3.3.1. Physical Parameters in Water Samples
The river water samples in the dry season exhibited an acidic, neutral, and slightly alkaline pH range of 5.77 ± 0.01 to 7.77 ± 0.01 (
Table 6). In the assessment, the results were compared against the established standards for water quality, particularly the ones outlined by the WHO and TBS for drinking water. This is crucial because, in many areas across Africa, untreated river water is directly utilized for various household needs, including drinking, sometimes without undergoing any preliminary treatment processes [
61].
The pH range of the water samples was 7.58 ± 0.01 to 8.24 ± 0.05, which is related to the pH ranges measured in the Pangani River [
19]. Upstream reaches exhibited lower pH levels of 6.12 ± 0.01 and 5.77 ± 0.01, respectively, during the dry season; these lower pH levels posed several implications to aquatic life [
62]. Typically, pH levels below 4 tend to amplify the toxicity of the majority of metals [
63], while the highest pH values (alkaline conditions) tend to reduce the mobility of toxic heavy metals [
48]. In the wet season, the highest values were 8.24 ± 0.05 at the headwater of Morogoro River at the Uluguru Mountains; this elevated pH level might be attributed to natural factors like geological features or the riparian forest ecosystem that might influence the organic matter decomposition in the river.
The PCA was conducted to identify and explain the variations in the physical parameters in the surface water datasets. The PCA resulted in two principal components, PC1 and PC2. PC1 and PC2, including eigenvalues surpassing one, accounted for a cumulative variance of 67.75% (
Table 5). The first principal component was loaded with TDS and conductivity, which accounted for 24.74% of the total variance and signified the influence of TDS in electrical conductivity due to an increase in the dissolved ions in the water, as reported by Kurkjian et al. [
64]. The pH and DO % were responsible for 14.89% of the total variance loaded in PC2. The correlation test proved a high positive correlation between TDS and conductivity, turbidity, and salinity, with a correlation coefficient value of 0.99, 0.99, and 0.09, followed by temperature and DO % with a coefficient of 0.83 (
Table 7).
The highest level of electrical conductivity, ranging between 1133.33 ± 1.53 µS/cm and 2446.33 ± 0.58 µS/cm, was observed from the midstream to the downstream during the dry season. A similar study performed by Kurkjian et al. [
64] reported that a higher level of electrical conductivity indicated the presence of inorganic dissolved solids acquired from anthropogenic activities. Through this study, it was noted that the river banks and floor are highly dominated by silt clay soil that influences a higher level of electrical conductivity. Similar findings were reported in the Mekong River water that runs through areas with silt clay soils, which tends to have higher conductivity because of the presence of materials that ionize when washed into the water [
65]. In the wet season, the highest recorded electrical conductivity was 445.33 ± 0.58 µS/cm and the lowest was 37.33 ± 2.08 µS/cm. The potential causes of the variability in the electrical conductivity in the wet and dry seasons might be associated with the effect of dilution, causing a lower level of EC in the wet season, while the higher EC in the dry season might be associated with the accumulation of dissolved ions in the river under the influence of excessive evaporation.
Water temperatures varied between 22.67 ± 0.06 °C and 32.0 °C. This observation is in agreement with the temperature ranges reported for the Angaw River and Limpopo River basins, respectively [
66,
67]. During the wet season, the water temperatures across all sampling stations were in line with the WHO standards (
Table 8), with the lowest temperature of 21.51 ± 0.03 °C and the highest temperature of 29.39 ± 0.07 as reported in Pangani River, Tanzania [
20]. Generally, the water temperature tends to influence the DO levels, as higher temperatures tend to decrease the amount of oxygen that water can hold. However, this association is subject to modifications caused by various factors such as changing hydro-meteorological conditions [
68].
A higher TDS concentration was observed during the dry season, particularly in the midstream and downstream reaches, and similar findings were recorded at the Ruvu River [
69] and in the Odzi River [
70]. A study conducted by Mato [
71] demonstrated that total dissolved solid (TDS) concentrations ranging from 0 to 1500 mg/L signify good quality freshwater. Furthermore, TDS values below 500 mg/L indicate excellent freshwater quality with potentially lower levels of pollution. Conversely, when the TDS values exceed 1500 mg/L, the water may have a salty taste, indicating a higher concentration of dissolved solids. The TDS concentrations across all sampling stations in the wet season aligned with the WHO standards, with the TDS concentrations ranging from 18.67 ± 0.58 mg/L to 222.67 ± 0.58 mg/L. This observation can be associated with the increase in the river discharge during the wet season which tends to amplify the dilution process, as the lowest TDS of 18.67 ± 0.58 mg/L was recorded at a point with a higher discharge of 3.727 m
3/s.
The findings showed that there was significant variability in the salinity in the two seasons of the sampling campaigns, with a high level of salinity in the dry season. Salinity in the water samples during the dry season was in the range of 0.02 ± 0 mg/L to 1.12 ± 0 mg/L, indicating a substantial surge in dissolved solutes from upstream to downstream zones situated in proximity to residential areas, agricultural fields, and industries. Other potential sources of elevated salinity might be associated with increased dissolved salt originating from agricultural runoff, discharges from the on-site sanitation systems, and contaminated runoff from the urban area [
72]. This finding aligns with the higher salinity observed in the river water, suggesting potential implications for human health due to the intake of saline river water [
73]. In the wet season, the average salinity levels in the Ngerengere River and its tributaries within Morogoro Municipality were lower compared to the dry season, with salinity levels ranging from 0.02 ± 0 mg/L upstream to 0.21 ± 0 mg/L downstream. The study findings showed variability in the turbidity across the sampling stations in each sampling campaign. The ideal state for river water is colorless [
74]; in the dry season, the study showed that the turbidity levels ranged from 2.33 ± 0.58 NTU in the upstream to 1034.67 ± 6.03 NTU in the downstream.
The turbidity levels of the surface water play a significant role in the aquatic ecosystem by influencing the amount of light penetrating the water, which can also affect the water temperature and overall habitat suitability for aquatic organisms. The average turbidity values in the wet season ranged from 0.02 ± 0.01 NTU to 92.97 ± 2.32 NTU, where the upstream stations were observed to have low turbidity levels. The lower turbidity observed in the upstream river water samples near the headwaters of Uluguru mountain can be attributed to the significant presence of forested areas in the region. Forest ecosystems act as natural buffers against sedimentation and pollutants, primarily through various mechanisms facilitated by dense vegetation.
During the dry season, the dissolved oxygen (DO) levels ranged from 2.067 ± 0.06% and 0.25 ± 0.01 mg/L to 4.53 ± 0.06% and 0.46 ± 0.01 mg/L, with temperature values of 31.33 ± 0.12 °C to 22.67 ± 0.06 °C, respectively. This trend is similar to the other previous studies [
64,
65]. This study revealed that the water flow rate data at the sampling stations have significant implications for the level of dissolved oxygen [
75]. During the wet season, the highest DO level was recorded at the upstream reaches. The study performed in the Rungiri reservoir observed the average DO of the dam to be 4.91 ± 0.49 mg/L, which is quite dissimilar to the findings of this study; there is no specific recommended limit for dissolved oxygen in drinking water. Nevertheless, a desirable dissolved oxygen level for a healthy water source is considered to be 5 mg/L [
76].
The water quality parameters in the Ngerengere River, as revealed by this study, showcase both similarities and distinctions when compared to other urban rivers globally. While the pH levels align with those observed in the other urban rivers of developing countries (
Table 9), it was observed that the Karnaphuli urban river experiences higher temperatures. The salinity levels in the Ngerengere River are considerably lower than the Mutangwi River in Limpopo Province, South Africa, pointing to a distinct freshwater nature. The electrical conductivity (EC) in the Ngerengere River spans a wide range, surpassing most other rivers except for Mutangwi. Dissolved oxygen (DO) levels in the Ngerengere River are lower than in several comparable rivers, suggesting potential concerns for aquatic life. Turbidity in the Ngerengere River is notably higher compared to the Ngong River, Mutangwi River, and Lower Danube.
The PCA produced two principal components, PC1 and PC2, for the variance of physical parameters in river water during the wet season. PC1 and PC2, including eigenvalues surpassing one, accounted for a cumulative variance of 86.14% (
Table 10). The first principal component was loaded with temperature, salinity, conductivity, turbidity, and TDS, which accounted for 61.745 of the total variances. DO, salinity, conductivity, TDS, and pH were responsible for 24.40% of the total variance loaded in PC2. The correlation test showed a high positive correlation between TDS and salinity, and conductivity and salinity, with correlation coefficient values of 0.999 and 0.999, respectively.
3.3.3. Variation in Heavy Metal Concentrations in Water and Sediments
The values of heavy metal concentrations in the river water samples during the dry and wet seasons across the sampling stations are represented in
Figure 5.
The study revealed that the order of magnitude of the heavy metal concentrations was Cu > Cr > Ni > Pb > Zn > Cd. During the dry season, the highest mean concentration of lead (Pb) was 0.08 ± 0, which was recorded at sampling station S11; the highest concentration of Pb might be associated with the nature of the activities, including garages, car washes, residential and commercial activities, and petrol station services. This research observed a positive relationship between Pb with Cr, similar to the study of Huang et al. [
87], as well as Pb with Cd, Cd with Cu [
30], Pb with Ni, Cr with Cd [
88], Cd with Ni, Cu with Zn, and Zn with Ni. The Pearson correlation matrix showed that Pb and Ni were moderately correlated, with an R-value of 0.514. Pb with Cr, Pb with Cd, Cr with Cd, Cd with Cu, Cd with Ni, Cu with Zn, and Zn with Ni were weakly correlated, with R-values of 0.32, 0.33, 0.46, 0.46, 0.06, 0.30, and 0.39, respectively (
Table 12). Furthermore, weak negative correlations were found between Pb with Cu, Pb with Zn, Cr with Cu, Cr with Zn, and Cr with Ni, as well as between Cd and Zn, and Cu with Ni.
During the dry season, the highest mean concentration of lead (Pb) was 0.08 ± 0, which was recorded at the Kikundi stream near its confluence with the Morogoro River; the highest concentration of Pb might be associated with the nature of the activities, including garages, car washes, residential and commercial activities, and petrol station services. The findings were not consistent with Liu et al. [
89], which reported higher lead concentrations in water bodies surrounding the mining sites. The lowest Pb concentration was 0.04 ± 0.01 mg/L, which was quite similar to Singh et al. [
24]. This study revealed that most of the upstream sampling stations were less polluted from lead concentrations. This observation is in line with the Tanzania standards for permissible lead limits in water, but is not consistent with the WHO guidelines. Chromium levels in the surface water were recorded to be within the WHO and TBS standards for most sampling stations, except for sampling stations S1 and S5, where the concentrations of chromium recorded were 0.06 ± 0 and 0.08 ± 0, respectively. The highest chromium concentration was recorded at the confluence of the Bigwa and Ngerengere Rivers. The potential attributes of high chromium concentrations might emanate from runoff and spillage from the Tanzam highway, which was observed during the sampling. Notably, most of the sampling stations were recorded to be less than below the detection limit. Chromium concentrations in most surface water ranged between 0 and 0.01 mg/L of chromium; however, these concentrations are usually influenced by the extent of the industrial activity [
11,
90].
The cadmium concentration in the dry season was recorded to be in the range below the detection limit. However, the highest mean concentration of cadmium was 0.03 ± 0.02 mg/L, which was located in the Mwele area, adjacent to car washing facilities and other commercial activities. The levels of cadmium in the Ngerengere River and its tributaries were in accordance with the standards set by both the World Health Organization (WHO) and Tanzania water quality standards. Other important sources of Cd pollution are the metal industry, plastics, and sewers. A major portion of Cd (30–50%) was contained in the most mobile fraction (either in exchangeable or carbonate bound), and therefore can easily enter the food chain [
91]. Amongst the different metals, the Cd concentration was the lowest, but the toxicity was high. It was found that Cd was significantly higher in the dry season compared to the other seasons. At selected river tributaries of the Mara River in Tanzania, Nkinda et al. [
88] reported that chromium concentrations ranged from 0.97 ± 0.49 mg/L to 2.58 ± 0.57 mg/L in the Somoche and Nyarusobindoro areas, citing the impacts of mining operations for the elevated level of chromium in the surface water [
3]. Overall, most of the sampling stations along the Ngerengere River and its tributaries were recorded with the lowest concentrations of copper, notably below the detection limit. The highest copper concentrations were 0.73 ± 0.04 mg/L and 0.32 ± 0.02 mg/L, and the lowest concentrations were recorded to be <0.01 in the most upstream points of the river and its tributaries. Wang and Bjorn [
90] highlighted the toxicity concerns of copper due to its exposure, citing gastrointestinal symptoms at lower exposure levels than those that cause chronic toxicity and other health implications, like neurological effects and memory impairment [
18]. A significant amount of copper is in the immobile form and can be found in reducible (Fe-Mn oxide) and residual fractions [
91]. Major sources of Cu pollution are the production of home tools, metals, manipulation, the timber industry, and ashes. The average concentration of zinc ranged from below the detection limit to 0.03 ± 0.02 mg/L. Zinc occurs in small amounts in almost all igneous rocks, and the major zinc ores are sulfides, including sphalerite and wurtzite. The natural zinc concentration in soils is estimated to be 1–300 mg/kg, while in the natural surface waters, the concentration of zinc is usually below 0.010 mg/L, and in groundwater is 0.01–0.04 mg/L [
11].
Furthermore, the principal component analysis (PCA) results revealed two principal components, collectively explaining 58.34% of the variability in the dataset (
Table 13). The initial principal component (PC1), responsible for 30.05% of the total variance, exhibited notably high positive loadings for Pb, Cd, and Cr, with a high loading of Cd followed by a moderate loading for Pb and Cr. It is well-established that chromium and cadmium are commonly linked in various rock types, suggesting their presence in soils derived from such geological formations [
92]. Our study reaffirmed this association, showing a correlation coefficient (r) of 0.42 between these elements. It is worth noting that, apart from natural processes, anthropogenic sources like industrial effluents, mismanagement of solid waste disposal, and other agricultural runoffs aggravate the concentrations of Cr and Cd [
93]. The second principal component, explaining 28.29% of the variance, exhibited a high positive loading for Ni, a moderate positive loading for Zn, and a low positive loading for Pb. According to Ahmed and Mokhtar [
92], the primary sources of Pb and Ni in the aquatic environment emanate from the natural weathering of minerals and widespread anthropogenic activities, which is reaffirmed by our results, showing a correlation coefficient (r) of 0.54.
The order of magnitude of heavy metal concentrations during the wet season across the sampling stations was as follows: Zn > Ni> Cr > Cu > Cd > Pb. The highest concentrations of Pb, Cr, Cd, Cu, Zn, and Ni were 0.01 ± 0 mg/L, 0.05 ± 0.04 mg/L, 0.02 ± 0 mg/L, 0.01 ± 0 mg/L, 4.07 ± 0.08 mg/L, and 3.07 ± 0.04 mg/L, respectively. This study indicated that the levels of Ni exceeded the WHO standards and TBS standards. Zn was higher than the maximum limits established by the WHO. The recoded values of Pb and Cu remain to be in line with the established WHO and Tanzania standards. The level of chromium was higher at S1, with a mean concentration of 0.05 ± 0.04. From the observed findings, it can be concluded that the midstream and downstream reaches of the urban catchment of the Ngerengere River have been highly impacted by heavy metal pollution. In the wet season, strong positive correlations were observed between Pb and Cd, Pb and Cu, Pb and Zn, Cd and Cu, Cd and Zn, and Cu and Zn, with R-values of 1.00, 0.99, 0.99, 0.99, 0.99, and 0.99 (
Table 12). Moderately positive correlations were observed between Pb and Cr, Cr and Cd, Cr and Cu, as well as Cr and Zn. Furthermore, weak negative correlations were found between Pb with Ni, Cr with Ni, Cd with Ni, Cu with Ni, and Zn with Ni. The principal component analysis (PCA) results revealed two significant components, collectively explaining 99.24% of the variance (
Table 14). The first principal component (PC1), responsible for 62.33% of the total variance, exhibited positive loadings for all heavy metals, with a high loading of Pb, Cd, Cu, and Zn, and followed by low loading for Cr and Ni. The second principal component, explaining 36.92% of the variance, exhibited a high positive loading for Cr and Ni, followed by moderate loading of Zn. Pb, Cd and Cu showed a negative loading.
3.3.5. Nutrient Loading in Water and Sediments
This study revealed that there was significant temporal and spatial variability in ammonia-nitrogen, nitrate nitrogen, nitrate nitrogen, and phosphate concentrations in water and sediments. In the dry season, the concentrations of ammonia-nitrite were higher at the downstream reach of the Ngerengere River in Morogoro Municipality at sampling, with readings of 1.63 ± 0.01 mg/L and 1.55 ± 0.05 mg/L (
Figure 7); this observation might be attributed by the presence of excreta in the river water, attributed by on-site sanitation systems and excreta from livestock [
66,
73]. The levels of ammonia were not in line with the Tanzania standards for drinking water supplies, per TZS 789: 2008. Nitrite nitrogen concentrations ranged from 0.08 ± 0.01 mg/L to 0.39 ± 0.53 mg/L, indicating nitrite nitrogen enrichment upstream compared to downstream.
The nitrate levels ranged from 0.19 ± 0.04 mg/L to 0.39 ± 0.30 and 0.46 ± 0.47 mg/L. Higher nitrate concentrations might be attributed to upstream farming activities that transport nitrate-enriched runoff to Mindu Dam, while, at S3, the potential attribute of the nitrate concentration is due to ongoing farming practices and on-site sanitation practices; other potential sources of nutrients in the river might be the atmospheric nitrogen gases, because the aforementioned sampling stations are situated in the proximity of Tanzam highway. This has been also reported in the study of Akhtar et al. [
94], which established the link of air–water interaction and the associated implications to the water quality. One potential public health consequence associated with elevated nitrate levels in the river is the increased risk of methemoglobinemia in infants, commonly known as “blue baby syndrome”. To prevent methemoglobinemia, the US Environmental Protection Agency (EPA) has established maximum permissible levels of 10 mg/L for nitrite-nitrogen and 1 mg/L for nitrate-nitrogen. Additionally, the river may face challenges related to ammonia toxicity to aquatic organisms, particularly when concentrations exceed 0.2 mg/L, especially in instances of elevated pH and ammonia levels. Mitigating ammonia toxicity involves maintaining a pH level below 8 and ammonia concentrations below 1 mg/L. From an environmental management perspective, nutrient enrichment in the river raises concerns about eutrophication, leading to compromised ecological integrity in surface waters, the potential extinction of fish populations, the proliferation of toxic cyanobacteria blooms, and a reduction in oxygen levels [
68]. The average phosphate concentration in river water ranged from 0.187 ± 0.038 mg/L at S1 to 0.456 ± 0.474.
The elevated phosphate concentration at S2 might be attributed to point sources and non-point/diffuse sources, possibly containing both organic and inorganic forms of this element; the water at the sampling station, being a dam with low water velocity, facilitates the gradual settling of suspended solids (SSs) along with particulate phosphorus (PP) [
95], and this phenomenon is responsible for eutrophication in surface water. Diffuse sources involve inputs from the leaching of geological rocks and land use, whereas point sources consist of industrial discharge [
96]. In surface waters, phosphate and polyphosphate inorganic compounds constitute the prevalent forms of phosphorus, while organic phosphorus arises from the life processes and decay of aquatic organisms, along with human activities that contribute to phosphorus release [
97].
The study also signifies those tributaries (Morogoro and Bigwa) might influence the nutrient transportation to the Ngerengere River, as in their confluence and downstream, the nutrient levels appeared to be higher; this has been observed in sampling stations S6, S5, S7, and S11 for ammonia-nitrogen, nitrite-nitrogen, nitrate-nitrogen, and phosphorus (phosphate), respectively. At this juncture, the concentration of nutrients in the downstream reach of the Ngerengere River within Morogoro Municipality can be influenced by water from Morogoro River. Similar findings were observed in the downstream reaches of Kilombero Valley compared to the upstream reaches due to excessive agricultural activities [
98]. In the wet season, the highest concentrations of ammonia, nitrite, nitrate, and phosphate in the river water were 2.05 ± 0.01 mg/L, 0.15 ± 0.01 mg/L, 0.53 ± 0.01 mg/L, and 0.63 ± 0.01 mg/L, respectively. The resulting increase in the nutrient loading in the wet season downstream was due to an increase in the surface runoff attributed to rainfall events within the catchment.
For a considerable period, sediments have been acknowledged as a repository for numerous pollutants released into surface water. The presence of contaminated sediments can lead to harmful ecological impacts on sediment-related organisms like macrophytes, benthos, and demersal fish, as well as on higher-level biota such as pelagic fish and aquatic birds [
99]. In this study, particularly in the dry season, high nutrient concentrations in the sediments were 2.21 ± 0.12 mg/kg, 0.48 ± 0.14 mg/kg, 1.82 ± 0.26 mg/kg, and 34.29 ± 0.55 mg/kg for ammonia-nitrogen, nitrite-nitrogen, nitrate-nitrogen, and phosphorus (phosphate), respectively (
Figure 8). Ammonium-N and nitrate-N are naturally present in water due to the decomposition of organic and inorganic matter, excretion by organisms, and the microbial reduction in atmospheric nitrogen [
98]. Nonetheless, the elevated ammonium-N observed at S11 may be attributed to on-site sanitation systems located near the sampling station. The study also indicated that the sediment at the downstream reach of the river has a higher phosphate concentration than the upstream reach. This study also revealed that higher phosphate concentrations in the Morogoro tributary, particularly at sampling station S5, might cause an increase in the elevated phosphate concentrations downstream of the Ngerengere River; this might be attributed to sediment transported from tributaries, especially the Morogoro River. The percentage of total carbon in the soil was higher at midstream and lower at the upstream reaches.
This study also showed that the sulphate concertation in the urban catchment of the Ngerengere River was higher at the midstream, at 255.43 ± 0.01 mg/kg, and lower at the upstream, at 52.16 ± 0.71 mg/kg. Chloride concentrations were higher in the sediments collected upstream at S13, located within the Uluguru Mountains, at 269.92 ± 32.56, which is likely attributed to weathering processes and geological formations; the lowest chloride concentration was lower at the midstream reaches, with a reading of 66.14 ± 0.34. In the wet season, the highest concentrations of ammonia, nitrite, nitrate, and phosphate in the river sediment were 2.64 ± 0.03 mg/kg, 0.63 ± 0.01 mg/kg, 1.46 ± 0.01 mg/kg, and 48.16 ± 0.01 mg/kg, respectively.
The findings from the hierarchical cluster analysis (HCA) further showed that the urban catchment of the Ngerengere River in Morogoro Municipality was divided into two pollution clusters (C1 and C2) for both water and sediments. The dendrogram in
Figure 9 summarizing the results of the HCA shows that the initial splitting of the tree forms two clusters for both water and sediments. The top cluster (Cluster 1) contains eleven stations (S1, S9, S10, S2, S3, S4, S5, S13, S11, and S12) and the bottom cluster (Cluster 2) contains two stations (S7 and S8) for water; for sediments, C1 contains S1, S10, S11, S3, S2, S4, S8, S5, S12, S6, and S7, and C2 contains S9 and S13. For the water samples, C1 and C2 entail the sampling stations of the middle–upstream and downstream, respectively. The nitrate concentrations of C2 were almost twice that of C1 (
Table 16), indicating that there were significant impacts of human activities in the downstream and midstream reaches of the river and tributaries. For the sediment samples, C1 and C2 include the sampling stations at the middle–downstream and upstream reaches. The phosphate concentrations of C2 (upstream) were almost twice to that of C1 (downstream), signifying phosphate binding onto sediment in oxic conditions [
100]. This was supported by this study, which recorded higher dissolved oxygen in the upstream reaches.
The Wilcoxon signed-rank non-parametric test compared the values of the nutrients in the water and sediments obtained between the two seasons and revealed that NH3 in the dry season was equal to NH3 in the wet season, NO2− in the dry season > NO2− in the wet season, NO3− in the dry season > NO3− in the wet season, and PO43− in the dry season was equal to PO43− in the wet season for the case of river water samples. Furthermore, in river sediments, NH3 in the dry season was equal to NH3 in the wet season, NO2− in the dry season < NO2− in the wet season, NO3− in the dry season was equal to NO3− in the wet season, and PO43− in the dry season > PO43− in the wet season.
Organic loading in the water showed that the (5-day Biochemical Oxygen Demand) BOD
5 concentrations in the dry season ranged from 24.76 ± 0.03mg/L to 277.52 ± 0.16 mg/L, which signifies that the downstream reaches of the river have a higher organic loading compared to the upstream reaches, which can be attributed to the accumulation of waste. Notably, the midstream reaches recorded relatively higher BOD
5 concentrations, which was linked to the existence of point sources of organic pollution like industries, on-site sanitation systems, and poor solid waste management marked by presence of the Mafisa dumpsite. This study revealed that domestic waste, industrial activities, and runoff from agricultural activities resulted in higher COD concentrations, which was due to higher COD concentration values of 123.11 ± 0.02 mg/L, 115.83 ± 0.08 mg/L, 100.19 ± 0.05 mg/L, and 102.16 ± 0.16 mg/L. Tanzania’s water quality standards specify the permissible limits for organic pollution introduced artificially and naturally in water bodies. In this study, we evaluated the total carbon in the water to accommodate the natural and artificial carbon in the water. This study revealed that the total carbon was higher downstream at 0.35 ± 0.03% and lower upstream at 0.13 ± 0.01%, which represented the pristine environment (headwater). Tanzania water quality standards have grouped sulphate and chloride ions together as salinity and hardness impact parameters. Sulphate concentrations ranged from 16.40 ± 0.91 mg/L to 116.79 ± 0.37, and these findings are quite related to the observations reported by Mbuligwe and Kasseva [
50] at Msimbazi River; according to the Tanzania standards, the lower and upper limits for sulphate in water is 200 and 600 mg/L, respectively. Chloride was observed to be higher downstream, at 119.28 ± 0.22, than upstream, at 26.37 ± 0.22 mg/L, which signified the elevated salinity of the river water.
This study also showed that the total carbon in the bottom sediments of the river and its tributaries was higher (5.23 ± 0.16 mg/kg) in the midstream area, which was covered by mixed types of pollution sources responsible for organic loading in the river, while the lowest total carbon was higher at the upstream reaches, which can be associated to the textural properties of the sediment and the reduced disturbance from anthropogenic pollution sources responsible for organic pollution. Higher phosphorus and nitrogen concentrations in the sediments were recorded at 34.29 ± 0.55 mg/kg, 1.82 ± 0.03 m/kg, 0.48 ± 0.14, and 2.21 ± 0.12 mg/kg for phosphate, nitrate-nitrogen, nitrite-nitrogen, and ammonia-nitrogen, respectively; for sulphate and chloride, higher concentrations were recorded at 255.43 ± 0.01 mg/kg and 269.92 ± 32.56 mg/kg. The lowest phosphorus and nitrogen concentrations in the sediments were 13.56 ± 0.69 mg/kg, 0.51 ± 0.05 m/kg, 0.20 ± 0.04, and 0.28 ± 0.01 mg/kg for phosphate, nitrate-nitrogen, nitrite-nitrogen, and ammonia-nitrogen, respectively. The spatial variations in nutrients are influenced by land-use practices and the extent of urban development [
73], where higher nitrogen and phosphorus concentrations usually occur in areas of urban and agricultural activities [
50], while the temporal variability of the nutrients in the sediment is influenced by geological processes and weather seasons, as higher nutrient levels are normal during the wet season due to the effects of runoff from agriculture and urban centers. In the wet season, higher BOD
5, COD, and total carbon concentrations in the river water were recorded at 287.39 ± 0.55 mg/L, 110.51 ± 0.51 mg/L, and 0.30 ± 0.02%, respectively. Furthermore, the level of organic loads explained by the total carbon percentage was higher in the midstream reaches, with a TC reading of 3.3875 ± 0.03%.