An investigation into the relations between some growth parameters and yield of barley

Twenty-five field experiments on barley were done at four sites from 1970 to 1975, with an additional site in 1975, comparing five rates of nitrogen application. The crops were sampled at c. 14-day intervals from about the four-leaf stage to maturity to follow changes with time in the dry weights of the constituent plant parts and to measure fertile tiller number, grain number per ear and grain weight. Some data have been selected from this body of information and regression analysis has been used to assess the possible importance of pre- and post-anthesis growth in determining the yield of barley. Ear emergence was taken as an approximate indicator of anthesis. Yield was closely related (r=+0–96) and almost equal to the amount of dry matter accumulated before ear emergence for twenty-one of the experiments, with a regression coefficient of 0–95. In two of the remaining experiments the regression coefficient was greater, 1–14; and smaller in the other two, o-8i. Plant population is also shown to affect the regression coefficient. Despite these anomalies grain yield was more closely related to plant dry weight at ear emergence than to the increase in weight after ear emergence (r =+0–79). The increase in plant dry weight after ear emergence was frequently less than the yield of grain, suggesting that the plant can compensate for inadequate photosynthesis during grain filling. The result of this compensation is a reduction in straw dry weight. This implies that previously assimilated dry matter is transported to the grain, or that respiratory losses from the straw are not replaced by current photosynthesis. These observations suggest that yield may be limited by sink capacity rather than by photosynthesis after ear emergence. The main component of sink capacity, grain number per m² was closely related to yield (r =+0–95) and is known to be determined at or before anthesis. Grain size was shown to be related to grain number per ear (r= 4- 0–99), suggesting that grain size is also, at least partially, determined at ear emergence. Therefore, all the yield components are determined, wholly or partly before ear emergence.     

Effects of Temperature Variation at Different Times on Growth and Yield of Sugar Beet and Barley

Sugar-beet and barley were grown in pots outdoors (environmentN) and, for five successive 4-week periods starting at sowing,batches of plants were transferred to three growth rooms whosetemperatures were either similar to the outdoor mean (environment^M), or 3° C hotter (environment H) or 3° C colder (environmentC). Some plants were harvested immediately after treatment;others were returned to environment N and harvested when mature. At the end of period 1, sugar-beet plants from environment Mhad more dry weight and leaf area than those outdoors. Immediatelyafter spending later periods in environment M, plants had smallerleaves and similar dry weight to those continuously outdoors.These differences disappeared by maturity. Warmth in the growthrooms (i.e. the difference H—C) during periods 1, 2, and3, while leaf area was increasing, increased the number andsize of leaves and usually also dry weight; in later periodsit had no effect. The effects induced during periods 2 and 3,but not period 1, persisted to maturity to give greater totaland root dry weight and yield of sugar. The final effects ondry weight were much larger than those immediately after treatment,and were the result of differences in growth outdoors aftertreatment which depended on differences in leaf area; the efficiencyof the leaves was not affected by previous treatment. Transferring barley to environment M from N had inconsistentimmediate effects on leaf area and dry weight which disappearedby the final harvest. Transfer during periods 2 and 3, beforethe ears had started emerging, increased shoot number and delayeddevelopment. The proportion of the ears that ripened and theyield of grain were usually less for plants that had spent aperiod in environment M than for plants permanently outdoors,which also had some green ears. Warmth in the growth rooms duringperiods 1 and 2 increased dry weight and leaf area immediately,but had negligible effects at maturity because the increasesin leaf area did not persist after ear emergence. Warmth laterhastened death of leaves, decreased total dry weight immediatelyand also at maturity, but increased the proportion of ears thatripened and hence usually grain weight. Variation in leaf areaduration after ear emergence (D), determined by effects on thetime the ears emerged and the rate the leaves died, accountedfor most of the variation in grain yield, but warmth after theears emerged decreased grain yield less than proportionallyto the decrease in D. Net assimilation rate (E) of sugar-beet was greater than ofbarley, and decreased less with age. E of both species was usuallygreater in environment M than outdoors in spite of less radiation.It was only slightly affected by temperature. Nitrogen and potassium uptake were increased by treatments thatincreased dry weight. The percentage contents suggest that extrauptake was a consequence and not a cause of the increase indry weight.     

Physiological Causes of Differences in Grain Yield between Varieties of Barley

In a field experiment on barley at Rothamsted with the highmean yield of 49 cwt. of grain per acre, the varieties Proctorand Herta produced 10—15 per cent, more grain than Plumage-Archeron plots that received no nitrogenous fertilizer. When nitrogenwas applied the difference was increased to about 30 per cent.,because the higher nitrogen supply caused the Plumage-Archercrop to lodge and did not increase its yield, while Proctorand Herta remained standing. The three varieties did not differ in leaf-area index nor innet assimilation rate before ear emergence, so that all hadthe same total dry weight. After ear emergence, the leaf-areaindices of Proctor and Plumage-Archer were nearly equal, butthat of Herta was smaller. Assuming that the photosyntheticefficiency of the leaves continued to be the same in all varieties,the higher grain yields of Proctor and Herta cannot be attributedto greater production of dry matter by the leaves, either beforeor after ear emergence. A pot experiment on plants with shadedears confirmed that the dry matter contributed to grain yieldby unit leaf area was nearly equal in all the varieties. The higher grain yield of Proctor and Herta than of Plumage-Archermust therefore have come from additional photosynthesis in partsof the plant other than the leaves, i.e. in the ears themselves.An attempt to demonstrate this directly in a pot experiment,by comparing the grain yields of plants with shaded or withunshaded ears, was unsuccessful because the varieties behaveddifferently in pots; Proctor and Herta produced only about 6per cent, more grain yield than Plumage-Archer, and though thedecrease in grain yield by shading the ears was slightly greaterfor Proctor and Herta, the differences were not significant. The sum of ear sizes (estimated from length and breadth measurements)per m.1 in the field experiment was greater for Proctor andHerta than for Plumage-Archer. Also the distribution of drymatter between developing ears and shoots apparently differedwith variety, so that at ear emergence the dry weight of earsper m.² was greater in the two higher yielding varieties. Theincreased amount of photosynthetic tissue in the ears of Proctorand Herta, as measured by size or weight, may not wholly explaintheir greater dry-matter production; ears of Herta may alsohave a higher photosynthetic efficiency. No differences in nutrient uptake that could account for thevarietal differences in grain yield were found. Plumage-Archerabsorbed more potassium, and Herta less phosphorus than theother varieties. About a quarter of the final content of nitrogen,and a third of the phosphorus, was absorbed after ear emergence,but the potassium content was nearly maximal at ear emergenceand later decreased. The pot experiment showed that, on the average of all varieties,26 per cent. of the dry matter in the grain at harvest originatedfrom photosynthesis in the ears, including 10 per cent, fromthe awns; 59 per cent, came from photosynthesis in the flag-leaflamina and sheath and peduncle, and 15 per cent, from partsof the shoot below the flag leaf.     

Sink Activity Estimation by Sink Size and Dry Matter Increase During the Ripening Stage of Barley (Hordeum vu/gare) and Rice (Oryza sativa)

During the ripening stage of barley and rice, the sink activitywas defined as the dry matter increase per units sink size,leaf area and time, as follows: NAR = A.SinkW+NAR', where NAR is the net assimilation rate (g d.wt dm^–2d^–1);A is the sink activity [g d.wt g^–1d.wt (ear) dm^–2d^–1]; Sink W is ear wt per plant at heading (g d.wt);and NAR' is net assimilation rate excluding the assimilate ofsink organ (g d.wt dm^–2 d^–1). Plant material with 16 combinations of mutually different sink(ear) and source (leaf) size were produced at heading for eachcrop: parts of each leaf and ear were removed to produce fourgrades in barley, and also a part of each leaf was removed producingfour grades for four rice varieties showing different ear size.NAR and NAR' were determined during 26 and 21 d in barley andrice after heading, respectively. Sink activity (A), representedas the assimilation rate induced by the sink organ, was estimatedfrom the relationship between SinkW and NAR using the previousequation. The sink activity was significantly higher in ricewith a value of 0–0.028 g d.wt g^–1 d.wt (ear) dm^–2d^–1 vs. 0–0.0017 in barley, suggesting that therelative role of leaves for grain filling is considerably higherin rice than in barley. The sink activity obtained in the studymight be introduced into a model to predict the yields of barleyand rice. Hordeum vulgare L, barley, Oryza saliva L, rice, dry matter, NAR, sink, source, sink activity, model     

Relationships between early vigour, grain yield, leaf structure and stable isotope composition in field grown barley

Fast growth and early development in barley are used in breeding programmes to improve the water use efficiency and transpiration efficiency of this crop in Mediterranean conditions. Here, we examine the use of several simple traits based on the structure and stable isotope composition of seedling leaves to assess differences in early vigour, phenology and grain yield, and also the interaction with low temperatures in barley. A set of 260 F₈ lines of two-row barley (Hordeum vulgare L.) derived from the cross of Tadmor and WI 2291 were cultivated in two locations in northwest Syria. Total chlorophyll content on an area basis (SPAD) and specific leaf dry weight (SLDW) were measured in recently fully expanded intact leaves of seedlings. Total leaf area and total dry weight per seedling were evaluated in the same seedlings. The stable isotope compositions of carbon and nitrogen (δ¹³C and δ¹⁵N, respectively) were analyzed in the same leaves on a subset of 75 genotypes. Number of days from planting to heading and grain yield were recorded at both sites. The grain yield measured at both locations was positively correlated with the SPAD value of seedlings, but showed no relationship with SLDW. Days to heading was negatively correlated with SPAD values. Regarding early vigour, a negative relationship between the SLDW and the total leaf area of seedlings was observed. However, no relationship between the δ¹³C of seedlings and early vigour was observed, except when only the genotypes most resistant to low temperatures (i.e. showing the highest SPAD values) were considered. This subset of genotypes showed negative relationships between δ¹³C and either total leaf area or total dry weight. In addition, δ¹⁵N was negatively correlated with SPAD only within the high-SPAD genotypes. This suggests that within the genotypes resistant to low temperatures, those with higher chlorophyll content assimilate more nitrogen from nitrate.     

Studies in the Diagnosis of Mineral Deficiency

Material from four fertilizer trials on barley in Hampshire was analysed with the principal purpose of comparing the extent to which the potassium content of different plant organs was diagnostic of potassium deficiency. Samples of older leaf blades and sheaths, young leaves, stems and ears were gathered at the time of ear emergence from each of the 108 plots, and analysed spectrographically for calcium, iron, magnesium, manganese, potassium and sodium.
Differences in composition between plants from the different sites were proportionately greater in the older leaf blades than in the other organs for calcium, the young leaves for manganese and sodium, and the older leaf blades and sheaths for potassium. Differences in sodium and manganese content at the different sites appeared to be related to the differences in potassium status.
Applications of muriate of potash increased the potassium content of all organs except the ears, and decreased the content of magnesium, manganese and sodium, and of iron at one site. The effect of potassium supply on manganese and sodium content was most marked in the young leaves. The proportional increases observed in potassium content as a result of application of muriate of potash were similar at all four sites, in spite of the fact that responses in growth and yield differed greatly.
As between the four sites, the responses to muriate of potash observed in the yields of grain are significantly correlated with the potassium content of the older leaf blades and the stems, and the following tentative limiting values are put forward, above which no increase in grain yield as a result of potassic manuring may be expected:
(a) in the older leaf blades at the time of ear emergence 0.92% potassium in dry matter, (b) in the stems at the time of ear emergence 1–01 % potassium in dry matter.     

Varietal Differences in Photosynthesis of Ears and Leaves of Barley

Rates of apparent photosynthesis of ears and of the combinedflag leaf and sheath and peduncle of Proctor barley grown inpots or in the field were similar to those of Plumage Archer,or slightly smaller when the dimensions of the ear and leafarea of Proctor were less than those of Plumage Archer. Thephotosynthesis rate of the ear—about 1.0 mg. CO₂ per earper hour—was similar or slightly less than the rate ofthe flag leaf and sheath and peduncle. These rates of photosynthesisindicated that 40-50 per cent, of the carbohydrate in the grainwas provided by photosynthesis in the shoot and about 40 percent, by photosynthesis in the ear. The total CO₂ fixed by theear was equivalent to about 60 per cent, of the grain weight,20 per cent, being lost by respiration. Shading the ear underestimatedthe total amount of CO₂ fixed by the ear and decreased dry weightof grain per ear of both Proctor and Plumage Archer by 26 percent., as in pots. The contribution of ear photosynthesis toyield of grain per acre was greater for Proctor than for PlumageArcher because Proctor had more ears. The rate of apparent photosynthesis per dm.² of leaves of Proctorwas similar to that of Plumage Archer both before and afterear emergence. Before ear emergence, the photosynthesis rateof a particular leaf decreased linearly with time and was slowerfor lower than for higher leaves on the shoot. Respiration ratesper g. dry weight of ears of Proctor and Plumage Archer weresimilar; in one experiment the leaves of Proctor respired slightlyfaster than those of Plumage Archer.     

Influence of sowing windows and genotypes on growth,radiation interception,conversion efficiency and yield of guar

Crop growth largely depends on radiation. Radiation is the main impetus for photosynthesis and movement of photosynthates from source to sink. Therefore, identification of the optimum sowing windows and suitable cultivars for efficient utilization of radiation is of prime importance. A field study was conducted in red clay soil during 2014 and 2015 Kharif season and the treatments consisted of three genotypes and three sowing windows by using randomized complete block design with three replications. The effect of genotypes and sowing windows was found significant with respect to number of trifoliate leaves, leaf area ratio, dry matter production, grain numbers, pod length, test weight, grain yield, and stover yield of guar during 2014 as compared to 2015 sown crop. Statistically significant plant height, number of trifoliate leaves, number of branches, leaf area ratio, absolute growth rate, leaf area index, dry matter, grain number, pod length, grain yield, stover yield and a higher cumulative radiation interception were recorded with 15th August sown crop as compared to other sowing windows. The plant height, number of trifoliate leaves, number of branches, leaf area ratio, absolute growth rate, leaf area index, dry matter, grain number, pod length, grain yield, stover yield and maximum cumulative interception of radiation were significant with RGC-1003 as compared to RGC-936 and HG-365. It is observed that the incident PAR to dry matter accumulation conversion efficiency was varied with cultivars and different sowing windows which ranges from 0.74 g MJ⁻¹ to 0.79 g MJ⁻¹.     

不同生态环境下水稻基因型产量形成与源库特性的比较研究

以日本和IRRI的9个水稻品种为材料,分别以武香粳9号和两优培九为对照,在江苏南京和云南丽江研究了不同水稻基因型干物质积累与源库形成特征及其在不同生态环境下的差异.结果表明,生态环境对水稻产量和干物质积累量影响显著.高产水稻品种积累了高额干物质量,且干物质生产优势在中后期.高产品种的总颖花量、LAI及群体生长速率(CGR)都较高.稻谷产量随干物质积累总量的增加而提高,与齐穗后干物质积累量、总颖花量和LAI呈极显著正相关,与粒叶比呈显著正相关.与云南丽江点相比,群体LAI、单位面积颖花量和抽穗后干物质积累量少及生长速率(CGR)低是南京点稻谷产量低的关键因素.     

干旱对东北春玉米生长发育和产量的影响

选取玉米品种丹玉39为供试材料,利用大型农田水分控制试验场,采用大田池栽方式,在玉米三叶-拔节期、拔节-吐丝期、吐丝-乳熟期分别开展中度干旱胁迫及复水控制对比试验,分析3个关键生育时期干旱胁迫对春玉米生长发育和产量的影响.结果表明：与水分适宜对照（CK）相比,三叶-拔节期遭受干旱胁迫后,全生育期推迟13 d,至拔节普遍期,株高偏低29.8%,叶面积偏小41.2%,复水后,株高和产量得到较大程度恢复,果穗性状和最终产量差异不大;拔节-吐丝期遭受干旱胁迫后,全生育期缩短7 d,至吐丝普遍期,株高偏低18.6%,叶面积偏小14.1%,果穗长、穗粒数、果穗干质量、穗粒质量分别下降6.9%、19.1%、28.1%和29.4%,空秆率增加13.3%;吐丝-乳熟期遭受干旱胁迫后,全生育期缩短15 d,生长至乳熟普遍期,株高偏低2.3%,叶面积偏小37.3%,果穗长、穗粒数、果穗干质量、穗粒质量分别下降9.2%、24.1%、30.8%和27.9%,空秆率增加24.5%.拔节-吐丝期、吐丝-乳熟期干旱胁迫处理并复水后,玉米株高恢复不明显,产量降幅显著.     

Effects of net blotch on growth and yield of spring barley

The effect of net blotch on the growth and yield of cv. Beatrice spring barley was examined in a greenhouse experiment. Separate inoculations at growth stages 21 and 34 reduced green leaf area, root weight, leaf sheath and stem weight and tiller number. The early inoculated plants, which responded and recovered more rapidly than later treated ones, suffered a loss in grain yield and this was related to the amount of disease, the loss in green leaf area and the reduction in unit leaf rate.     

Experiments with CCC on wheat: effects of spacing, nitrogen and irrigation

In experiments with spring and winter wheat at Rothamsted and Woburn during 4 years CCC increased yield at close spacing (4 in) (10 cm) more than at usual spacing (8 in) (20 cm), but there was no interaction between spacing and yield. Some experiments tested up to 2·4 cwt/acre (300 kg/ha) N to see whether yields continued to increase with more than usual amounts of N, when CCC prevented lodging. There was no evidence of this. When a short dry spell occurred at ear emergence, yield of spring wheat was increased by 6 cwt/acre (750 kg/ha) by CCC and 10 cwt (1250 kg) by irrigation. CCC probably improves yield in these conditions because the larger root system it causes enables more ear-bearing shoots to survive. CCC increases yield in two ways, either by increasing ears or grain per ear. In an unlodged crop CCC usually makes the grains smaller, but by preventing lodging it can also increase size. Usually CCC decreases the leaf area per shoot. The flag leaf may be smaller, unchanged or larger than those of untreated plants. There was no obvious connexion between flag-leaf area and grain yield; when CCC decreased flag-leaf area duration by 25 %, grain yield was unchanged. The results suggest that using CCC gives a more than even chance of a profitable yield increase.     

The Effects of Grain Nitrogen and Applied Nitrate on Growth, Photosynthesis and Protein Content of the First Leaf of Barley Cultivars

Five cultivars of barley with widely differing grain nitrogencontents were compared. In the absence of exogenous nitratesupply plants grown from high nitrogen grain showed a more rapidleaf emergence, greater leaf size, especially of the first leaf,higher photosynthetic rate and greater total souble proteinand Fraction 1 protein content of the first leaf, than plantsgrown from low nitrogen grain. However, early supply of nitrateto plants grown from low nitrogen grain enabled these to performas well as those from grain with a high nitrogen content. Regressionanalysis showed that Fraction 1 content of the first leaf isclosely correlated with grain nitrogen which exerts a progressivelygreater effect on content of this protein as application ofexogenous nitrate is delayed. The more rapid photosyntheticrate of plants grown with high nitrogen, and the consequentgreater rate of dry matter accumulation, is attributable mainlyto effects of nitrogen availability on leaf area and much lessto effects on leaf protein.     

Analysis of Growth and Yield of Winter and Spring Wheats

In a field experiment to investigate the physiological causesof variation in yield between autumn- and spring-sown wheatand between old and new varieties, the grain yields of the winterwheats were 3-15 per cent, greater than of the spring ones andthe new varieties Cappelle-Desprez and Jufy I yielded 40-70per cent, more than Squarehead's Master and Atle. Nitrogen fertilizerincreased the yields of Cappelle-Desprez and Jufy I more thanof Atle, and decreased the yield of Squarehead's Master by makingit lodge. Until ear emergence the winter varieties had greater leaf-areaindices (L) and dry weights, but smaller net assimilation rates(E), than the spring varieties. Square-head's Master had greaterL but smaller E, and similar dry weight to Cappelle-Desprez.Jufy I had similar E to Atlc, but greater L and dry weight.Nitrogen increased L and dry weight, but decreased E. All thedifferences in E between varieties and nitrogen treatments couldbe explained by the opposite effects on L, that is to say, thedifferences in E were caused by variation in mutual shadingarising from the differences in L and not by changes in leafphysiology. L of winter wheat reached its maximum at the end of May, butL of spring wheat continued to increase until ear emergence.Afterwards Ldecreased more rapidly for winter than for springwheat, so that eventually spring wheat had the greater L. Thesedifferences in the time changes of L partially compensated forthe shorter growth period of spring wheat, and tended to equalizethe grain yield from winter and spring sowings. After ear emergence total dry weight of winter varieties continuedto be greater than of spring ones, but the difference in dryweight of ears was much smaller because ear: shoot dry-weightratio was greater for the spring varieties. Total dry weight,ear dry weight and ear: shoot ratio were all greater in thenew than in the old varieties. Leaf area duration (D) afterear emergence was slightly greater for the winter than for thespring varieties and similar for old and new. The apparent efficiencyof this leaf area in grain production, measured by the grainleaf ratio (ratio of grain dry weight to D), was similar forwinter and spring varieties but greater for new than for old.This suggests that Cappelle-Desprez and Jufy I have higher grainyields because their ears photosynthesize more than do the earsof Squarehead's Master and Atle. Before ear emergence winter varieties had more shoots than springones, and old varieties more than new. After ear emergence therewere only small differences in numbers of ears; percentage survivalwas greater for spring than for winter and for new than forold varieties. Differences in dry weight between varieties were not causedby differences in nitrogen uptake.     

Survival of Tillers and Distribution of Dry Matter between Ear and Shoot of Barley Varieties

Plants of Plumage Archer barley grown in pots produced moreshoots than did Proctor, but had fewer ears at maturity, becausesome shoots died about 7 days before ear emergence. The numberand position on the plant of the shoots that died were consistentfor particular growing conditions. Shoots that died were notalways the last to be produced. There were no consistent differencesin dry weight, leaf area, nitrogen content, or apex developmentbetween shoots that did and did not survive; nor did removingthree developing ears on older shoots affect the survival ofother shoots. Growth of Plumage Archer plants was not checkedby death of shoots; dry matter, nitrogen, and leaf area wereredistributed so that increase in surviving shoots compensatedfor losses in the dead shoots. The dry-weight ratio of ear to shoot was smaller for Proctorthan for Plumage Archer at ear emergence and anthesis, but atmaturity it was greater for Proctor, both when ears were shadedto prevent them photosynthesizing and when they were unshaded.The varietal difference in ear: shoot dry-weight ratio was reversedbecause the relative growth-rate of ears of Proctor was greaterand because more dry matter was lost from its shoots. Both changesmay have been caused by translocation to the ear of a greaterproportion of the assimilate from the shoots of Proctor thanof Plumage Archer. Leaves of Proctor appeared to be more efficientin producing dry matter for the ear than those of Plumage Archer.     

Genotypic variation in response of barley to boron deficiency

Responses of a range of barley (Hordeum vulgare L.) genotypes to boron (B) deficiency were studied in two experiments carried out in sand culture and in the field at Chiang Mai, Thailand. In experiment 1, two barley genotypes, Stirling (two-row) and BRB 2 (six-row) and one wheat (Triticum aestivum L.) genotype, SW 41, were evaluated in sand culture with three levels of applied B (0, 0.1 and 1.0 μM B) to the nutrient solution. It was found that B deficiency depressed flag leaf B concentration at booting, grain number and grain yield of all genotypes. In barley Stirling, B deficiency also depressed number of spikes plant^-1, spikelets spike^-1 and straw yield. However, no significant difference between genotypes in flag leaf B concentration was found under low B treatments. Flag leaf B concentration below 4 mg kg^-1 was associated with grain set reduction and could, therefore, be used as a general indicator for B status in barley. In experiment 2, nine barley and two wheat genotypes were evaluated in the field on a low B soil with three levels of B. Boron levels were varied by applying either 2 t of lime ha^-1 (BL), no B (B0) or 10 kg Borax ha^-1 (B+) to the soil prior to sowing. Genotypes differed in their B response for grain spike^-1, grain spikelet^-1 and grain set index (GSI). The GSI of the B efficient wheat, Fang 60, exceeded 90% in all B treatments. The B inefficient wheat SW 41 and most of the barley genotypes set grain normally (GSI >80%) only at the B+. In B0 GSI of the barley genotypes ranged from 23% to 84%, and in BL from 19% to 65%. Three of the barley with severely depressed GSI in B0 and BL also had a decreased number of spikelets spike^-1. In experiment 3, 21 advanced barley lines from the Barley Thailand Yield Nursery 1997/98 (BTYN 1997/98) were screened for B response in sand culture with no added B. Grain Set Index of the Fang 60 and SW 41 checks were 98 and 65%, respectively, and GSI of barley lines ranged between 5 and 90%. One advanced line was identified as B efficient and two as moderately B efficient. The remaining lines ranked between moderately inefficient to inefficient. These experiments have established that there is a range of responses to B in barley genotypes. This variation in the B response was observed in vegetative as well as reproductive growth. Boron efficiency should be considered in breeding and selection of barley in low B soils. This revised version was published online in June 2006 with corrections to the Cover Date.     

Some effects of barley yellow dwarf virus on spring and winter cereals in glasshouse trials

The tolerance of spring and winter varieties of wheat, oats and barley to infection by barley yellow dwarf virus (BYDV) was examined in glasshouse tests. Severely affected plants were stunted and grain yields were considerably decreased because of decreases in both ear number and numbers and sizes of grains. Winter barley varieties were very susceptible and many were killed by BYDV infection. The winter wheat varieties were more widely tolerant than those of oats and barley. Individual seedling symptoms, although correlated with reductions in yield, could not be relied upon for accurate classification of all varieties in order of their susceptibility to infection. Symptoms of seedling infection incorporated into an index of infection permit estimates to be made o eventual decreases in yield by applying the formula DY = 1.4 × (SH+LA+LL)+18. Thus decrease in grain yield (DY) can be related to decreases in height (SH) and leaf length (LL) and increases in leaf area discoloured (LA) in seedling plants infected with BYDV.     

Commercially available plant growth regulators and promoters modify bulk tissue abscisic acid concentrations in spring barley, but not root growth and yield response to drought

Field and lysimeter experiments were conducted in 2002 to investigate the effects of an antigibberellin growth regulator (Moddus, active ingredient trinexapac‐ethyl, Syngenta Crop Protection UK Ltd, Whittlesford, Cambridge, UK) and an auxin‐stimulating (Route, active ingredient zinc ammonium acetate, De Sangosse Ltd, Swaffham Bulbeck, Cambridge, UK) growth promoter on root growth, soil water extraction and the drought response of spring barley. The effects on root growth and distribution were investigated in the field. The effects on the drought response were studied in 1.2‐m‐deep lysimeters packed with a loamy sand subsoil and sandy loam topsoil. Lysimeters were located under a fixed rain shelter, and drought was imposed by withholding irrigation. In both field and lysimeter experiments, growth regulator/promoters were applied to cv. Optic at early tillering according to the manufacturers’ recommendations. After withholding irrigation from lysimeters at Zadoks growth stage (GS) 21 (37 days after sowing), 50% of the profile available water had been depleted by flag leaf emergence (GS 37/39; 62 days after sowing). Drought significantly reduced stem biomass at ear emergence (GS 59; 78 days after sowing) but not leaf or ear dry weight; this was before there was any significant reduction in leaf water potential or stomatal conductance to water vapour. The reduction in stem biomass may reflect a change in partitioning between shoot and root in response to soil drying. When averaged over growth regulator/promoter treatments, drought reduced grain yield by approximately 1 t ha^?1. This was associated with a reduction in both ears per m² and grains per ear. The mean grain weight was not reduced by drought, in spite of significant reductions in stomatal conductance and canopy lifespan post‐anthesis. Route, and to a lesser extent Moddus, significantly increased abscisic acid accumulation in the stem base of droughted plants, and there was some indication of a possible delay in stomatal closure in Route‐treated plants as the soil moisture deficit developed. However, there was no significant effect on the amount of soil water extracted or grain yield under drought. Similarly, in field experiments, neither Route nor Moddus significantly altered total root length, biomass or distribution. There is little evidence from these experiments or in the literature to support the use of antigibberellin or auxin‐simulating growth regulator/promoters to modify root growth and drought avoidance of spring barley.     

Quantitative phenotypical expression of three mutant genes in barley and the basis for defining an ideotype for Mediterranean environments

Summary Three mutants induced in the two-rowed barley variety Beka and their three binary recombinants have been used in an attempt to define an ideotype suitable for Mediterranean agroclimatic conditions. Physiological methods (classical plant growth analysis) together with the study of genotype x environment interaction for grain yield were used to characterize the genotypes. That characterization brought out the huge phenotypical variation produced by only three mutant genes, suggesting that single Mendelian genes may alone explain the quantitative variation, including grain yield, without the necessity of using the polygenic concept. The genotype best adapted to the environments studied is later in heading and has shorter straw and denser spikes than Beka; it also has higher inverse of leaf area rate and grain: leaf area ratio, a lower rate of leaf senescence, and a shorter grain filling period than the original variety.     

Studies in the diagnosis of mineral deficiency; manganese deficiency in wheat

At fourteen sites where winter wheat was growing commercially, twelve of which were known or suspected to be deficient in manganese, a spray of manganese sulphate was applied late in the shooting stage of development, and the effect on yield of grain estimated. Samples of certain organs of unsprayed wheat plants were gathered on three occasions between tillering and ear emergence, and samples of weed leaves on the same occasions and after harvest; these samples were analysed spectrographically for manganese.
The results indicate that analysis of the wheat plant can be used to forecast its response to a manganese sulphate spray, and the following tentative limiting values for manganese content are put forward, above which no increase in grain yield as a result of treatment may be expected: (a) during tillering, 34 p.p.m. manganese in dry matter of lower leaf blades; (b) just prior to ear emergence, 36 p.p.m. manganese in dry matter of stems. The highest correlation obtained between response and manganese content was that with the values for stem samples gathered just prior to ear emergence.
Analysis of weed samples can only be expected to indicate gross differences in the manganese status of different sites.