The use of hydrochloric acid to improve the germination of sugar-beet seed

This study confirmed that steeping sugar-beet seed in 0.3 M hydrochloric acid for 2 h as the first part of a 12 h treatment, substantially improved performance under cold, wet conditions. Smaller benefits were also found in warmer, drier tests; no detrimental effects were found. Adding excess sodium hydroxide at the end of the acid steep further improved the growth of the inherently slower part of the population under cold, wet conditions. Steeping seed in acid or acid followed by alkali also controlled Phoma betae as effectively as the current commercial thiram step treatment.     

A seed treatment for the control of Pythium damping-off diseases and Peronospora parasitica on brassicas

In soil inoculated with Pythium ultimum or Pythium irregulare, seed treatment with either Apron 70 (=1 g metalaxyl and 1 g captan/kg seed) or thiram gave control of pre-emergence damping-off of Brussels sprout and cabbage seedlings. On cauliflower, Apron 70 was significantly more effective than thiram. No post-emergence damping-off occurred in either of these crops or in oil-seed rape following seed treatment with Apron 70 whilst post-emergence losses from untreated seed ranged from 10·2–19·4% and from thiram treated seed from 5·7-7·4%. Apron 70 gave complete control of Peronospora parasitica on cauliflower inoculated 10 days after sowing; thiram was ineffective. Following seed treatment with Apron 70, metalaxyl was detected in the cotyledons, true leaves and roots of cabbage seedlings up to 4 wk from sowing.     

Aerated-steam treatment for control of Alter nana tenuis on lobelia seed

Alternaria tenuis may cause severe seedling blight, damping-off and leaf spotting of the bedding plant lobelia. Disease transmission from seed naturally and artificially infected by A. tenuis was demonstrated and the pathogenicity of four isolates established. Soaking of lobelia seed in 0–2% thiram suspension at 30 ^oC for 12 h adversely affected the rate of germination and did not consistently reduce infection to acceptable levels. Treatment with aerated steam at 50–51 ^oC for 15–20 min reduced seed infection to undetectable or insignificant levels and caused only slight damage to the seed. In glasshouse trials seed treated with aerated steam performed significantly better than seed soaked in thiram suspension both in terms of germination and foliage production.     

Is KCl a reliable extractant of15NH 4 + added to coastal marine sediments?

The release of NH ₄ ⁺ and¹⁵N-labelled NH ₄ ⁺ by one-step KCl extraction was assessed in different types of coastal marine sediments. KCl was efficient to extract NH ₄ ⁺ from sandy sediments and less efficient in silt sediments, where an extended extraction period was required for obtaining a maximum NH ₄ ⁺ yield. Extraction at 0 or 20 °C had only a little effect on the efficiency of KCl. KCl gave always non complete recovery of¹⁵NH ₄ ⁺ in silt sediments. However, the added label could be fully recovered by addition of 80 mol·cm^–3 exogenous NH ₄ ⁺ prior to KCl, or when NaCl or ASW replaced KCl.¹⁵NH ₄ ⁺ was added to non-biological silt sediment, which was incubated at 0 °C up to 16 hours, to see the effect of physical processes on the partition of¹⁵NH₄ among porewater (29–49%) exchangeable (9–30%) and non-extractable, organic bound pools (24–42%). Total¹⁵N recovery was approximately 100%. KCl failed to remove¹⁵NH₄ which entered to unknown, bound pools in sediment. Only shortly after addition of¹⁵N (0.1 h), the extraction period resulted in significantly different¹⁵N recoveries (P < 0.05) in KCl extractable NH ₄ ⁺ , 17% versus 9% of label was recovered after 1 min or 60 min extraction of sediment, respectively. Two hours of incubation time were required for complete equilibrium of¹⁵NH ₄ ⁺ among porewater, exchangeable and organic bound pools. Sediments (silt) to which¹⁵NH ₄ ⁺ has been added in order to measure NH ₄ ⁺ turn-over and KCl is used as extractant, should be incubated for at least 2 hours, before taking a zero-time sample.     

Ce^3+和La^3+对人工老化沙葱种子活力及生理特性的影响

以未老化和人工老化后的沙葱(Allium mongolicum Regel.)种子为材料,采用氯化铈(Ce3+)和氯化镧(La3+)浸种,测定种子萌发和生理指标,探讨Ce3+和La3+浸种对种子萌发、老化种子活力和生理特性的影响。结果显示:(1)在老化0~5 h时,Ce3+和La3+处理可显著促进沙葱种子萌发,提高种子活力;在老化5 h后,Ce3+和La3+处理对种子萌发无明显促进作用。(2)在老化0~15 h时,Ce3+和La3+处理的沙葱种子中抗氧化酶活性和抗坏血酸(AsA)含量提高,其超氧阴离子自由基(O2-·)产生速率、过氧化氢(H2O2)含量和丙二醛(MDA)含量显著降低;在老化15 h后,Ce3+和La3+处理的种子抗氧化酶活性提高、AsA含量降低,O2-·产生速率和MDA含量提高。(3)在老化5 h时,沙葱种子呼吸速率发生跃变达到最大,Ce3+和La3+处理显著降低了种子呼吸速率。(4)Ce3+和La3+处理在老化0~5 h时提高了沙葱种子超弱发光(UWL)强度,但在老化5 h后沙葱种子的UWL强度降低。研究认为,在沙葱种子人工老化初期,Ce3+和La3+浸种处理可以诱导增强种子抗氧化酶活性和提高AsA含量,有效清除因老化产生积累的过量活性氧(ROS),减轻过氧化伤害,提高种子活力;种子老化中后期,其内部ROS产生与清除系统发生紊乱,加剧了ROS对种子结构的损伤,Ce3+和La3+浸种处理的缓解效应丧失。     

A C-NMR study on the influxes into the tricarboxylic acid cycle of a renal epithelial cell line, LLC-PK1/Cl4: the metabolism of [2-C]glycine, l-[3-C]alanine and l-[3-C]aspartic acid in renal epithelial cells

Perchloric acid extracts of LLC-PK₁/Cl₄ cells, a renal epithelial cell line, incubated with either [2-¹³C]glycine l-[3-¹³C]alanine, or d,l-[3-¹³C]aspartic acid were investigated by ¹³C-NMR spectroscopy. All amino acids, except labelled glycine, gave rise to glycolytic products and tricarboxylic acid cycle (TCA) intermediates. For the first time we also observed activity of γ-glutamyltransferase activity and glutathione synthetase activity in LLC-PK₁ cells, as is evident from enrichment of reduced glutathione. Time courseS showed that only 6% of the labelled glycine was utilized in 30 min, whereas 31% of l-alanine and 60% of l-aspartic acid was utilized during the same period. ¹³C-NMR was also shown to be a useful tool for the determination of amino acid uptake in LLC-PK₁ cells. These uptake experiments indicated that glycine alanine and aspartic acid are transported into Cl₄ cells via a sodium-dependent process. From the relative enrichment of the glutamate carbons, we calculated the activity of pyruvate dehydrogenase to be about 61% of when labelled l-alanine was the only carbon source for LLC-PK₁/Cl₄ cells. Experiments with labelled d,l-aspartic, however, showed that about 40% of C-3-enriched oxaloacetate (arising from a de-amination of aspartic acid) reached the pyruvate pool.     

Microbial population dynamics on seeds during drum and steeping priming

In the UK, seeds are primed commercially via drum or steeping priming processes to improve seed germination and seedling establishment but the microbial population dynamics occurring during these processes are unknown. Consequently, changes in culturable bacterial and fungal populations that occurred during laboratory and commercial scale drum priming of carrot, leek and parsnip seed and during laboratory scale and commercial scale steeping priming of carrot and sugar beet seed were investigated. Populations of bacteria and pseudomonads increased by 2 and 4 log₁₀ cfu g^–1 seed during priming to reach between 7 and 10 log₁₀ cfu g^–1 seed with less than 1 log₁₀ cfu g^–1 seed decrease after redrying, irrespective of seed type or priming process. Pseudomonads represented approximately 10% of the culturable bacterial population. Fungal populations also increased by between 1 and 3 log₁₀ cfu g^–1 seed during priming of carrot, leek and parsnip seed and were little affected by redrying. Addition of a tefluthrin coating (a standard commercial insecticide treatment) during the drying stage of commercial scale drum priming had little effect on microbial populations. During steeping priming, populations of bacteria and pseudomonads on sugar beet also increased by 2 and 4 log₁₀ cfu g^–1 seed with less than 1 log₁₀ cfu g^–1 seed decrease after redrying. However, fungi did not increase in the same manner on sugar beet, suggesting that the sugar beet seed itself may have an inhibitory effect on fungal growth. The presence of thiram in the steeping liquid (a standard commercial fungicide treatment) inhibited fungal proliferation on carrot and sugar beet seed. Spore forming bacteria generally occurred at low levels on all seeds (between 2 and 5 log₁₀ cfu g^–1seed) and did not exhibit any characteristic population changes during priming or redrying. Clearly some culturable populations of microorganisms can increase reproducibly during these priming processes and survive the redrying procedure, thereby demonstrating the potential for a novel method of introducing microbial inoculants onto seed.     

Anaerobic fermentative production of lactic acid using cheese whey and corn steep liquor

Cheese whey was the most suitable substrate for production of lactic acid under anaerobic conditions by Entercoccus flavescens which, on supplementating with corn steep liquor (5% v/v) and 10 mM CaCO₃ at pH 5.5, 37°C, yielded 12.6 g lactic acid/l in 36 h. Production was scaled up to a 10 l bioreactor under controlled pH and continuous CO₂ supply and gave 28 g lactic acid/l in 30 h resulting in a net 8.7-fold increase in production as compared to unoptimized conditions.     

Measurement of organic-35S and organic-S in lake sediments: Methodological considerations

Three protocols for the determination of inorganic and organic sulfur fractions were tested for their suitability to estimate total indigenous organic sulfur (S_org) and³⁵S_org formed from added³⁵SO₄ ^2– in sediments of chemically dilute lakes in the ELA. The protocols tested have all been reported in the literature. It was found that two protocols involving sequential analyses for S fractions following acid treatment gave estimates of both S_org and³⁵S_org up to 87% lower than a non-sequential protocol. The low estimates were largely due to hydrolysis and solubilization of solid phase S which was then removed in a rinsing step. The non-sequential protocol, in which total reduced inorganic sulfur and total sulfur were determined on separate aliquots, is recommended as the most reliable of the three. Individual analyses in this protocol were verified for these lake sediments using a variety of S standards.     

Zinc seed coating improves the growth,grain yield and grain biofortification of bread wheat

This study, comprising three independent experiments, was conducted to optimize the zinc (Zn) application through seed coating for improving the productivity and grain biofortification of wheat. Experiment 1 was conducted in petri plates, while experiment 2 was conducted in sand-filled pots to optimize the Zn seed coating using two sources (ZnSO₄, ZnCl₂) of Zn. In the first two experiments, seeds of two wheat cultivars Lasani-2008 and Faisalabad-2008 were coated with 0.25, 0.50, 0.75, 1.00, 1.25, 1.50, 1.75 and 2.00 g Zn kg^?1 seed using ZnSO₄ and ZnCl₂ as Zn sources. The results of experiment I revealed that seed coating with 1.25 and 1.50 g Zn kg^?1 seed using both sources of Zn improved the seedling emergence. However, seed coated with 1.25 and 1.50 g Zn kg^?1 seed using ZnSO₄ was better regarding improvement in seedling growth and seedling dry weight. The results of the second experiment indicated that seed coated with 1.25 and 1.50 g Zn kg^?1 seed using ZnSO₄ improved the seedling emergence and seedling growth of tested wheat cultivars. However, seed coating beyond 1.5 g Zn kg^?1 seed using either Zn source suppressed the seedling emergence. Third experiment was carried out in glass house in soil-filled earthen pots. Seeds of both wheat cultivars were coated with pre-optimized treatments (1.25, 1.50 g Zn kg^?1 seed) using both Zn sources. Seed coating with all treatments of ZnSO₄ and seed coating with 1.25 g Zn kg^?1 seed using ZnCl₂ improved the seedling emergence and yield-related traits of wheat cultivars. Seed coating with 1.25 g Zn kg^?1 seed also improved the chlorophyll a and b contents. Maximum straw Zn contents, before and after anthesis, were recorded from seed coated with 1.5 g Zn kg^?1 seed using either Zn source. Increase in grain yield from seed coating followed the sequence 1.25 g Zn kg^?1 seed (ZnSO₄) >1.25 g Zn kg^?1 seed (ZnCl₂) >1.5 g Zn kg^?1 seed (ZnSO₄). However, increase in grain Zn contents from seed coated was 1.5 g Zn kg^?1 seed (ZnCl₂) >1.25 and 1.5 g Zn kg^?1 seed (ZnCl₂, ZnSO₄) >1.25 g Zn kg^?1 seed (ZnSO₄). Seed coating with Zn increased the grain Zn contents from 21 to 35 %, while 33–55 % improvement in grain yield was recorded. In conclusion, wheat seeds may be coated with 1.25 g Zn kg^?1 seed using either source of Zn for improving the grain yield and grain Zn biofortification.     

Establishing the large scale osmotic priming of onion seeds by using enriched air

Onion seeds were primed in polyethylene glycol solutions (PEG) (-1.5 MPa) for 14 days at 15°C on filter paper and in bubble columns containing 50 g seed litre^-1 PEG using air or enriched air (75% O₂/25% N₂) to aerate and suspend the seeds. Compared with untreated seeds, priming seeds in bubble columns using enriched air increased the percentage seed germination but it did not when air was used, or when seeds were primed on filter paper. Mean germination times (t_m) were significantly reduced in all cases but the reduction was greatest using enriched air and least using air. The spread of germination times was significantly reduced only for seeds primed in enriched air. Drying seeds following priming reduced the percentage germination compared with untreated seeds, but only significantly for those primed in bubble columns using air. Drying also increased the mean germination times by 1.5 to 1.8 days (relative to primed seed which had not been dried). Seeds primed in enriched air were least affected. This increased time is that typically required for water re-imbibition after drying. Priming with enriched air followed by drying gave the same number of normal seedlings as untreated seeds.     

Chloride and potassium channels in U937 human monocytes

Summary Ionic channels in a human monocyte cell line (U937) were studied with the inside-out patch-clamp technique. A Ca²⁺-activated K⁺ channel and three Cl^–-selective channels were observed. The Ca²⁺-activated K⁺ channel had an inward-rectifying current-voltage relationship with slope conductance of 28 pS, and was not dependent on membrane potential. Among the three Cl^– channels, and outward-rectifying 28-pS channel was most frequently observed. The permeability ratio (Cl^–/Na⁺) was 4–5 and CH₃SO ₄ ^– was also permeant. The channel became less active with increasing polarizations in either direction, and was inactive beyond ±120 mV. The channel, observed as bursts, occasionally had rapid events within the bursts, suggesting the presence of another mode of kinetics. Diisothiocyanatostilbene-disulfonic acid (DIDS) blocked the channel reversibly in a dose-dependent manner. The second 328-pS Cl^– channel had a linear currentvoltage relationship and permeability ratio (Cl^–/Na⁺) of 5–6. This channel became less active with increasing polarizations and inactive beyond ±50 mV. DIDS blocked the channel irreversibly. The channel had multiple subconductance states. The third 15-pS Cl^– channel was least frequently observed and least voltage sensitive among the Cl^– channels. Intracellular Ca²⁺ or pH affected none of the three Cl^– channels. All three Cl^– channels had a latent period before being observed, suggesting inhibitory factor(s) presentin situ. Activation of the cells with interferon-, interferon-A or 12-O-tetradecanoylphorbol-13-acetate (TPA) caused no change in the properties on any of the channels.     

Pea seed infection by Mycosphaerella pinodes and Ascochyta pisi and its control by seed soaks in thiram and captan suspensions

Apparently normal pea seeds from pods bearing lesions of Mycosphaerella pinodes were often internally infected with the fungus. When infected seeds were sown in sterile grit almost all the seedlings showed disease lesions, at or below soil level, 4–6 weeks after sowing. Seed infected with Ascochyta pisi gave only 40% infection of seedlings: these showed lesions on the stem and first two leaves within 4 weeks of sowing. Infection of seeds by both pathogens could be eradicated by soaking the seeds for 24 hr. in 0.2% suspensions of thiram or captan at 30d?C. In laboratory or greenhouse tests these treatments did not check germination, but in the field the captan treatment reduced emergence. The treated seeds became fully imbibed but could be dried and stored: the thiram treatment was used for semi-commercial treatment of quantities of seed up to 3 cwt.     

Seasonal patterns of growth and nitrogen fixation in field-grown pea

The seasonal patterns of growth and symbiotic N₂ fixation under field conditions were studied by growth analysis and use of¹⁵N-labelled fertilizer in a determinate pea cultivar (Pisum sativum L.) grown for harvest at the dry seed stage. The patterns of fertilizer N-uptake were almost identical in pea and barley (the non-fixing reference crop), but more fertilizer-N was recovered in barley than in pea. The estimated rate of N₂ fixation in pea gradually increased during the pre-flowering and flowering growth stages and reached a maximum of 10 kg N fixed per ha per day nine to ten weeks after seedling emergence. This was the time of early pod-development (flat pod growth stage) and also the time for maximum crop growth rate and maximum green leaf area index. A steep drop in N₂ fixation rate occurred during the following week. This drop was simultaneous with lodging of the crop, pod-filling (round pod growth stage) and the initiation of mobilization of nitrogen from vegetative organs. The application of fertilizer-N inhibited the rate of N₂ fixation only during that period of growth, when the main part of fertilizer-N was taken up and shortly after. Total accumulation of fixed nitrogen was estimated to be 244, 238 and 213 kg N ha⁻¹ in pea supplied with nil, 25 or 50 kg NO ₃ ⁻ −N ha⁻¹, respectively. About one-fourth of total N₂ fixation was carried out during preflowering, one fourth during the two weeks of flowering and the remainder during post-flowering. About 55% of the amount of N present in pods at maturity was estimated to be derived from mobilization of N from vegetative organs. “Starter” N (25 or 50 kg NO ₃ ⁻ −N ha⁻¹) did not significantly influence either dry matter and nitrogen accumulation or the development of leaf area. Neither root length and root biomass determined 8 weeks after seedling emergence nor the yield of seed dry matter and nitrogen at maturity were influenced by fertilizer application.     

Structural characterization and reactivity of gamma-octamolybdate functionalized by proline

The reaction of molybdate and dl-proline at pH 3.4 results in the formation of a Na₄[Mo₈O₂₆(proO)₂] · 22H₂O complex (pro = proline) in which two proline ligands are attached to molybdenum(VI) ions via monodentate coordination of the carboxylate groups. The structure of the complex was determined by single crystal X-ray diffraction and by combination of ¹H, ¹³C and ⁹⁵Mo NMR spectroscopy techniques in solution. The structure of the complex is strongly dependant on the pH. At native pH 3.4 the octamolybdate-type structure seems to be present in solution, but the increase of pH to 5.8 resulted in a rearrangement of the structure to a heptamolybdate-type structure. At physiological pH, the polyoxometalate framework was completely dissociated into the monomeric unit. The reactivity of the Na₄[Mo₈O₂₆(proO)₂] · 22H₂O towards the hydrolysis of ATP was tested at different pH values. While in solution at pH 3.4 the hydrolysis proceeded to yield AMP (adenosine monophosphate) and ADP (adenosine diphosphate) in nearly equal amounts, reaction mixture at pH 5.8 gave ADP as the only product of hydrolysis after 24 h of reaction. At neutral pH, the hydrolysis of ATP was slower, but it proceeded to yield 75% of ADP after 48 h of reaction.     

Role of protein kinase C in the regulation of cytosolic Ca2+ in A431 cells: Separation of growth factor and bradykinin pathways

Summary Calcium signaling systems in nonexcitable cells involve activation of Ca²⁺ entry across the plasma membrane and release from intracellular stores as well as activation of Ca²⁺ pumps and inhibition of passive Ca²⁺ pathways to ensure exact regulation of free cytosolic Ca²⁺ concentration ([Ca²⁺] _i ). A431 cells loaded with fura-2 cells were used as a model system to examine regulation of Ca²⁺ entry and intracellular release. Epidermal growth factor (EGF) and transforming growth factor alpha (TGF-) both stimulated Ca²⁺ entry and release while bradykinin appeared only to release Ca²⁺ from intracellular stores. The possible role of protein kinase C (PKC) in modulating the [Ca²⁺] _i response to these agonists was examined by four methods. Low concentrations of TPA (2×10^–10 m) had no effect on Ca²⁺ release due to EGF, TGR- or bradykinin but resulted in a rapid return of [Ca²⁺] _i to baseline levels for EGF or TGF-. Addition of the PKC inhibitor staurosporine (1 and 10nm)_completely inhibited the action of TPA on EGF-induced [Ca²⁺] _i changes. An inhibitor of diglyceride kinase (R59022) mimicked the action of TPA. Down-regulation of PKC by overnight incubation with 0.1 or 1 m TPA produced the converse effect, namely prolonged Ca²⁺ entry following stimulation with EGF or TGF-. To show that one effect of TPA was on Ca²⁺ entry, fura-2 loaded cells were suspended in Mn²⁺ rather than Ca²⁺ buffers. Addition of EGF or TGF- resulted in Ca²⁺ release and Mn²⁺ entry. TPA but not the inactive phorbol ester, 4--phorbol-12,13-didecanoate, inhibited the Mn²⁺ influx. Thus, PKC is able to regulate Ca²⁺ entry due to EGF or TGF- in this cell type. A431 cells treated with higher concentrations of TPA (5×10^–8 m) inhibited not only Ca²⁺ entry but also Ca²⁺ release due to EGF/TGF- but had no effect on bradykinin-mediated Ca²⁺ release, suggesting differences in the regulation of the intracellular stores responsive to these two classes of agonists. Furthermore, sequential addition of EGF or TGF- gave a single transient of [Ca²⁺] _i , showing a common pool of Ca²⁺ for these agonists. In contrast, sequential addition of EGF (or TGF-) and bradykinin resulted in two [Ca²⁺] _i transients equal in size to those obtained with a single agonist. Ionomycin alone was able to fully deplete intracellular Ca²⁺ stores, whereas ionomycin following either EGF (or TGF-) or bradykinin gave an elevation of the [Ca²⁺] _i signal equal to that of the second agonist. These data indicate that there are separate pools of intracellular Ca²⁺ for EGF-mediated Ca²⁺ release which also respond differently to TPA.     

Stimulation of sugar-beet hypocotyl extension with potassium nitrate

Steeping sugar-beet seeds in an aqueous thiram suspension, as now used commercially in the UK, makes seedling emergence more rapid and increases the number of plants established. This study investigated whether the potassium and nitrate, removed by steeping, were needed to stimulate subsequent hypocotyl growth. Experiments under controlled conditions showed that re-incorporation of KNO₃ by adding the salt to the steeping solution or, less wastefully during pelleting, slightly slowed root protrusion but made hypocotyl extension more rapid, particularly under dry conditions. There were indications that placement of KNO₃ under the seed would be better. Nevertheless, in the field where recommended amounts of fertiliser were applied, incorporation of about 5 g KNO₃/kg seed during pelleting was consistently beneficial following the four sowings. This amount decreased the time to half-final emergence by 0.3 days, gave 3% more established plants and, with the later sowings, increased dry weight in mid-May by 10%.     

Responses of dormant heather (Calluna vulgaris) seeds to light, temperature, chemical and advancement treatments

Two seed lots of Calluna vulgaris were obtainedfrom English Nature (seed of Cornish provenance) (EN) and John ChambersWildflower Seeds (JCWS). In laboratory tests, under continuous light untreatedseeds of both seed lots were partially dormant at temperatures between14–35 °C, but JCWS seeds were more deeply dormant thanENseeds. The optimum temperature for germination for both lots was ca 18°C. Germination of EN seeds was much lower in the dark than inthe light at all temperatures; JCWS seeds did not germinate in the dark. In thelight at 22 °C, dormancy of both seed lots was broken whenseeds were incubated in GA_4/7 solution(2×10^–4 M). Dormancy ofJCWSseeds at 22 °C in the light was broken when seeds wereincubated in four different smoke solutions but more so when used incombinationwith GA_4/7. Soaking seeds for 4h insmoke/GA_4/7solutions before sowing improved both the speed andpercentage germination in pot experiments on a mist bench in the glasshouse byat least 10-fold. Soaking with GA_4/7 alone produced a 5-fold increasein germination but seedlings were more etiolated than with thesmoke/GA_4/7 mixtures. A seed advancement treatment modified from thatused commercially on sugar beet seeds also promoted germination in bothlaboratory and glasshouse tests. This entailed soaking seeds in 0.2% thiramsuspension for 4h followed by incubation in excess solution at 22°C for 4 days. This treatment was not as effective as thesmoke/GA_4/7 seed soaks.     

Photosynthetic Efficiency of Plants of Brassica Juncea,Treated with Chlorosubstituted Auxins

The leaves of 29-d-old plants of Brassica juncea Czern & Coss cv. Varuna were sprayed with 10^–6 or 10^–8 M aqueous solutions of indole-3-yl-acetic acid (IAA) or its substituted derivatives 4-Cl-IAA, 7-Cl-IAA, and 4,7-Cl₂-IAA. All the auxins improved the vegetative growth and seed yield at harvest compared with those sprayed with de-ionised water (control). 4-Cl-IAA was most prominent in its effect, generating 21.6, 39.7, 61.0, 35.0, 65.5, and 56.2% higher values for dry mass, leaf chlorophyll content, carbonic anhydrase (E.C. 4.2.1.1) and nitrate reductase (E.C. 1.6.6.1) activities, net photosynthetic rate, and carboxylation efficiency, respectively, in 60-d-old plants. It also enhanced the seed yield by 31.1% over the control. The order of response of the plants to various auxins was 4-Cl IAA 7-Cl IAA > 4,7-Cl₂ IAA = IAA > control.     

Infection of the flowers and seed of parsnip by Itersonilia pastinacae

Seeding parsnip plants on four commercial holdings in Essex showed not only the root cankers and leaf spots associated with infection by Itersonilia pastinacae, but also extensive lesions on the petioles and necrosis of the inflorescences. These last-named symptoms were proved to be caused by I. pastinacae which could also be found on some of the seeds. Seed infection, though largely superficial, was sometimes more deep-seated. It could be eliminated by soaking the seed in an aqueous suspension of 0·2% thiram at 30 °C for 24 h. Heavily infected seed gave a low percentage of seedlings bearing cotyledon lesions: it is uncertain whether hypocotyl lesions, which also occurred, were caused directly by the fungus. An outdoor test failed to show that infected seed gave rise ultimately to roots bearing Itersonilia cankers: the significance of this and other possible sources of infection is discussed.