3.2. Comparison of the Outflow Water Qualities
Table 2 shows the summary statistics of the outflow water quality variables for the indoor and outdoor rigs. The variability of pH was relatively low; maximum standard deviations for both the indoor and outdoor rigs were up to 0.36. Mean values ranged between 7.1 and 7.5. In contrast, the maximum standard deviations for conductivity ranged between 41.8 and 85.9 μS for the indoor and between 32.9 and 90.1 μS for the outdoor rig, respectively. However, the most significant variability was recorded for suspended solids with respect to the outdoor bin 1 and indoor bin 5; standard deviations reached concentrations of 369.5 mg/L and 199.9 mg/L respectively (
Table 2).
Mean dissolved oxygen concentrations were similar for both rigs, ranging between 6.4 and 7.6 mg/L, and between 5.8 and 8.3 mg/L for the indoor and outdoor rig respectively (
Table 2). Overall reductions in dissolved oxygen for both systems ranged between 1% and 35%. However, the oxygen distribution profile varied considerably within the system. Lowest values were measured near the geotextile and at the bottom, indicating high microbiological activity. The BOD reductions were between 77% and 100%, which indicates a high biodegradation potential [
13].
Figure 5,
Figure 6 and
Figure 7 highlight nutrient distributions and show that the ortho-phosphate-phosphorus, ammonia-nitrogen and nitrate-nitrogen concentrations increase considerably with the addition of dog faeces. High reductions of ortho-phosphate-phosphorus (
Figure 5) and ammonia-nitrogen (
Figure 6) were observed after treatment. For the indoor system, ortho-phosphate-phosphorus mean concentrations were less than 1.4 mg/L (corresponding reduction of 79%). For the outdoor system, concentrations fluctuated between 0.2 and 3.5 mg/L with corresponding reduction rates between 58% and 95%. Ammonia-nitrogen concentrations from urban runoff ranges from 0.1 mg/L–10 mg/L, whilst average concentrations are approximately 25 mg/L from untreated urban domestic wastewater. Hence, the influent concentrations of NH
4 matched that of urban stormwater and not domestic wastewater. Ammonia-nitrogen reductions were up to 98% for both systems and the corresponding mean concentrations ranged between 0.07 and 1.09 mg/L for the indoor and between 0.03 and 1.06 mg/L for the outdoor system respectively. The findings indicate relatively high nutrient reductions and/or transformations, which were accelerated during the heating period. However, the mean weekly effluent of nutrients (ammonia-nitrogen, nitrate-nitrogen, nitrite-nitrogen and ortho-phosphate-phosphorous) showed no statistical differences for ANOVA from the heat cycle to the cooling cycle (
p > 0.05). Similar results occurred for BOD
5 and suspended solids outflow concentrations. Nitrate-nitrogen concentrations varied as a result of organic nitrogen present in the gully pot liquor being converted to NO
3-N.
Table 2.
Summary statistics of the outflow water quality for the rigs located indoors and outdoors.
Table 2.
Summary statistics of the outflow water quality for the rigs located indoors and outdoors.
Variable | Statistics | Bin Number |
---|
| | 1 * | 2 ** | 3 ** | 4 * | 5 ** | 6 ** |
Indoor Rig (Sample Number, n = 110) |
Five-days at 20 °C Biochemical oxygen demand (mg/L) | Mean | 0.8 | 1.2 | 0.9 | 0.6 | 0.9 | 0.5 |
SD | 1.5 | 1.7 | 0.7 | 0.5 | 1.0 | 0.5 |
Suspended solids (mg/L) | Mean | 145.1 | 139.4 | 173.3 | 120.3 | 132.7 | 115.5 |
SD | 154.1 | 189.9 | 195.3 | 118.3 | 200.0 | 125.4 |
Total dissolved solids (mg/L) | Mean | 182.7 | 180.4 | 151.8 | 197.6 | 176.3 | 171.6 |
SD | 22.8 | 33.2 | 34.7 | 21.1 | 27.1 | 42.7 |
Dissolved oxygen (mg/L) | Mean | 6.5 | 7.3 | 7.6 | 7.0 | 6.4 | 7.2 |
SD | 1.8 | 2.2 | 2.4 | 1.8 | 1.9 | 2.1 |
pH (-) | Mean | 7.2 | 7.5 | 7.5 | 7.4 | 7.4 | 7.5 |
SD | 0.3 | 0.2 | 0.2 | 0.3 | 0.3 | 0.3 |
Conductivity (μS) | Mean | 365.5 | 361.4 | 308.1 | 396.2 | 354.2 | 344.1 |
SD | 46.8 | 66.8 | 70.9 | 41.8 | 53.9 | 86.0 |
Ammonia-nitrogen (mg/L) | Mean | 0.1 | 0.1 | 0.1 | 0.1 | 0.1 | 0.1 |
SD | 0.2 | 0.1 | 0.1 | 0.1 | 0.2 | 0.1 |
Nitrate-nitrogen (mg/L) | Mean | 18.4 | 5.9 | 4.5 | 17.6 | 3.2 | 4.7 |
SD | 16.7 | 5.0 | 3.2 | 18.1 | 3.0 | 4.1 |
Ortho-phosphate-phosphorus (mg/L) | Mean | 1.4 | 0.4 | 0.3 | 1.3 | 0.3 | 0.3 |
SD | 0.7 | 0.3 | 0.4 | 0.7 | 0.4 | 0.4 |
Outdoor Rig (Sample Number, n = 110) |
Five-days at 20 °C Biochemical oxygen demand (mg/L) | Mean | 2.3 | 0.8 | 0.5 | 0.9 | 0.6 | 0.7 |
SD | 3.2 | 1.6 | 0.7 | 1.2 | 0.7 | 0.9 |
Suspended solids (mg/L) | Mean | 255.8 | 105.9 | 105.0 | 103.0 | 97.4 | 70.3 |
SD | 369.5 | 115.0 | 131.2 | 101.9 | 124.6 | 64.7 |
Total dissolved solids (mg/L) | Mean | 212.2 | 166.5 | 156.3 | 187.6 | 164.6 | 153.0 |
SD | 40.0 | 23.7 | 16.4 | 15.8 | 22.1 | 16.2 |
Dissolved oxygen (mg/L) | Mean | 6.2 | 8.0 | 7.6 | 5.8 | 8.2 | 8.3 |
SD | 1.3 | 1.6 | 1.2 | 1.0 | 1.5 | 1.3 |
pH (-) | Mean | 7.1 | 7.3 | 7.3 | 7.1 | 7.4 | 7.4 |
SD | 0.2 | 0.4 | 0.2 | 0.3 | 0.2 | 0.2 |
Conductivity (μS) | Mean | 428.7 | 333.5 | 314.6 | 383.7 | 329.7 | 307.6 |
SD | 90.1 | 47.4 | 33.0 | 67.8 | 44.1 | 33.3 |
Ammonia-nitrogen (mg/L) | Mean | 0.1 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 |
SD | 0.1 | 0.0 | 0.0 | 0.1 | 0.0 | 0.1 |
Nitrate-nitrogen (mg/L) | Mean | 8.1 | 3.8 | 5.5 | 5.0 | 4.3 | 5.1 |
SD | 8.6 | 3.1 | 2.5 | 6.0 | 3.1 | 2.5 |
Ortho-phosphate-phosphorus (mg/L) | Mean | 1.0 | 0.3 | 0.2 | 1.5 | 0.2 | 0.2 |
SD | 0.9 | 0.2 | 0.2 | 0.8 | 0.3 | 0.2 |
Figure 5.
Ortho-phosphate-phosphorous concentrations for gully pot liquor and gully pot liquor and dog faeces (a) and outflow concentrations for the indoor and outdoor bins (b). The plots represent the 25th percentile, median and the 75th percentile. The whiskers represent the 10th and 90th percentiles; solid circles represents outliers and stars represents extreme outliers (n = 110).
Figure 5.
Ortho-phosphate-phosphorous concentrations for gully pot liquor and gully pot liquor and dog faeces (a) and outflow concentrations for the indoor and outdoor bins (b). The plots represent the 25th percentile, median and the 75th percentile. The whiskers represent the 10th and 90th percentiles; solid circles represents outliers and stars represents extreme outliers (n = 110).
Figure 6.
Ammonia-nitrogen concentrations for gully pot liquor and gully pot liquor and dog faeces (a) and outflow concentrations for the indoor and outdoor bins (b). The plots represent the 25th percentile, median and the 75th percentile. The whiskers represent the 10th and 90th percentiles; solid circles represents outliers and stars represents extreme outliers (n = 110).
Figure 6.
Ammonia-nitrogen concentrations for gully pot liquor and gully pot liquor and dog faeces (a) and outflow concentrations for the indoor and outdoor bins (b). The plots represent the 25th percentile, median and the 75th percentile. The whiskers represent the 10th and 90th percentiles; solid circles represents outliers and stars represents extreme outliers (n = 110).
Figure 7.
Nitrate-nitrogen concentrations for gully pot liquor and gully pot liquor and dog faeces (a) and outflow concentrations for the indoor and outdoor bins (b). The plots represent the 25th percentile, median and the 75th percentile. The whiskers represent the 10th and 90th percentiles; solid circles represents outliers and stars represents extreme outliers (n = 110).
Figure 7.
Nitrate-nitrogen concentrations for gully pot liquor and gully pot liquor and dog faeces (a) and outflow concentrations for the indoor and outdoor bins (b). The plots represent the 25th percentile, median and the 75th percentile. The whiskers represent the 10th and 90th percentiles; solid circles represents outliers and stars represents extreme outliers (n = 110).
This study continues analysis previously addressed by Scholz and Grabowiecki [
13] from 2007–2008 with greater details on the microbial and physiochemical water quality treatability. An increase in nitrate-nitrogen was recorded, as ammonia-nitrogen was broken down [
13]. For the indoor and outdoor bins, which received dog faeces, the highest releases of nitrate-nitrogen were recorded. This is likely due to the additional load of nitrogen found by Tota-Maharaj and Scholz [
19]. There was also an increase for the indoor bin 6 and the outdoor bin 6 (no faeces, and no heating or cooling). For both outdoor and indoor rigs, nitrate-nitrogen reductions were not observed, as several removal efficiencies were negative due to the low concentrations and reconversion of the nitrite ion to nitrates.
Carbon dioxide levels were similar for the indoor and outdoor rigs, indicating similar activities of microbes (
Figure 8). However, only two bins for each system were examined, resulting in 16 sampling points in total. The highest concentrations were recorded close to the first two (
i.e., shallowest) sampling points for each bin. This indicated that the most intensive microbial activity took place around the geotextile and the lowest part of the sub-base. Microbiological counts (
Table 3) varied considerably for the outdoor system. The spatial distributions of CO
2 concentrations generated in the rigs were similar to that reported by Scholz and Grabowiecki [
13]. Spatial profiles for PPS with geotextiles from the four horizontal sampling points showed highest concentrations (>2000 ppm) around the geotextile sub-base zone.
Table 3.
Mean colony forming unit (CFU/100 mL) counts (rounded to statistically significant numbers) for the rigs effluent of concentrated stormwater between March 2008 and April 2010 (sample number, n = 110).
Table 3.
Mean colony forming unit (CFU/100 mL) counts (rounded to statistically significant numbers) for the rigs effluent of concentrated stormwater between March 2008 and April 2010 (sample number, n = 110).
Rig Location | Indicator Bacteria | PPS Number | | Influent |
---|
1 | 2 | 3 | 4 | 5 | 6 | −Dog Faeces | + Dog Faeces |
---|
Indoor | Shigella sp. | 3.7 × 102 | 1.5 × 102 | 2.5 × 102 | 2.7 × 102 | 4.7 × 102 | 2.1 × 102 | 1.7 × 104 | 4.2 × 105 |
| Enterococus sp. | 9.0 × 102 | 1.6 × 102 | 1.8 × 102 | 1.9 × 102 | 6.0 × 101 | 1.4 × 102 | 2.1 × 102 | 3.3 × 104 |
| Escherichia coli | 7.8 × 103 | 1.1 × 103 | 2.8 × 103 | 9.6 × 103 | 7.0 × 103 | 2.9 × 103 | 1.1 × 105 | 1.7 × 106 |
| Total heterotrophs | 3.7 × 104 | 4.2 × 104 | 7.8 × 104 | 6.6 × 104 | 6.2 × 104 | 9.6 × 104 | 4.4 × 106 | 1.2 × 108 |
Outdoor | Shigella sp. | 3.5 × 102 | 3.1 × 102 | 2.0 × 102 | 3.7 × 102 | 2.2 × 102 | 2.0 × 102 | 3.2× 103 | 9.7 × 104 |
| Enterococus sp. | 5.0 × 102 | 1.3 × 102 | 5.0 × 102 | 6.0 × 102 | 1.6 × 102 | 2.2 × 102 | 4.1 × 102 | 2.5 × 104 |
| Escherichia coli | 1.5 × 105 | 5.7 × 104 | 2.9 × 104 | 1.2 × 105 | 5.8× 103 | 5.9× 103 | 6.7× 104 | 2.3 × 106 |
| Total heterotrophs | 4.9 × 105 | 1.2 × 105 | 3.6 × 104 | 9.6 × 104 | 1.7× 105 | 4.2× 104 | 7.6 × 106 | 3.4 × 101° |
Figure 8.
Carbon dioxide outflow concentrations for PPS 1 and PPS 5 (indoor and outdoor rig). The plots represent the 25th percentile, median and the 75th percentile. The whiskers represent the 10th and 90th percentiles; solid circles represents outliers (n = 110).
Figure 8.
Carbon dioxide outflow concentrations for PPS 1 and PPS 5 (indoor and outdoor rig). The plots represent the 25th percentile, median and the 75th percentile. The whiskers represent the 10th and 90th percentiles; solid circles represents outliers (n = 110).
3.3. Statistical Analysis
From
Table 4, the environmental parameters for all bins (both indoor and outdoor) followed a normal distribution if α > 0.05. On the contrary if α < 0.05, the distribution did not follow normality and was therefore transformed prior to statistical analysis.
Table 4 summarises the distribution of all water quality data (physical, chemical and microbiological) and how this data was distributed over the period of analysis. If the measured parameters followed a normal distribution curve the statistical parameter α > 0.05. It can be seen for water sample temperatures (°C), pH, and dissolved oxygen (mg/L) all followed a normal distribution whilst all other parameters did not. For the cases whereby water quality parameters did not form a normal distribution, the data was transformed prior to the analysis of variance statistical analysis.
One-way ANOVA which has one independent variable was used to test the entire group of Indoor (PPS 1 to PPS6)
versus the outdoor group (PPS1 to PPS6) (
Table 5) and the effects of carbon dioxide production with PPS 1
versus PPS 5 for both indoor and outdoor, respectively. To test the effects if any, for variations in pavement design for such as (i) treating gully pot liquor and gully pot liquor mixed with dog faeces; (ii) geotextile layer
versus geocomposites; and (iii) presence of GSHP, were all analysed with grouped paired ANOVA for a combined indoor and outdoor rigs respectively (
Table 6). Grouped pairwise ANOVA comparisons at a significant level of
p = 0.05 was applied to test the significant differences between heating and cooling cycles for all water quality parameters effluents within both indoor and outdoor rigs collectively (PPS1, PPS 2, PPS 4 and PPS 5). The statistical tests for pairwise analysis indicate that the water quality variables for each bin (PPS1, PPS2, PPS4, and PPS 5) outflow concentrations differ significantly from each other when
p < 0.05 during the heating and cooling cycles (
Table 7).
Table 4.
One-sample Kolmogorov-Smirnov test for normality. For significance α>0.05 sample follows a normal distribution (in bold).
Table 4.
One-sample Kolmogorov-Smirnov test for normality. For significance α>0.05 sample follows a normal distribution (in bold).
Parameters | Indoor Rig | Outdoor Rig |
---|
PPS 1 | PPS 2 | PPS 3 | PPS 4 | PPS 5 | PPS 6 | PPS 1 | PPS 2 | PPS 3 | PPS 4 | PPS 5 | PPS 6 |
---|
Water sample temperatures (°C) | 0.830 | 0.194 | 0.951 | 0.876 | 0.148 | 0.852 | 0.834 | 0.900 | 0.744 | 0.679 | 0.645 | 0.827 |
Geothermal heating/cooling temperatures (°C) | 0.000 | 0.000 | ¯ | 0.000 | 0.000 | ¯ | 0.000 | 0.000 | ¯ | 0.000 | 0.000 | ¯ |
pH | 0.062 | 0.078 | 0.606 | 0.071 | 0.163 | 0.731 | 0.560 | 0.079 | 0.697 | 0.872 | 0.123 | 0.052 |
Electroconductivity (μS/cm) | 0.000 | 0.000 | 0.003 | 0.002 | 0.001 | 0.000 | 0.000 | 0.083 | 0.000 | 0.000 | 0.002 | 0.182 |
Redox potential (mV) | 0.113 | 0.104 | 0.099 | 0.154 | 0.571 | 0.246 | 0.292 | 0.255 | 0.083 | 0.163 | 0.342 | 0.202 |
NO3-N (mg/L) | 0.000 | 0.000 | 0.000 | 0.000 | 0.000 | 0.000 | 0.000 | 0.002 | 0.000 | 0.000 | 0.001 | 0.000 |
NH4-N (mg/L) | 0.000 | 0.000 | 0.000 | 0.000 | 0.000 | 0.000 | 0.000 | 0.000 | 0.000 | 0.000 | 0.000 | 0.000 |
PO4-P mg/L | 0.027 | 0.000 | 0.000 | 0.047 | 0.000 | 0.000 | 0.067 | 0.000 | 0.000 | 0.046 | 0.000 | 0.001 |
Total dissolved solids (ppm) | 0.042 | 0.041 | 0.068 | 0.006 | 0.014 | 0.424 | 0.043 | 0.048 | 0.330 | 0.351 | 0.079 | 0.093 |
Suspended solids (mg/L) | 0.001 | 0.000 | 0.004 | 0.000 | 0.000 | 0.006 | 0.000 | 0.000 | 0.000 | 0.000 | 0.000 | 0.000 |
Turbidity (NTU) | 0.002 | 0.000 | 0.001 | 0.000 | 0.000 | 0.003 | 0.001 | 0.000 | 0.000 | 0.000 | 0.000 | 0.000 |
E. coli (CFU/100 mL) | 0.176 | 0.014 | 0.001 | 0.002 | 0.028 | 0.000 | 0.230 | 0.019 | 0.010 | 0.020 | 0.000 | 0.000 |
Enterococci sp (CFU/100 mL) | 0.138 | 0.008 | 0.000 | 0.000 | 0.000 | 0.000 | 0.240 | 0.018 | 0.002 | 0.001 | 0.015 | 0.000 |
Total coliforms (CFU/100 mL) | 0.175 | 0.015 | 0.001 | 0.001 | 0.019 | 0.000 | 0.233 | 0.019 | 0.010 | 0.002 | 0.029 | 0.000 |
Salmonella sp (CFU/100 mL) | 0.423 | 0.018 | 0.003 | 0.183 | 0.001 | 0.005 | 0.332 | 0.663 | 0.023 | 0.001 | 0.237 | 0.022 |
Shigella sp (CFU/100 mL) | 0.424 | 0.019 | 0.003 | 0.170 | 0.001 | 0.000 | 0.298 | 0.639 | 0.021 | 0.001 | 0.225 | 0.024 |
THB (CFU/100 mL) | 0.000 | 0.000 | 0.000 | 0.000 | 0.000 | 0.000 | 0.000 | 0.000 | 0.000 | 0.000 | 0.000 | 0.000 |
BOD (mg/L) | 0.000 | 0.000 | 0.000 | 0.000 | 0.000 | 0.000 | 0.000 | 0.000 | 0.001 | 0.000 | 0.001 | 0.000 |
COD (mg/L) | 0.002 | 0.000 | 0.003 | 0.003 | 0.001 | 0.000 | 0.051 | 0.000 | 0.017 | 0.000 | 0.001 | 0.001 |
Dissolved oxygen (mg/L) | 0.176 | 0.281 | 0.091 | 0.081 | 0.095 | 0.113 | 0.989 | 0.799 | 0.120 | 0.202 | 0.456 | 0.530 |
Carbon dioxide CO2 (ppm) | 0.000 | ¯ | ¯ | ¯ | 0.000 | ¯ | 0.000 | ¯ | ¯ | ¯ | 0.000 | ¯ |
ANOVA statistical results for BOD effluent concentrations between the indoor and outdoor rigs showed a strong statistical variation (
p < 0.01) (
Table 5). BOD effluent concentrations showed variations between (PPS 1 and PPS 4) and (PPS 2 and PPS 5) which compares the differences between the presence of geotextiles (PPS 4) and geocomposites (PPS 1). In addition, variations in concentrations of BOD occurred for (PPS 5
vs. PPS 6) (
p < 0.05) and not (PPS 2
vs. PPS 3) (
p > 0.05) which shows inconsistencies for BOD outflow concentrations when the pavements systems are integrated with GSHP. ANOVA analysis between PPS 4 and PPS 5 which treated different types of concentrated stormwater (inflows 1 and 2) saw statistical variations in BOD effluent concentrations (
p < 0.05) but not (PPS 1
vs. PPS 2). However, during the heating and cooling cycles for PPS 1, PPS 2, PPS 4 and PPS 5, there were no statistical differences for BOD outflow concentrations (
p > 0.05).
Table 5.
One way ANOVA between in indoor (PPS 1–PPS 6) and outdoor rig (PPS 1–PPS 6), significant values (p < 0.05) in bold.
Table 5.
One way ANOVA between in indoor (PPS 1–PPS 6) and outdoor rig (PPS 1–PPS 6), significant values (p < 0.05) in bold.
Water Quality Parameters | Indoor Rig & Outdoor Rig |
---|
Sum of Squares | Sum of Squares | Sum of Squares |
---|
pH | 7.45 | 133.98 | 0.000 |
Electroconductivity (μS/cm) | 4.031 × 104 | 2.75 | 0.098 |
Redox potential (mV) | 72.50 | 0.02 | 0.894 |
Nitrate-nitrogen (NO3-N mg/L) | 0.52 | 1.02 | 0.314 |
Ammonia-nitrogen (NH4-N mg/L) | 0.63 | 9.01 | 0.003 |
Ortho-phosphate-phosphorous (PO4-P mg/L) | 9.14 | 18.74 | 0.000 |
Total dissolved solids (ppm) | 1.749 × 104 | 17.35 | 0.000 |
Suspended solids (mg/L) | 1.561 × 103 | 3.26 | 0.072 |
Escherichia coli (Log10 CFU/100 mL) | 7.19 | 40.85 | 0.000 |
Enterococci sp. (Log10 CFU/100 mL) | 5.98 | 32.40 | 0.000 |
Shigella sp. (Log10 CFU/100 mL) | 5.53 | 56.04 | 0.000 |
Total heterotrophic bacteria (Log10 CFU/100 mL) | 12.36 | 1.07 | 0.302 |
Biochemical oxygen demand (BOD mg/L) | 349.39 | 26.88 | 0.000 |
Dissolved oxygen (mg/L) | 0.05 | 0.03 | 0.85 |
One-way ANOVA between indoor and outdoor rigs for the effluent NH
4-N (mg/L) concentrations showed statistical differences (
p < 0.05) (
Table 5). Furthermore, NH
4-N (mg/L) reductions saw significant variations between (PPS 1
vs. PPS 2) (
p < 0.05) with the variable being the type of urban runoff being treated. However, this was not the case for (PPS 4
vs. PPS 5) (
p > 0.05) which had similar layouts and treated inflows 1 and 2 separately (
Table 6). The presence of geotextiles made a significant contribution for the removal of NH
4-N (mg/L) with regards to (PPS 1
vs. PPS 4) and (PPS 2
vs. PPS 5) (
p < 0.05). The statistical analysis between the heating and cooling cycles (PPS 1, 2, 4 and 5) also showed significant differences for effluent NH
4-N (mg/L) concentrations (
p < 0.05) (
Table 7). One-way ANOVA between the indoor and outdoor rigs showed a strong statistical variation for
E. coli outflow concentrations (
p < 0.01), which shows the effects of temperature and environmental conditions on the decline of these bacterial cell colonies (
Table 5). With respect to the design variations in pavement systems, the presence of a geotextile membrane (PPS 1
vs. PPS 4) and (PPS 2
vs. PPS 5) for both indoor and outdoor rigs showed a significant difference of
E. coli effluent concentrations (
p < 0.05). The applications of geothermal heating and cooling (presence of GHP) also saw significant outflow concentrations between (PPS 2
vs. PPS 3) and (PPS 5
vs. PPS 6). In addition, the types of inflow 1 and 2 being treated by the same pavement design (PPS 1
vs. PPS 2) and (PPS 4
vs. PPS 5) showed significant variations for effluent
E. coli concentrations. This is expected as inflow 2 spiked with dog faeces contains a higher concentration of
E. coli bacterial cells than inflow 1 (gully pot liquor).
Table 6.
Paired ANOVA (Indoor and Outdoor rigs) between PPS structure variations and type of urban runoff treated, significant values (p < 0.05) in bold. a (Inflow 1 vs. Inflow 2); b (Geotextile membrane vs. Geocomposite); c (GSHP vs. no GSHP).
Table 6.
Paired ANOVA (Indoor and Outdoor rigs) between PPS structure variations and type of urban runoff treated, significant values (p < 0.05) in bold. a (Inflow 1 vs. Inflow 2); b (Geotextile membrane vs. Geocomposite); c (GSHP vs. no GSHP).
Water Parameters | PPS (Indoor and Outdoor) |
---|
a (1 vs. 2) | a (4 vs. 5) | b (1 vs. 4) | b (2 vs. 5) | c (2 vs. 3) | c (5 vs 6) |
---|
pH | 0.000 | 0.000 | 0.000 | 0.000 | 0.489 | 0.291 |
Electroconductivity (μS/cm) | 0.000 | 0.000 | 0.000 | 0.000 | 0.246 | 0.179 |
Redox potential (mV) | 0.719 | 0.196 | 0.154 | 0.234 | 0.351 | 0.406 |
NO3-N (mg/L) | 0.231 | 0.000 | 0.000 | 0.030 | 0.000 | 0.001 |
NH4-N (mg/L) | 0.017 | 0.112 | 0.042 | 0.026 | 0.428 | 0.881 |
PO4-P (mg/L) | 0.000 | 0.000 | 0.046 | 0.000 | 0.937 | 0.331 |
Total dissolved solids (ppm) | 0.095 | 0.000 | 0.000 | 0.000 | 0.000 | 0.063 |
Suspended solids (mg/L) | 0.245 | 0.086 | 0.048 | 0.000 | 0.579 | 0.016 |
E. coli (Log10 CFU/100 mL) | 0.000 | 0.000 | 0.000 | 0.000 | 0.000 | 0.000 |
Enterococci sp (Log10 CFU/100 mL) | 0.000 | 0.000 | 0.000 | 0.000 | 0.000 | 0.000 |
Shigella sp (Log10 CFU/100 mL) | 0.239 | 0.219 | 0.000 | 0.018 | 0.959 | 0.000 |
THB (Log10 CFU/100 mL) | 0.000 | 0.000 | 0.000 | 0.000 | 0.553 | 0.633 |
BOD (mg/L) | 0.372 | 0.022 | 0.000 | 0.000 | 0.164 | 0.000 |
Dissolved oxygen (mg/L) | 0.000 | 0.000 | 0.000 | 0.000 | 0.000 | 0.000 |
Table 7.
Paired ANOVA between heating and cooling cycles for PPS 1, 2, 4 and 5 (Indoor and Outdoor rigs), significant values (p < 0.05) in bold.
Table 7.
Paired ANOVA between heating and cooling cycles for PPS 1, 2, 4 and 5 (Indoor and Outdoor rigs), significant values (p < 0.05) in bold.
(A) Heating Cylces | (B) Cooling Cycles | Mean Difference (A-B) | Std. Error | Sig. |
---|
pH | 0.15 | 0.02 | 0.000 |
Electroconductivity (μS/cm) | 3.15 | 6.09 | 0.605 |
Redox potential (mV) | 33.63 | 4.31 | 0.000 |
PO4-P (mg/L) | 0.05 | 0.04 | 0.184 |
NH4-N (mg/L) | 0.04 | 0.02 | 0.009 |
NO3-N (mg/L) | 0.05 | 0.08 | 0.485 |
Total dissolved solids (ppm) | 3.79 | 2.14 | 0.077 |
Suspended solids (mg/L) | 6.46 | 1.48 | 0.000 |
Dissolved oxygen (mg/L) | 0.58 | 0.12 | 0.000 |
BOD (mg/L) | 0.15 | 0.23 | 0.512 |
Escherichia coli (Log10 CFU/100 mL) | 2.12 | 1.82 | 0.048 |
Enterococci sp (Log10 CFU/100 mL) | 1.47 | 1.13 | 0.026 |
Shingallae sp (Log10 CFU/100 mL) | 1.45 | 0.83 | 0.000 |
THB (Log10 CFU/100 mL) | 4.59 | 4.69 | 0.425 |
Throughout the heating and cooling cycles, a significant difference occurred (
p < 0.05) for
E. coli concentrations between (PPS 1, 2, 4 and 5) (
Table 7). For CO
2 measurements, ANOVA analysis showed a large significant difference (
p < 0.01) between PPS 1 and PPS 5 for both indoor and outdoor rigs regarding the CO
2 produced, respectively. The occurrence of higher concentrations of CO
2 (ppm) evolved for PPS 5 clearly demonstrates increased microbial activity in and around the geotextile level, when compared to the geocomposite layer in PPS 1. The results show that biodegradation does not only occur at the geotextile layer but evolves at a rapid rate when it is present. PPS 5 when compared to PPS 1 produced a higher percentage of approximately 35% CO
2 indicating an increase in microbial activities around this zone. These findings are corroborated by Newman
et al. [
20]; and Coupe
et al. [
21] who showed that just above and beneath the geotextile layer within the PPS structure the highest volume of CO
2 is produced and O
2 is reduced which indicates a higher respiration rate for protozoa and aerobes in the biodegradation process of pollutants.