1. Introduction
Microgreen is an emerging new specialty crop with high market value of USD 30–50 per pound (454 g) [
1]. It is a collective term for vegetable, herb, grain, or flower seedlings consumed at a young stage [
2,
3,
4,
5]. Microgreens are harvested 7–21 days after germination with expanding cotyledons or first pair of true leaves [
6]. A number of plant species in the families including Amaranthacea, Apiaceae, Asteraceae, Brassicaceae, Fabaceae, and Lamiaceae, have been grown as microgreens, among which
Brassica crops are of the most grown species [
7,
8,
9,
10,
11]. Microgreens are used by chef and consumers to enhance flavor, color, and texture in various foods and have become increasingly popular in recent years as consumer awareness of microgreen dietary value increases [
1,
3,
8]. The high market value, increasing customer demand, and short production cycle had drawn interest among vegetable growers to produce microgreens [
7].
Microgreens are reported to be four to six times nutrient denser than their mature counterparts [
12,
13,
14,
15]. They are considered functional food with high mineral nutrient concentrations and health-beneficial phytochemicals [
15]. Xiao et al. [
16] reported microgreen greens in the Brassicaceae family are most abundant in macronutrients of K and calcium (Ca) and micronutrients of iron (Fe) and zinc (Zn) after evaluating 30 varieties. They also contain high levels of antioxidant phytochemicals including ascorbic acid, carotenoids, glucosinolates, and polyphenols with substantial variations within and between species [
6]. Microgreen lettuce (
Lactuca sativa) have higher mineral concentrations including Ca, Magnesium (Mg), Fe, manganese (Mn), Zn, selenium (Se), and molybdenum (Mo) and lower nitrate concentration than mature lettuce [
10]. Basil (
Ocimum basilicum) microgreens can be biofortified with Se to satisfy the human dietary need for this micronutrient [
17]. There lacks standardized recommendations for cultural practices including species/variety and substrate choice, fertilization, and control of microenvironment in relation to shoot yield and nutrient compositions of microgreens [
4,
9,
18,
19].
Fertilization was considered optional in microgreen production since seeds have stored nutrient for initial seedling growth. However, fertilizer application, premixed in growing substrate, or applied post-emergent was reported to result in fast growth and high yield of microgreen shoots [
20]. The most economic fertilization treatments for arugula (
Eruca vesicaria subsp.
sativa) microgreens were daily post-emergent fertigation with 150 mg·L
−1 N or daily application of 75 mg·L
−1 N plus preincorporation of 1000 mg·L
−1 N [
18]. Preharvest daily spray of 10 mM calcium chloride solution on broccoli (
Brassica oleracea var.
italica) microgreens increased shoot biomass, Ca concentration, and improved visual quality during storage. Plant species/variety, slow versus fast growing, may differ in their requirements for fertilization [
1]. With an increasing number of species and varieties grown as microgreens, crop-specific fertilizer requirements with respect to microshoot yield and mineral nutrients largely remain unclear.
Microgreens can be produced with peat-based potting mix or hydroponic pads that are made from synthetic or recycled fibrous materials [
7]. A variety of hydroponic pads including biostrate (made from felt fiber), jute mat, and hemp mat are commercially available, some of which are compostable and can serve as a sustainable alternative to a peat-based substrate [
21,
22]. Physical and chemical properties including container capacity, air filled porosity, bulk density, pH, and electrical conductivity (EC) vary among substrate types and affect growth of microgreen crops [
21]. Efficacy of using hydroponic mats to grow microgreens is species or variety dependent. Hydroponic pads made from textile fibers and jute-kenaf fibers were reported to produce similar fresh shoot yield of rapini (
Brassica rapa L.) microgreens [
21]. Hydroponic substrate type also affects nutritional facts of microgreens and food safety in microgreen production due to the humid conditions and warm temperatures. The latter has become one of the most important concerns in microgreen production [
7], where hydroponic mat type was found to affect microbial populations on microgreens [
21].
The objective of this study was to investigate shoot production and mineral nutrients of five microgreens grown with four types of hydroponic pads as affected by post-emergent fertilization.
2. Materials and Methods
2.1. Plant Materials and Cultivation
Shoot growth and mineral nutrient concentrations of five microgreens were evaluated (
Table 1). Microgreen seeds of selected species were purchased from the True Leaf Market (Salt Lake City, UT, USA). Seed sowing rate for each microgreen was determined by supplier recommendation and summarized in
Table 1. Hundred-seed weight of each microgreen was measured with three replications. This study was conducted in a greenhouse at Mississippi State University, USA. (33.4552° N, 88.7944° W) and included two experiments with the first conducted on 29 January 2020 and then repeated on 25 February 2020. The temperature in the greenhouse was set at 25 °C with natural light.
Each microgreen was grown with four types of hydroponic pad including biostrate, hemp mat, micro-mats, and jute mat (
Table 2). Each hydroponic pad was precut or manually cut into the size of approximately 25 cm by 25 cm to fit the bottom of the growing tray. Black plastic trays without drainage holes (width 25.72 cm, length 25.72 cm, depth 6.03 cm; T.O. Plastics, Clearwater, MN, USA) were used to grow microgreens in this study. Hydroponic pads were then hydrated by soaking them into tap water, drained with excessive water, and placed into each growing tray. Seeds of appropriate weight were measured and manually sown onto the hydrated hydroponic pads, and covered with another black tray to provide a dark environment and maintain moisture during germination. Microgreen seeds were misted with a spray bottle every 12 h to moisturize the seeds and substrate, when the cover tray was removed shortly and put back on after misting. Four days after sowing, the cover tray was turned upside down with the bottom being placed on top of microgreen shoots for another 24–48 h. This practice was to provide some resistance and encourage microshoot elongation as recommended by the seed supplier. The cover tray was then removed at approximately 7 days after planting (DAP).
After covers were removed, half of the trays from each microgreen were fertigated once with 120 mL of water-soluble fertilizer 20N-8.7P-16.6K (Peters® Professional 20-20-20 General Purpose, also containing (wt/wt) 0.05% Mg, 0.05% Fe, 0.025% Mn, 0.013% boron (B), 0.013% copper (Cu), 0.005% Mo, and 0.025% Zn; ICL Specialty Fertilizers, Tel-Aviv, Israel) at a rate of 100 mg·L−1 N. The fertilizer solution had a pH of 6.56 and EC of 0.41 mS·cm−1. As a control to the fertilization treatment, the other half of trays were irrigated with the same volume of water (pH 7.54; EC 0.15 mS·cm−1).
2.2. Data Collection and Shoot Harvest
Plant height was measured in each tray before shoot harvest from the substrate surface to the highest point of shoot growth. Microgreen shoot in each tray were carefully harvested above the substrate surface, with the expanding cotyledons (microgreen stage 1) or with the first pair of true leaves (microgreen stage 2) as described by Waterland et al. [
5]. Fresh shoot weight of microgreens harvested from each tray was measured. Freshly harvested microgreen shoots were then oven dried at 60 °C until constant weight and measured for dry shoot weight (DW). Dry weight percentage (%) was also determined for each tray.
2.3. Mineral Nutrient Analyses
Dry microgreen samples were ground to pass a 1-mm sieve with a grinder (Wiley mini mill, Thomas Scientific, Swedesboro, NJ, USA) for mineral nutrient analyses. Combustion analysis was used for the determination of total N concentration with 0.25 g of dry tissue using an elemental analyzer (vario MAX cube; Elementar Americas Inc., Long Island, NY, USA). A dry tissue sample of 0.5 g was digested with 1 mL of 6 M hydrochloric acid (HCl) and 50 mL of 0.05 M HCl for the concentrations of P, K, Ca, Mg, Cu, Fe, Mn, Zn, and B using inductively coupled plasma optical emission spectrometry (SPECTROBLUE; SPECTRO Analytical Instruments, Kleve, Germany). Microgreen samples were tested at the Mississippi State University Extension Service Soil Testing Laboratory. Concentrations of macronutrients (mg·g−1) and micronutrients (µg·g−1) in microgreens were presented on a dry weight basis.
2.4. Experimental Design and Statistical Analyses
This experiment was conducted in a randomized complete block design with a factorial arrangement of treatments. Microgreens (5 species), hydroponic pad (4 types), and fertilization (fertilizer or not) were the three main factors contributing to 40 treatment combinations. Each treatment combination had five replications with an individual growing tray as the experimental unit. Significance of any main effect or the interaction among main factors were determined by analysis of variance (ANOVA) using PROC GLMMIX procedure of SAS (version 9.4; SAS Institute, Cary, NC, USA). Where indicated by ANOVA, means were separated by Tukey’s honest significant difference (HSD) at α ≤ 0.05. Data from the two experiments were compared as repeated measures. All statistical analyses were performed using SAS.
4. Discussion
Fresh shoot yield is of the most limiting factor in microgreen production [
4,
20,
23,
24,
25]. Microgreens varied in their fresh shoot yield, which was altered by hydroponic substrate type and fertilization treatment. Fresh, dry shoot weights, and dry weight percentage of tested microgreens in this current study are in similar ranges as our previous study when similar microgreen species/varieties were grown with a peat-based soilless substrate [
26], suggesting selection of high-yielding microgreen species or varieties can potentially be applied to different growing systems including using peat-based substrate, or hydroponic pads of various types. Microgreen shoot yield (fresh or dry) results are also in agreement with previously reported ranges [
9,
20,
21].
Microgreen yield varied between the two experiments, with higher fresh shoot weight, macro-, and micronutrient concentrations except for Cu in the January experiment than February (data not shown). This is likely due to the fluctuating microenvironment conditions in the greenhouse including temperature, relative humidity, and light conditions [
26]. Air temperature was set to be 25 °C in the greenhouse, and was observed to fluctuate within 8 °C of the setting. Relative humidity ranged from 20% to 80%, and daily light integral ranged from 3 to 15 mol·m
−2·d
−1 within the experiment duration. Producers could experience similar changes in microgreens between production cycles. Supplemental lighting may help offset such fluctuations.
Fresh microgreen yield was shown to increase with increasing seed sowing rate. However, as seeding rate increases, individual shoot weight decreases and production cost increases since seeds contribute to a significant portion of microgreen production cost [
4,
18]. The sowing rates used in this study was recommended by the seed supplier ranging from 60.5 g·m
−2 in mustard to 189 g m
−2 in radish (
Table 1), equivalent to 17,182 seeds per m
2 in radish to 33,611 seeds per m
2 in mustard. This sowing rate was generally in agreement with reported ranges of 10,000–40,000 seeds per m
2 for microgreens, yet crop-specific optimum sowing rate needs to be determined based on germination percentage, seed weight, and desired shoot density [
27]. Besides fresh shoot yield, choice of microgreen species is also affected by appearance, texture, flavor, nutritional values, and phytochemical compositions, with genetic variability between and within taxa for traits of interest [
9,
28].
Compared to a number of studies investigating the effect of light on minerals and phytochemical concentrations in microgreens [
19,
29,
30], there lacks standardization in cultural practices including fertilization application, or guidelines for microgreen quality [
4,
20,
24,
25]. One time post-emergent fertigation increased overall shoot height in both experiments, increased overall dry shoot weight and fresh shoot weight in kale and radish in January 2020, and increased various macronutrient concentrations in different microgreens. This is in agreement with our previous results evaluating ten microgreens using a peat-based soilless substrate, when one time post-emergent fertigation with 100 mg·L
−1 N also increased overall fresh shoot yield, macro-, and micronutrient concentrations in selected microgreen species. Murphy et al. [
4] recommended daily fertigation with 150 mg·L
−1 N for optimal yield in arugula microgreens [
18]. In addition to increased yield, large shoot height is a desirable characteristic in assisting with easy harvest of microgreens manually or mechanically [
11]. Hydroponic pads generally have lower water holding capacity than peat-based substrate [
21], microgreens grown in a hydroponic system may benefit from more frequent fertigation. Slow growing species may require more frequent fertilization than fast growing ones [
1].
Mineral nutrient profiles varied among microgreens. For example, radish and broccoli had the highest N concentrations and mustard had the highest P concentration when grown in three substrate types except for hemp. Mustard also had the lowest N concentration among tested microgreens when grown with each substrate type. Ranking of most other mineral nutrients between microgreens varied among hydroponic pad types, suggesting substrate type can affect nutrient profile of microgreens, which should be taken into consideration in microgreen production. Analyses of 30 varieties of
Brassica microgreens revealed that they are a rich source of mineral nutrients, especially K, Mg, Fe, and Zn [
16]. Concentrations of macro- and micronutrients in the current study were generally in consistent ranges with previous reports. The five tested microgreens had lower concentrations of K, Cu, Fe, and B in this study grown with hydroponic pads than when grown with a peat-based potting mix in our previous study [
26]. This agrees with Di Gioia et al. [
21] in that peat resulted in higher nitrate, potassium, and sodium concentrations in microgreen rapini than three hydroponic pads including Sure to Grow (made from polyethylene-terephthalate), textile fiber, and jute-kenaf fiber. This may result from the facts that water holding capacity of peat was tested to be higher than hydroponic pads, and that peat itself contains higher mineral nutrient concentrations than the hydroponic pads [
21]. Mineral nutrients may also change among harvest stages from microgreen stage 1, microgreen stage 2, baby leaf, to adult stage, with microgreen stages having higher mineral nutrient concentrations than the adult stage [
5].
An ideal hydroponic growing substrate should be readily available, relatively inexpensive, and derived from renewable materials [
21]. They should also have an adequate ratio between micropores to macropores to have high container capacity and sufficient air filled porosity. The four tested hydroponic pads are all constructed with biodegradable fibers with different physical and chemical characteristics. Hemp mat was superior in producing the highest shoot height, fresh and dry shoot weights in each microgreen species, or overall, in one or two experiments compared with the other three pad types. Hemp also resulted in the lowest N concentrations among substrate types in each microgreen in both experiments, which could result from the dilution effect of nutrient due to the highest fresh and dry shoot weights in microgreens. Fast growth and high yield of microgreens may benefit from fertilization with a high N formula, with caution on the balance between nitrate and ammonium forms of N since some microgreen crops like arugula tends to accumulate more nitrate [
20]. However, microgreens generally have lower nitrate concentrations than their mature counterparts [
10,
12]. Compared to the hemp mat, jute, and micro-mats have denser texture, likely contributing to a higher water holding capacity but less air filled porosity, while biostrate is thin and lose moisture easily as observed.
Hydroponic pads constructed with different fiber materials can be sources of certain mineral nutrients [
21]. A hemp mat could be a source of K and B, resulting in the highest K (in both experiments) and B concentrations (in January) in each microgreen. Highest micronutrient concentrations were mostly found in the jute or hemp mat if there was significant difference among substrate types, where the higher nutrient concentrations may also result from better shoot growth in these two substrate types. Further analyses of mineral compositions of different hydroponic pads will be required to confirm their effects on microgreen mineral nutrient concentrations.
Food safety concerns including microbial contamination by human pathogens in microgreen production has emerged with the expanding industry [
7]. Microbial contamination can be introduced through seeds, growing substrate, equipment, or a lack of hygienic practices by workers [
31]. Microgreens are more vulnerable to internalization of bacteria than mature vegetable plants [
32]. However, foodborne pathogen outbreaks have not been associated with microgreen consumption as much as in sprouts, where sprouts are generally grown in a dark and moist condition that are more conductive to microbial proliferation [
9,
33,
34,
35]. We did observe mold-like occurrence on hydroponic pads, with higher mold counts on micro-mats and hemp mats, less in our previous study using a peat-based substrate [
26]. It was recently reported that microgreens grown in a hydroponic system and soil-substitute are both subject to pathogen proliferation with contaminated seeds, with higher microbial population in the hydroponic system [
33,
36,
37]. Effective treatments for seed surface sterilization and antimicrobial action need to be developed for sustainable microgreen production [
9,
38]. Disinfecting practices should also be identified for hydroponic pads since they could be potential source of microbial contamination [
21]. Growers should also select reputable supplier for certified microgreen or sprout seeds with high germination quality and potentially lower health risks.