Growth enhancement of the highly prized tropical trees siamese rosewood and burma padauk
Introduction
The Fabaceae or Leguminosae, the family name of legumes, peas, and beans, is a large family of flowering plants having an economical and medicinal importance (Kuete et al., 2013), especially Dalbergia cochinchinensis (Siamese rosewood) and Pterocarpus indicus (Burma padauk). They are high-priced not only due to its beautifully-patterned wood, but also due to being the second conservation plant for Convention on International Trade in Endangered Species of Wild Fauna and Flora (CITES), found in the Indochina region. Because of being a commercially-valuable resource, these plants have been often illegally cut in Thailand for international trading purposes. The Royal Forest Department, Ministry of Natural Resources and Environment in Thailand, therefore, promote seedlings production by building a plantation forest to conserve genetic resources in degraded forest areas. However, plant seedlings grow quite slowly with low survival rate (Choosa-nga et al., 2017). The research on how to improve growth and survival rates of leguminosae seedlings has been extensively of interest.
Arbuscular mycorrhizal fungi (AMF) belonging to the Division Glomeromycotina (Sparafora et al., 2016) are symbiotic fungi that colonize in plant roots more than 80% of land plants (Boonlue et al., 2012). AMF symbiosis can be found in nearly all types of ecosystems and can be formed naturally by most plant species. It has beneficial effects on nutrient uptake, phosphorus (P), nitrogen (N), potassium (K), and micronutrients that help promote plant growth (Jeffries 1987). AMF can also help the plants to grow under unfavorable environmental conditions, such as arid conditions and prevent plant diseases in the root system. Mycorrhiza helper bacteria (MHB) are a group of organisms that form symbiotic associations specifically with the mycorrhiza, such as ectomycorrhiza and arbuscular mycorrhiza (Frey-Klett et al., 2007), but not with the plants (Rigamonte and Pylro 2010). Helper bacteria can enhance mycorrhizal functions, increase mycorrhizal growth, and improving phosphorus uptake to the plant (Visen et al., 2017). However, the bacterial diversity was found that closely related to soil phosphorus solubilizing, while pH, and potassium had an inverse correlation with bacterial diversity, which the Bacillus, Paenibacillus, Burkholderia, Pseudomonas, Acinetobacter, Agrobacterium and Stenotrophomonas are the main genera (Zhao et al., 2013; Altinkaynak and Ozkoc, 2020; Leal de Castilh et al., 2020) of plant growth-promoting helper bacteria. If mycorrhizal formation could be enhanced by co-inoculation with mycorrhizal helper bacteria (MHB) which promote rapid root colonization by specific mycorrhizal fungi, this would be of advantage to the popular forest industry (Zhao et al., 2013).
Furthermore, the AMF has effects on seedlings survival and growth under nursery conditions (Guissou et al., 2016), which healthy seedlings in the nursery raised are prerequisites. Because of the transplantation in natural fields, there are many factors that could make trees become weaker and die. In addition, various plant species have been reported on the relationship between their growth and the presence of AMF, while there is still no report on the co-inoculation of AMF together with MHB to promote the growth of siamese rosewood and burma padauk. The co-inoculation of AMF and MHB should be able to promote growth and enrich biomass of plants. Therefore, this study aims to evaluate the effects of AMF and MHB in promoting growth and biomass of the Leguminosae seedlings under pot trial.
Section snippets
Isolation of arbuscular mycorrhizal fungi
The AMF were collected from rhizosphere soils surrounding root of the burma padauk plant in the forest surrounding Chulabhorn Dam, Chaiyaphum province, Thailand. The AMF spores were separated by wet-sieving of different sizes i.e. 250 μm, 125 μm and 90 μm were used. Fifty grams of soil sample was thoroughly mixed in 500 mL water in a beaker and was allowed to settle. The sieves were placed in the following order 250 μm, 125 μm and 90 μm from top to bottom. The water in the beaker was decanted
Results
Two dominant species of AMF isolates named KKU−CLD−1 and PC2−2 were found in this study. The MHB was isolated from the spore of AMF dominant species. The 2 isolates of MHB which were KKU−CLD−1.1–3−1 and KKU−CLD−2.3–1–2 were obtained from AMF isolate KKU−CLD−1, while the 4 isolates of MHB which were KKU−CLD−4.1–3−3, KKU−CLD−4.1–1−1, KKU−CLD−4.3–1–2, and KKU−CLD−4.3–3−1 were obtained from AMF isolate PC2−2.
In order to screen for MHB strains showing high phosphate-solubilizing activity, 6 MHB
Discussion
The 2 AMF isolates were identified based on their morphology and molecular approach using 18S rDNA, ITS rDNA and partial 28S rDNA genes. The results showed that the sequences of isolate KKU−CLD−1 were 99% identical to the sequences of Glomus clarum (Accession No. FM865543.1), while the sequences of isolate PC2−2 were 95% identical to the sequences of Glomus proliferum (Accession No. FM992402.1). Therefore, AMF isolates KKU−CLD−1 and PC2−2 were named Glomus clarum KKU−CLD−1 and Glomus proliferum
Conclusions
This work presented the beneficial effects of AMF and MHB on the growth and biomass of siamese rosewood and burma padauk, which are economically important especially in Thailand. The co-inoculation of A. mellea KKU−NBP−SB−2 and S. maltophilia KKU−CLD−4.3–3−1 had significant effects on the growth and phosphorus uptake compared to other treatments. The co-inoculation of G. proliferum PC2−2 and S. maltophilia KKU−CLD−4.3–3−1 also had an effect on biomass in both plants. This is due to the positive
Declaration of competing interest
The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.
Acknowledgements
This study was funded by the Plant Genetic Conservation Project under The Royal Initiative of Her Royal Highness Princess Maha Chakri Sirindhorn, Khon Kaen University (FY 61002018, FY 62000120013). We would like to thank the Electricity Generating Authority of Thailand (EGAT) for field support and the Salt-tolerant Rice Research Group, and the Microbial Resources and Applications group at Faculty of Science, Khon Kaen University, Thailand for partial financial support.
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