Abstract
Purpose
Planting strategies can be effective mechanisms to reduce diffuse pollution from agricultural catchments reaching water bodies. Plants with antimicrobial properties such as mānuka (Leptospermum scoparium) demonstrated in controlled conditions the ability to inhibit nitrification and growth of pathogens in soils. This potential in a real on-farm setting was still to be investigated.
Methods
In a stock-excluded riparian area, planted with mānuka on a dry stock farm, synthetic excrement patches high in urea (950 kg N ha−1 equiv.) and Escherichia coli (7.9 × 109 cfu plant-1) underneath mānuka saplings and pasture were applied. Soil was sampled at three depths over 21 days after the excrement application and analysed for total C and N, inorganic N, pH, soil moisture and E. coli.
Results
There was no significant difference between the pasture and mānuka for total C and N, C:N ratio, and soil moisture. E. coli was only different between both at 20–30 cm deep. NO3− - N and NH4+ - N concentrations were significantly lower under mānuka compared to pasture for the upper two soil depths (NO3− - N: 109 mg kg−1 vs 205 mg kg−1 in the topsoil).
Conclusions
The results of this study indicate that mānuka may inhibit urease activity and nitrification and could reduce on-farm nitrate leaching, while also highlighting that field conditions make quantifying such phenomenon more complex.
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Introduction
As one of New Zealand’s largest export markets, pastoral agriculture is a vital part of the national economy and accounts for 40% of total land cover (Ministry for the Environment and StatsNZ 2018). However, agricultural intensification to meet export demands has come largely at the expense of well-functioning ecosystems and has resulted in declining freshwater quality across the country (Dymond et al. 2013; Julian et al. 2017; MacLeod and Moller 2006). Increased stocking rates and associated animal excreta as well as and nitrogenous fertilisers are leading causes of declining freshwater quality (Julian et al. 2017; Parfitt et al. 2006). Faecal contamination from overstocking, direct stock access to waterways, and farm effluent pose a health risk and limits New Zealanders’ capacity to enjoy water-based recreational activities (Collins et al. 2007; Houlbrooke et al. 2004).
The New Zealand setting is just one example of a worldwide crisis regarding the impact of agriculture intensification on water quality. Globally, over 87% of the N agricultural inputs are not used by plants or livestock, and forms the so-called N surplus (Galloway et al. 2003). Depending on the agricultural system, over 80% of the soil N surplus can be lost via leaching (Billen et al. 2013), which will consequently affect waterbodies. According to Billen et al. (2013), the 84% of the anthropogenic N is accumulated in basins that occupy only 43% of the global continental area. These “hot-spot” basins are located in Europe, North America, India, China, New Zealand, and small coastal basins in South America (Billen et al. 2013). According to Bain et al. (2014), 1.8 billion people globally are exposed to faecal contaminated drinking water, and most of faecal contaminated drinking water occurs in rural areas. In US, about 480,000 km of rivers and shorelines and 2 million ha of lakes are impaired by pathogenic contamination (Pandey et al. 2014).
Planting of riparian areas and creation of shelterbelts are effective mechanisms to minimise negative environmental impacts in agricultural regions (Billen et al. 2013). Riparian planting strategies have been shown to reduce nutrient runoff, microbial contamination, and erosion and sedimentation in small streams (McKergow et al. 2016). Shelterbelts have been shown to limit nitrate movement (Ryszkowski and Kędziora 2007) and reduce Escherichia coli run-off (McDowell et al. 2006). If riparian plantings or shelterbelts comprise native vegetation, there is also the potential to increase biodiversity in areas that are usually depauperate of it, and there is increasing demand and necessity for enhancing native biodiversity on farms (Lee et al. 2008).
Utilisation of mānuka (Leptospermum scoparium) in planting strategies is being investigated to further reduce negative environmental impacts. Mānuka is an indigenous pioneer shrub with ubiquitous presence across New Zealand (Stephens et al. 2005). It is well-known to thrive in extreme environmental conditions, such as low fertility soil, and acts as a colonising species in successional forest development (Stephens et al. 2005). Antimicrobial properties in mānuka honey, oils, and leaves has made the plant culturally significant to Māori for its use in rongoā (traditional Māori medicine) (Williams 1996) and also within modern medical practice with mānuka honey products incorporated into wound treatment and personal care products (Stephens et al. 2005).
The antimicrobial properties observed in essential oil products are postulated to have similar effects on pathogen survival within the root networks. Prosser et al. (2014) concluded that mānuka leaf, oil, and root extracts all either significantly reduced or inhibited growth of five bacterial species (both gram-positive and gram-negative), whereas ryegrass supported bacterial growth in all but one species. Similarly, Prosser et al. (2016) found in a subsequent study that potted mānuka significantly reduced E. coli counts, with a 90% reduction in eight days (compared to 93 days for ryegrass). Mishra (2018) also found mānuka root extracts showed inhibition of E. coli growth; however, the root system encouraged preferential flow and leaching down the soil profile at high irrigation schemes (14 mm d−1).
Comparable properties were observed with the effects of mānuka on nitrogen cycling and could be useful in biological nitrification inhibition (BNI), whereby traits of a natural ecosystem can control the nitrification process (Subbarao et al. 2006). Downward (2013) demonstrated that mānuka extracts inhibited nitrifying bacteria activity of Nitrosospira sp. cultures while pasture extracts did not. Likewise, a lysimeter study by Esperschuetz et al. (2017) found that following successive urea applications, mānuka significantly reduced nitrate leaching (2 kg ha−1) compared to pine (53 kg ha−1). Higher concentrations of ammonium under mānuka suggested inhibition of nitrification enzymes as the leading cause (Esperschuetz et al. 2017). In addition, reduced cumulative nitrous oxide emissions under mānuka compared to pine suggested inhibition of denitrification enzymes (Esperschuetz et al. 2017).
Use of mānuka in on-farm planting strategies has the potential to mitigate bacterial inputs from stock and reduced nitrate loading through BNI. However, to date these effects have been limited to laboratory-based studies, with a paucity of information on how the natural environment influences the response of mānuka to agricultural waste rich in nitrogen and bacteria pollution. In this work, we sought to address how these interactions occur in the natural riparian environment by testing the following hypotheses: (a) there is a difference in nitrogen speciation between mānuka and pasture, where there is less nitrate and more ammonium accumulation in soil under mānuka than under pasture, and (b) there is a faster reduction in E. coli counts with mānuka compared to pasture, and the reduction is impacted by preferential flow.
Materials and methods
Study site
The experiment was conducted in a newly planted mānuka riparian zone, situated on the western side of Lake Wairarapa, New Zealand (−41.183182°, 175.254344°) (Fig. 1). The riparian zone is a fenced-off band of variable width (20 m - 60 m), which borders a sheep and beef farm that uses sulphur, phosphate, and nitrogen fertilisers. The area is relatively flat and slopes gently to the edge of the lake. Soils underlying the study site are Orthic Brown (LandcareResearch 2018). An area of approximately 2500 m2 was planted with c.a. 4300 mānuka at 1-m spacing. Within the fenced-off zone, and at both sides of the mānuka planted area, there are unplanted areas (1800 m2 and 1010 m2) with plant cover consisting mostly of Lolium perenne (pasture).
Field experiment
To test the hypotheses, a field experiment was completed between October and November 2018, exposing mānuka and pasture to a worst-case scenario of a “synthetic” excrement patch with high concentration of urea and E. coli. At the time of the experiment, mānuka saplings had grown for 14 months and were around 1 m tall.
Within the mānuka planted area, fifteen saplings of similar size were randomly selected for the experiment. A circle of 15-cm radius (approximately 707 cm2) was marked out around each sapling for applying the “synthetic” excrement patch (Fig. 2a and c). Similarly, 15 random circles of the same size (707 cm2) were selected within the unplanted area to investigate the effect of pasture (Fig. 2b and d). The mānuka and pasture circles were placed in the central area of their respective zones to avoid potential influence from the other areas, and from the farm paddock.
Synthetic urea (CH4N2O) was applied at a rate to imitate cow urination to test the effects on nitrogen cycling. Average urine concentrations are typically 0.95 g N 100 mL−1, and the average urination event can range between 20 and 120 g N m−2 (Selbie et al. 2015). Therefore, 14.15 g of urea was added to 700 mL of distilled water, equating to 95 g N m−2. The 700 mL of diluted urea solutions were applied to each of the 30 marked areas (15 for each treatment).
Similarly, E. coli was applied at a rate to emulate a worst-case scenario of excrement with high numbers of E. coli. The E. coli strain used in this experiment was isolated from dairy shed effluent to represent a strain likely to be found in farm settings. Here, 100 μL of dairy shed effluent were plated into E. coli selective agar (Brilliance™) and grown overnight at 34 °C. Ten E. coli colonies were taken from the plate and grown together in 30 mL Luria broth at 34 °C for 24 h. The broth was then centrifuged at 2000 rpm for 1 h. The resulting pellet was washed twice with Ringer’s solution to form a seed stock and stored at 4 °C until it was used in the experiment within two weeks. The E. coli in the seed stock was enumerated by plating serial dilutions and the colony forming units (cfu) were used to calculate the numbers to be applied to the experiment. Given the median E. coli numbers in cow pats (6 × 106 cfu g−1) (Moriarty et al. 2008), and an average excrement weight for bovine cattle of 2 kg (Kormanovskii et al. 2017; Scheile et al. 2018), E. coli was added to the experiment at a rate of 7.2 × 109 cfu per ring in each of the 30 rings. E. coli from the seed stock was resuspended in Ringer’s solution and diluted to the required numbers to be applied to the field experiment. The E. coli cfu in the final solution were enumerated by plating serial dilutions to confirm that the added E. coli was the same than the calculated one.
Prior to application of urea and E. coli solutions, excessive grass growth around mānuka trees was cut back and the pasture in the unplanted area trimmed to 2 cm to allow solutions to reach root networks. The solutions were applied slowly over a period of three hours to allow percolation and avoid runoff out of the marked areas.
A baseline sampling was performed one month before the experiment started. After the “excrement” application, soil was sampled after 1 day, 3 days, 7 days, 14 days, and 21 days. At each of these time points, three mānuka and three pasture areas (out of the 15 treated with the “excrement”) were randomly selected and sampled. Soil samples were collected from both treatments at 0–10 cm, 10–20 cm, and 20–30 cm using a soil probe. Soil samples were transported on ice to the laboratory, kept at 4 °C overnight and processed the following day. This length of the experiment (21 days) was selected to be comparable with previous research by Esperschuetz et al. (2017), who found a quick response in ammonia oxidation and NO2 fluxes in soil in the first 18 days after urea application in their lysimeters, with a slower change until day 21. Similarly, Prosser et al. (2016) reported a significant reduction of E. coli under mānuka in a 7-day experiment, and Gutierrez-Gines et al. (2021) in a 21-day experiment.
Chemical and biological analysis
Fresh soil samples were sieved (2 mm) and analysed for soil moisture, inorganic nitrogen, and E. coli. NH4+-N and NO3−-N were extracted with 2 M KCl (Blakemore et al. 1987) and analysed by Flow Injection Analyser (Quikchem 8500). E. coli was enumerated using a 5-tube MPN procedure as described by Horswell et al. (2007). Enumeration was completed by comparing the results with a MPN table and calculated per gram of dry soil (Prosser et al. 2016). Soil moisture was determined after drying the samples at 104 °C for 48 h.
Samples were then dried at 60 °C for two weeks and homogenised again through a 2-mm sieve. Total organic carbon (TOC) and total nitrogen (TN) were analysed by a LECO TruMac Elementar analyser. pH was analysed in 1:2.5 soil:water ratio (Blakemore et al. 1987) with a Eutech pH 700 pH meter.
Data analysis
The results of the experiment, disregarding the baseline ones, were analysed for each soil depth independently. pH, NH4+-N and NO3−-N results were analysed with an analysis of covariance with Treatment (mānuka, pasture) and Day as independent variables. The assumptions of normality, homoscedasticity and linearity were assessed by plotting the residuals of the model. TOC, TN, soil moisture and C:N ratio did not fulfil the linearity assumptions and were analysed for differences between pasture and mānuka by t-tests for each day, and E. coli enumeration, by non-parametric Kruskal-Wallis. Similar to Prosser et al. (2016), linear regression between Log10(MPN) and Day were calculated to estimate decimal E. coli reductions in the soil. A correlation matrix between the variables was calculated using the non-parametric Kendall correlation. The analyses were performed with the stats package of the programme R (R Core Team 2018).
Results
Rainfall, weather conditions, and soil moisture
During the experiment, temperature varied from 9 °C to 24 °C (GWRC 2021). As shown in Fig. 3, conditions were relatively dry before baseline sampling (day 0) and soil moisture on Day 0 was not different between the two treatments (Fig. 4). A notable rain event was received during the days of the synthetic excrement application (day A) and the first sampling day (day 1). The next rain event happened after the seventh day of sampling and again at the end of the experiments. These rainfall conditions were reflected in the soil moisture during the experiment (Fig. 4), with an increase between baseline sampling and the first day of sampling after the excrement application, then a decline back to around baseline levels before a slight increase toward Day 21 (Fig. 4). Differences in soil moisture between treatments were only significant on the topsoil (0–10 cm) on days 3 and 7, with drier soil under mānuka (Fig. 4).
E. coli
The application of the synthetic excrement increased the numbers of E. coli in the topsoil (0–10 cm) after the first day from none to an average of 1.5 × 103 MPN g−1 and 2.3 × 103 MPN g−1 of dry soil under mānuka and pasture, respectively. In both treatments, E. coli slowly decreased over the remainder of the experiment without showing a difference between treatments (Fig. 4). Linear regressions of Log10(MPN) and Day calculated a 90% reduction (1 Log10 reduction) in E. coli in the topsoil on days 9 and 8.5 under mānuka and pasture, respectively. Only one day after the synthetic excrement application, E. coli was already detected in deeper soil below 10 cm and also below 20 cm (Fig. 4) in both treatments. There were only significant differences between mānuka and pasture in the 10–20 cm soil depth on day 14 and more consistent differences between treatments in the deeper soil at 20–30 cm, with higher E. coli numbers under mānuka than under pasture (Fig. 4). There was no relationship between E. coli numbers and any other soil variable (Kendall correlation <0.4).
Nitrogen and carbon
Total organic carbon and total nitrogen significantly increased in the soil after the application of the synthetic excrement (Fig. 5) and showed very little variation along the experiment in the three soil depths. There was no significant difference between mānuka and pasture. The C:N ratio decreased after the synthetic excrement application and did not significantly change along the experiment or between treatments (Fig. 5). Although total nitrogen was not different between mānuka and pasture, there were significant differences between them regarding the evolution of inorganic nitrogen over the experiment. Background concentration of NH4+ -N in the topsoil was 13 mg kg−1 and was not different between mānuka and pasture. Following a large increase of NH4+-N after synthetic excrement application (up to an average of 470 mg kg−1 in the topsoil), NH4+ -N concentration declined over the course of the experiment at 0–10 cm and 10–20 cm, with a significant influence by treatment in these two soil depths (Fig. 4 and Table 1). NH4+ -N at 20–30 cm was constant during the experiment and without difference between treatments. Background NO3− -N concentration in the topsoil was low (4.8 mg kg−1) and similar in the two treatments. NO3−-N significantly increased in the topsoil and at 10–20 cm throughout the experiment with a significantly higher rate in pasture than in mānuka (Fig. 4 and Table 1). At the end of the experiment NO3− -N concentrations in the topsoil were 109 mg kg−1 and 205 mg kg−1 under mānuka and pasture, respectively.
Soil pH
Background soil pH was different in the soil depths and slightly different between mānuka and pasture (p = 0.06). After the application of the synthetic excrement, pH increased in the topsoil and decreased along the experiment with significant influence by treatment (Fig. 5 and Table 1). At 10–20 cm, the effect of treatment was marginal, and at 20–30 cm, there was no significant effect.
Discussion
E. coli
In contrast to the results of Prosser et al. (2016) and Gutierrez-Gines et al. (2021), who found a 90% reduction in E. coli counts in 8 and 14 days under mānuka and 93 and 45 days under pasture, respectively, our experiment indicated there were no significant differences between the two plant covers in E. coli reduction in both, the topsoil and 10–20 cm. E. coli survival and mortality rates in the soil can be influenced by a multitude of factors including physical and chemical soil properties (e.g. water availability, pH), atmospheric conditions (e.g. temperature), and interactions between other organisms within soils (e.g. indigenous microflora) (van Elsas et al. 2011). Avery et al. (2004) showed a rapid decrease of E. coli in soil after organic waste application (over 1 Log10 decrease after one day, and about 2 Log10 after two days). Our results, however, are more similar to studies showing stable numbers for the first few days (Mubiru et al. 2000; Nicholson et al. 2005; Ogden et al. 2001), followed by a decrease which became slower with time, resulting in E. coli survival in the soil for 1–2 months depending on the climate and soil conditions (Avery et al. 2004; Horswell et al. 2007; Nicholson et al. 2005). The addition of organic carbon and nitrogen in the form of urea at the same time than the addition of E. coli, might have promoted the survival, or even re-growth, of this bacterium in the soil. In fact, Jamieson et al. (2002) and Horswell et al. (2010) showed that organic matter and nutrients are key factors for the survival of enteric bacterial in the soil. These factors demonstrate to be more important than root systems for the survival of E. coli in field conditions.
While E. coli reductions exist in all horizons, a rapid reduction in the 0–10 cm horizon and more gradual reductions in the 10–20 and 20–30 cm horizons, as well as the presence of E. coli in the 20–30 cm soil depth one day after the “excrement” application, could suggest E. coli movement down the soil profile was enhanced by rainfall during the first two days of the experiment. Gagliardi and Karns (2000) detected E. coli in leachates from lysimeters treated with E. coli-inoculated manure at the same levels as the inoculum for 8 h after steady rainfall (16.5 mm h−1). Moreover, higher E. coli counts in the mānuka treatment in the 20–30 cm horizon compared with pasture suggests preferential flow enhanced by pivoting mānuka roots, compared with the dense root system of pasture in the topsoil, as demonstrated also by Mishra (2018). Monitoring over a longer period would have given insights of the survival of E. coli under these conditions of soil moisture and nutrients, and in the different soil depths, above all if nutrients decreased over time. This is a limitation of the study, which will have to be addressed in further research.
Nitrogen
Significantly lower concentrations of NO3− -N in soil under mānuka compared to pasture supports the hypothesis that mānuka roots can inhibit nitrification of NH4+ to NO3− in soil. This corroborates the findings of Esperschuetz et al. (2017) who suggested that antimicrobial properties of mānuka roots may reduce the nitrifier bacteria populations in the soil, thus inhibit nitrification and the conversion from NH4+ to NO3−.
However, lower NO3− -N concentrations could also be attributed to the lower initial concentrations of NH4+ -N seen in the mānuka treatment, which indicates that there was less NH4+ available to transform into NO3−. The elevated NH4+ -N concentrations in the pasture compared with mānuka was an unanticipated result, as Esperschuetz et al. (2017) attributed the higher concentration of NH4+ under mānuka - in comparison to pine - to soil accumulation due to the lower nitrification rate in mānuka root systems.
Studies looking at the application of synthetic urinary nitrogen (15 N) by Clough et al. (1998) and Frase et al. (1994) found that plant uptake over one year was responsible for 43% and 21.6–31.4% of nitrogen reductions, respectively. Similarly, total nitrogen uptake to plant biomass was significantly greater under mānuka than pine (Esperschuetz et al. 2017), although no significant differences in total nitrogen in the soil were observed in that study. In our study, N plant uptake could only partially explain the large difference between NH4+ in mānuka and pasture on day 1 to 7. Assuming that the whole difference in NH4+ -N between mānuka and pasture (150 mg kg−1 on day 1 and 300 mg kg−1 on day 3) was due to plant uptake as well as luxury uptake of N by mānuka (Franklin et al. 2015), this species should have produced over 450 g more fresh weight than pasture in four days, which is unrealistic.
One unknown of the experiment is how ammonium volatilisation contributed to the differences in ammonium observed between the two treatments. Decau et al. (2003) concluded that around 12–25% of urinary nitrogen can be lost through ammonium volatilisation. Elevated soil moisture conditions observed in our study, as well as similar moisture under mānuka and pasture, suggests, however, that this is unlikely. Clough et al. (2003) suggested that urease enzymes rapidly hydrolyse urea to ammonium in moist soil conditions. Similarly, 10 mm of rainfall following application of synthetic urinary nitrogen was found to minimise excessive loss via volatilisation (Clough et al. 1998).
In addition to BNI, another potential contributor to nitrogen cycling in this experiment could be the inhibition of urease activity via the mānuka root networks. The use of synthetic urease inhibitors has been shown to reduce nitrogen losses through ammonium volatilisation and leachate following urea application (Gioacchini et al. 2002).
We cannot discard the possibility of losing N via preferential flow created by mānuka root systems, as it was discussed previously for E. coli. However, in contrast to E. coli results, there was no difference in inorganic nitrogen in the 20–30 cm depth between the two plants. It could be expected that if the differences in inorganic nitrogen between mānuka and pasture were due to N losses by plant uptake, ammonia volatilisation or leaching via preferential flow, there would be a different nitrogen concentration in the soil. However, total nitrogen and C:N ratio were not significantly different between the two plant types, which could imply that differences were mostly due to speciation (rather than losses), or that the differences in inorganic nitrogen were too small compared with the total nitrogen concentration, which would make the comparison difficult.
Wider implications and future directions
This study indicates that mānuka has a limited impact on reducing common agricultural pollutants (with a greater impact on nitrogen than E. coli) when compared to pasture from grazing riparian areas. Challenges were expected in attempting this study in a ‘real-world’ setting. However, the results – particularly for inorganic nitrogen – are promising. The elevated values of nitrate and ammonium under pasture are interesting and suggest a higher potential for nitrate leaching. However, further longitudinal studies with older mānuka stands, over different seasons, and including the quantification of nitrogen losses such as ammonia volatilisation and nitrogen leaching, are required to assess the validity of the results presented here, contributing to our understanding of the role mānuka plays in pollutant mitigation.
Agricultural catchments are considered responsible for the sharp rise of nitrate in surface water and groundwater systems, mainly from urine in grazed paddocks (Di and Cameron 2002). However, many of the proposed solutions to minimising losses involve lost production costs or are time intensive (de Klein 2001; Di and Cameron 2002). While planting mānuka would not be without costs (e.g. initial planting and maintenance during establishment), it is much less time intensive and would not involve major changes to on-farm practices. Depending on climate and land conditions, there is potential economic incentive through mānuka honey and oil production. The mānuka honey industry in particular is increasingly economically important, with a 35% increase in total honey exports from 2015 to 2016, fetching around 12–148 NZD kg−1 (MPI 2017). Similarly, mānuka essential oil production could benefit from the high fertility farm soils, with potential gross values of US$ 26,000 ha−1 (Seyedalikhani et al. 2019). These alternative mānuka uses would not only mitigate the effect of farming activities on water quality but diversify the farm incomes.
Although the use of plants with antimicrobial properties to reduce the migration of N and pathogens from farming areas into water bodies is still an incipient research line (Gutierrez-Gines et al. 2021), there is a wide opportunity worldwide given the large range of plant species with antibacterial activity being investigated (Chassagne et al. 2021). According to those authors, Lamiaceae, Fabaceae and Asteraceae are the families with the greatest number of species with known antimicrobial properties. These families present a wide distribution around the world, and most of them could potentially be a source of income for farmers with similar uses than those described for mānuka (i.e. Nieto 2017).
Data availability
The datasets generated during and/or analysed during the current study are available from the corresponding author on reasonable request.
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Acknowledgements
Planting of mānuka trees and site maintenance was supported by Greater Wellington Regional Council and local Māori indigenous community Ngāti Kahungunu ki Wairarapa. Thank you to Paul Smith, landowner of the Hinaburn Station, for access to his property to run this experiment. Statistical advice was provided by David Wood from the Institute of Environmental Science and Research. Dr. Brett Robinson and Dr. Kristin Bohm peer-reviewed this manuscript prior to submission.
Funding
This project was funded by the Centre for Integrated Biowaste Research, under The Institute of Environmental Science and Research Strategic Science Investment Fund from the Ministry of Business, Innovation and Employment, New Zealand (C03X1701). Further financial support was provided by Victoria University of Wellington.
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Halford, S., Gutiérrez-Ginés, M.J., Rees, A. et al. Effect of mānuka (Leptospermum scoparium) on nitrogen and Escherichia coli reductions in soils: a field experiment. Plant Soil 465, 491–502 (2021). https://doi.org/10.1007/s11104-021-05035-3
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DOI: https://doi.org/10.1007/s11104-021-05035-3