Abstract

Field experiments were conducted to evaluate plant population and N-fertilizer effects on yield and yield components of maize (Zea mays L.). Three levels of plant populations (53000, 66000, and 800000 plants ha−1 corresponding to spacings of 75 × 25, 60 × 25, and 50 × 25 cm) and 4 doses of N (100, 140, 180, and 220 kg ha−1) were the treatment variables. Results revealed that plant growth, light interception (LI), yield attributes, and grain yield varied significantly due to the variations in population density and N-rates. Crop growth rate (CGR) was the highest with the population of 80,000 ha−1 receiving 220 kg N ha−1, while relative growth rate (RGR) showed an opposite trend of CGR. Light absorption was maximum when most of densely populated plant received the highest amount of N (220 kg N ha−1). Response of soil-plant-analysis development (SPAD) value as well as N-content to N-rates was found significant. Plant height was the maximum at the lowest plant density with the highest amount of N. Plants that received 180 kg N ha−1 with 80,000 plants ha−1 had larger foliage, greater SPAD value, and higher amount of grains cob−1 that contributed to the maximum yield (5.03 t ha−1) and the maximum harvest index (HI) compared to the plants in other treatments.

1. Introduction

Maize (Zea mays L.) is the third most important grain crop in the world after wheat and rice [1] and has a great utility in agroindustry. It is also of interest to report that calorie yield in maize is two and halftimes higher than that in paddy-rice [2]. In Bangladesh, the cultivation of maize has been gaining popularity in recent years. It is now becoming an important cereal crop for its high productivity and diversified use. The agroclimatic condition of Bangladesh is favorable for its cultivation all year round. However, the average yield of local maize in the country is comparatively low (1.06 t ha−1), whereas the newly released varieties have the potential to produce more than 5.2 t ha−1 [3, 4]. Agronomic practices such as seed rate, plant population and fertilizer management are known to affect crop environment, which influence the growth and ultimately the yield [5]. Optimum population nitrogen (N) levels should be maintained to exploit maximum natural resources, such as nutrients, sunlight, and soil moisture, to ensure satisfactory growth and yield. High density is undesirable because it encourages inter plants competition for resources.

N has been found to be the most important nutrient for maize production [6]. Biomass production of a crop largely depends on the function of leaf area development and consequential photosynthetic activity [7]. Photosynthetic rate can substantially be increased with N-fertilization. Application of N-fertilizer has also been reported to have significant effect on grain yield and quality of maize [8]. Hardas and Karagianne-Hrestou [9] reported that 180 kg N ha−1 was optimum for maize, while Singh et al. [10] observed that application of 200 kg N ha−1 increased grain yield of maize. However, a substantial percentage of applied N is also lost due to volatilization, leaching, and denitrification. Therefore, N should be applied in such a way that would maximize its utilization for grain production. There are some reports on N-management [6] and the optimization of population density per unit area [11] for the maximum harvest of maize. However, the relationship between maize forage yield and plant density is not well established. Maize producers require more information on how N-fertilization and plant density practices affect dry-matter yield and quality.

Keeping the above information in view, the present study was conducted to (1) determine the growth and growth efficiency of maize at different levels of N-fertilizer and plant population and (2) determine the optimum N-fertilizer application and plant population density for the maize growing farmers. We examined the plant height, light interception (LI), leaf area index (LAI), total dry-matter (TDM), grain yield (GY), and harvest index (HI) of maize plants in treated soils. In addition, soil-plant-analysis development (SPAD) values, dry-mass (DM), and harvest index (HI) of maize plants were also evaluated. We believe that this work would therefore aid in the development of production systems (seed rate, fertilizing) and the profitability of the crop in Bangladesh as well as maize growing countries in the world.

2. Materials and Methods

2.1. Experimental Site and Land Preparation

Field experiments were conducted during the rabi season (November–February) in the experimental field of the BSMR Agricultural University at Gazipur in Bangladesh. The experimental site is geographically situated at 23°N latitude and 91°E longitudes with an elevation of 6 m from sea level at the eastern part of Bangladesh. The soil of the experimental plot before application of farm yard manure and nitrogen was silty clay loam having pH 6.5, organic C content was moderate, 1.13%, total N (%) 0.08, available P (Olsen) 9 ppm, exchangeable K (meq 100 g−1 soil) 0.20, exchangeable Ca (meq 100 g−1 soil) 4.5, available S 14 ppm, Zn 10 ppm, and Fe was 370 ppm. The experimental field was cleared, and weeds were manually removed. The soil was ploughed and harrowed with power-tiller, leveled carefully to get a well-pulverized soil, and divided into plots. Each plot was surrounded by 20 to 25 cm high mud plastered levee to prevent the entering of irrigation water. Recommended practices for disease and insect control were followed.

2.2. Experimental Design and Fertilization of Crop

Field plots (  m) were arranged in a split-plot factorial fitted to randomized complete block design (RCBD) with 3 replicates. Adjacent blocks were separated by a 2 m alley, and main plots were separated by a 1 m alley. Experimental treatments were repeated on the same  m plot area each year. The main-plot treatments were 3 plant populations (53000, 66000, and 80000 plants ha−1) and 4 rates of N (0, 100, 140, 180 and 220 kg N ha−1) as subplots. The treatment combinations for the experiment were shown in Table 1. Clean and healthy matured maize seeds (germination rate > 95%) were sown at the spacing of 75, 60, and 50 cm between rows and 25 cm within rows to give population density of 53,000, 66,000 and 80,000 plants ha−1. The variety of maize used for the experiment was Z. mays cv. “Mohor”. We chose “Mohor” because it is one of the popular maize varieties in Bangladesh.

The well-decomposed farmyard manure (FYM—a combination of animal manure, animal urine, and plant materials used for animal bedding and waste straw feed) at 10 t ha−1 was applied during the final land preparation. The land was fertilized (by hand) with 110 kg triple super phosphate (TSP), 50 kg muriate of potash (MP), 120 kg gypsum ha−1, respectively [12]. One third of the urea and the whole amount of TSP, MP and gypsum were applied at the time of final land preparation (i.e., 2 w prior to sowing), while the remaining urea was spitted equally and top-dressed at 28 and 53 days after sowing (DAS). Weeds were manually controlled and irrigation was done as and when necessary. Recommended practices for disease and insect control were followed as and when necessary.

2.3. Measurement of Plant Height

The height of five randomly selected plants was measured from the base of the plant to the tip of the tallest leaf. The height of each plant was recorded in cm, and the mean values of 5 plants for each plot were determined.

2.4. Determination of Leaf Area Index (LAI) and Light Interception (LI)

Leaf area index (LAI) was determined at 15-day intervals (35, 50, 65, and 80 DAS) by an automatic leaf area meter (Model AMM-8, Hayashi Denko Co. Ltd., Tokyo, Japan) using the following formula: LAI = total leaf area of a plant (m2)/ground area covered by a plant (m2), described by Pierce and Running [13].

Light interception (LI) by the crop community was recorded at five times, for example, 35, 50, 65, 80, and 95 DAS of maize by Sunfleck Ceptometer (Model Decagon, Pulman, Washington, USA) using the following formula: light transmission ratio , where ( ) is photosynthetically active radiation (PAR) received on the top of the canopy and is PAR at different depth of the canopy.

2.5. Measurement of Crop Growth Rate (CGR) and Relative Growth Rate (RGR)

Crop growth rate (CGR) is in the increase in plant dry materials per unit area of land per unit time. CGR values were estimated at 15-day interval as described by Hunt [14]. The following formula was used: CGR (g2 m−2 day−1) = , where is total dry weight at time and is the total dry weight at time .

Relative growth rate (RGR) is in the increase in plant materials per unit of materials present per unit time. RGR was determined using the following formula proposed by Hunt [14]: RGR (g g−1 day−1) , where is total dry weight at time , is total dry weight at time , and ln is natural logarithm.

2.6. Determination of Soil-Plant-Analysis Development (SPAD) Value

Leaf chlorophyll content may be used as an indirect indicator of crop N status. Chlorophyll meter values (SPAD) were taken using a portable SPAD meter (Model SPAD-502, Minolta crop, Ramsey, NJ) starting from 60 DAS with 15-day interval. The instrument measures transmission of red light at 650 nm, at which chlorophyll absorbs light, and transmission of infrared light at 940 nm, at which no absorption occurs. On the basis of these two transmission values, the instrument calculates a SPAD value that is well correlated with chlorophyll content [15].

2.7. Measurement of Grain Yield, Dry Matter and Harvest Index

After the final harvest, the cobs from each plot were separated, cleaned, dried, and weighed separately. Grain yield of each plot was recorded kg ha−1 individually and adjusted at 14% moisture content. Dry-mass (DM) of roots and shoots was determined after drying the samples at 72°C until the constant weight was attained.

The harvest index (HI) was computed as the ratio of grain yield (GY) to the total above ground DM yield. The following formula was used: HI (%) = (grain yield/total biological yield) × 100.

2.8. Chemical Analysis of Leaf

Leaves were collected and carried out in the laboratory of the Department of Soil Science, BSMRAU, Salna, Gazipur. Leaf N-content is an important physiological parameter that indicates the plant N status [16]. The total nitrogen concentration in maize leaves was determined by modified the Kjeldahl digestion colorimetric method as described by Cataldo et al. [17].

2.9. Statistical Analysis

All data collected were analyzed using analysis of variance (ANOVA) followed by protected Fisher’s least-significant difference (LSD) test. The means were separated by the LSD at the level of probability [18]. All the experiments were performed twice, and replicates (3) were averaged.

3. Results and Discussion

3.1. Plant Height

Figure 1 shows the plant height in response to different N levels and plant population over time. Plant height increased progressively over time attaining the highest at physiological maturity. The rate of increase, however, varied depending on the growth stages. A significant variation in plant height was observed due to planting density and N-rates except at 35 DAS. The influence of both planting density and N-rates was first apparent at 55 DAS, and the difference among them persisted throughout the growing period. Sparsely populated plants (53,000 ha−1) with 220 kg N ha−1 were the tallest and were statistically at par with that received 180 kg N ha−1.

This might be due to receiving sufficient amount of light and nutrients. On the contrary, densely populated plants with lower N-rates were shorter at all the growth stages. Our study supports the work of Pandey et al. [19] who observed that plant height of maize increased greatly when the seeds were planted sparsely and sufficient amount of N was applied.

3.2. Leaf Area Index (LAI)

LAI of maize with different levels of N-fertilizer and planting density showed substantial differences over the growth stages (Figure 2). LAI increased sharply reaching peak at 65 DAS and then decreased irrespective of treatment differences. The rate of decrease of LAI after attaining peak was more rapid. LAI decreased at 65 DAS reflecting the loss of some existing leaves through senescence. Among the planting densities, 53,000 plants ha−1 showed higher LAI throughout the growing period; however, maximum LAI was obtained from 220 kg N ha−1 with 53,000 plants ha−1 irrespective of growth stages. The increased LAI might be due to the increased availability of N under the higher levels of N-fertilizer with lower population, which resulted in larger leaves. From this result, it is evident that increasing population density tended to depress LAI irrespective of N-levels. Reduction of LAI might be due to an interplant competition (for nutrient and space) within the community. Similar trend in reduction of LAI was also reported in maize and forage maize by Gardner et al. [20] and Okpara and Omaliko [21].

3.3. Light Interception (LI)

Planting density and N-fertilizer application differed substantially in LI. LI varied from 58 to 80% at 35 DAS and increased maximum at 65 DAS and thereafter it declined (Figure 3). Combination of D3N4 ( ) was favorable for light penetration to the upper of the canopy, which resulted better LI and the lowest LI was found in D1N1 (53,000 plants   kg N ha−1). Higher light absorption by the treatment D3N4 (  plants  ) is presumably because of larger leaf surface availability for photosynthesis as evident by higher leaf dry-weight. Pepper [22] and Amanullah et al. [23] also reported that increased plant densities can promote utilization of solar radiation by maize canopies. On the contrary, it is reported that increased maize population/unit area decreased the availability of light into the maize canopy. This indicates that population is the main factor influencing the net radiation absorbed by the plants. Higher penetration of radiation below the canopy indicates lower interception of solar radiation at the canopy. The maximum light was intercepted at 65 DAS corresponded to higher LAI. The more the LAI, the greater the light interception. The LI was less at pretasseling and grain filling stages, which might be due to lower LAI in these stages of crop growth. However, efficiency of conversion of intercepted solar radiation into economic maize yields may decrease with high plant population density because of mutual shading of plants [24].

3.4. Crop Growth Rate (CGR)

Regardless of treatments, CGR increased progressively time reaching peak during 50 to 65 DAS and thereafter declined till maturity (Figure 4). Reduction in growth rate with plant age was probably due to cessation of vegetative growth, loss of leaves, and senescence. Similar reduction in the maize and in the late season of forage maize was also reported by Padmaja [25] and Okpara and Omaliko [21]. Treatment variation during the later growth periods was not significant though the differences were apparent in the initial 35 to 50 DAS up to 55 to 60 DAS. Among the N-levels, 220 kg N ha−1 showed maximum CGR throughout growth period followed by 180 kg N ha−1. The highest CGR was associated with the combination of D3N4 followed by D3N3, while the lowest CGR was in the plants at D1N1 treatment. In general, increase in planting density increased CGR in all the N-levels; CGR response to population density and N-rates followed a linear relationship suggesting that 97 and 99% of total variation in CGR could be accounted for by the linear function of N and population density, respectively (Figure 5). Therefore, the functional relationship suggests that higher the N-levels and population density, the greater was the CGR of maize plant.

3.5. Relative Growth Rate (RGR)

Irrespective of treatments, RGR was more at early stage (30 to 50 DAS) and showed a decreasing trend with the advancement of plant age (Figure 6). The decrease in RGR was probably due to the increase of metabolically active tissue, which contributed less to the plant growth. The decrease in RGR might be also due to the decrease in net assimilation rate (NAR). Variations in RGR across the treatments were not apparent in the later growth period, but the differences were observed in the early growth period. Sparsely populated plants with 100 kg N ha−1 (D1N1) gave the highest RGR, while the lowest PGR was found in densely populated plants (80,000 ha−1) with higher N-rates (220 kg ha−1). Similar results were reported for maize by Ahmad et al. [26] and for rice by Hussain et al. [27].

3.6. SPAD Values and N-Content in Maize Leaves

Regardless of treatment, SPAD values decreased with the plant age (Table 2). Maximum SPAD values were observed at 60 DAS which declined progressively reaching the lowest at 105 DAS. Similar trend was also observed in the case of N-content in leaves. The higher SPAD values and N-content of maize leaves at 60 DAS were probably due to the less sink demand for N from the source (leaf). Conversely, lower SPAD values and N-content at 75 DAS and afterwards might have been due to remobilization of N from leaves to reproductive organs as grain formation was started after 60 DAS. Planting density exerted significant influence on SPAD values and N-content in leaves. However, higher values of both the parameters were obtained from sparsely populated plants (53,000 ha−1) at 60 DAS compared to other populating densities. Response of SPAD value and N-contents to N-rates was also found significant. SPAD value and N-content in the maize leaves increased as N-level increased. Planting density and N-rates interaction effects on SPAD values and N-content were also statistically significant. SPAD values and N-content in leaves increased with the increase of N-levels irrespective of population density.

The highest SPAD value and N-content were found in the plants treated with 220 kg N ha−1 regardless of planting density followed by 180 kg N ha−1. Our results corroborated the findings of Feibo et al. [28] and Zhao et al. [29] who reported that high correlations were recorded between SPAD readings, total leaf chlorophyll, and higher level of N-fertilizers application in short- season cotton (24.2 to 25.0 kg ha−1) and winter wheat (180 kg ha−1).

The relationship between SPAD values and N-content is linearly associated at different growth stages (Figure 7), suggesting that as SPAD values were increased, N-content in leaves was also increased linearly. However, the functional relationship indicates that over 50 to 62% N-content variation in maize leaves can be attributed to the difference in SPAD values.

3.7. Total Dry Matter Production

Total dry matter production (TDM) increased progressively with the progressive increase in planting densities and N-levels. Densely populated plants (80,000 ha−1) had accumulated more DM than the sparsely (53,000 ha−1) planted ones (Table 3). Plants (80,000) grown with 220 kg N ha−1 produced maximum TDM followed by 140 and 180 kg N ha−1. This might be due to higher number of plants per unit area. The DM production was largely a function of photosynthetic surface, which was favorably influenced by N-fertilization. The increase (60%) in DM production of cotton was due to N-fertilization also reported by Oosterhuis et al. [30] and Dubeux et al. [31]. Our results were compared favorably with those of Lucus and Remison [32] who observed linear trends of dry matter production in maize to increasing population density.

3.8. Interrelationships among the Plant Characters

Table 4 shows the correlation between different plant characters of maize. GY had significant positive correlation with total biomass produced and LAI. LTR was found negatively correlated with grain yield. HI has correlated with SPAD value, N-content in leaf, and grain yield.

TDM was significantly associated with LTR and LAI. Contribution of leaf area and LTR for variation in TDM accumulation indicated that leaf area was the most influential factor for determining TDM than the other parameters. LAI was positively correlated with N-content in leaf and LTR. N-content in the leaf had significant positive influence on SPAD value.

4. Conclusion

The results of this study conclusively reveal that the plant height was higher in sparsely populated plants with varying doses of N. Plants grown with 180 kg N ha−1 with 80,000 plants ha−1 had larger foliage, greater light absorption, and growth efficiency that eventually resulted in higher grain yield. On the basis of the obtained results, we concluded that growth efficiency could substantially be increased by adjusting population density with sufficient amount of N-fertilizer. Further experiments should be conducted considering different combinations of major/minor nutrient elements to fully exploit the growth parameters of maize crop under local conditions.

Acknowledgments

The authors thank the authority of BSMRAU Agricultural University, Gazipur, Bangladesh, for providing the space for crop cultivation. This research was partly supported by the Universiti Putra Malaysia (UPM), Malaysia.