Eudontomyzon mariae (Berg, 1931)
Ukrainian brook lamprey
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عکس ها | تصوير گوگل
Eudontomyzon mariae
عکس از Artaev, O.
عکس ها | تصوير گوگل
عکس از Artaev, O.
رده بندی / نامها اسامي عام | مترادف | Catalog of Fishes(جنس, گونه ها) | ITIS | CoL | WoRMS | Cloffa
> Petromyzontiformes (Lampreys) > Petromyzontidae (Northern lampreys) > Lampetrinae
Etymology: Eudontomyzon: eu-, a Greek intensive (good, well or very); odontos (Gr.) tooth, referring to numerous radially arranged teeth of E. danfordi; myzon (Gr.), to suck (borrowed from Petromyzon), referring to their suctorial behavior (See ETYFish); mariae: In honor of Berg’s second wife Maria (née Ivanova), “who examined many thousands of river lampreys from the mouth of the Neva and other streams, falling into the Finnish Gulf” (See ETYFish).
Eponymy: Maria Mikhailovna Berg née Ivanova was (1922) the second wife of the author. [...] (Ref. 128868), visit book page.
More on author: Berg.
Etymology: Eudontomyzon: eu-, a Greek intensive (good, well or very); odontos (Gr.) tooth, referring to numerous radially arranged teeth of E. danfordi; myzon (Gr.), to suck (borrowed from Petromyzon), referring to their suctorial behavior (See ETYFish); mariae: In honor of Berg’s second wife Maria (née Ivanova), “who examined many thousands of river lampreys from the mouth of the Neva and other streams, falling into the Finnish Gulf” (See ETYFish).
Eponymy: Maria Mikhailovna Berg née Ivanova was (1922) the second wife of the author. [...] (Ref. 128868), visit book page.
More on author: Berg.
Taxonomic Remarks
This species needs a complete re-evaluation Renaud (2011; Re. 89241:41), and may be a complex of species. Please send references, or more studies are needed.
محیط زیست: محیط زیست / منطقه آب و هوایی / تغييرات عمق / محدوده توزیع بوم شناسي
; آب شيرين نزديك كف زي; رود رو. Temperate; 57°N - 41°N, 14°E - 49°E (Ref. 59043)
پراكنش سرزمینها | مناطق سازمان خوار و بار جهاني (FAO) | اکوسیستمها | ظهور | نقشه نقطه ای | معرفي | Faunafri
Europe: Drainages of the Baltic Sea (Odra, Vistula, Neman), northern Black Sea (Sava, Drava, Danube [except Tisza, Timis, and Cerna rivers], Prut, Dnieper, Dniester, Don, Kuban, and in rivers of Georgia from Bzyb' in south to Chorokhi in north), Aegean Sea (Vardar), and Caspian Sea (Volga - Sura River) (Ref. 58030). One record in the upper Morava system (Czechia) (Ref. 59043).
اندازه / وزن / سن
بلوغ: Lm ? range ? - ? cm
Max length : 22.2 cm TL جنس نر / بدون خواص جنسي; (Ref. 12283); common length : 18.0 cm TL جنس نر / بدون خواص جنسي; (Ref. 556); بيشينه سن گزارش شده: 7 سال ها (Ref. 12283)
Max length : 22.2 cm TL جنس نر / بدون خواص جنسي; (Ref. 12283); common length : 18.0 cm TL جنس نر / بدون خواص جنسي; (Ref. 556); بيشينه سن گزارش شده: 7 سال ها (Ref. 12283)
توصيف مختصر كليدهاي شناسايي | ريخت شناسي | ريخت ستجي بوسيله انداره گيري
خارهاي باله پشتي (کل) : 0; شعاع نرم باله پشتي (کل) : 0; خارهاي باله مخرجي: 0; شعاع نرم باله مخرجي: 0. Adults: 12.0-22.2 cm TL. Body wet weight of 37 individuals 13.1-19.5 cm TL, 3.61-12.69 g. Body proportions, as percentage of TL (based on 39 specimens measuring 12.3-19.5 cm TL): prebranchial length, 6.9-12.1; branchial length, 8.5-12.3; trunk length, 44.9-54.4; tail length, 24.3-31.3; cloacal slit length, 0.4-2.2; eye length, 0.7-2.1; disc length, 2.2-5.8; prenostril length, 2.5-6.5; snout length, 2.7-7.6; postocular length, 2.4-3.7. The urogenital papilla length, as a percentage of branchial length, in eight spawning males measuring 14.35-18.4 cm TL, 25.0-38.6. Trunk myomeres, 60-73. Dentition: Most labial teeth are villiform; supraoral lamina, usually only 2 unicuspid teeth, but in less than 10% of cases, 1-3 small unicuspid teeth may also be found on the bridge; infraoral lamina, 5-10 usually unicuspid teeth, but 1-2 lateralmost teeth may be bicuspid; usually 3 endolaterals on each side (83%), but 4 (11%), 1 (4%), and 2 (2%) also found; endolateral formula, typically 1-2-2 (26%), 1-2-1 (22%), 2-2-1 (13%), 2-2-2 (11%), but also 1-1-1, 2-2-3, 1-1-2-2 (each 6%), 2, 1-1-2-1 (each 4%), 1-2, 1-2-2-2 (each 2%) - Naseka et al. (2009) reported the following additional formulae from the syntypic series, including a count of 5 endolaterals: 1-1-2, 1-3-1, 2-1-1, 2-3-2, 1-2-2-1, 2-1-2-2, 1-1-2-1-1; 2-5 rows of anterials; first row of anterials, 5-10 unicuspid teeth, exceptionally, one lateralmost tooth may be bicuspid; 1-4 rows of exolaterals; rows of posterials, 0-3 (absent in 10% of individuals only); first row of posterials, either complete (continuous) with 12-20 unicuspid teeth (62% of individuals) or incomplete (discontinuous) with 1-12 unicuspid teeth (38% of individuals) or entirely absent (very rarely) - Naseka et al. (2009) reported the following additional counts from the syntypic series: complete row with 10 unicuspid and 1 bicuspid teeth; incomplete row with 13-17 unicuspid teeth and with 4 unicuspid and one bicuspid teeth; transverse lingual lamina, 3-7 unicuspid teeth, the median one enlarged (in 79% of individuals, the median cusp is both higher and wider, while in 21% of individuals it is wider, but not noticeably higher, than the flanking cusps); longitudinal lingual laminae each with 5-11 unicuspid teeth. Velar tentacles, 7-12, with tubercles. No dark blotch near the apex of the second dorsal fin. Lateral line neuromasts unpigmented or darkly pigmented, at least on the ventral aspect. Extent of caudal fin pigmentation (- = absence to trace; + = 1% to under 25%; ++ = 25% to under 75%; +++ = 75% or more): - (7%), + (3%), ++ (13%), +++ (77%). Caudal fin shape, spade-like (97% of individuals), rarely rounded. Oral fimbriae, 88-98 (Ref. 89241). With 62-73 trunk myomeres. The caudal fin is dark grey to black (Ref. 59043).
Body shape (shape guide): eel-like; Cross section: circular.
Body shape (shape guide): eel-like; Cross section: circular.
Adults are found in freshwater; in brooks, rivers, and lakes (Ref. 89241). They inhabit the mountain and foothill zones of watercourses containing clear water with a strong current and gravel-sand substrate. The ammocoetes larvae live in detritus-rich sand-mud substrates in areas of weak current, frequently beneath overhanging banks. Ammocoetes feed on diatoms and detritus; adults don't feed. Metamorphosis occurs in September in Poland and Slovakia and in July in the Ukraine. Ammocoetes used as live bait (Ref. 12283). Adults are preyed upon by Esox lucius (Ref. 89241), the chub (Leuciscus cephalus) and other predators in the period of their spawning (beginning of May to beginning of June). Mature individuals form spawning aggregations (Ref. 59043). Spawning occurs on gravel and sand substrates, also possibly over hard white clay (Ref. 58030), in late April - early May in the Ukraine. Fecundity, 1,950-7,106 eggs/female (Ref. 89241). Adults are nonparasitic. However, rare cases of ectoparasitism have been reported in Jelesná Brook, Slovakia and the Prut River, Ukraine (Ref. 89241).
چرخه زندگی و رفتار جفتگیری بلوغ | تولید مثل | تخم ریزی | تخم ها | باروری | توزاد ( لارو)
Spawning individuals come out in open day light. Males dig a shallow nest in areas with moderate current. Spawners form aggregations. Spawners die afterwards. Ammocoetes last 3.5 to 4.5 years. They metamorphose in September - December (Ref. 59043).
مآخذ اصلی
مراجع خود را بارگذاری کنید | مراجع | هماهنگ كننده | همكاران
Holcík, J. and C.B. Renaud, 1986. Eudontomyzon mariae (Berg, 1931). p. 165-185. In J. Holcík (ed.) The Freshwater fishes of Europe. Vol.1, Part I, Petromyzontiformes. (Ref. 12283)
وضعيت در فهرست قرمز IUCN (Ref. 130435: Version 2025-2 (Global))
حداقل نگرانی (LC) ; Date assessed: 03 February 2023
CITES
Not Evaluated
خطر برای انسان ها
Harmless
استفاده انسانی
ماهي گيري – شيلات: از بی علاقه گی; طعمه: usually
FAO - Publication: search | FishSource |
اطلاعات بيشتر
پویایی جمعیت
پارامترهای رشد
حداکثر سن/اندازه
نسبت طول-وزن.
طول-طول نسبی.
نوسانات طولی
تبدیل انبوه
بازسازی
فراواني
پارامترهای رشد
حداکثر سن/اندازه
نسبت طول-وزن.
طول-طول نسبی.
نوسانات طولی
تبدیل انبوه
بازسازی
فراواني
چرخه زندگی
تولید مثل
بلوغ
بلوغ/آبششها
باروری
تخم ریزی
تجمعات تخمریزی
تخم ها
نمو تخم
توزاد ( لارو)
پويايي لاروي
تولید مثل
بلوغ
بلوغ/آبششها
باروری
تخم ریزی
تجمعات تخمریزی
تخم ها
نمو تخم
توزاد ( لارو)
پويايي لاروي
آناتومی
منطقه آبششي
مغز
اتولیت
منطقه آبششي
مغز
اتولیت
فیزیولوژی
ترکیب بدن
مواد مغذی
مصرف اکسیژن
نوع شنا
سرعت شنا
رنگدانههای بصری
صدای ماهی
بیماریها و انگلها
سمیت (LC50s)
ترکیب بدن
مواد مغذی
مصرف اکسیژن
نوع شنا
سرعت شنا
رنگدانههای بصری
صدای ماهی
بیماریها و انگلها
سمیت (LC50s)
ابزارها
کتاب الکترونیکی | راهنماي صحرايي | كليدهاي شناسايي | امكان نرم افزاري بسامد طولي | ابزار تاريخ زيستي | نقشه نقطه ای |
گرفتن-MSY |
گزارش های ويژه
راجع به نگهداری آکواريم ملاحظه کنيد | برگه اطلاعات و مشخصات گونه ها را ملاحظه کنيد | برگه اطلاعات و مشخصات آبزی پروری را ببينيد
بارگيری XML
منابع اينترنتي
AFORO (otoliths) | Aquatic Commons | BHL | Cloffa | Websites from users | فيش واچر را ببينيد | CISTI | Catalog of Fishes: جنس, گونه ها | DiscoverLife | ECOTOX | FAO - Publication: search | Faunafri | Fishipedia | Fishtrace | GloBI | Google Books | Google Scholar | Google | IGFA World Record | پايگاه هاي داده ها | OneZoom | Open Tree of Life | Otolith Atlas of Taiwan Fishes | PubMed | Reef Life Survey | Socotra Atlas | TreeBase | Tree of Life | Wikipedia: برو, جستجو | World Records Freshwater Fishing | سوابق جانورشناسی
تخمینها بر اساس مدلها
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شاخص تنوع فیلوژنتیکی (مرجع 82804) |
PD50 = 0.5312 [Uniqueness, from 0.5 = low to 2.0 = high]. |
| Bayesian length-weight | a=0.00129 (0.00059 - 0.00283), b=2.98 (2.79 - 3.17), in cm total length, based on LWR estimates for this (Sub)family-body shape (Ref. 93245). |
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سطح تروفیک (مرجع 69278) |
3.7 ±0.6 se; based on size and trophs of closest relatives |
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جهندگی (مرجع 120179) |
پايين ، كم, كمينه زمان لازم براي دو برابر شدن جمعيت 5/4 – 14 سال (Semelparous species, assuming tm (= tmax) > 4). |
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آسیبپذیری ماهیگیری (Ref. 59153) |
Low to moderate vulnerability (31 of 100). 🛈 |