水稻穗内不同粒位间的矿质营养变化差异及其与籽粒植酸含量的关系

Positional variation in grain mineral nutrients within a rice panicle and its relation to phytic acid concentration 水稻穗内不同粒位间的矿质营养变化差异及其与籽粒植酸含量的关系 first-author corresp ‡Corresponding Author ‡Corresponding Author †E-mail:chengfm@zju.edu.cn †E-mail:chengfm@zju.edu.cn chengfm@zju.edu.cn College of Agriculture and Biotechnology, Zhejiang University, Hangzhou 310058, China College of Agriculture and Biotechnology, Zhejiang University, Hangzhou 310058, China Six japonica rice genotypes, differing in panicle type, grain density, and phytic acid (PA) content, were applied to investigate the effect of grain position on the concentrations of major mineral nutrients and its relation to PA content and grain weight within a panicle. Grain position significantly affected the concentrations of the studied minerals in both the vertical and horizontal axes of a rice panicle. Heavy-weight grains, located on primary rachis and top rachis, generally had higher mineral concentrations, but were lower in PA concentration and molar ratios of PA/Zn, compared with the small-weight grains located on secondary rachis and bottom rachis, regardless of rice genotypes. However, on the basis of six rice genotypes, no significant correlations were found among mineral elements, PA, and grain weight. These results suggested that some desired minerals, like Zn and Fe, and their bioavailability, can be enhanced simultaneously by the modification of panicle patterns, and it will be helpful in the selection of rice genotypes with low PA and high mineral nutrients for further breeding strategy without sacrificing their high yields. 研究目的 2 阐明水稻穗内不同粒位间的主要矿质营养元素和植酸含量差异、粒位分布特点及其与品种穗型间的联系。 创新要点 2 将水稻品种的穗型变化与稻米营养品质结合起来，从水稻穗粒结构角度，对同一稻穗内不同籽粒间的主要矿质营养元素与植酸含量差异、粒位分布特点及其与水稻品种穗型间的相互关系进行了较系统的探讨分析。 研究方法 2 以典型的直立穗型和弯穗型粳稻品种为材料，通过对两类水稻品种在相同栽培条件下籽粒矿质营养元素和植酸含量的测定分析，并依据水稻籽粒在稻穗上的着生部位，将同一稻穗内的不同籽粒划分为六个粒位，比较分析了两类品种同一稻穗内不同部位间矿质营养元素和植酸含量的差异变化及其粒位分布特点。 重要结论 2 水稻穗型虽然与品种间的籽粒矿质营养元素和植酸含量高低没有直接关系，但对其穗内不同籽粒间的主要矿质营养元素和植酸含量存在着较大影响；与稻穗中下部的弱势粒相比，同一稻穗内着生在稻穗上中部的强势粒通常具有相对较高的锌、铁矿质元素含量，而籽粒植酸含量和植酸/锌（铁）摩尔比则有所降低，稻米营养品质也相对较好；不同矿质营养元素相比，粒位效应对铁矿质营养的影响作用要略大于对钙和锌营养元素含量。 Grain position Minerals Phytic acid Rice Oryza sativa L. 水稻穗型 粒位效应 营养品质 矿质元素 植酸 Introduction 1 Micronutrient malnutrition, often called ‘Hidden Hunger’, now affects more than two billion people worldwide (McLaughlin et al., 1999 1999 ). Populations in developing countries are particularly at risk as they live largely on plant-based diets without sufficient micronutrients gained from meat, fruits, or vegetables (Frank et al., 2009 2009 ). The case is particularly severe for women, infants, and children (Umeta et al., 2005 2005 ). It is therefore imperative to improve the nutrient composition of plant food so as to alleviate the widespread micronutrient malnutrition (Ferguson et al., 1988 1988 ). Rice is one of the major cereal crops, consumed by nearly two billion people worldwide. As a primary dietary source of energy, especially for the low-income and rural population, rice plays an important role in providing plant proteins, carbohydrates, and other nutrients (Ferguson et al., 1988 1988 ). However, rice grain is relatively low in some micronutrients such as iron (Fe), zinc (Zn), and calcium (Ca), compared with other staple crops such as wheat, maize, and legumes (Adeyeye et al., 2000 2000 ). In the past few decades, great efforts have been made to elucidate the effects of genotype and environment on mineral uptake and accumulation in rice plants (Schachtman and Barker, 1999 1999 ). It has been demonstrated that mineral concentrations in rice grain vary greatly according to genotype, geographical location, and other environmental factors (Anandan et al., 2011 2011 ). Although the extent of difference is cultivar-dependent, the former studies showed that grain position within a panicle had a considerable impact on grain chemical composition, like protein or microelements (Calderini and Ortiz-Monasterio, 2003 2003 ; Liu et al., 2005a 2005a ), suggesting that the improvement of spikelet architecture and morphological pattern is possible for obtaining the cultivars with high yield and balanced nutrition (Calderini and Ortiz-Monasterio, 2003 2003 ). Large variation among rice grains in a panicle is unfavorable for commercial value and quality (Jeng et al., 2006 2006 ). Some research has been performed on the effect of grain position within a panicle on rice quality, so as to reduce the variation through improved agronomic practices, including application of plant growth regulators, and better water and fertilizer management (Jongkaewwattana and Geng, 1991 1991 ). It was reported that there were large variations in grain quality (chalky occurrence, palatability, amylose, protein, and amylographic characteristics) between primary and secondary rachides (Matsue et al., 1995 1995 ) and among the different positions within a rice panicle (Kobayasi et al., 2002 2002 ). However, to date, little research has been done on the positional variation of micronutrient concentration in relation to rice panicle morphology. Phytic acid (PA) in crops, including cereals and legumes, is an anti-nutritional factor for animals and human, as it can strongly chelate mineral nutrients such as Zn, Fe, Ca, and magnesium (Mg) (Raboy, 2001 2001 ), leading to a marked reduction in their bioavailability (Raboy et al., 1984 1984 ). Moreover, animals possibly excrete more phytates if they are given high PA feed, which poses a threat of contaminating water. Therefore, it was important to reduce PA concentration in rice grain for the improvement of crops’ nutritional quality (Raboy, 2001 2001 ). In this experiment, six japonica rice genotypes, differing in panicle type, grain density, and PA content, were used with the following objectives: (1) to investigate the effect of grain position on mineral elements (potassium (K), Mg, sodium (Na), Ca, Zn, Fe, manganese (Mn), and copper (Cu)), as well as PA concentration; (2) to identify the positional distribution of mineral elements in grains within a panicle as affected by the panicle morphology of rice genotypes; and, (3) to illustrate the relationships among mineral elements, PA content, and grain weight at different positions within a panicle. Materials and methods 1 Plant materials and field experiments 2 According to previous surveys on grain PA and panicle type of 56 rice cultivars and 32 breeding lines, collected from different locations of China (Liu et al., 2005a 2005a ; Cheng et al., 2007 2007 ), six japonica rice genotypes (98110, HIPj, Xiushui63, Xiushui994, Chunjiang15, and Xiushui11) were selected for the current study. All genotypes were seeded in late May and transplanted in late June at the experimental farm of the Huajiachi Campus of Zhejiang University, China. Each genotype was grown in two replicates of an eight-row plot, 2 m long and 20 cm wide between rows with nine hills in each row and three seedlings per hill. The trial was managed according to locally recommended agronomic practices. Grain sampling and analysis 2 Grains from six positions within a panicle, i.e., top primary, top secondary, middle primary, middle secondary, bottom primary, and bottom secondary rachides, were sampled for analysis. The classification of these positions for each genotype is shown in Table 1 1 . Panicle traits, including panicle length and bending degree of panicle (an angle from the tip of panicle to the extending top of stem), were determined at maturity with 20 individual measurements of main stems in each plot (Table 1 1 ). PL: panicle length; GPP: grains per panicle; GD: grain density; BD: bending degree of panicle 2 Cultivar 2 Total number of primary branches 3 Classification of rachis within a panicle 5 Panicle morphological character Upper rachis Middle rachis Lower rachis PL (cm) GPP GD (grain/cm) BD (°) Yield (kg/hm 2 ) 98110 14 4 5 5 16.2 151.2 9.3 9.0 8427.5 HIPj 14 4 5 5 16.0 148.7 9.3 9.2 8132.7 Xiushui63 12 3 5 4 15.8 126.5 8.0 9.7 7737.1 Xiushui994 14 4 5 5 15.4 132. 6 8.6 7.8 7945.3 Chunjiang15 12 4 4 4 21.5 103.7 4.8 76.2 6863.8 Xiushui11 12 4 4 4 19.2 110.0 5.7 86.1 7142.0 At maturity, 30 panicles were harvested from each replication. After being dried naturally, rice grains were collected separately from six positions, then husked, milled, and passed through a 0.5-mm sieve. The flour was then stored in a desiccator until analysis. The concentrations of K, Na, Mg, Ca, Zn, Fe, Mn, and Cu were determined by an atomic absorption spectrophotometer (Perkin-Elmer Model AA6300) after wet digestion with nitric acid. PA was determined as described by Miller et al. ( 1980 1980 ) with modification (Liu et al., 2005a 2005a ). Triplicate measurements were performed for each sample. Data analysis 2 Statistical analysis was performed using statistics software version SPSS 11.0. The data were submitted for variance analysis and the means were tested by least significant difference. Correlation analysis was conducted to characterize the relationships among eight mineral elements, PA content, and grain weight for different grain positions and six genotypes, respectively. Results 1 Positional variation in K, Mg, Na, Ca, Zn, Fe, Mn, and Cu concentrations within a panicle 2 As shown in Table 2 2 , grain position was an important source of variation for grain mineral concentrations. Of all eight minerals, there were significant differences among grains located on the different positions within a panicle. The grains on the top primary and middle primary rachides had substantially higher minerals concentrations than those on the bottom secondary and middle secondary rachides. The order of positional differences in mineral concentrations was: top primary rachides > middle primary rachides > bottom primary rachides/top secondary rachides > middle secondary rachides > bottom secondary rachides, although the extent of difference was genotype-dependent and varied largely with various mineral elements. This result clearly indicated that grain position affected the concentrations of all eight minerals in both vertical and horizontal axes of the rice panicle. In comparative terms, the effects of grain positions on Na, Fe, and Cu concentrations were more substantial than those on Ca and Zn concentrations, as reflected by their differences in coefficients of variation (CVs) and the variable range of different positions (Table 2 2 ). TPR: top primary rachis; TSR: top secondary rachis; MPR: middle primary rachis; MSR: middle secondary rachis; BPR: bottom primary rachis; BSR: bottom secondary rachis; CV: coefficient of variation. The values followed by the same letters within a column are not significantly different in term of the same cultivar ( P > 0.05) 2 Cultivar 2 Grain position 8 Concentration (μg/g) K Mg Na Ca Zn Fe Mn Cu 98110 TPR 1627a 1518a 260.6a 263.7a 25.28a 10.27a 24.82bc 2.780a TSR 1568b 1453ab 219.8ab 256.5b 24.58b 9.57c 24.20c 2.471b MPR 1468c 1398b 203.3bc 253.9bc 24.55b 9.89b 26.08a 2.425b MSR 1396d 1315c 191.7bcd 250.7bc 24.07c 9.31d 26.03a 2.273b BPR 1440cd 1378bc 170.4cd 247.8cd 23.48d 8.96e 25.19b 1.866c BSR 1314e 1324c 156.3d 242.3d 22.78e 8.59f 24.63c 1.671c Mean 1469 1398 200.4 252.5 24.12 9.43 25.16 2.248 CV 7.76% 5.56% 18.57% 2.93% 3.69% 6.49% 3.04% 18.28% HIPj TPR 1862a 1704a 265.6a 282.1a 26.76a 11.93a 31.62a 2.815a TSR 1732b 1585b 200.5cde 269.4b 25.97b 10.90c 28.78b 2.567bc MPR 1583c 1440c 241.7ab 267.7b 25.83b 11.33b 27.52c 2.688ab MSR 1285e 1321d 215.1bc 263.8c 25.29c 10.92c 25.55c 2.459cd BPR 1536d 1389c 192.6de 257.6d 24.75d 10.42d 26.81c 2.302d BSR 1328e 1329d 184.1e 253.1e 24.38d 9.88e 25.07d 2.022e Mean 1554 1461 216.6 265.6 25.50 10.90 27.56 2.476 CV 14.43% 10.47% 14.49% 3.83% 3.41% 6.53% 8.71% 11.49% Xiushui63 TPR 1836a 1757a 312.2a 290.1a 22.87a 9.68a 46.83a 2.505a TSR 1790a 1671ab 267.7b 283.2b 22.50a 9.42bc 43.27c 2.167b MPR 1802a 1655b 275.8b 281.8b 21.99b 9.33cd 45.03b 2.225b MSR 1570b 1415c 249.9bc 276.9c 21.28c 9.16d 38.87de 2.168b BPR 1737a 1715ab 209.7c 270.3d 20.88cd 8.70e 42.87c 2.010b BSR 1498b 1429c 191.9c 262.4e 20.44d 8.40f 38.73e 1.643c Mean 1706 1607 251.2 277.5 21.66 9.11 42.60 2.120 CV 8.12% 9.19% 17.66% 3.57% 4.39% 5.25% 7.66% 13.40% Xiushui994 TPR 1655a 1359a 312.2a 304.2a 20.84a 10.81a 36.88a 3.270a TSR 1587ab 1297ab 239.1b 296.1b 20.46ab 10.18b 32.36c 2.908b MPR 1492b 1305ab 218.4b 292.3c 19.89ab 10.23b 33.81b 2.868b MSR 1571ab 1245b 202.2bc 287.4d 19.75ab 9.76c 32.52c 2.673bc BPR 1514b 1291ab 167.6cd 282.7e 19.21b 9.17d 32.98c 2.442cd BSR 1465b 1225b 150.6d 276.1f 18.79b 8.96e 30.29d 2.198d Mean 1547 1287 215.0 289.8 19.82 9.85 33.14 2.727 CV 4.54% 3.68% 26.80% 3.44% 3.84% 7.09% 6.55% 13.84% Chunjiang15 TPR 1571a 1456a 228.9a 254.0a 24.81a 9.72a 34.02a 3.208a TSR 1308bc 1339b 179.9bc 247.8b 22.40b 9.26b 32.30b 2.975b MPR 1395b 1310bc 202.0abc 247.0b 21.55c 9.14b 31.93b 2.832b MSR 1336bc 1250c 218.7ab 240.2cd 22.40b 8.81c 31.22bc 2.870b BPR 1278c 1274bc 187.0abc 236.9d 21.26c 8.40d 30.84c 2.603c BSR 1285c 1375b 174.9c 231.6e 20.45d 8.18e 30.18c 2.525c Mean 1362 1334 198.7 242.9 22.15 8.92 31.75 2.836 CV 8.13% 5.59% 10.99% 3.37% 6.77% 6.41% 4.24% 8.78% Xiushui11 TPR 1527a 1458a 273.8a 229.6a 24.48a 11.71a 30.58a 2.868a TSR 1347bc 1343a 228.2b 223.9b 23.74a 11.42b 26.95b 2.672b MPR 1421ab 1333a 228.9b 218.8cd 24.04a 11.20c 25.15bc 2.568c MSR 1345bc 1365a 216.1bc 214.6d 23.49a 10.86d 24.30c 2.458d BPR 1276c 1368a 206.0bc 209.5e 22.33b 10.34e 24.06c 2.283e BSR 1098d 864b 191.5c 203.2f 21.92b 10.08f 22.65d 2.132f Mean 1336 1289 224.1 216.6 23.33 10.94 25.62 2.497 CV 10.81% 16.50% 12.57% 4.43% 4.29% 5.78% 10.99% 10.65% The ratio of the eight mineral concentrations was relatively stable or showed only slight variations among different grain positions in a rice cultivar (Table 2 2 ). However, relatively great variability in the ratio of various minerals was found among cultivars, although the concentrations of Zn, Fe, Mn, and Cu were found to be remarkably lower than those of K, Mg, Na, and Ca in rice grains, with the lowest values for Cu and Fe, and the highest for K and Mg. For instance, 98110 had much higher Ca and Mg concentrations than Xiushui11, whereas the concentrations of Fe, Mn, and Cu for 98110 were lower than those for Xiushui11, in terms of an average of six different positions. This result suggested that grain positions had a relatively small impact on the ratio of mineral concentrations compared with the rice genotypes, despite the different sensitivities to the effect of grain positions among different mineral elements. Considering the yield potential of rice genotypes (Table 1 1 ) and grain mineral concentrations (Table 2 2 ), little relationship was found between the eight mineral concentrations and rice genotypes, differing in grain density in a panicle and grain yield, in terms of average different positions. In contrast, the extent of positional variation in some mineral elements (K, Na, Fe, and Cu), particularly the variable range between top primary rachides and bottom secondary rachides, even tended to be more pronounced than that of the six rice genotype variations (Table 2 2 ). This implied that the concentrations of mineral elements in rice grains were not inherently related to the level of grain yield for different rice genotypes. Positional variation in PA content, grain weight, molar ratios of PA/Zn and PA/Fe within a panicle 2 From Table 3 3 , the marked differences among different positions were found in PA concentration, grain weight, and molar ratios of PA/Zn and PA/Fe. For grain weight, the grains located on the primary rachis (PR) and top rachis (TR) were significantly heavier than those on the secondary rachis (SR) and bottom rachis (BR), irrespective of rice genotype. On the other hand, the grains on PR and TR had somewhat lower PA concentrations relative to those on SR and BR. This result suggested that the grains with heavier weights were generally lower in PA concentrations in a comparison of different positions within a panicle, which was opposite to the effect of grain positions on mineral concentrations. However, the extent of positional variation in PA concentrations was considerably smaller compared with that in grain weight and most of minerals, in terms of their small CVs and narrow-range in PA among different grain positions for all six rice genotypes presented here (Tables 2 2 and 3 3 ). PR: primary rachis; SR: secondary rachis; TR: top rachis; MR: middle rachis; BR: bottom rachis. The crossing column between TR and PR means TPR (top primary rachis), and the corresponding expressions were for TSR (top secondary rachis, TR-SR), MPR (middle primary rachis, MR-PR), MSR (middle secondary rachis, MR-SR), BPR (bottom primary rachis, BR-PR), and BSR (bottom secondary rachis, BR-SR), respectively. Mean 1 is the average of three different positions for PR or SR; Mean 2 is the average of all six different positions; CV is the coefficient of variation. The values followed by the same letters within a column are not significantly different in term of the same cultivar ( P > 0.05) 2 Cultivar 2 Grain position 2 PA concentration (mg/g) 2 Grain weight (mg) 2 PA/Zn molar ratio 2 PA/Fe molar ratio PR SR PR SR PR SR PR SR 98110 TR 4.68b 4.55b 25.47a 20.12c 18.35c 18.34c 45.17e 47.09d MR 4.89a 4.49b 24.35a 20.63c 19.74b 18.50c 49.00c 47.81cd BR 5.07a 5.25a 22.16b 17.06d 21.39a 22.85a 56.02b 60.58a Mean 1 4.88 4.76 23.99 19.27 19.83 19.89 50.06 51.83 Mean 2 2 4.82 2 21.63 2 19.86 2 50.95 CV 2 6.24% 2 14.10% 2 9.48% 2 11.80% HIPj TR 4.54a 4.43ab 24.12a 19.05d 16.82a 16.90a 37.73c 40.26b MR 4.18c 4.32ab 23.16b 19.01d 16.03b 16.91a 36.54cd 39.17b BR 3.68d 4.23c 20.50c 18.09e 14.73c 17.17a 35.00d 42.39a Mean 1 4.13 4.32 22.59 18.72 15.86 16.99 36.42 40.61 Mean 2 2 4.23 2 20.65 2 16.43 2 38.52 CV 2 7.10% 2 11.89% 2 5.57% 2 6.90% Xiushui63 TR 5.64bc 5.60c 26.54a 23.04c 24.66d 25.24d 58.26c 60.30c MR 6.13a 6.06a 25.68ab 22.40c 27.88c 28.48b 65.70b 66.16b BR 5.97ab 5.98ab 25.26b 22.45c 28.59b 29.26a 68.62b 71.19a Mean 1 5.91 5.88 25.83 22.63 27.04 27.66 64.19 65.88 Mean 2 2 5.90 2 24.23 2 27.35 2 65.04 CV 2 3.77% 2 7.48% 2 7.01% 2 7.56% Xiushui994 TR 4.58ab 4.46b 25.71a 23.18ab 21.98c 21.80c 42.37d 43.81c MR 4.28c 4.36c 24.14a 18.62c 21.52c 22.07c 41.84d 44.67c BR 4.43bc 4.64a 20.29bc 17.57c 23.06b 24.69a 48.31b 51.78a Mean 1 4.43 4.49 23.28 19.79 22.19 22.85 44.17 46.75 Mean 2 2 4.46 2 21.58 2 22.52 2 45.46 CV 2 3.01% 2 15.04% 2 5.27% 2 8.47% Chunjiang15 TR 4.87bc 4.90b 27.69a 21.41d 19.63c 21.88b 50.10c 52.92bc MR 4.98ab 5.09a 26.51ab 25.07bc 23.11a 22.72b 54.49b 57.78a BR 4.85bc 4.75c 24.68c 21.03d 22.81b 23.23a 57.74a 58.07a Mean 1 4.90 4.91 26.29 22.50 21.85 22.61 54.11 56.26 Mean 2 2 4.91 2 24.40 2 22.23 2 55.18 CV 2 2.38% 2 11.01% 2 6.12% 2 5.90% Xiushui11 TR 4.23b 4.31a 29.00a 28.61ab 17.28c 18.15b 36.12c 37.74c MR 4.49a 4.25b 28.48ab 24.26c 18.68b 18.09b 40.09b 39.13b BR 4.51a 4.38a 27.49b 19.73d 20.21a 19.98a 43.62a 43.45a Mean 1 4.41 4.31 28.32 24.20 18.72 18.74 39.94 40.11 Mean 2 2 4.36 2 26.26 2 18.73 2 40.03 CV 2 2.74% 2 13.84% 2 6.14% 2 7.57% The molar ratio of PA/Zn was commonly considered as an important parameter for the evaluation of Zn bioavailability in cereal and legumes (Raboy et al., 1984 1984 ). As shown in Table 3 3 , the average molar ratio of PA/Zn ranged from 18.73 (Xiushui11) to 27.35 (Xiushui63) among the six genotypes, and the extent of positional variation in the molar ratio of PA/Zn was much larger than that in PA concentrations among different grains within a panicle, as reflected by their CVs. In general, PR and TR tended to have lower molar ratio of PA/Zn relative to SR and BR, which was almost consistent with the tendency of positional differences in PA concentration. This result implied that grain position was closely related to Zn bioavailability in rice grains, with relatively high Zn bioavailability noted for PR and TR within a panicle. The average molar ratio of PA/Fe ranged from 38.52 to 65.04 among all six genotypes, wider variation compared with that of average molar ratio of PA/Zn (Table 3 3 ). Moreover, the extent of the variation in the molar ratio of PA/Fe among different grain positions was also somewhat greater than that in the molar ratio of PA/Zn, despite the similar trend for difference between PR and SR for both molar ratios of PA/Fe and PA/Zn. Correlations among K, Mg, Na, Ca, Zn, Fe, Mn, Cu, PA contents and grain weight 2 The Pearson correlation coefficients among eight minerals, PA and grain weight were calculated for six different grain positions in a panicle (Table 4 4 ). There were highly positive correlations ( P < 0.01) between Zn and Fe, and statistically positive correlations ( P < 0.05 or P < 0.01) among Ca, Zn, Fe, and Cu, regardless of genotypes. However, the statistical significance varied greatly with rice genotype for most of their correlations among other mineral concentrations, and also among minerals, PA, and grain weight. Generally, there were positive correlations among eight minerals, and between minerals and grain weight, but negative correlations between minerals and PA content. Correlation is significant at the 0.05 level (2-tailed) Correlation is significant at the 0.01 level (2-tailed) 2 Cultivar 2 Feature 10 Correlation coefficient K Mg Na Ca Zn Fe Mn Cu PA GW 10 98110 K 1.000 Mg 0.960 ** ** 1.000 Na 0.932 ** ** 0.889 * * 1.000 Ca 0.953 ** ** 0.891 * * 0.991 ** ** 1.000 Zn 0.904 * * 0.810 0.959 ** ** 0.981 ** ** 1.000 Fe 0.856 * * 0.796 0.936 ** ** 0.955 ** ** 0.981 ** ** 1.000 Mn −0.302 −0.430 −0.151 −0.092 0.064 0.143 1.000 Cu 0.874 * * 0.777 0.962 ** ** 0.971 ** ** 0.993 ** ** 0.970 ** ** 0.054 1.000 PA −0.577 −0.353 −0.662 −0.677 −0.730 −0.612 −0.117 −0.768 1.000 GW 0.702 0.663 0.711 0.770 0.794 0.854 * * 0.361 0.733 −0.315 1.000 10 HIPj K 1.000 Mg 0.963 ** ** 1.000 Na 0.601 0.650 1.000 Ca 0.816 * * 0.891 * * 0.880 * * 1.000 Zn 0.826 * * 0.886 * * 0.859 * * 0.990 ** ** 1.000 Fe 0.709 0.751 0.951 ** ** 0.957 ** ** 0.953 ** ** 1.000 Mn 0.961 ** ** 0.982 ** ** 0.744 0.923 ** ** 0.907 * * 0.825 * * 1.000 Cu 0.743 0.753 0.883 * * 0.934 ** ** 0.956 ** ** 0.978 ** ** 0.812 * * 1.000 PA 0.351 0.567 0.512 0.665 0.669 0.537 0.492 0.492 1.000 GW 0.684 0.624 0.902 * * 0.744 0.729 0.839 * * 0.741 0.795 0.161 1.000 10 Xiushui63 K 1.000 Mg 0.938 ** ** 1.000 Na 0.746 0.541 1.000 Ca 0.807 0.614 0.985 ** ** 1.000 Zn 0.821 * * 0.651 0.953 ** ** 0.972 ** ** 1.000 Fe 0.753 0.533 0.984 ** ** 0.994 ** ** 0.963 ** ** 1.000 Mn 0.956 ** ** 0.925 ** ** 0.763 0.782 0.800 0.718 1.000 Cu 0.780 0.618 0.947 ** ** 0.963 ** ** 0.881 * * 0.947 ** ** 0.767 1.000 PA −0.473 −0.531 −0.483 −0.533 −0.661 −0.503 −0.477 −0.433 1.000 GW 0.789 0.836 * * 0.552 0.547 0.503 0.465 0.896 * * 0.634 −0.201 1.000 10 Xiushui994 K 1.000 Mg 0.669 1.000 Na 0.880 * * 0.853 * * 1.000 Ca 0.848 * * 0.875 * * 0.978 ** ** 1.000 Zn 0.879 * * 0.807 0.963 ** ** 0.989 ** ** 1.000 Fe 0.772 0.819 * * 0.961 ** ** 0.979 ** ** 0.962 ** ** 1.000 Mn 0.734 0.924 ** ** 0.873 * * 0.852 * * 0.780 0.830 * * 1.000 Cu 0.827 * * 0.865 * * 0.974 ** ** 0.995 ** ** 0.977 ** ** 0.990 ** ** 0.872 * * 1.000 PA 0.142 −0.053 0.056 −0.110 −0.098 −0.179 −0.081 −0.164 1.000 GW 0.587 0.945 ** ** 0.862 * * 0.909 * * 0.854 * * 0.898 * * 0.834 * * 0.905 * * −0.162 1.000 10 Chunjiang15 K 1.000 Mg 0.690 1.000 Na 0.805 0.191 1.000 Ca 0.802 0.460 0.607 1.000 Zn 0.869 * * 0.542 0.792 0.850 * * 1.000 Fe 0.820 * * 0.488 0.641 0.993 ** ** 0.881 * * 1.000 Mn 0.888 * * 0.618 0.655 0.967 ** ** 0.933 ** ** 0.971 ** ** 1.000 Cu 0.818 * * 0.480 0.715 0.944 ** ** 0.949 ** ** 0.972 ** ** 0.956 ** ** 1.000 PA 0.111 −0.567 0.575 0.309 0.251 0.329 0.161 0.367 1.000 GW 0.764 0.124 0.863 * * 0.592 0.615 0.567 0.602 0.540 0.439 1.000 10 Xiushui11 K 1.000 Mg 0.871 * * 1.000 Na 0.921 ** ** 0.690 1.000 Ca 0.916 * * 0.751 0.938 ** ** 1.000 Zn 0.944 ** ** 0.733 0.887 * * 0.940 ** ** 1.000 Fe 0.909 * * 0.714 0.911 * * 0.990 ** ** 0.970 ** ** 1.000 Mn 0.842 * * 0.645 0.973 ** ** 0.938 ** ** 0.813 0.892 * * 1.000 Cu 0.928 ** ** 0.744 0.950 ** ** 0.998 ** ** 0.955 ** ** 0.992 ** ** 0.938 ** ** 1.000 PA −0.337 −0.189 −0.507 −0.503 −0.458 −0.500 −0.548 −0.522 1.000 GW 0.838 * * 0.882 * * 0.709 0.804 0.734 0.771 0.700 0.782 0.041 1.000 Table 5 5 presents the correlations among the eight minerals, PA and grain weight for six genotypes. The correlation coefficients among the minerals were statistically significant only for K-Ca ( r =0.833), but no significant correlations ( P > 0.05) were observed among PA and minerals, except for PA-Mn ( r =0.818). Furthermore, grain weight was poorly correlated with minerals and PA. This result implied that grain PA concentration was relatively independent of grain weight and most metal minerals for different rice genotypes. Correlation is significant at the 0.05 level (2-tailed) Correlation is significant at the 0.01 level (2-tailed) 2 Feature 10 Correlation coefficient K Mg Na Ca Zn Fe Mn Cu PA GW K 1.000 Mg 0.801 1.000 Na 0.670 0.657 1.000 Ca 0.833 * * 0.403 0.270 1.000 Zn −0.195 0.200 −0.210 −0.444 1.000 Fe −0.216 −0.269 0.076 −0.304 0.490 1.000 Mn 0.724 0.621 0.699 0.597 −0.611 −0.562 1.000 Cu −0.573 −0.759 −0.590 −0.112 −0.318 0.036 −0.236 1.000 PA 0.562 0.726 0.568 0.285 −0.339 −0.744 0.818 * * −0.543 1.000 GW −0.420 −0.133 0.316 −0.661 −0.209 −0.057 0.153 0.030 0.285 1.000 Discussion 1 The yield potential of a rice cultivar is closely related to grain number per panicle and grain weight (Cheng et al., 2007 2007 ). However, it was practically difficult to make a balance of grain number and grain weight for a rice panicle owing to the limiting assimilation supply from leaves (Mohapatra and Sahu, 1991 1991 ). In the past two decades, the enhancement of yield level for newly released japonica cultivars was mostly attributable to the elevated grain number per panicle (Padmajarao, 1995 1995 ), and there was a narrow variation of grain weight between modern japonica cultivars and landraces (He et al., 2011 2011 ). In fact, the japonica cultivars now being widely planted in China were mainly characterized by compact and erect or semi-erect panicles with more grains per panicle (Cheng et al., 2007 2007 ). On the other hand, the compact-panicle cultivars were often found to show a great variation in floret development and grain filling among different rachides within a panicle (Liu et al., 2005b 2005b ; Wang et al., 2006 2006 ); also there were dramatic differences in protein composition, amylose content, grain weight, and chalkiness among different positional grains (Cheng et al., 2007 2007 ). In our current study, grain position significantly affected the concentrations of minerals in both vertical and horizontal axes of the rice panicle. The grains located on top primary and middle primary rachides were substantially higher than those on bottom secondary rachides and middle secondary rachides for all measured minerals (K, Mg, Na, Ca, Mn, Zn, Fe, and Cu). This result was generally in agreement with several previous findings, which demonstrated that the levels of Zn and Fe concentrations in wheat grain decreased at grain positions far distal from rachis (Calderini and Ortiz-Monasterio, 2003 2003 ), and the heavy-weight grains had higher Zn and Fe concentrations relative to the small-weight grains within a wheat spike (Liu et al., 2006 2006 ). However, little association was found between mineral concentrations and the rice yield for the rice genotypes differing in grain density and grain weight (Table 2 2 ), and between grain weight and the mineral concentrations, in term of an average of six different grain positions (Table 5 5 ). The results indicated the feasibility of enhancing the desirable mineral concentrations in rice grains without causing reduction in grain weight and yield level by appropriate breeding strategies and agronomic management for the compact rice cultivars. Moreover, in light of the fact that the high yield potentials of compact rice cultivars were mostly achieved by high grain density and floret numbers in a panicle (Wang et al., 2006 2006 ; Cheng et al., 2007 2007 ), it might be practically efficient to increase grain mineral concentrations of whole rice panicles, with the variation of mineral concentration among grains within a panicle being simultaneously decreased, through the modification of their rachis patterns in a panicle, i.e., reducing grain number on the secondary rachis, or increasing grain number on the secondary rachis at the top rachis instead of at the bottom rachis. Previous studies have showed that the enhancement of yield potentials could cause a significant reduction in nitrogen (N) and phosphoros (P) concentrations of wheat (Calderini et al., 1995 1995 ), rice (Jongkaewwattana and Geng, 1991 1991 ), maize (Simmonds, 1995 1995 ), and sunflower grains (López Pereira et al., 2000 2000 ). Additionally, initial findings indicated that grain weight was negatively related to grain PA, prolamin, glutelin, and total protein contents among different positions in a wheat spike (Herzog and Stamp, 1983 1983 ; Ishimaru et al., 2005 2005 ) or a rice panicle (Matsue et al., 1995 1995 ; Liu et al., 2005b 2005b ). Our present research concluded that the heavy-weight grains in a rice panicle generally had lower PA relative to the light ones (Table 3 3 ), which coincided well with previous reports (Liu et al., 2005b 2005b ). Interestingly, our experimental results revealed that Fe and Zn concentrations of heavy-weight grains were generally higher than those of light-weight grains (Table 2 2 ), but the positional variations in Fe and Zn concentrations were poorly related to those in grain PA concentration for the different rachides within a rice panicle (Table 4 4 ). Thavarajah et al. ( 2010 2010 ) investigated the impact of environmental temperature on PA, Zn and Fe concentrations in lentil seeds, concluding that high PA content was independent of the increase in total Zn and Fe concentrations in lentil seeds for high temperature regimes. Furthermore, Iwai et al. ( 2012 2012 ) revealed that total Fe, Zn, and K concentrations in filling grains increased constantly with rice grain development, and the well-developed mature grains had higher concentrations of Fe, Zn, and K minerals than the poorly-developed filling grains. According to our findings, the heavy-weight grains in a rice panicle generally had higher Fe and Zn concentrations relative to the small ones (Table 2 2 ). This trend was basically similar to the results reported previously by Thavarajah et al. ( 2010 2010 ) and Iwai et al. ( 2012 2012 ), but it was contradictory to a previous hypothesis, which presumed that the low N and P concentrations in heavy-weight grains were partially caused by the dilution of additional starch accumulation to other chemical components (Calderini and Ortiz-Monasterio, 2003 2003 ). Nevertheless, these discordant phenomena did not exclude the possibility that grain N and P concentrations were quite different from many metal minerals in their positional variations within a panicle/spike, which could be caused by their difference in the translocation and accumulation in the rice plant and grain location (Schachtman and Barker, 1999 1999 ; Vasconcelos et al., 2003 2003 ). Considering the extent of variation in grain mineral concentration among different positions within a rice panicle, the effect of grain position was more substantial for Na, Fe, and Cu than for Ca and Zn (Table 2 2 ). For rice breeding strategies, the different sensitivities to the effect of grain position on these metal minerals suggested that the improvement of panicle architecture and morphological pattern should be attended to more carefully if the deficiency of desired minerals was caused by low Fe concentration rather than low Zn and Ca concentrations in a compact rice cultivar. However, it should be stressed that the effect of grain position on the concentrations of PA and metal minerals (e.g., Fe, Zn, and Ca) was somewhat variable, depending on rice cultivars, and also the extent of positional variations in PA and metal minerals within a panicle was, in many cases, not so great as the cultivar-dependent difference in PA and metal minerals (Tables 2 2 and 3 3 ). For instance, Xiushui11 had relatively higher Fe, but inherently lower Ca concentration in rice grains than Chunjiang15, irrespective of grain position in the rice panicle. Thus, the selection of rice genotypes with low PA and high desirable minerals was an effective approach to directly reduce grain PA and to enhance the desirable mineral concentrations in rice grains for the improvement of its nutritional quality. The inhibitory effect of PA on mineral absorption can be estimated by molar ratios of PA/mineral concentrations. The molar ratio of PA/Zn was most widely applied to evaluate Zn bioavailability for human and animal absorption (Raboy et al., 1984 1984 ). The molar ratios of PA/Zn for cereals and legumes, maize, wheat, sorghum, and rice ranged approximately from 20 to 40, and were relatively high compared with millet and soybean. In our study, the molar ratio of PA/Zn in brown rice grains was very close to those reviewed by Adeyeye et al. ( 2000 2000 ), but it was slightly lower than the previous report of Wei et al. ( 2012 2012 ), possibly owing to differences in PA and mineral determination methods. Considering the variations of the molar ratios of PA/Zn and PA/Fe among different grain positions, PR and TR generally were lower in both the molar ratios of PA/Zn and PA/Fe compared with BR and SR (Table 3 3 ), and also there was a significantly positive association between Zn and Fe concentrations for different grain positions within a panicle (Table 4 4 ) and positive correlation for various rice cultivars (Table 5 5 ). Our result was in agreement with the previous finding that transgenic rice with the ferritin gene enhanced Zn accumulation in rice grains (Vasconcelos et al., 2003 2003 ). Therefore, it could be concluded that grain position had a large impact not only on grain Zn and Fe concentrations, but also on their bioavailability. Meanwhile, the lower PA and higher Zn or Fe concentrations for the heavier weight grains within a panicle implied that grain Zn and Fe concentrations in rice grains and their bioavailability could be concomitantly enhanced by a selection of good panicle architecture and morphological pattern for the rice genotypes, particularly for the compact rice genotypes with high grain density and yield levels. References EI Adeyeye , LA Arogundade , ET Akintayo , 等 . Calcium, zinc and phytate interrelationship in some foods of major consumption in Nigeria . Food Chem , 2000 . 71 ( 4 ): 435 - 441 . DOI: 10.1016/S0308-8146(00)00159-X http://doi.org/10.1016/S0308-8146(00)00159-X . Calcium, zinc and phytate interrelationship in some foods of major consumption in Nigeria A Anandan , G Rajiv , R Eswaran , 等 . Genotypic variation and relationships between quality traits and trace elements in traditional and improved rice ( Oryza sativa L.) genotypes . J Food Sci , 2011 . 76 ( 4 ): H122 - H130 . 22417360 DOI: 10.1111/j.1750-3841.2011.02135.x http://doi.org/10.1111/j.1750-3841.2011.02135.x . Genotypic variation and relationships between quality traits and trace elements in traditional and improved rice (Oryza sativa L.) genotypes DF Calderini , I Ortiz-Monasterio . Grain position affects grain macronutrient and micronutrient concentrations in wheat . Crop Sci , 2003 . 43 ( 1 ): 141 - 151 . DOI: 10.2135/cropsci2003.0141 http://doi.org/10.2135/cropsci2003.0141 . Grain position affects grain macronutrient and micronutrient concentrations in wheat DF Calderini , S Torresleon , GA Slafer . Consequences of wheat breeding on nitrogen and phosphorus yield, grain nitrogen and phosphorus concentration and associated traits . Ann Bot (London) , 1995 . 76 ( 3 ): 315 - 322 . DOI: 10.1006/anbo.1995.1101 http://doi.org/10.1006/anbo.1995.1101 . Consequences of wheat breeding on nitrogen and phosphorus yield, grain nitrogen and phosphorus concentration and associated traits FM Cheng , Y Liu , ZH Liu , 等 . Positional variation in chalky occurrence within a rice panicle and its relation to grain nutritional quality . Aust J Agric Res , 2007 . 58 ( 2 ): 95 - 103 . . Positional variation in chalky occurrence within a rice panicle and its relation to grain nutritional quality EL Ferguson , RS Gibson , LU Thompson , 等 . Phytate, zinc, and calcium contents of 30 East African foods and their calculated phytate:Zn, Ca:phytate and [Ca][phytate]/[Zn] molar ratios . J Food Compos Anal , 1988 . 1 ( 4 ): 316 - 325 . DOI: 10.1016/0889-1575(88)90031-2 http://doi.org/10.1016/0889-1575(88)90031-2 . Phytate, zinc, and calcium contents of 30 East African foods and their calculated phytate:Zn, Ca:phytate and [Ca][phytate]/[Zn] molar ratios T Frank , R Habernegg , FJ Yuan , 等 . Assessment of the contents of phytic acid and divalent cations in low phytic acid ( lpa ) mutants of rice and soybean . J Food Compos Anal , 2009 . 22 ( 4 ): 278 - 284 . DOI: 10.1016/j.jfca.2008.11.022 http://doi.org/10.1016/j.jfca.2008.11.022 . Assessment of the contents of phytic acid and divalent cations in low phytic acid (lpa) mutants of rice and soybean XH He , Y Sun , D Gao , 等 . Comparison of agronomic traits between rice landraces and modern varieties at different altitudes in the paddy fields of Yuanyang terrace, Yunnan province . J Resour Ecol , 2011 . 2 ( 1 ): 46 - 50 . DOI: 10.3969/j.issn.1674-764x.2011.01.007 http://doi.org/10.3969/j.issn.1674-764x.2011.01.007 . Comparison of agronomic traits between rice landraces and modern varieties at different altitudes in the paddy fields of Yuanyang terrace, Yunnan province H Herzog , P Stamp . Dry matter and nitrogen accumulation in grains at different ear positions in ‘gigas’, semidwarf and normal spring wheats . Euphytica , 1983 . 32 ( 2 ): 511 - 520 . DOI: 10.1007/BF00021463 http://doi.org/10.1007/BF00021463 . Dry matter and nitrogen accumulation in grains at different ear positions in ‘gigas’, semidwarf and normal spring wheats T Ishimaru , T Hirose , T Matsuda , 等 . Expression patterns of genes encoding carbohydrate-metabolizing enzymes and their relationship to grain filling in rice ( Oryza sativa L.) comparison of caryopses located at different positions in a panicle . Plant Cell Physiol , 2005 . 46 ( 4 ): 620 - 628 . 15701658 DOI: 10.1093/pcp/pci066 http://doi.org/10.1093/pcp/pci066 . Expression patterns of genes encoding carbohydrate-metabolizing enzymes and their relationship to grain filling in rice (Oryza sativa L.) comparison of caryopses located at different positions in a panicle T Iwai , M Takahashi , K Oda , 等 . Dynamic changes in the distribution of minerals in relation to phytic acid accumulation during rice seed development . Plant Physiol , 2012 . 160 ( 4 ): 2007 - 2014 . 23090587 DOI: 10.1104/pp.112.206573 http://doi.org/10.1104/pp.112.206573 . Dynamic changes in the distribution of minerals in relation to phytic acid accumulation during rice seed development TL Jeng , TH Tseng , CS Wang , 等 . Yield and grain uniformity in contrasting rice genotypes suitable for different growth environments . Field Crop Res , 2006 . 99 ( 1 ): 59 - 66 . DOI: 10.1016/j.fcr.2006.03.005 http://doi.org/10.1016/j.fcr.2006.03.005 . Yield and grain uniformity in contrasting rice genotypes suitable for different growth environments S Jongkaewwattana , S Geng . Effect of nitrogen and water management on panicle development and milling quality of California rice ( Oryza sativa L.) . J Agron Crop Sci , 1991 . 167 ( 1 ): 43 - 52 . DOI: 10.1111/j.1439-037X.1991.tb00932.x http://doi.org/10.1111/j.1439-037X.1991.tb00932.x . Effect of nitrogen and water management on panicle development and milling quality of California rice (Oryza sativa L.) K Kobayasi , Y Horie , T Imaki . Relationship between apical dome diameter at panicle initiation and the size of panicle components in rice grown under different nitrogen conditions during the vegetative stage . Plant Prod Sci , 2002 . 5 ( 1 ): 3 - 7 . DOI: 10.1626/pps.5.3 http://doi.org/10.1626/pps.5.3 . Relationship between apical dome diameter at panicle initiation and the size of panicle components in rice grown under different nitrogen conditions during the vegetative stage ZH Liu , FM Cheng , GP Zhang . Grain phytic acid content as affected by cultivar and environment and its relation to protein content . Food Chem , 2005 . 89 ( 1 ): 49 - 52 . DOI: 10.1016/j.foodchem.2004.01.081 http://doi.org/10.1016/j.foodchem.2004.01.081 . Grain phytic acid content as affected by cultivar and environment and its relation to protein content ZH Liu , FM Cheng , WD Cheng , 等 . Positional variations in phytic acid and protein content within a panicle of japonica rice . J Cereal Sci , 2005 . 41 ( 3 ): 297 - 303 . DOI: 10.1016/j.jcs.2004.09.010 http://doi.org/10.1016/j.jcs.2004.09.010 . Positional variations in phytic acid and protein content within a panicle of japonica rice ZH Liu , HY Wang , XE Wang , 等 . Genotypic and spike positional difference in grain phytase activity, phytate, inorganic phosphorus, iron, and zinc contents in wheat ( Triticum aestivum L.) . J Cereal Sci , 2006 . 44 ( 2 ): 212 - 219 . DOI: 10.1016/j.jcs.2006.06.001 http://doi.org/10.1016/j.jcs.2006.06.001 . Genotypic and spike positional difference in grain phytase activity, phytate, inorganic phosphorus, iron, and zinc contents in wheat (Triticum aestivum L.) M López Pereira , N Trápani , VO Sadras . Genetic improvement of sunflower in Argentina between 1930 and 1995: Part III. Dry matter partitioning and grain composition . Field Crop Res , 2000 . 67 ( 3 ): 215 - 221 . DOI: 10.1016/S0378-4290(00)00096-4 http://doi.org/10.1016/S0378-4290(00)00096-4 . Genetic improvement of sunflower in Argentina between 1930 and 1995: Part III. Dry matter partitioning and grain composition Y Matsue , K Odahara , M Hiramatsu . Differences in amylose content, amylographic characteristics and storage proteins of grains on primary and secondary rachis branches in rice ( Oryza Sativa ) . Jpn J Crop Sci , 1995 . 64 ( 3 ): 601 - 606 . DOI: 10.1626/jcs.64.601 http://doi.org/10.1626/jcs.64.601 . Differences in amylose content, amylographic characteristics and storage proteins of grains on primary and secondary rachis branches in rice (Oryza Sativa) MJ McLaughlin , DR Parker , JM Clarke . Metals and micronutrients—food safety issues . Field Crop Res , 1999 . 60 ( 1-2 ): 143 - 163 . DOI: 10.1016/S0378-4290(98)00137-3 http://doi.org/10.1016/S0378-4290(98)00137-3 . Metals and micronutrients—food safety issues GA Miller , VL Youngs , ES Oplinger . Environmental and cultivar effects on oat phytic acid concentration . Cereal Chem , 1980 . 57 ( 3 ): 189 - 191 . . Environmental and cultivar effects on oat phytic acid concentration PK Mohapatra , SK Sahu . Heterogeneity of primary branch development and spikelet survival in rice panicle in relation to assimilates of primary branches . J Exp Bot , 1991 . 42 ( 7 ): 871 - 879 . DOI: 10.1093/jxb/42.7.871 http://doi.org/10.1093/jxb/42.7.871 . Heterogeneity of primary branch development and spikelet survival in rice panicle in relation to assimilates of primary branches S Padmajarao . Yield and high density grain as influenced by crop density and N levels in scented rice . Madras Agric J , 1995 . 82 ( 2 ): 108 - 112 . . Yield and high density grain as influenced by crop density and N levels in scented rice V Raboy . Seeds for a better future: ‘low phytate’ grains help to overcome malnutrition and reduce pollution . Trends Plant Sci , 2001 . 6 ( 10 ): 458 - 462 . 11590064 DOI: 10.1016/S1360-1385(01)02104-5 http://doi.org/10.1016/S1360-1385(01)02104-5 . Seeds for a better future: ‘low phytate’ grains help to overcome malnutrition and reduce pollution V Raboy , DB Dickinson , FE Below . Variation in seed total phosphorus, phytic acid, zinc, calcium, magnesium, and protein among lines of Glycine max and G. soja . Crop Sci , 1984 . 24 ( 3 ): 431 - 434 . DOI: 10.2135/cropsci1984.0011183X002400030001x http://doi.org/10.2135/cropsci1984.0011183X002400030001x . Variation in seed total phosphorus, phytic acid, zinc, calcium, magnesium, and protein among lines of Glycine max and G. soja DP Schachtman , SJ Barker . Molecular approaches for increasing the micronutrient density in edible portions of food crops . Field Crops Res , 1999 . 60 ( 1-2 ): 81 - 92 . DOI: 10.1016/S0378-4290(98)00134-8 http://doi.org/10.1016/S0378-4290(98)00134-8 . Molecular approaches for increasing the micronutrient density in edible portions of food crops NW Simmonds . The relation between yield and protein in cereal grain . J Sci Food Agric , 1995 . 67 ( 3 ): 309 - 315 . DOI: 10.1002/jsfa.2740670306 http://doi.org/10.1002/jsfa.2740670306 . The relation between yield and protein in cereal grain D Thavarajah , P Thavarajah , CT See , 等 . Phytic acid and Fe and Zn concentration in lentil ( Lens culinaris L.) seeds is influenced by temperature during seed filling period . Food Chem , 2010 . 122 ( 1 ): 254 - 259 . DOI: 10.1016/j.foodchem.2010.02.073 http://doi.org/10.1016/j.foodchem.2010.02.073 . Phytic acid and Fe and Zn concentration in lentil (Lens culinaris L.) seeds is influenced by temperature during seed filling period M Umeta , CE West , H Fufa . Content of zinc, iron, calcium and their absorption inhibitors in foods commonly consumed in Ethiopia . J Food Compos Anal , 2005 . 18 ( 8 ): 803 - 817 . DOI: 10.1016/j.jfca.2004.09.008 http://doi.org/10.1016/j.jfca.2004.09.008 . Content of zinc, iron, calcium and their absorption inhibitors in foods commonly consumed in Ethiopia M Vasconcelos , K Datta , N Oliva , 等 . Enhanced iron and zinc accumulation in transgenic rice with the ferritin gene . Plant Sci , 2003 . 164 ( 3 ): 371 - 378 . DOI: 10.1016/S0168-9452(02)00421-1 http://doi.org/10.1016/S0168-9452(02)00421-1 . Enhanced iron and zinc accumulation in transgenic rice with the ferritin gene F Wang , FM Cheng , GP Zhang . The relationship between grain filling and hormone content as affected by genotype and source-sink relation . Plant Growth Regul , 2006 . 49 ( 1 ): 1 - 8 . DOI: 10.1007/s10725-006-0017-3 http://doi.org/10.1007/s10725-006-0017-3 . The relationship between grain filling and hormone content as affected by genotype and source-sink relation YY Wei , MJ Shohag , Y Wang , 等 . Effect of zinc sulfate fortification in germinated brown rice on seed zinc concentration, bioavailability, and seed germination . J Agric Food Chem , 2012 . 60 ( 7 ): 1871 - 1879 . 22273463 DOI: 10.1021/jf205025b http://doi.org/10.1021/jf205025b . Effect of zinc sulfate fortification in germinated brown rice on seed zinc concentration, bioavailability, and seed germination Compliance with ethics guidelines Da SU, Faisal SULTAN, Ning-chun ZHAO, Bing-ting LEI, Fu-biao WANG, Gang PAN, and Fang-min CHENG declare that they have no conflict of interest. This article does not contain any studies with human or animal subjects performed by any of the authors. 10.1631/jzus.B1400157 Project supported by the National Natural Science Foundation of China (Nos. 31071366 and 31271655) 2014-06-05 2014-10-11 2014-09-17 2022-01-05 Copyright © Zhejiang University and Springer-Verlag Berlin Heidelberg 2014 2014 Journal of Zhejiang University-SCIENCE B (Biomedicine and Biotechnology) 11 15