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Soilless Production of Lettuce (Lactuca sativa) in the Atacama Desert Using Fog Water: Water Quality and Produce Mineral Composition

1
Centro UC Desierto de Atacama, Pontificia Universidad Católica de Chile, Santiago 8331150, Chile
2
Departamento de Ciencias Vegetales, Facultad de Agronomía y Sistemas Naturales, Pontificia Universidad Católica de Chile, Santiago 8331150, Chile
3
Instituto de Geografía, Pontificia Universidad Católica de Chile, Santiago 8331150, Chile
4
Escuela de Gobierno, Universidad Mayor, Santiago 8580745, Chile
*
Author to whom correspondence should be addressed.
Horticulturae 2024, 10(9), 957; https://doi.org/10.3390/horticulturae10090957 (registering DOI)
Submission received: 7 August 2024 / Revised: 30 August 2024 / Accepted: 6 September 2024 / Published: 7 September 2024
(This article belongs to the Special Issue Soilless Culture in Vegetable Production)

Abstract

:
Soilless vegetable production in the Atacama Desert of Northern Chile is spreading since it is perceived as an alternative that requires much less water than open field soil production. However, strong competition between mining and urban use for human population consumption exists, forcing growers to use alternative water sources. Fog is commonly present in the coastal areas of Northern Chile; however, little information exists with regards to its chemical composition and the effect on nutrient quality of the produce. To address this knowledge gap, a set of experiments was carried out in Chañaral, a small town located in the Atacama Desert of Northern Chile. There, a 200 m2 greenhouse equipped with twenty deep flow pools was used in two consecutive growing cycles. Water for the mixing of the nutrient solution was collected from the fog using fog-catchers and later stored in 2000-L tanks. Fog water quality (electrical conductivity, pH and mineral content) was monitored directly from the storage tanks. Two types of lettuce, green butterhead and red oak leaf, were compared on their yield and accumulation of nutrients and heavy metals. The results indicate that fog water is of good quality for soilless production, with an electrical conductivity value of 0.65 ± 0.18 and low content of heavy metals. Plants’ heavy metal accumulation is below the recommendation of Food and Agriculture Organization and World Health Organization. Fog water presents as a viable water source for soilless production in Northern Chile.

1. Introduction

The Atacama Desert in Northern Chile is considered one of the driest places in the world, with mean annual precipitation as low as 0.8 mm in locations such as Iquique [1]. The extreme aridity limits agricultural production to small valleys where surface or groundwater can be found; however, due to the reduction in precipitation in the Andes mountains during the last decade, water is becoming less available year after year, forcing the use of alternative water sources and innovative cultivation methods [2]. Every year, more growers are becoming attracted to soilless production, since they understand that considerably less water is required for vegetable production in comparison to open field soil production [3]. Growers in Northern Chile mostly rely on tap water for mixing the nutrient solution, but the electrical conductivity (EC) of this water commonly exceeds 1.5 dS m−1, which impairs produce quality [4]. Using low-volume reverse osmosis systems is becoming the preferable method for water treatment in this area, with the consequent cost in energy and the disposal of brine.
An underused water resource is fog. Fog is commonly present in the coastal areas of Northern Chile, since it forms by the condensation of moisture within the cold marine layer that is trapped under the subsidence of warm air masses related to the Hadley cell [5]. The result is a low-altitude stratocumulus cloud that interacts with the coastal mountains next to the seashore [1]. Then, using fog catchers (low-cost devices built with a rigid frame that holds a 32 m2 mesh through which fog flows capturing and condensing water droplets, Figure 1) an average of 100 L per day can be harvested [1]. These devices are in use in several locations across the globe, mainly in arid or semi-arid region like Oman, Namibia, South Africa, or Saudi Arabia [6].
Little information is available with regards to the chemical quality of fog water, especially on the EC values. However, most concerns arise with regards to the presence of heavy metals in this water source, since they can accumulate in the produce, becoming a threat for human health [7].
In a previous publication [1], our research group presented the results of water yield from fog collectors located along the Atacama Desert. However, knowledge gaps in relation to water quality remained unanswered. Here, we present the preliminary results of water quality analysis and heavy metal accumulation on two lettuce genotypes cultivated under greenhouse conditions in the Atacama Desert using only water collected from fog.

2. Materials and Methods

The study was conducted in Northern Chile in a location named Falda Verde (26°17′ S/70°37′ W). The location is known as a wasteland due to the severe accumulation of mining wastes on the banks of the Salado River, including high concentrations of lead, copper, and arsenic [8]. A 200 m2 passive plastic greenhouse was set up where the ventilation was naturally occurring by opening the sides and upper vents (Figure 2). Ten independent deep flow hydroponic pools each with a surface of 2.7 m2 were installed and connected to an air pump with a flow rate of 70 L min−1. Energy for the air pumps was obtained from photovoltaic panels installed outside the greenhouse. On top of the hills, twelve 32 m2 fog collectors were installed and they supplied water to a set of five 2000 L tanks. Water was drawn to the deep flow pools by means of hoses by gravity.
Water samples were taken before the start of the experiment and were sent to a commercial laboratory to determine pH, EC and mineral content. With the results, the amount of fertilizers required to mix a half-strength Hoagland solution (7.5 mM N, 0.5 mM P, 3 mM K, 2.5 mM Ca, 1 mM Mg, and 1 mM S) was determined. Nutrient solution pH was adjusted to 5.8 using phosphoric acid, and the initial EC value was 2.32 dS m−1.
Two lettuce varieties, a green butterhead (Fabietto, Rijk Zwaan) and a red oak leaf (Mondaï, Rijk Zwaan), were sown in plastic trays containing peat and perlite at a 9:1 rate. The trays were irrigated daily only with fog water. Once the plants reached the four true leaves stage, they were transplanted into the floating systems at a density of 30 plants per m2. Three weeks after the transplant, the fresh weight (FW) was recorded, and the leaf samples were taken to a commercial laboratory for the determination of mineral content. The results are expressed in a dry weight (DW) basis and the conversion to FW basis was calculated by dividing for the percentage of dry biomass. This experiment was replicated twice. The first experiment ran from 2 May 2024 to 23 May 2024, with average minimum and maximum temperatures of 12.61 ± 0.32 and 28.74 ± 0.80 °C, respectively. Mean daily light integral reached 11.31 ± 0.69 MJ m−2. The second experiment took place between 13 June and 4 July 2024, reaching an average mininmum temperature of 10.53 ± 0.21 °C, an average maximum temperature of 2.56 ± 0.54 °C, and a mean daily light integral of 6.42 ± 0.17 MJ m−2.
Differences in nutrients and heavy metals in leaf dry biomass between both genotypes (treatments) were analyzed by ANOVA and mean separation was carried out by LSD.

3. Results

Fog water is slightly acidic with a pH of 6.74 ± 0.54, and it presents a low content of dissolved solids expressed as an EC of 0.65 ± 0.18 (Table 1). The highest mineral content found corresponds to chloride followed by sodium, where the sum of both elements represents 75% of the total dissolved solids present in the water samples. Small concentrations of arsenic were detected but the heavy metal in higher concentration was copper. The concentration of cadmium, mercury, molybdenum, and lead were below the equipment detection limit.
After three weeks of growth in the deep flow system, plants reached an average fresh weight of 68.18 ± 4.01 g plant−1 and 55.25 ± 5.14 g plant−1 for the green and red varieties, respectively. Both varieties presented a similar mineral nutrient composition, except for the content of potassium which was higher in the red oak leaf variety and calcium which was higher in the green butterhead genotype. Both genotypes presented a significant accumulation of chloride and sodium (Table 2).
With regards to heavy metals, the largest content corresponds to manganese, zinc, and copper, with no differences between both varieties (Table 3).

4. Discussion

Fog water collected in the experimental site presents an average EC value of 0.65 ± 0.18 dS m−1, which is mainly attributed to the content of sodium and chloride (Table 1). Chloride accounts for 49% of total dissolved solids (TDS) present in the water samples while sodium represents 26% followed by sulphate, bicarbonate, magnesium, calcium, nitrate, potassium, and ammonium, which account for 11%, 5%, 3%, 3%, 2% 1%, and 1%, respectively. This is in agreement with the results presented in the literature regarding the study of aerosols formed from the sea surface as the result of water evaporating directly from the sea [9,10,11]. However, the concentration of these compounds may vary throughout the year, mainly because of dust deposition on the fog collectors, as reported by Shanyengana et al. [12], who described variations between 70 and 1000 mg TDS L−1, equivalent to EC values of 0.1 and 1.5 dS m−1, in fog water samples collected in the Namib Desert. In our first experiment, the water EC average value was 0.83 ± 0.11 dS m−1, while in the second experiment, the value dropped to 0.48 ± 0.15. Therefore, further research is required to understand the variations in TDS throughout the year and make the required adjustments in the fertilizer dosage for the nutrient solution mix.
Although the EC value is above the 0.5 dS m−1 threshold recommended for hydroponics [4], fog water contains significant amounts of essential mineral elements for crops, such as magnesium, calcium, and sulfur (Table 1). Therefore, the supply of these elements needs to be adjusted in the fertilizer formula in order to keep the EC within an adequate range. Our results indicate that fog water supplies 8% of Ca, 45% of Mg, and 36% of S required in a half-strength Hoagland’s solution [13].
The boron content in fog water is remarkably low (0.15 ppm), which is an advantage in comparison to other water sources available in the Atacama Desert. For instance, Pincetti-Zuñiga et al. [14] reported concentrations of above 2.5 mg L−1 in 64% of 90 samples of the surface and drinking water collected in Northern Chile (Azapa and Lluta valleys) and Figueroa et al. [15] reported concentrations of between 0.6 and 16 mg L−1 in the irrigation water used for olive production in the same area. Therefore, boron is commonly found in water sources from Northern Chile beyond the recommended standard of 0.7 mg L−1 [16]. Concentrations beyond this value result in yield reduction because of leaf damage and the generation of reactive oxygen species [17].
With regards to the content of heavy metals in the water, the most abundant element is copper with an average value around 1.5 mg L−1. Thus, the copper content in fog water is above the recommendation of 0.2 mg L−1 for irrigation water, according to the U.S. Environmental Protection Agency [18]. However, copper accumulation in the plant’s biomass depends upon plant species, and our results indicate that lettuce leaves present a concentration of between 27 and 43 mg kg−1 DW, equivalent to 1.35–2.15 mg Cu per kg of fresh biomass. These values are below the maximum permissible value (73 mg Cu kg−1 FW) recommended by FAO/WHO [19,20].
Although no cadmium, mercury or lead were detected in the water samples, they were present in the leaf biomass. Then, it is necessary to identify the source of these elements, since they could be present in the water at extremely low concentrations and accumulate in the leaves due to plant evapotranspiration [21] or can deposit on the leaves by air currents carrying them from the sediments on the coast [22]. Nonetheless, the content of cadmium in the biomass is below the FAO/WHO recommended threshold (4.0 mg kg−1 DW), as well as lead (6.0 mg kg−1 DW) [23].
The presence of arsenic in the leaves of our experiment is around 0.4 mg kg−1 DW equivalent to 0.02 mg kg−1 FW. This value is below the recommended maximum of 0.1 mg kg−1 FW set by the European Union [24]. In the case of mercury, the only recommendation found in the literature comes from the China Food and Drug Administration, providing a maximum level of 0.01 mg kg−1 FW, equivalent to 0.2 mg kg−1 DW [25]. Then, the content found in our experiment is considered permissible.
Finally, the yield achieved in both cultivation cycles demonstrates the suitability of soilless production using fog water. Our results indicate fresh biomass accumulation of 68.18 ± 4.01 and 55.25 ± 5.14 g plant−1 in the green and red varieties, respectively. These values are in agreement with those reported in the literature under similar temperature and radiation conditions [26,27]. Then, fog water presents as a viable water source that can be easily obtained in the coastal areas of the Atacama Desert at low cost.

5. Conclusions

Our results indicate that water collected from marine fog in the Atacama Desert is suitable for use in lettuce soilless production. It presents a low EC value and low concentration of heavy metals. Good yield can be achieved using this water source for hydroponic lettuce, and the accumulation of heavy metals is within the safe range defined by the international health authorities. Further studies are required to test its suitability for other vegetable crops grown under soilless methods. Overall, fog water collection presents as a viable alternative for agricultural production in arid lands.

Author Contributions

Conceptualization, F.A.; methodology, F.A., I.V., C.d.R. and V.C.; investigation, I.V.; writing—original draft preparation, F.A.; writing—review and editing, F.A., I.V., C.d.R. and V.C.; project administration, F.A. All authors have read and agreed to the published version of the manuscript.

Funding

This research and the APC was funded by National Agency of Research and Development (ANID—Chile), grant number FONDECYT Exploracion 13220028.

Data Availability Statement

The original contributions presented in the study are included in the article, and further inquiries can be directed to the corresponding author.

Acknowledgments

The authors acknowledge the contribution of the Association Atrapanieblas de Atacama for granting access to the study site.

Conflicts of Interest

The authors declare no conflicts of interest.

References

  1. Albornoz, F.; del Río, C.; Carter, V.; Escobar, R.; Vásquez, L. Fog Water Collection for Local Greenhouse Vegetable Production in the Atacama Desert. Sustainability 2023, 15, 15720. [Google Scholar] [CrossRef]
  2. Sarricolea, P.; Meseguer, O.; Romero-Aravena, H. Precipitation Trends in the Chilean Norte Grande and its Relationship with Climate Change Projections. Diálogo Andino 2017, 54, 41–50. [Google Scholar] [CrossRef]
  3. Fussy, A.; Papenbrock, J. An Overview of Soil and Soilless Cultivation Techniques—Chances, Challenges and the Neglected Question of Sustainability. Plants 2022, 11, 1153. [Google Scholar] [CrossRef] [PubMed]
  4. Schwarz, D.; Grosch, R.; Gross, W.; Hoffmann-Hergarten, S. Water quality assessment of different reservoir types in relation to nutrient solution use in hydroponics. Agric. Water Manag. 2005, 71, 145–166. [Google Scholar] [CrossRef]
  5. del Río, C.; Lobos-Roco, F.; Latorre, C.; Koch, M.A.; García, J.; Osses, P.; Lambert, F.; Alfaro, F.; Siegmund, A. Spatial Distribution and Interannual Variability of Coastal Fog and Low Clouds Cover in the Hyperarid Atacama Desert and Implications for Past and Present Tillandsia landbeckii Ecosystems. Plant Syst. Evol. 2021, 307, 58. [Google Scholar] [CrossRef]
  6. Azeem, M.; Noman, M.T.; Wiener, J.; Petru, M.; Louda, P. Structural Design of Efficient Fog Collectors: A Review. Environ. Technol. Innov. 2020, 20, 101169. [Google Scholar] [CrossRef]
  7. Bonnail, E.; Cunha Lima, R.; Martínez Turrieta, G. Trapping fresh sea breeze in desert? Health status of Camanchaca, Atacama’s fog. Environ. Sci. Pollut. Res. 2018, 25, 18204–18212. [Google Scholar] [CrossRef] [PubMed]
  8. Mesías, S.; Martínez, L.; Yohannessen, K.; Alvarado, S.; Klarian, J.; Mateo, M.; Costilla, R.; Fuentes, M.; Caceres, D. Trace element contents in fine particulate matter (PM2.5) in urban school microenvironments near a contaminated beach with mine tailings, Chañaral, Chile. Environ. Geochem. Health 2018, 40, 1077–1091. [Google Scholar] [CrossRef]
  9. Hu, P.; Xu, S.; Xie, C.; Hu, S.; Cao, Y.; Zheng, F. Aerosol particles with NaCl-inlay in coastal haze-fog episodes. Air Qual. Atmos. Health 2021, 15, 59–71. [Google Scholar] [CrossRef]
  10. Xiao, H.W.; Xiao, H.Y.; Shen, C.Y.; Zhang, Z.Y.; Long, A.M. Chemical Composition and Sources of Marine Aerosol over the Western North Pacific Ocean in Winter. Atmosphere 2018, 9, 298. [Google Scholar] [CrossRef]
  11. Sun, J.; Jin, Z.; Chang, H.; Zhang, W. A review of chloride transport in concrete exposed to the marine atmosphere zone environment: Experiments and numerical models. J. Build. Eng. 2024, 84, 108591. [Google Scholar] [CrossRef]
  12. Shanyengana, E.S.; Henschel, J.R.; Seely, M.K.; Sanderson, R.D. Exploring Fog as a Supplementary Water Source in Nambia. Atmos. Res. 2002, 64, 251–259. [Google Scholar] [CrossRef]
  13. Albornoz, F.; Lieth, H. Daily Macronutrient Uptake Patterns in Relation to Plant Age in Hydroponic Lettuce. J. Plant Nutr. 2016, 39, 1357–1364. [Google Scholar] [CrossRef]
  14. Pincetti-Zuñiga, G.P.; Richards, L.A.; Daniele, L.; Boyce, A.J.; Polya, D.A. Hydrochemical Characterization, Spatial Distribution, and Geochemical Controls on Arsenic and Boron in Waters from Arid Arica and Parinacota, Northern Chile. Sci. Total Environ. 2022, 806, 150206. [Google Scholar] [CrossRef]
  15. Figueroa, L.; Tapia, L.; Bastias, E.; Escobar, H.; Torres, A. Levels of Boron in Irrigation Waters and Soils Cultivated with Olives in Northern Chile. Idesia 1994, 13, 63–68. [Google Scholar]
  16. Ayers, R.S.; Westcot, D.W. Water Quality for Agriculture; FAO Irrigation and Drainage Paper 29; Food and Agriculture Organization of the United Nations: Rome, Italy, 1994. [Google Scholar]
  17. Brdar-Jokanović, M. Boron Toxicity and Deficiency in Agricultural Plants. Int. J. Mol. Sci. 2020, 21, 1424. [Google Scholar] [CrossRef]
  18. Singleton, H.J. Copper Water Quality Guideline for the Protection of Wildlife, Livestock Watering and Irrigation; Water Quality Guideline Series, WQG-05; Ministry of Environment and Climate Change Strategy: Victoria, BC, Canada, 2019.
  19. Mensah, E.; Kyei-Baffour, N.; Ofori, E.; Obeng, G. Influence of Human Activities and Land Use on Heavy Metal Concentrations in Irrigated Vegetables in Ghana and Their Health Implications. In Appropriate Technologies for Environmental Protection in the Developing World; Yanful, E.K., Ed.; Springer: New York, NY, USA, 2009; pp. 9–14. [Google Scholar]
  20. FAO/WHO. Codex General Standard for Contaminants and Toxins in Food and Feed. Available online: https://www.fao.org/fileadmin/user_upload/livestockgov/documents/1_CXS_193e.pdf (accessed on 2 August 2024).
  21. Eckenfelder, M. Water Quality: Amient Water Quality Guidelines for Mercury; Ministry of Environment and Climate Change Strategy: Victoria, BC, Canada, 2001. Available online: https://www2.gov.bc.ca/assets/gov/environment/air-land-water/water/waterquality/water-quality-guidelines/approved-wqgs/bc_env_mercury_waterqualityguideline_overview.pdf (accessed on 2 August 2024).
  22. Xu, Z.; Peng, J.; Zhu, Z.; Yu, P.; Wang, M.; Huang, Z.; Huang, Y.; Li, Z. Screening of Leafy Vegetable Varieties with Low Lead and Cadmium Accumulation Based on Foliar Uptake. Life 2022, 12, 339. [Google Scholar] [CrossRef] [PubMed] [PubMed Central]
  23. He, L.; Wang, S.; Liu, M.; Chen, Z.; Xu, J.; Dong, Y. Transport and Transformation of Atmospheric Metals in Ecosystems: A Review. J. Hazard. Mater. Adv. 2023, 9, 100218. [Google Scholar] [CrossRef]
  24. Shandana; Khan, A.; Waqas, M.; Nawab, J.; Idress, M.; Kamran, M.; Khan, S. Total Arsenic Contamination in Soil, Vegetables, and Fruits and its Potential Health Risks in the Chitral Valley, Pakistan. Int. J. Sediment Res. 2024, 39, 257–265. [Google Scholar]
  25. China Food and Drug Administration. Standard for Maximum Levels of Contaminants in Foods. 2017. Available online: https://www.fsis.usda.gov/sites/default/files/media_file/2021-02/GB-2762-2017.pdf (accessed on 2 August 2024).
  26. Miller, A.; Langenhover, P.; Nemali, K. Maximizing Productivity of Greenhouse-Grown Hydroponic Lettuce during Winter. HortScience 2020, 55, 1963–1969. [Google Scholar] [CrossRef]
  27. Djidonou, D.; Leskovar, D.I. Seasonal Changes in Growth, Nitrogen Nutrition, and Yield of Hydroponic Lettuce. HortScience 2019, 54, 76–85. [Google Scholar] [CrossRef]
Figure 1. Fog catchers used for the collection of water in the experimental site. The devices consist of a rigid frame made of wood that holds a mesh in the center through which fog flows. This allows the collection of fresh water which is channeled to a storage tank for later use.
Figure 1. Fog catchers used for the collection of water in the experimental site. The devices consist of a rigid frame made of wood that holds a mesh in the center through which fog flows. This allows the collection of fresh water which is channeled to a storage tank for later use.
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Figure 2. Experimental set up within the greenhouse. Twenty independent floating system pools were randomly distributed inside the greenhouse. Natural ventilation was carried out by lifting the sides of the greenhouse and the ceiling vent. Anti-aphid mesh was used on the vents to avoid the entrance of insects.
Figure 2. Experimental set up within the greenhouse. Twenty independent floating system pools were randomly distributed inside the greenhouse. Natural ventilation was carried out by lifting the sides of the greenhouse and the ceiling vent. Anti-aphid mesh was used on the vents to avoid the entrance of insects.
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Table 1. Chemical characterization of fog water before the addition of fertilizers. Values represent average ± standard error of four replicates.
Table 1. Chemical characterization of fog water before the addition of fertilizers. Values represent average ± standard error of four replicates.
ParameterUnitsValueRecommended Maximum Value [8]
pH 6.74 ± 0.546.5–8.4
ECdS m−10.65 ± 0.18 0.7
CalciummEq L−10.43 ± 0.07<20.0 *
MagnesiummEq L−10.91 ± 0.30<5.0 *
PotassiummEq L−10.08 ± 0.03<0.05 *
SodiummEq L−13.60 ± 1.103.0
ChloridemEq L−14.50 ± 1.303.0
SulphatemEq L−10.72 ± 0.20<20.0 *
BicarbonatemEq L−10.28 ± 0.031.5
Ammoniummg L−11.80 ± 0.20<5.0 *
Nitratemg L−15.60 ± 0.90<10.0 *
Aluminummg L−10.12 ± 0.025.0
Arsenicmg L−10.04 ± 0.010.10
Boronmg L−10.15 ± 0.080.7
Cadmiummg L−1<0.010.01
Coppermg L−11.50 ± 0.080.20
Ironmg L−10.09 ± 0.055.0
Manganesemg L−10.04 ± 0.000.20
Mercurymg L−1<0.010.02 **
Molybdenummg L−1<0.010.01
Leadmg L−1<0.015.0
Zincmg L−10.012.0
* Common values found in irrigation water [8]. ** Maximum recommendation value according to the Ministry of Environment, Canada [9].
Table 2. Leaf mineral nutrient composition. Values represent average ± standard error of ten replicates. Different letters in the same row denote significant differences (p < 0.05) between both genotypes.
Table 2. Leaf mineral nutrient composition. Values represent average ± standard error of ten replicates. Different letters in the same row denote significant differences (p < 0.05) between both genotypes.
NutrientGreen LeafRed Leaf
Nitrogen (%)3.03 ± 1.01 a3.25 ± 0.56 a
Phosphorus (%)0.50 ± 0.04 a0.45 ± 0.01 a
Potassium (%)1.41 ± 0.09 b2.08 ± 0.29 a
Calcium (%)0.49 ± 0.02 a0.36 ± 0.03 b
Magnesium (%)0.27 ± 0.01 a0.26 ± 0.01 a
Sulfur (%)0.08 ± 0.00 a0.08 ± 0.00 a
Chloride (%)3.33 ± 0.14 a2.83 ± 0.56 a
Sodium (%)1.05 ± 0.23 a0.96 ± 0.02 a
Iron (mg kg−1 DW)129 ± 27 a137 ± 33 a
Boron (mg kg−1 DW)29 ± 7 a44 ± 12 a
Manganese (mg kg−1 DW)79 ± 48 a76 ± 43 a
Molybdenum (mg kg−1 DW)0.21 ± 0.06 a0.15 ± 0.02 a
Table 3. Leaf heavy metal content. Values represent average ± standard error of five replicates. Different letters in the same row denote significant differences (p < 0.05) between genotypes analyzed on a dry weight basis.
Table 3. Leaf heavy metal content. Values represent average ± standard error of five replicates. Different letters in the same row denote significant differences (p < 0.05) between genotypes analyzed on a dry weight basis.
Heavy MetalMineral Content (mg kg−1 DW)
Green LeafRed Leaf
Zinc49 ± 23 a49 ± 24 a
Copper43 ± 24 a27 ± 7 a
Arsenic0.40 ± 0.00 a0.44 ± 0.03 a
Cadmium0.10 ± 0.00 a0.10 ± 0.01 a
Mercury0.02 ± 0.00 a0.02 ± 0.00 a
Lead0.47 ± 0.02 a0.31 ± 0.01 b
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Albornoz, F.; Vilches, I.; del Río, C.; Carter, V. Soilless Production of Lettuce (Lactuca sativa) in the Atacama Desert Using Fog Water: Water Quality and Produce Mineral Composition. Horticulturae 2024, 10, 957. https://doi.org/10.3390/horticulturae10090957

AMA Style

Albornoz F, Vilches I, del Río C, Carter V. Soilless Production of Lettuce (Lactuca sativa) in the Atacama Desert Using Fog Water: Water Quality and Produce Mineral Composition. Horticulturae. 2024; 10(9):957. https://doi.org/10.3390/horticulturae10090957

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Albornoz, Francisco, Inés Vilches, Camilo del Río, and Virginia Carter. 2024. "Soilless Production of Lettuce (Lactuca sativa) in the Atacama Desert Using Fog Water: Water Quality and Produce Mineral Composition" Horticulturae 10, no. 9: 957. https://doi.org/10.3390/horticulturae10090957

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