A small-volume multiplexed pumping system for automated, high-frequency water chemistry measurements in volume-limited applications

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Abstract

An automated multiplexed pumping system (MPS) for high-frequency water chemistry measurements at multiple locations previously showed the ability to increase spatial and temporal data resolution and improve understanding of biogeochemical processes in aquatic environments and at the land-water interface. The design of the previous system precludes its use in volume-limited applications in which highly frequent measurements requiring a large sample volume would significantly affect observed processes. A small-volume MPS was designed to minimize the sample volume while still providing high-frequency data. The system was tested for cross-contamination between multiple sources, and two applications of the technology are reported. Cross-contamination from multiple sources was shown to be negligible when using recommended procedures. Short-circuiting of flow in a bioreactor was directly observed using high-frequency porewater sampling in a well network, and the small-volume MPS showed high seasonal and spatial variability of nitrate removal in stream sediments, enhancing data collected from in situ mesocosms. The results show it is possible to obtain high-frequency data in volume-limited applications. The technology is most promising at the reach or transect scale for observing porewater solute dynamics over daily timescales, with data intervals < 1 h for up to 12 locations.

Figures

  • Figure 1 – Graphical depiction of small volume multiplexed pumping system (MPS) configurations which include 1) DI water source, 2) 12 port intake valve, 3 & 4) waste or air purge, 5) fractional volume collector (FVC), 6) bidirectional peristaltic pump, and 7) spectrophotometer with cuvette housing. An Arduino microcontroller actuates a series of 3 way valves to move between separate configurations described in Sec. 2.2.1 – 2.2.5. 5
  • Figure 2 - Changes in NO3- concentrations in low ([NO3]low) and high ([NO3]high) concentration sources (0.5 L) resulting from residual volumes purged to the alternate source. Greater concentration or dilution effects were seen with increasing differences in initial NO3- concentrations of the sources during Trials (a) – (d).
  • Figure 3 – Nitrate concentration at inlet wells before and during the KNO3 injection. Color indicates bioreactor inlet and depth of sampling wells, shape indicates the position of the well transect (centerline or near side wall).
  • Figure 4 – Nitrate concentration at outlet wells before and during the KNO3 injection. Color indicates bioreactor outlet and depth of sampling wells, shape indicates the position of the well transect (centerline or near side wall).
  • Table 1 - Results of testing cross contamination of cuvette. Treatment indicates the volume of sample pumped from the current source for cuvette rinsing relative to cuvette volume (Vcuvette), and whether or not a prior DI rinse was used. *** indicates that the 5 protocol used resulted in no significant difference between the initial NO3- concentration and subsequent measurements (α=0.05).
  • Table 2: Initial NO3- concentrations, calculated effective residual volumes (Vres) and 95% confidence interval (C.I.) from source contamination Trials (a) – (d).
  • Table 3 – Zero order NO3- removal rates, k, at eight well locations during five experimental trials. Zero order kinetics model was fitted to time series of NO3- concentrations after flow was stopped to the lab bioreactor.
  • Table 4 – Time series of NO3- concentrations in Sediment mesocosms were fitted to zero and first order kinetics models. Results indicate that for this short duration experiment (<24 hr) and at the observed range of NO3- concentrations (2-6 mg NO3-N L-1), removal was described equally well by either model, although first order kinetics better fitted NO3- time series during trials with large changes in NO3- concentration. 5

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APA

Maxwell, B. M., Birgand, F., Smith, B., & Aveni-Deforge, K. (2018). A small-volume multiplexed pumping system for automated, high-frequency water chemistry measurements in volume-limited applications. Hydrology and Earth System Sciences, 22(11), 5615–5628. https://doi.org/10.5194/hess-22-5615-2018

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