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Alosa fallax (Lacepède, 1803)

Twaite shad
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Alosa fallax   AquaMaps   Data sources: GBIF OBIS
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Alosa fallax
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分類 / Names 共通名の | 類義語 | Catalog of Fishes(部類, ) | ITIS | CoL | WoRMS | Cloffa

> Clupeiformes (Herrings) > Alosidae (Shads and Sardines)
Etymology: Alosa: Latin, alausa = a fish cited by Ausonius and Latin, halec = pickle, dealing with the Greek word hals = salt; it is also the old Saxon name for shad = "alli" ; 1591 (Ref. 45335).
More on author: Lacepède.

Issue
5 subspecies known.

Environment: milieu / climate zone / depth range / distribution range 生態学

; 新鮮な水; 汽水性の; 昇流魚 (Ref. 51243); 深さの範囲 10 - 400 m (Ref. 2945). Temperate; 66°N - 27°N, 25°W - 42°E

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Northeast Atlantic: Atlantic coasts from southern and western Iceland to northern Morocco (Ref. 188, 6683), including North Sea (Ref. 6683), Baltic Sea (Ref. 188, 6683); also Mediterranean Sea (Ref. 188, 3397, 6683) and Black Sea (Ref. 188, 3397, 26334). Several subspecies have been recognized based on the number of gill rakers and geographical location (Ref. 10541); some have since been given species-status (Ref. 59043).

Length at first maturity / サイズ / 重さ / 年齢

Maturity: Lm 32.5  range ? - ? cm
Max length : 60.0 cm SL オス/雌雄の選別がない; (Ref. 35388); common length : 40.0 cm SL オス/雌雄の選別がない; (Ref. 2945); 最大公表体重: 1.5 kg (Ref. 188); 最大記録サイズ: 25 年 (Ref. 556)

簡単な記述 検索表 | 形態学 | 形態計測学

背面の脊椎 (合計) : 0; 背鰭 (合計) : 16 - 22; 肛門の骨: 0; 臀鰭: 19 - 26; 脊つい: 49 - 59. Diagnosis: Body somewhat compressed, moderately deep with depth at pectoral fin less than head length, scutes apparent along belly (Ref. 188). Upper jaw notched, lower jaw fitting into it; no teeth on palatine and vomer; gillrakers fairly short and stout, total 30 to 80, shorter than gill filaments (Ref. 188, 59043). Usually a series of 4-8 black blotches behind gill opening, but sometimes a single blotch, the others faint or absent (Ref. 188, 40476, 59043). Alosa fallax resembles Alosa alosa, which has more and longer gillrakers and at most only 3 dark spots on flank (Ref. 188).

生物学     用語集 (例 epibenthic)

Amphihaline species (Ref. 51442), schooling and strongly migratory, but apparently not penetrating far up rivers (Ref. 188, 6683). Adults are usually found in open waters along the coast (Refs. 59043, 89486); juveniles are usually found along estuaries and near the shore (Ref. 59043), possibly making vertical diurnal movements synchronized with the tides; they remain in estuaries for over one year (Ref. 89630). Several landlocked (lake) non-migratory populations exist (Ref. 10541). Mostly anadromous, entering river mouths in March (Italy) or early June (northenr European rivers) to spawn in or above the tidal reaches; adults probably return to sea not long after spawning (Ref. 188, 6683). Eggs are demersal and widely scattered among sand or gravel on river bed (Ref. 118, 6683). Ichthyophagous, feeds on small fishes and crustaceans, the young taking the fry of herrings, sprats and gobies (Ref. 188, 51442). Females grow faster and are always larger than males of the same age (Ref. 10541). Very locally distributed due to pollution and impoundment of large rivers throughout Europe and most populations declined during the first decade of the 20th century, but seem to have stabilized at a low level since then (Ref. 59043). It has been suggested that members of the genus Alosa are hearing specialists with the American shad (Alosa sapidissima) having been found to detect and respond to sounds up to at least 180 kHz (Ref. 89631). This may aid in predator avoidance (e.g. cetaceans) (Ref. 89632). Hybridization between this species and the allis shad (Alosa alosa) has been reported from the Rhine (Ref. 89633) as well as rivers in France and Algeria (Ref. 10541). There is some evidence that indicates that shad hybrids may reproduce (Ref. 27567).

Life cycle and mating behavior 成熟 | 繁殖 | 放精 | | 生産力 | 幼生

Adults in the sea begin to congregate near mouths of estuaries in April. Enter estuaries and ascend rivers in May and June when water temperature is between 10-14 °C (Refs. 188, 51442, 59043, 89636). Males begin such movements at 2-3 years, females at 3-4 years (Ref. 59043). Although movement upstream is usually limited to a few kilometres above the brackish zone (Refs. 59043, 89486), spawning has also been reported in non-tidal freshwater areas up to 400 km upstream (Ref. 89637). Gametogenesis occurs in the estuaries. Early arrivals in the rivers are mostly males, with the sex ratio becoming more equal with the later arrivals (Ref. 42360). Spawning movements occur with spring tides and peak when river discharge levels are high (Refs. 89636, 89638). However, when flows are too high, movements upstream become limited (Refs. 89636, 89639). Spawn when water temperature is anywhere between 12-22 °C (Ref. 10541). Move to riverine spawning grounds at night; spawn in large, very noisy schools near surface and leave these areas before daybreak (Ref. 10541). Spawning sites consist of sand and gravel areas with flowing water (Ref. 10541). Spent adults return to the sea and may spawn for 3-4 seasons throughout their lifetime (Refs. 30578, 51442, 59043). Most individuals will have lost 22 % of their body weight after spawning (Ref. 89640). There is some evidence that most individuals return to their natal rivers to spawn (Refs. 10541, 59043). Eggs either drift with the current or sink to the bottom (Ref. 59043, 89641). Eggs hatch after 2-8 days, depending on water temperature (optimal 15-25 °C) (Refs. 35387, 41851). Larvae and juveniles move towards the estuaries and river mouths during their first summer and to the sea at the end of their second year (Ref. 59043). Males mature mainly between the ages of 2-5 years, females between 3-7 years (Ref. 188, 2163, 10541). Length at maturity is between 30-40 cm total length (Ref. 88187).

主な参考文献 Upload your references | 参考文献 | コーディネーター | 協力者

Whitehead, P.J.P., 1985. FAO Species Catalogue. Vol. 7. Clupeoid fishes of the world (suborder Clupeoidei). An annotated and illustrated catalogue of the herrings, sardines, pilchards, sprats, shads, anchovies and wolf-herrings. FAO Fish. Synop. 125(7/1):1-303. Rome: FAO. (Ref. 188)

IUCNのレッドリストの状況は (Ref. 130435: Version 2024-1)

  軽度懸念 (LC) ; Date assessed: 01 January 2008

CITES

Not Evaluated

CMS (Ref. 116361)

Not Evaluated

人間に対する脅威

  Harmless





Human uses

水産業: 少数商業の
FAO - 水産業: landings; Publication: search | FishSource | 私達の周りの海

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インターネットの情報源

Estimates based on models

Preferred temperature (Ref. 123201): 8.7 - 19.3, mean 10.8 °C (based on 522 cells).
Phylogenetic diversity index (Ref. 82804):  PD50 = 0.5000   [Uniqueness, from 0.5 = low to 2.0 = high].
Bayesian length-weight: a=0.00562 (0.00474 - 0.00667), b=3.06 (3.02 - 3.10), in cm total length, based on LWR estimates for this species (Ref. 93245).
栄養段階 (Ref. 69278):  4.0   ±0.4 se; based on diet studies.
Generation time: 3.1 (2.2 - 4.8) years. Estimated as median ln(3)/K based on 14 growth studies.
回復力 (Ref. 120179):  手段, 1.4年~4.4年の倍増期間の最小個体群 (K=0.21-0.38; tm=2-7; tmax=25; Fec>10,000).
Fishing Vulnerability (Ref. 59153):  Moderate to high vulnerability (50 of 100).
Climate Vulnerability (Ref. 125649):  Moderate vulnerability (44 of 100).
価格帯 (Ref. 80766):   Low.
Nutrients (Ref. 124155):  Calcium = 9.95 [4.94, 51.06] mg/100g; Iron = 0.495 [0.207, 1.198] mg/100g; Protein = 19.5 [17.1, 22.4] %; Omega3 = 1.53 [0.81, 2.92] g/100g; Selenium = 14.3 [7.1, 31.3] μg/100g; VitaminA = 14.2 [3.7, 52.6] μg/100g; Zinc = 0.288 [0.182, 0.505] mg/100g (wet weight); based on nutrient studies.