Cited by 344Plant nutrient uptake and metabolismPlant Micronutrient Interactions and EffectsPlant Molecular Biology Research

The DOI matches its Crossref record; 307 of the 307 references it cites were found in a registry or an index.

Comparative physiology of elemental distributions in plants

Open access

Conn, Simon, Gilliham, Matthew·2010·Annals of Botany

DOI 10.1093/aob/mcq027PMC PMC2887064

Open this paper in CoChat — free account Open PDF

Abstract

BACKGROUND: Plants contain relatively few cell types, each contributing a specialized role in shaping plant function. With respect to plant nutrition, different cell types accumulate certain elements in varying amounts within their storage vacuole. The role and mechanisms underlying cell-specific distribution of elements in plants is poorly understood. SCOPE: The phenomenon of cell-specific elemental accumulation has been briefly reviewed previously, but recent technological advances with the potential to probe mechanisms underlying elemental compartmentation have warranted an updated evaluation. We have taken this opportunity to catalogue many of the studies, and techniques used for, recording cell-specific compartmentation of particular elements. More importantly, we use three case-study elements (Ca, Cd and Na) to highlight the basis of such phenomena in terms of their physiological implications and underpinning mechanisms; we also link such distributions to the expression of known ion or solute transporters. CONCLUSIONS: Element accumulation patterns are clearly defined by expression of key ion or solute transporters. Although the location of element accumulation is fairly robust, alterations in expression of certain solute transporters, through genetic modifications or by growth under stress, result in perturbations to these patterns. However, redundancy or induced pleiotropic expression effects may complicate attempts to characterize the pathways that lead to cell-specific elemental distribution. Accumulation of one element often has consequences on the accumulation of others, which seems to be driven largely to maintain vacuolar and cytoplasmic osmolarity and charge balance, and also serves as a detoxification mechanism. Altered cell-specific transcriptomics can be shown, in part, to explain some of this compensation.

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

Integrity signals

Registry

Crossref · 10.1093/aob/mcq027

Cites

307 of 307 references verified0 citation errors · 0 not checkable

Statistics

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Mineral Nutrition of Higher Plants
(1995) · Elsevier eBooks · doi:10.1016/b978-0-12-473542-2.x5000-7 · Cited by 19,895
Mechanisms of Salinity Tolerance
Munns, R., & Tester, M. (2008) · Annual Review of Plant Biology · doi:10.1146/annurev.arplant.59.032607.092911 · Cited by 13,792
Na+ Tolerance and Na+ Transport in Higher Plants
Tester, M. A. (2003) · Annals of Botany · doi:10.1093/aob/mcg058 · Cited by 3,312
Cellular mechanisms for heavy metal detoxification and tolerance
Hall, J. L. (2002) · Journal of Experimental Botany · doi:10.1093/jexbot/53.366.1 · Cited by 2,968
Salinity tolerance in halophytes*
Flowers, T. J., & Colmer, T. D. (2008) · New Phytologist · doi:10.1111/j.1469-8137.2008.02531.x · Cited by 2,789
Visualizing secretion and synaptic transmission with pH-sensitive green fluorescent proteins
Miesenböck, G., Angelis, D. A. D., & Rothman, J. E. (1998) · Nature · doi:10.1038/28190 · Cited by 2,569
An “Electronic Fluorescent Pictograph” Browser for Exploring and Analyzing Large-Scale Biological Data Sets
Winter, D., Vinegar, B., Nahal-Bose, H. K., Ammar, R., Wilson, G., & Provart, N. J. (2007) · PLoS ONE · doi:10.1371/journal.pone.0000718 · Cited by 2,564
Calcium in Plants
White, P. J. (2003) · Annals of Botany · doi:10.1093/aob/mcg164 · Cited by 2,487
Biofortification of crops with seven mineral elements often lacking in human diets – iron, zinc, copper, calcium, magnesium, selenium and iodine
White, P. J., & Broadley, M. R. (2009) · New Phytologist · doi:10.1111/j.1469-8137.2008.02738.x · Cited by 2,178
Toxic metal accumulation, responses to exposure and mechanisms of tolerance in plants
Clemens, S. (2006) · Biochimie · doi:10.1016/j.biochi.2006.07.003 · Cited by 2,098
The Mechanism of Salt Tolerance in Halophytes
Flowers, T. J., Troke, P. F., & Yeo, A. R. (1977) · Annual Review of Plant Physiology · doi:10.1146/annurev.pp.28.060177.000513 · Cited by 1,942
Control of Stochasticity in Eukaryotic Gene Expression
Raser, J. M., & O'Shea, E. K. (2004) · Science · doi:10.1126/science.1098641 · Cited by 1,425
Molecular mechanisms of plant metal tolerance and homeostasis
Clemens, S. (2001) · Planta · doi:10.1007/s004250000458 · Cited by 1,417
CALCIUM OXALATE IN PLANTS: Formation and Function
Franceschi, V. R., & Nakata, P. A. (2005) · Annual Review of Plant Biology · doi:10.1146/annurev.arplant.56.032604.144106 · Cited by 1,304
The Putative Plasma Membrane Na + /H + Antiporter SOS1 Controls Long-Distance Na + Transport in Plants
Shi, H., Quintero, F. J., Pardo, J. M., & Zhu, J. (2002) · The Plant Cell · doi:10.1105/tpc.010371 · Cited by 1,295
Potassium transport and plant salt tolerance
Shabala, S. N., & Cuin, T. A. (2008) · Physiologia Plantarum · doi:10.1111/j.1399-3054.2007.01008.x · Cited by 1,266
A Gene Expression Map of the Arabidopsis Root
Birnbaum, K. D., Shasha, D. E., Wang, J. Y., Jung, J. W., Lambert, G. M., Galbraith, D. W., & Benfey, P. N. (2003) · Science · doi:10.1126/science.1090022 · Cited by 1,260
Phylogenetic Relationships within Cation Transporter Families of Arabidopsis
Mäser, P., Thomine, S., Schroeder, J. I., Ward, J. M., Hirschi, K. D., Sze, H., Talke, I. N., Anna Amtmann, A., Maathuis, F. J. M., Sanders, D., et al. (2001) · PLANT PHYSIOLOGY · doi:10.1104/pp.126.4.1646 · Cited by 1,257
Calcium at the Crossroads of Signaling
Sanders, D., Pelloux, J., Brownlee, C., & Harper, J. F. (2002) · The Plant Cell · doi:10.1105/tpc.002899 · Cited by 1,217
The ZIP family of metal transporters
Guerinot, M. L. (2000) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/s0005-2736(00)00138-3 · Cited by 1,200
Plant roots. The hidden half
Barlow, P. W., & Phil, D.-C. N. (1992) · Environmental and Experimental Botany · doi:10.1016/0098-8472(92)90065-a · Cited by 1,132
Transgenic salt-tolerant tomato plants accumulate salt in foliage but not in fruit
Zhang, H., & Blumwald, E. (2001) · Nature Biotechnology · doi:10.1038/90824 · Cited by 1,123
Calcium and Plant Development
Hepler, P. K., & Wayne, R. (1985) · Annual Review of Plant Physiology and Plant Molecular Biology · doi:10.1146/annurev.pp.36.060185.002145 · Cited by 985
Overexpression of a plasma membrane Na+/H+ antiporter gene improves salt tolerance in Arabidopsis thaliana
Shi, H., Lee, B., Wu, S.-J., & Zhu, J. (2002) · Nature Biotechnology · doi:10.1038/nbt766 · Cited by 949
Metals and micronutrients – food safety issues
McLaughlin, M. J., Parker, D. R., & Clarke, J. M. (1999) · Field Crops Research · doi:10.1016/s0378-4290(98)00137-3 · Cited by 938
Cadmium and iron transport by members of a plant metal transporter family in Arabidopsis with homology to Nramp genes
Thomine, S., Wang, R., Ward, J. M., Crawford, N. M., & Schroeder, J. I. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.97.9.4991 · Cited by 932
The biochemistry of environmental heavy metal uptake by plants: implications for the food chain.
Peralta-Videa, J. R., Lopez, M. L., Narayan, M., Saupe, G., & Gardea-Torresdey, J. (2009) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2009.03.005 · Cited by 926
Dynamic and quantitative Ca 2+ measurements using improved cameleons
Miyawaki, A., Griesbeck, O., Heim, R., & Tsien, R. Y. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.5.2135 · Cited by 829
Evolution of metal hyperaccumulation required cis-regulatory changes and triplication of HMA4
Hanikenne, M., Talke, I. N., Haydon, M. J., Lanz, C., Nolte, A., Motte, P., Kroymann, J., Weigel, D., & Krämer, U. (2008) · Nature · doi:10.1038/nature06877 · Cited by 812
The IRT1 protein from Arabidopsis thaliana is a metal transporter with a broad substrate range
Korshunova, Y. O., Eide, D., Clark, W. G., Guerinot, M. L., & Pakrasi, H. B. (1999) · Plant Molecular Biology · doi:10.1023/a:1026438615520 · Cited by 801
Heavy metal toxicity: cadmium permeates through calcium channels and disturbs the plant water status
Perfus‐Barbeoch, L., Leonhardt, N., Vavasseur, A., & Forestier, C. (2002) · The Plant Journal · doi:10.1046/j.1365-313x.2002.01442.x · Cited by 789
Mechanisms to cope with arsenic or cadmium excess in plants
Verbruggen, N., Hermans, C., & Schat, H. (2009) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2009.05.001 · Cited by 778
Shaping the calcium signature
McAinsh, M. R., & Pittman, J. K. (2008) · New Phytologist · doi:10.1111/j.1469-8137.2008.02682.x · Cited by 759
Cell Identity Mediates the Response of Arabidopsis Roots to Abiotic Stress
Dinneny, J. R., Long, T. A., Wang, J. Y., Jung, J. W., Mace, D., Pointer, S., Barron, C., Brady, S. M., Schiefelbein, J., & Benfey, P. N. (2008) · Science · doi:10.1126/science.1153795 · Cited by 746
A Role for the AKT1 Potassium Channel in Plant Nutrition
Hirsch, R. E., Lewis, B. D., Spalding, E. P., & Sussman, M. R. (1998) · Science · doi:10.1126/science.280.5365.918 · Cited by 717
Structure and function of metal chelators produced by plants
Rauser, W. E. (1999) · Cell Biochemistry and Biophysics · doi:10.1007/bf02738153 · Cited by 694
Genome-Wide Association Scan Meta-Analysis Identifies Three Loci Influencing Adiposity and Fat Distribution
Hunter, D. J., Peltonen, L., Guiducci, C., Crawford, G., Hirschhorn, J. N., Lyon, H. N., & Speliotes, E. K. (2009) · DSpace@MIT (Massachusetts Institute of Technology) · Cited by 687
Cellular compartmentation of cadmium and zinc in relation to other elements in the hyperaccumulator Arabidopsis halleri
Küpper, H., Lombi, E., Zhao, F.-J., & McGrath, S. P. (2000) · Planta · doi:10.1007/s004250000366 · Cited by 685
Root-to-shoot Cd translocation via the xylem is the major process determining shoot and grain cadmium accumulation in rice
Uraguchi, S., Mori, S., Kuramata, M., Kawasaki, A., Arao, T., & Ishikawa, S. (2009) · Journal of Experimental Botany · doi:10.1093/jxb/erp119 · Cited by 666
Engineering salt-tolerant Brassica plants: Characterization of yield and seed oil quality in transgenic plants with increased vacuolar sodium accumulation
Zhang, H., Hodson, J. N., Williams, J. P., & Blumwald, E. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.231476498 · Cited by 651
Enhanced salt tolerance mediated by AtHKT1 transporter‐induced Na + unloading from xylem vessels to xylem parenchyma cells
Sunarpi, Horie, T., Motoda, J., Kubo, M., Yang, H., Yoda, K., Horie, R., Chan, W., Leung, H., Hattori, K., et al. (2005) · The Plant Journal · doi:10.1111/j.1365-313x.2005.02595.x · Cited by 645
The Vegetative Vacuole Proteome of Arabidopsis thaliana Reveals Predicted and Unexpected Proteins[W]
Carter, C. J., Pan, S., Zouhar, J., Avila, E. L., Girke, T., & Raikhel, N. V. (2004) · The Plant Cell · doi:10.1105/tpc.104.027078 · Cited by 639
Ionomics and the Study of the Plant Ionome
Salt, D. E., Baxter, I. R., & Lahner, B. (2008) · Annual Review of Plant Biology · doi:10.1146/annurev.arplant.59.032607.092942 · Cited by 609
Physiological roles of nonselective cation channels in plants: from salt stress to signalling and development
Demidchik, V. V., & Maathuis, F. J. M. (2007) · New Phytologist · doi:10.1111/j.1469-8137.2007.02128.x · Cited by 603
Metal tolerance in plants
Ernst, W. H. O., Verkleij, J. A. C., & Schat, H. (1992) · Acta Botanica Neerlandica · doi:10.1111/j.1438-8677.1992.tb01332.x · Cited by 588
Differential expression and function of Arabidopsis thaliana NHX Na+/H+ antiporters in the salt stress response
Yokoi, S., Quintero, F. J., Cubero, B., Ruiz, M. T. G., Bressan, R. A., Hasegawa, P. M., & Pardo, J. M. (2002) · The Plant Journal · doi:10.1046/j.1365-313x.2002.01309.x · Cited by 587
Overexpression of AtHMA4 enhances root‐to‐shoot translocation of zinc and cadmium and plant metal tolerance
Verret, F., Gravot, A., Auroy, P., Leonhardt, N., David, P., Nussaume, L., Vavasseur, A., & Richaud, P. (2004) · FEBS Letters · doi:10.1016/j.febslet.2004.09.023 · Cited by 578
Shoot Na+ Exclusion and Increased Salinity Tolerance Engineered by Cell Type–Specific Alteration of Na+ Transport in Arabidopsis
Møller, I. S., Gilliham, M., Jha, D., Mayo, G. M., Roy, S. J., Coates, J. C., Haseloff, J. P., & Tester, M. A. (2009) · The Plant Cell · doi:10.1105/tpc.108.064568 · Cited by 563
Self-citation
IMPROVING THE NUTRIENT COMPOSITION OF PLANTS TO ENHANCE HUMAN NUTRITION AND HEALTH
Grusak, M. A., & DellaPenna, D. (1999) · Annual Review of Plant Physiology and Plant Molecular Biology · doi:10.1146/annurev.arplant.50.1.133 · Cited by 530
Iron deficiency enhances cadmium uptake and translocation mediated by the Fe 2+ transporters OsIRT1 and OsIRT2 in rice
Nakanishi, H., Ogawa, I., Ishimaru, Y., Mori, S., & Nishizawa, N. K. (2006) · Soil Science & Plant Nutrition · doi:10.1111/j.1747-0765.2006.00055.x · Cited by 527
Calcium-Related Physiological Disorders of Plants
Bangerth, F. K. (1979) · Annual Review of Phytopathology · doi:10.1146/annurev.py.17.090179.000525 · Cited by 513
THE GENERATION OF Ca2+ SIGNALS IN PLANTS
Hetherington, A. M., & Brownlee, C. (2004) · Annual Review of Plant Biology · doi:10.1146/annurev.arplant.55.031903.141624 · Cited by 499
Root Plasma Membrane Transporters Controlling K+/Na+ Homeostasis in Salt-Stressed Barley
Chen, Z., Pottosin, I. I., Cuin, T. A., Fuglsang, A. T., Tester, M. A., Jha, D., Jazo, I. Z., Zhou, M., Palmgren, M. B., Newman, I. A., et al. (2007) · PLANT PHYSIOLOGY · doi:10.1104/pp.107.110262 · Cited by 487
Extracellular Ca2+ Ameliorates NaCl-Induced K+ Loss from Arabidopsis Root and Leaf Cells by Controlling Plasma Membrane K+-Permeable Channels
Shabala, S. N., Demidchik, V. V., Shabala, L., Cuin, T. A., Smith, S. J., Miller, T., Davies, J. M., & Newman, I. A. (2006) · PLANT PHYSIOLOGY · doi:10.1104/pp.106.082388 · Cited by 486
Expression of Arabidopsis CAX2 in Tobacco. Altered Metal Accumulation and Increased Manganese Tolerance
Hirschi, K. D., Korenkov, V. D., Wilganowski, N. L., & Wagner, G. J. (2000) · PLANT PHYSIOLOGY · doi:10.1104/pp.124.1.125 · Cited by 482
The pathways of calcium movement to the xylem
White, P. J. (2001) · Journal of Experimental Botany · doi:10.1093/jexbot/52.358.891 · Cited by 456
Calcium Signaling during Abiotic Stress in Plants
Knight, H. (1999) · International review of cytology · doi:10.1016/s0074-7696(08)62707-2 · Cited by 450
Genomic scale profiling of nutrient and trace elements in Arabidopsis thaliana
Lahner, B., Gong, J., Mahmoudian, M., Smith, E. L., Abid, K. B., Rogers, E. E., Guerinot, M. L., Harper, J. F., Ward, J. M., McIntyre, L. M., et al. (2003) · Nature Biotechnology · doi:10.1038/nbt865 · Cited by 446
Cellular Compartmentation of Zinc in Leaves of the Hyperaccumulator Thlaspi caerulescens1
Küpper, H., Zhao, F. J., & McGrath, S. P. (1999) · PLANT PHYSIOLOGY · doi:10.1104/pp.119.1.305 · Cited by 444
The Calcium Conundrum. Both Versatile Nutrient and Specific Signal
Hirschi, K. D. (2004) · PLANT PHYSIOLOGY · doi:10.1104/pp.104.046490 · Cited by 432
Cell‐type‐specific calcium responses to drought, salt and cold in the Arabidopsis root
Kiegle, E., Moore, C. A., Haseloff, J. P., Tester, M. A., & Knight, M. R. (2000) · The Plant Journal · doi:10.1046/j.1365-313x.2000.00786.x · Cited by 410
HKT1;5-Like Cation Transporters Linked to Na + Exclusion Loci in Wheat, Nax2 and Kna1
Byrt, C. S., Platten, J. D., Spielmeyer, W., James, R. A., Lagudah, E. S., Dennis, E. S., Tester, M. A., & Munns, R. (2007) · PLANT PHYSIOLOGY · doi:10.1104/pp.106.093476 · Cited by 398
Genomic Comparison of P-Type ATPase Ion Pumps in Arabidopsis and Rice
Baxter, I. R., Tchieu, J. H., Sussman, M. R., Boutry, M., Palmgren, M. B., Gribskov, M., Harper, J. F., & Axelsen, K. B. (2003) · PLANT PHYSIOLOGY · doi:10.1104/pp.103.021923 · Cited by 389
The calcium sensor CBL10 mediates salt tolerance by regulating ion homeostasis in Arabidopsis
Kim, B., Waadt, R., Cheong, Y. H., Pandey, G. K., Domínguez‐Solís, J. R., Schültke, S., Lee, S. C., Kudla, J., & Luan, S. (2007) · The Plant Journal · doi:10.1111/j.1365-313x.2007.03249.x · Cited by 385
Death Don't Have No Mercy and Neither Does Calcium: Arabidopsis CYCLIC NUCLEOTIDE GATED CHANNEL2 and Innate Immunity
Ali, R., Ma, W., Lemtiri‐Chlieh, F., Tsaltas, D., Leng, Q., von Bodman, S., & Berkowitz, G. A. (2007) · The Plant Cell · doi:10.1105/tpc.106.045096 · Cited by 385
Cadmium accumulation in populations of Thlaspi caerulescens and Thlaspi goesingense
Lombi, E., Zhao, F. J., Dunham, S. J., & McGrath, S. P. (2000) · New Phytologist · doi:10.1046/j.1469-8137.2000.00560.x · Cited by 384
Vacuolar cation/H + exchange, ion homeostasis, and leaf development are altered in a T‐DNA insertional mutant of AtNHX1 , the Arabidopsis vacuolar Na + /H + antiporter
Apse, M. P., Sottosanto, J. B., & Blumwald, E. (2003) · The Plant Journal · doi:10.1046/j.1365-313x.2003.01871.x · Cited by 364
Arabidopsis Calcium-Dependent Protein Kinase AtCPK32 Interacts with ABF4, a Transcriptional Regulator of Abscisic Acid-Responsive Gene Expression, and Modulates Its Activity
Choi, H.-I., Park, H.-J., Park, J. H., Kim, S., Im, M.-Y., Seo, H.-H., Kim, Y.-W., Hwang, I., & Kim, S. Y. (2005) · PLANT PHYSIOLOGY · doi:10.1104/pp.105.069757 · Cited by 361
Transcriptional Profile of the Arabidopsis Root Quiescent Center
Nawy, T., Lee, J., Colinas, J., Wang, J. Y., Thongrod, S. C., Malamy, J. E., Birnbaum, K. D., & Benfey, P. N. (2005) · The Plant Cell · doi:10.1105/tpc.105.031724 · Cited by 359
Cellular compartmentation of nickel in the hyperaccumulators Alyssum lesbiacum, Alyssum bertolonii and Thlaspi goesingense
Küpper, H., Lombi, E., Zhao, F. J., Wieshammer, G., & McGrath, S. P. (2001) · Journal of Experimental Botany · doi:10.1093/jexbot/52.365.2291 · Cited by 359
Isolation of a strong Arabidopsis guard cell promoter and its potential as a research tool
Yang, Y., Costa, A., Leonhardt, N., Siegel, R. S., & Schroeder, J. I. (2008) · Plant Methods · doi:10.1186/1746-4811-4-6 · Cited by 353
Differential Metal Selectivity and Gene Expression of Two Zinc Transporters from Rice
Ramesh, S. A., Shin, R., Eide, D. J., & Schachtman, D. P. (2003) · PLANT PHYSIOLOGY · doi:10.1104/pp.103.026815 · Cited by 350
Forms of Zinc Accumulated in the HyperaccumulatorArabidopsis halleri
Géraldine Sarret, B., Saumitou‐Laprade, P., Bert, V., Proux, O., Hazemann, J., Traverse, A., Marcus, M. A., & Manceau, A. (2002) · PLANT PHYSIOLOGY · doi:10.1104/pp.007799 · Cited by 347
Low-Temperature Microscopy and Analysis
Echlin, P. (1992) · Springer eBooks · doi:10.1007/978-1-4899-2302-8 · Cited by 346
Molecular physiology of zinc transport in the Zn hyperaccumulator Thlaspi caerulescens
Lasat, M. M., Pence, N. S., Garvin, D. F., Ebbs, S. D., & Kochian, L. V. (2000) · Journal of Experimental Botany · doi:10.1093/jexbot/51.342.71 · Cited by 344
Root Suberin Forms an Extracellular Barrier That Affects Water Relations and Mineral Nutrition in Arabidopsis
Baxter, I. R., Hosmani, P. S., Rus, A. M., Lahner, B., Borevitz, J., Balasubramaniam, M., Mickelbart, M. V., Schreiber, L., Franke, R. B., & Salt, D. E. (2009) · PLoS Genetics · doi:10.1371/journal.pgen.1000492 · Cited by 332
Zinc hyperaccumulation and cellular distribution in Arabidopsis halleri
Zhao, F. J., Lombi, E., Breedon, T., & McGrath, S. P. (2000) · Plant Cell & Environment · doi:10.1046/j.1365-3040.2000.00569.x · Cited by 329
Moving cationic minerals to edible tissues: potassium, magnesium, calcium
Karley, A. J., & White, P. J. (2009) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2009.04.013 · Cited by 328
Cadmium‐induced inhibition of photosynthesis and long‐term acclimation to cadmium stress in the hyperaccumulator Thlaspi caerulescens
Küpper, H., Aravind, P., Leitenmaier, B., Trtílek, M., & Šetlík, I. (2007) · New Phytologist · doi:10.1111/j.1469-8137.2007.02139.x · Cited by 326
Identification of Thlaspi caerulescens Genes That May Be Involved in Heavy Metal Hyperaccumulation and Tolerance. Characterization of a Novel Heavy Metal Transporting ATPase
Papoyan, A., & Kochian, L. V. (2004) · Plant Physiology · doi:10.1104/pp.104.044503 · Cited by 322
Single-Cell Measurements of the Contributions of Cytosolic Na+ and K+ to Salt Tolerance
Carden, D. E., Walker, D. J., Flowers, T. J., & Miller, T. (2003) · PLANT PHYSIOLOGY · doi:10.1104/pp.011445 · Cited by 310
A Predicted Interactome for Arabidopsis
Geisler-Lee, J., O’Toole, N., Ammar, R., Provart, N. J., Millar, A. H., & Geisler, M. J. (2007) · PLANT PHYSIOLOGY · doi:10.1104/pp.107.103465 · Cited by 309
Transcriptome analysis of root transporters reveals participation of multiple gene families in the response to cation stress
Maathuis, F. J. M., Filatov, V., Herzyk, P., Krijger, G. C., Axelsen, K. B., Chen, S., Green, B. J., Li, Y., Madagan, K. L., Sánchez‐Fernández, R., et al. (2003) · The Plant Journal · doi:10.1046/j.1365-313x.2003.01839.x · Cited by 309
The leaf ionome as a multivariable system to detect a plant's physiological status
Baxter, I. R., Vitek, O., Lahner, B., Muthukumar, B., Borghi, M., Morrissey, J., Guerinot, M. L., & Salt, D. E. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0804175105 · Cited by 305
Engineering crop plants: getting a handle on phosphate
Brinch‐Pedersen, H., Sørensen, L. D., & Holm, P. B. (2002) · Trends in Plant Science · doi:10.1016/s1360-1385(01)02222-1 · Cited by 303
Tissue- and Age-Dependent Differences in the Complexation of Cadmium and Zinc in the Cadmium/Zinc Hyperaccumulator Thlaspi caerulescens (Ganges Ecotype) Revealed by X-Ray Absorption Spectroscopy
Küpper, H., Mijovilovich, A., Meyer‐Klaucke, W., & Kroneck, P. M. H. (2004) · PLANT PHYSIOLOGY · doi:10.1104/pp.103.032953 · Cited by 298
CAX1, an H+/Ca2+ antiporter from Arabidopsis.
Hirschi, K. D., Zhen, R. G., Cunningham, K. W., Rea, P. A., & Fink, G. R. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.16.8782 · Cited by 294
Loss of Halophytism by Interference with SOS1 Expression
Oh, D., Leidi, E. O., Zhang, Q., Hwang, S.-M., Li, Y., Quintero, F. J., Jiang, X., D’Urzo, M. P., Lee, S. Y., Zhao, Y., et al. (2009) · PLANT PHYSIOLOGY · doi:10.1104/pp.109.137802 · Cited by 293
The plant cDNA LCT1 mediates the uptake of calcium and cadmium in yeast
Clemens, S., Antosiewicz, D. M., Ward, J. M., Schachtman, D. P., & Schroeder, J. I. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.20.12043 · Cited by 293
Induction of Salt and Osmotic Stress Tolerance by Overexpression of an Intracellular Vesicle Trafficking Protein AtRab7 (AtRabG3e)
Mazel, A., Leshem, Y., Tiwari, B. S., & Levine, A. (2004) · PLANT PHYSIOLOGY · doi:10.1104/pp.103.025379 · Cited by 292
Calcium transport between tissues and its distribution in the plant
Clarkson, D. T. (1984) · Plant Cell & Environment · doi:10.1111/j.1365-3040.1984.tb01435.x · Cited by 290
A root's ability to retain K+ correlates with salt tolerance in wheat
Cuin, T. A., Betts, S. A., Chalmandrier, R., & Shabala, S. N. (2008) · Journal of Experimental Botany · doi:10.1093/jxb/ern128 · Cited by 290
T ONOPLAST T RANSPORTERS : Organization and Function
Maeshima, M. (2001) · Annual Review of Plant Physiology and Plant Molecular Biology · doi:10.1146/annurev.arplant.52.1.469 · Cited by 286
Distribution of cadmium in shoot and root tissues1
Lozano-Rodríguez, E., Hernández, L. E., Bonay, P., & Carpena‐Ruiz, R. O. (1997) · Journal of Experimental Botany · doi:10.1093/jxb/48.1.123 · Cited by 286
Cellular mechanisms for heavy metal detoxification and tolerance
Hall, J. L. (2002) · Journal of Experimental Botany · doi:10.1093/jxb/53.366.1 · Cited by 285
Uptake and transport of zinc in the hyperaccumulator Thlaspi caerulescens and the non‐hyperaccumulator Thlaspi ochroleucum
SHEN, Z. G., ZHAO, F. J., & McGRATH, S. P. (1997) · Plant, Cell & Environment · doi:10.1046/j.1365-3040.1997.d01-134.x · Cited by 278
A Cellular Hypothesis for the Induction of Blossom-End Rot in Tomato Fruit
HO, L. C. (2005) · Annals of Botany · doi:10.1093/aob/mci065 · Cited by 277
Expression of Arabidopsis CAX1 in Tobacco: Altered Calcium Homeostasis and Increased Stress Sensitivity
Hirschi, K. D. (1999) · The Plant Cell · doi:10.1105/tpc.11.11.2113 · Cited by 276
The NRAMP6 metal transporter contributes to cadmium toxicity
Cailliatte, R., Lapeyre, B., Briat, J., Mari, S., & Curie, C. (2009) · Biochemical Journal · doi:10.1042/bj20090655 · Cited by 271
A role for HKT1 in sodium uptake by wheat roots
Laurie, S., Feeney, K. A., Maathuis, F. J. M., Heard, P. J., Brown, S. J., & Leigh, R. A. (2002) · The Plant Journal · doi:10.1046/j.1365-313x.2002.01410.x · Cited by 268
Detoxification of cadmium in tobacco plants: formation and active excretion of crystals containing cadmium and calcium through trichomes
Choi, Y.-E., Harada, E., Wada, M., Tsuboi, H., Morita, Y., 智之, 草., & Sano, H. (2001) · Planta · doi:10.1007/s004250000487 · Cited by 266
Expression of an Arabidopsis Vacuolar Sodium/Proton Antiporter Gene in Cotton Improves Photosynthetic Performance Under Salt Conditions and Increases Fiber Yield in the Field
He, C., Yan, J., Shen, G., Fu, L., Holaday, A. S., Auld, D. L., Blumwald, E., & Zhang, H. (2005) · Plant and Cell Physiology · doi:10.1093/pcp/pci201 · Cited by 266
Ion accumulation in the cell walls of rice plants growing under saline conditions: evidence for the Oertli hypothesis
Flowers, T. J., HAJIBAGHERP, M. A., & Yeo, A. R. (1991) · Plant Cell & Environment · doi:10.1111/j.1365-3040.1991.tb01507.x · Cited by 265
Potassium activities in cell compartments of salt-grown barley leaves
Cuin, T. A. (2003) · Journal of Experimental Botany · doi:10.1093/jxb/erg072 · Cited by 246
Subcellular imaging of intramitochondrial Ca2+ with recombinant targeted aequorin: significance for the regulation of pyruvate dehydrogenase activity.
Rutter, G. A., Burnett, P., Rizzuto, R., Brini, M., Murgia, M., Pozzan, T., Tavaré, J. M., & Denton, R. M. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.11.5489 · Cited by 243
Functional Association of Arabidopsis CAX1 and CAX3 Is Required for Normal Growth and Ion Homeostasis
Cheng, N., Pittman, J. K., Shigaki, T., Lachmansingh, J., LeClere, S., Lahner, B., Salt, D. E., & Hirschi, K. D. (2005) · PLANT PHYSIOLOGY · doi:10.1104/pp.105.061218 · Cited by 243
Imaging and speciation of trace elements in biological environment
Łobiński, R., Moulin, C., & Ortega, R. B. (2006) · Biochimie · doi:10.1016/j.biochi.2006.10.003 · Cited by 240
Arabidopsis thaliana Cyclic Nucleotide Gated Channel 3 forms a non-selective ion transporter involved in germination and cation transport
Gobert, A., Park, G., Anna Amtmann, A., Sanders, D., & Maathuis, F. J. M. (2006) · Journal of Experimental Botany · doi:10.1093/jxb/erj064 · Cited by 238
The Arabidopsis cax1 Mutant Exhibits Impaired Ion Homeostasis, Development, and Hormonal Responses and Reveals Interplay among Vacuolar Transporters
Cheng, N., Pittman, J. K., Barkla, B. J., Shigaki, T., & Hirschi, K. D. (2003) · The Plant Cell · doi:10.1105/tpc.007385 · Cited by 228
Localization of Zinc and Cadmium in Thlaspi caerulescens (Brassicaceae), a Metallophyte that can Hyperaccumulate both Metals
Vázquez, M. D., Barceló, J. A., Poschenrieder, C., Mádico, J., Hatton, P. V., Baker, A. J. M., & Cope, G. H. (1992) · Journal of Plant Physiology · doi:10.1016/s0176-1617(11)81091-6 · Cited by 227
Ion Channels in the Xylem Parenchyma of Barley Roots (A Procedure to Isolate Protoplasts from This Tissue and a Patch-Clamp Exploration of Salt Passageways into Xylem Vessels
Wegner, L. H., & Raschke, K. (1994) · PLANT PHYSIOLOGY · doi:10.1104/pp.105.3.799 · Cited by 224
Regulation of macronutrient transport
Amtmann, A., & Blatt, M. R. (2008) · New Phytologist · doi:10.1111/j.1469-8137.2008.02666.x · Cited by 221
Phylogenetic variation in heavy metal accumulation in angiosperms
Broadley, M. R., Willey, N., Wilkins, J. C., Baker, A. J. M., Mead, A., & White, P. J. (2001) · New Phytologist · doi:10.1046/j.0028-646x.2001.00238.x · Cited by 218
The putative glutamate receptor 1.1 (AtGLR1.1) functions as a regulator of carbon and nitrogen metabolism in Arabidopsis thaliana
Kang, J., & Turano, F. J. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1030961100 · Cited by 217
Potassium nutrition, sodium toxicity, and calcium signaling: connections through the CBL–CIPK network
Luan, S., Lan, W., & Lee, S. C. (2009) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2009.05.003 · Cited by 215
Polyamines prevent NaCl‐induced K+ efflux from pea mesophyll by blocking non‐selective cation channels
Shabala, S. N., Cuin, T. A., & Pottosin, I. I. (2007) · FEBS Letters · doi:10.1016/j.febslet.2007.04.032 · Cited by 215
Salinity tolerance in Hordeum vulgare: ion concentrations in root cells of cultivars differing in salt tolerance**
Flowers, T. J., & Hajibagheri, M. A. N. (2001) · Plant and Soil · doi:10.1023/a:1010372213938 · Cited by 214
The Arabidopsis Circadian Clock Incorporates a cADPR-Based Feedback Loop
Dodd, A. N., Gardner, M. J., Hotta, C. T., Hubbard, K., Dalchau, N., Love, J., Assie, J.-M., Robertson, F. C., Jakobsen, M. K., Gonçalves, J. M., et al. (2007) · Science · doi:10.1126/science.1146757 · Cited by 214
The role of monovalent cation transporters in plant responses to salinity
Maathuis, F. J. M. (2005) · Journal of Experimental Botany · doi:10.1093/jxb/erj001 · Cited by 214
Photosynthetic capacity is related to the cellular and subcellular partitioning of Na+, K+ and Cl‐ in salt‐affected barley and durum wheat
James, R. A., Munns, R., von Caemmerer, S., Trejo, C., Miller, C., & Condon, T. (2006) · Plant Cell & Environment · doi:10.1111/j.1365-3040.2006.01592.x · Cited by 209
Genetic basis of Cd tolerance and hyperaccumulation in Arabidopsis halleri
Bert, V., Meerts, P., Saumitou‐Laprade, P., Salis, P., Grüber, W., & Verbruggen, N. (2003) · Plant and Soil · doi:10.1023/a:1022580325301 · Cited by 208
Molecular and functional characterization of a novel low-affinity cation transporter (LCT1) in higher plants
Schachtman, D. P., Kumar, R., Schroeder, J. I., & Marsh, E. L. (1997) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.94.20.11079 · Cited by 202
Nutrient loading of developing seeds
Zhang, W., Zhou, Y., Dibley, K. E., Tyerman, S. D., Furbank, R. T., & Patrick, J. W. (2007) · Functional Plant Biology · doi:10.1071/fp06271 · Cited by 202
Identification of Three Distinct Phylogenetic Groups of CAX Cation/Proton Antiporters
Shigaki, T., Rees, I., Nakhleh, L. K., & Hirschi, K. D. (2006) · Journal of Molecular Evolution · doi:10.1007/s00239-006-0048-4 · Cited by 196
Cadmium tolerance in Thlaspi caerulescensII. Localization of cadmium in Thlaspi caerulescens
Wójcik, M., Vangronsveld, J., DAHAEN, J., & TUKIENDORF, A. (2005) · Environmental and Experimental Botany · doi:10.1016/s0098-8472(04)00047-4 · Cited by 194
Molecular aspects of higher plant P-type Ca2+-ATPases
Geisler, M. M., Axelsen, K. B., Harper, J. F., & Palmgren, M. B. (2000) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/s0005-2736(00)00131-0 · Cited by 193
Overexpression of the AtGluR2 Gene Encoding anArabidopsis Homolog of Mammalian Glutamate Receptors Impairs CalciumUtilization and Sensitivity to Ionic Stress in TransgenicPlants
Kim, S. A., Kwak, J. M., Jae, S., Wang, M., & Nam, H. (2001) · Plant and Cell Physiology · doi:10.1093/pcp/pce008 · Cited by 191
AtGLR3.4, a glutamate receptor channel-like gene is sensitive to touch and cold
Meyerhoff, O., Müller, K., Roelfsema, M. R. G., Latz, A., Lacombe, B., Hedrich, R., Dietrich, P., & Becker, D. (2005) · Planta · doi:10.1007/s00425-005-1551-3 · Cited by 187
Leaf variations in Elaeagnus angustifolia related to environmental heterogeneity
Klich, M. G. (2000) · Environmental and Experimental Botany · doi:10.1016/s0098-8472(00)00056-3 · Cited by 182
Thellungiella halophila, a salt‐tolerant relative of Arabidopsis thaliana, has specific root ion‐channel features supporting K+/Na+ homeostasis under salinity stress
Volkov, V. S., & Amtmann, A. (2006) · The Plant Journal · doi:10.1111/j.1365-313x.2006.02876.x · Cited by 181
The Requirement for Sodium as a Micronutrient by Species Having the C4 Dicarboxylic Photosynthetic Pathway
Brownell, P. F., & Crossland, C. J. (1972) · PLANT PHYSIOLOGY · doi:10.1104/pp.49.5.794 · Cited by 181
A calcium-dependent protein kinase can inhibit a calmodulin-stimulated Ca 2+ pump (ACA2) located in the endoplasmic reticulum of Arabidopsis
Hwang, I., Sze, H., & Harper, J. F. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.97.11.6224 · Cited by 180
The impact of mineral nutrients in food crops on global human health
Welch, R. M. (2002) · Springer eBooks · doi:10.1007/978-94-017-2789-1_6 · Cited by 177
Characterization of Cd Translocation and Identification of the Cd Form in Xylem Sap of the Cd-Hyperaccumulator Arabidopsis halleri
Ueno, D., Iwashita, T., Zhao, F. J., & Ma, J. F. (2008) · Plant and Cell Physiology · doi:10.1093/pcp/pcn026 · Cited by 177
Increased Calcium Levels and Prolonged Shelf Life in Tomatoes Expressing Arabidopsis H+/Ca2+ Transporters
Park, S., Cheng, N. H., Pittman, J. K., Yoo, K. S., Park, J., Smith, R. H., & Hirschi, K. D. (2005) · PLANT PHYSIOLOGY · doi:10.1104/pp.105.066266 · Cited by 176
The impact of mineral nutrients in food crops on global human health
Welch, R. M. (2002) · Plant and Soil · doi:10.1023/a:1021140122921 · Cited by 175
Compartmentation of Zinc in Roots and Leaves of the Zinc Hyperaccumulator Thlaspi caerulescens J & C Presl
Vázquez, M. D., Poschenrieder, C., Barceló, J. A., Baker, A. J. M., Hatton, P. V., & Cope, G. H. (1994) · Botanica Acta · doi:10.1111/j.1438-8677.1994.tb00792.x · Cited by 170
Variation in the shoot calcium content of angiosperms
Broadley, M. R. (2003) · Journal of Experimental Botany · doi:10.1093/jxb/erg143 · Cited by 167
Placing metal micronutrients in context: transport and distribution in plants
Puig, S., & Peñarrubia, L. (2009) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2009.04.008 · Cited by 160
Diverse Functions and Molecular Properties Emerging for CAX Cation/H+ Exchangers in Plants
Shigaki, T., & Hirschi, K. D. (2006) · Plant Biology · doi:10.1055/s-2006-923950 · Cited by 157
Micro-scaled high-throughput digestion of plant tissue samples for multi-elemental analysis
Hansen, T. H., Laursen, K. H., Persson, D. P., Pedas, P., Husted, S., & Schjoerring, J. K. (2009) · Plant Methods · doi:10.1186/1746-4811-5-12 · Cited by 157
Transgenic salt‐tolerant sugar beet ( Beta vulgaris L.) constitutively expressing an Arabidopsis thaliana vacuolar Na + /H + antiporter gene, AtNHX3 , accumulates more soluble sugar but less salt in storage roots
Liu, H., Wang, Q., YU, M., Zhang, Y., Wu, Y., & Zhang, H. (2008) · Plant Cell & Environment · doi:10.1111/j.1365-3040.2008.01838.x · Cited by 155
Temporal and Spatial Development of the Cells of the Expanding First Leaf ofArabidopsis thaliana(L.) Heynh
Pyke, K. A., Marrison, J., & LEECH, A. M. (1991) · Journal of Experimental Botany · doi:10.1093/jxb/42.11.1407 · Cited by 155
Flux an important, but neglected, component of functional genomics
Fernie, A. R., Geigenberger, P., & Stitt, M. (2005) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2005.01.008 · Cited by 153
Salt-tolerant transgenic perennial ryegrass (Lolium perenne L.) obtained by Agrobacterium tumefaciens-mediated transformation of the vacuolar Na+/H+ antiporter gene
Wu, Y., Chen, Q., Chen, M., Chen, J., & Wang, X. (2005) · Plant Science · doi:10.1016/j.plantsci.2005.02.030 · Cited by 150
Cadmium effects on influx and transport of mineral nutrients in plant species
Yang, X., Baligar, V. C., Martens, D. C., & Clark, R. B. (1996) · Journal of Plant Nutrition · doi:10.1080/01904169609365148 · Cited by 146
Uptake of sodium in protoplasts of salt-sensitive and salt-tolerant cultivars of rice, Oryza sativa L. determined by the fluorescent dye SBFI
Kader, M. A., & Lindberg, S. M. (2005) · Journal of Experimental Botany · doi:10.1093/jxb/eri312 · Cited by 145
Vacuolar calcium channels
Pottosin, I. I., & Schönknecht, G. (2007) · Journal of Experimental Botany · doi:10.1093/jxb/erm035 · Cited by 145
A roadmap for zinc trafficking in the developing barley grain based on laser capture microdissection and gene expression profiling
Tauris, B., Borg, S., Gregersen, P. L., & Holm, P. B. (2009) · Journal of Experimental Botany · doi:10.1093/jxb/erp023 · Cited by 141
Where do all the ions go? The cellular basis of differential ion accumulation in leaf cells
Karley, A. J., Leigh, R. A., & Sanders, D. (2000) · Trends in Plant Science · doi:10.1016/s1360-1385(00)01758-1 · Cited by 138
The use of microelectrodes to investigate compartmentation and the transport of metabolized inorganic ions in plants
Miller, T., Cookson, S. J., Smith, S. J., & Wells, D. M. (2001) · Journal of Experimental Botany · doi:10.1093/jxb/52.356.541 · Cited by 135
Nutritional impact of elevated calcium transport activity in carrots
Morris, J., Hawthorne, K. M., Hotze, T., Abrams, S. A., & Hirschi, K. D. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0709005105 · Cited by 133
Partitioning of nutrient transport processes in roots
Tester, M. A., & Leigh, R. A. (2001) · Journal of Experimental Botany · doi:10.1093/jexbot/52.suppl_1.445 · Cited by 131
Measurement of Fluxes across Membranes
Walker, N. A., & Pitman, M. G. (1976) · Springer eBooks · doi:10.1007/978-3-642-66227-0_5 · Cited by 127
Remobilization of cadmium in maturing shoots of near isogenic lines of durum wheat that differ in grain cadmium accumulation
Harris, N. S., & Taylor, G. J. (2001) · Journal of Experimental Botany · doi:10.1093/jexbot/52.360.1473 · Cited by 127
The Arabidopsis cax3 mutants display altered salt tolerance, pH sensitivity and reduced plasma membrane H+-ATPase activity
Zhao, J. H., Barkla, B. J., Marshall, J., Pittman, J. K., & Hirschi, K. D. (2007) · Planta · doi:10.1007/s00425-007-0648-2 · Cited by 126
Using synchrotron X-ray fluorescence microprobes in the study of metal homeostasis in plants
Punshon, T., Guerinot, M. L., & Lanzirotti, A. (2009) · Annals of Botany · doi:10.1093/aob/mcn264 · Cited by 126
Purdue Ionomics Information Management System. An Integrated Functional Genomics Platform
Baxter, I. R., Ouzzani, M., Orçun, S., Kennedy, B., Jandhyala, S. S., & Salt, D. E. (2006) · PLANT PHYSIOLOGY · doi:10.1104/pp.106.092528 · Cited by 125
Shaping in plant cells
Martin, C. R., Bhatt, K., & Baumann, K. (2001) · Current Opinion in Plant Biology · doi:10.1016/s1369-5266(00)00213-2 · Cited by 124
The cyclic nucleotide‐gated channel, AtCNGC10, influences salt tolerance in Arabidopsis
Guo, K., Babourina, O., Christopher, D. A., Borsics, T., & Rengel, Z. (2008) · Physiologia Plantarum · doi:10.1111/j.1399-3054.2008.01157.x · Cited by 122
Comparison of essential and non‐essential element distribution in leaves of the Cd/Zn hyperaccumulator Thlaspi praecox as revealed by micro‐PIXE
Vogel‐Mikuš, K., Simčič, J., Pelicon, P., Budnar, M., Kump, P., Nečemer, M., Mesjasz‐Przybyłowicz, J., Przybyłowicz, W. J., & Regvar, M. (2008) · Plant Cell & Environment · doi:10.1111/j.1365-3040.2008.01858.x · Cited by 122
Differential toxicity of heavy metals is partly related to a loss of preferential extraplasmic compartmentation: a comparison of Cd‐, Mo‐, Ni‐ and Zn‐stress
Brune, A., Urbach, W., & Dietz, K. (1995) · New Phytologist · doi:10.1111/j.1469-8137.1995.tb04310.x · Cited by 121
Investigating glutamate receptor‐like gene co‐expression inArabidopsis thaliana
Roy, S. J., Gilliham, M., Berger, B., Essah, P. A., Cheffings, C. M., Miller, T., Davenport, R. J., Liu, L.-H., Skynner, M., Davies, J. M., et al. (2008) · Plant Cell & Environment · doi:10.1111/j.1365-3040.2008.01801.x · Cited by 120
Self-citation
Tolerance, accumulation and distribution of zinc and cadmium in hyperaccumulator Potentilla griffithii
Hu, P., Qiu, R., Senthilkumar, P., Jiang, D., Chen, Z.-W., Tang, Y., & Liu, F. (2009) · Environmental and Experimental Botany · doi:10.1016/j.envexpbot.2009.02.014 · Cited by 119
Enhanced Cd2+-selective root-tonoplast-transport in tobaccos expressing Arabidopsis cation exchangers
Korenkov, V. D., Park, S., Cheng, N.-H., Sreevidya, C. S., Lachmansingh, J., Morris, J., Hirschi, K. D., & Wagner, G. J. (2006) · Planta · doi:10.1007/s00425-006-0352-7 · Cited by 118
Overexpression of LCT1 in tobacco enhances the protective action of calcium against cadmium toxicity
Antosiewicz, D. M., & Hennig, J. (2003) · Environmental Pollution · doi:10.1016/j.envpol.2003.10.025 · Cited by 116
De‐regulated expression of the plant glutamate receptor homolog AtGLR3.1 impairs long‐term Ca 2+ ‐programmed stomatal closure
Cho, D., Kim, S. A., Murata, Y., Lee, S., Jae, S., Nam, H. G., & Kwak, J. M. (2009) · The Plant Journal · doi:10.1111/j.1365-313x.2009.03789.x · Cited by 116
A Cyclic Nucleotide-Gated Ion Channel, CNGC2, Is Crucial for Plant Development and Adaptation to Calcium Stress
Chan, C. W. M., Schorrak, L. M., Smith, R. K., Bent, A. F., & Sussman, M. R. (2003) · PLANT PHYSIOLOGY · doi:10.1104/pp.102.019216 · Cited by 115
Manganese Specificity Determinants in the ArabidopsisMetal/H+ Antiporter CAX2
Shigaki, T., Pittman, J. K., & Hirschi, K. D. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m209952200 · Cited by 113
Sub‐cellular localization of Ni in the hyperaccumulator, Hybanthus floribundus (Lindley) F. Muell
Bidwell, S. D., Crawford, S., Woodrow, I. E., Sommer‐Knudsen, J., & Marshall, A. T. (2004) · Plant Cell & Environment · doi:10.1111/j.0016-8025.2003.01170.x · Cited by 112
Glutamate Receptor Subtypes Evidenced by Differences in Desensitization and Dependence on theGLR3.3andGLR3.4Genes
Stephens, N. R., Qi, Z., & Spalding, E. P. (2007) · PLANT PHYSIOLOGY · doi:10.1104/pp.107.108134 · Cited by 112
The involvement of the transpirational bypass flow in sodium uptake by high‐ and low‐sodium‐transporting lines of rice developed through intravarietal selection
YADAV, R., Flowers, T. J., & Yeo, A. R. (1996) · Plant Cell & Environment · doi:10.1111/j.1365-3040.1996.tb00255.x · Cited by 112
QUANTITATIVE FLUORESCENCE MICROSCOPY: From Art to Science
Fricker, M. D., Runions, J., & Moore, I. R. (2006) · Annual Review of Plant Biology · doi:10.1146/annurev.arplant.57.032905.105239 · Cited by 105
Shining light on signaling and metabolic networks by genetically encoded biosensors
Lalonde, S., Ehrhardt, D. W., & Frommer, W. B. (2005) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2005.09.015 · Cited by 104
The expression of the endogenous vacuolar Na+/H+ antiporters in roots and shoots correlates positively with the salt resistance of wheat (Triticum aestivum L.)
Saqib, M., Zörb, C., Rengel, Z., & Schubert, S. (2005) · Plant Science · doi:10.1016/j.plantsci.2005.07.001 · Cited by 101
Effect of salt stress on growth and cation compartmentation in leaves of two plant species differing in salt tolerance
Mühling, K. H., & Läuchli, A. (2002) · Journal of Plant Physiology · doi:10.1078/0176-1617-00701 · Cited by 100
Impact of AtNHX1, a vacuolar Na+/H+ antiporter, upon gene expression during short- and long-term salt stress in Arabidopsis thaliana
Sottosanto, J. B., Saranga, Y., & Blumwald, E. (2007) · BMC Plant Biology · doi:10.1186/1471-2229-7-18 · Cited by 99
Concentrations of inorganic and organic solutes in extracts from individual epidermal, mesophyll and bundle-sheath cells of barley leaves
Fricke, W., Leigh, R., & Tomos, A. D. (1994) · Planta · doi:10.1007/bf00198565 · Cited by 98
Cell‐specific localization of Na+ in roots of durum wheat and possible control points for salt exclusion
Läuchli, A., James, R. A., Huang, C. X., McCully, M. E., & Munns, R. (2008) · Plant Cell & Environment · doi:10.1111/j.1365-3040.2008.01864.x · Cited by 97
Single cell technology
Kehr, J. (2003) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2003.09.002 · Cited by 96
Fluxes and Compartmentation in Plant Cells
MacRobbie, E. A. C. (1971) · Annual Review of Plant Physiology · doi:10.1146/annurev.pp.22.060171.000451 · Cited by 96
Molecular physiology of zinc transport in the Zn hyperaccumulator Thlaspi caerulescens
Lasat, M. M., Pence, N. S., Garvin, D. F., et al. (2000) · Journal of Experimental Botany · doi:10.1093/jxb/51.342.71 · Cited by 96
Protein synthesis in halophytes: The influence of potassium, sodium and magnesium in vitro
Flowers, T. J., & Dalmond, D. (1992) · Plant and Soil · doi:10.1007/bf00012008 · Cited by 95
Methods for Transcriptional Profiling in Plants. Be Fruitful and Replicate
Meyers, B. C., Galbraith, D. W., Nelson, T. M., & Agrawal, V. (2004) · PLANT PHYSIOLOGY · doi:10.1104/pp.104.040840 · Cited by 95
Transport of Cadmium via Xylem and Phloem in Maturing Wheat Shoots: Comparison with the Translocation of Zinc, Strontium and Rubidium
HERREN, T. (1997) · Annals of Botany · doi:10.1006/anbo.1997.0492 · Cited by 94
Root‐selective expression of AtCAX4 and AtCAX2 results in reduced lamina cadmium in field‐grown Nicotiana tabacum L.
Korenkov, V. D., King, B., Hirschi, K. D., & Wagner, G. J. (2009) · Plant Biotechnology Journal · doi:10.1111/j.1467-7652.2008.00390.x · Cited by 94
Spatial distribution of cadmium in leaves of metal hyperaccumulating Thlaspi praecox using micro‐PIXE
Vogel‐Mikuš, K., Regvar, M., Mesjasz‐Przybyłowicz, J., Przybyłowicz, W. J., Simčič, J., Pelicon, P., & Budnar, M. (2008) · New Phytologist · doi:10.1111/j.1469-8137.2008.02519.x · Cited by 94
The intercellular distribution of vacuolar solutes in the epidermis and mesophyll of barley leaves changes in response to NaCl
Fricke, W., Leigh, R. A., & Tomos, A. D. (1996) · Journal of Experimental Botany · doi:10.1093/jxb/47.9.1413 · Cited by 94
CLC-mediated anion transport in plant cells
Angeli, A. D., Monachello, D., Ephritikhine, G., Frachisse, J., Thomine, S., Gambale, F., & Barbier‐Brygoo, H. (2008) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2008.0128 · Cited by 94
Calcium protects Trifolium repens L. seedlings against cadmium stress
Wang, C., & Song, H. (2009) · Plant Cell Reports · doi:10.1007/s00299-009-0734-y · Cited by 93
Mapping of QTLs associated with cadmium tolerance and accumulation during seedling stage in rice (Oryza sativa L.)
Xue, D., Chen, M., & Zhang, G. (2008) · Euphytica · doi:10.1007/s10681-008-9785-3 · Cited by 93
Heavy Metal Uptake by Plants and Cyanobacteria
Küpper, H., & Kroneck, P. M. H. (2005) · CRC Press eBooks · doi:10.1201/9780849346071-5 · Cited by 92
Root structure and cellular chloride, sodium and potassium distribution in salinized grapevines
STOREY, R., Schachtman, D. P., & Thomas, M. R. (2003) · Plant Cell & Environment · doi:10.1046/j.1365-3040.2003.01005.x · Cited by 91
Comparative analysis of CAX2-like cation transporters indicates functional and regulatory diversity
Edmond, C., Shigaki, T., Ewert, S., Nelson, M. D., Connorton, J. M., Chalova, V. I., Noordally, Z. B., & Pittman, J. K. (2008) · Biochemical Journal · doi:10.1042/bj20081814 · Cited by 90
Identification of a calmodulin‐regulated autoinhibited Ca 2+ ‐ATPase (ACA11) that is localized to vacuole membranes in Arabidopsis
Lee, S. M., Kim, H. S., Han, H. J., Moon, B. C., Kim, C. Y., Harper, J. F., & Chung, W. S. (2007) · FEBS Letters · doi:10.1016/j.febslet.2007.07.023 · Cited by 90
IsBrassica junceaa suitable plant for phytoremediation of cadmium in soils with moderately low cadmium contamination? – Possibility of using other plant species for Cd-phytoextraction
Ishikawa, S., Ae, N., Murakami, M., & Wagatsuma, T. (2006) · Soil Science & Plant Nutrition · doi:10.1111/j.1747-0765.2006.00008.x · Cited by 90
Different effects of calcium and lanthanum on the expression of phytochelatin synthase gene and cadmium absorption in Lactuca sativa
He, Z., Li, J., Zhang, H., & Ma, M. (2004) · Plant Science · doi:10.1016/j.plantsci.2004.07.001 · Cited by 88
A novel yeast two‐hybrid approach to identify CDPK substrates: Characterization of the interaction between AtCPK11 and AtDi19, a nuclear zinc finger protein1
Rodríguez-Milla, M. Á., Uno, Y., Chang, I., Townsend, J. B., Maher, E. A., Quilici, D. R., & Cushman, J. C. (2006) · FEBS Letters · doi:10.1016/j.febslet.2006.01.013 · Cited by 87
Characterization of plant phenotypes associated with loss-of-function of AtCNGC1, a plant cyclic nucleotide gated cation channel
Ma, W., Ali, R., & Berkowitz, G. A. (2006) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2006.08.007 · Cited by 87
Manganese accumulation in the leaf mesophyll of four tree species: a PIXE/EDAX localization study
Fernando, D. R., Bakkaus, E., Perrier, N., Baker, A. J. M., Woodrow, I. E., Batianoff, G. N., & Collins, R. N. (2006) · New Phytologist · doi:10.1111/j.1469-8137.2006.01783.x · Cited by 87

Flagged first, then by citations

Research works printed but not linked: 5

Amtmann, 2005, Comparative analysis of ion transport in Arabidopsis related species differing in salt tolerance, Comparative Biochemistry and Physiology Part A: Molecular & Integrative Physiology, 141, S339
Boursiac, 2007, The mutation of two Ca2+ pumps ACA4 and ACA11 provides evidence for communication between the tonoplast and plasma membrane in the regulation of Ca2+ signals leading to a programmed cell death, 18th New Phytologist Symposium Calcium-based Signalling Systems in Plants
Chaney, 2000, Transfer of cadmium through plants to the food chain
Clarkson, 1991, Root structure and sites of ion uptake
Wu, 2009, Physiological characterization of co-expressing of a CAX1 calcium transporter and a CRT calcium-binding protein in planta, In vitro Cellular & Developmental Biology – Plant, 45, 511

Sorted by citations

Salinity tolerance of crops – what is the cost?
Munns, R., & Gilliham, M. (2015) · New Phytologist · doi:10.1111/nph.13519 · Cited by 1,303
Self-citation
Plant nutrition for sustainable development and global health
White, P. J., & Brown, P. H. (2010) · Annals of Botany · doi:10.1093/aob/mcq085 · Cited by 1,204
Unravelling cadmium toxicity and tolerance in plants: Insight into regulatory mechanisms
Gallego, S. M., Pena, L. B., Barcia, R. A., Azpilicueta, C. E., Iannone, M. F., Rosales, E. P., Zawoznik, M. S., Groppa, M. D., & Benavides, M. P. (2012) · Environmental and Experimental Botany · doi:10.1016/j.envexpbot.2012.04.006 · Cited by 1,221
Evaluating physiological responses of plants to salinity stress
Negrão, S., Schmöckel, S. M., & Tester, M. A. (2016) · Annals of Botany · doi:10.1093/aob/mcw191 · Cited by 1,200
Root responses to cadmium in the rhizosphere: a review
Lux, A., Martinka, M., Vaculik, M., & White, P. J. (2011) · Journal of Experimental Botany · doi:10.1093/jxb/erq281 · Cited by 1,100

See all 344

Authors: Conn, S., & Gilliham, M.
Affiliations: The University of Adelaide (AU)
ORCID: Conn, Simon
Gilliham, Matthew
Venue: Annals of Botany
Publisher: Oxford University Press (OUP)
Published: 2010-04-21
Volume: 105
Issue: 7
Pages: 1081-1102
ISSN: 0305-7364 (ISSN-L)
1095-8290
DOI: 10.1093/aob/mcq027
PMC: PMC2887064
OpenAlex: W2122748132
Cited by: 344
References: 305
Citations by year: 2026: 17 · 2025: 13 · 2024: 16 · 2023: 20 · 2022: 23 · 2021: 22 · 2020: 25 · 2019: 35 · 2018: 23 · 2017: 17 · 2016: 21 · 2015: 15 · 2014: 23 · 2013: 22 · 2012: 27
FWCI: 2.27
Type: journal article
Language: en
Open access: bronze
doi.org
Locations: Annals of Botany (publishedVersion)
Europe PMC (PubMed Central) (publishedVersion)
PubMed Central (publishedVersion)
PubMed (publishedVersion)
Adelaide Research & Scholarship (AR&S) (University of Adelaide) (submittedVersion)
Topics: Life Sciences › Agricultural and Biological Sciences › Plant Science › Plant nutrient uptake and metabolism
Life Sciences › Agricultural and Biological Sciences › Plant Science › Plant Micronutrient Interactions and Effects
Life Sciences › Agricultural and Biological Sciences › Plant Science › Plant Molecular Biology Research
Keywords: plant vacuole, calcium, cadmium, sodium, ion transporters, solute transporters, osmolarity, charge balance, detoxification, stress-responsive gene expression, plant nutrition
MeSH terms: Elements, Physiology, Comparative, Plants

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

Comparative physiology of elemental distributions in plants

Abstract

Overview

Integrity signals

Verification

Claims the paper makes

Claims other papers make about this one

Self-check

Citations

Cites

Cited by

Related

Metadata

Record

About these checks