groups.
The red knot or just knot is a medium-sized shorebird which breeds in tundra and the Arctic Cordillera in the far north of Canada, Europe, and Russia. It is a large member of the Calidris sandpipers, second only to the great knot. Six subspecies are recognised.
Callinectes sapidus, the blue crab, Atlantic blue crab, or, regionally, the Maryland blue crab, is a species of crab native to the waters of the western Atlantic Ocean and the Gulf of Mexico, and introduced internationally.
Horseshoe crabs are marine and brackish water arthropods of the family Limulidae and the only living members of the order Xiphosura. Despite their name, they are not true crabs or crustaceans: they are chelicerates, most closely related to arachnids such as spiders, ticks, and scorpions.
Xiphosura is an order of arthropods related to arachnids. They are more commonly known as horseshoe crabs. They first appeared in the Hirnantian. Currently, there are only four living species. Xiphosura contains one suborder, Xiphosurida, and several stem-genera.
Limulus is a genus of horseshoe crab, with one extant species, the Atlantic horseshoe crab. One fossil species is currently assigned to the genus though several other species have been named, which have since been assigned to other genera.
Limulus amebocyte lysate (LAL) is an aqueous extract of motile blood cells (amebocytes) from the Atlantic horseshoe crab Limulus polyphemus. LAL reacts with bacterial endotoxins such as lipopolysaccharides (LPS), which are components of the bacterial capsule, the outermost membrane of cell envelope of gram-negative bacteria. This reaction is the basis of the LAL test, which is widely used for the detection and quantification of bacterial endotoxins.
The Jonah crab is a marine brachyuran crab that inhabits waters along the east coast of North America from Newfoundland to Florida. Jonah crabs possess a rounded, rough-edged carapace with small light spots, and robust claws with dark brown-black tips. The maximum reported carapace width for males is 222 mm, while females rarely exceed 150 mm. It is the closest relative to the European brown crab in the Western Atlantic.
The mangrove horseshoe crab, also known as the round-tailed horseshoe crab, is a species of horseshoe crab, a chelicerate arthropod found in tropical marine and brackish waters of India, Bangladesh, and Southeast Asia. It may also occur in Sri Lanka, Myanmar and the Philippines, but confirmed records are lacking. It is the only species in the genus Carcinoscorpius.
Tachypleus tridentatus, commonly known as the Chinese horseshoe crab, Japanese horseshoe crab, or tri-spine horseshoe crab, is a species of horseshoe crab found in Southeast and East Asia, with records from China, Indonesia, Japan, South Korea, Malaysia, the Philippines, Taiwan, and Vietnam. It is found in coastal marine and brackish waters, and tolerates colder temperatures than the other Asian horseshoe crabs, although juveniles still need water warmer than 22 °C (72 °F) to moult.
An amebocyte or amoebocyte is a motile cell in the bodies of invertebrates including cnidaria, echinoderms, molluscs, tunicates, sponges, and some chelicerates.
Apposition eyes are the most common form of eye, and are presumably the ancestral form of compound eye. They are found in all arthropod groups, although they may have evolved more than once within this phylum. Some annelids and bivalves also have apposition eyes. They are also possessed by Limulus, the horseshoe crab, and there are suggestions that other chelicerates developed their simple eyes by reduction from a compound starting point. Some caterpillars appear to have evolved compound eyes from simple eyes in the opposite fashion.
Synziphosurina is a paraphyletic group of chelicerate arthropods previously thought to be basal horseshoe crabs (Xiphosura). It was later identified as a grade composed of various basal euchelicerates, eventually excluded from the monophyletic Xiphosura sensu stricto and only regarded as horseshoe crabs under a broader sense. Synziphosurines survived at least since early Ordovician to early Carboniferous in ages, with most species are known from the in-between Silurian strata.
Tachypleus gigas, commonly known as the Indo-Pacific horseshoe crab, Indonesian horseshoe crab, Indian horseshoe crab, or southern horseshoe crab, is one of the four extant (living) species of horseshoe crab. It is found in coastal water in South and Southeast Asia at depths to 40 m (130 ft).
Coagulin is a gel-forming protein of hemolymph that hinders the spread of bacterial and fungal invaders by immobilizing them. It is produced in the coagulogen form before being cleaved into the active form through a serine proteinase cascade. It has been most extensively studied in horseshoe crabs. It has also been produced by other organisms, such as Bacillus coagulans I4 in a plasmid location. In human medicine, coagulation of coagulin is the basis of detection of bacterial endotoxin through the Limulus amebocyte lysate test for parenteral medications.
Limulus clotting factor overbar C is an enzyme. This enzyme catalyses the following chemical reaction
Limulus clotting enzyme is an enzyme. This enzyme catalyses the following chemical reaction:
H. Jane Brockmann is an emeritus professor at the University of Florida known for her research on animal behavior, especially in the mating and nesting behavior of horseshoe crabs. In 2008, she was elected a fellow of the American Association for the Advancement of Science.
Jack Levin is an American physician-scientist and hematologist who, with Fred Bang, developed the Limulus amebocyte lysate (LAL) test for bacterial endotoxins.
1 2 3 Heard, Willie (Fall 2001). "Coast"(PDF). Project Oceanography: 81–91. Archived from the original(PDF) on 19 February 2017. Retrieved 5 July 2008.
↑ King, T.L.; Eackles, M.S.; Spidle, A.P.; Brockmann, H.J. (2005). "Regional differentiation and sex-biased dispersal among populations of the horseshoe crab Limulus polyphemus". Transactions of the American Fisheries Society. 134 (2): 441–465. Bibcode:2005TrAFS.134..441K. doi:10.1577/T04-023.1.
1 2 Koichi Sekiguchi; Carl N. Shuster Jr (2009). "Limits on the Global Distribution of Horseshoe Crabs (Limulacea): Lessons Learned from Two Lifetimes of Observations: Asia and America". In Tanacredi, John T.; Botton, Mark L.; Smith, David (eds.). Biology and Conservation of Horseshoe Crabs. Springer. pp.5–24. ISBN978-0-387-89959-6.
↑ Elizabeth Quinn; Kristen Paradise & Jelle Atema (1998). "Juvenile Limulus polyphemus generate two water currents that contact one proven and one putative chemoreceptor organ". The Biological Bulletin. 195 (2): 185–187. doi:10.2307/1542829. JSTOR1542829. PMID28570188.
↑ Mürer, EH; Levin, J; Holme, R (December 1975). "Isolation and studies of the granules of the amebocytes of Limulus polyphemus, the horseshoe crab". Journal of Cellular Physiology. 86 (3 Pt 1): 533–42. doi:10.1002/jcp.1040860310. PMID413. S2CID24546343.
↑ Shuster, Carl N. Jr. (1982). "A Pictorial Review of the Natural History and Ecology of the Horseshoe Crab Limulus polyphemus, With Reference to Other Limulidae". Physiology and Biology of Horseshoe Crabs: Studies on Normal and Environmentally Stressed Animals. Liss. p.22. ISBN0-8451-0081-5.
↑ "About ERDG". horseshoecrab.org. ERDG. Retrieved 31 January 2015.
↑ Molly Murray (May 5, 2006). "Seafood dealer wants to harvest horseshoe crabs (subtitle: Regulators look at 2-year ban on both sides of Delaware Bay)". The News Journal. pp.B1, B6.
↑ "Horseshoe Crabs in Political Pinch Over Bird's Future / Creature is Favored Bait On Shores of Delaware; Red Knot Loses in Court". The Wall Street Journal. June 11, 2007. pp.A1, A10.
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