Cyphocharax aninha Wosiacki & Miranda, 2014
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drawing shows typical species in Curimatidae.
Google image
drawing shows typical species in Curimatidae.
Klassificering / Namn Populärnamn | synonymer | Catalog of Fishes(Släkte, Arter) | ITIS | CoL | WoRMS | Cloffa
> Characiformes (Characins) > Curimatidae (Toothless characins)
Etymology: Cyphocharax: Greek, kyphos = curved, humpback + Greek, charax = a marine fish without identification (Ref. 45335); aninha: The specific name refers to the nickname of Ana Prudente (MPEG), wife of the first authors and pays tribute to her contributions towards the understanding of the Neotropical fauna, specifically the systematics of snakes.
Etymology: Cyphocharax: Greek, kyphos = curved, humpback + Greek, charax = a marine fish without identification (Ref. 45335); aninha: The specific name refers to the nickname of Ana Prudente (MPEG), wife of the first authors and pays tribute to her contributions towards the understanding of the Neotropical fauna, specifically the systematics of snakes.
Miljö: miljö / Klimatzon / djupintervall / distributionsområde Ekologi
; sötvatten bentopelagisk. Tropical
Utbredning Territorier | FAO områden | Ekosystem | Förekomster | Prickkarta | Utplanteringar | Faunafri
South America: Rio Mopeco, a left tributary of the Rio Parui in Pará, Brazil.
Storlek / Vikt / Ålder
Kort beskrivning Bestämningsnycklar | Morfologi | Morfometri
Mjukstrålar i ryggfenan (totalt) : 11 - 12; Mjukstrålar i analfenan: 9 - 10; Ryggkotor: 29 - 30. Cyphocharax aninha is distinguished from its congeners with the exception of C. vexillapinnus, C. gangamon, C. signatus, and C. punctatus, by the absence of or having extremely reduce infraorbital sensory canal, when present, in largest specimens (30.0 mm SL), to a fleshy or osseous canal in the fifth infraorbital (vs. canal always present and complete). It further differs from its congeners (except C. saladensis, C. vexillapinnus, C. signatus, C. punctatus, and juveniles of C. gangamon) by the possession of four to nine, modally seven, pored scales on lateral line (vs. more than ten). It can be further distinguished from its congeners, except C. santacatarinae, by having a large, ellipsoid, vertically oriented spot almost forming a bar at the rear of the caudal peduncle and over the base of the caudal-fin rays (vs. absence of a spot in C. abramoides, C. aspilos, C. derhami, C. festivus, C. leucostictus, C. magdalenae, C. microcephalus, C. multilineatus, C. nagelii, C. nigripinnis, C. notatus, C. platanus, C. pinnileps, C. plumbeus, C. stilboleps, C. vexillapinnus, or circular or lozenge-shaped, horizontally oriented, spot typically concentrated on the center of the caudal peduncle and not reaching the dorsal and ventral margins of the peduncle in C. biocellatus, C. gangamon, C. gilbert, C. gillii, C. gouldingi, C. helleri, . laticlavius, C. meniscaprorus, C. mestomyllon, C. modestus, C. oenas, C. pantostictos, C. punctatus, C. signatus, C. spilotus, C. piluropisis, C. spilurus, C. vanderi, and C. voga). It is also distinguished from C. helleri, C. laticlavius, C. multilineatus, and C. pantostictos by the absence of series of longitudinal dark continuous or discontinuous lines on the body (vs. presence of such pigmentation). It is can be separated from C. notatus and . vexillapinnus by the absence of a spot on the dorsal fin (vs. presence); and from C. biocellatus, C. punctatus, C. vanderi, and C. voga by the absence of circular or ellipsoid spots on the flanks (vs. presence). It can be diagnosed from its congeners, except C. signatus, in having 10-12, rarely 13 or 14 branched pectoral-fin rays (vs. 13 -17). It can be further distinguished from C. signatus by the tip of last branched ray of anal fin not reaching the base of the caudal-fin rays (vs. reaching). It further differs from C. saladensis by the caudal-peduncle height 10.4-14.4% SL (vs. 15.0-17.0)% SL), and the interorbital width 33.1-43.8% HL (vs. 44.0-50.0)% HL); from C. spilotus by the distance from snout to anus 67.2-77.7% CP (vs. 78.0-82.0% CP); from C. santacatarinae in the orbital diameter 32.2-43.3% HL (vs. 26.0-30.0% HL) and by having 30 or 31 total vertebrae (vs. 32-34); and from C. pinnilepis by having 9 or 10 middorsal scales from the supraoccipital process to the dorsal-fin origin (vs. 11-13) (Ref. 94769).
Body shape (shape guide): elongated.
Body shape (shape guide): elongated.
Livscykel och parningsbeteende Könsmognad | Reproduktion | Lek | Ägg | Fekunditet | Larver
Huvudreferens
Ladda upp dina referenser | referenser | Koordinator : Vari, Richard P. | Medarbetare
Wosiacki, W.B. and D.P. da Silva Miranda, 2013. Description of a new small species of the genus Cyphocharax (Characiformes: Curimatidae) from the Lower Amazon basin. Copeia 2013(4):627-633. (Ref. 94769)
Status på IUCN:s rödlista (Ref. 130435: Version 2025-2 (Global))
Least Concern (LC) ; Date assessed: 15 June 2020
CITES
Not Evaluated
Hot mot människor
Harmless
Mänskliga användningsområden
FAO - Publication: search | FishSource |
Ytterligare information
Trofisk ekologi
Livsmedelsartiklar (preys)
Födosammansättning
Födointag
Matransoner
Predatorer
Livsmedelsartiklar (preys)
Födosammansättning
Födointag
Matransoner
Predatorer
Populationsdynamik
Tillväxtparametrar
Max. åldrar / storlekar
Längd-vikt rel.
Längd-längd rel.
Längd-frekvenser
Massakonvertering
Rekrytering
Abundans
Tillväxtparametrar
Max. åldrar / storlekar
Längd-vikt rel.
Längd-längd rel.
Längd-frekvenser
Massakonvertering
Rekrytering
Abundans
Livscykel
Reproduktion
Könsmognad
Mognad/Gills rel.
Fekunditet
Lek
Lekande aggregat
Ägg
Utveckling av ägg
Larver
Larvdynamik
Reproduktion
Könsmognad
Mognad/Gills rel.
Fekunditet
Lek
Lekande aggregat
Ägg
Utveckling av ägg
Larver
Larvdynamik
Anatomi
Gälyta
Hjärna
Otolit
Gälyta
Hjärna
Otolit
Fysiologi
Kroppssammansättning
Näringsämnen
Syreförbrukning
Typ av simning
Simhastighet
Visuella pigment
Ljud från fisk
Sjukdomar & Parasiter
Toxicitet (LC50)
Kroppssammansättning
Näringsämnen
Syreförbrukning
Typ av simning
Simhastighet
Visuella pigment
Ljud från fisk
Sjukdomar & Parasiter
Toxicitet (LC50)
Genetik
Genom
Genetik
Heterozygositet
Ärftlighet
Genetisk mångfald
Genom
Genetik
Heterozygositet
Ärftlighet
Genetisk mångfald
Människorelaterad
Vattenbrukssystem
Vattenbruksprofiler
Avelslinjer
Ciguatera-fall
Frimärken, mynt, diverse.
Vattenbrukssystem
Vattenbruksprofiler
Avelslinjer
Ciguatera-fall
Frimärken, mynt, diverse.
Verktyg
Särskilda rapporter
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Internet-källor
AFORO (otoliths) | Aquatic Commons | BHL | Cloffa | Websites from users | Check FishWatcher | CISTI | Catalog of Fishes: Släkte, Arter | 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: Go, sök | World Records Freshwater Fishing | Zoobank | Zoologiskt register
Uppskattningar baserade på modeller
|
Index för fylogenetisk mångfald (Ref. 82804) |
PD50 = 0.5000 [Uniqueness, from 0.5 = low to 2.0 = high]. |
| Bayesian length-weight | a=0.01413 (0.00618 - 0.03226), b=3.03 (2.86 - 3.20), in cm total length, based on LWR estimates for this Genus-body shape (Ref. 93245). |
| 0 | |
|
Resiliens (Ref. 120179) |
Hög, lägsta populationsfördubblingstid mindre än 15 månader (Preliminary K or Fecundity.). |
|
Sårbarhet i fisket (Ref. 59153) |
Low vulnerability (10 of 100). 🛈 |