Genotypic variation in phosphorus utilisation of soybean [Glycine max (L.) Murr.] grown in various sparingly soluble P sources
C. Tang A D , Y. F. Qiao B , X. Z. Han B and S. J. Zheng CA Department of Agricultural Sciences, La Trobe University, Bundoora (Melbourne), Vic 3086, Australia.
B Northeast Institute of Geography and Agricultural Ecology, Chinese Academy of Sciences, Harbin, China.
C College of Life Sciences, Zhejiang University, Hangzhou 310058, China.
D Corresponding author. Email: c.tang@latrobe.edu.au
Australian Journal of Agricultural Research 58(5) 443-451 https://doi.org/10.1071/AR06280
Submitted: 25 August 2006 Accepted: 12 January 2007 Published: 11 May 2007
Abstract
This study compared the utilisation of sparingly soluble P among soybean genotypes selected from 3 geographical regions with contrasting soil pH. Plants of 5 genotypes from each region were grown for 72 days in soil columns supplied with hydroxyapetite (Ca-P), AlPO4 (Al-P), or FePO4 (Fe-P) at a rate of 25 mg P/kg soil. NaH2PO4 (Na-P) was used as control at the same rate. Shoot weights ranged from 2.4 to 5.9 g/plant. On average, the genotypes selected from calcareous soils of north-west China produced the highest shoot biomass whereas those from neutral soils of the north-east region the least. Root biomass and root surface area followed the same trend. In contrast, the root-to-shoot weight ratio was highest in Fe-P and lowest in Na-P while root length in Na-P and Fe-P was greater than in the other P forms. The genotypes from the north-east region had higher P concentration in the shoot than those from the other 2 regions. Total P uptake ranged from 9.0 to 15.9 mg/plant for Na-P, and from 6.3 to 12.4 for the sparingly soluble P. Average total P uptake was the highest for the genotypes from the north-west region, and was greatest in Na-P and lowest in Fe-P. The genotypes from the north-east region displayed the greatest ability to use sparingly soluble P, and those from the north-west the least relative to Na-P. Total P uptake from the sparingly soluble P correlated highly with plant biomass production, N2 fixation and nodulation, and seed P, while the relative P uptake correlated highly with P concentration in shoots but neither correlated with root carboxylate release nor leachate pH. The results suggest that there is a substantial genotypic variation in utilisation of sparingly soluble P, which is related to early vigour, nodulation, and seed P reserve but not to origin site pH or root exudation.
Additional keywords: breeding, local variety, organic acids, P deficiency, phosphorus acquisition, rhizosphere pH, root exudates, selection site pH.
Acknowledgment
We thank Prof. G. X. Pan for soil classification, and Chinese Academy of Sciences (KSCX2-YW-N-002) and Natural Science Foundation of China (30671217) for financial support.
Ding H, Li SX
(1997) Genotypic differences of phosphorus accumulation and utilization efficiency between soybean varieties. Chinese Journal of Oil Crops 19, 52–54.
Ding H, Li SX
(1998) Genetic differences in tolerance to low phosphorus and response to phosphorus fertilizer for soybean varieties. Journal of Plant Nutrition and Fertilizers 4, 257–263.
Fredeen AL,
Madhusudana Rao I, Terry N
(1989) Influence of phosphorus nutrition on growth and carbon partitioning in Glycine max. Plant Physiology 89, 225–230.
| PubMed |
Hinsinger P,
Plassard C,
Tang C, Jaillard B
(2003) Origins of root-mediated pH changes in the rhizosphere and their responses to environmental constraints — a review. Plant and Soil 248, 43–59.
| Crossref | GoogleScholarGoogle Scholar |
Nian H,
Ahn SJ,
Yang ZM, Matsumoto H
(2003) Effect of phosphorus deficiency on aluminium-induced citrate exudation in soybean (Glycine max). Physiologia Plantarum 117, 229–236.
| Crossref | GoogleScholarGoogle Scholar |
Ohwaki Y, Hirata H
(1992) Differences in carboxylic acid exudation among P-starved leguminous crops in relation to carboxylic acid contents in plant tissues and phospholipid level in roots. Soil Science and Plant Nutrition 38, 235–243.
Raghothama KG
(1999) Phosphate acquisition. Annual Review of Plant Physiology and Molecular Biology 50, 665–693.
| Crossref | GoogleScholarGoogle Scholar |
Sas L,
Rengel Z, Tang C
(2001) Root morphology, excess cation uptake, and extrusion of proton and organic acid anions in Lupinus albus L. under phosphorus deficiency. Plant Science 160, 1191–1198.
| Crossref | GoogleScholarGoogle Scholar | PubMed |
Shane MW, Lambers H
(2005) Cluster roots: a curiosity in context. Plant and Soil 274, 101–125.
| Crossref | GoogleScholarGoogle Scholar |
Shen J,
Rengel Z,
Tang C, Zhang FS
(2003) Role of phosphorus nutrition in development of cluster roots and release of carboxylates in soil-grown Lupinus albus. Plant and Soil 248, 109–206.
| Crossref | GoogleScholarGoogle Scholar |
Song C,
Han XZ, Tang C
(2007) Changes in phosphorus fractions, sorption and release in Unic Mollisols under different ecosystems. Biology and Fertility of Soils (In press) ,
Tang C,
Fang RY, Raphael C
(1998) Factors affecting soil acidification under legumes: II. Effect of phosphorus supply. Australian Journal of Agricultural Research 49, 657–664.
| Crossref | GoogleScholarGoogle Scholar |
Thomson BD,
Bell RW, Bolland MDA
(1992) Low seed phosphorus concentration depresses early growth and nodulation of narrow-leafed lupin (Lupinus angustifolius cv. Gungurru). Journal of Plant Nutrition 15, 1193–1214.
Tong XJ,
Yan X,
Lu YG,
Nian H, Zheng SL
(1999) Study on characteristics of phosphorus efficiency of soybean native germplasm in Guangdong Province: 1. Differences of soybean genotypes in characteristics of phosphorus efficiency and relationship between phosphorus efficiency and content of soil availability phosphorus. Acta Pedologica Sinica 36, 404–412.
Watt M, Evans JR
(2003) Phosphorus acquisition from soil by white lupin (Lupinus albus L.) and soybean (Glycine max L.), species with contrasting root development. Plant and Soil 248, 271–283.
| Crossref | GoogleScholarGoogle Scholar |
Yan F,
Zhu Y,
Müller C,
Zörb C, Schubert S
(2002) Adaptation of H+-pumping and plasma membrane H+ ATPase activity in proteoid roots of white lupin under phosphate deficiency. Plant Physiology 129, 50–63.
| Crossref | GoogleScholarGoogle Scholar | PubMed |
Yang ZM,
Sivaguru M,
Horst WJ, Matsumoto H
(2000) Aluminum toleranceis achieved by exudation of citric acid from roots of soybean (Glycine max). Physiologia Plantarum 110, 72–77.
| Crossref | GoogleScholarGoogle Scholar |