Microcosm analysis of salinity effects on coastal lagoon plankton assemblages

A microcosm experiment was conducted to assess the effects of salinity on coastal lagoon plankton assemblages. Five salinity levels were replicated four-fold in 3801 fiberglass tanks. Salinity levels used were 0, 8.5, 17, 34 and 51 ppt, or 0, 25, 50, 100 and 150 percent seawater. These were achieved by mixing concentrated lagoon water and tapwater in different proportions. Tanks were inoculated with plankton collected from San Dieguito Lagoon (Del Mar, San Diego County, California) and other fresh and saline waterbodies in the area. Selected physical-chemical variables, phytoplankton, zooplankton, and other invertebrate populations were monitored on five sampling dates over a 114 day period (13 August–5 December 1986).Total phytoplankton abundance increased with salinity, for salinities >17 ppt. Most taxa showed marked effects of salinity, though the pattern of the effects often varied greatly from date to date. Chlorophytes tended to be most abundant at 51 ppt. Pyrrhophytes were most abundant at 0 or 51 ppt, and least abundant at 8.5 or 17 ppt. Cryptophytes increased with increasing salinity. Euglenophytes exhibited no salinity effect on any date. Bacillariophytes were most abundant at 8.5–34 ppt and least abundant at 51 ppt, with individual taxa showing maxima at 0–17 ppt (Navicula, Synedra), 8.5–34 ppt (Surirella, Amphora), and 34 ppt (Cylindrotheca).Total zooplankton abundance decreased with salinity, for salinities > 17 ppt. The dominant taxa were protozoans, rotifers, cladocerans, and copepods, and all but the first group showed strong salinity effects. Protozoan abundance was unaffected by salinity. Rotifers were most abundant at 0 ppt (Keratella, Filinia) or 8.5 ppt (Brachionus). With few exceptions, cladocerans (Alona, Ceriodaphnia, Scapholeberis) were found only at 0 ppt. Abundance of calanoid copepods decreased with increasing salinity, with individual taxa showing maxima at 0 ppt (Diaptomus), 8.5–17 ppt (Pseudodiaptomus, Eurytemora), and 34 ppt (Acartia). Cyclopoid copepods were most abundant at 17 ppt, with individual taxa showing maxima at 0 ppt (Eucyclops), 8.5 ppt (Halicyclops), and 17 ppt (Oithona). Harpacticoid copepods (Cletocamptus, Tachidius) were most abundant at 17–34 ppt. Ostracods and mosquito (Culex) larvae were most abundant at 8.5 ppt and absent at 34 and 51 ppt. Polychaetes generally were most abundant at 17–34 ppt, and water boatmen (Trichocorixa) at 8.5–34 ppt. Various physical and chemical variables also showed significant variations with salinity. Tending to increase with salinity were temperature, ammonia and orthophosphate concentrations. Decreasing with salinity were pH, dissolved oxygen and silica concentrations. The causes and interrelationships of these salinity effects are discussed.     

The influence of pre‐settlement and early post‐settlement processes on the adult distribution and relative dominance of two invasive mussel species

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The Reaction of Mytilus trossulus Larvae (Bivalvia,Mytilidae) to Desalination and Increase of Water Column Temperature

Under homogeneous salinity and temperature conditions and uniform daylight, the early larvae of the Pacific mussel Mytilus trossulus (blastulae and trochophores) accumulated in the uppermost layer of water column, while the late larvae tend to concentrate at the bottom. In a water column with a temperature or salinity gradient, the early larvae accumulated at the surface even when the salinity and temperature conditions were incompatible with their life activity. The distribution of the late larvae was different as they were able to leave water of unfavorable temperature and salinity and accumulate at the bottom.     

Effects of increases in salinity on phytoplankton in the Broadwater of the Myall Lakes, NSW, Australia

The Broadwater of the Myall Lakes system is highly susceptible to cyanobacterial bloom formation after heavy rain events. During prolonged low flow periods, saline intrusion from the lower Myall River increases salinity levels and effectively controls some bloom forming algal taxa. To assess the effect of low-to-moderate increases in salinity (up to 4 ppt) on phytoplankton chlorophyll a, cell abundance, diversity and assemblage structure, salinity enhancement experiments were conducted on Broadwater samples collected in June 2005 (salinity 1.5 ppt), October 2005 (4 ppt) and January 2006 (12 ppt). Natural phytoplankton assemblages were incubated in the laboratory for 10 days, under different treatments of salinity (no addition, +2 ppt, + 4 ppt) and nutrient conditions (no addition, excess N+P). The greatest impact of salinity enhancement in N+P enriched samples was observed in June (1.5–5.5 ppt); chlorophyll a was significantly reduced in samples with the highest salinity treatment, and the taxon most negatively affected by an elevation in salinity to 5.5 ppt was Anabaena circinalis. Taxonomic richness and diversity (Shannon–Wiener index) were unexpectedly significantly higher at 5.5 ppt than at 1.5 ppt. This result, in part, explains the observed significant differences in phytoplankton assemblage structure over this salinity range. In October, the main effect of elevating salinity levels from 4 ppt to 8 ppt was a reduction in the abundance of chlorophytes, particularly Scenedesmus. Phytoplankton samples that were collected when the lake salinity level was 12 ppt were little affected by salinity increases of 2 ppt and 4 ppt, most likely because field samples were already relatively high in salt content. We suggest that further investigations focus on phytoplankton responses to salinity under a range of nutrient regimes that are common to coastal lakes.     

Tolerance of Pinus taeda and Pinus serotina to low salinity and flooding: Implications for equilibrium vegetation dynamics

Questions: 1. Do pine seedlings in estuarine environments display discrete or continuous ranges of physiological tolerance to flooding and salinity? 2. What is the tolerance of Pinus taeda and P. serotina to low salinity and varying hydrologic conditions? 3. Are the assumptions for ecological equilibrium met for modeling plant community migration in response to sea‐level rise? Location: Albemarle Peninsula, North Carolina, USA. Methods: In situ observations were made to quantify natural pine regeneration and grass cover along a salinity stress gradient (from marsh, dying or dead forest, to healthy forest). A full‐factorial greenhouse experiment was set up to investigate mortality and carbon allocation of Pinus taeda and P. serotina to low‐salinity conditions and two hydrology treatments over 6 months. Treatments consisted of freshwater and two salinity levels (4 ppt and 8 ppt) under either permanently flooded or periodically flushed hydrologic conditions. Results: Natural pine regeneration was common (5–12 seedlings per m²) in moderate to well‐drained soils where salinity concentrations were below ca. 3.5 ppt. Pine regeneration was generally absent in flooded soils, and cumulative mortality was 100% for 4 and 8 ppt salinity levels under flooded conditions in the greenhouse study. Under weekly flushing conditions, mortality was not significantly different between 0 and 4 ppt, confirming field observations. Biomass accumulation was higher for P. taeda, but for both pine species, the root to shoot ratio was suppressed under the 8 ppt drained treatment, reflecting increased below‐ground stress. Conclusions: While Pinus taeda and P. serotina are commonly found in estuarine ecosystems, these species display a range of physiological tolerance to low‐salinity conditions. Our results suggest that the rate of forest migration may lag relative to gradual sea‐level rise and concomitant alterations in hydrology and salinity. Current bioclimate or landscape simulation models assume discrete thresholds in the range of plant tolerance to stress, especially in coastal environments, and consequently, they may overestimate the rate, extent, and timing of plant community response to sea‐level rise.     

Effects of salinity on growth and survival of African sharptooth catfish (clarias gariepinus) larvae

Growth and survival of replicate batches of African sharptooth catfish (Clarias gariepinus) larvae were monitored in 0, 2.5, 5.0, 7.5 and 10 ppt salinity. No significant differences in mortality or growth rate were evident between 0 and 5 ppt salinity. At 7.5 ppt mortality rate was higher and larval growth rate declined in comparison to the lower salinities. At 10 ppt all larvae died within 48 hours. The condition factor of the larvae similar between 0–2.5 ppt and displayed a declining trend between 2.5–7.5 ppt. Osmoconcentratkm of blood plasma of C. gariepinus in fresh water was 280 ± 20 mOsm/kg which is equivalent to 9.5 ppt salinity. It was concluded that 0–2.5 ppt is the optimal sclinity range for larval rearing and that short-term exposure to higher salinities (2.5–7.5 ppt) could be effective in the treatment of ectoparasitic diseases.     

Tissue Distribution, Effects of Salinity Acclimation, and Ontogeny of Aquaporin 3 in the Marine Teleost, Silver Sea Bream (Sparus sarba)

The purpose of the present study was to ascertain the tissue-specific expression of the water channel protein, aquaporin 3 (AQP3), during salinity acclimation and larval development of silver sea bream (Sparus sarba). A cDNA fragment encoding aquaporin 3 (aqp3) from silver sea bream gill was cloned and from the deduced amino acid sequence a polyclonal antibody was prepared. AQP3 was found to be present in gill, kidney, liver, brain, heart, and spleen but not in whole blood. The abundance of AQP3 was significantly highest in gills of hypoosmotic (6 ppt) and isoosmotic (12 ppt) acclimated sea bream when compared to seawater (33 ppt) and hypersaline (50 ppt)- acclimated sea bream. Spleen tissue also displayed significantly high levels of AQP3 protein in hypoosmotic and isoosmotic salinities whereas the AQP3 abundance in brain, liver, heart, and kidney remained unchanged across the range of salinities tested. The ontogenetic profile of AQP3 was also investigated from developing sea bream larvae and AQP3 was first detected at 14 days posthatch (dph) and increased steadily up to 28–46 dph. In conclusion, this study has demonstrated that AQP3 expression is modulated in gill and spleen tissue of salinity acclimated sea bream and that it can be detected relatively early during larval development.     

A starvation test to determine optimal salinities for larval freshwater prawns,Macrobrachium rosenbergii

• 1.1. A starvation test was conducted in small beakers with stage 1 (S1) and stage 2 (S2) Macrobrachium rosenbergii larvae to determine optimal salinities.
• 2.2. Experiments were first performed with S2 larvae at 13 ppt to identify a suitable medium made with artificial sea salts.
• 3.3. A broad-range (0–35 ppt) and a subsequent narrow-range (9–16 ppt) salinity experiment with S2 larvae were used to identify 13 ppt as the optimal salinity, with 12 ppt as the next best; this agrees well with most previous estimates of optimal salinities for rearing larvae.
• 4.4. S1 larvae were also tested in a narrow-range salinity experiment but were not used further because, unlike starved S2 larvae, they molted during the experiment.
• 5.5. Identification of the optimal salinity was not affected by 50% daily water exchange or by bright light.
• 6.6. Exposure of larvae to three different salinities—7, 13 and 19 ppt—during S1 influenced the width of the optimal salinity range for S2 larvae.

     

Salinity tolerance of stable fly (Diptera: Muscidae)

Effects of salinity on the survival, growth, and development of stable fly, Stomoxys calcitrans (L.), were investigated in the laboratory. Larvae failed to develop to pupation when reared in media containing a salinity of 40 parts per thousand (ppt) sodium chloride (NaCl). Maximum salinity supporting larval development equaled the salinity of seawater (34 ppt); the larval LC90 was 24.2 ppt. Deleterious effects of high salinity decreased as larvae matured. Six-day-old larvae reared at a salinity of 34 ppt weighed 79% less than controls, compared with a 36% difference in 9-d-old larvae; by pupation, the difference was only 24%. Salinity did not influence the duration of larval, pupal, or adult stages. Survival of pupae was unimpaired despite a slight increase in number of pupal deformities, and normal adults emerged. Eggs were highly tolerant to saline. They hatched at salinity concentrations lethal to larvae; greater than 50% hatch occurred even when eggs were maintained at 80 ppt NaCl. Sensitivity of larvae to salinities close to that of seawater might be important for control of stable flies inhabiting marine areas.     

Determining the optimum temperature and salinity for larval culture,and describing a culture protocol for the conservation aquaculture for European smelt Osmerus eperlanus (L.)

Populations of anadromous European smelt Osmerus eperlanus (L.) are declining across its geographical range in northern Europe, but no practical culture techniques exist to develop stock enhancement programmes for this species. In this study, a culture protocol is described to rear fish from fertilised eggs to mature adults in 2 years involving the use of ‘green water’, live feed and artificial diets. The sequence of embryonic development for eggs incubated at 10°C/0 ppt was described and photographed. To determine the optimum conditions for larval culture, fertilised eggs were reared at a range of salinities (0–20 ppt) and temperatures (5–18°C) until first feeding. Best hatching success (ca. 97%), size at hatch (ca. 0.8 mm) and survival to first feeding (ca. 96%) of larvae were achieved under combined conditions of low salinity (0–0 ppt) and temperature (5–10°C). No larvae survived a salinity of 20 ppt. The time taken from fertilisation to hatch (FtH) and hatching duration (HD) were temperature-dependent ranging from 42 days FtH and 10 days HD at 5ºC, to 10 days FtH and 2 days HD at 18°C irrespective of salinity. The results indicate that conservation programmes could utilise existing salmonid hatchery facilities (i.e. freshwater, ≤10°C water temperature) for stock enhancement. Since on-growing of smelt involves the logistical and technical problems of live feed production, it is recommended that smelt enhancement programme utilise freshwater hatchery facilities to rear fish until hatching, and then stock out onto known spawning grounds in rivers allowing hatched larvae to drift into estuaries to complete the larval and juvenile phases. This approach would minimise the time spent in the hatchery post-hatching, eliminate the need for live food production, prevent the development of predator-naïve fish, and hence would mimic the natural life cycle of the species as closely as possible.     

Morphological and physiological responses of Scaevola sericea (Goodeniaceae) seedlings to salt spray and substrate salinity

The effects of substrate salinity and salt spray upon seedlings of Scaevola sericea were examined in this study. Three levels of substrate salinity: 0.0 ppt, 3.0 ppt, and 10.0 ppt were examined in conjunction with three levels of salt spray: zero, medium (200 mg m^-2mdd^-1), and high (1200–1500 mg-m^-2mdd^-1). Leaf surface area, root to shoot ratio, as well as leaf, stem, and root mass decreased significantly (P 0.05) with increasing substrate salinity. Biomass accumulation was very low at 10.0 ppt substrate salinity, suggesting that higher levels of substrate salinity cannot be tolerated by the seedlings. Salt spray had a substantial effect on several of these variables, however its effects were less pronounced than those of substrate salinity. Cell sap osmolarity, leaf thickness, and leaf specific mass increased significantly (P 0.05) with both increasing substrate salinity and salt spray levels. Leaf carbon isotope ratios (δ^l3C) became more positive with increasing salinity, indicating an enhancement of the intrinsic water use efficiency of the seedlings at higher salinities. Scaevola sericea is one of the dominant plants found at the leading edge of strand communities in the Hawaiian archipelago and throughout much of the tropical Pacific. Since substrate salinity and salt spray increase with proximity to the ocean, the two factors may act together to limit the seaward expansion of S. sericea in coastal habitats.     

Effect of cadmium on survival,osmoregulation and gill structure of the Sunda prawn,Macrobrachium sintangense (de Man), at different salinities

The prawn Macrobrachium sintangense is likely to be subjected to occasional exposure to combined metal and saline stressors in its natural environment. This research evaluated the acute toxicity (96?h LC₅₀) of cadmium (Cd) on the prawn M. sintangense, with respect to the osmoregulatory capacity (OC) of prawns and to document histological changes in the gills after exposure to sublethal Cd concentrations at different salinities. The 96?h LC₅₀ of Cd to M. sintangense decreased with increasing salinity. The 96?h LC₅₀ values were 89.12 (72.53–109.50), 681.26 (554.20–837.46) and 825.37 (676.99–1006.27) μg CdL^?1 at 0, 10 and 20 ppt, respectively. The OC of prawns exposed to 30?μg?CdL^?1 at 0 ppt and to 300?μg?CdL^?1 at10 ppt decreased significantly compared with that of control prawns exposed to 0 and 10 ppt respectively. Swelling, hyperplasia and necrosis of gill lamellae resulting in the loss of marginal canals were observed in the gills of prawns exposed to 30?μg?CdL^?1 at 0 ppt and to 300?μg?CdL^?1 at 10 ppt for 7?days.     

The salinity tolerance of the invasive golden apple snail (Pomacea canaliculata)

We exposed snails of an invasive species of golden apple snail (Pomacea canaliculata) to five artificial sea water treatments at salinity levels of 0, 5, 10, 15 or 20 parts per thousand (ppt) to assess their salinity tolerance. We observed the behaviour, heart rate, total haemocyte counts, haemolymph ionic concentration and Na⁺/K⁺-ATPase activity in the mantle at 0, 12, 24, 48, 72 and 96 h post salinity exposures. The heart rate declined with increasing salinity, while Na⁺/K⁺-ATPase activity in the mantle presented a reverse trend, possibly to maintain normal osmolality. A trend of rising total haemocyte count was observed from 0 ppt and 5 ppt to 10 ppt salinities, while a sudden increase in the count was observed at 15 ppt and 20 ppt salinity groups. Furthermore, haemolymph Cl^?, Na⁺ and K⁺ concentrations increased directly with elevated salinity. An additional trial was performed to assess the growth performance of the snails under exposure to low salinities. During a 1 month trial, snails grew better at 5 ppt salinity treatment. Taken together, our results demonstrate that P. canaliculata can tolerate salt stress to some extent. The finding also obviously implies a possible invasive risk to estuaries.     

Comparative survival and growth of embryos,larvae, and juveniles of pejerrey Odontesthes bonariensis and O. hatcheri* at different salinities

The hatching of fertilized eggs and the survival and growth of larvae and juveniles of the inland‐water atherinids Odontesthes bonariensis (Valenciennes 1835) and O. hatcheri (Eigenmann 1909) were examined at salinities of 0, 5, 10, 20, and 30 ppt. In addition, a limited study compared the salinity responses of O. bonariensis eggs and larvae from different origins. Overall, embryos, larvae, and juveniles of both species were euryhaline, although best survival and growth rates were obtained at the intermediate salinities. Survival of O. bonariensis at 0 ppt varied from very good to very poor. Comparison of the salinity responses of eggs and larvae of O. bonariensis from the current Japanese strain with newly introduced strains from three locations in Argentina did not reveal a clearly superior strain for freshwater culture. In general, O. hatcheri showed higher survival and growth rates and better adaptability to fresh water compared with O. bonariensis. Although both species are commonly regarded as freshwater species, the results of this study emphasize the importance of millimolar quantities of salts in the rearing water for improved survival and growth.     

THE BIOLOGY AND FUNCTIONAL MORPHOLOGY OF MYTILOPSIS SALLEI (RECLUZ) (BIVALVIA: DREISSENACEA) FOULING VISAKHAPATNAM HARBOUR, ANDHRA PRADESH, INDIA

Mytilopsis sallei (Récluz) (Dreissenacea) has been introducedinto Visakhapatnam harbour, India. The normal distribution ofthe species is Central America and it is here contended thatthe species has been introduced into the Indo-Pacific via thePanama canal (opened in 1915) attached to the hulls of ships.M. allyneana (Hertlein & Hanna) with a distribution restrictedto Fiji is considered synonymous with M. sallei. The literature on M. sallei is reviewed and it is shown thatthe species has wide temperature, salinity and oxygen tolerancesand thus transport across a variety of water masses is entirelyfeasible. The species also possesses a fast rate of growth,a high fecundity and matures early. It is an opportunistic specieswhich free from the restraints that normally hold it in checkin its natural environment, poses a serious fouling threat toharbours throughout the Indo-Pacific and to the endemic fauna. The morphological adaptations of M. sallei are also describedand compared with those of Dreissena polymorpha (Pallas) inparticular and other fouling bivalves in general. The speciesis ideally adapted to life in turbid estuaries experiencingwide variations in temperature, salinity, oxygen and turbulence.A warning against further introductions is given. (Received 14 December 1979;     

Growth and physiological parameters of whiting (Sillaginodes punctata) in relation to salinity

This study assessed the impact of salinity on whiting (Sillaginodes punctata) in an attempt to understand the mechanisms by which salinity could potentially influence habitat selection and growth of King George whiting in southern Australia. The experiment included whiting of two age classes, young of the year (YOY) and 2⁺ year, at three salinities (30, 40, 50 ppt). YOY whiting showed no significant difference in length or weight gain, specific growth rate, feed intake, food conversion ratio or condition factor when exposed to the three salinities for 72 day. Plasma osmolality of YOY whiting was not significantly different at any salinity, although it was significantly lower than that of 2⁺ year whiting. The 2⁺ year whiting showed significantly higher plasma osmolality than the YOY. Blood plasma potassium and chloride levels of 2⁺ year fish at 50 ppt were significantly higher than those at 30 ppt and 40 ppt. Blood sodium levels at 50 ppt were significantly higher than at 30 ppt but the sodium level at 40 ppt was not different from 30 ppt or 50 ppt. Haematocrit of 2⁺ whiting was significantly higher at 30 than at 50 ppt while haematocrit at 40 ppt was not different from 30 or 50 ppt. The 2⁺ year‐old whiting had a more pronounced increase in plasma osmolality and plasma ions at high salinities, indicating poorer osmoregulatory capacity in older fish. This study provides physiological evidence to partially explain habitat occupancy and growth in relation to salinity of different age groups of whiting in southern Australia.     

Reproduction of the Endangered Killifish Aphanius iberus at Different Salinities

Adult fish of a freshwater population of the Iberian endangered cyprinodontid Aphanius iberus, were induced to reproduce at salinities of 5, 15, 30, 45 and 60ppt. For each salinity five 30l aquaria were used, each one including a male and two females. Maturity and spawning outside the natural season, were obtained at conditions of 22 to 28°C and a photoperiod of 14L:10D. The larvae were fed with rotifers Brachionus plicatilis and Synchaeta cecilia valentina. Experiment lasted 40 days. The first spawning occurred on the 17th day at 45ppt of salinity and the first embryos hatched on the 34th day at 5 and 15ppt salinity. The final average number of larvae per aquarium ranged from 5.2 (45ppt salinity) to 10.8 (15ppt salinity). No significant differences were found between the average values at different salinities (p<0.01).     

Effect of different salinity on serum osmolality,ion levels and hematological parameters of East Java strain tilapia Oreochromis niloticus

This study evaluated the effect of different salinity levels on the physiology of East Java strain tilapia (Oreochromis niloticus) by measuring the serum osmolalities (SO), ion levels and hematological parameters. Their SOs above the external medium (hyper-osmotic) at 0 and 5 ppt, becoming iso-osmotic at 10 ppt and hypo-osmotic at 15 ppt. The concentrations of serum Na⁺, K⁺, Cl^? and Ca²⁺ in fish acclimated in 0 and 5 ppt were not significantly different. The levels of Na⁺, Cl^– and Ca²⁺ in fish exposed to 10 and 15 ppt were higher than those in fish acclimated at 0 and 5 ppt. In contrast, the levels of K⁺ in fish exposed to 10 and 15 ppt were lower than those in fish exposed to 0 and 5 ppt. The levels of red blood cell, hematocrit and hemoglobin of fish exposed to salinity of 0, 5, 10 and 15 ppt were not significantly different. The levels of white blood cell increased significantly at fish exposed to 10 and 15 ppt. These data provide useful information for future reference and farming practice.     

The effect of cadmium on plasma melanocyte-stimulating hormone and morphological changes of melanophores in the cichlid fish Oreochromis niloticus,at different salinity levels

ABSTRACT

The effects of cadmium concentration (0, 2.5 and 5 mg L^?1) on melanocyte-stimulating hormone (MSH), melanophore index (MI), and melanophore number (MN), as well as a microscopic examination of scale melanocytes in tilapia (Oreochromis niloticus Linnaeus, 1757) was evaluated at different salinity levels (0, 5 and 15 ppt). The levels of MSH, MI, and MN were lower in Cd-exposed fish than in control fish (not exposed to Cd) at salinity level of 0 and 5 ppt. In ppt, however these levels of MSH, MI and MN in control and Cd-exposed fish were not significantly different. In the media without Cd, the levels of MSH, MI and MN were not significantly different at all salinities. The morphological changes of melanophores were higher in Cd-exposed fish than in control fish at salinity 0 and 5 ppt, respectively. These morphological changes were not significantly different in the control fish at all salinities as well as in fish exposed to 0–5 mg L^?1 Cd at salinity of 15 ppt. This study therefore demonstrates that the toxic effect of Cd on MSH levels and melanophore morphology decreased with increasing salinity. Further, due to the sensitivity of chromatophores to Cd, melanophore morphology is proposed as a biomarker of Cd exposure in aquatic ecosystems.