Features

Diversity

All seahorses belong to the genus Hippocampus of the family Syngnathidae . As of 2020, there are 42 recognized species of seahorses, at least 10 of which are under the “Vulnerable” or “Endangered” category of the International Union for Conservation of Nature (IUCN)'s Red List. Threats to seahorses include habitat degradation and exploitation by humans. The highest diversity of species is located in the Indo-Pacific region. Seahorses likely evolved around 20 million years ago in the Indo-Pacific region, following tectonic plate movement and periodic sea-level changes that increased the amount of shallow-water grassland habitats. Incidents of vicariance, dispersal, and founder colonization are suspected to account for the diversity of species in the Atlantic Ocean. Defining clear phylogenetic relationships between species in the genus Hippocampus has been challenging due to the lack of fossil evidence and conflict between leading hypotheses. However, species are generally divided into two groups: smooth seahorses and spiny seahorses. Within each group, species exhibit morphological diversity due to sexual selection and differences in primary habitat.

Geographic Range

Seahorses occupy tropical and temperate marine environments, anywhere between 50° north to 50° south, and live in shallow areas, often between 40 and 100 m deep. They primarily occupy the benthic zone, where they can hide among corals or vegetation, such as seagrasses, mangroves, and filamentous algae.

Habitat

Seahorses are small and have limited mobility most of their life. Soft-bottom habitats with seagrass or corals provide seahorses with abundant prey and vertical structure that is ideal for hiding from larger predators. Most tropical seahorses inhabit coral reefs, whereas species in temperate areas inhabit areas dominated by seagrasses or filamentous algae. Habitat selection varies between species depending on regional differences in food availability and predation risk. Most species use a sit-and wait feeding strategy, where individuals grasp their tails onto coral or vegetation and wait for small planktonic or benthic prey to pass by. As they develop, many seahorses exhibit changes in habitat selection. Most species maintain small home ranges in areas where their colors and ornamentations provide camouflage. Seahorses are not territorial, but individuals with overlapping home ranges do develop social structures. Some seahorse species maintain a home range as adults, but have a planktonic juvenile stage that is subject to dispersal. Other species perform seasonal migrations as adults, while others engage in rafting behavior, traveling long distances by attaching to floating mats of vegetation.

Systematic and Taxonomic History

The genus Hippocampus is a monophyly within the family Syngnathidae , and they are distinguished from other genera by three main synapomorphies: head-to-trunk angle, caudal fin structure, and the presence of brood pouch. The genus name Hippocampus is derived from the Greek words for “horse” and “sea animal”, and it was first defined by T. Rafinesque in 1810. Pipefishes and seadragons (subfamily Sygnathinae ) are the closest relatives to seahorses. They share a similar brooding style, but pipefishes and seadragons lack the pouch structure of seahorses. Taxonomic relationships between seahorse species are still under debate, as there is limited fossil evidence and historical knowledge regarding the genus. Early studies classified species based on morphological characteristics. However, morphological variation among species, poor type descriptions, homonyms, and the ability of some seahorses to change color make it difficult to identify systematic relationships and taxonomic origins based on morphology. More recent studies have introduced techniques to organize species relationships based on genetic information. Mitochondrial studies support the ancestral roles of Longsnout seahorses ( Hippocampus reidi ) and Pacific seahorses ( H. ingens ) in the Atlantic and Pacific Oceans, respectively. Extant seahorse species are suspected to have radiated from a common ancestor some time during the Late Pliocene. There are competing hypotheses with regards to the geographic area in which seahorses evolved. There is higher diversity in the Indo-Pacific region compared to the Atlantic Ocean, which may be indicative of an origin in the Pacific Ocean. However, there is no evidence that conclusively supports one hypothesis over the other. Episodes of vicariance or dispersal observed in some Hippocampus species suggest the need for further investigation of seahorse evolutionary patterns due to variance in biogeographic distributions.

Physical Description

Seahorses are small, with body lengths ranging from 1.5 to 35.0 cm. Unlike other groups in the family Syngnathidae , seahorses have heads that form a right angle with their bodies. Seahorses have thin skin and lack scales, but they have a series of bony rings in their bodies and tails that serve as body armor. Some seahorse species develop bony protrusions from these body rings that help them blend in with surrounding environment. Some seahorse species are capable of changing their skin color to camouflage with their environment or communicate with conspecifics during courtship. Female seahorses are usually larger than males, but they lack the brood pouch structure that males use to carry fertilized eggs.

  • Sexual Dimorphism
  • sexes shaped differently

Development

Body proportions of seahorses change during their development; juvenile seahorses usually have heads that are proportionally larger than their bodies when compared to adults. Other than their small size and relatively larger heads, juvenile seahorses closely resemble adults. In some seahorse species, males and females differ in length, size, or even body proportions. For instance, some males have longer tails and some females have longer bodies. Adult male seahorses develop a brood pouch, where they store fertilized eggs until they develop and hatch. Typically, newly hatched seahorses remain in the paternal brood pouch, where they develop for several days before they are released. However, in some species embryos hatch from eggs without fully undergoing embryogenesis. There are also a few species where juveniles are reported to hatch with vestigial caudal fins, which disappear within a few days after birth. These vestigial caudal fins demonstrate the evolutionary relationship between seahorses and other fish clades.

Reproduction

Most species of seahorses are reported to be monogamous for at least one brooding cycle, although pairs may remain together through multiple seasons. Some seahorse species engage in serial or social monogamy, wherein individuals switch or return to mates between brooding cycles. During copulation, female seahorses release unfertilized eggs and males bring the eggs into their brood pouch before fertilizing them. Eggs develop inside parental brood pouches until they hatch, or even a few days after hatching.

Seahorse species have different breeding seasons depending on their geographic location and surrounding environmental factors, such as water temperature or access to sunlight. Tropical species generally have longer breeding seasons than temperate species. Seahorses perform courtship rituals prior to copulation. Courtship displays in some species are complex, with up to four distinct phases. Complicated courtship rituals are typically initiated by males, and they are suspected to help mating pairs synchronize their reproductive cycle from the previous mating seasons. Males carry fertilized eggs in their brood pouches until the eggs hatch, which can take between 9 and 30 days, depending on the species. Shortly after they hatch, juveniles are released from their parental brood pouch, at which point they are fully independent. Depending on the species, seahorse reach adulthood between 4 and 12 months after hatching.

Males seahorses usually go through more than one pregnancy per breeding season. Females deposit their eggs into the brood pouch of their mate, which then provides all necessary protection for the fertilized embryos. Male seahorse can release around 100 to 300 hatchlings at a time, although brood size can range from as few as five in smaller species to approximately 2,000 individuals in larger species. Pregnancy last between 10 and 25 days, depending on the species. Generally, longer and larger males can carry larger broods of eggs.

  • Parental Investment
  • male parental care
  • pre-fertilization
    • provisioning
    • protecting
      • male
  • pre-hatching/birth
    • provisioning
      • male
    • protecting
      • male
  • pre-independence
    • provisioning
      • male
    • protecting
      • male
  • post-independence association with parents

Lifespan/Longevity

In captivity, smaller seahorse species can live up to one year, while larger species can live up to five years. Longevity in wild seahorses ranges from one to five years. Seahorses experience different rates of mortality in different life stages, due to changing predation risk, fishing risk, and disease susceptibility. Newly hatched seahorses are small and planktivorous, and they are subjected to higher predation risk. As they reach adulthood, seahorses settle down in small, well-protected ranges of seagrass or coral habitat. They also develop bony spines and cryptic camouflage, which help them deter and avoid predators. For most seahorse species, fewer than 1% of a brood survive until maturity. Seahorse mortality is also impacted by habitat loss, fishery by-catch events, and overexploitation by commercial seahorse fishing and sale.

Behavior

Seahorses have low mobility as adults, spending much of their lives in small areas of benthic habitat. Seahorses have not been observed to defend territories, in contrast to the behavior of most other sedentary benthic fish. Although seahorses usually remain within a small home range, some species migrate seasonally or exhibit "rafting" behavior, traveling long distances by attaching to floating mats of vegetation.

Seahorses exhibit a high level of mate fidelity, often selecting the same mate for multiple successive mating seasons. They are asocial outside of breeding season, although multiple individuals may have overlapping home ranges. Seahorses are ambush predators, waiting in an area for small planktonic or benthic organisms to come near enough to be caught. Seahorses have cryptic coloration that helps them hide from prey and predators, though they will flee an area if they feel threatened. Because they have such low mobility, younger and smaller seahorses are often observed "hitch hiking" by attaching to larger adults, which seem to be remarkably tolerant of smaller individuals.

Communication and Perception

Seahorses communicate and perceive their environment using a combination of visual, chemical, and physical cues. Most intraspecific communication occurs between mating pairs, which perform elaborate courtship behaviors during the breeding season. Courtship displays vary in complexity between species, but many involve visual and tactile communication between the two mating individuals. Some species also make clicking sounds by stridulating, or producing sounds by rubbing bones in their heads together. Stridulation has been observed in males and females during copulation. Seahorses also release chemical pheromones that are important to communicating reproductive status.

Seahorses are ambush predators, relying primarily on visual cues to detect and capture prey. Their eyes are capable of moving independently from each other, which helps them search for both prey and predators. Seahorses have lateral lines, which help them detect nearby movement or changes in water pressure. They are also sensitive to chemical cues from predators and prey in their environment.

Food Habits

Seahorses are ambush predators, eating any planktonic or benthic organisms that they can catch, including crustaceans, other invertebrates, and small fishes. They rely heavily on eyesight while hunting, and so most foraging occurs during the day. Seahorses spend much of their foraging time latched onto corals or seagrass, visually scanning for prey. Once they locate a prey item, they move close enough to capture it by generating suction with their mouths.

Predation

Seahorses, in general, are relatively small - the largest species, pot-bellied seahorses ( Hippocampus abdominalis ), reach a maximum size of 35 cm - so they serve as prey for larger marine fishes, mammals, sea turtles, and water birds. Seahorses are also eaten by benthic predators, such as crabs and shrimps. Predation risk is highest for planktonic juveniles, which are very small (~10 mm) and highly vulnerable to piscivorous fish and planktivorous organisms. Because adult seahorses are planktivorous, cannibalism of juveniles by adults is relatively common. Seahorses mostly rely on camouflage and habitat choice to avoid predators. When threatened, seahorses react by bending their heads and withdrawing their tails.

Ecosystem Roles

Seahorses serve important roles as secondary consumers in various coral, mangrove, and seagrass habitats. They are primarily planktivorous, eating the juvenile or larval forms of aquatic invertebrates and small fishes. Seahorses also serve as prey items for large fishes, marine mammals, sea turtles, and seabirds.

Mutualist Species
  • Marine plants and corals

Economic Importance for Humans: Positive

While seahorse sale and trade is internationally restricted, some species are believed to have medicinal properties, and so both live and dried specimens are sold illegally, often at high prices. Seahorses are also caught as bycatch from shrimp trawling ships, and these individuals are often sold as exotic pets.

Economic Importance for Humans: Negative

Seahorses are used in traditional medicinal practices. They have the potential to transmit zoonotic diseases to humans when ingested.

Conservation Status

Seahorses exhibit slow population growth, in part due to their monogamous reproductive strategy and long period of parental investment. As a result, seahorses are vulnerable to the negative impacts of climate change, habitat loss, disease, and anthropogenic activities. Although exact rates of seahorse bycatch in shrimp trawling are unknown due to the difficulty of monitoring trawlers, the similarity in size and habitat between shrimps and seahorses means that seahorses are likely to be caught in trawling nets. Seahorses are also an important ingredient in some traditional medicines, as they are believed to cure or improve several health issues. Although seahorse aquacultural is present, it occurs at levels that are insufficient to support the demand for traditional medicines. Consequently, wild seahorses are captured and sold illegally, which is leading to population declines for several seahorse species. Humans not only pose a threat to seahorse survival; interactions with humans can also disrupt breeding behaviors. The selective capture of seahorses for sale as exotic pets can separate pair-bonded individuals, thereby reducing reproductive rates.

As of 2023, more than 10 species of seahorse are listed as vulnerable or endangered on the IUCN list, with many of these species confirmed to have declining populations. Current seahorse conservation methods include captive breeding and reintroduction programs, as well as broader habitat protection measures. The ranges of some seahorse species overlap with marine protected areas (MPAs), which benefit entire marine communities by protecting them from fishing and other destructive human activities.

Encyclopedia of Life

Contributors

Trang Nguyen (author), Colorado State University, Genevieve Barnett (editor), Colorado State University, Galen Burrell (editor), Special Projects.

Atlantic Ocean

the body of water between Africa, Europe, the southern ocean (above 60 degrees south latitude), and the western hemisphere. It is the second largest ocean in the world after the Pacific Ocean.

World Map

Pacific Ocean

body of water between the southern ocean (above 60 degrees south latitude), Australia, Asia, and the western hemisphere. This is the world's largest ocean, covering about 28% of the world's surface.

World Map

temperate

that region of the Earth between 23.5 degrees North and 60 degrees North (between the Tropic of Cancer and the Arctic Circle) and between 23.5 degrees South and 60 degrees South (between the Tropic of Capricorn and the Antarctic Circle).

tropical

the region of the earth that surrounds the equator, from 23.5 degrees north to 23.5 degrees south.

saltwater or marine

mainly lives in oceans, seas, or other bodies of salt water.

pelagic

An aquatic biome consisting of the open ocean, far from land, does not include sea bottom (benthic zone).

benthic

Referring to an animal that lives on or near the bottom of a body of water. Also an aquatic biome consisting of the ocean bottom below the pelagic and coastal zones. Bottom habitats in the very deepest oceans (below 9000 m) are sometimes referred to as the abyssal zone. see also oceanic vent.

reef

structure produced by the calcium carbonate skeletons of coral polyps (Class Anthozoa). Coral reefs are found in warm, shallow oceans with low nutrient availability. They form the basis for rich communities of other invertebrates, plants, fish, and protists. The polyps live only on the reef surface. Because they depend on symbiotic photosynthetic algae, zooxanthellae, they cannot live where light does not penetrate.

monogamous

Having one mate at a time.

sexual

reproduction that includes combining the genetic contribution of two individuals, a male and a female

fertilization

union of egg and spermatozoan

internal fertilization

fertilization takes place within the female's body

ovoviviparous

reproduction in which eggs develop within the maternal body without additional nourishment from the parent and hatch within the parent or immediately after laying.

male parental care

parental care is carried out by males

natatorial

specialized for swimming

motile

having the capacity to move from one place to another.

sedentary

remains in the same area

solitary

lives alone

visual

uses sight to communicate

tactile

uses touch to communicate

chemical

uses smells or other chemicals to communicate

stores or caches food

places a food item in a special place to be eaten later. Also called "hoarding"

cryptic

having markings, coloration, shapes, or other features that cause an animal to be camouflaged in its natural environment; being difficult to see or otherwise detect.

pet trade

the business of buying and selling animals for people to keep in their homes as pets.

food

A substance that provides both nutrients and energy to a living thing.

drug

a substance used for the diagnosis, cure, mitigation, treatment, or prevention of disease

carnivore

an animal that mainly eats meat

piscivore

an animal that mainly eats fish

bilateral symmetry

having body symmetry such that the animal can be divided in one plane into two mirror-image halves. Animals with bilateral symmetry have dorsal and ventral sides, as well as anterior and posterior ends. Synapomorphy of the Bilateria.

tactile

uses touch to communicate

chemical

uses smells or other chemicals to communicate

References

Anderson, P. 2012. Sexual Dimorphism in Morphometry and Allometry of the Adult Lined Seahorse, Hippocampus erectus. Copeia , 3: 389-393. Accessed February 03, 2020 at http://doi.org/10.1643/CG-11-003 .

Bergert, B., P. Wainwright. 1997. Morphology and kinematics of prey capture in the syngnathid fishes Hippocampus erectus and Syngnathus floridae. Marine Biology , 127.4: 563–570. Accessed March 02, 2020 at https://doi.org/10.1007/s002270050046 .

Boehm, J., L. Woodall, B. Teske, S. Lourie, C. Baldwin, J. Waldman, M. Hickerson. 2013. Journal of Biogeography. Marine dispersal and barriers drive Atlantic seahorse diversification , 40(10): 1839–1849. Accessed February 09, 2020 at https://doi.org/10.1111/jbi.12127 .

Fonseca, T., F. David, F. Ribeiro, A. Wainberg, W. Valenti. 2017. Technical and economic feasibility of integrating seahorse culture in shrimp/oyster farms. Aquaculture Research , 48(2): 655-664. Accessed March 25, 2020 at https://doi.org/10.1111/are.12912 .

Foster, S., A. Vincent. 2004. Life history and ecology of seahorses: implications for conservation and management. Journal of Fish Biology , 61(1): 1-61. Accessed February 03, 2020 at https://doi.org/10.1111/j.0022-1112.2004.00429.x .

Hamilton, H., N. Saarnam, G. Short, A. Sellas, B. Moore, T. Hoang, C. Grace, M. Gomon, K. Crow, B. Simison. 2017. Molecular phylogeny and patterns of diversification in syngnathid fishes. Molecular Phylogenetics and Evolution , 107: 388-403. Accessed April 12, 2020 at https://doi.org/10.1016/j.ympev.2016.10.003 .

Herald, E. 1959. From pipefish to seahorse — a study of phylogenetic relationships. Proceedings of the California Academy of Sciences, 4th series. , 29(4): 465-473. Accessed March 25, 2020 at https://archive.org/details/cbarchive_123159_frompipefishtoseahorseastudyof1956/page/n9/mode/2up .

IerecĂȘ, R., A. RĂŽmulo,2 M,5 S,3 M,4 PR,6 and Mara C Nottingham7, B. Kallyne, M. JosĂ©, O. Frederico, T. Oliveira, M. Nottingham. 2005. Fishers' knowledge and seahorse conservation in Brazil. Journal of Ethnobiology and Ethonomedicine , 1: 12. Accessed March 02, 2020 at doi: 10.1186/1746-4269-1-12 .

James, P., K. Heck. 1994. The effects of habitat complexity and light intensity on ambush predation within a simulated seagrass habitat. Journal of Experimental Marine Biology and Ecology , 176(2): 187-200. Accessed March 02, 2020 at https://doi.org/10.1016/0022-0981(94)90184-8 .

LOURIE, S., R. POLLOM, S. FOSTER. 2016. A global revision of the Seahorses Hippocampus Rafinesque 1810 (Actinopterygii: Syngnathiformes): Taxonomy and biogeography with recommendations for further research. Zootaxa - Magnolia Press Auckland, New Zealand , 4146(1): 1-66. Accessed March 26, 2020 at http://doi.org/10.11646/zootaxa.4146.1.1 .

Lourie, S., S. Foster, E. Cooper, A. Vincent. 2004. "A Guide To The Identification Of Seahorses" (On-line). Project Seahorse and TRAFFIC North America, Washington, D.C. Accessed February 03, 2020 at https://static1.squarespace.com/static/55930a68e4b08369d02136a7/t/560323e2e4b0d28c82499865/1443046370329/Seahorse_ID_Guide_2004.pdf .

Lourie, S., J. Pritchard, S. Casey, S. Truong, H. Hall, A. Vincent. 1999. The taxonomy of Vietnam’s exploited seahorses (family Syngnathidae). Biological Journal of the Linnean Society , 66(2): 231–256. Accessed March 25, 2020 at https://doi.org/10.1006/bijl.1998.9999 .

Masonjones, H., S. Lewis. 1996. American Society of Ichthyologists and Herpetologists. Courtship Behavior in the Dwarf Seahorse, Hippocampus zosterae , 1996(3): 634-640. Accessed February 16, 2020 at https://doi.org/10.2307/1447527 .

Novelli, B., F. Otero-Ferrer, A. Socorro, M. Caballero, A. Segade-Botella, L. Molina DomĂ­nguez. 2017. Fish Physiology and Biochemistry. Development of short-snouted seahorse (Hippocampus hippocampus, L. 1758): osteological and morphological aspects , 43(3): 833-848. Accessed February 16, 2020 at https://doi.org/10.1007/s10695-017-0339-2 .

Ofelio, C., A. Díaz, G. Radaelli, . Planas. 2018. Journal of Fish Biology. Histological Development of the Long‐snouted Seahorse Hippocampus Guttulatus During Ontogeny , 92(1): 72-87. Accessed February 16, 2020 at https://doi-org.ezproxy2.library.colostate.edu/10.1111/jfb.13668 .

Randall, J., S. Lourie. 2003. A New Pygmy Seahorse, Hippocampus denise (Teleostei: Syngnathidae), from the Indo-Pacific. Zoological Studies , 42(2): 284-291. Accessed February 03, 2020 at http://zoolstud.sinica.edu.tw/Journals/42.2/284.pdf .

Salin, K., T. Yohannan, C. Mohanakumaran Nair. 2005. Fisheries and trade of seahorses, Hippocampus spp., in southern India. Fisheries Management and Ecology , 12(4): 269-273. Accessed February 03, 2020 at https://doi.org/10.1111/j.1365-2400.2005.00450.x .

Short, G., R. Smith, H. Motomura, D. Harasti, H. Hamilton. 2018. Hippocampus japapigu, a new species of pygmy seahorse from Japan, with a redescription of H. pontohi (Teleostei, Syngnathidae). ZooKeys , 779(779): 27-49. Accessed February 03, 2020 at https://doi.org/10.3897/zookeys.779.24799 .

Smith, R., A. Grutter, I. Tibbetts. 2012. Extreme habitat specialisation and population structure of two gorgonian-associated pygmy seahorses. Marine Ecology Progress , 444: 195-206. Accessed February 03, 2020 at http://dx.doi.org/10.3354/meps09471 .

Stephen, C., H. Hall, H. Stanley, A. Vincent. 2004. Molecular Phylogenetics and Evolution. The origin and evolution of seahorses (genus Hippocampus): a phylogenetic study using the cytochrome b gene of mitochondrial DNA , 30(2): 261–272. Accessed February 09, 2020 at https://doi.org/10.1016/j.ympev.2003.08.018 .

Storero, L., A. GonzĂĄlez. 2008. Feeding habits of the seahorse Hippocampus patagonicus in San Antonio Bay (Patagonia, Argentina). Journal of the Marine Biological Association of the United Kingdom , 88(7): 1503-1508. Accessed February 03, 2020 at https://doi.org/10.1017/S0025315408002506 .

Ternes, M., L. Gerhardinger, A. Schiavetti. 2016. Seahorses in focus: local ecological knowledge of seahorse-watching operators in a tropical estuary. Journal of Ethnobiology and Ethnomedicine , 12.1: 52. Accessed March 02, 2020 at doi:10.1186/s13002-016-0125-8. .

Vincent, A., S. Foster, H. Koldewey. 2011. Conservation and management of seahorses and other Syngnathidae. Journal of Fish Biology , 78 (6): 1681–1724. Accessed March 08, 2020 at https://doi-org.ezproxy2.library.colostate.edu/10.1111/j.1095-8649.2011.03003.x .

Vitturi, R., A. Libertini, M. Campolmi, F. Calderazzo, A. Mazzola. 2005. Conventional karyotype, nucleolar organizer regions and genome size in five Mediterranean species of Syngnathidae (Pisces, Syngnathiformes). Journal of Fish Biologylogy , 52(4): 677–687. Accessed March 25, 2020 at https://doi.org/10.1111/j.1095-8649.1998.tb00812.x .

Wang, X., Y. Zhang, H. Zhang, G. Qin, Q. Lin. 2019. Complete mitochondrial genomes of eight seahorses and pipefishes (Syngnathiformes: Syngnathidae): insight into the adaptive radiation of syngnathid fishes. BMC Evolutionary Biology , 19(1): 1-11. Accessed April 12, 2020 at https://doi.org/10.1186/s12862-019-1430-3 .

Wilson, A., A. Vincent, I. Ahnesjö, A. Meyer. 2001. Male Pregnancy in Seahorses and Pipefishes (Family Syngnathidae): Rapid Diversification of Paternal Brood Pouch Morphology Inferred From a Molecular Phylogeny. Journal of Heredity , 92(2): 159-166. Accessed March 25, 2020 at https://doi.org/10.1093/jhered/92.2.159 .

Woodall, L., H. Koldewey, P. Shaw. 2011. Serial monogamy in the European long-snouted seahorse Hippocampus guttulatus. Conservation Genetics , 12(6): 1645-1649. Accessed February 03, 2020 at https://doi.org/10.1007/s10592-011-0253-6 .

Woods, C. 2000. New Zealand Journal of Marine and Freshwater Research. Preliminary observations on breeding and rearing the seahorse Hippocampus abdominalis (Teleostei: Syngnathidae) in captivity , 34(3): 475-485. Accessed February 16, 2020 at https://doi.org/10.1080/00288330.2000.9516950 .

Xiong, Z., A. Vincent. 2018. Diversity and Distributions. Predicting Distributions, Habitat Preferences and Associated Conservation Implications for a Genus of Rare Fishes, Seahorses (Hippocampus Spp.) , 24(7): 1005-1017. Accessed February 09, 2020 at https://doi.org/10.1111/ddi.12741 .

Dr. Richard Smith. 2020. "Pigmy Seahorse Species" (On-line). Ocean Realm Images. Accessed February 03, 2020 at http://oceanrealmimages.com/pygmy-seahorses/species/ .

2020. "Search result: Hippocampus" (On-line). The IUCN Red List. Accessed February 04, 2020 at https://www.iucnredlist.org/search?query=Hippocampus&searchType=species .

To cite this page: Nguyen, T. 2025. "Hippocampus" (On-line), Animal Diversity Web. Accessed {%B %d, %Y} at https://animaldiversity.org/accounts/Hippocampus/

Last updated: 2025-27-30 / Generated: 2025-10-03 01:03

Privacy Consent Preference

This website uses some essential cookies to make it work. We’d like to set additional analytics cookies to analyze site usage. We won’t set these additional cookies unless you accept them.