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Brief Summary

provided by EOL authors
The Nile tilapia, Oreochromis niloticus, is a cichlid fish native to North, East and Central Africa, and Israel. Like other tilapia species, O. niloticus is easily and inexpensively farmed and was introduced (and subsequently established itself) in much of the tropical and subtropical world via aquaculture mainly between 1960-80 as a highly desirable alternative to the earlier (between 1940-60) introduced Mozambique tilapia O. mossambicus. Omnivorous, tolerant of wide temperature and water quality and salinity ranges, fast-breeding with an effective reproductive strategy of mouthbreeding to protect and transport its young, and difficult to eradicate, the Nile tilapia, like other tilapia species, has profoundly and negatively effected the biodiversity, ecology and water quality of many ecosystems outside its native range. (Food and Agriculture Organization of the United Nations, factsheet; Global Invasive Species Database, Invasive Species Specialist Group (ISSG), 2008; Wikipedia 2011)
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Benefits

provided by FAO species catalogs
Caught with seines, gillnets and trawls. Cultured in hot spring areas. The total catch reported for this species to FAO for 1999 was 230 445 t. The countries with the largest catches were Egypt (112 811 t) and Thailand (53 000 t). Marketed fresh and frozen.

Brief Summary

provided by FAO species catalogs
Occurs at a temperature range of 8& to 42&C, in a wide variety of freshwater habitats. Is mainly diurnal.Feeds mainly on phytoplankton or benthic algae. Eggs and larvae nursed in mouth of female. Omnivorous, but relying more heavily on plants.

Size

provided by FAO species catalogs
To 62 cm; weight 3.650 g (reported age 9 years).

Diagnostic Description

provided by FAO species catalogs
Body compressed; caudal peduncle depth equal to length. Scales cycloid. A knob-like protuberance absent on dorsal surface of snout. Upper jaw length showing no sexual dimorphism. First gill arch with 27 to 33 gillrakers. Lateral line interrupted. Spinous and soft ray parts of dorsal fin continuous. Dorsal fin with 16 - 17 spines and 11 to 15 soft rays. Anal fin with 3 spines and 10-11 rays. Caudal fin truncated. Colour in spawning season, pectoral, dorsal and caudal fins becoming reddish; caudal fin with numerous black bars.

Diseases and Parasites

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Trichodina Infestation 10. Parasitic infestations (protozoa, worms, etc.)
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Diseases and Parasites

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Trichodina Infection 1. Parasitic infestations (protozoa, worms, etc.)
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Diseases and Parasites

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Trichodina Infestation 9. Parasitic infestations (protozoa, worms, etc.)
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Diseases and Parasites

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Trichodina Infestation 8. Parasitic infestations (protozoa, worms, etc.)
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Diseases and Parasites

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Cichlidogyrus Infestation 4. Parasitic infestations (protozoa, worms, etc.)
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Diseases and Parasites

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Cichlidogyrus Infestation 3. Parasitic infestations (protozoa, worms, etc.)
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Diseases and Parasites

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Cichlidogyrus Infestation 2. Parasitic infestations (protozoa, worms, etc.)
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Diseases and Parasites

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Tripartiella Infestation 2. Parasitic infestations (protozoa, worms, etc.)
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Diseases and Parasites

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Ichthyophthirius Disease. Parasitic infestations (protozoa, worms, etc.)
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Diseases and Parasites

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Cichlidogyrus Infestation. Parasitic infestations (protozoa, worms, etc.)
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Diseases and Parasites

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Ergasilus Disease 3. Parasitic infestations (protozoa, worms, etc.)
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Diseases and Parasites

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Cristaria Infestation. Parasitic infestations (protozoa, worms, etc.)
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Diseases and Parasites

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Trichodina Infection 5. Parasitic infestations (protozoa, worms, etc.)
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Diseases and Parasites

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Tripartiella Infestation. Parasitic infestations (protozoa, worms, etc.)
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Diseases and Parasites

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Enterogyrus Infestation. Parasitic infestations (protozoa, worms, etc.)
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Diseases and Parasites

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Gyrodactylus Infestation 1. Parasitic infestations (protozoa, worms, etc.)
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Diseases and Parasites

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Gyrodactylus Infestation 2. Parasitic infestations (protozoa, worms, etc.)
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Diseases and Parasites

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Lamproglena Infestation. Parasitic infestations (protozoa, worms, etc.)
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Diseases and Parasites

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Epitheliocystis. Bacterial diseases
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Diseases and Parasites

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Trichodinosis. Parasitic infestations (protozoa, worms, etc.)
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Diseases and Parasites

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Skin Flukes. Parasitic infestations (protozoa, worms, etc.)
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Diseases and Parasites

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Yellow Grub. Parasitic infestations (protozoa, worms, etc.)
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Diseases and Parasites

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Edwardsiellosis. Bacterial diseases
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Life Cycle

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Sexual maturity is reached at 3-6 months depending on temperature, reaching about 30 g. Reproduction occurs only when temperatures are over 20°C. Several yearly spawnings every 30 days. Females incubate eggs inside their mouths (approximately for a week) where larvae hatch and remain until the vitellus is reabsorved. Egg size 1.5 mm, larval length at hatching 4 mm.Spawns in firm sand in water from 0.6 to 2 m deep of lakes (Ref. 2) and inshore waters (Ref. 55624). Males set up and defend territory which are visited by the females. Courtship lasts several hours. A single male probably fertilises the eggs of more than one female (Ref. 55624). Eggs are shed in batches in shallow nest and fertilized by male. Each batch of eggs is picked up into oral cavity by female. Females solely involved in broodcare. Female carries up to 200 eggs in her mouth where the larvae hatch and remain until after the yolk-sac is absorbed.
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Migration

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Potamodromous. Migrating within streams, migratory in rivers, e.g. Saliminus, Moxostoma, Labeo. Migrations should be cyclical and predictable and cover more than 100 km.
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Morphology

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Dorsal spines (total): 15 - 18; Dorsal soft rays (total): 11 - 13; Analspines: 3; Analsoft rays: 9 - 11; Vertebrae: 30 - 32
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Threats

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Least Concern (LC) , IUCN Grouper and Wrasse Specialist Group
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Trophic Strategy

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Inhabit the littoral zone of lakes and are abundant in Lakes Turkana (Rudolf) and Albert. Although a freshwater species they are also found in brackish water like in the Nile Delta. The area occupied by the species extends from 8° S to 32° N and from 6000 ft (1830 m) to sea level. O. niloticus of Lake Edward form very large schools of 100 sq.m or more at the lake surface when feeding. The species takes epiphytic algae, diatoms or plankton according to conditions. (See also Ref. 3736).
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Diseases and Parasites

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Alitropus Infestation. Parasitic infestations (protozoa, worms, etc.)
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Diagnostic Description

provided by Fishbase
Diagnosis: A large deep-bodied tilapia, with a relatively small head (Ref. 118638). Jaws of mature male not greatly enlarged, length of lower jaw 29-37% of head length; genital papilla of breeding male not tassellated (Ref. 2). Body depth 36-50% of SL (Ref. 28714). Most distinguishing characteristic is the presence, at all life stages, of regular vertical stripes throughout depth of caudal fin (Ref. 4967, 53405, 118638). In smaller fishes, these are relatively wide and form an arc, and start at the base of the caudal fin (Ref. 118638). Males are bluish pink, sometimes with a dark throat, belly, anal and pelvic fins; females are usually brownish, silvery/white beneath with around 10 thin vertical bars (Ref. 118638).Description: Lower pharyngeal bone longer than broad, its anterior part longer than toothed part; outer jaw teeth bicuspid, inner jaw teeth tricuspid, posterior pharyngeal teeth bicuspid and stout; 3-4 rows of teeth in jaws (3-5, rarely 6, in specimens over 200 mm SL); micro-gillrakers present; scales cycloid (Ref. 53405).Coloration: margin of dorsal fin grey or black; vertical bars in caudal fin 7-12 (Ref. 2). Regular black cross bars on caudal fin; ground colour greyish, relatively dark in adults; back olivaceous-green, sides paler, with 6-9 rather indistinct cross bars; belly whitish; upper lip pale green or white, lower lip white; dorsal and anal fins greyish, sometimes with very narrow red margin, soft part of fin with vertical lines (or with aligned light spots resembling striped pattern); pelvic fins grey, pectorals transparent; "tilapian" spot lacking in adults but very distinct in fingerlings which also have more distinct cross bars and very prominent black spot on upper part of caudal peduncle; throat, belly and unpaired fins black in mature males (Ref. 53405). Head and trunk in breeding male suffused with red (Ref. 28714).
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Diseases and Parasites

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Fish tuberculosis (FishMB). Bacterial diseases
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Diseases and Parasites

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Contracaecum Disease (larvae). Parasitic infestations (protozoa, worms, etc.)
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Diseases and Parasites

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Gnathostoma Disease (larvae). Parasitic infestations (protozoa, worms, etc.)
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Allan Palacio
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Diseases and Parasites

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Cichlidogyrus Infestation 5. Parasitic infestations (protozoa, worms, etc.)
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Diseases and Parasites

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Fish Tuberculosis 2. Parasitic infestations (protozoa, worms, etc.)
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Diseases and Parasites

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Trypanosoma Infestation 2. Parasitic infestations (protozoa, worms, etc.)
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Diseases and Parasites

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Dilepid Cestode larvae Infestation (general sp.). Parasitic infestations (protozoa, worms, etc.)
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Diseases and Parasites

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Cichlidogyrus Infestation 10. Parasitic infestations (protozoa, worms, etc.)
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Diseases and Parasites

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Myxobacterial Infections. Bacterial diseases
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Diseases and Parasites

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Dactylosoma Infection 1. Parasitic infestations (protozoa, worms, etc.)
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Diseases and Parasites

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Aeromonosis. Bacterial diseases
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Diseases and Parasites

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Amplicaecum Infection (Larvae). Parasitic infestations (protozoa, worms, etc.)
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Diseases and Parasites

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Whirling Viral Disease of Tilapia Larvae. Viral diseases
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Diseases and Parasites

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Aeromonasis in Tilapia. Bacterial diseases
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Diseases and Parasites

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Turbidity of the Skin (Freshwater fish). Parasitic infestations (protozoa, worms, etc.)
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Diseases and Parasites

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Caligus Infestation 3. Parasitic infestations (protozoa, worms, etc.)
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Diseases and Parasites

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Transversotrema Infestation. Parasitic infestations (protozoa, worms, etc.)
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Diseases and Parasites

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Sporozoa-infection (Myxobolus sp.). Parasitic infestations (protozoa, worms, etc.)
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Diseases and Parasites

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False Fungal Infection (Epistylis sp.). Parasitic infestations (protozoa, worms, etc.)
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Diseases and Parasites

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False Fungal Infection (Apiosoma sp.). Parasitic infestations (protozoa, worms, etc.)
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Diseases and Parasites

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Cryptobia Infestation. Parasitic infestations (protozoa, worms, etc.)
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Diseases and Parasites

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Trypanosoma Infection. Parasitic infestations (protozoa, worms, etc.)
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Diseases and Parasites

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Dactylogyrus Gill Flukes Disease. Parasitic infestations (protozoa, worms, etc.)
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Diseases and Parasites

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Acanthogyrus Infestation. Parasitic infestations (protozoa, worms, etc.)
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Diseases and Parasites

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Cichlidogyrus Disease. Parasitic infestations (protozoa, worms, etc.)
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Diseases and Parasites

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Iridovirosis. Viral diseases
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Diseases and Parasites

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Fish louse Infestation 1. Parasitic infestations (protozoa, worms, etc.)
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Biology

provided by Fishbase
Occurs in a wide variety of freshwater habitats like rivers, lakes, sewage canals and irrigation channels (Ref. 28714). Does not do well in pure salt water, but is able to survive in brackish water (Ref. 52307). Mainly diurnal. Feeds mainly on phytoplankton or benthic algae. Additionally, insect larvae are of some importance, as are aufwuchs and detritus; juveniles tend to be more omnivorous than adults (Ref. 52307). Oviparous (Ref. 205), ovophilic (Ref. 52307). A maternal mouthbrooder (Ref. 2, 28714, 52307, 118638), males dig simple pits in shallow water (Ref. 118638). May mature early (about 11 cm TL females, 14 cm TL males) (Ref. 28714). Globally, the most important tilapia species in fish farming and supports major capture fisheries where established; generally highly invasive and known to hybridise with many other Oreochromis species and for this reason further stocking has been banned in a number of countries, e.g. South Africa, Malawi and Zambia (Ref. 118638). Extended temperature range 8-42 °C, natural temperature range 13.5 - 33 °C (Ref. 3). Maximum depth from Ref. 34290. Marketed fresh and frozen (Ref. 9987).
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Importance

provided by Fishbase
fisheries: highly commercial; aquaculture: commercial
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分布

provided by The Fish Database of Taiwan
原產於非洲,現因人工養殖之故,已被引進世界上的許多地區,包括台灣在內。本種魚易於與同屬它種魚雜交,故在野外較難發現純種魚。目前台灣純種尼羅口孵非鯽主要存在於水產試驗所及其它少數水產研究機構或養殖場,而廣泛分布於各地低海拔之河川、池沼及溝渠等水域,實為無法區分之雜交種。
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臺灣魚類資料庫

利用

provided by The Fish Database of Taiwan
以其易於雜交之特性而廣為世界各國引進養殖的一種魚類。肉質鮮美細嫩,骨刺少,經濟價值高。
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臺灣魚類資料庫

描述

provided by The Fish Database of Taiwan
體呈橢圓形,側扁;背部輪廓隆起。頭中大。口中大,後端不及眼眶前緣。吻圓鈍,唇厚。上下頜各具3-4行細小而扁薄的葉狀齒;鋤骨和腭骨均無齒。下枝鰓耙20-26。體被大櫛鱗,頭部除吻部和頦部外均被鱗;側線平直,在背鰭第4-5軟條下方中斷,形成上下二側線。背鰭單一,無缺刻,硬棘XV-XVIII(通常為XVII),軟條數10-14;臀鰭硬棘III,軟條數10-11;胸鰭側位,鰭條頗長,末端達臀鰭起點上方;腹鰭胸位,末端達肛門;尾鰭截形。體色隨環境而異,一般為暗褐色,背部暗綠,腹部銀白;鰓蓋上緣具一藍灰色斑點;一般體側具8-12條暗色橫帶。背、臀及尾鰭具許多灰色小點,尾鰭具多條垂直橫紋;成熟雄魚在生殖期間,體側暗色橫帶消失,背和尾鰭具淡紅之鰭緣。
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臺灣魚類資料庫

棲地

provided by The Fish Database of Taiwan
廣鹽性魚類,可存活於淡水及海水中,對環境的適應性很強,能耐高鹽度、低溶氧及混濁水,但耐寒力差,適宜生存溫度在16-35℃,溫度低於10℃以下,或高於40℃以上皆不利生存;繁殖能力強,生長快速,對疾病的抵抗性高,故廣被養殖業者引進繁殖。雜食性,以浮游生物、藻類、水生植物碎屑等為食。
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Nile tilapia

provided by wikipedia EN

The Nile tilapia (Oreochromis niloticus) is a species of tilapia, a cichlid fish native to parts of Africa and the Levant, particularly Israel and Lebanon.[2] Numerous introduced populations exist outside its natural range.[1][3] It is also commercially known as mango fish (not to be confused with mango tilapia, or Sarotherodon galilaeus), nilotica, or boulti.[4]

Description

The Nile tilapia reaches up to 60 cm (24 in) in length,[2] and can exceed 5 kg (11 lb).[5] As typical of tilapia, males reach a larger size and grow faster than females.[5]

Wild, natural-type Nile tilapias are brownish or grayish overall, often with indistinct banding on their body, and the tail is vertically striped. When breeding, males become reddish, especially on their fins.[5][6] It is commonly confused with the blue tilapita (O. aureus); that species lacks the striped tail pattern, has a red edge to the dorsal fin (this edge is gray or black in Nile tilapia), and males are bluish overall when breeding. The two species can also be separated by meristics.[6] Because many tilapia in aquaculture and introduced around the world are selectively bred variants and/or hybrids, identifying them using the standard features that can be used in the wild, natural types is often not possible.[6] The virtually unknown O. ismailiaensis has a plain tail, but otherwise closely resembles (and may only be a variant of) the Nile tilapia.[7] Regardless, O. ismailiaensis might be extinct, as its only known habitat in northeastern Egypt has disappeared,[8] although similar-looking individuals (perhaps the same) are known from the vicinity.[7]

Nile tilapia can live for more than 10 years.[5]

Range and habitat

The Nile tilapia is native to larger parts of Africa, except Maghreb and almost all of Southern Africa. It is native to tropical West Africa, the Lake Chad basin, and much of the Nile system, including lakes Tana, Albert and EdwardGeorge, as well as lakes Kivu, Tanganyika, and Turkana, and the Awash and Omo Rivers. In Israel, it is native to coastal river basins.[1][2] It has been widely introduced elsewhere, both in Africa and other continents, including tens of countries in Asia, Europe, North America, and South America. In these places, it often becomes highly invasive, threatening the native ecosystems and species.[1][2] However, some introduced populations historically labelled as Nile tilapia either are hybrids or another species; the Nile tilapia and blue tilapia especially often have been confused.[6]

The Nile tilapia can be found in most types of freshwater habitats, such as rivers, streams, canals, lakes, and ponds, and ranging from sea level to an altitude of 1,830 m (6,000 ft).[1][2] It also occurs in brackish water, but is unable to survive long-term in full salt water.[2] The species has been recorded at water temperatures between 8 and 42 °C (46 and 108 °F), although typically above 13.5 °C (56.5 °F),[2] and the upper lethal limit usually is at 39–40 °C (102–104 °F).[1] Also, some variations occur depending on the population. For example, those in the northern part of its range survive down to the coldest temperatures, while isolated populations in hot springs in the Awash basin and at Suguta River generally live in waters that are at least 32–33 °C (90–91 °F).[8] Although Nile tilapia can survive down to relatively cold temperatures, breeding generally only occurs when the water reaches 24 °C (75 °F).[5]

Subspecies

O. n. niloticus

Although FishBase considers the species as monotypic,[2] several distinctive populations often are recognized as valid subspecies:[1][8][9]

  • O. n. niloticus (Linnaeus, 1758) – most of species' range
  • O. n. baringoensis Trewavas, 1983Lake Baringo in Kenya
  • O. n. cancellatus (Nichols, 1923) – Awash basin in Ethiopia
  • O. n. eduardianus (Boulenger, 1912)Albertine Rift Valley lakes
  • O. n. filoa Trewavas, 1983 – hot springs in Awash basin in Ethiopia
  • O. n. sugutae Trewavas, 1983 – Karpeddo soda springs at Suguta River in Kenya
  • O. n. tana Seyoum & Kornfield, 1992 – Lake Tana in Ethiopia
  • O. n. vulcani Trewavas, 1933 – Lake Turkana in Ethiopia and Kenya

While the species is overall very widespread and common, the IUCN considers O. n. baringoensis as endangered, O. n. sugutae as vulnerable, and O. n. filoa as data deficient.[1]

A population found in Lake Bogoria appears to be an undescribed subspecies.[8]

The forms referred to as Oreochromis (or Tilapia) nyabikere and kabagole seem to belong to this species, too. An undescribed population found at, for example, Wami River, Lake Manyara, and Tingaylanda seems to be a close relative.[10]

Behavior

Feeding

The Nile tilapia is mostly a herbivore, but with omnivorous tendencies, especially when young.[2] They mostly feed on phytoplankton and algae, and in some populations other macrophytes also are important.[1] Other recorded food items are detritus and aquatic insect larvae,[2] including those of mosquitoes, making it a possible tool in the fight against malaria in Africa.[11] However, when introduced outside its native range, it often becomes invasive, threatening more localized species.[2]

The Nile tilapia typically feeds during daytime, which suggests that, similar to trout and salmon, it exhibits a behavioral response to light as a main factor contributing to feeding activity. Due to its fast reproductive rate, however, overpopulation often results within groups of Nile tilapia. To obtain the necessary nutrients, night feeding may also occur due to competition for food during daylight. A recent study found evidence that, contrary to popular belief, size dimorphism between the sexes results from differential food conversion efficiency rather than different amounts of food consumed. Hence, although males and females eat equal amounts of food, males tend to grow larger due to a higher efficiency of converting food to body weight.[12]

Social organization

Groups of Nile tilapia establish social hierarchies in which the dominant males have priority for both food and mating. Circular nests are built predominantly by males through mouth digging to become future spawning sites. These nests often become sites of intense courtship rituals and parental care.[13] Like other fish, Nile tilapia travel almost exclusively in schools. Although males settle down in their crafted nesting zones, females travel between zones to find mates, resulting in competition between the males for females.

Like other tilapias, such as Mozambique tilapia, dominance between the males is established first through noncontact displays such as lateral display and tail beats. Unsuccessful attempts to reconcile the hierarchy results in contact fighting to inflict injuries. Nile tilapia have been observed to modify their fighting behavior based upon experiences during development. Thus, experience in a certain form of agonistic behavior results in differential aggressiveness among individuals.[14] Once the social hierarchy is established within a group, the dominant males enjoy the benefits of both increased access to food and an increased number of mates. However, social interactions between males in the presence of females results in higher energy expenditures as a consequence of courtship displays and sexual competition.[12]

Reproduction

Typical of most fish, Nile tilapia reproduce through mass spawning of a brood within a nest made by the male. In such an arrangement, territoriality and sexual competition amongst the males lead to large variations in reproductive success for individuals in a group. The genetic consequence of such behavior is reduced genetic variability in the long run, as inbreeding is likely to occur among different generations due to differential male reproductive success.[15] Perhaps driven by reproductive competition, tilapias reproduce within a few months after birth. The relatively young age of sexual maturation within Nile tilapia leads to high birth and turnover rates. Consequently, the rapid reproductive rate of individuals can actually have a negative impact on growth rate, leading to the appearance of stunted tilapia as a result of a reduction in somatic growth in favor of sexual maturation.[16]

Female Nile tilapia, in the presence of other females either visually or chemically, exhibit shortened interspawning intervals. Although parental investment by a female extends the interspawning period, female tilapia that abandon their young to the care of a male gain this advantage of increased interspawning periods. One of the possible purposes behind this mechanism is to increase the reproductive advantage of females that do not have to care for young, allowing them more opportunities to spawn.[17] For males, reproductive advantage goes to the more dominant males. Males have differential levels of gonadotropic hormones responsible for spermatogenesis, with dominant males having higher levels of the hormone. Thus, selection has favored larger sperm production with more successful males. Similarly, dominant males have both the best territory in terms of resources and the greatest access to mates.[18] Furthermore, visual communication between Nile tilapia mates both stimulates and modulates reproductive behavior between partners such as courtship, spawning frequency, and nest building.[13]

Parental care

Species belonging to the genus Oreochromis typically care for their young through mouthbrooding, oral incubation of the eggs and larvae. Similar to other tilapia, Nile tilapia are maternal mouthbrooders and extensive care is, therefore, provided almost exclusively by the female. After spawning in a nest made by a male, the young fry or eggs are carried in the mouth of the mother for a period of 12 days. Sometimes, the mother pushes the young back into her mouth if she believes they are not ready for the outside. Nile tilapias also demonstrate parental care in times of danger. When approached by a danger, the young often swim back into the protection of their mother's mouth.[19] However, mouthbrooding leads to significant metabolic modifications for the parents, usually the mother, as reflected by fluctuations in body weight and low fitness. Thus, parental-offspring conflict can be observed through the costs and benefits of mouthbrooding. Protection of the young ensures passage of an individual's genes into the future generations, but caring for the young also reduces an individual's own reproductive fitness.[16]

Since female Nile tilapia exhibiting parental care show extended interspawning periods, one of the benefits is slowing down vitellogenesis (yolk deposition) to increase the survival rate of one's own young. The size of spawned eggs correlates directly with advantages concerning hatching time, growth, survival, and onset of feeding, since increased egg size means increased nutrients for the developing young. Thus, one of the reasons behind a delayed interspawning period by female Nile tilapia may be for the benefit of offspring survival.[17][20]

Aquaculture

An Egyptian New Kingdom amulet in the shape of a tilapia hieroglyph from circa 1350/1320 BC

Tilapia, likely the Nile tilapia, was well known as food fish in Ancient Egypt and commonly featured in their art (paintings and sculptures). This includes a 4000-year-old tomb illustration that shows them in man-made ponds, likely an early form of aquaculture.[5][21] In modern aquaculture, wild-type Nile tilapia are not farmed very often because the dark color of their flesh is undesirable for many customers, and because of the reputation the fish has as being a trash fish.[22] However, they are fast-growing and produce good fillets; leucistic ("red") breeds which have lighter meat have been developed to counter the consumer distaste for darker meat.

Hybrid stock is also used in aquaculture; Nile × blue tilapia hybrids are usually rather dark, but a light-colored hybrid breed known as "Rocky Mountain White" tilapia is often grown due to its very light flesh and tolerance of low temperatures.[22]

As food

Live pla nin on a table at a Thai market

The red-hybrid Nile tilapia is known in the Thai language as pla thapthim (Thai: ปลาทับทิม), meaning "pomegranate fish" or "ruby fish".[23] This type of tilapia is very popular in Thai cuisine, where it is prepared in a variety of ways.[24]

The black-and-white-striped tilapia pla nin (Thai: ปลานิล), some says was mispronounce from "Nile fish", some media says is name of Akihito (仁) who give this fish to Bhumibol, has darker flesh and is commonly either salted and grilled or deep-fried, and it can also be steamed with lime (pla nin nueng manao).[25]

Nile tilapia, called بلطي bulṭī in Arabic, is (being native to Egypt) among the most common fish in Egyptian cuisine, and probably the most common in regions far from the coast. It is generally either battered and pan-fried whole (بلطي مقلي bulṭī maqlī [bʊltˤiː maʔliː]) or grilled whole (بلطي مشوي bulṭī mashwī [bʊltˤiː maʃwiː]). Like other fish in Egypt, is generally served with rice cooked with onions and other seasonings to turn it red.

In Israel, Nile tilapia is commonly fried, grilled or baked with vegetables herbs and spices and eaten with rice or bulgur pilafs. It is also baked in the oven with tahini sauce drizzled over it with potatoes, onions, asparagus, sweet peppers or tomatoes and flavored with sumac and dried mint.

Tilapia, often farmed, is a popular and common supermarket fish in the United States.

In India, Nile tilapia is the most dominant fish in some of the South Indian reservoirs and available throughout the year. O. niloticus grows faster and reaches bigger sizes in a given time. The littoral areas of Kelavarappalli Reservoir are full of nests of Nile tilapia and they breed during south-west monsoon (July–September). The fish mainly feed on detritus. Zooplankton, phytoplankton, and macrophytes also were recorded occasionally from the gut of Nile tilapia. The demand is heavy, especially from local poor people, as this fish is affordable to the lowest income group in this area.[26]

See also

  • Nile perch — a similar-named but different fish that grows much larger and is highly predatory

References

  1. ^ a b c d e f g h i Diallo, I.; Snoeks, J.; Freyhof, J.; Geelhand, D.; Hughes, A. (2020). "Oreochromis niloticus". IUCN Red List of Threatened Species. 2020: e.T166975A134879289. doi:10.2305/IUCN.UK.2020-3.RLTS.T166975A134879289.en. Retrieved 19 November 2021.
  2. ^ a b c d e f g h i j k Froese, Rainer; Pauly, Daniel (eds.) (2015). "Oreochromis niloticus" in FishBase. November 2015 version.
  3. ^ Azevedo-Santos, V.M.; O. Rigolin-Sá; and F.M. Pelicice (2011). "Growing, losing or introducing? Cage aquaculture as a vector for the introduction of non-native fish in Furnas Reservoir, Minas Gerais, Brazil". Neotropical Ichthyology. 9 (4): 915–919. doi:10.1590/S1679-62252011000400024.
  4. ^ Ibrahim, A. A.; El-Zanfaly, H. T. (1980). "Boulti (Tilapia nilotica Linn.) fish paste 1. Preparation and chemical composition". Zeitschrift für Ernährungswissenschaft. 19 (3): 159–162. doi:10.1007/BF02018780. PMID 7445573. S2CID 31199737.
  5. ^ a b c d e f Nico, L.G.; P.J. Schofield; M.E. Neilson (2019). "Oreochromis niloticus (Linnaeus, 1758)". Food and Agriculture Organization, United Nations. Retrieved 5 November 2019.
  6. ^ a b c d Nico, L.G.; P.J. Schofield; M.E. Neilson (2019). "Oreochromis niloticus (Linnaeus, 1758)". U.S. Geological Survey, Nonindigenous Aquatic Species Database. Retrieved 5 November 2019.
  7. ^ a b Neumann, D.; H. Obermaier; T. Moritz (2016). "Annotated checklist for fishes of the Main Nile Basin in the Sudan and Egypt based on recent specimen records (2006-2015)". Cybium. 40 (4): 287–317. doi:10.26028/cybium/2016-404-004.
  8. ^ a b c d Ford, A.G.P.; et al. (2019). "Molecular phylogeny of Oreochromis (Cichlidae: Oreochromini) reveals mito-nuclear discordance and multiple colonisation of adverse aquatic environments" (PDF). Mol. Phylogenet. Evol. 136: 215–226. doi:10.1016/j.ympev.2019.04.008. PMID 30974200. S2CID 109938635.
  9. ^ Trewavas, E. (1983). Tilapiine Fishes of the genera Sarotherodon, Oreochromis and Danakilia. Natural History Museum, London.
  10. ^ Nagl, Sandra; Tichy, Herbert; Mayer, Werner E.; Samonte, Irene E.; McAndrew, Brendan J.; Klein, Jan (2001). "Classification and Phylogenetic Relationships of African Tilapiine Fishes Inferred from Mitochondrial DNA Sequences". Molecular Phylogenetics and Evolution. 20 (3): 361–374. doi:10.1006/mpev.2001.0979. PMID 11527464.
  11. ^ "Nile tilapia can fight malaria mosquitoes", BBC News, 8 August 2007.
  12. ^ a b TOGUYENI, A; FAUCONNEAU, B; BOUJARD, T; FOSTIER, A; KUHN, E; MOL, K; BAROILLER, J (1 August 1997). "Feeding behaviour and food utilisation in tilapia, Oreochromis Niloticus: Effect of sex ratio and relationship with the endocrine status". Physiology & Behavior. 62 (2): 273–279. doi:10.1016/S0031-9384(97)00114-5. PMID 9251968. S2CID 25867399.
  13. ^ a b Castro, A.L.S.; Gonçalves-de-Freitas, E.; Volpato, G.L.; Oliveira, C. (1 April 2009). "Visual communication stimulates reproduction in Nile tilapia, Oreochromis niloticus (L.)". Brazilian Journal of Medical and Biological Research. 42 (4): 368–374. doi:10.1590/S0100-879X2009000400009. PMID 19330265.
  14. ^ Barki, Assaf; Gilson L. Volpato (October 1998). "Early social environment and the fighting behaviour of young Oreochromis niloticus (Pisces, Cichlidae)". Behaviour. 135 (7): 913–929. doi:10.1163/156853998792640332.
  15. ^ Fessehaye, Yonas; El-bialy, Zizy; Rezk, Mahmoud A.; Crooijmans, Richard; Bovenhuis, Henk; Komen, Hans (15 June 2006). "Mating systems and male reproductive success in Nile tilapia (Oreochromis niloticus) in breeding hapas: A microsatellite analysis". Aquaculture. 256 (1–4): 148–158. doi:10.1016/j.aquaculture.2006.02.024.
  16. ^ a b Peña-Mendoza, B.; J. L. Gómez-Márquez; I. H. Salgado-Ugarte; D. Ramírez-Noguera (September 2005). "Reproductive biology of Oreochromis niloticus (Perciformes: Cichlidae) at Emiliano Zapata dam, Morelos, Mexico". Revista de Biología Tropical. 53 (3/4): 515–522. doi:10.15517/rbt.v53i3-4.14666. PMID 17354460.
  17. ^ a b Tacon, P. (1 November 1996). "Relationships between the expression of maternal behaviour and ovarian development in the mouthbrooding cichlid fish Oreochromis Niloticus". Aquaculture. 146 (3–4): 261–275. doi:10.1016/S0044-8486(96)01389-0.
  18. ^ Pfennig, F.; Kurth, T.; Meissner, S.; Standke, A.; Hoppe, M.; Zieschang, F.; Reitmayer, C.; Gobel, A.; Kretzschmar, G.; Gutzeit, H. O. (26 October 2011). "The social status of the male Nile tilapia (Oreochromis niloticus) influences testis structure and gene expression". Reproduction. 143 (1): 71–84. doi:10.1530/REP-11-0292. PMID 22031714.
  19. ^ "Oreochromis niloticus (Nile tilapia)" (PDF). UWI.
  20. ^ Rana, Kausik J. (1986). "Parental influences on egg quality, fry production and fry performance in Oreochromis niloticus (Linnaeus) and O. mossambicus (Peters)". University of Stirling.
  21. ^ Soliman, N.F.; D.M.M. Yacout (2016). "Aquaculture in Egypt: status, constraints and potentials". Aquaculture International. 24 (5): 1201–1227. doi:10.1007/s10499-016-9989-9. S2CID 16767145.
  22. ^ a b "Tilapia". Archived from the original on 2012-10-16. Retrieved 2007-07-12.
  23. ^ https://web.archive.org/web/20170623071944/http://www.fishtech.mju.ac.th/FishNew1/OSS/files/ByBUzsfTue53948.pdf Management Guidelines of Red Tilapia Culture in Cages, Trang Province (in Thai)
  24. ^ "Recipes for Thaptim Fish". Archived from the original on 2009-09-10. Retrieved 2013-10-05.
  25. ^ Fish breeding in Thailand
  26. ^ Feroz Khan, M.; Panikkar, Preetha (2009). "Assessment of impacts of invasive fishes on the food web structure and ecosystem properties of a tropical reservoir in India". Ecological Modelling. 220 (18): 2281–2290. doi:10.1016/j.ecolmodel.2009.05.020.

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Nile tilapia: Brief Summary

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The Nile tilapia (Oreochromis niloticus) is a species of tilapia, a cichlid fish native to parts of Africa and the Levant, particularly Israel and Lebanon. Numerous introduced populations exist outside its natural range. It is also commercially known as mango fish (not to be confused with mango tilapia, or Sarotherodon galilaeus), nilotica, or boulti.

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