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💧 Freshwater 🌡️ Tropical

Emerald green tetra

Hyphessobrycon comodoro Dagosta, Seren, Ferreira & Marinho, 2022
Max Length
3.9 cm
Max Weight
-
Lifespan
-
Trophic Level
2.9
Depth
0–2 m
Climate
Tropical
Resilience
High
Vulnerability
10.00/100
Typical Length
-
Depth Zone
-

📖 Overview

Collection areas are impoundments of tributaries of the rio Mutum formed by the road building, where the water is transparent, with maximum widths ranging 50-60 m and depth 0.3-2 m. The substrate is formed by sand, silt, and organic matter, with the presence of submerged aquatic macrophytes and large amounts of filamentous algae. The only other species collected syntopically was Hoplerythrinus unitaeniatus (Spix & Agassiz, 1829), which is probably a predator of the H. comodoro. The streams that form the lagoons are small, 2-4 m wide and 0.5-2 m deep, with clear rapid waters and a bottom composed of sand and leaf litter. Local vegetation is composed of secondary forest. The other known locality lies at the rio Mutum itself, downstream to the other two and here the new species occurs syntopically with Hyphessobrycon hexastichos and Hasemania nambiquara. The diet was mainly composed of resources autochthonous (91.6% of the volume of food items), mainly vegetable fragments (57.7%) and aquatic insects (32.7%). The vegetable fragments were composed of aquatic macrophyte structures and the aquatic insects were fragments of adults, larvae, and pupae of Diptera and larvae of Trichoptera, and Odonata). Specimens analyzed were collected in a region under moderate anthropogenic pressure, which may influence the diet of fish species. Further, damming streams to road building changes the taxonomic and functional of fish assemblages and limits the longitudinal dispersion. The transformation from lotic to lentic environments, with an increase in the width of the canopy-opening channel, creates pelagic and benthic areas that allow the proliferation of macrophytes and algae. Biological data taken from regions impacted by human action has high scientific value, but in the case of this species, it is crucial that the data also be available from less impacted environments .

Scientific Name
Hyphessobrycon comodoro
Authority
Dagosta, Seren, Ferreira & Marinho, 2022
Habitat
Freshwater
Climate
Tropical
Max Length
3.9 cm
Depth Range
0–2 m
Trophic Level
2.9
Resilience
High
Vulnerability
10.00/100
Salinity
0–0.5 ppt

🐟 Physical Description

This species is distinguished from all its congeners, except Hyphessobrycon cachimbensis, H. cyanotaenia, H. fernandezi, H. melanostichos, H. nigricinctus, H. paucilepis, H. petricolus, H. piranga, H. psittacus, H. scholzei, H. sovichthys, H. stegemanni, H. taphorni, H. tuyensis and H. vilmae by having a well-defined and relatively narrow dark midlateral stripe on body, extending from head to the middle caudal-fin rays (vs. no well-defined longitudinal stripe or stripe wider than the orbit, or stripe starting approximately vertically through the origin of the dorsal fin or stripe blurred posteriorly); differs from the aforementioned species, except H. cachimbensis, H. cyanotaenia, H. melanostichos, H. nigricinctus, H. petricolus, by having a humeral blotch (vs. no humeral blotch absent); differs from H. cachimbensis, H. cyanotaenia by having the distal profile of the anal fin falcate in males (vs. approximately straight or convex) and from H. cachimbensis, H. petricolus, H. nigricinctus by having 13-16 branched anal-fin rays (vs. 17-26); differs further from H. cyanotaenia by lacking concentration of black pigmentation on longest rays of dorsal, pelvic, and anal fins (vs. pigmentation present); differs from H. melanostichos (the most similar congener) by having 11 or 12 horizontal scale rows around caudal peduncle (vs. 14), fewer branched pelvic-fin rays 6 (vs. 7), humeral blotch wider than deep, with pigmentation much more intense than the dark midlateral band, with well-defined edges (vs. humeral blotch deeper than wide, with pigmentation similar to the dark midlateral band, without well-defined edges); differs from H. melanostichos by having 13-15 (mode 14, rarely 16 (only 3 of 30 specimens), branched anal-fin rays (vs. 16–18, mode 16) .Cross section: compressed.

🌀 Behaviour

Behavioural data for Emerald green tetra is currently being reviewed.

🦐 Diet

aquatic invertebrates
small fish
algae
detritus

🥚 Reproduction

🐣 Oviparous
Spawning Season
spring
Spawn Location
Substrate
Fertilization
External

🌍 Habitat & Distribution

Freshwater; benthopelagic; depth range 0 - 2 m . Tropical South America: Brazil.

🌿 Ecology

Zone Preferences
💧 Freshwater
Trophic Level
2.9±0.3

📐 Morphometrics

Length–Weight Relationship: W = 0.00661 × L3.12 (TL)
Max TL
3.9cm

🌡️ Water Parameters & Tolerance

Salinity Range
0–0.5ppt

📊 Population Risk & Fisheries

Population Resilience
High
Minimum doubling time
Fishing Vulnerability
10.00/100
Low vulnerability
Trophic Level
2.9
Omnivore / Planktivore
Climate Zone
Tropical
Described By
Dagosta, Seren, Ferreira & Marinho, 2022

🦠 Common Diseases

The following diseases are known to affect Emerald green tetra.

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