Ranking of 11 coastal halophytes from salt marshes in northwest Turkey according their salt tolerance

Salt-affected soils with high electrolyte contents limit the development of the majority of plants and serve as a habitat only for such species (halophytes) that can survive the conditions. To date, there is still much that is unknown about the physiological mechanisms, including ion relationships, that make plants salt-resistant. The primary aim of this study was to evaluate a method of ranking plants for their salt tolerance. A total of 11 coastal halophytes of the Kavak Delta were evaluated for their ability to cope with different soil salinities. For this, electrical conductivities of soils (of up to 135 dS m(-1)) were recorded and a total of 100 plant samples, including plant roots, were taken from a depth of 0-15 cm in the soil. The halophytes were ranked in the following order from highest to moderate salt tolerance: Halocnemum strobilaceum >= Salicornia fragilis >= Arthrocnemum fruticosum = Suaeda prostrata >= Salsola kali = Petrosimonia brachiata >= Juncus maritimus = Aeluropus littoralis >= Halimione portulacoides = Limonium graecum >= Artemisia santonicum. The Na+/K+ ratios of leaves perfectly reflected the salinity tolerance ranking of all halophytic species examined. It proved possible to rank the salt tolerance of halophytes by assessment of the electrical conductivity of the soil in which they grew naturally; tolerance was well predicted by the Na+/K+ ratio in the shoots

Is chloride toxic to seed germination in mixed-salt environments? A case study with the coastal halophyte Suaeda maritima in the presence of seawater

Abstract Most salt tolerant plants, halophytes, use seed germination for natural regeneration. However, germination in mixed-salt environments such as seawater is poorly understood and ion toxicity by Cl−, the most highly concentrated ion in seawater, is rarely considered over Na+. Here, we investigate Cl− toxicity in the germination of the halophyte Suaeda maritima in the presence of artificial seawater (ASW). Seeds were germinated at 15/5 °C in dilutions of ASW and at concentrations of NaCl, MgCl2, CaCl2 and KCl as found in ASW. Solutions of polyethylene glycol (PEG) were used for osmotic comparison. Germination percentage and normal seedlings were quantified. Non-germinated seeds were tested for recovery on water. Germination rate (1/t50) was used in a halotime model to quantify the maximum concentration of Cl− (Cl−max) and Na+ (Na+max) for germination. Germination was most negatively affected when all salts were combined in the concentrations found in ASW. Recovery of non-germinated seeds from all salt treatments on water was low, but all germinated seeds formed normal seedlings. Germination on ASW was higher than on iso-osmotic solutions of PEG. The 1/t50 decreased with increasing Cl− and Na+ concentration, indicating maximum thresholds to germination at 1381 mM (Cl−max) and 1262 mM (Na+max). The results indicate that ASW does not produce an osmotic limitation to the germination of S. maritima, and exposure to salt ions can even promote germination. However, ion toxicity is the major limitation, with Cl− similarly as toxic as Na+. In mixed-salt environments such as seawater, Cl− toxicity should not be overlooked

Salt tolerance in rice: seedling and reproductive stage QTL mapping come of age

Key message Reproductive stage salinity tolerance is most critical for rice as it determines the yield under stress. Few studies have been undertaken for this trait as phenotyping was cumbersome, but new methodology outlined in this review seeks to redress this deficiency. Sixty-three meta-QTLs, the most important genomic regions to target for enhancing salinity tolerance, are reported. Abstract Although rice has been categorized as a salt-sensitive crop, it is not equally affected throughout its growth, being most sensitive at the seedling and reproductive stages. However, a very poor correlation exists between sensitivity at these two stages, which suggests that the effects of salt are determined by different mechanisms and sets of genes (QTLs) in seedlings and during flowering. Although tolerance at the reproductive stage is arguably the more important, as it translates directly into grain yield, more than 90% of publications on the effects of salinity on rice are limited to the seedling stage. Only a few studies have been conducted on tolerance at the reproductive stage, as phenotyping is cumbersome. In this review, we list the varieties of rice released for salinity tolerance traits, those being commercially cultivated in salt-affected soils and summarize phenotyping methodologies. Since further increases in tolerance are needed to maintain future productivity, we highlight work on phenotyping for salinity tolerance at the reproductive stage. We have constructed an exhaustive list of the 935 reported QTLs for salinity tolerance in rice at the seedling and reproductive stages. We illustrate the chromosome locations of 63 meta-QTLs (with 95% confidence interval) that indicate the most important genomic regions for salt tolerance in rice. Further study of these QTLs should enhance our understanding of salt tolerance in rice and, if targeted, will have the highest probability of success for marker-assisted selections

Elliptic curves, modular forms, and sums of Hurwitz class numbers

Let H(N) denote the Hurwitz class number. It is known that if $p$ is a prime, then {equation*} \sum_{|r|<2\sqrt p}H(4p-r^2) = 2p. {equation*} In this paper, we investigate the behavior of this sum with the additional condition $r\equiv c\pmod m$. Three different methods will be explored for determining the values of such sums. First, we will count isomorphism classes of elliptic curves over finite fields. Second, we will express the sums as coefficients of modular forms. Third, we will manipulate the Eichler-Selberg trace for ula for Hecke operators to obtain Hurwitz class number relations. The cases $m=2,3$ and 4 are treated in full. Partial results, as well as several conjectures, are given for $m=5$ and 7.Comment: Preprint of an old pape

Tissue tolerance: an essential but elusive trait for salt-tolerant crops

For a plant to persist in saline soil, osmotic adjustment of all plant cells is essential. The more salt-tolerant species accumulate Na+ and Cl– to concentrations in leaves and roots that are similar to the external solution, thus allowing energy-efficient osmotic adjustment. Adverse effects of Na+ and Cl– on metabolism must be avoided, resulting in a situation known as ‘tissue tolerance’. The strategy of sequestering Na+ and Cl– in vacuoles and keeping concentrations low in the cytoplasm is an important contributor to tissue tolerance. Although there are clear differences between species in the ability to accommodate these ions in their leaves, it remains unknown whether there is genetic variation in this ability within a species. This viewpoint considers the concept of tissue tolerance, and how to measure it. Four conclusions are drawn: (1) osmotic adjustment is inseparable from the trait of tissue tolerance; (2) energy-efficient osmotic adjustment should involve ions and only minimal organic solutes; (3) screening methods should focus on measuring tolerance, not injury; and (4) high-throughput protocols that avoid the need for control plants and multiple Na+ or Cl- measurements should be developed. We present guidelines to identify useful genetic variation in tissue tolerance that can be harnessed for plant breeding of salt tolerance

Space Transportation System (STS)-117 External Tank (ET)-124 Hail Damage Repair Assessment

Severe thunderstorms with associated hail and high winds struck the STS-117 stack on February 26, 2007. Peak winds were recorded at 62 knots with hail sizes ranging from 0.3 inch to 0.8 inch in diameter. As a result of the storm, the North Carolina Foam Institute (NCFI) type 24-124 Thermal Protection System (TPS) foam on the liquid oxygen (LO2) ogive acreage incurred significant impact damage. The NCFI on the ET intertank and the liquid hydrogen (LH2) acreage sustained hail damage. The Polymer Development Laboratory (PDL)-1034 foam of the LO2 ice frost ramps (IFRs) and the Super-Lightweight Ablator (SLA) of the LO2 cable tray also suffered minor damage. NASA Engineering and Safety Center (NESC) was asked to assess the technical feasibility of repairing the ET TPS, the reasonableness of conducting those repairs with the vehicle in a vertical, integrated configuration at the Kennedy Space Center (KSC) Vehicle Assemble Building (VAB), and to address attendant human factors considerations including worker fatigue and the potential for error. The outcome of the assessment is recorded in this document

A New Algorithm for Supernova Neutrino Transport and Some Applications

We have developed an implicit, multi-group, time-dependent, spherical neutrino transport code based on the Feautrier variables, the tangent-ray method, and accelerated ${\bf \Lambda}$ iteration. The code achieves high angular resolution, is good to O($v/c$), is equivalent to a Boltzmann solver (without gravitational redshifts), and solves the transport equation at all optical depths with precision. In this paper, we present our formulation of the relevant numerics and microphysics and explore protoneutron star atmospheres for snapshot post-bounce models. Our major focus is on spectra, neutrino-matter heating rates, Eddington factors, angular distributions, and phase-space occupancies. In addition, we investigate the influence on neutrino spectra and heating of final-state electron blocking, stimulated absorption, velocity terms in the transport equation, neutrino-nucleon scattering asymmetry, and weak magnetism and recoil effects. Furthermore, we compare the emergent spectra and heating rates obtained using full transport with those obtained using representative flux-limited transport formulations to gauge their accuracy and viability. Finally, we derive useful formulae for the neutrino source strength due to nucleon-nucleon bremsstrahlung and determine bremsstrahlung's influence on the emergent $\nu_{\mu}$ and $\nu_{\tau}$ neutrino spectra.Comment: 58 pages, single-spaced LaTeX, 23 figures, revised title, also available at http://jupiter.as.arizona.edu/~burrows/papers, accepted for publication in the Ap.