1. Introduction
Application of biochar in agricultural and environmental contexts has increased recently, partially due to advantages in terms of mitigating climate change, carbon sequestration, soil fertility (increased water holding capacity, nutrient retention, bulk density), and remediation of air, soil, and water. Biochar is produced by pyrolysis—the thermal degradation and carbonization of a carbonaceous material in the absence of oxygen. In addition to biochar, other materials are generated, including pyroligneous acid (PA), tar, and syngas (a fuel mixture of hydrogen, carbon monoxide, and often, some carbon dioxide).
PA (also referred to as wood vinegar, pyroligneous liquor, pyroligneous extract, pyrolysis oil, or aqueous phase bio-oil) is a liquid material with condensed and highly oxygenated organic acids, arising from reactions between volatile elements generated during thermal decomposition. PA is composed of water (80–90%) and more than 200 organic compounds, including acids, alcohols, phenols, aldehydes, and esters (10–20%) depending on pyrolysis conditions [
1,
2,
3,
4,
5]. Some of these compounds have antioxidant properties and can be developed into a range of useful products [
6,
7,
8,
9,
10].
Due to this antioxidant activity, in agriculture, PA is recognized as a valuable antimicrobial agent and bio-insecticide. For example, the high concentration of phenol compounds in PA can enhance plant protection mechanisms [
11]. In addition, PA contains other chemical compounds which may act as biodegradable herbicides, including 5-aminolevulinic acid (ALA) [
12].
Additional benefits of PA for agriculture include promotion of plant growth [
1] and soil health [
13,
14]. Application of PA has been observed to increase seed germination and root growth [
15], perhaps the result of organic acids converting unavailable soil P into phosphoric acid for nutrient uptake [
16]. According to Wang et al. [
17], several plant-growth promoting mechanisms may be triggered in parallel by PA application: (1) accumulation of proteins involved in different pathways of secondary metabolism, stress response, and carbohydrate metabolism; (2) accumulation of antioxidant enzymes, and (3) decreased reactive oxygen species (ROS) and malonaldehydes in root tissue [
17]. These pathways are essential for proper molecular regulation of plant growth in response to stress.
However, knowledge regarding PA application in agriculture is mostly derived from limited studies focusing on plant growth effects. Detailed information regarding chemical compound content within PA and identification of optimal chemical profiles for growth promotion in different crop species is essential for application to be effective. For example, PA is reported to contain humic substance (complex heterogeneous organic compounds) mixtures, consisting of fulvic and humic acids. Humic substances are well-known plant-growth biostimulants [
18], but more research is needed. It is also important to characterize exact chemical composition as PA is often assumed to be a biodegradable material [
19], with little concern for environmental effects following application. Spectroscopic techniques may be used for better characterization of PA chemical composition and effects on plant growth [
20].
Another challenge is to define optimal PA concentrations for specific crops. For example, Zulkaramai et al. [
21] compared the effect of four concentrations of PA (0, 10, 20, and 30%) and found that although 30% was toxic to rockmelon (
Cucumis melo L.
cv.), a concentration of 10% was beneficial for plant growth.
Finally, biochar and PA are often applied in tandem for various uses, such as enhancing seed germination and growth [
22], enhancement of protection against microbial activity [
23], and the degradation of herbicide [
24]. Previously, Pan et al. [
25] hypothesized that positive effects of combined application might be due to several factors, including increased soil fertility and nutrient supply. It is therefore important to monitor changes in soil nutrients after the addition of PA and/or biochar.
This work reports on the effect of combined applications of chemical fertilizer, biochar, and PA on plant growth in a pot experiment (treatments described in
Table 1). To characterize chemical profiles of the organic inputs, four spectroscopic measurements of fluorescence excitation were utilized—excitation-emission matrix (EEM) [
5,
10], ion chromatography [
26], high-performance liquid chromatography (HPLC) [
20], and gas chromatography-mass spectrometry (GC-MS) [
8,
26,
27]. The effect of inputs on growth of Komatsuna plants (
Brassica rapa var.
perviridis, Japanese mustard spinach) was examined with three factors: (1) Two dilution rates of PA (200-fold and 800-fold); (2) Four levels of chemical fertilizer rates (100%, 75%, 50%, and 0%), and (3) biochar addition. This work aims to evaluate the effect of PA application on growth of
Komatsuna in combination with biochar.
3. Materials and Methods
3.1. Pyrolysis Process
Biochar and PA materials were generated in the laboratory of Meiwa Co., Ltd. (Kanazawa, Japan). Biochar was generated with pyrolysis using a continuous-type rotary kiln (Carbon Hero, Kanazawa City, Ishikawa, Meiwa Co., Ltd., Japan). Wood chips of Cryptomeria japonica (Japanese cedar; Kidagen Lumber mill, Nomi, Japan) were used as kiln feedstock. Raw materials were dried and chopped before pyrolysis.
Pyrolysis temperature and duration was between 400 and 500 °C, for 20 to 30 min. Following pyrolysis, the biochar was sieved (2 mm) for homogeneity. Electroconductivity (EC) and pH of the biochar was 10.1 ms cm−1 and 3.2. Average surface area and porosity were 2.9052 × 102 m2 g−1 and 0.68 nm, respectively. C, N, P, and K concentrations were 74.3%, 1.1%, 0.5%, and 1.7%, respectively. The C:N ratio was 67.5. Cation exchange capacity was 22 cmol(+) kg−1.
PA was also generated with pyrolysis using pine feedstock (Pinus thunbergiana); 40 kg of pine wood (moisture content of 10 to 20%) yielded approximately 3000 mL after 3 h under the same pyrolysis conditions used for biochar production. The sample was then analyzed with EEM, SEC-HPLC, CG-MS, and ion chromatography.
3.2. Spectrometric Analysis and Chromatography
3.2.1. Excitation Emission Matrix (EEM) Spectroscopy
A light path length of 10 mm (quartz cell, F10-SQF-10, GL Sciences, Tokyo, Japan) was used for EEM measurements. Fluorescence intensity was measured with a spectrophotometer (F07100, Hitachi, Tokyo, Japan), using a 5 nm interval. Excitation wavelength (Ex) and fluorescence wavelength (Em) ranged from 200–500 nm and 250–550 nm, respectively. Scan speed was between 30,000 nm min−1 and 60,000 nm min−1. The excitation and fluorescence slit was set to 5 nm and 10 nm, respectively. Voltage was 400 V. EEM equipment was allowed to settle for more than 1 h to stabilize the xenon lamp excitation source. A low temperature circulator (CTP-1000, EYELA, Queenstown, Singapore) was used to keep water temperature stable at 25 °C. MilliQ H2O and quinine sulfate were used as controls before and after measurement of the samples. Relative fluorescence intensity (RFI) was calculated based on quinine sulfate results, ranging between Ex/Em = 455 nm/350 nm. Measurements were replicated at least twice. Data analysis was performed with FL Solutions, version 4.2 (Hitachi, Tokyo, Japan).
3.2.2. Size Exclusion Chromatography—High-Performance Liquid Chromatography (SEC–HPLC)
Gel permeation chromatography (GPC) columns (GL-W530, 10.7 mm × 300 mm, Hitachi) with an exclusion limit of 50,000 Da were utilized, based on the method of Nagao et al. (2001). An HPLC system equipped with an L-2130 intelligent pump (Hitachi) allowed for SEC mobile phases, with a flow rate of 1.0 mL min−1 was used. A column oven allowed temperature to be fixed at 30 °C. An L-2485 (Hitachi) chromatography detector was used. A calibration curve was generated by analyzing blue dextran (50,000 Da), polyethylene glycol (C2nH4n+2On+1), 1 Amino-2-hydroxymethyl-1,3-propanediol (C4H11NO3(0.01 M)), and NaCl (0.01 M) with a differential refractometer. pH was adjusted to 8.00 ± 0.03 with 1.0 M HCL. The machine was purged to remove bubbles and avoid salt precipitation, and the apparatus was left to settle for over 1 h; 1840, 6450, 1010, 400, 194, 106 Da, acetone (molecular size: 58 Da), MilliQ H2O, and fulvic acid (10 mg L−1) were used as controls of the HPLC system. Volume, peak area, and height were calculated with an HPLC system manager (D-7000, Hitachi). Measurements were replicated at least twice. Six peaks were observed with molecular weights of 8970, 5190, 1650, 790, 670, and 280 Da, inferred from a calibration curve generated using standard material.
3.2.3. Ion Chromatography
Samples were diluted with ultrapure H2O, and purified to high levels of specification. Later, the samples were filtered through a 0.45 νm pore size filter (Merck KGaA, Darmstadt, Germany) before analysis. Organic acids (lactic acid, acetic acid, citric acid, malic acid, formic acid, and succinic acid) were analyzed using a Dionex ICS-2100 ion chromatography system and Ion Pac AS20 4 × 250 mm column (Thermo Fisher Scientific Inc., Waltham, MA, USA). Compounds were detected and quantified by measuring the magnitude of conductivity in the eluted fractions.
3.2.4. Gas Chromatography-Mass Spectrometry (GC-MS)
An Agilent/JEOL gas chromatograph was used to identify organic components contained in the sample of the refined PA. A 30 m × 0.25 mm × 0.25 μm capillary column (Ultra ALLOY, Frontier Lab, Fukushima, Japan) was used. The injection volume and port temperature was 1.0 μL and 220 °C, respectively. Split injection was performed at a rate of 50:1. The carrier gas was helium, with a stable flow rate of 3.00 mL min−1. Column temperature was maintained at 40 °C for 2 min, then raised to 360 °C at a heating rate of 20 °C min−1, for 12 min. Electron impact (El) source energy was 70 eV, source temperature was 230 °C, and the scanning range was 35–400 amu s−1. The National Institute of Standards and Technology (NIST) mass spectrometry library was used for analysis. Corresponding peak areas were used to determine the relative compound content within PA samples.
3.3. Field Trial
Komatsuna (
Brassica rapa var.
perviridis) (Takii & Co., Ltd., Kyoto, Japan) plants were cultivated in a randomized complete block design pot experiment. Plants were grown in a plastic greenhouse on an experimental farm at Meiwa Co. Ltd., Japan (36°37′24.7″ N, 136°37′58.7″ E). In July, Komatsuna seeds were sowed into plastic pots (0.038 m
2) filled with 3.9 L of field soil. Three pots (9 plants per pot) were randomly selected for downstream experiments. The full experiment design is outlined in the
Supplementary Materials (Table S1; Figure S1).
Chemical fertilizer and biochar were mixed into the soil at different rates. For the control pot (full fertilizer treatment, zero biochar, zero PA), the recommended rate of chemical fertilizer for Ishikawa prefecture was applied, equivalent to 2.13 g of 16:10:14 NPK fertilizer per pot. Within the treatment plots, 0, 50, 75, or 100% of inorganic fertilizer was replaced with biochar and/or PA. PA was diluted with water at two ratios: 1 part pyroligneous acid and 200 parts water (PA200), and 1 part pyroligneous acid and 800 parts water (PA800). After dilution, 200 mL of PA was mixed into the soil. To control for moisture content, 200 mL of water was supplied to the other treatments. pH and EC of the soil was 6.5 and 0.106 mS cm
−1. Rates of chemical fertilizer, biochar, and PA applied to each control and treatment plot are shown in
Table 1.
Ten days after sowing (DAS), seedlings were thinned to 4 plants per pot, and the remaining plants were harvested at 44 DAS. Temperature and humidity were monitored. All treatments were irrigated twice per day with 50 mL. After harvest, plants were gently washed and dried with tap water and paper towels. Plants were separated into two parts: leaves (above ground organs) and roots. Fresh weight was measured with a balance. Plant height was recorded as length from the base of the leaf stalk, to the tip of the longest leaf. Chlorophyll levels were recorded with a SPAD meter (Soil Plant Analysis: Development; SPAD-502, Konica Minolta, Osaka, Japan) at 23, 26, and 31 DAS. Chlorophyll levels were recorded in triplicate from the center of the smallest and largest leaf.
3.4. Fertility/Nutrition Analysis
3.4.1. Soil
Soil sampling was performed at harvest. Soils were air-dried, ground, and passed through a 2 mm sieve prior to chemical analysis. pH was measured using the glass electrode method with a soil and water ratio of 1:2.5 [
49]. To determine soil exchangeable cation capacity, extraction was performed with 1 M NH
4OAc at pH 7 [
50], then measured with a multitype inductive coupled plasma (ICP) emission spectrometer (ICPE-9000, Shimadzu Co, Kyoto, Japan). Concentrations of available micronutrients (Fe, Zn, Cu, and Mn) were measured by mixing 10 g of soil with 20 mL of diethylene triamine pentaacetic acid (DTPA-TEA) solution [
51]. Available P was extracted with the Truog method quantified by using molybdenum blue [
52].
3.4.2. Plant
Above-ground organs were oven-dried at 60 °C, weighed for dry biomass, and homogenized in agate grinding jars with a mixer mill (MM200, Retsch GmbH, Haan, Germany); 0.5 g of the sample was digested with 1 mL HNO
3 within Teflon vessels oven-heated to 160 °C for 4 h. Samples were left to rest overnight [
53]. Concentrations of Ca, Mg, K, Na, P, Fe, Zn, Cu, and Mn were determined with a multitype ICP emission spectrometer (ICPE-9000, Shimadzu Co., Kyoto, Japan).
3.5. Statistical Analysis
All experiments were conducted in duplicate or triplicate. ANOVA tests (p < 0.05) were used to determine significant effects on plant height, fresh biomass, SPAD, and nutrient content in soil and plant tissues. The Shapiro–Wilk test was used to verify normality of the data. The three factors for the ANOVA tests were: PA dilution (200-fold, 800-fold, control); biochar level (0 g and 5 g); chemical fertilizer rate (0, 50, 75, and 100%). Statistical analyses were conducted with R (Rstudio 3.5.1 version, RStudio, Boston, MA, USA). Significant differences were verified at p < 0.05.