Oxygen consumption remains stable while ammonia excretion is reduced upon short time exposure to high salinity in Macrobrachium acanthurus (Caridae: Palaemonidae), a recent freshwater colonizer

• Published in: Zoologia (Curitiba, Brazil) Brazil), 2017-01, Vol.34, p.1-9
• Main Authors: Arruda Freire, Carolina, Rios, Leonardo de P., Giareta, Eloísa P., Castellano, Giovanna C.
• Format: Article
• Language: English
• Subjects: Aeration; Ammonia; Animal behavior; Aquaria; Aquariums; Aquatic habitats; Brackish water; Catabolism; Cell size; Coastal ecology; Coastal zone; Containers; Crustaceans; Decapoda; Dissolved oxygen; Drinking water; Euryhalinity; Excretion; Experiments; Exposure; Freshwater; Freshwater environments; Habitats; Hemolymph; Inland water environment; lactate; Lactic acid; Macrobrachium acanthurus; Marine biology; Marine fishes; Metabolism; Moisture content; Muscles; osmoregulation; Oxygen; Oxygen consumption; palaemonidae; Perfusion; pH effects; Physiology; Proteins; Salinity; Salinity effects; Salts; Shellfish; Shrimps; Shutdowns; Tissue; Tropical climate; Uptake; Ventilation; Water content; ZOOLOGY
• ISSN: 1984-4689; 1984-4670; 1984-4689
• DOI: 10.3897/zoologia.34.e20173

Palaemonid shrimps occur in the tropical and temperate regions of South America and the Indo-Pacific, in brackish/freshwater habitats, and marine coastal areas. They form a clade that recently (i.e., ~30 mya) invaded freshwater, and one included genus, Macrobrachium Bate, 1868, is especially successful in limnic habitats. Adult Macrobrachium acanthurus (Wiegmann, 1836) dwell in coastal freshwaters, have diadromous habit, and need brackish water to develop. Thus, they are widely recognized as euryhaline. Here we test how this species responds to a short-term exposure to increased salinity. We hypothesized that abrupt exposure to high salinity would result in reduced gill ventilation/perfusion and decreased oxygen consumption. Shrimps were subjected to control (0 psu) and experimental salinities (10, 20, 30 psu), for four and eight hours (n = 8 in each group). The water in the experimental containers was saturated with oxygen before the beginning of the experiment; aeration was interrupted before placing the shrimp in the experimental container. Dissolved oxygen (DO), ammonia concentration, and pH were measured from the aquaria water, at the start and end of each experiment. After exposure, the shrimp’s hemolymph was sampled for lactate and osmolality assays. Muscle tissue was sampled for hydration content (Muscle Water Content, MWC). Oxygen consumption was not reduced and hemolymph lactate did not increase with increased salinity. The pH of the water decreased with time, under all conditions. Ammonia excretion decreased with increased salinity. Hemolymph osmolality and MWC remained stable at 10 and 20 psu, but osmolality increased (~50%) and MWC decreased (~4%) at 30 psu. The expected reduction in oxygen consumption was not observed. This shrimp is able to tolerate significant changes in water salt concentrations for a few hours by keeping its metabolism in aerobic mode, and putatively shutting down branchial salt uptake to avoid massive salt load, thus remaining strongly hyposmotic. Aerobic metabolism may be involved in the maintainance of cell volume, concomitant with reduced protein/aminoacid catabolism upon increase in salinity. More studies should be conducted to broaden our knowledge on palaemonid hyporegulation.