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Fate of tebuthiuron and hexazinone in green-cane harvesting system Thiago Antônio Pinheiro Toniêto, Letícia Pierri, Valdemar Luiz Tornisielo, and Jussara Borges Regitano J. Agric. Food Chem., Just Accepted Manuscript • DOI: 10.1021/acs.jafc.5b04665 • Publication Date (Web): 05 Jan 2016 Downloaded from http://pubs.acs.org on January 10, 2016
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Journal of Agricultural and Food Chemistry
Fate of tebuthiuron and hexazinone in green-cane harvesting system
Thiago Antônio Pinheiro Toniêto†, Letícia de Pierri†, Valdemar Luiz Tornisielo‡, Jussara Borges Regitano*† †
Department of Soil Science, University of São Paulo (USP/ESALQ), Av. Pádua Dias 11, 13418-260,
Piracicaba (SP), Brazil, Tel: +55 019 34172126,
[email protected]; ‡ Laboratory of Ecotoxicology, University of São Paulo (USP/CENA), Av. Centenário 303, 13400-970, Piracicaba (SP), Brazil.
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ASTRACT
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In Brazil, fire prior to sugarcane harvesting has to be phased out by 2017, but it was
3
already phased out in up to 85-90 % of the cropped area. This new system is called
4
green cane and entirely changed weed management practices. The main goal of this
5
study was to evaluate the effects of the straw presence as well as humic acid (HA),
6
formulation, soil type, and aging on the sorption and leaching of
7
hexazinone. Both herbicides presented low sorption for all treatments (Kd,app ≤ 3.25 L
8
kg-1), but it was higher for tebuthiuron in the clayer soil (LVd). Straw and aging only
9
slightly enhanced sorption. The HA effects were not clear. Sorption was mostly affected
10
by herbicide and soil type. Straw may promote physical trapping (∼31% of applied
11
amount) which cannot be accessed by "batch" sorption (∼15 % of the applied amount is
12
sorbed) attenuating leaching of highly mobile herbicides in green cane systems. In order
13
to properly access leaching through straw residues under laboratory condition, rainfall
14
distribution is very important.
15
Keywords
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Straw, humic acid, fire, pesticides, mobility, groundwater pollution.
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C-tebuthiuron and
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INTRODUCTION
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Sugarcane (Saccharum officinarum) became particularly important in Brazil
19
after the National Alcohol Program (PROALCOOL) creation in the 70’s. The goal was
20
to replace fossil fuels by ethanol on large scale. Currently (2013/2014), sugarcane
21
represents ∼2 % of Brazilian GDP and yield surpasses 680 million tons.1 However,
22
according to the new environmental protocol signed,2 the use of fire prior to harvesting
23
should be phased out by 2017 (this will be called “green-cane” harvesting system). It
24
should change weed control management practices that correspond to one of the major
25
costs involved on sugarcane production. As a matter of fact, the use of herbicides
26
increased abruptly in the last ten years. It matched with the beginning of the green-cane
27
likely due to lower herbicide transposition through the straw resulting in lower efficacy3
28
and natural selection of large seed weeds (e.g., Ipomoea spp.) having sufficient reserves
29
(energy) to emerge.4
30
The green-cane system provides about 5 to 20 Mg ha-1 year-1 of straw on the soil
31
top, which increases soil organic carbon content and agrochemicals interception, mainly
32
fertilizers and pesticides.4-7 A straw layer of 7 Mg ha-1 is capable to retain up to 200 L
33
of a herbicide spray in tropical systems8 and herbicide transposition decreases with
34
straw amounts.3,9,10 Moreover, sugarcane straw degrades slowly due to its high C/N
35
ratio, i.e. only ∼30 % of the original dry matter degraded 3 y after harvesting.11 The
36
straw ability to cover the soil for long periods may favor chemical or physical
37
entrapment of the herbicide decreasing its efficacy or degradation.5
38
Tebuthiuron (N-[5-(1,1-dimethylethyl)-1,3,4-thiadiazol-2-yl]-N,N’-dimethylurea) and
39
hexazinone [3-cyclohexyl-6-(dimethylamino)-1-methyl-1,3,5-triazine-2-4(1H,3H)dione] are
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pre-emergent herbicides heavily used for weed control in sugarcane (Table 1). Both of
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them show high persistence (half-lives = 12-15 mo for tebuthiuron and up to 9 mo for
42
hexazinone), moderate to extremely high toxicity,12 low sorption (Kd = 0.002-3.6 L kg-1
43
for tebuthiuron and 0.07-1.65 L kg-1 for hexazinone),13-15 and high water solubility (Sw
44
= 2,500 mg L-1 for tebuthiuron and 33,000 mg L-1 for hexazinone), which point out
45
their high leaching potential in soils.16 Indeed, they have been frequently reported in
46
groundwaters.17-19
47
Pesticide interactions with soil particles enhance with aging.20-24 Aging refers to
48
pesticide residence time in the soil. Although not yet fully understood, it happens due to
49
enhancement in binding energy and diffusion over time5,22. These interactions may
50
become so strong that is no longer possible to extract part of them by traditional
51
methods (this fraction is called “non-extractable”).25 Thus, aging before the first rain
52
may considerably decrease leaching to groundwater,5,20 mainly for those herbicides
53
with high solubility and low sorption, such as tebuthiuron and hexazinone. In other
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words, herbicide leaching is usually overestimated when aging is disregarded.21
55
Humic acids (HA) have been applied to agricultural areas to enhance soil
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environmental quality and crop yieds.26,27 However, HA effect on the environmental
57
behavior of pesticides are not yet fully elucidated. HA functional groups may interact
58
with pesticides serving as sorption sites thus reducing their mobility;28-31 but they may
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also act as co-solvent28 or hydrophobic sites for partitioning in the liquid phase thus
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enhancing their mobility28,32, mainly in soils with high permeability. In addition, HA
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may compete with pesticides for sorption sites in the soils,31,32 which also enhance
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leaching. To the best of our knowledge, there are no reports regarding HA effects on the
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environmental fate of herbicides in green-cane harvesting systems.
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Therefore, the main goals of this work were to evaluate the effects of sugarcane
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straw as well as of HA, formulation, and aging on the sorption and leaching of
66
tebuthiuron and hexazinone in contrasting tropical soils under laboratory conditions.
67
The presence of the straw is critical for weed control in the new green cane harvesting
68
system adopted in Brazil.
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MATERIALS AND METHODS
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The surveys were conducted at the Center for Nuclear Energy in Agriculture
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(CENA-USP), Piracicaba-SP, Brazil, using sorption33 and leaching34 protocols with
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small modifications.
74 75
Chemicals, soils and treatments
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Analytical standards and radiolabeled forms (14C-UL) of tebuthiuron (specific
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activity = 3.01 MBq mg-1, purity > 98%) and hexazinone (specific activity = 3.14 MBq
78
mg-1, purity > 98%) were adopted.
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Soil samples of a sandy clay loam and a clay Oxisols (LVA and LVd according
80
to Brazilian Soil Classification System, respectively)35 (coordinates 22° 40’20'' S and
81
47° 37’ 31” W, respectively) were selected because they are very representative of the
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sugarcane areas in São Paulo state, Brazil, and present contrasting texture. The soil
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samples were collected at 0-20 cm layer, air-dried, sieved in 2-mm mesh, and
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conditioned at room temperature. Particle size was measured by the hydrometer method
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and chemical attributes according to Raij et al.36 Briefly, pH was determined in
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CaCl2 0.01 mol L-1 (soil:solution ratio = 1:2.5); calcium, magnesium and potassium
87
were extracted by an ion exchange resin and Ca2+ and Mg2+determined by atomic
88
absorption spectrophotometry and K+ by flame photometry; potential acidity (H + Al)
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was determined by pH-SMP; and total soil organic carbon by combustion in an
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elementary autoanalyzer.
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Sugarcane straw samples (variety SP 90-2032) were collected after third ratoon
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harvesting, oven dried at 65 °C, and cut into 2.5-cm pieces. HA source and application
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rate followed manufacturer’s recommendations (150 L ha-1). Soils, straw, and HA
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attributes are presented on table 2.
95 96
Sorption experiment
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The treatments comprehended two straw rates (0 and 10 Mg ha-1), two HA rates
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(0 and 150 L ha-1), two herbicides (tebuthiuron and hexazinone), two incubation periods
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(0 and 21 d), two soils (LVA and LVd), and two formulations (with commercial
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formulation (CF) and without (AI = active ingredient only)), which were completely
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randomized and arranged in a factorial design, in duplicate.
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About 60 mg of sugarcane straw (= 10 Mg ha-1 straw, assuming bulk density =
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1.2 g cm-3 and soil depth = 10 cm) were added to 5 g soil (air dried) in centrifuge tubes
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(Teflon, 50 mL) and soil moisture adjusted to 75 % of the field capacity. For time zero
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(t0), 10-ml aliquots of 0.005 mol L-1 CaCl2 solution were added to the tubes immediately
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after herbicides application to attain maximum recommended field rates (tebuthiuron =
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1000 g a.i. ha-1 and hexazinone = 500 g a.i. ha-1, both with radioactive concentration ∼
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135 Bq mL-1), which were weighed, shaken horizontally (160 rpm) for 24 h, and
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centrifuged (830 g for 15 min). Then, 1-mL aliquots of the supernatants were analyzed
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by liquid scintillation spectrometry (LSS) to determine soil-solution equilibrium
111
concentration (Ce). For 21 d (t21), the tubes were placed in a semi-dark room at 25 ± 2°C
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and the soil moisture maintained by gravimetry. Then, the previous procedure was
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repeated to evaluate sorption. This period was adopted because most pesticide reaction
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with soil particles happens within this period, although sugarcane cycle comprehends
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12-15 mo.
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Then, the supernatants were discarded and the tubes placed in a ventilation oven
117
(40°C, 48 h). After drying, a few tubes were weighed and the slurries removed,
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macerated, and oxidized (0.20 g) in a biological oxidizer (900°C for 3 min), in
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triplicates, to determine herbicides sorbed concentration to the soil (S) and mass
120
balance. The 14CO2 released was captured by the monoethanolamine solution and the
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radioactivity determined by LSS. The recovery ranged from 90 to 110 % of the applied
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radioactivity, which allowed calculating S by the difference between initial (Ci) and
123
equilibrium (Ce) concentrations. Afterwards, the apparent sorption distribution
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coefficients (Kd,app= S / Ce) were calculated for a single concentration.24 It is reasonable
125
since our previous work showed that initial concentrations for both herbicides were
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within linear isotherm range and therefore allow comparing soil’s sorption.37
127 128
Leaching experiment
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This experiment was completely randomized in a factorial design, in triplicates,
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comprehending two HA rates (0 and 150 L ha-1), two herbicides (tebuthiuron and
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hexazinone), and two herbicide formulations (AI and CF), but just in the sandier soil
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(LVA) in order to represent the worst case scenario, totalizing 24 columns.
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Glass columns (length = 30 cm, diameter of inner conical sphere = 5 cm) were
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used for soil packaging. Fiberglass and sterilized sand with HCl were added to the
135
column bottoms to serve as a support. Soil packaging was manually performed (height
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= 5 cm and soil density ∼ 1.78 g cm-3) and then aliquots of 11-g of straw were added to
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the topsoils (= 16 Mg ha-1 of straw (82 kg m-3) determined based on field
138
measurements). This straw mass was subdivided into three even layers of about 2.5-cm
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separated by fiber glasses (packing density = 0.08 g cm-3). At the very top, another thin
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layer of fiber glass was added in order to promote homogeneous dispersion of the
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aqueous solution and avoid surface disturbance. Afterwards, the soil columns were
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saturated by capillarity with 0.005 mol L-1 CaCl2, the “aqueous solution” excess let
143
percolate for ∼ 2 h, and then the herbicides solutions applied to attain the maximum
144
recommended field rates (radioactivity ∼ 30 Bq g-1 of soil). The columns were placed in
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a semi-dark room at 25 ± 2oC and the rainfall was simulated in two stages of 50 mm
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with 0.005 mol L-1 CaCl2 solution (6 and 30 h after herbicide application), applied in
147
continuous flow for 2 h with the aid of a peristaltic pump. Since rainfall distribution
148
affects leaching, it was simulated using one- (flow rate = 0.8 mL min-1 channel-1) and
149
four-drop (flow rate = 0.2 mL min-1 channel-1) channels per column, always totalizing
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100 mm of rain.
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Leachates were collected immediately after each rain simulation, and 10-mL
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aliquots were analyzed by LSS. Further, straw and soil samples were removed from the
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columns using pressurized air and placed into aluminum containers to air dry. These
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materials were further ground and homogeneously mixed. Subsequently, subsamples of
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0.10-g of straw and 0.20-g of soil were oxidized in a biological oxidizer (900 °C for 3
156
min), in triplicate, and radioactivity determined by LSS. Recovery ranged from 89 and
157
117 %.
158 159
Statistical analysis
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All experimental data were submitted to variance analysis within each herbicide
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and soil type. When interactions were observed, the factors were outspread and their
162
significance compared by Tukey test (p ≤ 0.05).
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RESULTS AND DISCUSSION
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Sorption of tebuthiuron and hexazinone
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Apart of the treatment, tebuthiuron and hexazinone showed low sorption in all
168
soils (Kd,app ≤ 3.25 and 1.76 L kg-1, respectively) (Table 3), which is consistent with
169
previous studies.15,37,38 The greater sorption of tebuthiuron compared to hexazinone was
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expected due to intrinsic molecule properties, such as its lower water solubility.
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Moreover, sorption was considerably higher in the clay soil (LVd, Table 3).
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Across all treatments, 24 and 14% of the applied tebuthiuron and hexazinone were
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sorbed to the LVA whereas 56 and 41 % of them were sorbed to the LVd, respectively.
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In other words, the LVd presented Kd,app even 16 times higher than the LVA. It is well
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known that clay soils have the ability to accumulate more carbon in relation to sandy
176
soils39 since clay promotes physical protection and chemical stabilization of SOC,40
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especially in tropical soils, as corroborated by its higher initial SOC (Table 2). It
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contributes to higher soil CEC and buffer capacity. In addition, clayer tropical soils
179
have considerable amounts of Fe and Al oxides and hydroxides that may work as
180
sorption sites for these molecules. Our previous work has already shown that organic
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carbon content was the soil attribute that better correlated with these herbicides
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sorption, but the addition of Fe oxide contents helped in their sorption prediction.37
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These should favor hidrophobic partitioning and sorption processes.24
184
Straw addition only slightly enhanced sorption of both herbicides, but the
185
increase was more abrupt for tebuthiuron in the sandier soil (LVA) when freshly applied
186
(Table 3). Across all treatments, sorption in this soil increased from 15 to 24% for
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tebuthiuron and from 9 to 12% for hexazinone when freshly applied. On the other side,
188
it increase from 28 to 30% for tebuthiuron, but slightly decreased from 18 to 17 % for
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hexazinone when aged for 21 d (Table 3). In the LVd, the influence of straw addition
190
was most noticeable for hexazinone when freshly applied. In this case, sorption
191
enhanced from 36 to 42% in the presence of the straw whereas it enhanced only from 42
192
to 44 % when aged. For tebuthiuron, independent of the residence time, sorption
193
enhanced by 2% (from 55 to 57%), on average, in the presence of the straw.
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Although literature reports increase in pesticides sorption with HA addition,29-31
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that was not the case here. HA addition did not appear to significantly influence these
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herbicides sorption. It only slightly reduced tebuthiuron sorption (Kd,app) when freshly
197
applied to the LVd (Table 3). In this case, sorption reduced from 55 to 52% of the
198
applied amount (Table 3). Sorption reversibility due to soluble organic compounds
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addition to soils is observed primarily when molecule sorption is low, but also depends
200
on herbicide properties.41 In other words, interactions between pesticides and soluble
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organic materials are conditioned by hydrophobicity/hydrophilicity properties of
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both,32,42 but may also involve specific or non-specific sorption mechanisms. The high
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solubilities and moderately polar structures of these herbicides and HA co-solvent
204
properties and competition for the sorption sites31-32 should favor desorption and explain
205
part of our results, especially when the herbicide is freshly applied, although
206
competition for sorption sites was proved for compounds different than ours.
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Aging enhanced sorption of both herbicides in all treatments and soil types.
208
Overall, sorption enhanced from 20 to 29 and from 53 to 58% for tebuthiuron in the
209
LVA and LVd, respectively, and from 10 to 18 and from 39 to 43% for hexazinone,
210
respectively. It is clear that the aging effects were most significant for the herbicide with
211
lower sorption (hexazinone) in the soil with lower buffer capacity (LVA). However, to
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better predict pesticides fate in soils, the residence time must be considered.20,24
213
Moreover, in the absence of sugarcane straw, aged Kd,app values increased mostly after
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HA addition (Table 3), which may preclude leaching of highly soluble herbicides,
215
particularly hexazinone. This result was most prominent for commercial formulation,
216
mainly in the LVA, likely due to the presence of certain vehicles on its formulation that
217
facilitate diffusion to less accessible sorption sites and increase herbicide sorption over
218
time. 22
219
Regardless of treatment and soil type, it is possible to conclude that tebuthiuron
220
and hexazinone always showed high leaching potential (Kd,app < 5.0 L kg-1) (Table 3).
221
However, the methodology adopted (“batch” experiment) disregards the physical barrier
222
created by the straw,24 which may overestimate pesticide mobility in green-cane
223
systems. Considering a completely different molecule and another substrate, it was
224
observed ∼50% reduction in simazine leaching by the presence of wheat straw on the
225
soil surface.43 The authors were unable to identify if leaching reduction was held by
226
herbicide sorption or by its interception to the straw, or both. Our results suggest that it
227
was likely due to wheat straw interception.
228 229
Leaching of hexazinone and tebuthiuron
230
According to the literature, the adoption of one drop channel at the center of the
231
soil columns to simulate rainfall events, as recommended by OECD protocol (for soils),
232
underestimated leaching of both herbicides, most likely due to lack of rainfall
233
interception. Across all treatments, in this case, ∼57 and 42 % of the applied amounts of
234
tebuthiuron and hexazinone were retained in the first 2.5 cm straw layer and ∼28 and 43
235
% were leached, respectively (Figure 1). Rainwater distribution is a crucial factor
236
dictating pesticides environmental fate since it is the vehicle by which the molecule is
237
transferred from the straw to the soil in green-cane systems.3 The intensity and shape of
238
the rain and the aging effects directly influence molecules transfer into soil and, hence,
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its efficacy and fate.22,44,45 Furthermore, the ligno-cellulosic nature of the sugarcane
240
straw and its lack of capillarity (differently from soils) favor water preferential flow at
241
the center of the column,3 avoiding herbicide contact with water and, therefore, its
242
subsequent percolation.24 In addition, water into contact with lignin induces stress in the
243
glassy core of the polymer and, at the same time, promotes expansion in rubbery region,
244
resulting in a pressure between the lignin subunits and, consequently, cracking its
245
structure.46 These cracks eventually may also facilitate water preferential flow itself.3
246
Therefore, leaching experiments were repeated dividing rain simulation into four
247
dropping channels per column in order to reproduce rainfall distribution more
248
realistically (Figure 2). At this scenario, also across all treatments, ∼ 33 and 31 % of
249
tebuthiuron and hexazinone applied amounts were retained in the first 2.5 cm straw
250
layer, respectively, and ∼ 44 % were equally leached for both molecules (Figure 2).
251
However, ∼ 19 and 24 % of the applied tebuthiuron and hexazinone reached the soil,
252
respectively. In the previous approach (one drop), only ∼ 9 and 6 % of the applied
253
amounts reached the soil, respectively. Although tebuthiuron presented higher sorption,
254
it showed similar soil profile distribution to hexazinone when rainfall was better
255
distributed (four drops) (Figure 2). We may not forget that tebuthiuron sorption was
256
higher, but still very low mainly in the LVA. Even after 100 mm of rain, ∼ 40 % of both
257
applied herbicides remained intercepted in the straw, which differs from sorption
258
expectations, mainly for hexazinone (Figure 2). Therefore, the straw left on soil surface
259
in green-cane harvesting systems seems advantageous from the environmental point of
260
view since it attenuates groundwater contamination risks by highly mobile herbicides,
261
such as tebuthiuron and hexazinone.47 These results were in disagreement with those
262
from sorption suggesting that straw presence did not considerably affect our herbicides
263
mobility.
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HA application appeared to have increased hexazinone retention to the straw
265
and, as a result, decreased its leaching apart of the formulation (although differences
266
were not statistically significant). Hexazinone straw retention was enhanced by about
267
11-12 % in the presence of HA (it changed from 35 to 47 % and from 29 to 40 % of the
268
applied amount for the AI and CF, respectively) (Figure 2). For tebuthiuron, it seems
269
that the presence of HA may have increased AI solubility and; therefore, decreased
270
straw retention (from 49 to 36 %) and increased its leaching (from 37 to 50 %), but the
271
same was not observed for the CF (Figure 2). Tebuthiuron results were in accordance to
272
those of the sorption study (Kd,app was lower in the presence of HA when tebuthiuron
273
was freshly applied) and agreed with those attained by other authors.28,32 Nevertheless,
274
such contrasting results do not allow drawing a final conclusion regarding the
275
treatments employed. Therefore, many times here the data was treated as an average
276
value across all treatments.
277
We could conclude that sugarcane straw only slightly enhanced tebuthiuron and
278
hexazinone sorption, which was always low apart of chemical formulation, HA
279
application, pesticide aging, and soil type. HA application and CF seems to have little
280
influence on sorption of highly soluble herbicides, such as ours. Aging enhanced
281
sorption mainly for hexazinone in the soil sandier soil (LVA), but soil type was the
282
parameter that mostly affected sorption. In order to properly access leaching through
283
straw residues under laboratory condition, rainfall distribution is very important. One
284
drop channel to simulate rainfall event, as proposed by OECD Guideline for soils,
285
underestimated leaching. The presence of sugarcane straw worked as a physical barrier
286
for herbicides trapping, capable to retain ∼ 30 % of the applied herbicides, thus either
287
avoiding or retarding leaching. Although tebuthiuron presented higher sorption,
288
leaching amounts were similar to those for hexazinone. Considering that we worked
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with the worst case scenario regarding leaching purposes, i.e. a sandy soil with low OC
290
content, heavy rain, very mobile herbicides, and no aging, these results would be
291
expected.
292 293
Aknowledgements
294 295
The authors thank FAPESP for the research financial support (Process Number:
296
2012/15843-0); CNPq for granting the first author a Master’s degree scholarship;
297
Fabrício G. Giore for reviewing the project ideas; and Carlos Alberto Dorelli and
298
Rodrigo Pompinato for their technical support.
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UNICA - Industry Union of Sugarcane. Institutional folder. 2011. São Paulo.
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plant residue management systems. Weed Sci. 1997, 45, 307-320. (6)
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FIGURE CAPTIONS Figure 1 – Percentages of tebuthiuron and hexazinone leached after 100-mm rainfall simulation with one-drop channel per column. Bars represent the significant difference by Tukey test (p ≤ 0.05, n = 3).
Figure 2 – Percentages of tebuthiuron and hexazinone leached after 100-mm rainfall simulation with four-drop channels per column. Bars represent the significant difference by Tukey test (p ≤ 0.05, n = 3).
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TABLES Table 1. Structural formulas and chemical classifications of tebuthiuron and hexazinone. Attributes
Tebuthiuron
Hexazinone
C9H16N4OS Substituted urea
C12H20N4O2 Triazine
Structural formula Molecular formula Chemical family
Table 2. Soils, straw, and humic acid’s chemical and physical attributes. ----------- Soil atributes ----------a b LVA LVd c pH 4.5 4.3 d
SOC
-3
g dm
-3
P
mg dm mmolc dm-3
+
K
2+
Ca
2+
Mg Al
3+
H + Al SB CEC
Sand
23
3
10
0.7
-1
g kg
1.3
5
37
2
7
3.0
6.6
11
f
g
8
45
18.9
124 284
Silt
18
123
Clay
226
593
a c
a
pH
C/N ratio CEC
5.9
-
34/1 -1
mmolc kg
density e
WHC
-
g dm ³ %
350 0.08 215
---------- Humic acid attributes ----------
79
8.2 756
------------- Straw attributes -------------
pH C/N ratio
7.2
-
2/1 -1
density
g mL
total C
-1
gL
1.09 14
b
LVA = sandy clay loam Oxisol; LVd = clay Oxisol pH CaCl2 0.01 mol L-1; dsoil organic carbon; ewater holding capacity; fsum of bases; fcation exchange capacity.
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Table 3. Effects of soil type (LVA and LVd), sugarcane straw (0 and 10 Mg ha-1), formulation (AI and CF), humic acid (0 and 150 L ha-1), and aging (0 and 21 d) on the apparent sorption distribution coefficients (Kd,app) of tebuthiuron and hexazinone. Values inside parenthesis refer to sorbed herbicide amounts (% of applied). Values followed by same uppercase in the columns and lowercase in the rows do not differ statistically (Tukey test, p ≤ 0.05). Treatments formulation
straw (Mg ha-1)
CF CF + HA AI AI + HA
0 10 0 10 0 10 0 10
a
without straw with straw c without HA d with HA e aging b
CF CF + HA AI AI + HA a
without straw with straw c without HA d with HA e aging b
0 10 0 10 0 10 0 10
Tebuthiuron 0d
Hexazinone
21 d
Mean 0d 21 d Mean -1 Kd,app (L kg ) -------------------------------------- LVA --------------------------------------
0.36 (15) 0.79 (28) 0.09 (4) 0.34 (15) 0.56 (22) 0.93 (32) 0.18 (8) 0.42 (17) 0.61 (23) B 0.37 (14) 0.24 (11) 0.61 (23) 0.18 (8) 1.00 (30) 0.62 (23) 0.78 (28) 0.34 (15) 0.38 (16) 0.44 (18) 0.83 (29) 0.28 (12) 0.32 (14) 0.66 (25) 0.88 (31) 0.72 (26) A 0.32 (14) 0.46 (19) 0.33 (14) 0.83 (29) 0.22 (10) 0.35 (15) 0.43 (18) 0.77 (28) 0.92 (31) 0.26 (11) 0.41 (17) 0.37 (15) Bb 0.76 (28) Ba 0.57 (22) 0.19 (9) 0.50 (18) 0.35 (13) 0.27 (12) 0.42 (17) 0.35 (14) 0.65 (24) Ab 0.88 (30) Aa 0.77 (27) 0.51 (20) 0.86 (30) 0.68 (25) 0.22 (10) 0.39 (16) 0.30 (13) 0.52 (20) 0.79 (28) 0.65 (24) 0.25 (11) 0.34 (19) 0.29 (15) 0.51 (20) 0.82 (29) 0.66 (25) 0.23 (10) b 0.46 (18) a 0.34 (14) -------------------------------------- LVd -------------------------------------2.24 (52) 2.84 (58) 1.13 (35) 1.76 (46) 2.62 (56) 2.87 (58) 2.54 (55) B 1.69 (45) 1.61 (44) 1.45 (41) 1.95 (48) 2.76 (57) 1.13 (35) 1.22 (35) 2.27 (52) 2.79 (57) 1.35 (39) 1.74 (46) 2.52 (55) 2.92 (58) 1.23 (37) 1.54 (43) 2.58 (55) 3.17 (60) 2.78 (57) A 1.41 (41) 1.64 (44) 1.49 (42) 2.20 (51) 2.99 (59) 1.20 (37) 1.72 (45) 2.58 (56) 3.25 (61) 1.65 (44) 1.55 (43) 2.23 (52) 2.88 (58) 2.56 (55) B 1.18 (36) 1.56 (42) 1.37 (39) B 2.51 (55) 3.02 (59) 2.77 (57) A 1.52 (42) 1.64 (44) 1.58 (43) A 1.37 (40) 1.64 (44) 1.50 (42) 2.49 (55) Ab 2.95 (59) Aa 2.72 (57) 2.25 (52) Bb 2.95 (59) Aa 2.60 (56) 1.33 (39) 1.56 (42) 1.44 (40) 2.37 (53) 2.95 (58) 2.66 (56) 1.35 (39) b 1.60 (43) a 1.47 (41)
a
mean values for all treatments without straw addition (0 Mg ha-1); mean values for all treatments with straw addition (10 Mg ha-1); c mean values for all treatments without HA application; d mean values for all treatments with HA application; e mean values for all treatments for each incubation time (0 and 21 d). b
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FIGURES (Figure 1)
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FIGURES (Figure 2)
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TABLE OF CONTENTS GRAPHIC
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The authors declare no competing financial interest in publishing this paper.
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