Steindachnerina seriata

Steindachnerina seriata Netto-Ferreira & Vari, 2011

muatnaik fotos/gambar dan video
Gambar | imej Google
Image of Steindachnerina seriata
Steindachnerina seriata
foto/gambar oleh Sabaj Pérez, M.H.

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

> Characiformes (Characins) > Curimatidae (Toothless characins)
Etymology: Steindachnerina: Named after Franz Steindachner, 1876; naturalist, ichthyologist that studied the fauna of Galápagosseriata: Name from Latin 'seriata' meaning arranged in a series; referring to multiple series of narrow dark stripes situated along the scale row margins on the lateral and dorsolateral surface of the body in the species.
Eponymy: Franz Steindachner (1834–1919) was an Austrian zoologist who specialised in herpetology and ichthyology. [...] (Ref. 128868), visit book page.
More on authors: Netto-Ferreira & Vari.

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

; air tawar pelagis, permukaan. Tropical; 7°S - 8°S, 55°W - 56°W

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

South America: known only from two localities that lie relatively close to each other in the Rio Jamanxim, a right bank tributary of the Rio Tapajo´s in the eastern portions of the Amazon basin. Further sampling is necessary in order to determine whether S. seriata has a restricted range as proposed for various groups of Brazilian freshwater fishes by Nogueira et al. (2010). Alternatively, the apparent limited distribution for the species might reflect the undersampling of the Rio Tapajo´s ichthyofauna as evidenced by the recent discovery of S. seriata and S. fasciata in that catchment (Ref. 88964).

Ukuran / Berat / umur

Kematangan: Lm ?  range ? - ? cm
Max length : 8.3 cm SL jantan/; (Ref. 88964)

deskripsi pendek Kunci identifiaksi (pengenalan) | Morfologi | Morfometrik

Steindachnerina seriata is distinguished from all congeners with the exception of S. fasciata by the presence of multiple narrow, dark stripes extending along the lateral and dorsolateral portion of the body. It differs from S. fasciata in the position on the scales of the dark stripes extending along the body (positioned along the areas of contact of proximate horizontal scale rows versus situated along the middle of the scales of each row, respectively), in the pigmentation pattern of the lateral surface of the caudal peduncle (the absence of a horizontally elongate, midlateral, dark stripe on the caudal peduncle versus the presence of such pigmentation, respectively), the distance from the tip of the snout to the origin of the anal fin (79.2–82.7% versus 84.1–88.9% of SL, respectively), the distance from the tip of the snout to the anus (76.2–78.0% versus 78.8–83.9% of SL, respectively), the length of the snout (33.5–34.6% versus 28.9–32.3% of HL, respectively), and the length of the postorbital portion of the head (36.3–38.8% versus 39.7–43.6% of HL, respectively). Steindachnerina seriata can be further distinguished from S. argentea, S. bimaculata, S. binotata, S. conspersa, S. leucisca, and S. notograptos in the form of the fleshy lining of the roof of the oral cavity (the presence of a distinct series of multiple very fleshy folds extending ventrally from the dorsal surface of the oral cavity versus the presence of only three weakly to moderately developed longitudinal folds in that region, respectively), from S. gracilis, S. hypostoma, S. planiventris, and S. quasimodoi in the transverse form of the prepelvic region (obtusely flattened versus distinctly flattened, respectively) and the number of scales across the transversely flattened prepelvic region immediately anterior to the insertion of the pelvic fins (3 or 4 versus 5 or 6 scales, respectively), from S. binotata, S. corumbae, S. dobula, S. hypostoma, S. insculpta, S. leucisca, S. notograptos, and S. varii in the pigmentation of the dorsal fin (the presence of a spot of dark pigmentation on the basal portions of the fin versus the absence of such pigmentation on the fin throughout ontogeny, respectively), from S. amazonica, S. argentea, S. atratoensis, S. biornata, S. brevipinna, S. conspersa, S. dobula, S. elegans, S. fasciata . S. guentheri, S. hypostoma, S. insculpta, S. notonota, and S. varii in the pigmentation pattern along the midlateral portions of the body and caudal fin (the absence of distinct dark pigmentation along the midlateral surface of the body and caudal fin versus the presence of a dark midlateral stripe extending along the lateral line and/or a patch of horizontally elongate dark pigmentation along the caudal peduncle and/or dark pigmentation along the middle caudal-fin rays, respectively) (Ref. 88964).

Biologi     Daftar kata (contoh epibenthic)

Collected in flooded areas along the margin of the river among stands of dense aquatic vegetation (Ref. 88964).

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

rujukan utama Unggah referensi Anda | Acuan | Koordinator : Vari, Richard P. | mitra

Netto-Ferreira, A.L. and R.P. Vari, 2011. New species of Steindachnerina (Characiformes: Curimatidae) from the Rio Tapajós, Brazil, and review of the genus in the Rio Tapajós and Rio Xingu basins. Copeia 2011(4):523-529. (Ref. 88964)

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

  kekurangan data (DD) ; Date assessed: 07 November 2018

CITES

Not Evaluated

CMS (Ref. 116361)

Not Evaluated

ancaman kepada manusia

  Harmless





penggunaan manusia

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=0.01445 (0.00647 - 0.03228), b=3.01 (2.84 - 3.18), in cm total length, based on LWR estimates for this Genus-body shape (Ref. 93245).
0
Kerentanan Penangkapan Ikan
(Ref. 59153)
Low vulnerability (16 of 100). 🛈