Labeobarbus nzadimalawu

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Labeobarbus nzadimalawu Vreven, Musschoot, Decru, Wamuini Lunkayilakio, Obiero, Cerwenka & Schliewen, 2018

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Image of Labeobarbus nzadimalawu
No image available for this species;
drawing shows typical species in Cyprinidae.

klasifikasi / Nama Nama-nama umum | Sinonim (persamaan) | Catalog of Fishes(Marga, Jenis) | ITIS | CoL | WoRMS | Cloffa

> Cypriniformes (Carps) > Cyprinidae (Minnows or carps) > Torinae
Etymology: nzadimalawu: Before the Christian missionaries arrived, the Inkisi River was locally referred to as the 'Nzadi malawu' in Kikongo (Kintandu/Kindibu dialects), which means 'the river that brings good luck; the part of the river towards the northern border of Angola still bears this name; species name referring to this ancient name of the river basin to which it seems endemic; a noun in apposition, making its gender ending unchangeable (Ref. 127934).

Lingkungan: lingkungan / zona iklim / kisaran kedalaman / jangkauan distribusi Ekologi

; air tawar bentopelagis. Tropical

Penyebaran Wilayah | Daerah-daerah FAO | Ekosistem | Kemunculan | peta titik | Introduksi | Faunafri

Africa: Inkisi River, Lower Congo River basin above the Zongo Falls, in Democratic Republic of the Congo (Ref. 127934).

Ukuran / Berat / umur

Kematangan: Lm ?  range ? - ? cm
Max length : 21.3 cm SL jantan/; (Ref. 127934)

deskripsi pendek Kunci identifiaksi (pengenalan) | Morfologi | Morfometrik

Duri punggung (Keseluruhan (total)) : 0; duri punggung lunak (Keseluruhan (total)) : 13 - 15; Duri dubur: 0; Sirip dubur lunak: 9; vertebrata, bertulang belakang: 36 - 38. Diagnosis: Within the Congo basin Labeobarbus nzadimalawu can be distinguished from L. altipinnis, L. ansorgii, L. batesii, L. brauni, L. cardozoi, L. caudovittatus, L. dartevellei, L. fasolt, L. habereri, L. humphri, L. iphthimostoma, L. iturii, L. jubbi, L. longidorsalis, L. longifilis, L. lufupensis, L. macroceps, L. macrolepidotus, L. macrolepis, L. mawambi, L. mawambiensis, L. mirabilis, L. nanningsi, L. oxyrhynchus, L. paucisquamatus, L. stappersii, L. trachypterus, L. upembensis and L. wittei by its high number of lateral line scales, 35-41 vs. les than 34; from L. leleupanus by its low number of lateral line scales, 35-41 vs. 45-47; from L. tropidolepis and L. platyrhinus by its low number of scales between the lateral line and the dorsal and ventral midline, 4.5-6.5 and 5.5-6.5 vs. 7.5-8.5 and 7.5-9.5 in L. tropidolepis and 6.5-7.5 and 6.5-8.5 in L. platyrhinus, and from the latter by its low number of circumpeduncular scales as well, 12-16 vs. 16-18; from L. robertsi by the absence of papillae on the anterior edge of the lower jaw vs. with numerous well identifiable papillae; from L. pellegrini by the presence of two pair of well-developed barbels vs. a single pair of minute posterior barbels in L. pellegrini; from L. progenys by its non-prognathous lower jaw vs. prognathous; from L. altianalis and L. gestetneri by the last unbranched dorsal-fin ray not being transformed into a well-developed spine, but instead being clearly segmented for about half of its length, 42.8-57.7% of dorsal-fin height, vs. transformed into a spine, clearly segmented only at its most distal end, less than 30.0% of dorsal-fin height; and from L. somereni, by its high total number of gill rakers on the first gill arch, 18-22 vs. 11, and a, positively allometric, narrow mouth width, 16.1-26.5% of head length vs. 31.3% (Ref. 127934). Further, L. nzadimalawu can be distinguished from both the other members of the Inkisi complex, L. ndazinkisi and the intermediate/hybrid specimens by the presence of a free mental lobe, vs. no mental lobe but instead a cornified Varicorhinus real cutting edge on the outer edge of the lower jaw in L. nzadinkisi and no or only a rudimentary or attached mental lobe in hybrid specimens; in addition, L. nzadimalawu can be distinguished from L. nzadinkisi by its narrow mouth width, 16.1-26.5% of head length vs. 26.8-50.5%, long head length, 23.0-26.4% of standard length vs. 20.1-22.1%; short dorsal-fin base length, 12.1-16.0% of standard length vs. 14.4-17.9%; and long prepectoral distance, 22.6-26.0% of standard length vs. 20.0-22.1%; finally, L. nzadimalawu can be distinguished from Acapoeta tanganicae by its low number of lateral line scales, 35-41 vs. 57-67 (Ref. 127934). Within the adjacent Lower Guinea ichthyofaunal province L. nzadimalawu can be distinguished from L. axelrodi, L. batesii, L. brevispinis, L. cardozoi, L. caudovittatus, L. compiniei, L. habereri, L. fimbriatus, L. jaegeri, L. malacanthus, L. mariae, L. mbami, L. micronema, L. mungoensis, L. roylii, L. sandersi, L. semireticulatus, L. steindachneri, L. tornieri, L. versluysii and L. werneri by its higher number of lateral line scales, 35-41 vs. less than 34; from L. aspius, L. lucius and L. progenys by its non-prognathous lower jaw vs. lower jaw clearly prognathous; and from L. rocadasi by its last unbranched dorsal-fin ray not being transformed into a well-developed spine, but instead being clearly segmented over approximately half its length, 42.8-57.7% of dorsal-fin height vs. last unbranched dorsal-fin ray transformed into a spine, clearly segmented only at its most distal end; finally, L. ndazimalawu can be distinguished from Sanagia velifera by its high number of lateral line scales, 35-41 vs. 22-24 (Ref. 127934). Within the adjacent Quanza ichthyofaunal province, L. nzadimalawu can be distinguished from L. ansorgii, L. gulielmi, L. jubbi, L. nanningsi, L. rhinopterus, L. rosae and L. roylii by its high number of lateral line scales, 35-41 vs. less than 34; from L. clarkeae, L. ensifer and L. varicostoma by the absence of papillae on the anterior edge of the lower jaw vs. with well identifiable papillae; from L. lucius and L. progenys by its non-prognathous lower jaw vs. lower jaw clearly prognathous; and from L. boulengeri, L. ensis, L. girardi, L. steindachneri, L. stenostoma and L. rocadasi by its last unbranched dorsal-fin ray not being transformed into a well-developed spine, but instead being clearly segmented over approximately half its length, 42.8-57.7% of dorsal-fin height vs. last unbranched dorsal-fin ray transformed into a spine, clearly segmented only at its most distal end (Ref. 127934).


Biologi     Daftar kata (contoh epibenthic)

Siklus hidup dan perilaku kawin Kematangan | Reproduksi, perkembang biakan | Pemijahan | telur-telur | Fekunditas | Larva

rujukan utama Unggah referensi Anda | Acuan | Koordinator | mitra

Vreven, E.J.W.M.N., T. Musschoot, E. Decru, S. Wamuini Lunkayilakio, K. Obiero, A.F. Cerwenka and U.K. Schliewen, 2018. The complex origins of mouth polymorphism in the Labeobarbus (Cypriniformes: Cyprinidae) of the Inkisi River basin (Lower Congo, DRC, Africa): insights from an integrative approach. Zool. J. Linn. Soc. 186:414-482. (Ref. 127934)

Status IUCN Red List (Ref. 130435: Version 2025-2 (Global))


CITES

Not Evaluated

CMS (Ref. 116361)

Not Evaluated

ancaman kepada manusia

  Harmless





penggunaan manusia

Perikanan: tidak ada kepentingan
FAO - Publication: search | FishSource |

informasi lanjut

Ekologi trofik
Item makanan (mangsa)
Komposisi makanan
Konsumsi makanan
Ransum makanan
Pemangsa
Ekologi
Ekologi
Dinamika populasi
Parameter pertumbuhan
Maks. usia / ukuran
Panjang-berat rel.
Panjang-panjang rel.
ukuran frekuensi
Konversi massa
pemulihan
Kelimpahan
Siklus hidup
Reproduksi, perkembang biakan
Kematangan
Kedewasaan / insang rel.
Fekunditas
Pemijahan
Agregasi pemijahan
telur-telur
pekembangan telor
Larva
Dinamika larva
Penyebaran
Wilayah
Daerah-daerah FAO
Ekosistem
Kemunculan
Introduksi
BRUVS - Video
Anatomi
Area insang
Otak
Otolith
Fisiologi
Komposisi tubuh
Nutrisi
Konsumsi oksigen
Jenis renang
Kecepatan berenang
Pigmen visual
Suara ikan
Penyakit & Parasit
Toksisitas (LC50)
Genetika
genom
Genetika
Heterozigositas
Diturunkan
Keanekaragaman Genetik
Yang berhubungan dengan manusia
Sistem akuakultur
profil budidaya air
Strain
Kasus Ciguatera
Perangko, koin, dll.
Penjangkauan
mitra
Taksonomi
Nama-nama umum
Sinonim (persamaan)
Morfologi
Morfometrik
Gambar
Acuan
Acuan

Alat, peralatan

laporan khas

muat turun XML

Sumber internet

AFORO (otoliths) | Aquatic Commons | BHL | Cloffa | Websites from users | semak peneliti ikan | CISTI | Catalog of Fishes: Marga, Jenis | DiscoverLife | ECOTOX | FAO - Publication: search | Faunafri | Fishipedia | Fishtrace | GloBI | Google Books | Google Scholar | Google | IGFA World Record | OneZoom | Open Tree of Life | Otolith Atlas of Taiwan Fishes | PubMed | Reef Life Survey | Socotra Atlas | TreeBase | Tree of Life | Wikipedia: pergi, Cari | World Records Freshwater Fishing | Zoobank | Catatan Zoologi

Estimasi berdasarkan model

Indeks keanekaragaman filogenetik (Acuan 82804):  PD50 = 0.5000   [Uniqueness, from 0.5 = low to 2.0 = high].
Bayesian length-weight: a=0.00468 (0.00218 - 0.01003), b=3.10 (2.90 - 3.30), in cm total length, based on LWR estimates for this (Sub)family-body shape (Ref. 93245).
Tingkat Trofik (Acuan 69278):  3.2   ±0.5 se; based on size and trophs of closest relatives
Daya lenting (Acuan 120179):  sedang, Waktu penggandaan populasi minimum 1.4 - 4.4 tahun (Preliminary K or Fecundity.).
Kerentanan Penangkapan Ikan (Ref. 59153):  Low vulnerability (16 of 100). 🛈