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Habitat

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These fish are found in lagoons and seaward reefs (Fautin and Allen, 1992; Myers, 1991). They are non-migratory fish living in brackish marine water with depths ranging up to 38 meters and temperatures around 25°C. These fish live in symbiotic relationships with various sea anenomes including Heteractis crispa, Hetaractis magnifica, Macrodactyla doreensis and Stichodactyla gigantea. Amphiprion perideraion often occurs in the same environment with the closely related Amphiprion akallopison, often in the same anemone (Kuiter and Tonozuka, 2001).

Range depth: 1 to 38 m.

Habitat Regions: tropical ; saltwater or marine

Aquatic Biomes: reef ; coastal

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Lamb, D. 2006. "Amphiprion perideraion" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Amphiprion_perideraion.html
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David Lamb, University of Michigan-Ann Arbor
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Kevin Wehrly, University of Michigan-Ann Arbor
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Tanya Dewey, Animal Diversity Web
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Conservation Status

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This species is not listed as endangered or threatened and there are no immediately forseeable plans to place it on the IUCN Red List.

US Federal List: no special status

CITES: no special status

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Lamb, D. 2006. "Amphiprion perideraion" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Amphiprion_perideraion.html
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David Lamb, University of Michigan-Ann Arbor
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Kevin Wehrly, University of Michigan-Ann Arbor
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Behavior

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Communication among Amphiprion perideraion is not well-understood. They perceive their environment through visual, chemical, and tactile cues and are likely to use these modes of perception in communication.

Perception Channels: visual ; tactile ; chemical

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Lamb, D. 2006. "Amphiprion perideraion" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Amphiprion_perideraion.html
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David Lamb, University of Michigan-Ann Arbor
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Associations

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Amphiprion perideraion are preyed on by large, predatory fish, notably groupers (Serranidae). The primary defense used by these fish is their ability to survive within sea anemones. The toxic stings of anemones protects resident fish from predators.

Known Predators:

  • groupers (Serranidae)
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Lamb, D. 2006. "Amphiprion perideraion" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Amphiprion_perideraion.html
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David Lamb, University of Michigan-Ann Arbor
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Life Cycle

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Once the eggs of A. perideraion hatch, they take on a planktonic form where they are carried from the natal host anemone and float in the water column.

At the end of their larval period, A. perideraion enter a juvenile stage where they metamorphose. Metamorphosis involves the development of the white bands as well as a general migration to different depths of water and host anemones. Evidence suggests that juveniles progressively forage in a smaller area as they become adults.

Members of the genus Amphiprion occupy a single anemone for their entire life, rarely swimming more than several meters from their host. These groups consist of one female, but many include several males. The female is the largest member of the colony and the dominant male is the next largest. The others, while male, are functionally sterile unless one of the two dominant fishes die.

Development - Life Cycle: metamorphosis ; indeterminate growth

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Lamb, D. 2006. "Amphiprion perideraion" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Amphiprion_perideraion.html
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David Lamb, University of Michigan-Ann Arbor
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Benefits

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There are no known adverse effects of Amphiprion perideraion on humans. They are considered harmless.

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Lamb, D. 2006. "Amphiprion perideraion" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Amphiprion_perideraion.html
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David Lamb, University of Michigan-Ann Arbor
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Kevin Wehrly, University of Michigan-Ann Arbor
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Benefits

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Amphiprion perideraion is a common aquarium fish and is thus of economic value to humans. They are quite appealing to divers, and their presence may encourage ecotourism.

Positive Impacts: pet trade ; ecotourism

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Lamb, D. 2006. "Amphiprion perideraion" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Amphiprion_perideraion.html
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David Lamb, University of Michigan-Ann Arbor
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Kevin Wehrly, University of Michigan-Ann Arbor
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Associations

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Amphiprion perideraion live with their host anemone in a symbiotic relationship. These fish are coated with a mucus which helps to protect them from the sting of the anemone. The toxic stings of anemones protect anemone fish from predators and anemones obtain food particles in the water column as a result of anemone feeding.

Species Used as Host:

  • Heteractis crispa
  • Heteractis magnifica
  • Macrodactyla doreensis
  • Stichodactyla gigantea

Mutualist Species:

  • Heteractis crispa
  • Heteractis magnifica
  • Macrodactyla doreensis
  • Stichodactyla gigantea
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Lamb, D. 2006. "Amphiprion perideraion" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Amphiprion_perideraion.html
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David Lamb, University of Michigan-Ann Arbor
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Kevin Wehrly, University of Michigan-Ann Arbor
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Trophic Strategy

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A. perideraion use suction feeding. The maxilla pushes the premaxilla forward, which causes an area of low pressure inside the mouth, resulting in suction.

Amphiprion perideraion exploit a wide range of phytoplankton (blue-green algae and diatoms), zooplankton and zoobenthos. This makes them omnivorous generalists. Amphiprion perideraion collect food from surrounding areas near their host anemones. They have also been known to consume food leftover from their host.

Studies have shown that Amphiprion melanopus experience a rapid growth during their juvenile stage. This rate is affected by contact with sunlight, likely due to a higher abundance of plankton. It's likely that there's selective pressure for larger fish, as smaller ones do not have the chance to mate.

Animal Foods: aquatic or marine worms; aquatic crustaceans; other marine invertebrates; zooplankton

Plant Foods: algae; phytoplankton

Primary Diet: omnivore ; planktivore

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Lamb, D. 2006. "Amphiprion perideraion" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Amphiprion_perideraion.html
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David Lamb, University of Michigan-Ann Arbor
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Kevin Wehrly, University of Michigan-Ann Arbor
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Distribution

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Amphiprion perideraion are distributed throughout tropical regions in the western Pacific and Indian Oceans. Their range includes the Gulf of Thailand, Cocos Islands and Christmas Island in the eastern Indian Ocean. In the Indo-Australian Archipelago in the Pacific, they are found from Samoa and Tongo, north to the Ryukyu Islands, Fiji, and Micronesia, extending southward to the Great Barrier Reef and New Caledonia.

Biogeographic Regions: oriental (Native ); indian ocean (Native ); pacific ocean (Native )

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Lamb, D. 2006. "Amphiprion perideraion" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Amphiprion_perideraion.html
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David Lamb, University of Michigan-Ann Arbor
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Kevin Wehrly, University of Michigan-Ann Arbor
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Life Expectancy

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Currently, there is very little available data regarding the lifespan of Amphiprion. Some data suggests that the lifespan is around ten years. Amphiprion percula have a record of 18 years in captivity.

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Lamb, D. 2006. "Amphiprion perideraion" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Amphiprion_perideraion.html
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David Lamb, University of Michigan-Ann Arbor
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Kevin Wehrly, University of Michigan-Ann Arbor
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Morphology

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Amphiprion perideraion are typically pink to pinkish orange in color. Fins are pale to transparent. They have a very distinct white dorsal stripe extending from the head to the caudal tail. A second, vertical, stripe is observed between the head and the rest of the body. Amphiprion perideraion have 9 or 10 well-developed dorsal spines and 2 anal spines. They have 16 or 17 dorsal soft rays and 12 or 13 anal soft rays. Likewise, they have highly developed pharyngeal teeth and a premaxilla with an ascending process, resulting in very effective suction feeding.

They reach a maximum length of 10 cm (Lieske and Myers, 1994; Fautin and Allen, 1992).

Similar species include A. nigripes, A. leucokranos, A. akallopisos and A. sandaracinos. Amphiprion nigripes can be distinguished by a black belly, pelvic area and anal fins and a more reddish color. Amphiprion leucokranos have much wider and broader stripes which don't extend the full lenth of the body. The remaining two species lack the white head bar present in A. perideraion.

Females are slightly longer than males at 5.5 cm (compared to 4.6 cm) at maturity.

Range length: 10 (high) cm.

Average length: 4.6-5.5 cm.

Other Physical Features: ectothermic ; bilateral symmetry

Sexual Dimorphism: female larger

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Lamb, D. 2006. "Amphiprion perideraion" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Amphiprion_perideraion.html
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David Lamb, University of Michigan-Ann Arbor
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Kevin Wehrly, University of Michigan-Ann Arbor
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Reproduction

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Amphiprion perideraion are monogamous fish where only two of the representatives of a group are actually involved in the mating. The female and dominant male are strictly monogamous. When the female dies, the largest male undergoes a sex change and becomes the mating female. After this, the second largest male actively becomes involved in mating.

In spawning, male A. ocellaris chase females, passing over the nest. With each pass, the female lays a line of eggs which adhere to the rock surface. The male then fertilizes the eggs and protects them from predators.

Mating System: monogamous

Amphiprion perideraion spawn several times between April and August, but sometimes as early as February, depending on the conditions. In this species, the largest fish is always the female and the second largest fish is always the male. Fish are male first until the female dies (protandrous). During a year, the pair may produce between 2000 and 4000 eggs. Both males and females reach maturity between 1.75 and 1.83 years of age.

While little research has actually been done on the reproductive mechanisms of A. perideraion, a similar species Ampiprion ocellaris showed several interesting reproductive mechanisms. Females control males through agression and chase away other females. Dominant males build a nest on a bare rock face near an anemone. Courtship behavior in A. ocellaris includes the extension of spines, biting, and chasing.

Breeding interval: Amphiprion perideraion will breed several times a year with no obvious peak season.

Breeding season: They breed between April and August.

Range number of offspring: 2000 to 4000.

Range age at sexual or reproductive maturity (female): 1.75 to 1.83 years.

Range age at sexual or reproductive maturity (male): 1.75 to 1.83 years.

Key Reproductive Features: iteroparous ; seasonal breeding ; gonochoric/gonochoristic/dioecious (sexes separate); sequential hermaphrodite (Protandrous ); sexual ; fertilization (External ); oviparous

Male Amphiprion perideraion protect the developing eggs while they are attached to the substrate just outside of the host anemone, for about 6 to 8 days. When the eggs hatch, the larvae leave the host anemone.

Parental Investment: pre-fertilization (Provisioning); pre-hatching/birth (Protecting: Male)

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Lamb, D. 2006. "Amphiprion perideraion" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Amphiprion_perideraion.html
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David Lamb, University of Michigan-Ann Arbor
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Kevin Wehrly, University of Michigan-Ann Arbor
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Diagnostic Description

provided by Fishbase
Description: Color orange. Fins transparent. One white stripe following the dorsal contour from snout to caudal peduncle. One white vertical stripe between head and trunk (Ref. 237). Body depth 2.1-2.7 in SL (Ref. 90102).
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Recorder
Rainer Froese
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Diseases and Parasites

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Skin Fungi (Saprolegnia sp.). Fungal diseases
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Allan Palacio
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Diseases and Parasites

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Coral fish Disease. Parasitic infestations (protozoa, worms, etc.)
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Life Cycle

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Oviparous, distinct pairing during breeding (Ref. 205). Monogamous mating is observed as both obligate and social (Ref. 52884). Eggs are demersal and adhere to the substrate (Ref. 205). Males guard and aerate the eggs (Ref. 205). One pair spawns several times per year. Annual fecundity is estimated to be 2,000 to 4,000 eggs. Size at sex change = 5.4 cm TL (Ref. 55367). Also Ref. 240, 7471.
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Morphology

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Dorsal spines (total): 9 - 10; Dorsal soft rays (total): 16 - 17; Analspines: 2; Analsoft rays: 12 - 13
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Trophic Strategy

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Occurs inshore (Ref. 75154). Adults inhabit lagoon and seaward reefs (Ref. 1602). Lives together with sea anemones inhabiting coral reefs. Feeds predominantly on benthic algae and zooplankton (Ref. 237). Diurnal species (Ref. 113699).
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Biology

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Adults inhabit lagoon and seaward reefs (Ref. 1602). Mainly diurnal. Non-burrowing. Monogamous (Ref. 52884). A protandrous hermaphrodite (Ref. 32166). Oviparous, distinct pairing during breeding (Ref. 205). Eggs are demersal and adhere to the substrate (Ref. 205). Males guard and aerate the eggs (Ref. 205). Associated with the anemones: Heteractis magnifica (usually), Heteractis crispa, Macrodactyla doreensis, and Stichodactyla gigantea (Ref. 5911). In Bali they occur together with the closely related Indian Ocean species A. akallopison and have even been found sharing the same anemone (Ref. 48636). Has been reared in captivity (Ref. 35413, 35418, 35420).
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Importance

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fisheries: of no interest; aquarium: commercial
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分布

provided by The Fish Database of Taiwan
分布於印度-太平洋區,由聖誕島至薩摩亞和東加,北至琉球群島,南至大堡礁及新加勒多尼亞。台灣主要分布於南部、西南部、東南部、小琉球和綠島等海域。
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利用

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本身體色豔麗以及與海葵共生之習性,使其成為受歡迎之水族觀賞魚。目前已能人工繁殖。
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描述

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體呈橢圓形而側扁,標準體長為體高之 1.9-2.2倍。吻短而鈍。眼中大,上側位。口小,上頜骨末端不及眼前緣;齒單列,圓錐狀。眶下骨及眶前骨具放射性鋸齒;各鰓蓋骨後緣皆具鋸齒。體被細鱗;側線之有孔鱗片 32-43個。背鰭單一,軟條部不延長而略呈圓形,硬棘IX-X,軟條 16-17;臀鰭硬棘II,軟條12-13;胸鰭鰭條16-18;雄、雌魚尾鰭皆呈圓形。體一至呈橘紅色,各鰭淡色。頭部及軀幹部間具一白色窄垂直白色;體背由吻部沿背鰭基底延伸至尾柄另具一白窄帶。
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棲地

provided by The Fish Database of Taiwan
主要棲息於潟湖及珊瑚礁區,棲息深度可達約38公尺。和海葵具共生之行為,喜歡共生的海葵有/Heteractis magnigica/、/Heteractis crispa/及/Macrodactyla doreensis /等,體表之黏液可保護自己不被海葵傷害。行一夫一妻制。偶有與克氏海葵魚同時出現,但無克氏海葵魚的攻擊性,而僅是緊依著海葵叢不離開。雜食性,以藻類和浮游生物為食。
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Amphiprion perideraion ( Catalan; Valencian )

provided by wikipedia CA
 src=
Amphiprion perideraion
 src=
Exemplars d'Amphiprion perideraion al Parc Nacional de Komodo
 src=
Dos Amphiprion perideraion en una anemone de mar
 src=
Un exemplar a Osprey Reef, al mar del Corall
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Un Amphiprion perideraion dins d'una anemone gegant, Heteractis magnifica
 src=
Anemones amb Amphiprion perideraion

Amphiprion perideraion és una espècie de peix de la família dels pomacèntrids i de l'ordre dels perciformes.[4]

Morfologia

  • Els mascles poden assolir 10 cm de llargària total.
  • És de color taronja.
  • Té les aletes transparents.[5][6]

Reproducció

És monògam i hermafrodita.[7][8]

Depredadors

A les Illes Marshall és depredat per serrànids.[9]

Hàbitat

Viu a zones de clima tropical (25°C-25°C; 34°N-22°S, 96°E-156°E), associat als esculls de corall, a 1-38 m de fondària i en simbiosi amb les anemones Heteractis magnifica (normalment), Heteractis crispa, Macrodactyla doreensis i Stichodactyla gigantea.[10][5]

Distribució geogràfica

Es troba des del Golf de Tailàndia fins a Samoa, Tonga, les Illes Ryukyu, la Gran Barrera de Corall i Nova Caledonia.[5]

Costums

Observacions

Es pot criar perfectament en captivitat.[12][13][14]

Referències

  1. Bloch M. E. & Schneider J. G. 1801. M. E. Blochii, Systema Ichthyologiae iconibus cx illustratum. Post obitum auctoris opus inchoatum absolvit, correxit, interpolavit Jo. Gottlob Schneider, Saxo. Berolini. Sumtibus Auctoris Impressum et Bibliopolio Sanderiano Commissum. Systema Ichthyol.. i-lx + 1-584. Pls. 1-110.
  2. Bleeker, P. 1855. Bijdrage tot de kennis der ichthyologische fauna van het eiland Groot-Obij. Natuurkd. Tijdschr. Neder. Indië v. 9: 431-438.
  3. «Amphiprion perideraion». Catalogue of Life. (anglès) (anglès)
  4. The Taxonomicon (anglès)
  5. 5,0 5,1 5,2 5,3 FishBase (anglès)
  6. Lieske, E. i R. Myers 1994. Collins Pocket Guide. Coral reef fishes. Indo-Pacific & Caribbean including the Red Sea. Haper Collins Publishers, 400 p.
  7. Whiteman, E.A. i I.M. Côté 2004. Monogamy in marine fishes. Biol. Rev. 79:351-375.
  8. Moyer, J.T. i A. Nakazono 1978. Protandrous hermaphroditism in six species of the anemonefish genus Amphiprion in Japan. Jap. J. Ichthyol. 25(2):101-106.
  9. FishBase (anglès)
  10. Fautin, D.G. i G.R. Allen 1992. Field guide to anemonefishes and their host sea anemones. Western Australian Museum, Francis Street, Perth.
  11. Kuiter, R.H. i T. Tonozuka 2001. Pictorial guide to Indonesian reef fishes. Part 2. Fusiliers - Dragonets, Caesionidae - Callionymidae. Zoonetics, Australia. 304-622 p.
  12. Gardner, T.R. 1997. Commercial breeding of the dottybacks. Seascope 14:1-2.
  13. Miyagawa, K. 1989. Experimental analysis of the symbiosis between anemonefishes and sea anemones. Ethology 80:19-46.
  14. Moe, A.M. Jr. 1992. The marine aquarium handbook. Beginner to breeder. Green Turtle Publication, Florida, Estats Units. 318 p.


Bibliografia

  • Allen, G.R. 1975. The anemone fishes. Their classification and biology. Segona edició. T.F.H. Publications, Inc., Neptune City, Nova Jersey.
  • Allen, G.R. i R.C. Steene 1988. Fishes of Christmas Island Indian Ocean. Christmas Island Natural History Association, Christmas Island, Indian Ocean, 6798, Austràlia. 197 p.
  • Allen, G.R. 1991. Damselfishes of the world. Mergus Publishers, Melle, Alemanya. 271 p.
  • Allen, G.R. i W.F. Smith-Vaniz 1994. Fishes of the Cocos (Keeling) Islands. Atoll Res. Bull. 412:21 p.
  • Allen, G.R. i P.L. Munday 1994. Kimbe Bay rapid ecological assessment: the coral reefs of Kimbe Bay (West New Britain, Papua New Guinea), Volum 3: Fish diversity of Kimbe Bay. The Nature Conservancy, South Pacific program Office, Auckland, Nova Zelanda. 107 p.
  • Allen, G.R. i M. Adrim 2003. Coral reef fishes of Indonesia. Zool. Stud. 42(1):1-72.
  • Allsop, D.J. i S.A. West 2003. Constant relative age and size at sex change for sequentially hermaphroditic fish. J. Evol. Biol. 16(2003):921-929.
  • Balon, E.K. 1990. Epigenesis of an epigeneticist: the development of some alternative concepts on the early ontogeny and evolution of fishes. Guelph Ichthyol. Rev. 1:1-48.
  • Bassleer, G. 2000. Diseases in marine aquarium fish: causes, development, symptoms, treatment. Bassleer Biofish, Westmeerbeek, Bèlgica, 96 p.
  • Calumpong, H.P., L.J. Raymundo i E.P. Solis-Duran (eds.) 1994. Resource and ecological assessment of of Sogod Bay, Leyte, Philippines - Final Report Vol.1 Fisheries Assessment. Siliman University Marine Laboratory.
  • Chen, J.-P., K.-T. Shao i C.-P. Lin 1995. A checklist of reef fishes from the Tungsha Tao (Pratas Island), South China Sea. Acta Zoologica Taiwanica 6(2):13-40.
  • Eschmeyer, William N.: Genera of Recent Fishes. California Academy of Sciences. San Francisco, Califòrnia, Estats Units. iii + 697. ISBN 0-940228-23-8 (1990).
  • Eschmeyer, William N., ed. 1998. Catalog of Fishes. Special Publication of the Center for Biodiversity Research and Information, núm. 1, vol. 1-3. California Academy of Sciences. San Francisco, Califòrnia, Estats Units. 2905. ISBN 0-940228-47-5.
  • Foale, S. 1998. What's in a name? An analysis of the West Nggela (Solomon Islands) fish taxonomy. SPC Traditional Marine Resource Management and Knowledge Information Bulletin #9:3-19.
  • Froese, R. i C. Papasissi 1990. The use of modern relational databases for identification of fish larvae. J. Appl. Ichthyol. 6:37-45.
  • Hardy, J.D. Jr. 2003. Coral reef fish species. NOAANational Oceanographic Data Center. NODC Coral Reef Data and Information Management System. Estats Units. 537 p.
  • Helfman, G., B. Collette i D. Facey: The Diversity of Fishes. Blackwell Science, Malden, Massachusetts (Estats Units), 1997. ISBN 1-4051-2494-6.
  • Herre, A.W.C.T. 1953. Check list of Philippine fishes. Res. Rep. U.S. Fish Wild. Serv., (20):977 p.
  • Huang, Z. 2001. Marine species and their distribution in China's seas. p. 404- 463. Vertebrata. Smithsonian Institution, Florida. 598 p.
  • Kailola, P.J. 1987. The fishes of Papua New Guinea: a revised and annotated checklist. Vol. II Scorpaenidae to Callionymidae. Research Bulletin Núm. 41, Research Section, Dept. of Fisheries and Marine Resources, Papua Nova Guinea.
  • Kulbicki, M. i J.T. Williams 1997. Checklist of the shorefishes of Ouvea Atoll, New Caledonia. Atoll Res. Bull. 444:26 p.
  • Masuda, H. i G.R. Allen 1993. Meeresfische der Welt - Groß-Indopazifische Region. Tetra Verlag, Herrenteich, Melle. 528 p.
  • Mohsin, A.K.M. i M.A. Ambak 1996. Marine fishes and fisheries of Malaysia and neighbouring countries. University of Pertanian Malaysia Press, Serdang, Malàisia. 744 p.
  • Monkolprasit, S., S. Sontirat, S. Vimollohakarn i T. Songsirikul 1997. Checklist of Fishes in Thailand. Office of Environmental Policy and Planning, Bangkok. 353 p.
  • Moyle, P. i J. Cech.: Fishes: An Introduction to Ichthyology, 4a edició, Upper Saddle River, Nova Jersey, Estats Units: Prentice-Hall. Any 2000. ISBN 0-13-011282-8.
  • Nelson, J.S. 2006: Fishes of the world. Quarta edició. John Wiley & Sons, Inc. Hoboken, Nova Jersey, Estats Units. 601 p. ISBN 0-471-25031-7.
  • Pauly, D. 1978. A preliminary compilation of fish length growth parameters. Ber. Inst. Meereskd. Christian-Albrechts-Univ. Kiel (55):1-200.
  • Randall, J.E., G.R. Allen i R.C. Steene 1990. Fishes of the Great Barrier Reef and Coral Sea. University of Hawaii Press, Honolulu, Hawaii. 506 p.
  • Robins, C.R., R.M. Bailey, C.E. Bond, J.R. Brooker, E.A. Lachner, R.N. Lea i W.B. Scott 1991. World fishes important to North Americans. Exclusive of species from the continental waters of the United States and Canada. Am. Fish. Soc. Spec. Publ. (21):243 p.
  • Thresher, R.E. 1984. Reproduction in reef fishes. T.F.H. Publications, Inc. Ltd., Neptune City (Estats Units). 399 p.
  • Wass, R.C. 1984. An annotated checklist of the fishes of Samoa. Natl. Ocean. Atmos. Adminis. Tech. Rept., Natl. Mar. Fish. Serv., Spec. Sci. Rept. Fish. (781).
  • Werner, T.B i G.R. Allen 1998. Reef fishes of Milne Bay Province, Papua New Guinea. A T. Werner i G. Allen (eds). A rapid biodiversity assessment of the coral reefs of Milne Bay Province, Papua New Guinea. RAP Working Papers 11, Conservation International, Washington DC.
  • Werner, T.B. i G.R. Allen 2000. A rapid marine biodiversity assessment of the Calamianes Islands, Palawan province, Philippines. RAP Bulletin of Biological Assessment 17. Washington DC:Conservation International.
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  • White, A. i H. Calumpong 1993. Saving Tubbataha Reef: Earthwatch expedition to the Philippines '92. Silliman J. 36(2):77-105.
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Amphiprion perideraion: Brief Summary ( Catalan; Valencian )

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 src= Amphiprion perideraion  src= Exemplars d'Amphiprion perideraion al Parc Nacional de Komodo  src= Dos Amphiprion perideraion en una anemone de mar  src= Un exemplar a Osprey Reef, al mar del Corall  src= Un Amphiprion perideraion dins d'una anemone gegant, Heteractis magnifica  src= Anemones amb Amphiprion perideraion

Amphiprion perideraion és una espècie de peix de la família dels pomacèntrids i de l'ordre dels perciformes.

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Halsband-Anemonenfisch ( German )

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Der Halsband-Anemonenfisch (Amphiprion perideraion) lebt in den Korallenriffen Südostasiens, Neuguineas, Melanesiens, Mikronesiens, von der Küste Nordaustraliens bis zu den Ryūkyū-Inseln. Bei Bali lebt er zusammen mit dem sehr nah verwandten Weißrücken-Anemonenfisch (Amphiprion akallopisos) und wurde schon in derselben Anemone wie dieser gefunden.

Merkmale

Der Körper des Fisches ist orange. Ein schmaler, weißer Querstreifen zieht sich vor dem Kiemendeckel über den Kopf. Ein weißer Längsstreifen beginnt an der Schnauze und zieht sich entlang der Basis der weißen Rückenflosse bis zum Schwanzstiel. Auch die Schwanzflosse ist weiß. Die übrigen Flossen sind transparent. Die Rückenflosse hat neun bis zehn Hart- und 16 bis 17 Weichstrahlen, die Afterflosse zwei Hart- und 12 bis 13 Weichstrahlen. Amphiprion perideraion wird bis zu 10 Zentimeter lang. Er wurde schon im Aquarium nachgezüchtet.

Die Fische akzeptieren vier Symbioseanemonenarten als Partner.

Quellen

Weblinks

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Halsband-Anemonenfisch: Brief Summary ( German )

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Der Halsband-Anemonenfisch (Amphiprion perideraion) lebt in den Korallenriffen Südostasiens, Neuguineas, Melanesiens, Mikronesiens, von der Küste Nordaustraliens bis zu den Ryūkyū-Inseln. Bei Bali lebt er zusammen mit dem sehr nah verwandten Weißrücken-Anemonenfisch (Amphiprion akallopisos) und wurde schon in derselben Anemone wie dieser gefunden.

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Pink skunk clownfish

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The pink skunk clownfish (Amphiprion perideraion), also known as the pink anemonefish, is a species of anemonefish that is widespread from northern Australia through the Malay Archipelago and Melanesia.[2] Like all anemonefishes, it forms a symbiotic mutualism with sea anemones and is unaffected by the stinging tentacles of the host. It is a sequential hermaphrodite with a strict size-based dominance hierarchy; the female is largest, the breeding male is second largest, and the male nonbreeders get progressively smaller as the hierarchy descends.[3] They exhibit protandry, meaning the breeding male changes to female if the sole breeding female dies, with the largest nonbreeder becoming the breeding male.[2]

Description

The body of A. perideraion is pink to peach. It has the white stripe along the dorsal ridge that is common to all members of the skunk complex and a white head bar running vertically just behind the eye.[2] While the largest species of anemonefish can reach a length of 18 cm (7.1 in), A. perideraion is one of the smallest species, with females growing to a length of 10 cm (3.9 in).[2]

Color variations

Some anemonefish species have color variations based on geographic location, sex, and host anemone. A. perideraion, like other members of the skunk complex, does not show any of these variations.[2]

Similar species

A. perideraion is included in the skunk complex, so has similarities with other species in this complex. The combination of dorsal stripe and head bar distinguishes it from most other species. A. akallopisos, A. sandaracinos, and A. pacificus all lack a white head bar, while A. nigripes lacks the dorsal stripe and has black belly and black pelvic and anal fins. The hybrid A. leucokranos has a broader head bar and the dorsal stripe does not extend the full length of the dorsal ridge.[2]

Distribution and habitat

A. perideraion is found throughout the Malay Archipelago and Melanesia, in the west Pacific Ocean from the Great Barrier Reef and Tonga, north to the Ryukyu Islands of Japan and in the eastern Indian Ocean from Ningaloo Reef, Western Australia, through the Rowley Shoals, Scott and Ashmore Reefs, Cocos and Christmas Islands to Sumatra. It inhabits reef lagoons and outer reef slopes.[4] A. perideraion has been thought to be found at depths of 3–20 m,[4] but surveys using autonomous underwater vehicles of mesophotic reefs at Viper Reef and Hydrographers Passage in the central Great Barrier Reef observed A. perideraion at depths between 50 and 65 m.[5] A. perideraion and A. clarkii are the only anemonefish found on both the east and west coasts of Australia.[2]

While the morphological features of A. perideraion are consistent throughout its range, genetic analysis of fish in the Indo-Malay Archipelago has shown a genetic break between the Java Sea population (Karimun Java) and all other locations. A north-to-south connection exists from the Philippines to the rest of the archipelago and a mixing of central populations along the strong current of the Indonesian throughflow.[6]

Host anemones

The relationship between anemonefish and their host sea anemones is not random and instead is highly nested in structure.[7] A. perideraion is a generalist, consistent with its widespread distribution, being hosted by the following four of the 10 host anemones: [2][4][7]

Unusually for anemonefish, A. perideraion has been observed sharing a host with other species, including A. clarkii [8] and A. akallopisos.[9]

Diet

The natural diet of anemonefish includes zooplankton, (diatoms and copepods), benthic worms, tunicates, and algae. A. perideraion is the only species of anemonefish to primarily feed on algae. [2]

Conservation status

Anemonefish and their host anemones are found on coral reefs and face similar environmental issues. Like corals, anemones contain intracellular endosymbionts, zooxanthellae, and can suffer from bleaching due to triggers such as increased water temperature or acidification. Local populations and genetic diversity remain vulnerable to high level of exploitation of these species and their host anemones by the global ornamental fish trade.[10] This species was not evaluated in the 2012 release of the IUCN Red List.

In aquaria

It has successfully been bred in an aquarium.[9] In an aquarium, hobbyists have fed the species brine shrimp, mysis shrimp, chopped shellfish, and dried algae.[9][11]

Gallery

References

  1. ^ Jenkins, A.; Carpenter, K.E.; Allen, G.; Yeeting, B. & Myers, R. (2017). "Amphiprion perideraion". IUCN Red List of Threatened Species. 2017: e.T188340A1860821. doi:10.2305/IUCN.UK.2017-2.RLTS.T188340A1860821.en. Retrieved 19 February 2022.
  2. ^ a b c d e f g h i Fautin, Daphne G.; Allen, Gerald R. (1997). Field Guide to Anemone Fishes and Their Host Sea Anemones. Western Australian Museum. ISBN 9780730983651. Archived from the original on 18 October 2014.
  3. ^ Buston PM (May 2004). "Territory inheritance in clownfish". Proc. Biol. Sci. 271 (Suppl 4): S252–4. doi:10.1098/rsbl.2003.0156. PMC 1810038. PMID 15252999.
  4. ^ a b c Bray, Dianne. "Pink Anemonefish, Amphiprion perideraion". Fishes of Australia. Retrieved 30 September 2014.
  5. ^ Bridge, T.; Scott. A.; Steinberg, D. (2012). "Abundance and diversity of anemonefishes and their host sea anemones at two mesophotic sites on the Great Barrier Reef, Australia". Coral Reefs. 31 (4): 1057–1062. Bibcode:2012CorRe..31.1057B. doi:10.1007/s00338-012-0916-x. S2CID 9154493.
  6. ^ Dohna, T.; Timm, J.; Hamid, L.; Kochzius M. (April 2015). "Limited connectivity and a phylogeographic break characterize populations of the pink anemonefish, Amphiprion perideraion, in the Indo-Malay Archipelago: inferences from a mitochondrial and microsatellite loci". Ecology and Evolution. 5 (8): 1717–1733. doi:10.1002/ece3.1455. PMC 4409419. PMID 25937914.
  7. ^ a b Ollerton J; McCollin D; Fautin DG; Allen GR. (2007). "Finding NEMO: nestedness engendered by mutualistic organization in anemonefish and their hosts". Proc R Soc B Biol Sci. 274 (1609): 591–598. doi:10.1098/rspb.2006.3758. PMC 1766375. PMID 17476781.
  8. ^ Hattori, A. (April 1995). "Coexistence of two anemonefishes, Amphiprion clarkii and A. perideraion, which utilize the same host sea anemone" (PDF). Environmental Biology of Fishes. 42 (4): 345–353. doi:10.1007/BF00001464. S2CID 23522414.
  9. ^ a b c Tristan Lougher (2006). What Fish?: A Buyer's Guide to Marine Fish. Interpet Publishing. p. 19. ISBN 978-1-84286-118-9.
  10. ^ Madduppa, H.HT.; Timm, J.; Kochzius M. (February 2014). "Interspecific, Spatial and Temporal Variability of Self-Recruitment in Anemonefishes". PLOS ONE. 9 (2): e90648. Bibcode:2014PLoSO...990648M. doi:10.1371/journal.pone.0090648. PMC 3938785. PMID 24587406.
  11. ^ "Pink Skunk Clownfish". Animal-World.com. Retrieved 29 September 2015.

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wikipedia EN

Pink skunk clownfish: Brief Summary

provided by wikipedia EN

The pink skunk clownfish (Amphiprion perideraion), also known as the pink anemonefish, is a species of anemonefish that is widespread from northern Australia through the Malay Archipelago and Melanesia. Like all anemonefishes, it forms a symbiotic mutualism with sea anemones and is unaffected by the stinging tentacles of the host. It is a sequential hermaphrodite with a strict size-based dominance hierarchy; the female is largest, the breeding male is second largest, and the male nonbreeders get progressively smaller as the hierarchy descends. They exhibit protandry, meaning the breeding male changes to female if the sole breeding female dies, with the largest nonbreeder becoming the breeding male.

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Amphiprion perideraion ( Spanish; Castilian )

provided by wikipedia ES
 src=
A. perideraion entre los tentáculos de H. magnifica, Koh Phangan, Tailandia

El pez payaso rosa (Amphiprion perideraion) es una especie de peces marinos de la familia Pomacentridae.

Pertenecen a los denominados peces payaso, o peces anémona, y viven en una relación mutualista con anémonas Heteractis crispa, Heteractis magnifica, Macrodactyla doreensis y Stichodactyla gigantea.[2]

Morfología

Es de color rosado o naranja rosado, y tiene una línea blanca distintiva recorriendo la espalda, desde el hocico hasta el pedúnculo caudal. También tiene otra fina línea blanca vertical que separa cabeza y tronco. Las aletas son pálidas a transparentes.[3]

Cuenta con 9-10 espinas y 16-17 radios blandos dorsales; 2 espinas y 12-13 radios blandos anales.[4]

Las hembras pueden llegar alcanzar los 10 cm de longitud total. Los machos alcanzan la madurez con 4,6 cm, y las hembras con 5,5 cm de longitud.[5]

Reproducción

Es monógamo y hermafrodita secuencial protándrico,[5]​ esto significa que todos los alevines son machos, y que tienen la facultad de convertirse en hembras, cuando la situación jerárquica en el grupo lo permite, siendo el ejemplar mayor del clan el que se convierte en la hembra dominante, ya que se organizan en matriarcados.[6]

Su género es algo fácil de identificar, ya que la hembra, teóricamente es la más grande del clan. Cuando ésta muere, el pequeño macho dominante se convierte en una hembra.

Son desovadores bénticos. Los huevos son demersales, de forma elíptica, y adheridos al sustrato.[7]​ La reproducción se produce en cuanto comienza a elevarse la temperatura del agua, aunque, como habitan en aguas tropicales, se pueden reproducir casi todo el año. El macho prepara el lugar de la puesta, en un sustrato duro en la base de una anémona, y, tras realizar las maniobras del cortejo, espera a que la hembra fije los huevos allí, y los fertiliza. Posteriormente, agita sus aletas periódicamente para oxigenar los embriones, y elimina los que están en mal estado.

Tras un periodo de 6-7 días, cuando los alevines se liberan, no reciben atención alguna de sus padres. Deambulan en aguas superficiales en fase larval durante 8 a 12 días, posteriormente descienden al fondo en busca de una anémona, y mutan a su coloración juvenil.

Alimentación

Come copépodos, isópodos y crustáceos planctónicos, larvas de tunicados, ascidias, gusanos, diatomeas, y algas bénticas, como Dictyota friabilis.[8]

Depredadores

En las Islas Marshall es depredado por meros, de la familia Serranidae.[9]

Hábitat y comportamiento

Es un pez de mar, de clima tropical (25°C-25°C; 34°N-22°S, 96°E-156°E), y asociado a los arrecifes de coral. Los adultos frecuentan las lagunas y arrecifes exteriores hacia mar adentro.[10]

Su rango de profundidad es entre 1-38 metros, aunque se reportan localizaciones hasta 41 metros de profundidad, y en un rango de temperatura entre 25.16 y 28.35ºC.[11]​ Es principalmente diurno.

Vive en simbiosis con las anémonas Heteractis crispa, Heteractis magnifica, Macrodactyla doreensis y Stichodactyla gigantea. En Bali se les ve compartiendo anémona con su pariente Amphiprion akallopisos.[12]

Distribución geográfica

Se encuentra desde el Golfo de Tailandia hasta Samoa, Tonga, las Islas Ryukyu, la Gran Barrera de Coral y Nueva Caledonia.

Está presente en la isla de Andamán, Australia, Camboya, China, Cocos, Filipinas, Fiyi, Guam, Indonesia, Japón, Kiribati, Malasia, islas Marianas del Norte, islas Marshall, Micronesia, isla Navidad, Nueva Caledonia, Palaos, Papúa Nueva Guinea, islas Ryukyu, islas Salomón, Samoa, Singapur, Sri Lanka, Tailandia, Taiwán, Tonga, Vanuatu y Vietnam.[13]

Observaciones

Puede ser criado en cautividad.[14][15]

Galería

Referencias

  1. Bailly, N. (2015). Amphiprion perideraion Bleeker, 1855. In: Froese, R. and D. Pauly. Editors. (2015) FishBase. Accessed through: World Register of Marine Species at http://www.marinespecies.org/aphia.php?p=taxdetails&id=278403 Registro Mundial de Especies Marinas. Consultado el 20 de mayo de 2015.
  2. Fautin, D.G. and G.R. Allen, (1992) (en inglés) Field guide to anemonefishes and their host sea anemones. Western Australian Museum, Francis Street, Perth.
  3. Allen, G.R., (1975) (en inglés) The anemone fishes. Their classification and biology. Second edition. T.F.H. Publications, Inc., Neptune City, New Jersey.
  4. "Amphiprion perideraion". En FishBase (Rainer Froese y Daniel Pauly, eds.). Consultada en mayo de 2015. N.p.: FishBase, 2015.
  5. a b Allsop, D.J. and S.A. West, (2003) (en inglés) Constant relative age and size at sex change for sequentially hermaphroditic fish. J. Evol. Biol. 16(2003):921-929.
  6. Allen, G.R., (1986) (en inglés) Pomacentridae. p. 670-682. In M.M. Smith and P.C. Heemstra (eds.) Smiths' sea fishes. Springer-Verlag, Berlin.
  7. Breder, C.M. and D.E. Rosen, (1966) (en inglés) Modes of reproduction in fishes. T.F.H. Publications, Neptune City, New Jersey. 941 p.
  8. http://www.fishbase.org/TrophicEco/FoodItemsList.php?vstockcode=2221&genus=Amphiprion&species=perideraion FishBase: Lista de alimentos de A. perideraion. Consultado el 20 de mayo de 2015.
  9. http://www.fishbase.org/TrophicEco/PredatorSummary.php?vpredatstage=juv.%2Fadults&genusname=Amphiprion&speciesname=perideraion&vstockcode=2221&vpreystage=juv.%2Fadults&vpredatorgroup=Serranidae&vpredatorname=groupers FishBase: Predadores de A. perideraion. Consultado el 20 de mayo de 2015.
  10. Myers, R.F., (1991)(en inglés) "Micronesian reef fishes. Second Ed". Coral Graphics, Barrigada, Guam. 298 p.
  11. http://www.iobis.org/mapper/?taxon_id=401420 IOBIS: Sistema de Información Biogeográfica Oceánica. Consultado el 20 de mayo de 2015.
  12. Kuiter, R.H. and T. Tonozuka, (2001) (en inglés) Pictorial guide to Indonesian reef fishes. Part 2. Fusiliers - Dragonets, Caesionidae - Callionymidae. Zoonetics, Australia. 304-622 p.
  13. http://www.fishbase.org/Country/CountryList.php?ID=2024&GenusName=Amphiprion&SpeciesName=perideraion FishBase: Lista de países de A. perideraion. Consultado el 20 de mayo de 2015.
  14. Gardner, T.R., (1997) (en inglés) Commercial breeding of the dottybacks. Seascope 14:1-2.
  15. Miyagawa, K., (1989) (en inglés) Experimental analysis of the symbiosis between anemonefishes and sea anemones. Ethology 80:19-46.

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Amphiprion perideraion: Brief Summary ( Spanish; Castilian )

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 src= A. perideraion en Heteractis magnifica. Gran Barrera de Arrecife Australiana  src= A. perideraion entre los tentáculos de H. magnifica, Koh Phangan, Tailandia

El pez payaso rosa (Amphiprion perideraion) es una especie de peces marinos de la familia Pomacentridae.

Pertenecen a los denominados peces payaso, o peces anémona, y viven en una relación mutualista con anémonas Heteractis crispa, Heteractis magnifica, Macrodactyla doreensis y Stichodactyla gigantea.​

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Amphiprion perideraion ( Basque )

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Amphiprion perideraion Amphiprion generoko animalia da. Arrainen barruko Pomacentridae familian sailkatzen da.

Banaketa

Erreferentziak

  1. Froese, Rainer & Pauly, Daniel ed. (2006), Amphiprion perideraion FishBase webgunean. 2006ko apirilaren bertsioa.

Ikus, gainera

(RLQ=window.RLQ||[]).push(function(){mw.log.warn("Gadget "ErrefAurrebista" was not loaded. Please migrate it to use ResourceLoader. See u003Chttps://eu.wikipedia.org/wiki/Berezi:Gadgetaku003E.");});
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Amphiprion perideraion: Brief Summary ( Basque )

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Amphiprion perideraion Amphiprion generoko animalia da. Arrainen barruko Pomacentridae familian sailkatzen da.

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Amphiprion perideraion ( French )

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Poisson-clown à collier

Le Poisson-clown à collier (Amphiprion perideraion), est une espèce de poissons clowns, de la famille des Pomacentridae qui regroupe les poissons-clowns et les demoiselles.

Répartition

Ce poisson peuple les eaux du centre de la région Indo-Pacifique et ce jusqu'à une profondeur de 3 à 30 mètres[1].

Habitat

 src=
Poissons-clown à collier

Comme tous les poissons-clowns, Amphiprion perideraion vit en association étroite (mutualisme) avec une grande anémone de mer, principalement Heteractis magnifica. Moins souvent, on peut également le trouver dans Heteractis crispa, Macrodactyla doreensis et Stichodactyla gigantea[2]. Dans une anémone vit habituellement un couple reproducteur et plusieurs subadultes immatures.

Reproduction

Les poissons de l'espèce Amphiprion perideraion sont des hermaphrodites protandriques. Ils sont tous mâles à la naissance. Selon les circonstances certains changeront de sexe et deviendront femelles. Ils sont en outre monogames, c'est-à-dire qu'ils n'ont qu'un seul partenaire pour leur vie, à moins qu'un des deux décède. Si la femelle du couple meurt, alors le mâle reproducteur peut devenir femelle s'il se trouve un autre compagnon[3]. La différenciation sexuelle se ferait en fonction de la taille des animaux en présence[4]. Lorsque la femelle est prête à pondre ses œufs, le mâle nettoie un pan de rocher, à proximité de l’anémone, où la femelle dépose se œufs. La femelle peut pondre de 300 à 700 œufs.

Taille

À l'âge adulte, Amphiprion perideraion mesure un maximum de 8 cm[1].

Régime alimentaire

De prime abord, il est omnivore. Lorsqu'il est domestique (en aquarium), il peut manger des morceaux de moules, crues ou cuites. Il peut aussi manger des petits morceaux de crevettes, des artemia et d'autres petits invertébrés.

Notes et références

  1. a et b « Amphiprion perideraion summary page », sur FishBase (consulté le 18 août 2020).
  2. D.G Fautin et G.R. Allen, Field guide to anemonefishes and their host sea anemones, Perth, Western Australian Museum, Francis Street, 1992
  3. Amphiprion perideraion sur Aquaportail.com
  4. Poisson Clown sur Terra Nova

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Amphiprion perideraion: Brief Summary ( French )

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Poisson-clown à collier

Le Poisson-clown à collier (Amphiprion perideraion), est une espèce de poissons clowns, de la famille des Pomacentridae qui regroupe les poissons-clowns et les demoiselles.

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Amphiprion perideraion ( Italian )

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Il pesce pagliaccio rosa o pesce pagliaccio crociato (Amphiprion perideraion Bleeker, 1855) è un pesce d'acqua salata appartenente alla famiglia Pomacentridae. Come tutti i pesci pagliaccio è noto per la simbiosi con alcune specie di anemoni di mare.

Descrizione

Presenta un corpo di forma ovaloide, compresso ai fianchi. La pinna dorsale è bassa e lunga, le pettorali ampie, le altre pinne hanno forma arrotondata. La livrea è semplice: una stretta striscia bianca va dalla punta del muso, lungo la parte posteriore del delicato corpo rosa dorato, fino alla fine del peduncolo caudale. Una più stretta banda bianca bordata di scuro attraversa il corpo verticalmente, coprendo l'opercolo. L'occhio scuro ha un cerchio dorato attorno alla pupilla e le pinne arrotondate sono più chiare del corpo. Le pinne dorsale e caudale dei maschi hanno il bordo arancione.
Raggiunge una lunghezza massima di 10 cm.

Biologia

Riproduzione

È una specie ermafrodita proterandrica (nasce maschio e invecchiando - con taglia sui 5,4 cm - trasmuta in femmina) e monogama. Ogni coppia si riproduce più volte l'anno. La femmina depone annualmente 2000-4000 uova. I maschio rimangono nel luogo di deposizione per curare e ossigenare le uova.

Mutualismo

Si associa alle specie di anemoni Heteractis magnifica (in prevalenza), Heteractis crispa, Macrodactyla doreensis e Stichodactyla gigantea.

Alimentazione

Si nutre di fitoplancton (diatomee), zooplancton e anellidi.

Predatori

Questa specie è preda abituale dei pesci della famiglia Serranidae.

Distribuzione e habitat

Questa specie è diffusa nel Pacifico orientale, dal Golfo di Thailandia alla Grande Barriera Corallina, fino alle coste della Nuova Caledonia. Vive nelle lagune atollifere e nelle barriere coralline.

 src=
Un gruppo di pesci pagliaccio rosa nell'anemone magnifica (Heteractis magnifica)

Acquariofilia

Il pesce pagliaccio rosa è allevato in acquari pubblici e privati. Questo pesce ha bisogno di valori dell'acqua ben precisi: Temp. 26° / 30 °C; Densità 1018 / 1022; PH 8,4. Abbastanza difficile da ambientare in quanto inizialmente soffre di parassitosi della pelle, Oodinuim e micosi; sarebbe sempre consigliabile acquistare esemplari già perfettamente acclimatati e quarantenati; una volta ben ambientato è onnivoro, predilige mangime surgelato, artemie o chironomus e mysis, liofilizzato o secco in granuli di piccolo diametro. Necessita di una vasca relativamente piccola, anche per le sue dimensioni, in quanto non è un grande nuotatore e preferisce restare nelle vicinanze del suo territorio, spesso incentrato su di un'attinia (in acquario vanno benissimo le specie del genere Radianthus). È purtroppo poco resistente alle malattie. Per il suo ottimale mantenimento in acquario sono necessarie vasche con acqua ben filtrata ed ossigenata, preparata con sali marini sintetici di ottima qualità; abbondanti cambi parziali con un'accurata sifonatura del fondo, regolari trattamenti con ozono ed aggiunte settimanali di Oligoelementi e Bioelementi. Molto adatto agli acquari di barriera con pesci pacifici ed invertebrati, del tipo Mini Reef.

Bibliografia

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Amphiprion perideraion: Brief Summary ( Italian )

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Il pesce pagliaccio rosa o pesce pagliaccio crociato (Amphiprion perideraion Bleeker, 1855) è un pesce d'acqua salata appartenente alla famiglia Pomacentridae. Come tutti i pesci pagliaccio è noto per la simbiosi con alcune specie di anemoni di mare.

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Rausvasis skunkinis jūrų klounas ( Lithuanian )

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Binomas Amphiprion perideraion
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Rausvasis skunkinis jūrų klounas (lot. Amphiprion perideraion, angl. Pink anemonefish) – vienuolžuvinių (Pomacentridae) šeimos žuvis. Kūnas iki 10 cm ilgio, rausvai rožinis, su baltomis juostomis, einančiomis burnos šonais ir išilgai nugaros. Nugarinis pelekas baltas.

Gyvena koraliniuose rifuose simbiozėje su aktinijomis, 3-30 m gylyje. Maitinasi bentosiniais dumbliais ir zooplanktonu.

Paplitęs Ramiajame vandenyne nuo Filipinų iki pietų Australijos.

Nuorodos

Vikiteka

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Rausvasis skunkinis jūrų klounas: Brief Summary ( Lithuanian )

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Rausvasis skunkinis jūrų klounas (lot. Amphiprion perideraion, angl. Pink anemonefish) – vienuolžuvinių (Pomacentridae) šeimos žuvis. Kūnas iki 10 cm ilgio, rausvai rožinis, su baltomis juostomis, einančiomis burnos šonais ir išilgai nugaros. Nugarinis pelekas baltas.

Gyvena koraliniuose rifuose simbiozėje su aktinijomis, 3-30 m gylyje. Maitinasi bentosiniais dumbliais ir zooplanktonu.

Paplitęs Ramiajame vandenyne nuo Filipinų iki pietų Australijos.

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Amphiprion perideraion ( Dutch; Flemish )

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Vissen

Amphiprion perideraion is een straalvinnige vissensoort uit de familie van rifbaarzen of koraaljuffertjes (Pomacentridae).[1] De wetenschappelijke naam van de soort is voor het eerst geldig gepubliceerd in 1855 door Bleeker.

Bronnen, noten en/of referenties
  1. (en) Amphiprion perideraion. FishBase. Ed. Ranier Froese and Daniel Pauly. 10 2011 version. N.p.: FishBase, 2011.
Geplaatst op:
22-10-2011
Dit artikel is een beginnetje over biologie. U wordt uitgenodigd om op bewerken te klikken om uw kennis aan dit artikel toe te voegen. Beginnetje
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Amfiprion złoty ( Polish )

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Amphiprion perideraion.jpg

Amfiprion złoty[1] (Amphiprion perideraion) – gatunek ryby okoniokształtnej z rodziny garbikowatych (Pomacentridae).

Występowanie

Ocean Indyjski i Pacyfik, od Zatoki Perskiej przez Zatokę Tajlandzką i Wyspy Kokosowe po Wyspy Riukiu, Samoa, Tonga, Wielką Rafę Koralową i Nową Kaledonię.

Żyje na rafach koralowych na głębokości 1–38 m w wodach o temperaturze ok. 25 °C. Wiąże się z ukwiałami z gatunków Heteractis magnifica (zazwyczaj), Heteractis crispa, Macrodactyla doreensis i Stichodactyla gigantea. Prowadzi głównie dzienny tryb życia. Na Bali współżyje razem ze spokrewnionym gatunkiem Amphiprion akallopisos, czasem nawet w tym samym ukwiale.

Cechy morfologiczne

Osiąga do 10 cm długości. Wzdłuż linii bocznej 50–59 łusek, linia boczna składa się z 32–43 otworów; pionowo poniżej linii bocznej 3–4 łuski, poniżej 19–20. Na pierwszej parze łuków skrzelowych 17–20 wyrostków filtracyjnych. W płetwie grzbietowej 9–10 twardych i 16–17 miękkich promieni, w płetwie odbytowej 2 twarde i 12–13 miękkich promieni. W płetwach piersiowych 16–18 promieni.

Ubarwienie cała pomarańczowe. Na grzbiecie, od pyska do ogona, biegnie biały pasek. Pionowy pasek z tyłu głowy. Płetwy przezroczyste. Tęczówka oka biała.

Odżywianie

Żywi się planktonem.

Rozród

Dojrzewa płciowo przed drugim rokiem życia przy długości 4,7–5,6 cm. Jest monogamiczny, jedna para trze się kilka razy do roku, samica składa rocznie około 2–4 tys. jaj.

Znaczenie i hodowla

Hodowany w akwariach. Rozmnaża się w niewoli.

Przypisy

  1. Stanisław Rutkowicz: Encyklopedia ryb morskich. Gdańsk: Wydawnictwo Morskie, 1982. ISBN 83-215-2103-7.

Bibliografia

  • Amphiprion perideraion. (ang.) w: Froese, R. & D. Pauly. FishBase. World Wide Web electronic publication. www.fishbase.org [dostęp 19 marca 2011]
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Amfiprion złoty: Brief Summary ( Polish )

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Amphiprion perideraion.jpg

Amfiprion złoty (Amphiprion perideraion) – gatunek ryby okoniokształtnej z rodziny garbikowatych (Pomacentridae).

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Amphiprion perideraion ( Ukrainian )

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Опис

Досягають довжини 10 см. Тіло риби помаранчевого кольору. Тонка біла поперечна смуга проходить через головою перед зябровою кришкою. Біла довга смуга починається на морді і тягнеться уздовж білого спинного плавця до основи хвоста. Хвостовий плавець білий. Інші плавці прозорі. У спинному плавці 9-10 жорстких променів і 16-17 м'яких. Анальний плавець складається з двох жорстких і 12-13 м'яких променів.

Поширення і спосіб життя

Мешканці коралових рифів Південно-Східної Азії, Нової Гвінеї, Меланезії, Мікронезії, від узбережжя північної Австралії до островів Рюкю. Біля острова Балі він живе разом з близькоспоріднених видом Amphiprion akallopisos поруч з тією ж актинією. Риби живуть у симбіозі з 4 видами актиній:Macrodactyla doreensis, Heteractis crispa, Heteractis magnifica й Stichodactyla gigantea.

Література

  • Daphne G. Fautin, Gerald R. Allen. Anemonenfische und ihre Wirte. — Melle: Tetra-Verlag, 1994. ISBN 3-89356-171-4

Галерея


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Cá hề hồng ( Vietnamese )

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Cá hề hồng (danh pháp khoa học: Amphiprion perideraion) là một loài cá hề được tìm thấy ở phía tây Thái Bình Dương. Chúng có thể được tìm thấy ở ngoài khơi quần đảo Cocosđảo Phục Sinh ở đông Ấn Độ Dương[1]. Giống như các loài cá hề khác, nó sống cộng sinh với hải quỳ.

Chú thích

Tham khảo


Hình tượng sơ khai Bài viết chủ đề bộ Cá vược này vẫn còn sơ khai. Bạn có thể giúp Wikipedia bằng cách mở rộng nội dung để bài được hoàn chỉnh hơn.
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Cá hề hồng: Brief Summary ( Vietnamese )

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Cá hề hồng (danh pháp khoa học: Amphiprion perideraion) là một loài cá hề được tìm thấy ở phía tây Thái Bình Dương. Chúng có thể được tìm thấy ở ngoài khơi quần đảo Cocosđảo Phục Sinh ở đông Ấn Độ Dương. Giống như các loài cá hề khác, nó sống cộng sinh với hải quỳ.

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Amphiprion perideraion ( Russian )

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Царство: Животные
Подцарство: Эуметазои
Без ранга: Вторичноротые
Подтип: Позвоночные
Инфратип: Челюстноротые
Группа: Рыбы
Группа: Костные рыбы
Подкласс: Новопёрые рыбы
Инфракласс: Костистые рыбы
Надотряд: Колючепёрые
Серия: Перкоморфы
Подотряд: Губановидные
Семейство: Помацентровые
Подсемейство: Рыбы-клоуны (Amphiprioninae Allen, 1975)
Вид: Amphiprion perideraion
Международное научное название

Amphiprion perideraion Bleeker, 1855

Синонимы
  • Amphiprion amamiensis Mori, 1966
  • Amphiprion rosenbergii Bleeker, 1855
  • Prochilus perideraion Bleeker, 1855
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Систематика
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Изображения
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ITIS 170145NCBI 80973EOL 225746

Amphiprion perideraion (лат.) — вид рыб из семейства помацентровых (Pomacentridae). Достигают длины 10 см[1]. Тело рыбы оранжевого цвета. Тонкая белая поперечная полоса проходит через всю голову перед жаберной крышкой. Белая длинная полоса начинается на рыле и тянется вдоль основания белого спинного плавника до основания хвостового плавника. Хвостовой плавник белый. Остальные плавники прозрачные. В спинном плавнике 9—10 жёстких лучей и 16—17 мягких. В анальном плавнике два жёстких и 12—13 мягких лучей.

Обитатели коралловых рифов Юго-Восточной Азии, Новой Гвинеи, Меланезии, Микронезии, от побережья северной Австралии до островов Рюкю. У острова Бали он живёт вместе с близкородственным видом Amphiprion akallopisos рядом с той же актинией. Рыбы живут в симбиозе с 4 видами актиний: Macrodactyla doreensis, Heteractis crispa, Heteractis magnifica и Stichodactyla gigantea.

Примечания

  1. Amphiprion perideraion (англ.) в базе данных FishBase.
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Amphiprion perideraion: Brief Summary ( Russian )

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Amphiprion perideraion (лат.) — вид рыб из семейства помацентровых (Pomacentridae). Достигают длины 10 см. Тело рыбы оранжевого цвета. Тонкая белая поперечная полоса проходит через всю голову перед жаберной крышкой. Белая длинная полоса начинается на рыле и тянется вдоль основания белого спинного плавника до основания хвостового плавника. Хвостовой плавник белый. Остальные плавники прозрачные. В спинном плавнике 9—10 жёстких лучей и 16—17 мягких. В анальном плавнике два жёстких и 12—13 мягких лучей.

Обитатели коралловых рифов Юго-Восточной Азии, Новой Гвинеи, Меланезии, Микронезии, от побережья северной Австралии до островов Рюкю. У острова Бали он живёт вместе с близкородственным видом Amphiprion akallopisos рядом с той же актинией. Рыбы живут в симбиозе с 4 видами актиний: Macrodactyla doreensis, Heteractis crispa, Heteractis magnifica и Stichodactyla gigantea.

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颈环双锯鱼 ( Chinese )

provided by wikipedia 中文维基百科
二名法 Amphiprion perideraion
Bleeker, 1855[1]

颈环双锯鱼学名Amphiprion perideraion)为輻鰭魚綱鱸形目隆頭魚亞目雀鲷科双锯鱼属鱼类,俗名粉红海葵鱼背带双锯齿盖鱼

分布

本魚分布于西太平洋區,包括印度尼西亚菲律宾日本台湾岛以及南海诸岛海南岛等海域。该物种的模式产地在Grootobi。[1]

深度

水深1至38公尺。

特徵

本魚體側扁,口小,體色橘黃色至粉紅色。由頭頂沿背部至尾柄有一白色細縱帶,鰓蓋前亦有一白色橫帶,尾鰭圓形,背鰭硬棘9至10枚,背鰭軟條16至17枚,臀鰭硬棘2枚,臀鰭軟條12至13枚,體長可達10公分。

生態

本魚棲息在珊瑚礁區,與海葵共生,繁殖期極具領域性,產黏著卵,仔稚魚具漂浮期,屬雜食性,以藻類、小型底棲無脊椎動物為食。

經濟利用

為高價值的觀賞魚,不供食用。

参考文献

  1. ^ 1.0 1.1 中国科学院动物研究所. 颈环双锯鱼. 中国动物物种编目数据库. 中国科学院微生物研究所. [2009-04-16]. (原始内容存档于2016-03-05).

扩展阅读

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颈环双锯鱼: Brief Summary ( Chinese )

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颈环双锯鱼(学名:Amphiprion perideraion)为輻鰭魚綱鱸形目隆頭魚亞目雀鲷科双锯鱼属鱼类,俗名粉红海葵鱼、背带双锯齿盖鱼。

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