Research Article

Influence of NaCl and NaHCO3 upon Salix Sungkianica Seed Germination and Seedling Growth  

Shurong Ma , Qian Lu , Meijiao Zhang , Shenkui Liu
Alkali Soil Natural Environmental Science Center (ASNESC), Stress Molecular Biology Laboratory, Northeast Forestry University, Harbin, 150040, P.R. China
Author    Correspondence author
Molecular Soil Biology, 2015, Vol. 6, No. 2   doi: 10.5376/msb.2015.06.0002
Received: 13 Jan., 2015    Accepted: 20 Jan., 2015    Published: 23 Mar., 2015
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This is an open access article published under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Preferred citation for this article:

Ma et al., 2015, Influence of NaCl and NaHCO3 upon Salix Sungkianica Seed Germination and Seedling Growth, Molecular Soil Biology, 6(2): 1-6 (doi: 10.5376/msb.2015.06.0002)

Abstract

The present study used the seeds and newborn seedings of Salix sungkianica as material, examining the influence of NaCl and NaHCO3 solutions of different concentrations on the seed germination and anatomical structure of the roots and lamina of the seedings. The results indicate such facts: (1) The presents of NaCl and NaHCO3 have a depressant effect on the seed germination, while a light concentration of NaHCO3 could accelerate the sprout. (2) S.sungkianica seedings show strong endurance under the stress of 50 mmon/L NaCl and 10 mmon/L NaHCO3 solutions, the seedings growth are better in 10 mmon/L NaHCO3. (3) Under the stress of such solutions of high concentration, certain degrees of endurance also present in the roots and lamina, with the anatomical results like the thicken of root endodermis, the enlargement of vascular bundle in diameter, the vanish of aerenchyma tissures and the closure of lamina stoma.

Keywords
Salix sungkianica; Saline–alkali stress; Seed germination; Seeding growth; Anatomical structure

Salix sungkianica is a species of Salicaceae Salix deciduous shrub. It is native only to China, where it occurs throughout the country`s northern provinces like Heilongjiang. A sun species which usually inhabit in moisture environment like wet sand of the river bank. The plant primarily reproduction modes are through seed and cuttaging. The tree has a soft texture, a gentle and slender branch, which could be used as weaving material. A graceful tree form and strong resistance make it suitable for landscaping (Zhang, 2009). It`s deep-rootness and flood enduring character makes it the optimized species for dyke strengthening and bank protection (Cao et al., 2013). In all, S. sungkianica has a excellent application prospect.

Salix linearistipularis is among the few ligneous plants originally inhibited in the saline-alkali soil (SAL) of Songnen plain (Liu, 2006). Therefore, it proces a high degree of saline-alkaline tolerance. Whether S. sungkianica as a sibling species of S. linearistipularis, also process some degrees of tolerance towards SAL and, whether it coult be planted in such an environment are still unknown. To answer such questions, this study used S. sungkianica seeds and newborn seedings as material, by simulating natural conditions, to investigate the stress effects of NaCl and NaHCO3 upon seed germination and the structure of lamina and roots of newborn seedings and; to examine the germination capacity, the growth of seedings and the structural changes of S. sungkianica roots and lamina in adverse situation like SAL. Therefore, to dertermine the adaptability of S. sungkianica towards SAL. The research itself will generate a theoretical significance on the development and utilization of wild S. sungkianica resources and, ecologically speaking, contribute to the enrichment of plant population in SAL.

1 Result and Discussion
1.1 Influence of NaCl on germination of S. sungkianica seeds and sapling structure

1.1.1 Influence of NaCl on the germination of S. sungkianica seeds
The germination rate and potential, germination index (GI), vital index (VI) and seeding length of S. sungkianica seeds are on the declining curve as the concentration of NaCl rise, due to the stress effects (Table 1A ) low concentration of NaCl suppress seed germination. The germination rate was 55.50±2.81% when NaCl=50 mmol/L, far lower than the control group (0 mmol/L, 77.00±2.12%) (P<0.01), the same with other indicators. And, germination happened on the second day when NaCl≤200 mmol/L; the third day when NaCl=250 mmol/L at a rate of 7.00±0.12%, with no growth of radicle though the cotyledon were unfolded. It is thus clear that the present of NaCl will significantly postpone seed germination and suppress the growth of sapling. Linear regression analysis was adopted to analyze the different NaCl concentrationsand relative germination rates. The linear regression equation is y=-0.319x+94.174, R2=0.974. The salt-tolerance limit, semi-lethal salt concentration, and salt concentration of S. sungkianica seeds are 216.84, 138.47, and 60.11 mmol/L, respectively. Most seeds treated with NaCl had gone dark-brown. In the re-germination test, those which colorhad changed showed no sign of re-germination while the unchanged ones did. And the re-germination rate dropped as the concentration rose. Therefore a deduction can be made that the stress effects of NaCl could be the combination of infiltration effect and ion effect (Andre et al., 2014; Zeng et al., 2006). 
 


Table 1 Effect of NaCl on the growth of the seedlings of S. sungkianica

 

1.1.2 Influence of NaCl upon anatomical structure of S. sungkianica root
Root plays a significant role in the vegetation process of plants. When the environmental condition becomes worse, the external form and internal structure would be modified to accommodate the change (Wang et al., 1997). Figure 1A shows the anatomical structure of S. sungkianica root. From out to core, the cross section is divided by epidermis, cortex and vascular bundle. The cortex contains exodermis, cortex, parenchymatous tissue and endodermis. The exodermis contains one or two layers of tightly aligned parenchymal cell. When the epidermis is destroyed, the exodermis become the defensive tissue, then the cortex and so on. Parenchymal cell is small and less regular shaped, some of them go rupture and becomes the aerenchyma, which is a peculiar structure of hydrophyte and hygrophyte. The S. sungkianica, which always grow along the river or in wetland, also process the aerenchyma. In recent years, research on halophyte has gaining some progress. Plants grow on saline-alkali land have difficulty in obtaining oxygen from the hardening soil, which also happens on hydrophyte and hygrophyte. To counter this adversity, the parenchymal cell go rupture, or separate from middle lamella, and the intercellular space among the biggish cell becomes connected, thus a clear aerenchyma comes into shape which ensures a normal respiratory metabolism (Werner et al., 1990; Wang, 2008). Therefore the S. sungkianica process a degree of salt-resistance. Endodermis contains several layers of small parenchymal cells. Vascular bundle includes primary xylem and primary phloem. When NaCl=50 mmon/L (Figure 1B), no significant difference is observed compare with the control group, the root maintains it's structure integrity with no obvious injury, only the endodermis has the tendency to intensified. Hence the S. sungkianica illustrates a strong salt-resistance when the concentration of NaCl is below 50 mmol/L. When NaCl=100 mmon/L (Figure 1C), the epidermis and exodermis vanished and the parenchymal cell of the cortex becomes the protective tissue. Together with the disappear of aerenchyma, a intensification of endodermis through the thickening of radial wall and inner-tangential wall of endodermis cells. Since the mould solute is absorbed by the root and transformed crosswise into the vessels in stele then the overground part.This structure will prevent toxic and pernicious ions into the plants, thus alleviate the harmful effects enforced by the salt-contained soil (Poppet et al., 1993). 
 

 
Figure 1 The effect of different concentrations of NaCl stress on root structure of S. sungkianica ×40

 

1.1.3 Influence of NaCl upon anatomical structure of seeding lamina
Lamina is the place where photosynthesis and respiration happens, and the morphosis of lamina will be altered under salt or alkali environments (Bai et al., 2013). Figure 2A shows the anatomical structure of S. sungkianica lamina of the control group, of which includes the upper epidermis, mesophyll tissue, lower epidermis, with no epidermal hair but covered with cuticle. The epidermis are made by monolayer cell, with most of its stomata open and concentrate in a particular area. The number of stoma is highly related with the conduction of water and air, and have an effect on photosynthesis and respiration. When the environment is suitable, the high density of stoma is good for photosynthesis; when the concentration of salt or alkali increase, some of the stomata closed in order to prevent water from over evaporation (Yang et al., 2011). After one month of growth, the mesophyll tissue (palisade and spongy parenchym) of the seedings have not completed it’s differentiation. When NaCl=50 mmol/L (Figure 2B), the lamina cells line up accordingly, and show a deepen of its color when dying with fast green, which means the cell walls have been thickened, the same goes with the control group (Wang, 2008). That all indicate a low concentration of NaCl presents no significant influence on lamina growth. When NaCl=100 mmol/L (Figure 2C), the structure of blade is damaged, with no clear vision of mesophyll cell and a shrinkage of upper and lower epidermis cell; but resistance like the thicken of cuticle is well observed, which reduce water evaporation as well as providing structural support when the blade is dehydrated and wilting; and most of the stomata are closed to prevent water from over-evaporation (Yang et al., 2011). 
 

 
Figure 2 The effect of different concentrations of NaCl stress on leaf structure of S. sungkianica ×40

 

1.2 Influence of NaHCO3 upon S. sungkianica seeds germination and seeding growth
1.2.1 Influence of NaHCO3 upon seed germination
All S. sungkianica seeds germinated on the second day regardless the difference of NaHCO3 concentration, which means the initial germination has no relation with it.For most plant species, seed germination rate is highest when it happens in pure water; and drops with the increase of NaHCO3. In a low NaHCO3 environment, however, some alkali-resistant seeds show a higher germination rate than they are in pure water (Zeng et al., 2014; A.El-Keblawy et al., 2005). Table 2 shows the S. sungkianica germination rate first rises then falls with the increase of NaHCO3, when NaHCO3=10 mmol/L, the number is 80.50± 3.14%, which is higher than the control group (0 mmol/L, 77.00±2.12%), and shows no signs of significant differences (P>0.05). Other indexes like seeding length, germination potential, GI and VI all reach their highest points when NaHCO3 =10 mmol/L, while the numbers are much lower in the control group (P<0.01). When NaHCO3=30 mmol/L, the germination rate, thus 62.50 ± 1.99%, much lower than the control group; nonetheless, the rate was still as high as 18.00±0.83% when NaHCO3=50 mmol/L. The linear regression equation is y=-1.298x+113.159, R2=0.954, The alkali-tolerance limit, semi-lethal alkali concentration, and alkali concentration of S. sungkianica seeds are 67.92, 48.66, and 29.39 mmol/L, respectively. In the re-germination experiment, which all the un-germinated seeds were put into pure water, result shows that seeds under stress treatment mostly turn dark-brown and lose its germination ability; those color remain unchanged, however, can re-germinate. And the rate of dark-brown seed rose with the increase of NaHCO3 concentration. 
 

 
Table 2 Effect of NaHCO3 on the growth of the seedlings of S. sungkianica

 

1.2.2 Influence of NaHCO3 upon anatomical structure of seeding roots
Figure 3A is the anatomical structure of S. sungkianica root. From out to core, the cross section is divided by epidermis, cortex and vascular bundle, with the presence of aerenchyma. The S. sungkianica showed a strong resistance when NaHCO3 = 10 mmol/L (Figure 3B), the anatomical structure is still intact, with no significant differences with that of the control group. When NaHCO3=30 mmol/L (Figure 3C), the epidermis and exodermis all disappear while the parenchymatous become the protective tissue, and the aerenchyma is also disappear; the radial and tangential walls of the cortical cell show a tendency of thicken, as for vascular bundle, the number of vessels in primary xylem decrease but enlarged in diameter, which is good for the water transportation and the physiological metabolism of plants (Wang, 2012).
 

 

Figure 3 The effect of different concentrations of NaHCO3 stress on root structure of S. sungkianica ×40

 

1.2.3 Influence of NaHCO3 upon the anatomical structure of seeding lamina
Figure 4A shows the anatomical structure of S. sungkianica lamina of the control group, of which includes upper epidermis, mesophyll tissue and lower epidermis, with no epidermal hair but covered with cuticle. When NaHCO3=10 mmol/L (Figure 4B), compare to control group, the lamina structure remains intact, lamina and both upper and lower epidermis cells are thickened, which means the lamina grew better in this condition (Werner et al., 1990); when NaHCO3 = 30 mmol/L (Figure 4C), both upper and lower epidermis cells become shrunk and the mesophyll cells are damaged, while most stomas are closed and section condition, it shows that concentration of NaHCO3 presents significant wreck influence on lamina structure.In conclusion, S. sungkianica seeds process a certain degree of salt-alkali resistance; when the concentration of NaCl is below 50 mmon/L or, NaHCO3 under 10 mmon/L, the saplings are highly adaptable and a low concentration of NaHCO3 could accelerate seeds germination and seedings development; under the suppress of a high concentration of salt or alkali, the anatomic results show that the roots and lamina of S. sungkianica all present a certain degree of resistance. Hence the thought of using S. sungkianica as reproducing tress species on salt-alkali soil is reasonable, of which should take full advantage of wild S. sungkianica resources and improves the quality of salt-alkali soil.
 

 
Figure 4 The effect of different concentrations of NaHCO3 stress on leaf structure of S. sungkianica ×40

 

2 Materials and methods
2.1 Acquisition and preservation of seeds

The S. sungkianica seeds were collected in late May, 2013, from S. sungkianica trees along the bank of Songhuajiang river of Harbin city. Only the most voluptuous and non-verminous were selected and preserved in -80 degree for further test.

2.2 Seed germination test
NaCl concentration was set at 0, 50, 100, 150, 200, and 250 mmol/L, and NaHCO3 concentration was divided into six gradients, namely, 0, 10, 20, 30, 40, and 50 mmol/L.Put 50 seeds from each of these concentrations on a culture dish, which is 10cm in diameter and filled only with 0.8% of agar. All the dishes were placed in the ZPQ-400 intelligent climatron.The illumination time was set as 12 h/d, intensity 5 grade, humidity 19-23 % and temperature 25℃. Four dishes were prepared for each concentration. A seed was germinated when 1mm of the radicle was observed breaking out of seed coat. Phenomena was recorded every day. All stress treatments were removed on the fourth day when 20 saplings were randomly selected from each dishes for the measuring and calculating of their length, raw weight, germination rate (%), germination potential (%), germination index (GI), vital index (VI) and salt-resistance. Non-germinating seeds were placed in a container with distilled water and subjected to germination experiment, and germinative number was then recorded (Guan et al., 2009).

2.3 Seeding cultivation
Based on the experiments of seed germination, the seeding cultivation test was conducted in five groups, the control group 0 (CK), two groups with NaCl was 50 and 100 mmon/L, and another two groups which contend 10 and 30 mmon/L NaHCO3 .Each plant pot was filled with a mixture of compost and vermiculite (1:1), the seedings were planted uniformly and covered with a thin layer of soil, while all pots were covered with plastic wrap to prevent water from over-evaporation. Then each pot was irrigated at fixed intervals with specific treating fluid, maintaining the soil`s water content at 100%. Each group with six samples. After 30 days, the seedings were picked up and cleaned, then treated with FAA stationary liquid for 48h for the final preparation of paraffin section.

2.4 Anatomical observation of root and lamina     
The samples were made from taproot and central lamina, paraffin section were prepared with general method, staining with sarranine-fast green (counter-dying). All sections were observed with Olympus optical microscope (BX41) and photoed by camera (Wang et al., 2010).

2.5 Data analysis method
All data were plotted and analyzed with Excel 2003, significance of difference and correlation analysis are examined with SPSS 19.0. If analysis of variance was significance, then doing multiple comparative studies via Duncan method and equation of linear regression (Yan et al., 2013).

 

Acknowledgments

This work was supported by the Special Fund for Forest Scientific Research in the Public Welfare (201404220), Program for Changjiang Scholars and Innovative Research Team in University (IRT13053), and National High Technology Research and Development Program (863 Project, 2013AA102701-7).

 
Reference
Andre S., Efisio M., and Luca F., 2014, Light temperature dry after-ripening and salt stress effects on seed germination of Phleum sardoum (Hackel) Hackel, Plant Species Biology, 29: 300-305
http://dx.doi.org/10.1111/1442-1984.12018

Bai X., Li Y., Shu S.P., and Zhao X.X., 2013, Response of leaf anatomical characteristics of Nitraria tangutorum Bobr. from different populations to habitats, Northwest Plant, 33(10): 1986-1993
Cao W., and Wu Y.Y., 2013, State key laboratory of forest and soil ecology, Institute of Applied Ecology, 24(2): 326-330

El-Keblawy A., and Al-Rawai A., 2005, Effects of salinity temperature and light on germination of invasive Prosopis juliflora (Sw.) D.C., Journal of Arid Environments, 61: 555-565
http://dx.doi.org/10.1016/j.jaridenv.2004.10.007

Guan B., Zhou D., Zhang H., Tian Y., Japhet W., and Wang P., 2009, Germination responses of Medicago ruthenica seeds to salinity, alkalinity, and temperature, Journal of Arid Environments, 73: 135-138
Guan F.C., Liang Z.W., and Huang L.H., 2009, Principle of agro-biological management and countermeasure of agricultural industrialization on saline-alkalized land in western Songnen Plain, Research of Agricultural Modernization, 30: 85-89
http://dx.doi.org/10.1016/j.jaridenv.2008.08.009

Li Y.H., 2005, Botany, The Second Press, Shanghai Science and Technology Press, Shanghai, China
Liu S.K., 2006, Saline plant in northeast China primaries illustrations, Northeast Forestry University Press, Harbin, China

Poppet et al., 1993, Physiological adaption to different salinity levels in mangroves, Toward the rational of high salinity tolerance plant, Plant and Soil, 148(1):217-224

Wang B.S., Zhao K.F., and Zou Q.,1997, Advances in crop salt tolerance mechanism and measures to improve crop salt resistance, Bulletin of Botany, 14(suppl): 25-30

Wang X.L., and Ma J., 2010, A study on leaf-structure and the diversity of xerophytes ecology adaption, Acta Ecologica Sinica, 19(6): 787-792

Wang Y., 2012, Contrasts and observations of dissecting construction of three drought-resistant plant leaf slices, Sichuan Forest Science, 24(1): 64-67

Wang Z.W., 2008, Study of comparing about evolved structure between Populusx canadensis Moench. and Salix matsudana Koidz. under salt and mesophytic environment, Northeast Normal University, Jilin, China

Werner A., and Stezer R., 1990, Physiological response of the mangrove Rhizophora mangle growth in the absence and presence of NaCl, Plant Cell and Environ, 13: 243-225
http://dx.doi.org/10.1111/j.1365-3040.1990.tb01309.x

Yang Z.P., Liu Q., and Li Z.J., 2011, Leaf blade comparative anatomy between the female and the male of Populus euphratica Oliv., Northwest Plant, 31(1): 79-83

Zeng Y.J., Wang Y.R., Baskin C.C., and Baskin J.M., 2014, Testing seed germination responses to water and salinity stresses to gain insight on suitable micro habitats for restoration of cold desert shrubs, Journal of Arid Environments, 100-101: 89-92
http://dx.doi.org/10.1016/j.jaridenv.2013.10.010

Zeng Y.L., Cai Z.Z., Ma J., Zhang F.C., and Wang B., 2006, Effects of salt and water stress on seed germination of halophytes Kalidium foliatum and Halostachys caspica, Chinese Journal of Ecology, 25: 1014-1018

Zhang J.L., 2009, Study on the plant landscape of sunny island, Northeast Forestry University, Heilongjiang, China

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