Introduction
Soybeans are an internationally important food, fodder and industrial crop and a useful source of vegetable oil and protein. Traditional Japanese food culture has developed with soybeans, making it an irreplaceable crop that can be connected directly with Japanese life. However, the current self-sufficiency rate (calorie base) for soybean in Japan is 6%, which is remarkably lower than that for paddy rice, which is also a staple of Japanese food culture. The Ministry of Agriculture, Forestry and Fisheries of Japan proposed a policy that the targeted self-sufficiency rate for soybeans in 2020 be raised to 17% (Ministry of Agriculture, Forestry and Fisheries of Japan, 2010); however, many problems related to production have blocked such an increase.
The effect of a policy of reduction of the acreage under rice cultivation since 1970 in Japan promoted the conversion to field from paddy field. Presently, over 80% of domestic soybean production comes from converted paddy fields following changes in paddy rice production (Ministry of Agriculture, Forestry and Fisheries of Japan, 2012). One of the problems for soybean production is closely related to the traits of these converted fields. The soil of converted fields includes a high fraction of heavy clay, reflecting their paddy field origin. Although soybean is more tolerant of excess moisture than other upland crops, flooding injury of soybean occurs and is affected by the duration of flooding (Scott et al., Reference Scott, Deangulo, Daniels and Wood1989), the ambient temperature (Wuebker et al., Reference Wuebker, Mullen and Koehler2001), the coexistence of pathogens (Kato et al., Reference Kato, Minamida, Tojo, Kokuryu, Hamaguchi and Shimada2013), the selection of cultivars (VanToai et al., Reference VanToai, Hoa, Hue, Nguyen, Shannon and Rahman2010), drought conditions after flooding (Ministry of Agriculture, Forestry and Fisheries of Japan, 2005), and growth stage. Heavy, prolonged rain just after seeding can cause very conspicuous flooding injury in soybean seed, and drastically reduce soybean yield as a result of poor germination (Arihara et al., Reference Arihara, Tian, Nakayama, Saito and Kanno2000).
Some current practices can avoid serious injury under these circumstances. Soybean seeds with a cracked seed coat are prone to non-germination under excess soil moisture; therefore, germination could be improved by removing cracked seeds before seeding (McDonald et al., Reference McDonald, Vertucci and Roos1988). Since quantitative trait locus (QTL) analysis of seed coat cracking or physiological factors has been advancing (Sayama et al., Reference Sayama, Nakazaki, Ishikawa, Yagasaki, Yamada, Hirota, Hirata, Yoshikawa, Saito, Teraishi, Okumoto, Tsukiyama and Tanisaka2009; Oyoo et al., Reference Oyoo, Benitez, Matsuura and Takahashi2010), future genetic improvements are expected. If the depth of the water table in a converted field can be freely controlled in soybean cultivation, the productivity can be stable. The FOEAS (Farm-Oriented Enhancing Aquatic System) is a field-engineering practice based on this idea (Matsuo et al., Reference Matsuo, Takahashi, Nakano, Fukami, Tsuchiya, Morita, Kitagawa, Nakano, Nakamoto and Tasaka2013). Soaking soybean seeds in hypertonic solution before planting has been found to be an artificial pre-treatment that improves the flooding tolerance of seeds (Woodstock and Taylorson, Reference Woodstock and Taylorson1981). Also, ‘high-moisture treatment’ for soybean seed has attracted attention for a long time as an effective and simple pre-treatment that has the same effect as the hypertonic method (Obendorf and Hobbs, Reference Obendorf and Hobbs1970; Vertucci and Leopold, Reference Vertucci and Leopold1984). Flooding injury could be reduced by moisture treatment in which the moisture content of seeds is raised to approximately 15% (Toledo et al., Reference Toledo, Cavariani, França-Neto and Nakagawa2010). Such technological improvements are useful in avoiding flooding injury, but further improvements and progress are needed. However, debatably, scientific breeding for flooding tolerance in susceptible cultivars could be important. Basic information on the injury-causing mechanism is essential for this, but there are still many unknowns.
Generally, the progress of seed germination has multiple phases (Weitbrecht et al., Reference Weitbrecht, Müller and Leubner-Metzger2011). Phase I begins just after water is absorbed by a seed, and consists of two processes: the first involves the rapid uptake of water (imbibition) and the second involves a linear increase in seed moisture content. After phase I, seeds almost entirely cease water uptake in phase II, and radicle emergence begins in the post-germination stage of phase III. In this report, we focused on the first process (phase I) because the rapid water influx during this phase occurs in dead seeds (Krishnan et al., Reference Krishnan, Joshi, Nagarajan and Moharir2004).
The cause of soybean seed flooding injuries has been examined in many studies. What is known about the mechanism is that sudden and rapid imbibition begins just after flooding of the seed, and imbibition induces the collapse of the cotyledons and the embryonic axis, preventing germination (Woodstock and Taylorson, Reference Woodstock and Taylorson1981; Nakayama and Komatsu, Reference Nakayama and Komatsu2008). The damage is greater in low-moisture than in high-moisture seeds (Ishibashi et al., Reference Ishibashi, Nakamoto, Hamabe, Zheng, Nabeta and Iwaya-Inoue2005). Furthermore, some other factors related to soybean seed flooding injury include low oxygen conditions (Tian et al., Reference Tian, Nakamura and Kokubun2005) and the induction of pathogens by leakage from damaged cells (Kato et al., Reference Kato, Minamida, Tojo, Kokuryu, Hamaguchi and Shimada2013).
Differences in the flooding injury of soybean seeds have been reported (Hou and Thseng, Reference Hou and Thseng1991; Tian et al., Reference Tian, Nakamura and Kokubun2005), and the key factor affecting the injury is the difference among cultivars and the seed water-absorbing rate (Hou and Thseng, Reference Hou and Thseng1991; Tian et al., Reference Tian, Nakamura and Kokubun2005). The consistent tendency is for the rate of imbibition to be slower in flooding-tolerant cultivars than in susceptible cultivars. That is, the imbibition is slow enough so that the cotyledons will not break. Furthermore, the imbibition behaviour of soybean seeds can be affected by substances on the seed coat (Mullin and Xu, Reference Mullin and Xu2001; Shao et al., Reference Shao, Meyer, Ma, Peterson and Bernards2007; Ranathunge et al., Reference Ranathunge, Shao, Qutob, Gijzen, Peterson and Bernards2010; Zhou et al., Reference Zhou, Sekizaki, Yang, Sawa and Pan2010), the seed coat colour (Hou and Thseng, Reference Hou and Thseng1991; Chachalis and Smith, Reference Chachalis and Smith2000), the region of the seed surface (Meyer et al., Reference Meyer, Steudle and Peterson2007; Muramatsu et al., Reference Muramatsu, Kokubun and Horigane2008), the micro-structure (Yaklich et al., Reference Yaklich, Vigil and Wergin1986; Ma et al., Reference Ma, Cholewa, Mohamed, Peterson and Gijzen2004) or the inner layer (Koizumi et al., Reference Koizumi, Kikuchi, Isobe, Ishida, Naito and Kano2008) of the seed coat, the adhesion between the seed coat and cotyledon (Chachalis and Smith, Reference Chachalis and Smith2000; Nakayama and Komatsu, Reference Nakayama and Komatsu2008) and the hydraulic conductivity of the seed coat (Meyer et al., Reference Meyer, Steudle and Peterson2007). Based on these findings, it is possible that seed traits that affect imbibition behaviour might determine the flooding tolerance of soybeans. Although there could be multiple strategies for soybean cultivars against excess soil moisture, a complete analysis of the mechanisms causing flooding injury is not available at present.
In the present study, we have attempted to clarify the relationship between flooding injury of soybean seeds and imbibition, as well as the traits that influence imbibition. For this purpose, we used moisture-treated soybean seeds of seven cultivars and compared their flooding tolerance, imbibition behaviour and seed traits, and determined their relationships.
Materials and methods
Plant materials and moisture treatment
To investigate the flooding tolerance of moisture-treated soybean (Glycine max (L.) Merr.) seeds, seven soybean cultivars were studied (Table 1). Coloured, stained, wounded or otherwise abnormal seeds were removed, and the normal seeds were stored in a refrigerator at 4°C. We checked that these normal seeds of all cultivars had a 90–100% germination rate with incubation on a wet Petri dish at 25°C in the dark for 3 d.
Basic information about the seeds of the seven soybean cultivars used in this study
a Cultivars are displayed in order of seed mass (see Table 2).
b Flooding tolerance derived from previous research (Tian et al., Reference Tian, Nakamura and Kokubun2005; our unpublished data).
c –, unknown.
As a pre-treatment before all experiments, seeds were moisture treated either in high- or low-moisture conditions for adjustment of their moisture content. In the case of high-moisture treatment, 60 seeds were incubated in a sealed plastic container with a plate containing 15 ml water at 25°C in the dark for 3 d. Low-moisture treated seeds were created by incubation of 60 seeds with 15 g of fresh silica gel particles.
Flooding treatment and germination test
The flooding tolerance of soybean seeds was elucidated in detail for various flooding durations using the paper towel method, basically according to the International Seed Testing Association rules (ISTA, 1985). After the moisture treatment, seeds were immediately immersed in distilled water for 10 min, 1 h, 3 h or 24 h at 25°C in the dark. Seeds without a flooding treatment were prepared as control samples. All these seeds were coated with Benlate T (Sumitomo Kagaku Co., Ltd, Tokyo, Japan) for sterilization before the germination test. Ten seeds were arranged on one piece of paper towel with sticky-tape, a part of the paper towel was soaked with tap water, and this was incubated at 25°C in the dark for a week. The germination rate was calculated by counting the normally germinating plantlets, defined as those with no damage to the cotyledons and with normal elongation of the infant root. The germination test was conducted with three replicates (ten seeds per replicate) in a complete randomized block design.
Seed moisture content and seed volume
Some of the moisture-treated seeds were weighed to obtain their fresh weight and dry weight. To measure dry weight, seeds were dried completely at 80°C for 2 d or more. The moisture content of the seeds was calculated from the fresh and dry weight after the moisture treatment. The measurements of fresh and dry weights were repeated with three replicates each (ten seeds per replicate).
The fresh weight of the seeds was also used for measuring the volume after the moisture treatment. To measure seed volume, ten seeds were put into a water-filled 50-ml measuring cylinder, and the increased volume of the water was measured. Although the method was not very sensitive, air bubbles on the seed surface were removed before measurement to maximize the accuracy as much as possible. The volume measurement was repeated three times with ten seeds per replicate.
Passive imbibition
In the present study, we measured two types of imbibition behaviour: passive imbibition, that which occurred in submerged (flooded) seeds, and capillary imbibition, where seeds absorbed water by capillarity. As we also wanted to compare two types of imbibition behaviour, we devised a methodology for measuring passive imbibition separately in six regions (Fig. 1A) of the seed surface and defined the passive imbibition as the average ratio of the regions. First, seeds were coated with water-repellent resin (silicon lacquer spray, Kanpe-hapio Co., Ltd, Oosaka, Japan) except for the seed surface region where imbibition would take place. After the seed coating, a circle-shaped area 2–5 mm in diameter was left exposed on the intact seed coat of each seed. The exposed seed coats in the circle were checked for a normal appearance with a microscope, and only normal seeds were moisture-treated before the measurement of passive imbibition. The low-moisture seeds were weighed and then promptly immersed in distilled water. Subsets of the seeds were removed from the water after 10 min, 30 min, 1 h and 3 h. The water adhering to lifted seeds was carefully wiped off with Kimwipes, and the seeds were weighed with an electric balance with a sensitivity of 0.01 mg (R180D, Sartorius AG, Göttingen, Germany). The passive imbibition was expressed as the water volume per average fresh seed weight and unit time [μl (g FW)− 1min− 1]. The measurement of passive imbibition was repeated eight times with ten seeds per replicate.
Photograph showing each separate part used to measure imbibition behaviour, using a ‘Hayahikari’ seed as a model (A), and a diagram of the instrument used to measure the hydraulic conductance of seed coats (B). In B, distilled water was incorporated into a bag in a pressure chamber. A seed coat was sandwiched with O-rings, a metal washer and a nylon filter, and then the assembly was tightened by compression screwing. Water was forced into the upper part by pressure from an air compressor. Water that passed through the seed coat and nylon filters was absorbed by cotton, which was then weighed.
Capillary imbibition
Capillary imbibition was also measured separately for the six regions (Fig. 1A) and averaged among them, using the bottom water supply method (Nakayama and Komatsu, Reference Nakayama and Komatsu2008). The low-moisture seeds were weighed and promptly placed on water-saturated cotton touching a certain seed partial surface that let the area imbibe. Subsets of the seeds were taken off the cotton after 10 min, 30 min, 1 h, 3 h and 6 h, and were weighed and calculated in the same way as for passive imbibition. We defined the seed-specific capillary imbibition as the average ratio of the regions of the seed. The measurement of capillary imbibition was repeated five times with one seed per replicate.
Hydraulic conductance of the seed coat
We measured the hydraulic conductance of the seed coat because the permeability of the seed coat to water would be of great importance for the imbibition behaviour of soybean seeds. In the present study, we measured the hydraulic conductance of the seed coat directly using a modified pressure chamber (Fig. 1B). A piece of the seed coat from the abaxial surface of a low-moisture seed was cut to 5 mm in diameter using a cork borer. The disc of the specimen was hydrated with distilled water until setting it up in the chamber lid of a pressure chamber. To protect the seed coat against uneven pressure, each disc was sandwiched between nylon discs (NRS-050, aperture: 50 μm; wire diameter: 38 μm; Nippon Rikagaku Kikai Co., Ltd, Tokyo, Japan), and was attached to the lid with metal washers and O-rings to make the chamber airtight. In the lid, a water-filled tube was placed by the seed coat disc so that the water would come up to the disc during pressurization. Pressure in the chamber was gradually increased to 100 kPa and maintained for 5 min, using a commercial air compressor (AM02-04N, Fujiwara Sangyo Co., Ltd, Hyogo, Japan). We trapped the water discharged through the seed coat for 5 min using pre-weighed cotton. The cotton was weighed with an electric balance with a sensitivity of 1 mg (VIC212, ACCULAB, Sartorius AG). The hydraulic conductance of the seed coat was represented as the water volume per unit time and pressure (μl kPa− 1min− 1). The measurement was conducted six times with a single seed coat disc per replicate.
Seed osmolarity
We also measured the osmolarity inside soybean seeds as a factor that could affect the capillary imbibition behaviour. After moisture treatment, a 5-mm cube of the cotyledonary centre was cut from the seed, and the fresh weight was measured. The fraction of the cotyledon was put into a 0.5-ml Eppendorf tube with 200 μl of Mili Q water, and frozen at − 80°C. After thawing, the tube was treated with ultrasonic cleaning equipment (CS-20, OMRON Co., Kyoto, Japan) for 10 min to release the water-soluble substances into solution from the cotyledonary tissue. Ten microlitres of the solution was loaded in an osmometer (VAPRO type 5600, Wescor Inc., Logan, Utah, USA) to measure the osmolarity. The osmolarity was expressed as the value per gram fresh weight of cotyledonary tissue [mol kg− 1(g FW seed)− 1]. The measurement was conducted ten times with one cotyledonary cube from a seed per replicate.
Statistical analysis
The experimental arrangement was based on a complete randomized design with 3–10 replicates, depending on the measurement. A Student's t-test, Tukey–Kramer's test, analysis of variance (ANOVA) and Pearson's correlation coefficient were conducted using the statistics software SPSS (v. 20.0, IBM SPSS, Tokyo, Japan).
Results
Effect of moisture treatment on basic traits of soybean seeds
Seeds after moisture treatment were measured for seed mass (weight of 100 seeds), moisture content and seed volume (Table 2). ANOVA showed that the effects of cultivar or treatment on all seed traits were significant, as well as the interactive effects between cultivar and treatment on seed mass (P < 0.05). In comparing the two moisture treatments, low-moisture seeds had lower moisture content (P < 0.01) and smaller seed mass (P < 0.001) than high-moisture seeds. The seed volume also swelled in the high-moisture seeds (P < 0.001). In comparing among cultivars, significant differences in all seed traits were detected (P < 0.001). Initial moisture content in seeds was adjusted to about 5% (low) and 13% (high) water (fresh mass basis). However, the magnitude of difference in weight and volume between the two moisture treatments depended upon cultivar. The differences related to the swelling ratio of the seed volume, which varied from 1.075 (NSe) to 1.255 (SMa).
Basic information about the moisture-treated seeds of the seven soybean cultivars
a Cultivars are displayed according to averaged seed mass.
b Moisture treatment for high (H) or low (L) moisture seed conditions.
c Ratio of volume high/low moisture treatment.
d Values in parentheses represent standard errors.
e ***, **, *, and † represent significant differences between H and L at the 0.1%, 1%, 5% and 10% levels, respectively (n= 3).
f ANOVA was performed with the data set 7 cultivars (C) × 2 treatments (T) × 3 replicates (blocks) with a complete randomized design. df, degrees of freedom; MS, mean square; F, F value; and P, P value.
Effect of moisture treatment on soybean seed survival under flooding
We checked seed survival, that is, the rate of germination into normal seedlings, after the various durations of flooding treatment for the different moisture-treated seeds (Fig. 2). Survival decreased with increased flooding duration up to 24 h for low-moisture seeds, but high-moisture seeds were not affected by flooding. There were significant cultivar-specific differences in the survival of low-moisture seeds after 3 h of flooding. After 3 or 24 h of flooding, NSe and TMu displayed lower survival. In contrast, SMa and PKi had higher survival rates as compared with the other cultivars. According to the hypothesis that the flooding injury was induced by mechanical damage to cotyledons during imbibition, this indicated that the cultivar-specific differences in survival were induced by imbibition until 3 h of flooding. Next, we checked the time-lapse shifting of imbibition behaviour of low-moisture seeds, focusing particularly on passive imbibition during 3 h of flooding.
Changes in the survival of moisture-treated soybean seeds after flooding. The left and right figures show the results for high- and low-moisture seeds, respectively. Seven cultivars are represented by different symbols: ●, TMu ‘Toyomusume’; □, ERe ‘Enrei’; ■, FYu ‘Fukuyutaka’; ◇, HHi ‘Hayahikari’; ♦, NSe ‘Nakasennari’; △, SMa ‘Suzumaru’ and ▲, PKi ‘Peking’. These symbols are arranged according to seed size (average weight of 100 seeds) shown in Table 1. Each value represents the mean of three replicates, and bars show standard errors. *** and ** accompanied by rectangles with a dotted boundary represent significant differences at the 0.001 and 0.01 probability level, respectively, among cultivars in the same duration of flooding, and the values with different small letters in rectangles are significantly different at the 0.05 probability level among the seven cultivars by a Tukey–Kramer's test (n= 3); ns denotes no significant difference. The averaged values are shown underneath rectangles, with standard errors in parentheses calculated from all values in the rectangle. Values with different capital letters underneath rectangles are significantly different at the 0.05 probability level by a Tukey–Kramer's test among the durations of the flooding treatment (n= 3).
Passive imbibition behaviour of low-moisture soybean seeds under flooding
Passive imbibition rate was measured separately in six regions of the seed surface (Fig. 1A) to conform to measurements of capillary imbibition. No significant difference of imbibition rate was observed in the different surface regions just after submergence, during which the imbibition rate was fastest [passive imbibition: P= 0.227 (not significant, ns); capillary imbibition: P= 0.913 (ns), n= 56, data not shown]. Thus, the results indicate that the effect of the seed surface region was small. The imbibition rates at different regions were then averaged and used for subsequent analysis.
Examining the shifts in passive imbibition rate during the first 3 h of flooding for low-moisture seeds, there was evidence of cultivar-specific differences in imbibition rate for flooding durations of 10–30 min (Fig. 3). Although there were cultivar-specific significant differences at the 0.05 level, a substantial difference could only be detected between TMu and PKi. The correlation between passive imbibition rate under flooding of 10–30 min and survival after 3 h of flooding, was not significant [R 2= 0.3215 (ns), n= 7, data not shown], even though both showed significant cultivar-specific differences. Additionally, there was no duration of passive imbibition rate in any duration of flooding that showed a significant correlation with survival after 3 h of flooding. Thus, a conventional hypothesis that a single effect accompanied by passive imbibition rate closely affected the flooding injury of soybean seeds could not be demonstrated in this study. Thus, we investigated another trait of imbibition behaviour of seeds, namely capillary imbibition.
Changes in the passive imbibition rate of low-moisture soybean seeds during the flooding treatment. Seven cultivars are represented by symbols: ●, TMu; □, ERe; ■, FYu; ◇, HHi; ♦, NSe; △, SMa and ▲, PKi. The arrangement of symbols is the same as for Fig. 1. Each value represents the mean of eight replicates, and bars show standard errors. * accompanied by rectangles with a dotted boundary represents a significant difference at the 0.05 probability level among cultivars in the same duration of flooding treatment, and the values with different small letters are significantly different at the 0.05 probability level among the seven cultivars by a Tukey–Kramer's test (n= 8); ns denotes no significant difference. The averaged values are shown above rectangles, with standard errors in parentheses calculated from all values in a rectangle. Values with different capitals above rectangles are significantly different at the 0.05 probability level by a Tukey–Kramer's test among the durations of the flooding treatment (n= 8).
Capillary imbibition behaviour of low-moisture soybean seeds with bottom water supply
Capillary imbibition behaviour was anticipated, because the seeds were allowed to absorb water from the bottom by capillarity. Therefore, we checked for capillary imbibition of low-moisture seeds at flooding durations of 6 h. The trend of shifts in capillary imbibition in low-moisture seeds showed evidence of cultivar-specific differences in imbibition for all flooding durations, except for those of 10–30 min (Fig. 4). A remarkable cultivar-specific difference was shown in SMa, which tended to imbibe water faster than the other cultivars. However, the other cultivars with distinct seed flooding tolerances, i.e. TMu, NSe and PKi, did not display distinct capillary imbibition rates. Similarly to the case of passive imbibition rate, the correlation between capillary imbibition rate under flooding of 0–10 min and survival after 3 h of flooding, was not significant [R 2= 0.2738 (ns), n= 7, data not shown], even though both showed significant cultivar-specific differences. And there was no duration of capillary imbibition rate in any duration of flooding that showed a significant correlation with survival after 3 h of flooding.
Changes in the capillary imbibition rate of low-moisture soybean seeds during the flooding treatment. Seven cultivars were represented by symbols: ●, TMu; □, ERe; ■, FYu; ◇, HHi; ♦, NSe; △, SMa and ▲, PKi. The arrangement of symbols is the same as for Fig. 1. Each value represents the mean of five replicates, and bars show standard errors. * accompanied by rectangles with dotted boundaries represents a significant differences at the 0.05 probability level among cultivars in the same duration of the flooding treatment, and the values with different small letters are significantly different at the 0.05 probability level among the seven cultivars by a Tukey–Kramer's test (n= 5); ns denotes no significant difference. The averaged values are shown above rectangles, with standard errors in parentheses calculated from all values in a rectangle. These values with different capitals above rectangles are significantly different at the 0.05 probability level by a Tukey–Kramer's test among the periods of flooding treatment (n= 5).
Ratio of passive and capillary imbibition rate
To further analyse the relationship between imbibition behaviour and seed flooding tolerance, we calculated the balance of two imbibition rates (passive/capillary ratio) related to survival after 3 h of flooding, using the ratio of passive imbibition to capillary imbibition (passive imibibition rate/capillary imbibition rate) with 20 combinations among four levels of passive imbibition and five levels of capillary imbibition. Four significantly negative correlations with survival after 3 h of flooding were found with passive/capillary ratio where the capillary imbibition during 0–10 min was used as the denominator [0–10 min, R 2= 0.6586 (P< 0.05); 10–30 min, R 2= 0.7292 (P< 0.05); 30 min–1 h, R 2= 0.5264 (P< 0.1); 1–3 h, R 2= 0.6106 (P< 0.05), n= 7, data not shown]. The remaining 16 combinations of passive and capillary imbibition did not show significant correlations with survival after 3 h of flooding. The relationship between the survival after 3 h of flooding and the passive/capillary ratio (passive imbibition at 10–30 min/capillary imbibition at 0–10 min) was the combination that showed the largest correlation coefficient with survival after 3 h of flooding (Fig. 5). The combination of passive/capillary ratio showed also a closer relationship with survival after 24 h of flooding. As is shown in Fig. 5, the susceptible cultivars such as NSe or TMu had a high passive/capillary ratio and low survival; in contrast, the tolerant cultivars like SMa or PKi had a low passive/capillary ratio and high survival. The ratio of imbibition rates suggests that the flooding injury of soybean seeds may become serious in cases of high passive imbibition or low capillary imbibition.
Relationships between passive imbibition rate at 10–30 min/capillary imbibition rate at 0–10 min and survival after 3 h of flooding (A), and survival after 24 h of flooding (B). Closed circle symbols represent each value, and the abbreviations of cultivars accompany these symbols. Data represents means from three replicates for survival. Bars show standard errors. A regression line shows a formula with significance at the 0.05 and 0.001 probability level (* and ***, respectively), by Pearson's correlation coefficient.
Seed traits affected two imbibition behaviours each
Next, we were interested in what kind of seed properties determined the extent of passive and capillary imbibition of soybean seeds. Among the various seed traits, the hydraulic conductivity of the seed coat and seed osmolarity surfaced as factors of particular interest. There were positive correlations between hydraulic conductivity of the seed coat and passive imbibition [0–10 min, R 2= 0.7493 (P< 0.05) (Fig. 6A); 10–30 min, R 2= 0.7138 (P< 0.05); 30 min–1 h, R 2= 0.0929 (ns); 1–3 h, R 2= 0.3404 (ns), n= 7] and between seed osmolarity and capillary imbibition [0–10 min, R 2= 0.4831 (P< 0.1); 10–30 min, R 2= 0.9086 (P< 0.001) (Fig. 6B); 30 min–1 h, R 2= 0.5947 (P< 0.05); 1–3 h, R 2= 0.6526 (P< 0.05); 3–6 h, R 2= 0.2227 (ns) n= 7].
Relationships between the conductivity of the seed coat and passive imbibition rate at 0–10 min (A), between seed osmolarity and capillary imbibition rate after 10–30 min (B), between capillary imbibition rate at 0–0 min and passive imbibition rate at 10–30 min (C), and between the conductivity of the seed coat and seed osmolarity (D). Closed circle symbols represent each value with 3–10 replicates (5 for capillary imbibition rate, 6 for seed conductivity, 8 for passive imbibition rate, 10 for seed osmolarity), and the abbreviations of cultivars accompany these symbols. Bars show standard errors. Regression lines show the formulas marked by *** and * indicating significance at the 0.001 and 0.05 probability levels, respectively, by Pearson's correlation coefficients; ns denotes no significant difference.
To ensure the independence of each relationship, we checked the relationship between the two imbibition behaviours that were used as parameters of the passive/capillary ratio, and between the hydraulic conductivity and seed osmolarity, and in both cases the results were non-significant (Fig. 6C and D). Additionally, the correlation between hydraulic conductivity and passive imbibition was not significant [0–10 min, R 2= 0.0078 (ns); 10–30 min, R 2= 0.1581 (ns); 30 min–1 h, R 2= 0.0033 (ns); 1–3 h, R 2= 0.1027 (ns); 3–6 h, R 2= 0.0350 (ns), n= 7, data not shown]. Although correlations between hydraulic conductivity and passive imbibition were subtly detected [0–10 min, R 2= 0.4831 (P< 0.1); 10–30 min, R 2= 0.2105 (ns); 30 min–1 h, R 2= 0.0454 (ns); 1–3 h, R 2= 0.5031 (P< 0.1), n= 7, data not shown], the relationship with capillary imbibition seemed to be specific to seed osmolarity.
Discussion
Importance of moisture treatment for soybean seed germination after flooding
High-moisture treatment for soybean seeds before planting has a remarkable positive effect on later germination (Obendorf and Hobbs, Reference Obendorf and Hobbs1970; Toledo et al., Reference Toledo, Cavariani, França-Neto and Nakagawa2010). In the seven cultivars used for the present study, the effect of moisture treatments on the seed moisture content was clear, and the differences among treatments were all significant (Table 2). Further, flooding injury was detected in low-moisture seeds in certain cultivars, but not in high-moisture seeds in any cultivars (Fig. 2). These results indicate that high-moisture treatment could improve germination after flooding, as reported in past studies. It was also reported that the threshold for the effective moisture content to inhibit flooding injury was approximately 15% (Toledo et al., Reference Toledo, Cavariani, França-Neto and Nakagawa2010). On the other hand, Vertucci and Leopold (Reference Vertucci and Leopold1984) suggested that imbibition damage of soybean seed was moderate between a seed moisture content of 8 and 24%. From our results, we found that moisture contents ranging from 12.6% (Nakasennari) to 13.2% (Toyomusume) could also inhibit flooding injury (Table 2, Fig. 2). The results from the evaluation of soybean seed flooding injury after moisture treatments simply indicate that the cultivar-specific differences in flooding injury must appear in low-moisture seeds. The key factor affecting the flooding injury of soybean seeds is the seed water-absorption rate – imbibition (Hou and Thseng, Reference Hou and Thseng1991; Tian et al., Reference Tian, Nakamura and Kokubun2005). For the next step, we focused on the behaviour of dried seeds.
Flooding injury affected by the combination of both types of imbibition
Low-moisture seeds showed remarkable symptoms of flooding injury in Toyomusume and Nakasennari, but not in Peking, Suzumaru or Hayahikari (Fig. 2). We could evaluate the former and the latter as susceptible and tolerant cultivars, respectively. These categories are almost in agreement with the evaluation for flooding tolerance in past research (Table 1). In low-moisture seeds, the significant difference in survival among cultivars was first detected after 3 h of flooding (P < 0.001). Based on these results, we inferred that a specific biophysical event did not occur in seeds of tolerant cultivars but did occur in seeds of susceptible cultivars within 3 h of flooding, and this reduced survival. We defined the cultivar-specific survival reduction by flooding within 3 h as the vital reaction triggered by imbibition.
To quantify seed imbibition behaviour, we used the parameter of the water-absorption rate, further defined separately into passive and capillary rates. A past report evaluated the flooding tolerance of soybean seeds under complete flooding conditions that induced passive imbibition with submergence (Hou and Thseng, Reference Hou and Thseng1992), and another report investigated soybean seed imbibition from a substrate water supply associated with capillary imbibition (Nakayama and Komatsu, Reference Nakayama and Komatsu2008). In an actual converted field, the complete flooding situation for seeds can be imagined to occur if heavy rain occurs just after seeding. However, just before and after the flooding situation, there should also be a slow, but constant, water supply via soil particles touching the seed surface. In other words, both behaviours, passive and capillary imbibition, could occur in soybean cultivation in a converted field. Therefore, we measured these imbibition rates separately, and evaluated each separately and their combination.
When soybean seeds experienced unhindered imbibition, water was absorbed from the whole seed surface (Ma et al., Reference Ma, Cholewa, Mohamed, Peterson and Gijzen2004), from a fixed specific region (McDonald et al., Reference McDonald, Vertucci and Roos1988; Pietrzak et al., Reference Pietrzak, Fregeau-Reid, Chatson and Blackwell2002), or from a specific region that changed over time (Meyer et al., Reference Meyer, Steudle and Peterson2007). In a preliminary analysis of the imbibition according to every partial region of seed surfaces, a multiple comparison procedure with a Tukey–Kramer's test did not show significant differences among five separate seed surface regions (Fig. 1A) during 0–10 min of flooding for either passive imbibition (P= 0.227 > 0.1, n= 56) or capillary imbibition (P= 0.913 > 0.1, n= 35). Therefore, we concluded that the effect of region-specific imbibition on whole-seed imbibition would not be relevant, and averaged the imbibition measured from separate seed surface regions. Additionally, although we tried to carefully remove abnormal seeds during the first seed sorting, seeds with heterogeneous swelling were often observed under flooding. Probably, seeds with tiny cracks or wounds remained even after careful sorting, and water absorbance would be concentrated in the specific regions under constant water pressure. The methodology for the imbibition measurement that we adopted in the present study included checking for the appearance of a normal seed coat and averaging regional imbibition. These were done so that we might be able to avoid the risk of irregularities from abnormal seed coats.
Thus, we carefully measured two types of imbibition; however, there were no close relationships between the flooding tolerance of soybean seeds and either type of imbibition in our methods and samples. We analysed the balance of two imbibition rates (passive/capillary ratio, which was calculated as the passive imbibition rate at 10–30 min/capillary imbibition rate at 0–10 min). This parameter showed a close relationship with cultivar-specific flooding tolerance (Fig. 5). The soybean cultivars that showed slower capillary imbibition, namely the susceptible Toyomusume and Nakasennari, nevertheless had faster passive imbibition, and therefore had a higher passive/capillary ratio. In contrast, soybean cultivars with a lower passive/capillary ratio were tolerant, i.e. Peking and Suzumaru. In this case, the slower passive imbibition in Peking and the faster capillary imbibition in Suzumaru seemed to lower the passive/capillary ratio (Figs 3, 4 and 5). From these results, we concluded that the reduced flooding injury of soybean seeds might be caused by their ability for capillary water absorbance, and for the restraint of forced water inflow under flooding, and that this complex behaviour was independently affected by the two types of imbibition (Fig. 6C), as reflected in the passive/capillary ratio.
Two seed traits independently affect the two types of imbibition
This study suggested that two different seed traits were independently linked to the two different types of imbibition behaviour. As a result, significant relationships were detected between the hydraulic conductivity of the seed coat and passive imbibition rate, and between the seed osmolarity and capillary imbibition rate (Fig. 6A and B). Furthermore, these two relationships were independent, since passive imbibition rate and seed osmolarity had no relation with capillary imbibition and hydraulic conductivity, respectively (Fig. 6C and D). Considering these two relationships with cultivar-specific traits, we could interpret that Peking, whose seed coat permeability was lower, had slower passive imbibition (Fig. 6A), and that Suzumaru, which had higher osmolarity, absorbed water positively (Fig. 6B). We could also hypothesize that the seed coat had a defensive role as the barrier for imbibition in the former example, and that the rich soluble substances induced the positive water-drawing capacity for imbibition in the latter example. The swelling ratio during moisture treatment was largest in Suzumaru (Table. 2) and must be linked with the high capacity for water influx. Actually, the swelling ratio had a significant positive correlation with the capillary imbibition rate [R 2= 0.6972 (P= 0.0194 < 0.05), n= 7, data not shown].
In general, soluble carbohydrates are thought to be the component mainly affecting the osmolarity of the extract solution from soybean cotyledons. Sucrose accounts for the largest part of the soybean cotyledons as a water-soluble monosaccharide, followed by stachyose and raffinose (Liu, Reference Liu1997). Among the water-soluble polysaccharides in the cell wall of soybean cotyledons are the pectin-like structures, rhamnogalacturonans, with side chains of neutral carbohydrates (Nakamura et al., Reference Nakamura, Furuta, Maeda, Nagamatsu and Yoshimoto2001). Although we did not identify the substances that affected seed osmolarity in this study, the carbohydrates described above might increase the seed osmolarity in some specific soybean cultivars.
An investigation using a pressure chamber reported that the soybean seed coats that were impermeable had five times lower hydraulic conductivity than permeable seed coats (Meyer et al., Reference Meyer, Steudle and Peterson2007). We also measured the hydraulic conductivity of seed coats with a modified pressure chamber method. In the present study, the region of the seed coat for measurement of hydraulic conductivity was limited to the abaxial surface (Fig. 1A, areas 5 and 6), because a flat region 3 mm in diameter was needed to fit the hole-size of the lid of the pressure chamber, and preparation of the disk was difficult for cultivars with smaller seeds, such as Peking and Suzumaru. Thus, the hydraulic conductivity of seed coats was limited to the abaxial surface; however, a close relationship between high conductivity and greater passive imbibition was shown. It is reasonable to assume that when the hydraulic conductivity of the seed coat was lower, passive imbibition was also smaller and, hence, the passive/capillary ratio tended to be lower, and the flooding tolerance became stronger. Clearly, seed coat resistance made water influx slow enough, so that the cotyledons would not break. However, the reason why seeds with a seed coat of high hydraulic conductivity showed a fast passive imbibition rate, remained unclear. Information about the traits of soybean seed coats related to hydraulic conductivity has already been reported. Imbibition induced the seed region of the seed coat not to adhere with the abaxial surface of the cotyledons (Chachalis and Smith, Reference Chachalis and Smith2000; Nakayama and Komatsu, Reference Nakayama and Komatsu2008). In addition, impermeable seed coats had fewer pore- or crack-like structures than permeable seed coats (Yaklich et al., Reference Yaklich, Vigil and Wergin1986; Ma et al., Reference Ma, Cholewa, Mohamed, Peterson and Gijzen2004). It was proposed that the cuticle that formed on the seed coat determined the permeability via the number of cracks (Ranathunge et al., Reference Ranathunge, Shao, Qutob, Gijzen, Peterson and Bernards2010). Thus, seed hardness was influenced by the cuticle (Shao et al., Reference Shao, Meyer, Ma, Peterson and Bernards2007), the hemicelluloses (Mullin and Xu, Reference Mullin and Xu2001) or the phenolics (Zhou et al., Reference Zhou, Sekizaki, Yang, Sawa and Pan2010). On the other hand, it has been suggested that the aleurone layer (Tian et al., Reference Tian, Nakamura and Kokubun2005) or inner layer (Koizumi et al., Reference Koizumi, Kikuchi, Isobe, Ishida, Naito and Kano2008) in the seed coat affected the permeability.
From the present study we conclude that: (1) the cultivar-specific seed flooding tolerance originates from decreasing survival of low-moisture seeds in susceptible cultivars; (2) the decreasing survival after 3 h of flooding is due to the balance of two types of imbibition rate (passive/capillary imbibition rate); (3) the two imbibition rates would be influenced independently by the hydraulic conductivity of the seed coat and by seed osmolarity, respectively. We will investigate in detail the positional relationship between the seed coat and the cotyledons, and the linkage between the structure of the seed coat and hydraulic conductivity. Understanding of the mechanism causing soybean seed flooding injury will be advanced by these basic investigations.
Acknowledgements
Appreciation is extended to the gene bank of the National Institute of Agrobiological Science for providing experimental seeds (user number: 2759); and to Professor J. Abe of the Research Faculty of Agriculture, Hokkaido University for advice on the experimental progress. We also thank Mr S. Ichikawa of the Field Science Centre for the Northern Biosphere, Hokkaido University, for assistance in seed multiplication.
Financial support
This study was supported by a Grant-in-Aid for Scientific Research from the Japan Society for the Promotion of Science (grant number: 24658013).
Conflicts of interest
None.
