Differences In Salinity Tolerance Research Articles

Tolerance of extreme salinity in two stem-succulent halophytes (Tecticornia species).

Communities of Tecticornia on the margins of ephemeral salt lakes in Australia often exhibit species zonation, such as at Hannan Lake (Western Australia) where Tecticornia indica subsp. bidens (Nees) K.A.Sheph. and Paul G.Wilson occupies the less saline dune habitat on lake margins and Tecticornia pergranulata (J.M.Black) K.A.Sheph. and Paul G.Wilson subsp. pergranulata occupies both the dunes and the more saline and moist lake playa. Here we tested the hypothesis that these two species differ in tolerance to extreme salinity. Plants were grown in drained sand cultures with treatments of 10-2000mM NaCl for 85 days. Both species were highly salt tolerant, maintaining growth at treatments of up to 2000mM NaCl, although the death of two replicates of T. indica at 2000mM NaCl suggests this salinity is close to the species tolerance limit. Both Tecticornia species maintained a favourable gradient in tissue water potential via osmotic adjustment as external salinity increased, also with reduced tissue water content at very high external salinity. Regulated accumulation of Na+ and Cl-, maintenance of net K+ to Na+ selectivity, high tissue concentrations of glycinebetaine and presumed cellular solute compartmentation, would have contributed to salt tolerance. The growth rate of T. pergranulata was 11-29% higher than T. indica suggesting, in addition to these moderate differences in salinity tolerance, other factors are likely to contribute to species zonation at salt lakes. The higher water use efficiency of the C4 T. indica compared with the C3 T. pergranulata may provide an advantage in the drier dune habitat on salt lake margins. An additional experiment confirmed the hypothesis that survival of T. pergranulata seedlings is enhanced by the duration of reduced salinity after germination, as would occur following significant rainfall, as older seedlings maintained higher growth rates during subsequent increases in salinity.

Differences in salinity tolerance of genetically distinct Phragmites australis clones

Different clones of the wetland grass Phragmites australis differ in their morphology and physiology, and hence in their ability to cope with environmental stress. We analysed the responses of 15 P. australis clones with dis- tinct ploidy levels (PLs) (4n ,6 n ,8 n ,1 0n ,1 2n) and geographic origins (Romania, Russia, Japan, Czech Republic, Australia) to step-wise increased salinity (8, 16, 24, 32, 40, 56 and 72 ppt). Shoot elongation rate, photosynthesis and plant part- specific ion accumulation were studied in order to assess if traits associated with salinity tolerance can be related to the genetic background and the geographic origin of the clones. Salt stress affected all clones, but at different rates. The maximum height was reduced from 1860 mm in control plants to 660 mm at 40 ppt salinity. The shoot elongation rate of salt-exposed plants varied significantly between clones until 40 ppt salinity. The light-saturated photosynthesis rate (Pmax) was stimulated by a salinity of 8 ppt, but decreased significantly at higher salinities. The stomatal conduct- ance (gs) and the transpiration rate (E) decreased with increasing salinity. Only three clones survived at 72 ppt salinity, although their rates of photosynthesis were strongly inhibited. The roots and basal leaves of the salt-exposed plants accumulated high concentrations of water-extractable Na + (1646 and 1004 mmol g 21 dry mass (DM), respectively) and Cl 2 (1876 and 1400 mmol g 21 DM, respectively). The concentrations of water-extractable Mg 2+ and Ca 2+ were reduced in salt-exposed plants compared with controls. The variation of all the measured parameters was higher among clones than among PLs. We conclude that the salinity tolerance of distinct P. australis clones varies widely and can be partially attributed to their longitudinal geographic origin, but not to PL. Further investigation will help in improving the under- standing of this species' salt tolerance mechanisms and their connection to genetic factors.

Effect of salinity on water relations of four turfgrasses

Information on the degrees and patterns of ion accumulation in various parts of a plant is important in evaluating salinity tolerance, as well as salinity tolerance mechanisms. ‘Challenger’ Kentucky bluegrass (Poa pratensis L.) (KBG), ‘Arid’ tall fescue (Festuca arundinacea Schreb) (TF), ‘Fults’ alkaligrass (Puccinellia distans (L.) Parl.) (AG), and a saltgrass (Distichlis spicata (Torr.) Beetle) (SG) collection were grown under various salinity levels in greenhouse hydroponic experiments. Salinity treatments were applied using 1NaCl:1CaCl 2 solution at different concentrations. . Ion concentrations in shoots and roots of each grass grown at different salinity levels were examined. As salinity increased, Na + , Cl , and Ca ++ concentrations increased linearly, while Mg ++ and K + concentrations decreased in shoots, sap, and roots of all species. Salinity tolerance of these species was associated with their ability to exclude Na + and Cl from shoots and maintain a relatively high level of K + . Potassium to sodium ratio in all species was higher in shoots than in roots, indicating these plants achieved K + selectivity via multiple processes in multiple locations. Maintenance of a K + /Na + ratio close to or above 1 was important for plant survival. Results indicated that, SG, AG, TF, and KBG could maintain a shoot K + /Na + ratio of 1 when salinity levels were less than 22.3, 13.6, 7.4, and 3.7 dS/m, respectively. Leaf ion secretion rate of SG increased as salinity level increased, reaching 5.05, 6.86, and 1.22 mg/g dw/day for Na + , Cl , and Ca ++ , respectively, at 23.5 dS/m. No Mg ++ or K + were secreted. Regulation of ion concentrations (via ion restriction, exclusion or secretion) and maintenance of higher K + /Na + ratio in shoots appeared to be important mechanisms contributing to the differences in salinity tolerance observed in these species. + /Na + ratio, ion secretion rate, salt glands, salinity tolerance.

Larval Tolerance to Salinity in Three Species of Australian Anuran: An Indication of Saline Specialisation in Litoria aurea

Recent anthropogenic influences on freshwater habitats are forcing anuran populations to rapidly adapt to high magnitude changes in environmental conditions or face local extinction. We examined the effects of ecologically relevant elevated salinity levels on larval growth, metamorphosis and survival of three species of Australian anuran; the spotted marsh frog (Limnodynastes tasmaniensis), the painted burrowing frog (Neobatrachus sudelli) and the green and golden bell frog (Litoria aurea), in order to better understand the responses of these animals to environmental change. Elevated salinity (16% seawater) negatively impacted on the survival of L. tasmaniensis (35% survival) and N sudelli (0% survival), while reduced salinity had a negative impact on L. aurea. (16% seawater: 85% survival; 0.4% seawater: 35% survival). L. aurea tadpoles survived in salinities much higher than previously reported for this species, indicating the potential for inter-populations differences in salinity tolerance. In L. tasmaniensis and L. aurea, development to metamorphosis was fastest in low and high salinity treatments suggesting it is advantageous for tadpoles to invest energy in development in both highly favourable and developmentally challenging environments. We propose that this response might either maximise potential lifetime fecundity when tadpoles experience favourable environments, or, facilitate a more rapid escape from pond environments where there is a reduced probability of survival.

Linking oxidative and salinity stress tolerance in barley: can root antioxidant enzyme activity be used as a measure of stress tolerance?

A causal relationship between salinity and oxidative stress tolerance and a suitability of using root antioxidant activity as a biochemical marker for salinity tolerance in barley was investigated. Net ion fluxes were measured from the mature zone of excised roots of two barley varieties contrasting in their salinity tolerance using non-invasive MIFE technique in response to acute and prolonged salinity treatment. These changes were correlated with activity of major antioxidant enzymes; ascorbate peroxidase, catalase, and superoxide dismutase. It was found that genotypic difference in salinity tolerance was largely independent of root integrity, and observed not only for short-term but also long-term NaCl exposures. Higher K+ retention ability (and, hence, salinity tolerance) positively correlated with oxidative stress tolerance. At the same time, antioxidant activities were constitutively higher in a sensitive but not tolerant variety, and no correlation was found between SOD activity and salinity tolerance index during large-scale screening. Although salinity tolerance in barley correlates with its oxidative stress tolerance, higher antioxidant activity at one particular time does not correlate with salinity tolerance and, as such, cannot be used as a biochemical marker in barley screening programs.

Interspecific divergence of ionoregulatory physiology in killifish: insight into adaptation and speciation

AbstractAdaptation to salinity is potentially a critical driving force of speciation in fishes. Here, we tested for differences in ion/osmoregulatory gene expression between two species of killifish Lucania goodei and L. parva that differ in salinity tolerance. Expression patterns of several genes encoding ion transport proteins were quantified for animals taken directly from populations that varied in salinity, as well as animals from a salinity transfer experiment. We found that L. parva, a euryhaline species, expressed higher levels of the genes involved in saltwater ion/osmoregulatory regulation than its stenohaline counterpart L. goodei (Na+/K+‐ATPase 1a and 1b, Na+‐K+‐2Cl‐ cotransporter 1 and glucocorticoid receptor) when exposed to a change in salinity in the laboratory. However, both species expressed similar levels for two of the three genes involved in freshwater osmoregulation (14‐3‐3a and V‐type H+‐ATPase). Surprisingly, we found little evidence for differential plasticity between L. parva and L. goodei in our salinity transfer experiment. Lucania parva expressed high levels of genes involved in both freshwater and saltwater ion/osmoregulation, while L. goodei only expressed high levels of genes involved in freshwater osmoregulation. These results indicate that L. parva may increase their transcript levels of osmoregulatory genes when faced with any type of salinity challenge. Thus, changes in ion/osmoregulatory physiology may be occurring post‐transcriptionally via differential RNA processing or enzyme activity. These findings provide unique insight into the ion/osmoregulatory physiology that underlies species and population differences in salinity tolerance.

Salinity Effect on Seed Germination and Growth of Two Warm-season Native Grass Species

Salinity tolerance of five buffalograss [Buchloe dactyloides (Nutt.) Englem.] cultivars (Texoka, Cody, Bison, Sharp's Improved II, and Bowie) and three blue grama [Bouteloua gracilis (Willd. ex Kunth) Lag. ex Griffiths] ecotypes (‘Lovington’, ‘Hachita’, and ‘Bad River’) was determined during in vitro seed germination and vegetative growth in a hydroponic system. Seeds were germinated on 0.6% agar medium supplemented with NaCl at 0, 5, 10, 15, and 20 g·L−1. Salinity reduced the final germination rate (FGR) and daily germination rate (DGR). Similarly, shoot dry weight (SDW), longest root length (LRL), and percentage of green tissue (PGT) of mature grasses declined with increasing salinity levels (NaCl = 0, 2.5, 5, 7.5, and 10 g·L−1). However, root dry weight (RDW) was not significantly affected by salinity. Blue grama exhibited a lower reduction in FGR and DGR than buffalograss at salinity levels lower than 10 g·L−1. Germination of all buffalograss cultivars and ‘Hachita’ blue grama was inhibited at salinity levels of 15 and 20 g·L−1 NaCl. However, buffalograss was more salt-tolerant than blue grama at the vegetative growth stage. Variations of salinity tolerance were observed within buffalograss cultivars and blue grama ecotypes, especially during the seed germination stage. Overall, buffalograss appeared to be salt-sensitive during germination but moderately salt-tolerant at the mature stage. However, blue grama was more salt-tolerant at the germination stage than the mature stage. Noticeable differences in salinity tolerance were observed between different germplasms. Therefore, salt tolerance of buffalograss and blue grama may be improved through turfgrass breeding efforts.

Transcriptional profiling analysis in Populus yunnanensis provides insights into molecular mechanisms of sexual differences in salinity tolerance

Physiological responses to abiotic stress in plants exhibit sexual differences. Females usually experience greater negative effects than males; however, little is known about the molecular mechanisms of sexual differences in abiotic stress responses. In the present study, transcriptional responses to salinity treatments were compared between male and female individuals of the poplar Populus yunnanensis. It was found that several functional groups of genes involved in important pathways were differentially expressed, including photosynthesis-related genes, which were mainly up-regulated in males but down-regulated in females. This gene expression pattern is consistent with physiological observations showing that salinity inhibited photosynthetic capacity more in females than in males. Furthermore, genes located in autosomes rather than in the female-specific region of the W chromosome are the major contributors to the sexual differences in the salinity tolerance of poplars. In conclusion, this study provided molecular evidence of sexual differences in the salinity tolerance of poplars. The identified sex-related genes in salinity tolerance and their functional groups will enhance our understanding of sexual differences in salinity stress at the transcription level.

Differences in Salinity Tolerance and Gene Expression Between Two Populations of Atlantic Cod (Gadus morhua) in Response to Salinity Stress

Populations of marine fish, even from contrasting habitats, generally show low genetic differentiation at neutral genetic markers. Nevertheless, there is increasing evidence for differences in gene expression among populations that may be ascribed to adaptive divergence. Studying variation in salinity tolerance and gene expression among Atlantic cod (Gadus morhua) from two populations distributed across a steep salinity gradient, we observed high mortality (45% North Sea cod and 80% Baltic Sea cod) in a reciprocal common garden setup. Quantitative RT-PCR assays for expression of hsp70 and Na/K-ATPase α genes demonstrated significant differences in gene regulation within and between populations and treatment groups despite low sample sizes. Most interesting are the significant differences observed in expression of the Na/K-ATPase α gene in gill tissue between North Sea and Baltic cod. The findings strongly suggest that Atlantic cod are adapted to local saline conditions, despite relatively low levels of neutral genetic divergence between populations.

Variations in salinity tolerance of malaria vectors of the Anopheles subpictus complex in Sri Lanka and the implications for malaria transmission

BackgroundAnopheles subpictus sensu lato, a widespread vector of malaria in Asia, is reportedly composed of four sibling species A-D based on distinct cytogenetic and morphological characteristics. However An. subpictus species B specimens in Sri Lanka are termed An. subpictus B/ An. sundaicus because of recent genetic data. Differences in salinity tolerance and coastal/inland prevalence of An. subpictus sibling species that were not previously established in Sri Lanka are presented here.ResultsSpecimens with morphological characteristics of all four Indian An. subpictus sibling species were found in Sri Lanka. Sibling species A, C and D tended to be predominant in inland, and An. subpictus species B/An. sundaicus, in coastal localities. Sibling species C was predominant in both adult and larval inland collections. Larvae of An. subpictus B/An. sundaicus were found in inland and coastal sites, including a lagoon, with salinity varying from 0 to 30 ppt. An. subpictus sibling species A, C and D larvae were present in water of salinity between 0 to 4 ppt. An. subpictus C, D and An. subpictus B/An. sundaicus larvae showed compatible differential salinity tolerance in laboratory tests. The first instar larvae of An. subpictus B/An. sundaicus showed 100% survival up to 15 ppt in comparison to species C and D where the corresponding values were 3 ppt and 6 ppt respectively. However all third instar larvae of An. subpictus B/An. sundaicus survived up to 30 ppt salinity whereas An. subpictus C and D tolerated up to 4 ppt and 8 ppt salinity respectively.ConclusionsThe results suggest that An. subpictus species B/An. sundaicus breed in fresh, brackish and nearly saline water while An. subpictus species C and D do so in fresh and less brackish waters in Sri Lanka, as in India. Because of the established role of An. sundaicus s.l. and An. subpictus s.l. as malaria vectors, the findings indicate a need for greater monitoring of brackish water breeding habitats in Asia. Tolerance to 15 ppt salinity may also constitute a simple method for differentiating An. subpictus B/An. sundaicus larvae from those of An. subpictus species C and D in field studies.

Salinity Tolerance of 12 Turfgrasses in Three Germination Media

Salinity tolerance of 12 turfgrasses in four groups, creeping bentgrass (Agrostis stolonifera L.), fescues (Festuca spp.), kentucky bluegrass (Poa pratesis L.), and alkaligrass [Puccinellia distans (Jacq.) Parl.], was evaluated using three germination methods. Seeds were germinated on 1% agar medium, on germination paper, or in a hydroponic system under salinity levels of 0, 5, 10, 15, or 20 g·L−1 NaCl. Germination rate and seedling growth of each grass were determined. Salinity reduced the final germination rate (FGR), daily germination rate (DGR), and seedling leaf area (LA) in all tests. On agar medium, no significant difference in salinity tolerance was observed among the four turf groups; however, ‘Turf Blue’ kentucky bluegrass with a corn starch-based coating (coated ‘Turf Blue’) showed a significant higher salinity tolerance than the uncoated one. Using germination paper, creeping bentgrass required the highest salinity level to cause 50% reduction in FGR followed by alkaligrass, fescues, and kentucky bluegrass. Kentucky bluegrass required the lowest salinity level (9.5 g·L−1) to reduce DGR by 50%. With the hydroponic system, alkaligrass required a salinity level of 26.3 g·L−1 to reduce FGR by 50%, the highest among the four groups. Alkaligrass showed again the highest salinity tolerance with an average of 12.7 g·L−1 needed to reduce LA by 50%. Among the grasses, coated ‘Turf Blue’ kentucky bluegrass, ‘Declaration’ creeping bentgrass, and ‘Fults’ alkaligrass showed the highest salinity tolerance when evaluated on agar medium, on germination paper, or in the hydroponic system, respectively. The present study determined the salinity tolerance of 12 turfgrasses at seed germination and early seedling growth stages and showed that the germination method was a factor affecting the evaluation result and it should be considered in a seed germination test of turfgrass for salinity tolerance.

Plasticity tradeoffs in salt tolerance mechanisms among desert Distichlis spicata genotypes.

We investigated genetic differences in salinity tolerance among 20 saltgrass (Distichlis spicata (L.) Greene) genotypes, including constitutive, gender-based and phenotypic plasticity traits, to better understand the basis of adaptation and acclimation by saltgrass in diverse environments. On average, the plants survived NaCl treatments up to ~1M, with reductions in growth and health that varied with genotype. For these 20 genotypes in a greenhouse study, we showed that greater plasticity in one salt tolerance mechanism was physiologically linked to lesser plasticity in another. Under various levels of constant salinity stress, genotypes employing a strategy of greater plasticity in foliar Na and lesser plasticity in both foliar K:Na and Na turnover rate were better able to substitute Na for K in some cellular functions, especially osmotic adjustment, leading to increased salinity tolerance. Although we observed gender segregation with salinity in the Owens (Dry) Lake Playa (Inyo County, CA, USA) population planted for dust control, from which the genotypes were collected, we did not observe gender differences in salinity tolerance in the greenhouse. Significant physiological plasticity tradeoffs among genotypes, however, did affect overall salinity tolerance and may be important for this species survival in diverse managed and natural habitats.

Salinity Tolerance of Cool-Season Turfgrass Cultivars Under Field Conditions

In order to utilize effluent or wastewater as irrigation on turfgrass sites it will require the identification of cool-season turfgrass cultivars with increased salinity tolerance. Evaluation of current cultivars and experimental selections for salinity tolerance is an important first step in making information available to turfgrass managers. An overhead irrigated field screening method was developed to closely mimic the challenges associated with irrigation of turf with saline water under summer stress conditions. A total 48 clones from each turfgrass cultivar were planted in a randomized complete block design with four replications (12 clones per replication) and were irrigated overhead with saltwater (EC =10 dS/m). This technique effectively identified differences in salinity tolerance, of Kentucky bluegrass, bentgrass, and perennial ryegrass cultivars and selections as measured by percent green ratings. The most salt tolerant cultivars included: Liberator, Eagleton, Diva, and Rhythm Kentucky bluegrasses; Declaration, Kingpin, and 007 creeping bentgrasses; and RKS, Gator 3, and MSH Comp perennial ryegrasses. Cultivars and selections exhibiting the least salinity tolerance were: RSP, A03-TB676, A03-84, and Julia Kentucky bluegrasses; EBM Comp and Tiger II colonial bentgrasses; SR7200 velvet bentgrass; and Fiesta III perennial ryegrass.

The salinity preference of members of the genus Macroplea (Coleoptera, Chrysomelidae, Donaciinae), fully aquatic leaf beetles that occur in brackish water

Reed beetles (Donaciinae) of the genus Macroplea Samouelle, 1819 live permanently submerged. Literature indicates that Macroplea mutica occurs in brackish water, whereas Macroplea appendiculata is restricted to freshwater. The salinity preference of these two species was tested in a linear and a circular device that offered a continuous salinity gradient. The distribution of animals in the devices was monitored over at least 3h in each of the 21 experiments. Both species preferred freshwater (salinity 0) over brackish water (salinity 10). In particular, this holds true for specimens collected in brackish water. Likewise, immediate reactions could be observed when during such experiments the direction of the gradient was reversed. While M. mutica can be regarded as a truly marine insect, this marine environment does not strictly reflect its fundamental niche with respect to salinity preference. This is in line with accumulating evidence that M. mutica can be found in freshwater habitats (and M. appendiculata in brackish water). This indicates that the species’ distribution might be influenced by other factors like host plant preference or dispersal mechanisms. It is discussed if—in spite of similar fundamental niches—differences in salinity tolerance (and hence performance in brackish water) may have contributed to speciation in the genus Macroplea.

THE EFFECT OF SALINITY ON THE GROWTH OF THE HALOPHYTE ATRIPLEX HORTENSIS (CHENOPODIACEAE)

The effect of salt stress on the growth of the Atriplex hortensis was determined by growing plants in soils receiving a one-time irrigation of nutrient solution containing low, medium, and high levels of NaCl. Atriplex plants were grown in sand culture under controlled greenhouse conditions. The experiment was compared to two varieties of A. hortensis. Growth and yield were progressively declined by increasing NaCl concentrations. Atriplex hortensis, an annual halophyte, exhibits significant reduction in height and biomass under saline stress conditions. The photosynthetic activity decreases when plants are grown under saline conditions leading to reduced growth and productivity. Low levels of salinity (5 g/l NaCl) did not cause substantial inhibition of growth but increasing concentrations of salt induced a progressive decline in length and weight of the plants. Salt stress induced a significant decrease in leaf area, but it had no significant effect on leaf water content. The results of present study indicate no differences in salinity tolerance in both Atriplex plants. Another possible conclusion is that improved tolerance to salt stress may be accomplished by decline in growth and photosynthetic activity. Based on

Calcium requirement of wheat in saline and non-saline conditions

Supplemental calcium (Ca2+) is used in hydroponic studies on salinity to lessen the potential for Ca2+ deficiency. However, the Ca2+ concentration and the sodium (Na+): Ca2+ ratio used vary considerably. The implications of using a wide range of Na+: Ca2+ ratios for studies of salinity tolerance in wheat are not known. Also, despite the risk of development of Ca2+ deficiency under salinity stress, there are few reliable reports on the critical level of Ca2+ which can be used to diagnose Ca2+ deficiency in wheat. Two experiments were conducted to examine Ca2+ requirements of wheat under saline and non-saline conditions and to derive a critical level for Ca2+. Four bread wheat genotypes (Triticum aestivum L.) and a durum wheat genotype [Triticum turgidum subsp. durum) (Desf.) Husn.] with known differences in salinity tolerance were grown at 100 mM NaCl for four weeks with varying levels of external Ca2+ which resulted in Na+:Ca2+ ratios of 30, 20, 15, 5 and 2. The critical Ca2+ concentration was defined in a second experiment by growing the same wheat genotypes at seven levels of Ca2+ (0.05, 0.1, 0.2, 0.5, 1, 2 and 10 mM) under non-saline conditions. When grown at 100 mM NaCl salinity tolerance was greatest when the Na+:Ca2+ ratio ranged from 5 to 15. Growing plants at lower or higher Na+:Ca2+ ratios induced nutrient imbalances and additional osmotic stress which reduced the growth of plants. Transient Ca2+ deficiency occurred at high Na+:Ca2+ ratios and low Mg2+ occurred at the lowest Na+:Ca2+ ratio. Adding NaCl raised the tissue Na+ concentration and reduced the Ca2+ concentration and the most appropriate Na+:Ca2+ ratio in the solution was that which resulted in tissue Ca2+ concentrations similar to those of non-salinised plants. The critical level of Ca2+ in the youngest fully emerged leaf blades was 15–23 mmol kg-1 DW (600–900 mg kg-1 DW).

Effects of pH on salinity tolerance of selected freshwater invertebrates

Salinization of freshwaters often co-occurs with other changes in the environment, including pH. We investigate the effect of pH on salinity tolerance in selected macroinvertebrates (Notalina fulva, Centroptilum sp. and Physa acuta--lethal effects only) and microinvertebrates (Paramecium caudatum and Hydra oligactis--lethal and sublethal effects). Despite seemingly plausible physiological arguments, no difference in salinity tolerance over 96-h period was detected between low (5 or 6 nominal) pH and circumneutral (7-8.2 nominal) pH. P. caudatum was more salt sensitive in pH 11 than in pH 5, 7, and 10 in terms of mortality, and in terms of a sublethal endpoint, number of individuals produced and survived over 72 h, more sensitive to salinity in pH 10 than in pH 5 and 7. No other effects of pH on salinity tolerance were detected. Acidification will likely have effects on freshwater organisms on its own, however, when combined with salinization (from saline waters approximating seawater) acidification level tested did not modify the direct effects of salinity on the sample of freshwater invertebrates tested from a range of taxonomic groups. Thus the risk of low (5 or 6) pH modifying the effect of salinity on freshwater invertebrates is not high. Logically, lower pH values might have modified the effect of salinity, but there is a limited scope for lower pH values that would keep the species studied alive. In contrast, alkaline pH may increase the effect of salinity in some freshwater invertebrates. It is possible that the effect of pH on salinity tolerance may, however, be increased in saline waters with low calcium concentrations.

Large variation in salinity tolerance in chickpea is explained by differences in sensitivity at the reproductive stage

Salinity is an ever-increasing problem in agriculture worldwide, especially in South Asia (India, Pakistan) and Australia. Improved genotypes that are well adapted to saline conditions are needed to enhance and sustain production in these areas. A screening of 263 accessions of chickpea, including 211 accessions from ICRISAT's mini-core collection (10% of the core collection and 1% of the entire collection), showed a 6-fold range of variation for seed yield under salinity (1.9 L of 80 mM NaCl per 7.5 kg Vertisol), with several genotypes yielding 20% more than a previously released salinity tolerant cultivar. The range of variation in yields under salinity was similar in both kabuli and desi chickpeas, indicating that breeding for salinity tolerance can be undertaken in both groups. A strong relationship ( r 2 = 0.50) was found between the seed yield under salinity and the seed yield under a non-saline control treatment, indicating that the seed yield under salinity was explained in part by a yield potential component and in part by salinity tolerance per se. Seed yields under salinity were therefore computed to separate the yield potential component from the residuals that accounted for salinity tolerance per se. Among the genotypes evaluated, desi genotypes had higher salinity tolerance than kabuli genotypes. The residuals were highly correlated to the ratio of seed yield under salinity to that of the control, indicating that both parameters can be used to assess salinity tolerance. A similar ratio was calculated for shoot dry weight at 50 days after sowing. However, no significant correlation was found between the shoot dry weight ratio and the yield ratio, indicating that differences in salinity tolerance among genotypes could not be inferred from measurements in the vegetative stage. The major trait related to salinity tolerance was the ability to maintain a large number of filled pods, whereas seed size was similar in tolerant and sensitive genotypes. Salinity tolerance was not related to the shoot Na + or K + concentrations.

Associations between anuran tadpoles and salinity in a landscape mosaic of wetlands impacted by secondary salinisation

Summary1. The secondary salinisation of wetlands is a global problem that poses a great threat to most freshwater biodiversity, including amphibians. We examined tadpole diversity in relation to wetland conductivity (our proxy for salinity) in wetlands in south‐eastern Australia to better understand (i) how salinity and amphibian diversity interact and (ii) the threat posed by secondary salinisation.2. Six tadpole species were trapped in 56 wetlands that reflected a typical salinity gradient for the study region. We developed Bayesian models to examine the relationships between conductivity and both the probability of species occupancy and expected number of species with the imperfect detection probability of species accounted for in the models.3. The probability of occupancy for all species and expected species number was negatively associated with wetland conductivity. Our results predict that conductivity should not limit tadpole presence below about 3000 μS cm−1 at 25 °C (approximately 6% seawater) in the region, but will largely exclude amphibian larvae beyond about 6000 μS cm−1 at 25 °C (approximately 12% seawater).4. We also detected subtle among‐species differences in salinity tolerance. The results reported here show that tadpoles in the study region are likely to be negatively affected by projected future increases in salinisation.

Contrasting patterns in genetic diversity following multiple invasions of fresh and brackish waters

Biological invasions may combine the genetic effects of population bottlenecks and selection and thus provide valuable insight into the role of such processes during novel environmental colonizations. However, these processes are also influenced by multiple invasions, the number of individuals introduced and the degree of similarity between source and receiving habitats. The amphipod Gammarus tigrinus provides a useful model to assess these factors, as its invasion history has involved major environmental transitions. This species is native to the northwest Atlantic Ocean, although it invaded both brackish and freshwater habitats in the British Isles after introduction more than 65 years ago. It has also spread to similar habitats in Western Europe and, most recently, to Eastern Europe, the Baltic Sea, and the Laurentian Great Lakes. To examine sources of invasion and patterns of genetic change, we sampled populations from 13 native estuaries and 19 invaded sites and sequenced 542 bp of the mitochondrial COI gene. Strong native phylogeographical structure allowed us to unambiguously identify three allopatrically evolved clades (2.3-3.1% divergent) in invading populations, indicative of multiple introductions. The most divergent clades occurred in the British Isles and mainland Europe and were sourced from the St Lawrence and Chesapeake/Delaware Bay estuaries. A third clade was found in the Great Lakes and sourced to the Hudson River estuary. Despite extensive sampling, G. tigrinus did not occur in freshwater at putative source sites. Some European populations showed reduced genetic diversity consistent with bottlenecks, although selection effects cannot be excluded. The habitat distribution of clades in Europe was congruent with the known invasion history of secondary spread from the British Isles. Differences in salinity tolerance among lineages were suggested by patterns of habitat colonization by different native COI clades. Populations consisting of admixtures of the two invading clades were found principally at recently invaded fresh and brackish water sites in Eastern Europe, and were characterized by higher genetic diversity than putative source populations. Further studies are required to determine if these represent novel genotypes. Our results confirm that biological invasions need not result in diminished genetic diversity, particularly if multiple source populations, each with distinctive genetic composition, contribute to the founding populations.