Effects of chemical-based fertilizer replacement with biochar-based fertilizer on albic soil nutrient content and maize yield
-
Dawei Yin
and Yu Lan
Abstract
Biochar-based fertilizers are used to improve soil’s physiochemical and biological properties and increase fertilizer utilization rate. Therefore, a technological model of biochar-based fertilizers is essential for the reduced application. This study was conducted to determine the effects of the different levels of biochar-based fertilizer applications on soil and plant nutrient content, as well as maize yield. Biochar-based fertilizer increased the total N content of maize stem and kernel and the total P content of maize axis and kernel. Biochar-based fertilizer increased the total P but decreased the total K of maize plants while increasing the fertilizer’s partial productivity. Treatment B1 (600.00 kg hm−2 of biochar-based fertilizer) increased the dry-matter weight of the maize at silking and filling stages by 1.60 and 15.83%. Treatment B1 increased the ear length, diameter, and plant height. Compared with BCK (600.00 kg hm−2 of conventional fertilizer), the yield of B1 was increased by 9.23%, and the difference was significant (p < 0.05). Biochar-based fertilizer treatments B2–B5 (biochar-based fertilizer reduced by 5–20%) reduced maize yield, but there was no significant difference between their yield and BCK. This study aimed to provide a basic understanding and reference for maize fertilizer reduction with good application prospects.
1 Introduction
To meet the increasing food requirements of the growing population, China is the largest chemical fertilizer consumer in the world (i.e., synthetic nitrogen (N), phosphorus (P), and potassium (K) fertilizer use were approximately 29, 30, and 26%, respectively, of the global total for agriculture from 2002 to 2019) [1]. However, the long-term overuse of chemical fertilizers can lead to increased N and P water pollution, soil degradation, and reductions in fertilizer-use efficiency and crop yield [2]. The major factors restricting the development of China’s maize industry are superfluous fertilizer input and low utilization of fertilizer; therefore, an urgent study for a new fertilizer application model is required [3]. Throughout the world, 32 countries or regions exhibit similar distributions of albic soil, and the total area of albic soil in China is approximately 5.273 million ha [4]. Owing to the severe problems caused by its dense physical structure, poor nutrient content, and low biological activity, albic soil is characterized as low-yielding [4,5]. Therefore, improving the low-yielding albic soil is strategically important to ensure food security.
Recently, biochar production and utilization have emerged as a widely recognized research area of great concern to experts and scholars worldwide. Biochar is rich in C and possesses a large surface area and strong adsorption capacity, several micropores, and other nutrient elements [6,7]. Straw and other biomasses are prepared as biochar and applied to the soil to considerably reduce soil bulk density; increase soil porosity; improve soil temperature, microecological environment, and nutrients; stimulate and promote soil microbial reproduction; and promote growth and development of a variety of crops [8,9].
Researchers have introduced biochar-based fertilizer to increase crop production and nutrient-use efficiency (NUE) as it has demonstrated great potential to be used as a slow-release fertilizer [10]. Biochar can be used as a carrier for nutrient delivery due to its unique physical and chemical properties, and various types of nutrients have been incorporated into the matrix of biochar [11,12,13]. Previous studies have demonstrated that biochar-based fertilizer could reduce the loss of nutrients and increase the NUE by the crops in the long term compared with conventional fertilizer [14,15,16].
Biochar-based fertilizer shows many advantages as compared with conventional fertilizer [15,17]. However, a few reports exist on biochar-based fertilizer applications to replace those of chemical fertilizers in the cold region of Northeast China. Therefore, this article studies the effects of biochar-based fertilizer instead of chemical fertilizer on the nutrient content of northeast albic soil, maize nutrient absorption, maize dry matter accumulation, and maize yield, and reveals the mechanism of biochar-based fertilizer reduction on maize yield, to provide theoretical basis and technical reference in innovating the technical model of maize-reduced fertilization.
2 Materials and methods
2.1 Overview of the test area
The test area is located in the Modern Agriculture Demonstration Park (45:43:59.40 N, 132:29:59.22E) of 850 Farm, Hulin City, Heilongjiang Province, China. It belongs to the temperate humid to subhumid continental monsoon climate (dry spring, humid, June to August), with an annual average temperature of 3.5°C and an annual average rainfall of 551.5 mm.
2.2 Test materials
The test soil type was albic soil of northeast meadow. The background values of basic soil nutrients were 34.8 g kg−1 organic matter, 1.70 g kg−1 total N, 0.877 g kg−1 total P, 162 mg kg−1 alkali-hydrolyzable N, 45.3 g kg−1 available P, and 97.0 g kg−1 available K in 0–20 cm surface soil. The values for pH and CEC were 5.35 and 10.16 cmol kg−1, respectively. Biochar-based fertilizer was provided by Shenyang Longtai Bioengineering Co., Ltd, Liaoning, China (total nutrient content ≥ 45%, i.e., N + P2O5 + K2O ≥ 45%). The maize variety was Kenyu 6 and was provided by the Maize Center of Heilongjiang Bayi Agricultural University.
2.3 Experimental design
The field experiment was laid out in a randomized block design with seven treatments, each replicated three times. The treatments imposed comprised: BKB (no fertilization); BCK (600.00 kg hm−2 of conventional fertilizer – 46% urea 225.00 kg hm−2, 64% diammonium phosphate 225.00 kg hm−2, and 60% potassium sulfate 150.00 kg hm−2); B1 (600.00 kg hm−2 of biochar-based fertilizer – with the same quality as the BCK treatment); B2 (biochar-based fertilizer reduced by 5%, 570.00 kg hm−2); B3 (biochar-based fertilizer reduced by 10%, 540.00 kg hm−2); B4 (biochar-based fertilizer reduced by 15%, 510.00 kg hm−2); and B5 (biochar-based fertilizer reduced by 20%, 480.00 kg hm−2). Each treatment plot area was 666.67 m2, and maize planting density was 52,500 plants/hm2, and the row spacing was 65 cm. Each treated fertilizer was used as base fertilizer, and no topdressing was required afterward. To avoid yield losses, conventional management practices were performed on the maize plants, weeds, insects, and diseases, controlled by either chemical or manual methods.
2.4 Sample collection
The soil sampling was carried out at the key growth stages of maize, which included the silking, grain-filling, and maturity stages. Maize rhizosphere soil with a depth of 0–20 cm was collected at the rice maturity stage using a stainless steel soil drill with a diameter of 2 cm, and 10 points were randomly selected from each treatment. After removing the roots, weeds, soil animals, and other impurities, they were mixed and used as a repeated soil sample for the same treatment. The soil sample was air-dried to analyze its chemical properties.
Ten maize plants were continuously investigated in each plot at their key growth stages to determine changes in dry matter weight. The maize plants were monitored continuously at the jointing and filling stages, and soil and plant analyzer development (SPAD) values of functional maize leaves (inverted three leaves) were measured. The yield of maize was measured at the maturity stage.
2.5 Soil nutrient determination
Soil pH was measured in 1:2.5 ratio soil solutions (with deionized water) using a pH meter. The soil organic matter (SOM) content was measured using the high temperature–volume method, with heating and oxidation by potassium dichromate. For total N, H2SO4 was used as an accelerator for digestion, and then the Kjeldahl analytic method was used. The soil alkali-hydrolyzable N was measured using the alkaline hydrolysis diffusion method. Available P was extracted using sodium bicarbonate and determined with ultraviolet spectrophotometry (TU-1810; Beijing Pgeneral Instrument Co. Ltd., Beijing, China). Total P was measured using the alkali fusion-molybdenum antimony anti-spectrophotometric method. Soil total K(TK) and available K (AK) were quantified using inductively coupled plasma-atomic emission spectrometry (ICPS-7500; Shimadzu, Japan). All the previously mentioned chemical indexes were measured according to Soil Agrochemical Analysis published by China Agriculture Press [18].
2.6 Calculations for fertilizer agronomic efficiency
Fertilizer agronomic efficiency and fertilizer partial productivity were calculated using the following formula [19]:
2.7 Measurement of dry matter weight, SPAD value, and actual yield of maize
Dry matter weight of stem, dry matter weight of sheath and leaf, dry matter weight of ear, and total dry matter weight of the abovementioned parts were determined by drying: each plant part was dried first in an oven at 105°C for 30 min and dried to constant weight at 80°C for moisture loss. SPAD values of functional maize leaves were measured using a SPAD-502 chlorophyll meter produced by Minolta Co., LTD (Tokyo, Japan). At the mature stage of maize, the area of each plot was determined to be 80m2, and the actual yield of maize was calculated.
2.8 Data analysis
SPSS 19.0 statistical software was used for variance analysis, LSD was used to test the significance of difference (p < 0.05), and Microsoft Excel 2010 was used for plotting.
3 Results
3.1 Effects of biochar-based fertilizer on SPAD value of maize
B1 and B2 increased the SPAD value of maize at silking stage (Table 1). The SPAD values of B1 and B2 increased by 7.56 and 1.33%, respectively, compared with that of BCK. However, all treatments reduced the SPAD value at the filling stage.
Effect of biochar-based fertilizer on SPAD value of maize
Treatment | Silking stage | Filling stage |
---|---|---|
BKB | 44.14 ± 2.37ab | 42.44 ± 3.91a |
BCK | 43.66 ± 1.46bc | 46.50 ± 0.80a |
B1 | 46.96 ± 1.96a | 41.98 ± 3.86a |
B2 | 44.24 ± 2.31ab | 41.50 ± 1.66a |
B3 | 43.50 ± 3.28bc | 42.54 ± 5.68a |
B4 | 46.14 ± 1.63ab | 44.84 ± 2.99a |
B5 | 40.74 ± 1.51c | 34.22 ± 3.15a |
Note: Letters a–c in the same column indicate significant difference at p < 0.05 (n = 10, LSD test). BKB (no fertilization); BCK (600.00 kg hm−2 of conventional fertilization); BCK kg hm−2, 64% diammonium phosphate 225.00 kg hm−2, and 60% potassium sulfate 150.00 kg hm−2); B1 (600.00 kg hm−2 of biochar-based fertilizer 150.00ion); BCK (600.00 maize the SPAD value at the filling stage. size of differenc kg hm−2); B3 (biochar-based fertilizer reduced by 10%, 540.00 kg hm−2); B4 (biochar-based fertilizer reduced by 15%, 510.00 kg hm−2); and B5 (biochar-based fertilizer reduced by 20%, 480.00 kg hm−2).
3.2 Effects of biochar-based fertilizer on soil nutrient content
Table 2 shows the effects of biochar-based fertilizer on soil nutrient contents at the growth stages of maize. Biochar fertilizer had no obvious effect on soil pH value at the silking and filling stages. Biochar-based fertilizer treatment had no obvious effect on the organic matter content of maize at the filling and maturity stages. The alkali-hydrolyzable N content in treatment B1 at the maturity stage showed an overall decreasing trend compared with BCK. The available P in the soil at silking, filling, and maturity stages of B1, increased by 0.93, 5.76, and 1.23%, compared with that of BCK. Compared with BCK, the available K content of B1 at silking and filling stages increased.
Effect of biochar-based fertilizer on soil nutrient content at maize critical growth stages
Growth stage | Treatment | pH | The organic matter (g kg−1) | Alkaline hydrolysis N (mg kg−1) | Available P (mg kg−1) | Available K (mg kg−1) |
---|---|---|---|---|---|---|
Silking stage | BKB | 5.54 ± 0.30a | 31.16 ± 2.11a | 180.00 ± 4.21c | 32.60 ± 8.72c | 84.00 ± 7.61c |
BCK | 5.13 ± 0.21ab | 31.31 ± 1.41a | 207.00 ± 5.00a | 53.50 ± 2.12a | 97.00 ± 3.20b | |
B1 | 4.91 ± 0.42b | 32.44 ± 2.83a | 200.00 ± 5.66a | 54.00 ± 4.24a | 117.00 ± 11.28a | |
B2 | 5.17 ± 0.37ab | 34.30 ± 2.53a | 192.00 ± 3.83b | 49.20 ± 2.61a | 89.00 ± 3.00c | |
B3 | 5.06 ± 0.26ab | 32.32 ± 1.63a | 192.00 ± 6.60b | 42.10 ± 3.19b | 119.00 ± 4.24a | |
B4 | 4.82 ± 0.28b | 34.44 ± 1.65a | 192.00 ± 8.80b | 42.30 ± 2.45b | 97.00 ± 4.69b | |
B5 | 5.10 ± 0.38ab | 34.93 ± 2.05a | 188.00 ± 8.50b | 42.40 ± 5.30b | 89.00 ± 8.20c | |
Filling stage | BKB | 5.36 ± 0.27a | 41.20 ± 3.02a | 188.00 ± 8.29a | 44.90 ± 2.37a | 84.00 ± 3.42a |
BCK | 5.18 ± 0.25a | 35.50 ± 1.93bc | 172.00 ± 3.35b | 43.40 ± 3.16abc | 87.00 ± 2.51a | |
B1 | 5.13 ± 0.30a | 33.30 ± 2.00c | 172.00 ± 2.83b | 45.90 ± 2.71a | 89.00 ± 2.87a | |
B2 | 5.01 ± 0.32a | 36.20 ± 2.03bc | 184.00 ± 8.55a | 44.50 ± 2.75ab | 89.00 ± 2.26a | |
B3 | 5.30 ± 0.29a | 34.40 ± 2.70bc | 168.00 ± 9.63b | 38.20 ± 3.04c | 84.00 ± 2.68a | |
B4 | 5.11 ± 0.27a | 37.70 ± 1.69ab | 184.00 ± 8.91a | 39.10 ± 4.85bc | 84.00 ± 4.16a | |
B5 | 5.12 ± 0.42a | 35.60 ± 2.40bc | 172.00 ± 8.64b | 38.10 ± 4.56c | 87.00 ± 3.89a | |
Maturity stage | BKB | 5.47 ± 0.24a | 33.20 ± 1.64a | 164.00 ± 4.56ab | 37.30 ± 7.40b | 89.00 ± 3.05a |
BCK | 5.31 ± 0.21ab | 33.00 ± 2.28a | 168.00 ± 4.20a | 48.60 ± 2.64a | 91.00 ± 2.51a | |
B1 | 4.91 ± 0.25ab | 30.30 ± 2.49a | 164.00 ± 4.56ab | 49.20 ± 3.04a | 91.00 ± 2.87a | |
B2 | 5.01 ± 0.21ab | 33.90 ± 2.65a | 168.00 ± 4.18a | 46.70 ± 2.18a | 89.00 ± 2.34a | |
B3 | 4.86 ± 0.31b | 33.90 ± 2.83a | 160.00 ± 4.75bc | 46.00 ± 3.02a | 89.00 ± 2.82a | |
B4 | 5.24 ± 0.38ab | 33.00 ± 1.50a | 153.00 ± 6.70c | 44.90 ± 2.37a | 89.00 ± 2.51a | |
B5 | 5.30 ± 0.36ab | 33.00 ± 1.79a | 153.00 ± 6.88c | 45.90 ± 2.66a | 89.00 ± 2.70a |
Note: Letters a–c in the same column indicate significant difference at p < 0.05 (n = 3, LSD test).
3.3 Effects of biochar-based fertilizer on dry matter accumulation of maize
Table 3 shows the dry matter weight of each part of maize at the growth stages. In the silking stage, the aboveground dry matter weights of B1, B2, and B4 increased by 1.60, 1.16, and 5.98%, respectively, compared with BCK. In the filling stage, treatments B1 and B5 increased the dry matter weight of maize aboveground. As a result, the aboveground dry matter weight of B1 was higher than that of BCK. In the mature stage of maize, the dry matter weights of B1–B5 showed a decrease compared with that of BCK. However, the differences were not significant.
Effect of biochar-based fertilizer on dry matter accumulation at maize critical growth stages
Growth stage | Treatment | Leaf weight | Sheath weight | Stem weight | Ear weight | Dry matter weight above ground |
---|---|---|---|---|---|---|
(g/plant) | (g/plant) | (g/plant) | (g/plant) | (g/plant) | ||
Silking stage | BKB | 34.66 ± 0.82b | 17.09 ± 0.53a | 41.54 ± 1.73a | 4.14 ± 1.00b | 97.43 ± 0.76a |
BCK | 36.49 ± 0.67ab | 18.09 ± 0.53a | 38.15 ± 1.17a | 6.11 ± 0.98ab | 98.83 ± 1.10a | |
B1 | 38.08 ± 0.09a | 16.97 ± 0.32a | 40.39 ± 0.19a | 4.97 ± 0.97ab | 100.41 ± 0.84a | |
B2 | 38.20 ± 1.44a | 17.64 ± 0.52a | 40.19 ± 4.15a | 3.95 ± 0.53b | 99.98 ± 5.29a | |
B3 | 35.69 ± 0.81ab | 17.27 ± 0.75a | 38.59 ± 2.07a | 4.66 ± 1.29b | 96.21 ± 4.45a | |
B4 | 36.96 ± 2.01ab | 17.79 ± 0.74a | 43.00 ± 2.56a | 7.00 ± 1.65a | 104.74 ± 6.66a | |
B5 | 34.66 ± 2.31b | 17.09 ± 1.11a | 41.54 ± 2.77a | 4.14 ± 1.96b | 97.43 ± 7.92a | |
Filling stage | BKB | 32.71 ± 5.12b | 15.31 ± 1.82b | 47.29 ± 4.70bc | 95.00 ± 16.75b | 190.30 ± 27.70b |
BCK | 42.40 ± 1.65a | 16.90 ± 1.57a | 55.31 ± 1.88abc | 127.50 ± 8.16a | 242.11 ± 12.25a | |
B1 | 41.99 ± 1.64a | 19.58 ± 0.86ab | 53.44 ± 2.65ab | 127.50 ± 7.59a | 242.51 ± 11.19a | |
B2 | 42.36 ± 2.42a | 20.15 ± 0.92a | 55.42 ± 2.38ab | 117.50 ± 6.61a | 235.43 ± 12.12a | |
B3 | 39.00 ± 3.30ab | 19.34 ± 1.64ab | 51.95 ± 2.66bc | 112.50 ± 2.39ab | 222.79 ± 7.82ab | |
B4 | 38.10 ± 3.02ab | 19.69 ± 1.65a | 56.97 ± 2.21ab | 110.00 ± 8.54ab | 224.76 ± 14.69a | |
B5 | 41.63 ± 1.33a | 20.10 ± 1.14a | 59.96 ± 1.71a | 125.00 ± 6.45a | 246.68 ± 9.27a | |
Maturity stage | BKB | 31.95 ± 8.49a | 11.73 ± 3.13b | 41.97 ± 7.12ab | 276.88 ± 47.03a | 362.53 ± 58.66a |
BCK | 31.65 ± 3.24a | 15.19 ± 1.98ab | 45.50 ± 5.47ab | 308.75 ± 63.24a | 401.09 ± 71.80a | |
B1 | 29.07 ± 9.00a | 15.50 ± 3.09ab | 45.44 ± 9.18ab | 300.63 ± 59.29a | 390.63a ± 72.59 | |
B2 | 31.55 ± 3.94a | 15.90 ± 4.46ab | 42.73 ± 4.85ab | 300.63 ± 30.94a | 390.80 ± 40.23a | |
B3 | 28.36 ± 3.35a | 13.10 ± 1.83ab | 38.23 ± 3.93b | 265.00 ± 26.90a | 344.70 ± 30.32a | |
B4 | 33.73 ± 6.62a | 15.32 ± 3.22ab | 43.84 ± 3.99ab | 308.13 ± 27.06a | 401.01 ± 35.86a | |
B5 | 34.61 ± 5.36a | 16.95 ± 2.75a | 50.36 ± 8.41a | 318.13 ± 56.79a | 420.04 ± 69.61a |
Note: Letters a–c in the same column indicate significant difference at p < 0.05 (n = 10, LSD test).
These results indicated that treatment B1 could increase the dry matter weight of maize shoot at silking and filling stages. This may be because biochar-based fertilizers delay nutrient release in soil. Consequently, the amount of nutrients released is basically consistent with the nutrient requirement of maize; thus, it promotes the accumulation of dry matter.
3.4 Effects of biochar-based fertilizer on the nutrient content of maize plants
Figure 1 shows the total N content in each organ of the maize plant. Biochar-based fertilizer treatments B1, B2, B4, and B5 reduced the total N content of maize leaves and sheaths. B1–B5 treatments increased the total N content of maize stem compared with BCK’s 3.90 g kg−1. Treatments B1 and B2 increased the total N content of the maize axis at 13.60 and 13.07 g kg−1. B1–B5 increased the total N content of maize grains compared with BCK’s 12.08 g kg−1.

Effect of biochar-based fertilizer on total N content in maize organs. Note: Different letters indicate significant difference of treatments at p < 0.05 (n = 3, LSD test).
Figure 2 shows the total P content in each maize organ. Treatments B1–B4 increased the total P content in maize stems compared with 1.51 g kg−1 in BCK. Treatments B1–B5 increased the total P content of the maize axis. B1–B5 increased the total P content of maize grains, and B1–B5 increased by 20, 24.88, 37.56, 1.95, and 62.93% compared with BCK, respectively.

Effect of biochar-based fertilizer on total P content in maize organs. Note: Different letters indicate significant difference of treatments at p < 0.05 (n = 3, LSD test).
Figure 3 shows the total K content in each organ of the maize plant. It can be seen that treatments B1, B2, B4, and B5 all reduced the total K content of maize organs.

Effect of biochar-based fertilizer on total K content in maize organs. Note: Different letters indicate significant difference of treatments at p < 0.05 (n = 3, LSD test).
As shown in Figure 4, each treatment of biochar-based fertilizer increased the total phosphorus content of maize plants, and treatments B1, B2, B4, and B5 increased the total nitrogen content of maize plants. However, each treatment of biochar-based fertilizer reduced the total K content of maize plants.

Effects of biochar-based fertilizer on total N, P, and K content of maize plants. Note: Different letters indicate significant difference of treatments at p < 0.05 (n = 3, LSD test).
3.5 Effects of biochar-based fertilizer on the nutrient utilization rate of maize
Table 4 shows the effects of biochar-based fertilizer on the nutrient utilization rate of maize. Biochar-based fertilizer treatment increased the agronomic efficiency of fertilizer on the whole (except B3 treatment). The total partial fertilizer productivity of B1–B5 increased by 39.64, 31.57, 35.28, 43.91, and 54.57%, respectively, compared with that of BCK. This indicates that conventional fertilizer treatment (BCK) of maize has certain drawbacks; a large number of fertilizers not only failed to achieve a significant yield increase but also caused fertilizer waste, greatly reducing the fertilizer utilization rate, but biochar-based fertilizer is more conducive to the absorption and utilization of nutrients for maize than conventional fertilizer.
Effects of biochar-based fertilizer on nutrient utilization rate of maize
Treatment | Fertilizer agronomic efficiency (kg kg−1) | Fertilizer partial productivity (kg kg−1) |
---|---|---|
BCK | 5.00 ± 1.40b | 33.60 ± 1.40e |
B1 | 10.36 ± 0.26a | 46.92 ± 0.26bc |
B2 | 5.72 ± 0.20b | 44.21 ± 0.20d |
B3 | 4.83 ± 0.00b | 45.25 ± 0.00 cd |
B4 | 5.34 ± 1.88b | 48.35 ± 1.88b |
B5 | 6.23 ± 1.28b | 51.94 ± 1.28a |
Note: Letters a–d in the same column indicate significant difference at p < 0.05 (n = 3, LSD test).
3.6 Effects of biochar-based fertilizer on maize agronomic traits
Table 5 shows the effects of biochar-based fertilizer on maize agronomic traits. The ear length of B1 and B3 increased by 5.43 and 1.23% compared with BCK. The ear diameter of maize under B1, B3, and B4 treatments increased by 2.47, 1.2, and 0.82% compared with BCK. The stem diameter of B1 was 2.09% higher than that of BCK. B1, B3, and B4 treatments increased the plant height of maize compared with BCK, respectively.
Effects of biochar-based fertilizer on agronomic traits of maize
Ear length (cm) | Ear coarseness (cm) | Thick stems (cm) | Plant height (cm) | |
---|---|---|---|---|
BKB | 20.50 ± 1.03ab | 4.79 ± 0.20a | 1.64 ± 0.13b | 255.50 ± 4.38a |
BCK | 20.25 ± 1.09ab | 4.85 ± 0.08a | 1.91 ± 0.17ab | 261.50 ± 6.69a |
B1 | 21.35 ± 1.25a | 4.97 ± 0.22a | 1.95 ± 0.20a | 264.50 ± 13.22a |
B2 | 19.15 ± 1.68b | 4.85 ± 0.12a | 1.76 ± 0.22ab | 254.00 ± 8.10a |
B3 | 20.50 ± 1.51ab | 4.91 ± 0.17a | 1.86 ± 0.25ab | 266.00 ± 9.37a |
B4 | 19.95 ± 0.96ab | 4.89 ± 0.13a | 1.88 ± 0.16ab | 265.50 ± 8.32a |
B5 | 19.95 ± 1.88ab | 4.85 ± 0.22a | 1.87 ± 0.23ab | 258.50 ± 19.73a |
Note: Letters a–b in the same column indicate significant difference at p < 0.05 (n = 10, LSD test).
3.7 Effects of biochar-based fertilizer on maize yield
Figure 5 shows the effect of biochar-based fertilizer on maize yield. The maize yield of B1 was 12386.25 kg hm−2, which was 9.23% higher than that of BCK (11340.00 kg hm−2), and the difference was significant (p < 0.05). The maize yields of B2, B3, B4, and B5 were 2.23, 4.76, 4.32, and 3.27% lower than those of BCK (11340.00 kg hm−2), but the difference was not significant. These results indicated that under the same quality application of biochar-based fertilizer as BCK, maize yield could be increased by using standard ridge mode (ridge spacing 65 cm). Under the condition of 5–20% reduction of biochar-based fertilizer application, maize could be in a stable yield level.

Effect of biochar-based fertilizer on maize yield. Note: Different letters indicate significant difference of treatments at p < 0.05 (n = 3, LSD test).
3.8 Correlation analysis of maize yield with soil nutrient content and dry matter accumulation
Table 6 shows the correlation analysis table of maize yield, soil nutrient content, and dry matter accumulation. The yield of maize was positively correlated with total N content and positively correlated with organic matter content at the jointing stage. There was a significant positive correlation between yield and alkali-hydrolyzed N content at the jointing stage. The yield was positively correlated with the available P and available K content at different stages.
Correlation analysis of maize yield with soil nutrient content and dry matter accumulation
Growth stage | Parameters | Yield | Ear length | Ear coarse | Stem stems | Plant height |
---|---|---|---|---|---|---|
Mature stage | Plant total N | 0.84** | −0.04 | 0.61 | 0.61 | 0.08 |
Plant total P | −0.26 | −0.07 | −0.28 | −0.30 | −0.46 | |
Plant total K | 0.07 | 0.40 | 0.17 | 0.39 | 0.64 | |
Dry matter accumulation | 0.39 | −0.30 | −0.01 | 0.42 | −0.14 | |
Jointing stage | SPAD value | 0.38 | 0.40 | 0.54 | 0.19 | 0.40 |
Filling stage | SPAD value | 0.03 | 0.14 | 0.09 | 0.06 | 0.34 |
Jointing stage | pH | −0.71* | −0.11 | −0.81* | −0.86** | −0.75* |
Organic matter | 0.15 | −0.59 | 0.12 | 0.19 | −0.08 | |
Hydrolyzable N | 0.78* | 0.2 | 0.52 | 0.78* | 0.45 | |
Available P | 0.91** | 0.1 | 0.58 | 0.73* | 0.25 | |
Available K | 0.6 | 0.63 | 0.88** | 0.65 | 0.81* | |
Filling stage | pH | −0.58 | 0.51 | −0.27 | −0.4 | 0.13 |
Organic matter | −0.87** | −0.26 | −0.80* | −0.84** | −0.51 | |
Hydrolyzable N | −0.57 | −0.42 | −0.57 | −0.74* | −0.56 | |
Available P | 0.21 | 0.24 | −0.04 | −0.26 | −0.41 | |
Available K | 0.73* | −0.07 | 0.3 | 0.33 | −0.3 | |
The mature stage | pH | −0.61 | −0.19 | −0.80* | −0.45 | −0.44 |
Organic matter | −0.70 | −0.75* | −0.64 | −0.51 | −0.35 | |
Hydrolyzable N | 0.15 | 0.04 | −0.12 | −0.23 | −0.39 | |
Available P | 0.91** | 0.06 | 0.7 | 0.87** | 0.43 | |
Available K | 0.72* | 0.57 | 0.44 | 0.59 | 0.31 |
Note: **, significantly different at 0.01 level; *, significantly different at 0.05 level.
4 Discussion
4.1 Effects of biochar-based fertilizer on the SPAD value of maize and soil nutrient content
Chlorophyll is the basic substance for photosynthesis in green plants and the main photosynthetic pigment of crop leaves. It affects the photosynthetic performance of crops, and its content reflects the senescence degree of leaves to a certain extent [20]. All treatments reduced the SPAD value at the filling stage, possibly because biochar-based fertilizer reduced the available N content in the soil at the mature stage of maize (Table 4) and the total N content in the leaves at the mature stage (Figure 1).
The results of Gao’s study showed that the biochar-based fertilizer increased soil pH value by 7.2% compared with NPK fertilizer treatment [21]. Yang et al. (2015) showed that the application of biochar-based fertilizer had no significant effect on soil pH value after three consecutive years [22]. In the mature stage of maize, biochar-based fertilizer reduces soil pH value. This may be due to the increase of maize root growth in different fertilization treatments. The massive growth of roots leads to an increase in the secretion of organic acids, which leads to a decrease in soil pH [23].
Yang et al. (2015) showed that biochar-based fertilizer for three consecutive years could increase SOM content [22]. Biochar-based fertilizer increased the organic matter content of albic soil in the silking stage of maize. This may be because the biochar input inhibits the mineralization of SOM and promotes the process of soil humification, leading to the increase of SOM content [24].
The results of Gao’s study showed that the application of biochar-based fertilizer was 2.1% lower than NPK treatment [21]. Wang (2020) found that biochar-based fertilizer can increase the content of soil available N [25]. The alkali-hydrolyzable N content of albic soil at maize maturity stage was decreased by biochar-based fertilizer compared with BCK. This is because under the condition of biochar reduction fertilization, the amount of N input to soil gradually decreased, and then reduced the content of alkali-hydrolyzed N. Biochar-based fertilizer may increase the ratio of C to N in soil [26], thus reducing the rate of soil microbial mineralization of soil organic N. After biochar-based fertilizer was applied to the soil, it disturbed the surface soil greatly, changed the pore structure of the soil, increased the aeration performance of the soil, and may accelerate the volatilization of NH3 in the fertilizer. Alternatively, the application of biochar-based fertilizer may promote the absorption and utilization of alkali-hydrolyzed N in maize.
Application of biochar-based fertilizer increased soil available P content compared with no fertilization [21]. Biochar-based fertilizer B1 increased the content of available soil P of albic soil. This may be because biochar enhances the adsorption of phosphate and soluble organophosphorus, effectively reduces the absorption of iron oxide on P, and reduces the leaching loss of available P [24]. Biochar, meanwhile, is itself an important source of P [27].
Previous studies have found that the content of available K in biochar-based fertilizer decreased by 1.3% compared with NPK treatment [21]. Biochar-based fertilizer B1 treatment is beneficial for increasing maize’s available K content. This is because biochar itself contains a large amount of K, which directly increases the content of available K in the soil after application. At the same time, biochar reduced K leaching. Biochar has a special pore structure that slows down the infiltration rate of water and enhances the cation exchange capacity of the soil, thus improving the adsorption capacity of soil for K+ in solution with strong mobility and easy leaching and reducing the leaching of K [21]. Biochar may enter the soil mineral layer and react and compete with fixed K ions, so that part of the inactive K can be converted into available K [28].
4.2 Effects of biochar-based fertilizer on the nutrient content of maize plants
Previous studies have found that biochar-based fertilizer can increase the N, P, and K contents of rice plants [11,29,30]. Biochar-based fertilizer treatments B1–B5 increase the total nitrogen and total phosphorus content of maize grains. Treatments B1–B2 and B4–B5 increased the total nitrogen content of maize plants, and treatments B1–B5 increased the total phosphorus content of maize plants. This is because the biochar-based fertilizer can promote the uptake and utilization of N and P nutrients in maize, which may be because biochar has a large amount of nutrient content and can improve soil fertility. Biochar has a large specific surface area, rich in pore structure and surface negative charge, which can effectively reduce the infiltration rate of water and strengthen the adsorption capacity of nutrient elements [31,32]. Biochar can promote the activities of soil microorganisms, enhance the activities of various soil enzymes, and improve soil nutrient cycling [33,34,35,36,37], thus promoting the absorption of soil N, P, and other nutrients by maize. However, each treatment of biochar-based fertilizer reduced the total K content of maize plants because the K content of biochar-based fertilizer was lower than that of BCK, which led to the decrease in the total K content of maize plants treated with biochar-based fertilizer.
4.3 Effects of biochar-based fertilizer on maize yield
The growth of maize is a process of dry matter accumulation. The dry matter quality expresses the accumulation of maize assimilation, and the accumulation of total dry matter determines yield to a certain extent [38]. Previous studies revealed that biochar-based fertilizer could increase dry matter accumulation at the maize seedling stage [39]. The biochar-based fertilizer could increase the agricultural utilization rate and partial productivity of N, P, and K fertilizer in rice [40]. Biochar-based fertilizer treatment B1 increases maize yield. The maize yield of B2, B3, B4, and B5 shows no significant difference compared with that of BCK, and fertilizer input was saved 5–20% by biochar-based fertilizer. That is because biochar carries many nutrients on its own. Biochar is usually rich in N, P, K, Ca, and Mg, effectively improving soil fertility levels, and is an important material basis for promoting maize yield increase [38]. Meanwhile, biochar has special physical and chemical properties. Biochar has a great specific surface area, pore structure, and high CEC. It can help enhance the soil’s ability to intercept nutrients and be suitable for the growth of soil microbial breeding habitats, improve the metabolic activities of microorganisms, and promote the soil nutrient cycle to increase yield [41,42]. By observing the growth trend of maize at the maturity stage, the author found that the application of biochar-based slow-release fertilizer (B1) could reduce the occurrence of premature senescence and maintain the green leaf area for a long time, which may also be an important reason to promote the increase of maize yield.
4.4 Application prospect of biochar-based fertilizer
In the past, excessive application of nitrogen and phosphorus fertilizers has caused a serious nutrient loss, resulting in a large amount of nitrogen and phosphorus into water, causing agricultural nonpoint source pollution [1]. Due to the high stability and strong adsorption performance of biochar, the coating material of conventional nitrogen and phosphorus fertilizer of biochar crops can be used to produce biochar-based fertilizer to realize low-carbon agriculture and nitrogen and phosphorus co-emission reduction and reduce fertilizer application amount [10]. Therefore, it is necessary to develop special biochar-based fertilizers with different nutrient release characteristics for different crop types, soil types, and climate conditions to meet the dual requirements of crop growth and agricultural environmental protection in different regions.
5 Conclusion
Biochar-based fertilizer increased the total P of maize plants and the fertilizer’s partial productivity. Treatment B1 increased the dry-matter weight of the maize at silking and filling stages. Compared with BCK, the yield of B1 increased by 9.23%. Biochar-based fertilizer treatments (B2–B5) reduced maize yield, but there was no significant difference between their yield and BCK. This study aimed to provide a basic understanding and reference for maize fertilizer reduction with good application prospects.
Acknowledgments
All individuals appreciate the partial support of Shenyang Agricultural University. We would like to thank Editage (www.editage.cn) for English language editing.
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Funding information: This work was funded by the Postdoctoral Foundation of Heilongjiang Province (LBH-Q20160) and the National Natural Science Foundation of China (31901479).
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Author contributions: This study was carried out in collaboration with all authors. D.Y. and X.Y. performed the experimental investigation. X.G., H.W., G.Y., G.D., S.W., and Z.W. performed the data curation and analysis and wrote the first draft of the manuscript. Corresponding author L.J. designed the study, performed the supervision, the writing – review and editing, and funding acquisition. Another corresponding author Y.L. performed the writing – review and the editing, and project administration. All authors have read and agreed to the published version of the manuscript.
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Conflict of interest: Authors state no conflict of interest.
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Data availability statement: The datasets generated during and/or analyzed during the current study are available from the corresponding author on reasonable request. Samples of the soil from the test area are available from the authors.
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- Selection and validation of reference genes for RT-qPCR analysis of different organs at various development stages in Caragana intermedia
- Cloning and expression analysis of SERK1 gene in Diospyros lotus
- Integrated metabolomic and transcriptomic profiling revealed coping mechanisms of the edible and medicinal homologous plant Plantago asiatica L. cadmium resistance
- A missense variant in NCF1 is associated with susceptibility to unexplained recurrent spontaneous abortion
- Assessment of drought tolerance indices in faba bean genotypes under different irrigation regimes
- The entire chloroplast genome sequence of Asparagus setaceus (Kunth) Jessop: Genome structure, gene composition, and phylogenetic analysis in Asparagaceae
- Food Science
- Dietary food additive monosodium glutamate with or without high-lipid diet induces spleen anomaly: A mechanistic approach on rat model
- Binge eating disorder during COVID-19
- Potential of honey against the onset of autoimmune diabetes and its associated nephropathy, pancreatitis, and retinopathy in type 1 diabetic animal model
- FTO gene expression in diet-induced obesity is downregulated by Solanum fruit supplementation
- Physical activity enhances fecal lactobacilli in rats chronically drinking sweetened cola beverage
- Supercritical CO2 extraction, chemical composition, and antioxidant effects of Coreopsis tinctoria Nutt. oleoresin
- Functional constituents of plant-based foods boost immunity against acute and chronic disorders
- Effect of selenium and methods of protein extraction on the proteomic profile of Saccharomyces yeast
- Microbial diversity of milk ghee in southern Gansu and its effect on the formation of ghee flavor compounds
- Ecology and Environmental Sciences
- Effects of heavy metals on bacterial community surrounding Bijiashan mining area located in northwest China
- Microorganism community composition analysis coupling with 15N tracer experiments reveals the nitrification rate and N2O emissions in low pH soils in Southern China
- Genetic diversity and population structure of Cinnamomum balansae Lecomte inferred by microsatellites
- Preliminary screening of microplastic contamination in different marine fish species of Taif market, Saudi Arabia
- Plant volatile organic compounds attractive to Lygus pratensis
- Effects of organic materials on soil bacterial community structure in long-term continuous cropping of tomato in greenhouse
- Effects of soil treated fungicide fluopimomide on tomato (Solanum lycopersicum L.) disease control and plant growth
- Prevalence of Yersinia pestis among rodents captured in a semi-arid tropical ecosystem of south-western Zimbabwe
- Effects of irrigation and nitrogen fertilization on mitigating salt-induced Na+ toxicity and sustaining sea rice growth
- Bioengineering and Biotechnology
- Poly-l-lysine-caused cell adhesion induces pyroptosis in THP-1 monocytes
- Development of alkaline phosphatase-scFv and its use for one-step enzyme-linked immunosorbent assay for His-tagged protein detection
- Development and validation of a predictive model for immune-related genes in patients with tongue squamous cell carcinoma
- Agriculture
- Effects of chemical-based fertilizer replacement with biochar-based fertilizer on albic soil nutrient content and maize yield
- Genome-wide identification and expression analysis of CPP-like gene family in Triticum aestivum L. under different hormone and stress conditions
- Agronomic and economic performance of mung bean (Vigna radiata L.) varieties in response to rates of blended NPS fertilizer in Kindo Koysha district, Southern Ethiopia
- Influence of furrow irrigation regime on the yield and water consumption indicators of winter wheat based on a multi-level fuzzy comprehensive evaluation
- Discovery of exercise-related genes and pathway analysis based on comparative genomes of Mongolian originated Abaga and Wushen horse
- Lessons from integrated seasonal forecast-crop modelling in Africa: A systematic review
- Evolution trend of soil fertility in tobacco-planting area of Chenzhou, Hunan Province, China
- Animal Sciences
- Morphological and molecular characterization of Tatera indica Hardwicke 1807 (Rodentia: Muridae) from Pothwar, Pakistan
- Research on meat quality of Qianhua Mutton Merino sheep and Small-tail Han sheep
- SI: A Scientific Memoir
- Suggestions on leading an academic research laboratory group
- My scientific genealogy and the Toronto ACDC Laboratory, 1988–2022
- Erratum
- Erratum to “Changes of immune cells in patients with hepatocellular carcinoma treated by radiofrequency ablation and hepatectomy, a pilot study”
- Erratum to “A two-microRNA signature predicts the progression of male thyroid cancer”
- Retraction
- Retraction of “Lidocaine has antitumor effect on hepatocellular carcinoma via the circ_DYNC1H1/miR-520a-3p/USP14 axis”
Articles in the same Issue
- Biomedical Sciences
- Effects of direct oral anticoagulants dabigatran and rivaroxaban on the blood coagulation function in rabbits
- The mother of all battles: Viruses vs humans. Can humans avoid extinction in 50–100 years?
- Knockdown of G1P3 inhibits cell proliferation and enhances the cytotoxicity of dexamethasone in acute lymphoblastic leukemia
- LINC00665 regulates hepatocellular carcinoma by modulating mRNA via the m6A enzyme
- Association study of CLDN14 variations in patients with kidney stones
- Concanavalin A-induced autoimmune hepatitis model in mice: Mechanisms and future outlook
- Regulation of miR-30b in cancer development, apoptosis, and drug resistance
- Informatic analysis of the pulmonary microecology in non-cystic fibrosis bronchiectasis at three different stages
- Swimming attenuates tumor growth in CT-26 tumor-bearing mice and suppresses angiogenesis by mediating the HIF-1α/VEGFA pathway
- Characterization of intestinal microbiota and serum metabolites in patients with mild hepatic encephalopathy
- Functional conservation and divergence in plant-specific GRF gene family revealed by sequences and expression analysis
- Application of the FLP/LoxP-FRT recombination system to switch the eGFP expression in a model prokaryote
- Biomedical evaluation of antioxidant properties of lamb meat enriched with iodine and selenium
- Intravenous infusion of the exosomes derived from human umbilical cord mesenchymal stem cells enhance neurological recovery after traumatic brain injury via suppressing the NF-κB pathway
- Effect of dietary pattern on pregnant women with gestational diabetes mellitus and its clinical significance
- Potential regulatory mechanism of TNF-α/TNFR1/ANXA1 in glioma cells and its role in glioma cell proliferation
- Effect of the genetic mutant G71R in uridine diphosphate-glucuronosyltransferase 1A1 on the conjugation of bilirubin
- Quercetin inhibits cytotoxicity of PC12 cells induced by amyloid-beta 25–35 via stimulating estrogen receptor α, activating ERK1/2, and inhibiting apoptosis
- Nutrition intervention in the management of novel coronavirus pneumonia patients
- circ-CFH promotes the development of HCC by regulating cell proliferation, apoptosis, migration, invasion, and glycolysis through the miR-377-3p/RNF38 axis
- Bmi-1 directly upregulates glucose transporter 1 in human gastric adenocarcinoma
- Lacunar infarction aggravates the cognitive deficit in the elderly with white matter lesion
- Hydroxysafflor yellow A improved retinopathy via Nrf2/HO-1 pathway in rats
- Comparison of axon extension: PTFE versus PLA formed by a 3D printer
- Elevated IL-35 level and iTr35 subset increase the bacterial burden and lung lesions in Mycobacterium tuberculosis-infected mice
- A case report of CAT gene and HNF1β gene variations in a patient with early-onset diabetes
- Study on the mechanism of inhibiting patulin production by fengycin
- SOX4 promotes high-glucose-induced inflammation and angiogenesis of retinal endothelial cells by activating NF-κB signaling pathway
- Relationship between blood clots and COVID-19 vaccines: A literature review
- Analysis of genetic characteristics of 436 children with dysplasia and detailed analysis of rare karyotype
- Bioinformatics network analyses of growth differentiation factor 11
- NR4A1 inhibits the epithelial–mesenchymal transition of hepatic stellate cells: Involvement of TGF-β–Smad2/3/4–ZEB signaling
- Expression of Zeb1 in the differentiation of mouse embryonic stem cell
- Study on the genetic damage caused by cadmium sulfide quantum dots in human lymphocytes
- Association between single-nucleotide polymorphisms of NKX2.5 and congenital heart disease in Chinese population: A meta-analysis
- Assessment of the anesthetic effect of modified pentothal sodium solution on Sprague-Dawley rats
- Genetic susceptibility to high myopia in Han Chinese population
- Potential biomarkers and molecular mechanisms in preeclampsia progression
- Silencing circular RNA-friend leukemia virus integration 1 restrained malignancy of CC cells and oxaliplatin resistance by disturbing dyskeratosis congenita 1
- Endostar plus pembrolizumab combined with a platinum-based dual chemotherapy regime for advanced pulmonary large-cell neuroendocrine carcinoma as a first-line treatment: A case report
- The significance of PAK4 in signaling and clinicopathology: A review
- Sorafenib inhibits ovarian cancer cell proliferation and mobility and induces radiosensitivity by targeting the tumor cell epithelial–mesenchymal transition
- Characterization of rabbit polyclonal antibody against camel recombinant nanobodies
- Active legumain promotes invasion and migration of neuroblastoma by regulating epithelial-mesenchymal transition
- Effect of cell receptors in the pathogenesis of osteoarthritis: Current insights
- MT-12 inhibits the proliferation of bladder cells in vitro and in vivo by enhancing autophagy through mitochondrial dysfunction
- Study of hsa_circRNA_000121 and hsa_circRNA_004183 in papillary thyroid microcarcinoma
- BuyangHuanwu Decoction attenuates cerebral vasospasm caused by subarachnoid hemorrhage in rats via PI3K/AKT/eNOS axis
- Effects of the interaction of Notch and TLR4 pathways on inflammation and heart function in septic heart
- Monosodium iodoacetate-induced subchondral bone microstructure and inflammatory changes in an animal model of osteoarthritis
- A rare presentation of type II Abernethy malformation and nephrotic syndrome: Case report and review
- Rapid death due to pulmonary epithelioid haemangioendothelioma in several weeks: A case report
- Hepatoprotective role of peroxisome proliferator-activated receptor-α in non-cancerous hepatic tissues following transcatheter arterial embolization
- Correlation between peripheral blood lymphocyte subpopulations and primary systemic lupus erythematosus
- A novel SLC8A1-ALK fusion in lung adenocarcinoma confers sensitivity to alectinib: A case report
- β-Hydroxybutyrate upregulates FGF21 expression through inhibition of histone deacetylases in hepatocytes
- Identification of metabolic genes for the prediction of prognosis and tumor microenvironment infiltration in early-stage non-small cell lung cancer
- BTBD10 inhibits glioma tumorigenesis by downregulating cyclin D1 and p-Akt
- Mucormycosis co-infection in COVID-19 patients: An update
- Metagenomic next-generation sequencing in diagnosing Pneumocystis jirovecii pneumonia: A case report
- Long non-coding RNA HOXB-AS1 is a prognostic marker and promotes hepatocellular carcinoma cells’ proliferation and invasion
- Preparation and evaluation of LA-PEG-SPION, a targeted MRI contrast agent for liver cancer
- Proteomic analysis of the liver regulating lipid metabolism in Chaohu ducks using two-dimensional electrophoresis
- Nasopharyngeal tuberculosis: A case report
- Characterization and evaluation of anti-Salmonella enteritidis activity of indigenous probiotic lactobacilli in mice
- Aberrant pulmonary immune response of obese mice to periodontal infection
- Bacteriospermia – A formidable player in male subfertility
- In silico and in vivo analysis of TIPE1 expression in diffuse large B cell lymphoma
- Effects of KCa channels on biological behavior of trophoblasts
- Interleukin-17A influences the vulnerability rather than the size of established atherosclerotic plaques in apolipoprotein E-deficient mice
- Multiple organ failure and death caused by Staphylococcus aureus hip infection: A case report
- Prognostic signature related to the immune environment of oral squamous cell carcinoma
- Primary and metastatic squamous cell carcinoma of the thyroid gland: Two case reports
- Neuroprotective effects of crocin and crocin-loaded niosomes against the paraquat-induced oxidative brain damage in rats
- Role of MMP-2 and CD147 in kidney fibrosis
- Geometric basis of action potential of skeletal muscle cells and neurons
- Babesia microti-induced fulminant sepsis in an immunocompromised host: A case report and the case-specific literature review
- Role of cerebellar cortex in associative learning and memory in guinea pigs
- Application of metagenomic next-generation sequencing technique for diagnosing a specific case of necrotizing meningoencephalitis caused by human herpesvirus 2
- Case report: Quadruple primary malignant neoplasms including esophageal, ureteral, and lung in an elderly male
- Long non-coding RNA NEAT1 promotes angiogenesis in hepatoma carcinoma via the miR-125a-5p/VEGF pathway
- Osteogenic differentiation of periodontal membrane stem cells in inflammatory environments
- Knockdown of SHMT2 enhances the sensitivity of gastric cancer cells to radiotherapy through the Wnt/β-catenin pathway
- Continuous renal replacement therapy combined with double filtration plasmapheresis in the treatment of severe lupus complicated by serious bacterial infections in children: A case report
- Simultaneous triple primary malignancies, including bladder cancer, lymphoma, and lung cancer, in an elderly male: A case report
- Preclinical immunogenicity assessment of a cell-based inactivated whole-virion H5N1 influenza vaccine
- One case of iodine-125 therapy – A new minimally invasive treatment of intrahepatic cholangiocarcinoma
- S1P promotes corneal trigeminal neuron differentiation and corneal nerve repair via upregulating nerve growth factor expression in a mouse model
- Early cancer detection by a targeted methylation assay of circulating tumor DNA in plasma
- Calcifying nanoparticles initiate the calcification process of mesenchymal stem cells in vitro through the activation of the TGF-β1/Smad signaling pathway and promote the decay of echinococcosis
- Evaluation of prognostic markers in patients infected with SARS-CoV-2
- N6-Methyladenosine-related alternative splicing events play a role in bladder cancer
- Characterization of the structural, oxidative, and immunological features of testis tissue from Zucker diabetic fatty rats
- Effects of glucose and osmotic pressure on the proliferation and cell cycle of human chorionic trophoblast cells
- Investigation of genotype diversity of 7,804 norovirus sequences in humans and animals of China
- Characteristics and karyotype analysis of a patient with turner syndrome complicated with multiple-site tumors: A case report
- Aggravated renal fibrosis is positively associated with the activation of HMGB1-TLR2/4 signaling in STZ-induced diabetic mice
- Distribution characteristics of SARS-CoV-2 IgM/IgG in false-positive results detected by chemiluminescent immunoassay
- SRPX2 attenuated oxygen–glucose deprivation and reperfusion-induced injury in cardiomyocytes via alleviating endoplasmic reticulum stress-induced apoptosis through targeting PI3K/Akt/mTOR axis
- Aquaporin-8 overexpression is involved in vascular structure and function changes in placentas of gestational diabetes mellitus patients
- Relationship between CRP gene polymorphisms and ischemic stroke risk: A systematic review and meta-analysis
- Effects of growth hormone on lipid metabolism and sexual development in pubertal obese male rats
- Cloning and identification of the CTLA-4IgV gene and functional application of vaccine in Xinjiang sheep
- Antitumor activity of RUNX3: Upregulation of E-cadherin and downregulation of the epithelial–mesenchymal transition in clear-cell renal cell carcinoma
- PHF8 promotes osteogenic differentiation of BMSCs in old rat with osteoporosis by regulating Wnt/β-catenin pathway
- A review of the current state of the computer-aided diagnosis (CAD) systems for breast cancer diagnosis
- Bilateral dacryoadenitis in adult-onset Still’s disease: A case report
- A novel association between Bmi-1 protein expression and the SUVmax obtained by 18F-FDG PET/CT in patients with gastric adenocarcinoma
- The role of erythrocytes and erythroid progenitor cells in tumors
- Relationship between platelet activation markers and spontaneous abortion: A meta-analysis
- Abnormal methylation caused by folic acid deficiency in neural tube defects
- Silencing TLR4 using an ultrasound-targeted microbubble destruction-based shRNA system reduces ischemia-induced seizures in hyperglycemic rats
- Plant Sciences
- Seasonal succession of bacterial communities in cultured Caulerpa lentillifera detected by high-throughput sequencing
- Cloning and prokaryotic expression of WRKY48 from Caragana intermedia
- Novel Brassica hybrids with different resistance to Leptosphaeria maculans reveal unbalanced rDNA signal patterns
- Application of exogenous auxin and gibberellin regulates the bolting of lettuce (Lactuca sativa L.)
- Phytoremediation of pollutants from wastewater: A concise review
- Genome-wide identification and characterization of NBS-encoding genes in the sweet potato wild ancestor Ipomoea trifida (H.B.K.)
- Alleviative effects of magnetic Fe3O4 nanoparticles on the physiological toxicity of 3-nitrophenol to rice (Oryza sativa L.) seedlings
- Selection and functional identification of Dof genes expressed in response to nitrogen in Populus simonii × Populus nigra
- Study on pecan seed germination influenced by seed endocarp
- Identification of active compounds in Ophiopogonis Radix from different geographical origins by UPLC-Q/TOF-MS combined with GC-MS approaches
- The entire chloroplast genome sequence of Asparagus cochinchinensis and genetic comparison to Asparagus species
- Genome-wide identification of MAPK family genes and their response to abiotic stresses in tea plant (Camellia sinensis)
- Selection and validation of reference genes for RT-qPCR analysis of different organs at various development stages in Caragana intermedia
- Cloning and expression analysis of SERK1 gene in Diospyros lotus
- Integrated metabolomic and transcriptomic profiling revealed coping mechanisms of the edible and medicinal homologous plant Plantago asiatica L. cadmium resistance
- A missense variant in NCF1 is associated with susceptibility to unexplained recurrent spontaneous abortion
- Assessment of drought tolerance indices in faba bean genotypes under different irrigation regimes
- The entire chloroplast genome sequence of Asparagus setaceus (Kunth) Jessop: Genome structure, gene composition, and phylogenetic analysis in Asparagaceae
- Food Science
- Dietary food additive monosodium glutamate with or without high-lipid diet induces spleen anomaly: A mechanistic approach on rat model
- Binge eating disorder during COVID-19
- Potential of honey against the onset of autoimmune diabetes and its associated nephropathy, pancreatitis, and retinopathy in type 1 diabetic animal model
- FTO gene expression in diet-induced obesity is downregulated by Solanum fruit supplementation
- Physical activity enhances fecal lactobacilli in rats chronically drinking sweetened cola beverage
- Supercritical CO2 extraction, chemical composition, and antioxidant effects of Coreopsis tinctoria Nutt. oleoresin
- Functional constituents of plant-based foods boost immunity against acute and chronic disorders
- Effect of selenium and methods of protein extraction on the proteomic profile of Saccharomyces yeast
- Microbial diversity of milk ghee in southern Gansu and its effect on the formation of ghee flavor compounds
- Ecology and Environmental Sciences
- Effects of heavy metals on bacterial community surrounding Bijiashan mining area located in northwest China
- Microorganism community composition analysis coupling with 15N tracer experiments reveals the nitrification rate and N2O emissions in low pH soils in Southern China
- Genetic diversity and population structure of Cinnamomum balansae Lecomte inferred by microsatellites
- Preliminary screening of microplastic contamination in different marine fish species of Taif market, Saudi Arabia
- Plant volatile organic compounds attractive to Lygus pratensis
- Effects of organic materials on soil bacterial community structure in long-term continuous cropping of tomato in greenhouse
- Effects of soil treated fungicide fluopimomide on tomato (Solanum lycopersicum L.) disease control and plant growth
- Prevalence of Yersinia pestis among rodents captured in a semi-arid tropical ecosystem of south-western Zimbabwe
- Effects of irrigation and nitrogen fertilization on mitigating salt-induced Na+ toxicity and sustaining sea rice growth
- Bioengineering and Biotechnology
- Poly-l-lysine-caused cell adhesion induces pyroptosis in THP-1 monocytes
- Development of alkaline phosphatase-scFv and its use for one-step enzyme-linked immunosorbent assay for His-tagged protein detection
- Development and validation of a predictive model for immune-related genes in patients with tongue squamous cell carcinoma
- Agriculture
- Effects of chemical-based fertilizer replacement with biochar-based fertilizer on albic soil nutrient content and maize yield
- Genome-wide identification and expression analysis of CPP-like gene family in Triticum aestivum L. under different hormone and stress conditions
- Agronomic and economic performance of mung bean (Vigna radiata L.) varieties in response to rates of blended NPS fertilizer in Kindo Koysha district, Southern Ethiopia
- Influence of furrow irrigation regime on the yield and water consumption indicators of winter wheat based on a multi-level fuzzy comprehensive evaluation
- Discovery of exercise-related genes and pathway analysis based on comparative genomes of Mongolian originated Abaga and Wushen horse
- Lessons from integrated seasonal forecast-crop modelling in Africa: A systematic review
- Evolution trend of soil fertility in tobacco-planting area of Chenzhou, Hunan Province, China
- Animal Sciences
- Morphological and molecular characterization of Tatera indica Hardwicke 1807 (Rodentia: Muridae) from Pothwar, Pakistan
- Research on meat quality of Qianhua Mutton Merino sheep and Small-tail Han sheep
- SI: A Scientific Memoir
- Suggestions on leading an academic research laboratory group
- My scientific genealogy and the Toronto ACDC Laboratory, 1988–2022
- Erratum
- Erratum to “Changes of immune cells in patients with hepatocellular carcinoma treated by radiofrequency ablation and hepatectomy, a pilot study”
- Erratum to “A two-microRNA signature predicts the progression of male thyroid cancer”
- Retraction
- Retraction of “Lidocaine has antitumor effect on hepatocellular carcinoma via the circ_DYNC1H1/miR-520a-3p/USP14 axis”