1. Introduction
Home gardens, often referred to as homestead agriculture, are increasingly recognized as vital components of sustainable food systems. They contribute significantly to food and nutritional security, income generation, and climate resilience worldwide [
1]. As one of the oldest forms of cultivation, homestead gardens continue to provide fresh produce and supplementary income, particularly during economic or environmental crises [
2]. For instance, the COVID-19 pandemic, which disrupted global food supply chains and disproportionately affected vulnerable populations, underscored the urgency of achieving Sustainable Development Goals (SDGs), particularly “No Poverty” and “Zero Hunger” [
3]. With more than 295 million people still facing chronic food insecurity and malnutrition [
4] and the global population projected to surpass 9 billion by 2050, food production systems must evolve to meet increasing demands. In this context, homestead agriculture plays a pivotal role by ensuring access to nutritious food. In Bangladesh, approximately 0.88 million hectares are dedicated to homestead gardening, contributing 3–44% of household caloric intake and 4–32% of protein intake [
5], while also supporting poverty alleviation and providing employment for women [
6].
Despite their importance, the sustainability and safety of homestead food production in Bangladesh are threatened by heavy metal contamination, particularly in industrially dense regions. Elevated concentrations of arsenic (As), Nickel (Ni), chromium (Cr), lead (Pb), and zinc (Zn) in agricultural soils often result from industrial effluents, untreated sewage, atmospheric deposition, agrochemicals, and contaminated irrigation water [
7,
8]. Industrial hubs engaged in textile manufacturing, battery recycling, metal plating, and e-waste processing tend to exhibit higher contamination levels than non-industrial areas, though agricultural runoff and waste mismanagement also contribute significantly [
9,
10]. Soil depth further influences contamination patterns: surface soils are directly exposed to deposition, while subsurface layers accumulate pollutants through leaching and percolation [
11]. The degradation of soil quality poses long-term risks to food safety and ecosystem, as heavy metals can enter crops and subsequently reach the human body via ingestion, dermal contact, or inhalation [
12]. In addition to human exposure pathways, pollutants from agricultural and industrial activities including excessive fertilizers, pesticides, waste dumping, and emissions further degrade soil, water, and air quality [
13], disrupt microbial communities, reduce soil fertility, and threaten biodiversity and ecosystem stability [
14].
Chronic exposure to heavy metals is associated with a wide range of severe health outcomes. As, a well-known carcinogen, is linked to cancers of the skin, lungs, and bladder, as well as liver damage and cardiovascular diseases [
15]. In Bangladesh, this issue is further aggravated by the use of arsenic-contaminated groundwater for irrigation, which facilitates its transfer into the food chain [
16]. Pb exposure from industrial sources is associated with neurological disorders, developmental delays, and cognitive impairment in children [
17]. Similarly, cadmium, Cr, Ni, and mercury are linked to kidney dysfunction, respiratory illness, and various cancers [
18]. As contamination becomes more widespread, these health risks have emerged as major public health concerns in both industrial and non-industrial regions.
Globally, numerous studies have reported heavy metal contamination in soils, crops, water bodies, and sediments, including research from Italy [
19], the United States [
20], China [
21], Croatia [
22], Africa [
23], and Bangladesh [
24]. However, comparatively little attention has been given to contamination in homestead agricultural soils in Bangladesh, even though produce from these systems is consumed directly by households without any commercial processing or safety checks. This knowledge gap is particularly concerning, given the vital role of homestead gardens in supporting rural food security.
Considering the clear links between environmental contamination and human health, regular monitoring of homestead agricultural soils is essential [
25]. Therefore, the present study aims to (i) quantify heavy metal concentrations in surface and subsurface soils of industrial and non-industrial homestead areas in Bangladesh, (ii) assess spatial variability in contamination, and (iii) evaluate ecological and human health risks using standardized pollution indices and risk assessment models. The findings from this research provide a deeper understanding of the environmental and public health risks posed by heavy metal contamination in homestead-based agricultural systems.
2. Materials and Methods
2.1. Study Area Description
This study was conducted across four districts surrounding the capital city Dhaka, Bangladesh: Savar, Narayanganj, Gazipur, and Mymensingh (
Figure 1). These sites were strategically selected to represent contrasting levels of industrial activity and their potential influence on homestead agriculture. Savar, Narayanganj, and Gazipur are heavily industrialized, whereas Mymensingh served as a non-industrial, agriculturally dominant control site.
Savar hosts diverse industries including tanneries, textiles, dyeing, and pharmaceuticals, often located near residential settlements. Narayanganj, one of the oldest industrial hubs, is renowned for textile, dyeing, and printing sectors. Gazipur has undergone rapid urbanization with growth in garment manufacturing, electronics, and plastics. The sampling locations were selected based on their proximity to major industrial zones. In these districts, homesteads are typically situated near industrial sites and are therefore highly vulnerable to contamination from multiple sources, including irrigation with polluted water, atmospheric deposition, and improper disposal of industrial effluents and solid wastes [
26]. Small and medium-scale industries lacking proper waste management further exacerbate this risk. In contrast, Mymensingh was selected as a control due to its minimal industrial activity and reliance on traditional agriculture with natural irrigation. Its rural setting, dominated by subsistence farming and homestead gardening, provides a baseline for comparing contamination in industrial and non-industrial contexts. The general features of the selected study areas are summarized in
Table 1.
2.2. Soil Sampling and Processing
Soil sampling was carried out in mid-July 2024, immediately after the monsoon season, to record the post-monsoon contamination status. Soil samples were collected from four districts, with three sampling sites per district. At each site, soils were sampled from two depths: surface (0–20 cm) and subsurface (21–50 cm). For each site depth combination, three subsamples were collected using a stainless-steel hand auger (country made), and homogenized to form one composite sample, resulting in a total 72 composite samples. All sampling tools were made of stainless steel to avoid contamination. The soil samples were air-dried, homogenized, and wrapped in laboratory-grade, acid-washed aluminum foil. Since the samples were completely dry and aluminum was not among the target analytes, the foil posed no risk of contamination. The wrapped samples were then placed in clean polyethylene containers for transport and storage to avoid external contamination, in compliance with phytosanitary regulations [
27,
28]. The general soil properties for each location and depth are presented in
Table 2.
In the laboratory, soil samples were cleaned, air-dried, and then ground and sieved using a mechanical shaker (AS 200-digit Retsch AS200, Retsch GmbH, Haan, Germany). The sieved samples were wrapped in aluminum foil and stored under refrigeration until analysis. Subsequently, the samples were oven-dried at 105 °C to a constant weight, further ground using an agate mortar, and passed through a 20 µm mesh to ensure homogenization. For digestion, 0.5 g of soil was treated with aqua regia (HNO
3:HCl = 1:3) [
29] and heated on hotplate (Zojirushi EA-DD10-TA, Zojirushi Corporation, Osaka, Japan) at 150 °C for approximately 90 min or until brown fumes ceased. The digested samples were then cooled, diluted with deionized water, filtered, and stored at 4 °C until heavy metal analysis (
Figure 2).
2.3. Heavy Metal Analysis
The concentrations of heavy metals in the soil samples were measured using Inductively Coupled Plasma Mass Spectrometry (ICP-MS; PerkinElmer NexION 350D, Shelton, CT, USA) at the Center for Environmental Science in Saitama, Japan (
Figure 2). The instrument was operated under standard conditions, including a plasma gas flow rate of 18.00 L/min, auxiliary gas flow of 1.20 L/min, nebulizer gas flow of 0.98 L/min, and plasma power of 1600 W. Prior to analysis, digested samples were diluted with 3% HNO
3 and spiked with an internal standard solution (Y). To ensure that heavy metal concentrations fell within the optimal detection range of the instrument (0.001–0.1 µg/L), the final digested solution was diluted tenfold with deionized water before measurement. The ICP-MS system was warmed up, tuned using a standard tuning solution, and its stability verified prior to analysis. Calibration curves were prepared using multi-element standard solutions (XSTC-662, Spex CertiPrep, Metuchen, NJ, USA), and only curves with R
2 > 0.999 were accepted for quantification.
2.4. Quality Assurance and Quality Control (QA/QC)
Comprehensive QA/QC procedures were implemented throughout soil sampling, preparation, digestion, and ICP-MS analysis to ensure data accuracy and reliability. Method blanks prepared with ultrapure water (Milli-Q) were included in each batch to monitor contamination during sample processing. All glassware was acid-washed and thoroughly rinsed with deionized water prior to use. Reagent blanks were digested using the same procedure as the soil samples and processed simultaneously. Analytical accuracy was evaluated using certified reference material (CRM), which was digested and analyzed in triplicate. Each digested sample solution was analyzed three times, and the relative standard deviation of repeated measurements remained below 5%. Elemental recoveries obtained from the CRM were within acceptable ranges for all analyzed metals. Therefore, QA/QC procedures including method blanks, reagent blanks, and CRM validation showed no evidence of contamination from storage materials. Additionally, we obtained excellent recovery percentages for the examined heavy metals from the CRMs, ranging from 93% to 104%. After every ten determinations, the instrument was recalibrated using standard solutions. The limits of detection (LOD) for Mn, Cr, Cu, Ni, Co, Zn, As, and Pb were 0.041, 0.018, 0.048, 0.088, 0.009, 0.067, 0.001, and 0.085 ng/mL, respectively, as previously reported [
30]. It is important to note that certain toxic metals such as mercury (Hg), despite their environmental significance [
31], were not analyzed due to methodological limitations.
2.5. Assessment of Contamination Levels
To comprehensively assess heavy metal contamination in homestead agricultural soils, several widely used indices were employed in this study. These include the Contamination Factor, Pollution Load Index, and Ecological Risk Index. Each was calculated relative to background concentrations of heavy metals, representing their natural geochemical abundance in soils and sediments. The accuracy and reliability of these assessments largely depend on the selection of appropriate background reference values [
32] (
Table 3).
In the absence of localized baseline data for homestead agricultural soils in Bangladesh, this study adopted globally recognized geochemical background values, as recommended [
41]. The background concentrations used were as follows: Cr (59.5 mg/kg), Mn (488 mg/kg), Ni (29 mg/kg), Zn (70 mg/kg), Cu (38.9 mg/kg), Pb (27 mg/kg), Co (11.3 mg/kg), V (82.4 mg/kg), and As (5.2 mg/kg). The
CF index assesses contamination from individual metals by expressing the ratio of observed concentration to background levels. In contrast, the
PLI and
Er provide integrated assessments of overall pollution levels and the potential ecological risks posed by multiple metals. These indices were chosen for their simplicity, interpretability, and applicability in various environmental contexts.
2.5.1. Contamination Factor
The Contamination Factor (
CF) is used to assess the degree of metal contamination in relation to its geochemical background and is calculated using the following equation [
42]:
where
concentration of the heavy metal in the soil, and
background value of the heavy metal mentioned in
Section 2.5. Based on its value,
CF can be categorized into four levels of contamination: when
CF values < 1 indicate low contamination, 1–3 moderate contamination, 3–6 considerable contamination, and > 6 very high contamination.
2.5.2. Pollution Load Index
The Pollution Load Index (
PLI) provides a cumulative indication of overall heavy metal pollution at a sampling site. It is calculated as the geometric mean of the
CF values for the metals assessed using the following formula:
where
CFn is the contamination factor of each individual metal and n is the number of metals evaluated. Interpretation of
PLI values:
PLI < 1: No pollution;
PLI = 1: Baseline (background) pollution level and
PLI > 1: Progressive site deterioration due to pollution.
2.5.3. Ecological Risk Assessment
The Ecological Risk Index (
Er) is used to assess the potential ecological threat posed by heavy metals in soil, indicating the level of environmental risk they may present to local ecosystems. This index accounts for both the contamination level and the toxicological characteristics of each metal [
42]. The Er value is calculated using the following formula:
where
Er is the ecological risk factor of a single metal;
Tr is the toxic response factor for a given heavy metal, and
CF is the contamination factor as previously described. The
Tr reflects the metal’s potential to cause ecological harm. The
Tr values used in this study are as follows: Cr = 2, Mn = 1, Pb = 5, Co = 5, Cu = 5, Ni = 5, Zn = 1, As = 10 and V = 2. Based on ecological risk factors, the classification is defined as follows:
Er < 40 indicates a low potential ecological risk; 40 ≤
Er < 80 represents a moderate potential ecological risk; 80 ≤
Er < 160 corresponds to a considerable ecological risk; 160 ≤
Er < 320 denotes a high ecological risk; and
Er > 320 reflects a very high ecological risk [
43].
2.6. Human Health Risk Assessment
Assessing the human health risks posed by heavy metals is essential for understanding the potential adverse effects they may have on both children and adults living in contaminated areas. This study evaluates the non-carcinogenic and carcinogenic health risks associated with exposure to heavy metals specifically Cr, Mn, Ni, Zn, Pb, Co, Cu, As, and V through three main exposure pathways: ingestion, inhalation, and dermal contact.
The risk assessment approach followed the guidelines and equations outlined by the United States Environmental Protection Agency (USEPA). So, Equations (4)–(17) were used to calculate average daily intake for each pathway, hazard quotient (HQ), hazard index (HI), and cancer risk (CR), allowing for a comprehensive evaluation of health hazards linked to heavy metal exposure in homestead agricultural soils.
These quantitative methods enable the identification of populations at risk and help prioritize contaminants requiring mitigation efforts in both industrial and non-industrial zones. Prolonged environmental exposure to heavy metals can lead to serious human health risks. To evaluate the potential health risks associated with exposure to heavy metals in the study area, both non-carcinogenic and carcinogenic risks were assessed following the standard methodology recommended by the United States Environmental Protection Agency [
44].
2.6.1. Estimated Daily Intake
Human exposure to heavy metals occurs predominantly via three pathways: ingestion, inhalation, and dermal contact, as supported by previous studies [
45,
46]. The Average Daily Dose (
ADD, mg·kg
−1·d
−1) for each pathway is calculated using the following equations:
Parameters: C = Concentration of heavy metal in soil (mg/kg), Ring, Rinh = Ingestion and inhalation rates (mg/day), EF = Exposure frequency (days/year), ED = Exposure duration (years), BW = Body weight (kg), AT = Averaging time (days), PEF = Particle emission factor, AF = Skin adherence factor (mg/cm2), SA = Exposed skin surface area (cm2), ABS = Dermal absorption factor.
2.6.2. Cancer Risk Assessment
The cancer risk associated with lifetime exposure to carcinogenic heavy metals was evaluated using the Lifetime Average Daily Dose (
LADD) and the Cancer Slope Factor (
CSF). The
LADD for ingestion, inhalation, and dermal contact was followed [
30,
47] and calculated using the following equations:
2.6.3. Non-Carcinogenic Risk
The Hazard Quotient (
HQ) is the ratio of the
ADD to the Reference Dose (
RfD) for each pathway. If HQ > 1, it suggests a potential for non-carcinogenic effects. The Hazard Index (
HI) is the sum of
HQ values across all pathways:
2.6.4. Carcinogenic Risk
The Carcinogenic Risk (
CR) estimates the probability of an individual developing cancer over a lifetime due to exposure to a carcinogen. The Cumulative Carcinogenic Risk (
CCR) is the sum of
CRs across all exposure pathways:
2.7. Statistical Analysis
Data were analyzed using IBM SPSS Statistics Version 20, Microsoft Excel 2013, and R software (version 4.3.2). The mean, minimum, and maximum, were used to summarize heavy metal concentrations in soils from industrial and non-industrial areas. Mean differences among sampling sites were evaluated using Duncan’s Multiple Range Test (DMRT). Pearson correlation analysis was performed to evaluate relationships among heavy metals and potential contamination sources. Additionally, principal component analysis (PCA) and Hierarchical cluster analysis (HCA) were conducted in R to identify major contributing factors and classify sampling sites based on their contamination profiles.
4. Conclusions
This study investigated the distribution of heavy metal contamination, pollution sources, ecological risks, and human health risks in homestead agricultural soils across industrial and non-industrial regions of Bangladesh. Nine heavy metals, namely Cr, Mn, Co, Ni, Cu, Zn, As, Pb, and V, were detected at varying concentrations. Industrial areas exhibited substantial enrichment of Cr, Ni, Cu, Zn, and Pb, whereas As contamination was more widespread in non-industrial regions. Higher As concentrations in surface soils compared to subsurface layers suggest ongoing inputs from industrial effluents, atmospheric deposition, agrochemical use, and wastewater irrigation.
Multivariate analyses revealed mixed contamination sources with clear site-specific variations, reflecting the influence of local anthropogenic activities on metal distribution. Ecological risk assessment identified As and Pb as the dominant contributors to ecological stress. Human health risk analysis further indicated that children are the most vulnerable population group, with ingestion identified as the primary exposure pathway, signaling potential health threats but the assessment of human health risks via consumption of crops grown in contaminated soil was not conducted in this study. Moreover, CCR results confirmed that As is the major driver of lifetime carcinogenic risk in homestead soils, followed by Cr, while contributions from other metals remain minimal.
Despite some limitations in conducting the study, such as the lack of evaluation of mitigation measures, the findings underscore the urgent need for site-specific monitoring, awareness-building initiatives, improved industrial waste management, and targeted mitigation strategies particularly the promotion of integrated pest management to safeguard food security and public health in studied areas of Bangladesh.