Hydrothermal time analysis of watermelon (<Emphasis Type="Italic">Citrullus vulgaris</Emphasis> cv. ‘Crimson sweet’) seed germination

This study evaluated the ability of a hydrothermal time model (HTT) to describe the kinetics of watermelon (Citrullus vulgaris cv. ‘Crimson sweet’) seed germination under different temperatures (T) and water potentials (ψ) and also to determine the cardinal temperatures of watermelon. Results indicated that ψ influenced germination rate and germination percentage. For this seed lot, cardinal temperatures were 10 °C for T _b, 28.34 °C for T _o and 40.8 °C for T _c in the control (0 MPa) treatment. There was a decrease in hydrotime constant (θ _H) when T was increased to T _o and then remained constant at supra-optimal temperatures (30 MPah^?1). Also, at temperatures above T _o, ψ _b(50) values increased linearly with T. The k _T value (the slope of the relationship between ψ _b(50) and T exceeds T _o) of this seed lot was calculated as 0.076 MPa°Ch^?1. Results this study show that when the HTT model is applied, it can accurately describe ψ _b(g) and the course of germination around Ts (R ² = 0.82). Moreover, the ψ _b(50) was estimated to be ?0.96 MPa based on this model. Consequently, the germination response of watermelon for all Ts and ψs can be adequately described by the HTT model and enabling it to be used as a predictive tool in watermelon seed germination simulation models.     

Using hydrothermal time concept to describe sesame (<Emphasis Type="Italic">Sesamum indicum</Emphasis> L.) seed germination response to temperature and water potential

To quantify both temperature (T) and water potential (ψ) effects on sesame (Sesamum indicum L.) seed germination (SG) and also to determine the cardinal T _s for this plant, a laboratory experiment was carried out using hydrothermal time model (HTT). For this purpose, four sesame cultivars (‘Asbomahalleh’, ‘Darab’, ‘Dashtestan’ and ‘Yellowhite’) were germinated at seven constant T _s (20, 25, 30, 35, 37, 39 and 43 °C) at each of the following ψ _s (0, ? 0.12, ? 0.24 and ? 0.36 MPa; provided by PEG 8000). Germination rate (GR) and germination percentage (GP) significantly influenced by ψ, T and their interactions in all cultivars (P ≤ 0.01). There was no significant difference, based on the confidence intervals of the model coefficients, between cultivars, so an average of cardinal T _s was 14.7, 35.4 and 47.2 °C for the minimum (T _b), optimum (T _o) and maximum (T _c) T _s, respectively, in the control condition (0 MPa). Hydrotime values in all cultivars decreased when T was increased to T _o and then remained constant at T _s > T _o (15 MPa h^?1). An average value of ψ _b(50) was estimated to be ? 1.23 MPa at T _s ≤ T _o and then increased linearly (0.1041 MPa°Ch^?1, the slope of the relationship between ψ _b(50) and supra-optimal T _s) with T when T _s increased above T _o and finally reached to zero at T _c. The T _b and T _o values were not influenced by ψ, but T _c value decreased (from 47.2 for zero to 43.5 °C for ? 0.36 MPa) at supra-optimal T _s as a result of the effect of ψ on GR. Based on our findings, this model (as a predictive tool) and or the estimated parameter values in this study can easily be used in sesame SG simulation models to quantitatively characterize the physiological status of sesame seed populations at different T _s and ψ _s.     

Modeling seed germination in Melisa officinalis L. in response to temperature and water potential

Seed germination is greatly influenced by both temperature (T) and water potential (ψ) and these factors largely determine germination rate (GR) in the field. Quantitative information about T and ψ effects on seed germination in lemon balm (Melisa officinalis L.) is scarce. The main objective of this study was to quantify seed germination responses of lemon balm to T and ψ, and to determine cardinal temperatures in a laboratory experiment. A segmented model was used to describe the effects of ψ (i.e., T) on GR and other germination parameters. The segmented model estimates were 7.2 °C for base (T _b), 28.9 °C for optimum (T _o), 40.1 °C for ceiling temperature (T _c) and 1.64 physiological days (f _o) (equivalent to a GR_max of 0.610 d^?1 and a thermal time of 35.6 °C days) to reach 50 % maximum germination in the control (0 MPa) treatment (R ² = 0.99, RMSE = 0.005 day^?1). The inherent maximum rate of germination (days) was calculated by the [GR_max = 1/f _o] model. ψ affected cardinal temperatures. From 0 to ?0.76 MPa, when ψ increased, T _b was a constant 7.2 °C to ?0.38 MPa and increased linearly to 20.1 °C as ψ decreased. T _o and f _o increased linearly from 28.9 to 30 °C, and from 1.64 to 5.4 day^?1, respectively as ψ decreased. However, there was no signification difference in T _o as ψ decreased nor did T _c decrease from 40.1 to 35 °C as ψ decreased. T _b, T _c and GR_max were the sole parameters affected by ψ and could be used to characterize differences between ψ treatments with respect to GR at various Ts. Therefore, the segmented model and its parameters can be used in lemon balm germination simulation models.     

Quantification of the Effect of Environmental Factors on Seed Germination and Seedling Growth of Eruca (Eruca sativa) Using Mathematical Models

Eruca (Eruca sativa; Brassicaceae) is an important industrial crop due to its ability to grow under a wide range of climatic conditions and in poor fertility lands and also for the quality of seed oil and protein. Seed germination (SG) is an important event in plant’s life history which can significantly be influenced by several environmental factors such as temperature (T), water potential (ψ), salinity, pH, and burial depth. Therefore, this study aimed (i) to investigate the effects of these environmental factors on SG behavior of Eruca using several mathematical models, (ii) to determine the cardinal Ts and tolerance threshold value for each trait (i.e., 50% reduction than its maximum value) affected by the environmental factor, and (iii) to quantify the response of Eruca seedling growth to each environmental factor. The results indicated that Eruca SG and seedling growth were significantly influenced by these factors (P < 0.05). The estimated cardinal Ts were 1 °C for the base T, 30 °C for the optimum T, and 40.8 °C for the ceiling T. The salt and drought tolerance threshold values were 257 mM NaCl and − 1.2 MPa for SG and 247 mM NaCl and − 1 MPa for the seedling growth, respectively, suggesting that the seedling growth was more sensitive than SG under both salt and drought stresses in Eruca. In addition, the maximum SG and seedling growth were observed at pH 7 and burial depth 1.9 cm. In general, the models used in this study could describe well the response of Eruca SG under different levels of environmental factors and also their parameters could easily be used in Eruca SG simulation models. This information also could help us to better manage the production of this plant under stressful conditions and/or to determine its geographic range expansion in the world.

     

Diversity in amylopectin structure, thermal and pasting properties of starches from wheat varieties/lines

Structural, thermal and pasting diversity of starches from Indian and exotic lines of wheat was studied. Majority of the starches showed amylose content ranging between 22% and 28%. Endotherm temperatures (T_o, T_p and T_c) of the starches showed a range between 56–57, 60 –61 and 65.5–66.5 °C, respectively. Exotherms with T_p between 87.0 and 88.2 °C were observed during cooling of heated starches, indicating the presence of amylose–lipid complexes. Exotherm temperatures were negatively correlated to swelling power. Amylopectin unit chains with different degree of polymerization (DP) were observed to be associated with pasting temperature, setback and thermal (endothermic T_o, T_p, and T_c) parameters. Amylopectin unit chains of DP 13–24 showed positive relationship with endothermic T_o, T_p and T_c. Pasting temperature showed positive correlation with short chains (DP 6–12) while negative correlation with medium chain (DP 13–24) amylopectins. Setback was positively correlated to DP 16–18 and negatively to DSC amylose–lipid parameters.     

Thermal buffering capacity of the germination phenotype across the environmental envelope of the Cactaceae

Recruitment from seeds is among the most vulnerable stage for plants as global temperatures change. While germination is the means by which the vast majority of the world's flora regenerate naturally, a framework for accurately predicting which species are at greatest risk of germination failure during environmental perturbation is lacking. Taking a physiological approach, we assess how one family, the Cactaceae, may respond to global temperature change based on the thermal buffering capacity of the germination phenotype. We selected 55 cactus species from the Americas, all geo‐referenced seed collections, reflecting the broad environmental envelope of the family across 70° of latitude and 3700 m of altitude. We then generated empirical data of the thermal germination response from which we estimated the minimum (T_b), optimum (T_o) and ceiling (T_c) temperature for germination and the thermal time (θ₅₀) for each species based on the linearity of germination rate with temperature. Species with the highest T_b and lowest T_c germinated fastest, and the interspecific sensitivity of the germination rate to temperature, as assessed through θ₅₀, varied tenfold. A left‐skewed asymmetry in the germination rate with temperature was relatively common but the unimodal pattern typical of crop species failed for nearly half of the species due to insensitivity to temperature change at T_o. For 32 fully characterized species, seed thermal parameters correlated strongly with the mean temperature of the wettest quarter of the seed collection sites. By projecting the mean temperature of the wettest quarter under two climate change scenarios, we predict under the least conservative scenario (+3.7°C) that 25% of cactus species will have reduced germination performance, whilst the remainder will have an efficiency gain, by the end of the 21st century.     

A hydrothermal time model explains the cardinal temperatures for seed germination

Temperature (T) and water potential (y) are two primary environmental regulators of seed germination. Seeds exhibit a base or minimum T for germination (T_b), an optimum T at which germination is most rapid (T_o), and a maximum or ceiling T at which germination is prevented (T_c). Germination at suboptimal T can be characterized on the basis of thermal time, or the T in excess of T_b multiplied by the time to a given germination percentage (t_g). Similarly, germination at reduced y can be characterized on a hydrotime basis, or t_g multiplied by the y in excess of a base or threshold y that just prevents germination (y_b). Within a seed population, the variation in thermal times to germination among different seed fractions (g) is based on a normal distribution of y_b values among seeds (y_b(g)). Germination responses across a range of suboptimal T and y can be described by a general hydrothermal time model that combines the T and y components, but this model does not account for the decrease in germination rates and percentages when T exceeds T_o. We report here that supra‐optimal temperatures shift the ψ_b(g) distribution of a potato (Solanum tuberosum L.) seed population to more positive values, explaining why both germination rates and percentages are reduced as T increases above T_o. A modified hydrothermal time model incorporating changes in ψ_b(g) at T > T_o describes germination timing and percentage across all T and ψ at which germination can occur and provides physiologically relevant indices of seed behaviour.     

Oceanibacterium hippocampi gen. nov., sp. nov., isolated from cutaneous mucus of wild seahorses (Hippocampus guttulatus)

A Gram-negative, aerobic, motile and slightly curved rod-shaped bacterium (BFLP-8^T) was isolated from cutaneous mucus of wild long-snouted seahorses (Hippocampus guttulatus) captured in northwest Spain (Toralla, Galicia). Strain BFLP-8^T grew at 10–35 °C and pH 5–9 (optimally at 25 °C and pH 7.0) and with 1–6 % (w/v) NaCl (optimally with 2 % NaCl). The predominant respiratory quinone (90 %) was ubiquinone with ten isoprene units (Q-10) and the major fatty acids identified were C_18:1 ω7c (54.8 % of the total), C_19:0 cyclo ω8c (11.6 %), C_16:0 (9.5 %), C_18:1 2-OH (7.1 %) and C_16:1 ω11c (6.7 %). The G+C content of the DNA was 57.8 mol%. Phylogenetic analysis based on 16S rRNA gene sequences showed that strain BFLP-8^T formed a distinct clade within the family Sneathiellaceae but is not specifically associated with any species in the family. On the basis of phenotypic, chemotaxonomic and phylogenetic data, strain BFLP-8^T represents a novel species within a new genus, for which the name Oceanibacterium hippocampi gen. nov., sp. nov. is proposed. The type strain is BFLP-8^T (=CECT 7691^T = DSM 23444^T).     

Design of a Frequency Reconfigurable Broadband THz Antenna Based on the Vanadium Dioxide

In this article, the design of a frequency reconfigurable broadband THz antenna based on vanadium dioxide (VO₂) is investigated. Instead of being fed by the microstrip line directly, a windmill-shaped feeding structure is designed to provide a proximity-coupled feeding method. Many modes with contiguous resonant frequencies can be excited to obtain the wideband performance. The proposed antenna combines gold with metamaterial VO₂. Thanks to insulator-metal phase transition characteristic of VO₂ at phase transition temperature (68 °C), we can change the length of the resonant branches to realize frequency reconfiguration by changing the external temperature (T). The simulated results illustrate that when T = 50 °C (State I), such an antenna has a bandwidth of 35.2% (7.01–10 THz) with S₁₁ below − 10 dB, and a maximum gain of 6.62 dBic. When T = 80 °C (State II), it has a bandwidth of 21.8% (5.77–7.18 THz) with S₁₁ below − 10 dB, and a maximum gain of 4.49 dBic. Thus, we realize a design of a proximity-coupled antenna with reconfigurable wideband over the THz band.

     

Local Osmosis and Isotonic Transport

Osmotically driven water flow, u (cm/s), between two solutions of identical osmolarity, c_o (300 mM in mammals), has a theoretical isotonic maximum given by u = j/c_o, where j (moles/cm²/s) is the rate of salt transport. In many experimental studies, transport was found to be indistinguishable from isotonic. The purpose of this work is to investigate the conditions for u to approach isotonic. A necessary condition is that the membrane salt/water permeability ratio, ε, must be small: typical physiological values are ε = 10⁻³ to 10⁻⁵, so ε is generally small but this is not sufficient to guarantee near-isotonic transport. If we consider the simplest model of two series membranes, which secrete a tear or drop of sweat (i.e., there are no externally-imposed boundary conditions on the secretion), diffusion is negligible and the predicted osmolarities are: basal = c_o, intracellular ≈ (1 + ε)c_o, secretion ≈ (1 + 2ε)c_o, and u ≈ (1 − 2ε)j/c_o. Note that this model is also appropriate when the transported solution is experimentally collected. Thus, in the absence of external boundary conditions, transport is experimentally indistinguishable from isotonic. However, if external boundary conditions set salt concentrations to c_o on both sides of the epithelium, then fluid transport depends on distributed osmotic gradients in lateral spaces. If lateral spaces are too short and wide, diffusion dominates convection, reduces osmotic gradients and fluid flow is significantly less than isotonic. Moreover, because apical and basolateral membrane water fluxes are linked by the intracellular osmolarity, water flow is maximum when the total water permeability of basolateral membranes equals that of apical membranes. In the context of the renal proximal tubule, data suggest it is transporting at near optimal conditions. Nevertheless, typical physiological values suggest the newly filtered fluid is reabsorbed at a rate u ≈ 0.86 j/c_o, so a hypertonic solution is being reabsorbed. The osmolarity of the filtrate c_F (M) will therefore diminish with distance from the site of filtration (the glomerulus) until the solution being transported is isotonic with the filtrate, u = j/c_F.With this steady-state condition, the distributed model becomes approximately equivalent to two membranes in series. The osmolarities are now: c_F ≈ (1 − 2ε)j/c_o, intracellular ≈ (1 − ε)c_o, lateral spaces ≈ c_o, and u ≈(1 + 2ε)j/c_o. The change in c_F is predicted to occur with a length constant of about 0.3 cm. Thus, membrane transport tends to adjust transmembrane osmotic gradients toward εc_o, which induces water flow that is isotonic to within order ε. These findings provide a plausible hypothesis on how the proximal tubule or other epithelia appear to transport an isotonic solution.     

Photosynthetic temperature response of the Antarctic vascular plants Colobanthus quitensis and Deschampsia antarctica

The photosynthetic temperature response of the Antarctic vascular plants Colobanthus quitensis and Deschampsia antarctica was examined by measuring whole-canopy CO₂ gas exchange and chlorophyll (Chl) a fluorescence of plants growing near Palmer Station along the Antarctic Peninsula. Both species had negligible midday net photosynthetic rates (P_n) on warm, usually sunny, days (canopy air temperature [T_c]> 20°C), but had relatively high P_n on cool days (T_c<10°C). Laboratory measurements of light and temperature responses of P_n showed that high temperature, not visible irradiance, was responsible for depressions in P_n on warm sunny days. The optimal leaf temperatures (T_l) for P_n in C. quitensis and D. antarctica were 14 and 10°C, respectively. Both species had substantial positive P_n at 0°C T_l, which were 28 (C. quitensis) and 32% (D. antarctica) of their maximal P_n, and we estimate that their low-temperature compensation points occurred at ?2°C T_l (C. quitensis) and ?3°C (D. antarctica). Because of the strong warming trend along the peninsula over recent decades and predictions that this will continue, we were particularly interested in the mechanisms responsible for their negligible rates of P_n on warm days and their unusually low high-temperature compensation points (i.e., 26°C in C. quitensis and 22°C in D. antarctica). Low P_n at supraoptimal temperature (25°C) appeared to be largely due to high rates of temperature-enhanced respiration. However, there was also evidence for direct impairment of the photosynthetic apparatus at supraoptimal temperature, based on Chl fluorescence and P_n/intercellular CO₂ concentration (c_i) response curve analyses. The breakpoint or critical temperature (T_cr) of minimal fluorescence (F_o) was ≈42°C in both species, which was well above the temperatures where reductions in P_n were evident, indicating that thylakoid membranes were structurally intact at supraoptimal temperatures for P_n. The optimal T_l for photochemical quenching (q_p) and the quantum yield of photosystem II (PSII) electron transfer (φ_PSII) were 9 and 7°C in C. quitensis and D. antarctica, respectively. Supraoptimal temperatures resulted in lower q_p and greater non-photochemical quenching (q_NP), but had little effect on F_o, maximal fluorescence (F_m) or the ratio of variable to maximal fluorescence (F_v/F_m) in both species. In addition, carboxylation efficiencies or initial slopes of their P_n/c_i response were lower at supraoptimal temperatures, suggesting reduced activity of ribulose-1,5-bisphosphate carboxylase/oxygenase (Rubisco). Although continued warming along the peninsula will increase the frequency of supraoptimal temperatures, T_c at our field site averaged 4.3°C and was below the temperature optima for P_n in these species for the majority of diurnal periods (86%) during the growing season, suggesting that continued warming will usually improve their rates of P_n.     

Hemoglobin senses body temperature

When aspirating human red blood cells (RBCs) into 1.3 μm pipettes (ΔP = −2.3 kPa), a transition from blocking the pipette below a critical temperature T _c = 36.3 ± 0.3°C to passing it above the T _c occurred (micropipette passage transition). With a 1.1 μm pipette no passage was seen which enabled RBC volume measurements also above T _c. With increasing temperature RBCs lost volume significantly faster below than above a T _c = 36.4 ± 0.7 (volume transition). Colloid osmotic pressure (COP) measurements of RBCs in autologous plasma (25°C ≤ T ≤ 39.5°C) showed a T _c at 37.1 ± 0.2°C above which the COP rapidly decreased (COP transition). In NMR T₁-relaxation time measurements, the T₁ of RBCs in autologous plasma changed from a linear (r = 0.99) increment below T _c = 37 ± 1°C at a rate of 0.023 s/K into zero slope above T _c (RBC T₁ transition). In conclusion: An amorphous hemoglobin–water gel formed in the spherical trail, the residual partial sphere of the aspirated RBC. At T _c, a sudden fluidization of the gel occurs. All changes mentioned above happen at a distinct T _c close to body temperature. The T _c is moved +0.8°C to higher temperatures when a D₂O buffer is used. We suggest a mechanism similar to a “glass transition” or a “colloidal phase transition”. At T _c, the stabilizing Hb bound water molecules reach a threshold number enabling a partial Hb unfolding. Thus, Hb senses body temperature which must be inscribed in the primary structure of hemoglobin and possibly other proteins. This article is dedicated to Ludwig Artmann who died on July 21, 2001 on a beautiful summer day during which we performed experiments far away. Ludwig Artmann was a man who encouraged us to be strong and to study hard no matter what were the costs.     

<Emphasis Type="Italic">Poseidonocella pacifica</Emphasis> gen. nov., sp. nov. and <Emphasis Type="Italic">Poseidonocella sedimentorum</Emphasis> sp. nov., novel alphaproteobacteria from the shallow sandy sediments of the Sea of Japan

The taxonomic study of two Gram-negative, aerobic, non-pigmented bacteria KMM 9010^T and KMM 9023^T isolated from a sandy sediment sample collected from the Sea of Japan seashore was performed. On the basis of the nearly complete 16S rRNA gene sequences, strains KMM 9010^T and KMM 9023^T clustered with the Roseobacter lineage (class Alphaproteobacteria) forming a distinct phylogenetic line adjacent to the genus Donghicola. Novel strains shared the highest sequence similarity of 96.4% to each other and lower than 96.1% similarities to other validly named genera of the class Alphaproteobacteria. In both strains, ubiquinone Q-10 was found to be the major respiratory quinone; phosphatidylcholine, phosphatidylglycerol, diphosphatidylglycerol, phosphatidic acid, and an unknown aminolipid were the major polar lipids and C_18:1ω7c and 11-methyl C_18:1ω7c were predominant fatty acids. The DNA G+C content was 60.5 mol% (KMM 9010^T) and 65.4 mol% (KMM 9023^T). Based on phenotypic properties and phylogenetic evidence, strains KMM 9010^T and KMM 9023^T should be classified as two novel species in a new genus, Poseidonocella gen. nov., with Poseidonocella pacifica sp. nov., the type species with the type strain KMM 9010^T (= NRIC 0794^T = JCM 17310^T), and Poseidonocella sedimentorum sp. nov. as the second species with the type strain KMM 9023^T (= NRIC 0796^T = JCM 17311^T).     

Deinococcus aestuarii sp. nov. and Deinococcus aquaedulcis sp. nov., two novel resistant bacteria isolated from pearl river estuary

Two novel species of the genus Deinococcus, designated SYSU M49105^T and SYSU M42101^T, were isolated from freshwater samples of the Pearl River estuary in Guangdong, China. Phylogenetic analysis using 16S rRNA gene sequence indicated that strains SYSU M49105^T and SYSU M42101^T showed the highest sequence similarities to Deinococcus aetherius JCM 11751 ^T (93.6%) and Deinococcus multiflagellatus NBRC 112888 ^T (97.3%), respectively. Cells of both strains were Gram-staining positive, aerobic, coccus-shaped, oxidase-negative and non-motile. The cell wall contained meso-diaminopimelic acid as their diagnostic diamino acid. MK-8 was the predominant respiratory quinone for both strains. The polar lipid profile of SYSU M49105^T contained two unidentified phosphoglycolipids, nine unidentified glycolipids, and five unidentified polar lipids. SYSU M42101^T had one unidentified phosphoglycolipid, nine unidentified glycolipids, one unidentified aminophospholipid and four unidentified polar lipids. The major fatty acids of strains SYSU M49105^T and SYSU M42101^T were summed feature 3 (C_16:1 ω7c and/ or C_16:1 ω6c) and C_16:0. The G?+?C contents of the novel isolates based on genomic DNAs were 69.6% and 67.4%, respectively. On the basis of phenotypic, genotypic and phylogenetic data, strains SYSU M49105^T and SYSU M42101^T should be considered to represent two novel species in the genus Deinococcus, for which the names Deinococcus aestuarii sp. nov. and Deinococcus aquaedulcis sp. nov. were proposed with the type strains SYSU M49105^T (=?KCTC 43258 ^T?=?CGMCC 1.18609 ^T) and SYSU M42101^T (=?KCTC 43257 ^T?=?CGMCC 1.18614 ^T), respectively.

     

Single-channel properties of a stretch-sensitive chloride channel in the human mast cell line HMC-1

A stretch-activated (SA) Cl⁻ channel in the plasma membrane of the human mast cell line HMC-1 was identified in outside-out patch-clamp experiments. SA currents, induced by pressure applied to the pipette, exhibited voltage dependence with strong outward rectification (55.1 pS at +100 mV and an about tenfold lower conductance at −100 mV). The probability of the SA channel being open (P _o) also showed steep outward rectification and pressure dependence. The open-time distribution was fitted with three components with time constants of τ_1o = 755.1 ms, τ_2o = 166.4 ms, and τ_3o = 16.5 ms at +60 mV. The closed-time distribution also required three components with time constants of τ_1c = 661.6 ms, τ_2c = 253.2 ms, and τ_3c = 5.6 ms at +60 mV. Lowering extracellular Cl⁻ concentration reduced the conductance, shifted the reversal potential toward chloride reversal potential, and decreased the P _o at positive potentials. The SA Cl⁻ currents were reversibly blocked by the chloride channel blocker 4,4′-diisothiocyanatostilbene-2,2′-disulfonic acid (DIDS) but not by (Z)-1-(p-dimethylaminoethoxyphenyl)-1,2-diphenyl-1-butene (tamoxifen). Furthermore, in HMC-1 cells swelling due to osmotic stress, DIDS could inhibit the increase in intracellular [Ca²⁺] and degranulation. We conclude that in the HMC-1 cell line, the SA outward currents are mediated by Cl⁻ influx. The SA Cl⁻ channel might contribute to mast cell degranulation caused by mechanical stimuli or accelerate membrane fusion during the degranulation process.     

Length to weight ratio of four fish species in estuary areas in the Northeast region of Brazil

The length to weight ratio (LWR) was used to estimate populations of four fish species sampled on the Amazon coast of the state of Maranhão, Brazil. The fishes were sampled in 2018 and 2019 by artisanal coastal fishing, using gillnets (0.20–0.60 mm). The parameters a and b of the equation W_T = a L_T^b were estimated. The obtained LWRs were W_T = 0.06LT^2.93, (r²) = .989 for Oligoplites saliens; W_T = 0.061L_T^2.57, (r²) = .982 for Peprilus crenulatus; W_T = 0.014L_T^2.80, (r²) = .985 for Bagre bagre; and W_T = 0.035L_T^3.21, (r²) = .981 for Nebris microps.     

<Emphasis Type="Italic">Alteromonas halophila</Emphasis> sp. nov., a new moderately halophilic bacterium isolated from a sea anemone

A pale yellow-colored, moderately halophilic, Gram-negative, catalase- and oxidase-positive, non-sporulating, rod-shaped, motile, aerobic bacterium, designated strain JSM 073008^T, was isolated from a sea anemone (Anthopleura xanthogrammica) collected from Naozhou Island, Leizhou Bay, South China Sea. The organism was able to grow with 1–20% (w/v) total salts (optimum, 5–10%), at pH 6.0–10.0 (optimum, pH 7.5) and 10–40°C (optimum, 25–30°C). The major cellular fatty acids were C_16:0, C_16:1 ω7c/iso-C_15:0 2-OH and C_18:1 ω7c. The polar lipids consisted of phosphatidylethanolamine, phosphatidylglycerol and an unidentified phospholipid. The predominant respiratory quinone was Q-8 and the genomic DNA G + C content was 47.5 mol%. Phylogenetic analysis based on 16S rRNA gene sequences indicated that strain JSM 073008^T should be assigned to the genus Alteromonas, being most closely related to Alteromonas hispanica F-32^T (sequence similarity 96.9%), followed by Alteromonas genovensis LMG 24078^T (96.6%) and Alteromonas litorea TF-22^T (96.4%). The sequence similarities between the novel isolate and the type strains of other recognized Alteromonas species ranged from 95.9% (with Alteromonas stellipolaris ANT 69a^T) to 94.5% (with Alteromonas simiduii BCRC 17572^T). The combination of phylogenetic analysis, phenotypic characteristics and chemotaxonomic data supported the view that strain JSM 073008^T represents a new species of the genus Alteromonas, for which the name Alteromonas halophila sp. nov. is proposed. The type strain is JSM 073008^T (=CCTCC AA 207035^T = KCTC 22164^T). The authors Yi-Guang Chen and Huai-Dong Xiao have contributed equally to this work.     

Leaf tensity: a method for rapid determination of water requirement information in Brassica napus L.

Water regulation caused by enzymes, such as carbonic anhydrase (CA), changes the water status, making it difficult to diagnose water deficit using leaf water potential (ψ_L) or stomatal conductance (g_s). Therefore, new methods for timely and accurately determining plant water status should be established. In this study, CA activity, ψ_L, leaf tensity (T_d), photosynthetic characteristics and plant growth of Brassica napus L. seedlings under drought and subsequent rewatering were analysed. Results indicated that T_d could reflect the plant water status better than ψ_L or g_s and played an important role in the photosynthesis of B. napus. B. napus exhibited good restorability at the 40?g?L^?1 polyethylene glycol level. The rewatering strategy for B. napus was excellent at 40?g?L^?1 (?0.15?MPa) →20?g?L^?1 (?0.11?MPa). T_d could be used for the rapid determination of water requirement information in B. napus during winter drought period.     

Microvirga splendida sp. nov., bacteria isolated from soil

Two bacterial strains, BT325^T and BT690, were isolated from soil samples collected in Korea. Both strains were Gram stain-negative, short rod-shaped, and formed light-pink colored colonies. The 16S rRNA sequence similarity of strains BT325^T and BT690 shared a sequence similarity of 99.7%. Both strains shared the highest 16S rRNA gene similarity of 98.6% with Microvirga arabica SV2184P^T, followed by Microvirga ossetica V5/3 M T (98.5% and 98.2%, respectively), Microvirga soli R491^T (98.3% and 98.2%, respectively), Microvirga aerilata (98.2% and 98.08%, respectively), Microvirga makkahensis (98.08% and 97.8%, respectively). Phylogenetic analyses based on 16S rRNA gene sequences revealed that strain BT325^T and BT690 were positioned in a distinct lineage within the family Methylobacteriaceae (order Rhizobiales, class Alphaproteobacteria). The genome size of strain BT325^T was 5,200,315 bp and the genomic DNA G?+?C content was 64.3 mol%. The sole respiratory quinone of strain BT325^T was Q-10 and the predominant cellular fatty acids were summed feature 3 (C_16:1 ω7c/C_16:1 ω6c) and summed feature 8 (C_18:1 ω7c/C_18:1 ω6c). The major polar lipids were diphosphatidylglycerol, phosphatidylglycerol, phosphatidylethanolamine, and phosphatidylcholine. Polyphasic taxonomic analysis of biochemical, chemotaxonomic, and phylogenetic analyses suggested that strains BT325^T represents a novel bacterial species within the genus Microvirga, for which the name Microvirga splendida is proposed. The type strain of Microvirga splendida is BT325^T (=?KCTC 72406 ^T?=?NBRC 114847 ^T).

     

Altererythrobacter flava sp. nov., a new member of the family Erythrobacteraceae,isolated from a surface seawater sample

A Gram-stain-negative, light yellow pigmented, non-motile and aerobic bacterial strain, designated HHU E2-1 ^T, was isolated from a surface seawater sample. The 16S rRNA gene sequence analysis indicated that HHU E2-1 ^T shared the highest sequence similarity to the type strain Qipengyuania gaetbuli DSM 16225 ^T (96.90%), which belongs to the family Erythrobacteraceae. Combined phylogeny of 288 single-copy orthologous gene clusters, analysis of average nucleotide identity (ANI) and digital DNA-DNA hybridization (dDDH), average amino acid identity (AAI) and evolutionary distances suggested that HHU E2-1 ^T can be considered as a member of the genus Altererythrobacter based on the recently proposed standard for defining genera of Erythrobacteraceae. Strain HHU E2-1 ^T grew at 15–35 °C and pH 5.0–8.0, with optimum growth at 28 °C and pH 7.0. Tolerance to NaCl was up to 4% (w/v) with optimum growth in 2–3% NaCl. The major fatty acids (>?10%) were C_18:1ω7c11-methyl, summed feature 3 (C_16:1ω7c and/or C_16:1ω6c), and summed feature 8 (C_18:1ω7c and/or C_18:1ω6c). The predominant isoprenoid quinone was ubiquinone-10. The genomic G?+?C content was 57.40%. On the basis of the phenotypic, phylogenetic and chemotaxonomic characterizations, HHU E2-1 ^T represents a novel species of the genus Altererythrobacter, for which the name Altererythrobacter flava sp. nov. is proposed. The type strain is HHU E2-1 ^T (=?CGMCC 1.17394 ^T?=?KCTC 72835 ^T?=?MCCC 1K04226^T).