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PLOS One logoLink to PLOS One
. 2014 Mar 11;9(3):e91767. doi: 10.1371/journal.pone.0091767

Evaluation of Chloropicrin as a Soil Fumigant against Ralstonia solanacarum in Ginger (Zingiber officinale Rosc.) Production in China

Liangang Mao 1,#, Qiuxia Wang 1,2,#, Dongdong Yan 1,2,#, Taotao Ma 1, Pengfei Liu 1, Jin Shen 1, Yuan Li 1,2, Canbin Ouyang 1,2, Meixia Guo 1,2, Aocheng Cao 1,2,*
Editor: A Mark Ibekwe3
PMCID: PMC3950219  PMID: 24618853

Abstract

Background

Chloropicrin (Pic) offers a potential alternative to methyl bromide (MB) against Ralstonia solanacarum in ginger (Zingiber officinale Rosc.) production. MB is scheduled to be withdrawn from routine use by 2015 in developing countries.

Methods

Pic treatments were evaluated in a laboratory study and in three commercial ginger fields.

Results

Laboratory studies showed that the EC50 value and EC80 value of Pic were 2.7 and 3.7 mg a.i. kg−1 soil, respectively. Field trials in highly infested soil revealed that treatments of Pic at the dose of 50 g m−2 covered with totally impermeable film (TIF) or polyethylene film (PE) sharply reduced Ralstonia solanacarum and maintained high ginger yields. Both of the Pic treatments provided results similar to, or in some cases slightly lower than, MB with respect to Ralstonia solanacarum control, plant survival, plant growth and yield. All of the fumigant treatments were significantly better than the non-treated control.

Conclusions

The present study confirms that the Pic is a promising alternative with good efficacy against Ralstonia solanacarum for ginger production and could be used in integrated pest management programs in China.

Introduction

In 2011 the total ginger production in China, the second largest ginger (Zingiber officinale Rosc.) producing country in the world, was 426,032.00 tonnes (t) and the area harvested was 36,007.00 hectare (ha) [1]. Due to successive monocropping of ginger, Ralstonia solanacarum, which was originally described by Smith (1896) as the causative agent of bacterial wilt of solanaceous plants [2], has the ability to reduce yields greatly in the cultivation of ginger in China. At present, methyl bromide (MB) is widely used in ginger cultivation in China as a preplant soil fumigant against R. solanacarum. MB, however, has to be phased out by 1 January 2015 in developing countries owing to its detrimental effects on the stratospheric ozone layer [3]. The withdrawal of MB from use as an agricultural fumigant has prompted a large amount of research aimed at finding effective and economically acceptable alternatives [4].

The pesticides currently applied against R. solanacarum in ginger in China include fumigants and other chemical or biological pesticides, such as chloropicrin (Pic), cupric hydroxide, and Bacillus cereus. Pic is becoming one of the most important fumigants for ginger production in China. There is much information in the literature on the ability of Pic to control various soilborne pests effectively in many crops, for example tomatoes [5][9], strawberries [10], peppers [11][13] and others. However, little information has been reported on Pic against R. solanacarum in ginger production.

The present work was initiated to test the effects of Pic on R. solanacarum in laboratory studies. In addition, three field trials were carried out to evaluate two different Pic treatments as a potential alternative to MB against R. solanacarum for ginger production in China.

Materials and Methods

Laboratory studies

The dose-responses of R. solanacarum to different Pic concentrations were studied in the laboratory. With the authorization of the institute of Fangshan agricultural science, Beijing, soil samples in the laboratory studies were collected from the top 20 cm of greenhouse soil in Nanhe village, Dashiwo town, Fangshan district, southwest of Beijing. The field studies site does not involve endangered or protected species and the GPS coordinates are 39°33′9.3″N, 115°49′34.1″E. The soil was composed of 61.48% sand, 37.20% silt, and 1.32% clay, with organic matter content 25.38 g kg−1 soil and pH 6.49. The soil was sieved through a 2-mm mesh, and then mixed together. The soil moisture was 12.37% (w/w). Particle size analyses were performed using the pipette method [14]. The organic carbon content was determined by wet oxidation using the method of Walkley and Black [15]. The pH was measured in a 1:2.5 soil to H2O extract. Soil moisture content was measured in the drying oven at 105±5°C until mass constancy was achieved [16]. The soil was sterilized at 121°C for 30 mins using the high-pressure steam sterilization pot. R. solanacarum, was grown on triphenyltetrazolium chloride (TTC) selective media and then quantitatively incorporated into the sterilized soil.

300 g R. solanacarum-infested soil was placed into each of 0.5 L glass jars [17][19]. The following treatments were applied with three replicates: Pic alone (1.0, 2.0, 4.0, 8.0, 16.0, 32.0, 64.0, 128.0, 256.0 mg a.i. kg−1 soil) and non-treated control. Pic was injected into the soil by pipette (Eppendorf, Germany) and then the jars were immediately sealed with covers. The jars were placed in incubators at 28°C for 7 days. The jars were opened to release the residual fumigant for a day and R. solanacarum was isolated from the soil quantitatively based on the method described by Kelman [20].

Field trials

In 2012 and 2013, with the authorization of Laiwu agriculture bureauthe, Shandong Province, three field experiments were conducted in three ginger fields located in Xiaoxia village, Zhaili town, Laiwu city, Shandong province, China (trial I: 36°17′31.9″N, 117°28′19.6″E), Hanwangxu village, Zhaili town, Laiwu city, Shandong province, China (trial II: 36°17′52.1″N, 117°26′07.4″E), and Caodaxia village, Zhaili town, Laiwu city, Shandong province, China (trial III: 36°16′30.8″N, 117°30′05.1″E), respectively. The field studies site does not involve endangered or protected species. And there are no specific permissions required for the field sites. All field sites are located in intensive ginger production areas of Laiwu, a region which has a long history of ginger production. However, R. solanacarum has become a big problem due to the continuous cropping. The major soil-borne disease is plant death caused by R. solanacarum. Details relevant to these trials are given in Table 1 and 2 .

Table 1. Soil characteristics in the experimental sites.

Site Soil moisture (%) pH (1:2.5) Organic matter (g kg−1) N/NH4 + (mg kg−1) N/NO3 (mg kg−1) Available K (mg kg−1) Available P (mg kg−1)
trial I 14.95 6.78 22.36 38.37 71.09 341.54 392.11
trial II 14.09 6.90 14.17 18.31 43.35 239.56 231.26
trial III 18.20 6.16 17.40 47.42 77.50 479.21 402.20

Table 2. Relevant trial dates and other details.

Site Fumigant application Tarp removal Ginger transplant Germination investigation Plant growth evaluationa End of the trial Preceding crop
trial I 02/11/12; 11/03/13 09/04/13 19/04/13 26/06/13 07/08/13 13/10/13 Ginger
trial II 03/11/12; 12/03/13 10/04/13 22/04/13 27/06/13 08/08/13 13/10/13 Ginger
trial III 03/11/12; 12/03/13 10/04/13 23/04/13 27/06/13 08/08/13 14/10/13 Ginger
a

Plant growth evaluation included ginger plant height and number of leaves per tiller.

The following fumigant products were used in the study: (a) Pic 99.5 LD (Dalian Dyestuffs & Chemicals Co., China), a commercial liquid product containing 99.5% Pic; (b) MB 98 TC (Lianyungang Dead Sea Bromine Co. Ltd, Jiangsu Province, China) containing 98% MB and 2% chloropicrin. The soil mulches were 0.04 mm polyethylene film (PE) (Baoding Baoshuo Plastic Co., Ltd., Hebei Province, China) and 0.04 mm totally impermeable film (TIF) (Jiahe Industrial Co., Ltd., Jiangsu Province, China).

Each Pic treated plot area was designed to 50 m2. Each MB treated plot area and untreated control plot area are both designed to 25 m2. The treatments were designed as randomized blocks with three replicates ( Table 3 ). The tested treatments were MB, used as a reference treatment, Pic, and untreated control. Pic liquid was injected into the soil at 15 cm depth via a manual injection machine at a rate of 50 g m−2 ( Figure 1 ). The Pic treatments were applied in two different seasons: one was applied in November 2012 (soil temperature at 5 cm depth was about 15 to 21°C during the day) and covered with TIF film; another was applied in March 2013 (soil temperature at 5 cm depth was about 13 to 19°C during the day) and covered with PE film ( Figure 1 ). MB was applied by using evaporating iron jars under a PE sheet and allowing it to vaporize in situ (cold method) at a rate of 40 g m−2 in March 2013, and a small arc tunnel (40 cm height) was constructed under the mulch with the aim of improving the fumigant distribution [21]. The ginger plants were 40 cm apart, planting distance 25 cm, about 6500 plants per mu. Traditional cultivation techniques were used in all plots.

Table 3. Experimental program of the field trials.

Trial Fumigant and formulationa Rate (g a.i. m−2) Tarpb Application method Fumigation date Abbreviation used for the treatment
trial I Pic 99 LD 50 TIF Injection 02/11/2012 Pic 50 TIF
Pic 99 LD 50 PE Injection 11/03/2013 Pic 50 PE
MB 98 TC 40 PE Cold method 11/03/2013 MB 40 PE
Untreated control 02/11/2012
trial II Pic 99 LD 50 TIF Injection 03/11/2012 Pic 50 TIF
Pic 99 LD 50 PE Injection 12/03/2013 Pic 50 PE
MB 98 TC 40 PE Cold method 12/03/2013 MB 40 PE
Untreated control 03/11/2012
trial III Pic 99 LD 50 TIF Injection 03/11/2012 Pic 50 TIF
Pic 99 LD 50 PE Injection 12/03/2013 Pic 50 PE
MB 98 TC 40 PE Cold method 12/03/2013 MB 40 PE
Untreated control 03/11/2012
a

Abbreviations: Pic  =  chloropicrin; MB  =  methyl bromide; TC  =  Technical.

b

Abbreviations: PE  =  polyethylene film; TIF  =  totally impermeable film.

Figure 1. Application of Pic in field trials:

Figure 1

(A) a manual injection machine was used to apply Pic in the soil; (B) the treatments were covered with PE or TIF film.

Soil R. solanacarum populations [colony-forming units (cfu) g−1 soil] were determined after fumigation from soil at the depth of 0–20 cm. Soil from each plot was sampled from 3 spots along the diagonal lines in a plot. R. solanacarum was determined using the same methods as the Laboratory studies.

Ginger germination was evaluated at 9 WAT (weeks after transplant). Plant growth (ginger plant height, tillers/plant and mortality) were evaluated at 15 WAT (weeks after transplant) (20 plants per plot). The yield, plant height and root disease severity in ginger were evaluated at the end of the trials. Twenty ginger plants were picked from each plot, and the severity of ginger root disease was assessed separately, based on a disease severity scale of 0–4, where 0  =  healthy plant and root, without disease; 1  =  black brown rotten roots comprising <25% of the entire root system; 2 = 26–50%; 3 = 51–75%; and 4 = 76–100% black brown rotten roots [22].

Statistical analyses

Laboratory studies

The bacterial control efficacy of treatments can be calculated according to the following equation.

graphic file with name pone.0091767.e001.jpg (1)

where Y is the control efficacy on bacteria, X1 is the bacteria population of the untreated control, X2 is the bacteria population of fumigant treatments.

The experimental design consisted of a randomized complete block with three replications. A nonlinear dose-response curve, which was analyzed with Origin (Origin Pro 8.0 for Windows), was used to describe the relationship between the R. solanacarum mortality (y) and the logarithm of the concentration of fumigant (x):

graphic file with name pone.0091767.e002.jpg (2)

Field trials

The control efficacy on bacteria was calculated using the same equation as the Laboratory studies.

The disease scores recorded for each plot were converted into disease indices (% DI) using the formula described by McKinney [22]

graphic file with name pone.0091767.e003.jpg (3)

where ƒ  =  number of plants in each class, v  =  class value, N  =  number of observed plants, and X  =  highest value in the evaluation scale.

Data were analyzed for ANOVA with SAS (SAS, version 8.0 for Windows). Significant differences among means were determined by Fisher's LSD test at P = 0.05 [23], [24]. Data for soil bacteria populations were transformed as necessary (square root transformations for small numbers [<100] and log10 for large numbers [> 100] for statistical analyses), but all data are reported as non-transformed values. The data in percentages (mortality and root disease index) were normalized with arcsine square root transformation prior to ANOVA.

Results

Laboratory studies

The nonlinear dose-response curve of R. solanacarum to different concentrations of Pic indicated a strong relationship between increases in fumigant concentration and mortality, with R 2 values≥0.994 ( Figure 2 ). A nonlinear curve fit model was expressed as follows:

graphic file with name pone.0091767.e004.jpg (4)

Figure 2. Response of R. solanacarum to different Pic concentrations after fumigation of a sandy loam soil for 7 days at 28°C.

Figure 2

The nonlinear curve fit (DoseResp) revealed that the concentrations required to control 50% (EC50) and 80% (EC80) of R. solanacarum were 2.7 and 3.7 mg a.i. kg−1 soil, respectively.

Field trials

Trial I

The untreated controls in trial I were heavily infested by R. solanacarum ( Table 4 and Figure 3 ). R. solanacarum levels were significantly lower in the chemical treatments compared with the untreated control, except for Pic 50 PE treatments applied in March. In trial I the greatest reduction of R. solanacarum was provided by MB 40 PE treatments (94.92%), followed by Pic 50 TIF treatments (85.27%) and Pic 50 PE treatments (75.93%) ( Table 4 ).

Table 4. Effects of soil fumigation on colony-forming units (cfu) of R. solanacearum on selective media of 1 g from soil after fumigation.
Site Treatmenta R. solanacearum
cfu/ga % reduction
trial I Pic 50 TIF 947b 85.27
Pic 50 PE 1547ab 75.93
MB 40 PE 327b 94.92
Untreated control 6427a
trial II Pic 50 TIF 1093b 84.25
Pic 50 PE 1667b 75.98
MB 40 PE 293c 95.77
Untreated control 6940a
trial III Pic 50 TIF 340bc 93.82
Pic 50 PE 583b 89.39
MB 40 PE 267c 95.15
Untreated control 5553a
a

In each column, data are means of three replication. Means followed by the same letter are not different (P = 0.05) according to the LSD test.

Figure 3. Ginger plants grown in plots treated with (A) Pic 50 TIF, (B) Pic 50 PE, (C) MB 50 PE and (D) Untreated control at the end of trials, respectively (trial I).

Figure 3

Ginger germination levels in all treatments were at least 96.97% at 9 WAT, and there was no significant difference between the chemical treatments and the untreated control at this stage ( Table 5 ). The fumigation treatments significantly affected plant height, number of leaves per tiller and plant mortality at 15 WAT ( Table 5 ). In trial I the ginger grown in MB PE treatment plots had the greatest plant height (91.0 cm), the largest number of leaves per tiller (15) and the lowest plant mortality (0.00%) at 15 WAT. However there was no significant difference between the three fumigant treatments with respect to plant mortality (which ranged from 0.0% to 0.5%), and all fumigant treatments substantially reduced plant mortality compared to the untreated control (60% mortality) ( Table 5 ).

Table 5. Effect of fumigation treatments on germination and plant growth during the ginger crop growth period.
Site Treatment Germination (%) Plant height (cm) Number of leaves/tillerb Mortality (%)
trial I Pic 50 TIF 99.56aa 80.0ab 11b 0.44b
Pic 50 PE 99.49a 78.3b 15ab 0.51b
MB 40 PE 98.10a 91.0a 15a 0.00b
Untreated control 96.97a 61.7c 5c 60.00a
trial II Pic 50 TIF 98.00a 87.3a 15a 0.00b
Pic 50 PE 98.46a 85.7a 15a 0.51b
MB 40 PE 100.00a 84.7a 16a 0.00b
Untreated control 97.76a 62.7b 5b 86.55a
trial III Pic 50 TIF 98.56ab 88.7a 13b 0.44b
Pic 50 PE 97.44ab 83.7a 17a 1.03b
MB 40 PE 100.00a 82.7a 14ab 0.00b
Untreated control 88.10b 57.3b 3c 70.85a
a

In each column, data are means of three replication. Means followed by the same letter are not different (P = 0.05) according to the LSD test.

b

Number of leaves/tiller were counted from the one who had the most leaves in the all tillers of one ginger plant.

Compared to the untreated control, fumigation treatments significantly affected plant height, number of tillers per plant, root disease index and yield at the end of the trials ( Table 6 ). Pic 50 TIF treatments produced the greatest plant height (99.8 cm) and the lowest root disease index (0.00%), followed by MB 40 PE and Pic 50 PE. Pic 50 TIF and MB 40 PE treatments showed no significant difference in plant height and root disease index ( Table 6 ). There was no significant difference in the number of tillers per plant in all chemical treatments. Ginger grown in the MB 40 PE plots had the lowest plant mortality (0.00%), followed by Pic 50 TIF and Pic 40 PE treatments, but there was no significant difference in plant mortality between MB 40 PE and Pic 50 TIF treatments ( Table 6 ). Ginger grown in the untreated plots had the lowest yield (1.50 Kg m−2). The plots treated with MB 40 PE provided the highest yield (6.69 Kg m−2), but this was not statistically different to the two Pic treatments ( Table 6 ).

Table 6. Effect of fumigation treatments on ginger plant height, tillers/plant, mortality, root disease, and yield at the end of the trials.
Site Treatment Plant height (cm) Tillers/plant Mortality (%) Root disease index (%) Yield (Kg m−2)
trial I Pic 50 TIF 99.8aa 15a 1.25c 0.00c 6.27a
Pic 50 PE 81.9b 14a 10.00b 26.88b 6.20a
MB 40 PE 97.9a 16a 0.00c 1.88c 6.69a
Untreated control 24.9c 2b 88.94a 93.13a 1.50b
trial II Pic 50 TIF 95.0a 15a 8.50b 12.50b 7.29a
Pic 50 PE 87.7a 13a 10.55b 12.50b 5.32b
MB 40 PE 98.4a 15a 0.00b 0.00b 6.24ab
Untreated control 0.0b 0b 100.00a 100.00a 0.00c
trial III Pic 50 TIF 90.6a 11b 10.00b 15.63b 4.99b
Pic 50 PE 93.1a 15ab 5.00b 6.25b 5.49ab
MB 40 PE 98.0a 17a 0.00b 0.00b 7.31a
Untreated control 42.2b 6c 90.85a 78.13a 1.87c
a

In each column, data are means of three replication. Means followed by the same letter are not different (P = 0.05) according to the LSD test.

Trial II

The untreated controls in trial II were also heavily infested by R. solanacarum ( Table 4 ). All chemical treatments reduced R. solanacarum at least 75.98%. The lowest level of R. solanacarum of was provided by MB 40 PE treatments, followed by Pic 50 TIF and Pic 50 PE treatments. However there was no significant difference in R. solanacarum levels between the two different Pic treatments ( Table 4 ).

Ginger germination levels in all treatments were at least 97.76% at 9 WAT, and there was no significant difference at this stage ( Table 5 ). Fumigation treatments significantly affected plant height, number of leaves per tiller and plant mortality at 15 WAT ( Table 5 ). Ginger grown in the untreated controls had the lowest plant height (62.7 cm), the least number of leaves per tiller (5) and the highest plant mortality (86.55%) at 15 WAT. Among the three fumigation treatments there was no statistical difference in plant height, number of leaves per tiller and plant mortality at 15 WAT, and all were significantly different to the control ( Table 5 ).

At the end of trial II, the fumigation treatments significantly affected plant height, number of tillers per plant, root disease index and yield ( Table 6 ). Plant height was significantly greater in all chemical treatments compared with the untreated control. The greatest plant height was observed in plots treated with MB 40 PE (98.4 cm), followed by Pic 50 TIF and Pic 50 PE. However, there was no significant difference in plant height between the Pic and MB treatments. Similarly, the plots treated with MB 40 PE provided the greatest number of tillers per plant (15), the lowest ginger mortality (0.00%), and the lowest ginger root disease index (0.00%), but these results were not statistically different from the Pic treatments.

Ginger grown in the untreated plots had the lowest yield (0.00 Kg m−2) ( Table 6 ). The plots treated with Pic 50 TIF provided the highest yield (7.29 Kg m−2), and this was not statistically different to the yield obtained with MB 40 PE but was significantly higher than the yield obtained with the Pic 50 PE treatment ( Table 6 ).

Trial III

Trial III also found that the untreated controls were heavily infested by R. solanacarum ( Table 4 ). All chemical treatments reduced R. solanacarum at least 89.39%. The lowest level of R. solanacarum was also provided by MB 40 PE treatments, followed by Pic 50 TIF and Pic 50 PE treatments. However, there was no significant difference in R. solanacarum levels between Pic 50 TIF and MB 40 PE treatments ( Table 4 ).

At 9 WAT there was no significant difference in ginger germination levels between the treatments except that the levels in MB 40 PE treatments (100%) were significantly higher than the untreated controls (88.10%) ( Table 5 ). Fumigation treatments significantly affected plant height, number of leaves per tiller and plant mortality at 15 WAT ( Table 5 ). Ginger grown in the untreated controls had the lowest plant height (57.3 cm), the least number of leaves per tiller (3) and the highest plant mortality (70.85%) at 15 WAT. The three fumigation treatments showed no significant difference in plant height, number of leaves per tiller and plant mortality ( Table 5 ).

At the end of the trials, fumigation treatments significantly affected plant height, number of tillers per plant, root disease index and yield ( Table 6 ). Plant height was significantly greater in all chemical treatments compared with the untreated control. The greatest plant height was observed in plots treated with MB 40 PE (98.0 cm), followed by Pic 50 PE and Pic 50 TIF, however there was no significant difference between the chemical treatments. Similarly, the plots treated with MB 40 PE provided the lowest ginger mortality (0.00%) and the lowest ginger root disease index (0.00%), but this was not statistically different from the Pic treatments. Ginger grown in the untreated plots had the lowest number of tillers per plant (6) and lowest yield (0.00 Kg m−2) ( Table 6 ). The plots treated with MB 40 PE provided the greatest number of tillers per plant (17) and the highest yield (7.31 Kg m−2); this was not statistically different from the yield obtained with Pic 50 PE but was significantly higher than the yield obtained with Pic 50 TIF ( Table 6 ).

Discussion

After three to five years' successive monocropping of ginger, ginger bacterial wilt caused by soil-borne R. solanacarum becomes greater and greater in China and the ginger producers have to plant other vegetables such as Chinese onion (Agrimonia fistulosum L.), garlic (Agrimonia sativum L.), Chinese cabbage (Brassica campestris L. spp.), radish (Raphanus sativus L.), maize (Zea mays L.) and others. Ginger has a relatively high economic value compared to other vegetables, so the application of a fumigant is regarded as an essential practice to protect ginger plants from soil-borne R. solanacarum in China. In our research, laboratory studies and three field trials were conducted to determine effects of several Pic treatments on R. solanacarum in ginger production.

Our laboratory studies showed that Pic can provide excellent control of R. solanacarum after fumigation of a sandy loam soil for 7 days at 28°C. The specific mechanism by which Pic controls R. solanacarum was not examined, however, the current laboratory results indicated that Pic is feasible and effective in controlling R. solanacarum.

In the present field trials, both Pic treatments (Pic 50 TIF applied in November, and Pic 50 PE applied in March) sharply reduced the colony-forming units (cfu) of R. solanacarum on media, and maintained high ginger yields in commercial production. Based on the present field results, the two different Pic treatments provided results similar to MB 40 PE in terms of R. solanacarum control after fumigation, plant growth at 15 WAT, plant height, plant mortality, root disease index and ginger yield at the end of the trials. The results confirmed that the two tested Pic treatments both provide an effective alternative to MB. However, based on our present field results, it is too soon to say which one of the Pic treatments is better, and more studies are needed in order to draw a definitive conclusion on this point. Generally speaking, the temperature must be between 4.4 to 26.7°C (40 to 80°F) at the depth of injection when Pic is applied [25]. In our filed trials, when Pic was applied, the soil temperatures at 5 cm depth during the day of two different Pic treatments (in November 2012 and in March 2013) was about 15 to 21°C and 13 to 19°C, respectively ( Figure 1 ). In November 2012 treatments, with the winter coming, the soil temperature will become lower and lower, and the lowest soil temperature will be about 0°C. Although from previous laboratory results, it would appear that chloropicrin is effective against Verticillium at low temperatures around 50°F±2°F (8.9 to 11.1°C) [26]. In the field application, whether and how low temperatures affect the effect of Pic on R. solanacarum is still unclear to us.

The soils in our three field trials were heavily infested by R. solanacarum, but at 9 WAT the fumigation treatments did not significantly affect ginger germination levels except for MB 40 PE treatments in trial III. This indicates that ginger bacterial blight did not generally appear in the initial growth stage of ginger, and this could be attributed to the relatively low temperature, low rainfall patterns and low soil moisture during the initial growth stage.

Pic is a strong eye irritant and has a pungent unpleasant smell, which can pose barriers to its adoption. Well-equipped commercial companies generally provide safe soil fumigation services in the United States, Europe, or Japan. However, soil fumigation in China is mostly conducted by individual farmers who generally lack essential application tools and personal protection equipment. Considering the environment emissions and potential human exposure, the gelatin capsule (gel cap) formulation of Pic will offer a promising solution [10], [27]. The use of TIF would allow greater retention of Pic than the conventional PE film, trapping the fumigant for a longer period near the soil surface and thereby increasing the dose and prolonging the exposure of soilborne pathogens to the fumigant [28], [29]. In the present field trials, Pic 50 TIF treatments applied in November were generally similar or even superior to Pic 50 PE treatments applied in March for controlling R. solanacarum and improving plant growth and ginger yield. However, we are not able to attribute this to the use of TIF before removing the effect of the different application seasons. Pic is normally applied in the spring (during March and April) about one month before ginger is transplanted in the field. The soil temperature is low (about 8 to 18°C during the day) during this fumigation period, so it would be desirable to examine in more detail the feasibity of applying Pic in the autumn (during October and November, just after the ginger harvest) when soil temperature is relatively high (about 15 to 25°C during the day).

In summary, our studies determined that the fumigant Pic had similar efficacy to MB in terms of controlling ginger bacterial blight caused by R. solanacarum, ginger germination, plant height, plant mortality, number of leaves per tiller and ginger yield. However, more detailed work to identify the most suitable application methods (formulation, rates, and application seasons) and appropriate combinations [30] with other fumigants or biological agents (for example Trichoderma asperellum, Bacillus subtilis or others) is necessary before Pic treatments can be recommended as an efficient alternative to methyl bromide for ginger production in China.

Acknowledgments

The authors give special thanks to Professor Jie Feng (Institute of Plant Protection, Chinese Academy of Agricultural Sciences) who in our laboratory studies provided Ralstonia solanacarum isolated from ginger grown in Shandong, China. We also thank Dr. Melanie Miller for editing the manuscript.

Funding Statement

This research was supported by the Program on Substituted Technology for Methyl Bromide in China (Special Finance of Chinese Ministry of Agriculture, 2110402) and UNDIO Project on Phasing-out of Methyl Bromide in Agriculture Sector in China (TF/CPR-A/08/003). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

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