Characteristics of bacterial community and ARGs profile in engineered goldfish tanks with stresses of sulfanilamide and copper.

Abuse of antibiotics in aquaculture have been alarming and might aggravate spread of resistance genes in the environment. Holistic ARGs proliferation checks require deeper analyses of coupled absolute abundances in 16S rRNA bacteria communities at the phylum level to detect biomarkers. Sulfanilamide (sul) and copper II sulfate (CuSO4 II) were, therefore, designed and added as separate or combined treatments in 9 replicate engineered goldfish tanks comprising 3 individual sul, 3 CuSO4 II, 3 (sul + CuSO4 II) combinations, and 3 controls within 180 days. The DNA from water and fish guts was sequenced under qPCR to determine 16S rRNA bacteria biomarkers co-occurring with the correspondent ARGs. Combined chemical addition at 0.8-1.5 mg sul + 0.5-1.0 mg CuSO4 II/3 L of tank waters reduced sequenced 16S rRNA bacteria absolute abundances in fish gut and water samples while portraying the biomarkers. Absolute abundances of the entire 16S rRNA bacteria was higher in fish guts (3.4 × 1014-4.9 × 108 copies/g) than water samples (1.5 × 109-2.6 × 1015 copies/L), respectively. Much as sul 1(log) were dominant over intl 1(log) genes, and their fundamental profiles were also higher in the fish guts than water samples; the Spearman's correlation analyses revealed positive relationship (p < 0.01 and r = 0.873) among the biomarkers of both ARG pairs at the phylum level and the physicochemical parameters. In the fish gut and water samples ratios, Bacteroidetes (10-85:12-85%) > Proteobacteria (10-50:15-65%) > Planktomycetes (10-52:8-25%) featured prominently based on LEfSe use as the hot-spotted biomarkers, hence justifying its higher prospects towards innovative environmental microbiological and biotechnological studies.

Effect of sheep manure-derived biochar on colloidal phosphorus release in soils from various land uses.

Colloidal phosphorus (CP) as an additional route of P mobilization in soil solution has gained much attention. A batch experiment was conducted to investigate the effect of sheep manure-derived biochar (SMB) on CP release from various land uses (paddy, vegetable, tea, and citrus) at a rate of 0% as a control treatment (CK), 1% as a low (L) level, 2% as a middle (M) level, and 4% as a high (H) level of SMB application. The CP and MRPcoll in the solution increased from 30.58 to 88.97% and from 2.45 to 55.54% of total P (TP), respectively. The SMB enhanced CP release in all the soils and all the treatments (except CK and L levels in tea soil; CK, L, and M levels in vegetable soil; and L and M levels in citrus soil). Multiple linear regression revealed a significant correlation between CP and MRPcoll and between colloidal iron, aluminum, calcium, and total organic carbon (Fecoll, Alcoll, Cacoll, and TOCcoll) and pH, which may play an important role as CP carriers that could depend on the pH. This study suggests that the application of SMB in the soil at an appropriate rate of 1 and 2% for tea and vegetable soils, respectively, could be beneficial to avoid the risk of CP release in water bodies.

Synergistic effects of anionic polyacrylamide and gypsum to control phosphorus losses from biogas slurry applied soils.

Excessive application of phosphorus (P) fertilizer to the agriculture soil can lead to the P loss to the aquatic ecosystem. Three soils from different land use (tea, paddy, and vegetable soils) were treated with biogas slurry (BS) at rate of 79.8 kg ha-1, anionic polyacrylamide (PAM) at rate of 12.5, 25 and 50 kg ha-1, Gypsum (Gy) at rate of 5t ha-1, and the control (Ck) without treatment, to control P losses in a laboratory batch experiment. The soil solution was analyzed for total P (TP), dissolved reactive P (DRP) and total dissolved P (TDP). Particulate P (PP) and dissolved unreactive P (DURP) were calculated by subtracting DRP from TP and TDP, respectively. The DRP was within a range of 68-98% of TP whereas PP varied in a range of 2-32% of TP and DURP was within a range of 0.1-19% of TP, depending on soil types and different treatments. The addition of PAM at a high rate and Gy together on the soil after BS application reduced the release of TP by 54, 46, and 51% and that of DRP by 61, 49, and 53% for tea, paddy and vegetable soils, respectively. However, the application of BS with PAM alone promoted the release of DRP by 77, 86, 70% for tea, paddy, and vegetable soils, respectively. This study suggests that the synergic application of PAM and Gy on soils after BS addition can be a good strategy to reduce P losses.

Nutrient retention by different substrates from an improved low impact development system.

The reuse of water in agriculture has become more common in water management worldwide. However, there is very limited information about nutrient retention in water reclamation management. In this study, an improved low impact development (LID) practice was constructed to investigate the synergistic effects of three substrates amendment on nitrogen (N) and phosphorus (P) retention under two irrigation modules: spray and drip irrigation. The orthogonal combination of the three substrates was controlled during four leaching events, with polyacrylamide (PAM), peat soil, and straw biochar application rates of 1, 2, and 4 g kg-1; 5, 10, and 20 g kg-1; and 10, 20, and 40 g kg-1, respectively. Results showed that the optimum treatments for N and P were 2 g kg-1 of PAM; 2 g kg-1 of PAM, 10 g kg-1 of peat soil, and 40 g kg-1 of straw biochar, respectively. The highest amounts of N and P retention under spray and drip irrigation were 83.12 mg N kg-1 and 50.09 mg N·kg-1, and 11.88 mg P·kg-1 and 7.47 mg P·kg-1, respectively. The analysis of variance indicated that PAM, biochar, and peat soil affected the retention of leachate, N, and P differently. PAM application could not only improve the water, N, P retention capacity of soil, but also significantly increase the content of ＞2 mm water-stable soil aggregate (WSA) (p＜0.05), and there is an advisable linear relation between N, P retention and the content of ＞2 mm WSA (R2 = 0.79, 0.67, respectively). Overall, this study concludes that a combined application of PAM and biochar could reduce P loss and increase the ＞2 mm WSA under leaching condition.

Phosphorus speciation and release kinetics of swine manure biochar under various pyrolysis temperatures.

Converting swine manure to biochar is an effective way to recycle valuable nutrients, but there are few reports on its feasibility as a phosphorus (P) source. The objective of this study was to clarify the unique nature, including P speciation, of manure biochar products under various pyrolysis temperatures. We used solution 31P nuclear magnetic resonance and P K-edge X-ray adsorption near-edge spectroscopy (P XANES) to characterize P species in swine manure biochar. For every 100 °C increment starting from 300 °C, the P content in manure biochar increased by 2.16 to 3.37 g kg-1. However, above 400 °C, organic P species did not appear anymore, and only inorganic P, including orthophosphate and pyrophosphate, existed. P K-edge XANES spectra further showed all biochar samples had higher percentages of Ca3 (PO4)2 and NaP2O7, and lower percentages of FePO4, AlPO4, and inositol hexaphosphate compared to manure. Interestingly, percentages of Ca3(PO4)2, FePO4, and AlPO4 in MB400 (indicating manure pyrolysed at 400 °C) were comparable with those in MB700 while the percentage of NaP2O7 was higher in MB400. Phosphorus release from MB400 maintained a relatively high level at 0.33 g kg-1 during the whole 300-h observation period. These results suggest that with a suitable pyrolysis temperature, it was feasible for manure biochar to be a P source alternative. Graphical abstract ᅟ.

A review of the identification and detection of heavy metal ions in the environment by voltammetry.

Currently, environmental pollution by heavy metals is a global problem. Therefore, it is crucial to develop effective detection techniques to determine the levels of heavy metal contamination in various mediums. Voltammetry is a highly sensitive electrochemical method used for the in situ detection of heavy metal ions. This study investigates the current trends related to electrode modification, developments in materials, and optimization of the experimental parameters. We discuss the sensing performance of four kinds of nanomaterials capable of inorganic modification (metal nanoparticles, metal oxides, carbonaceous nanomaterials, and their nanocomposites). The impact of several important factors, such as the deposition potential and time, buffer solution types, and pH on the sensitivity, reproducibility, stability, and anti-interference ability of the detection process, especially with regard to the co-detection of several heavy metal ions, was reviewed. We noted that in addition to the application of voltammetry to water-related issues, it is suitable for rapid and simple identification and analyses of heavy metals in polluted soil and other mediums. Thus, it is important to conduct additional research on the application of voltammetry to this area.