One of the current challenges in plant biology is the development of quantitative phenotyping approaches to link the genotype and the environment to plant structural, functional, and yield characteristics in order to meet the growing demands for sustainable food, feed, and fuel. The genotype of a plant consists of all of the hereditary information within the individual, whilst the phenotype, which represents the morphological, physiological, anatomical, and developmental characteristics, is the result of the interaction between the genotype and the environment. Understanding this interaction is one of the major challenges in plant sciences. In plant breeding, the ultimate goal is the improvement of traits of agricultural importance related to disease resistance, high yields, and the plant’s ability to grow in unfavourable environmental conditions. Currently, breeding approaches produce an annual yield increase of approximately 1% for major crops, which is below the over 2% increase needed to meet the global demands for food by 2050 (Ray et al., 2013).
Rapid developments in plant molecular biology and in molecular-based breeding techniques have resulted in an increasing number of species being sequenced and large collections of mutants, accessions, and recombinant lines allowing detailed analysis of gene functions. High-definition genotyping can now be carried out on thousands of plants in an automated way at continuously decreasing costs, thereby facilitating association genetics and the determination of multi-parental quantitative trait loci (QTLs) (Poland and Rife, 2012). For transcriptomic, proteomic, and metabolomic analyses large, often robotized, platforms are available allowing detailed characterization of the biochemical status of plants at a reasonable cost (Ehrhardt and Frommer, 2012). By contrast, an understanding of the link between genotype and phenotype has progressed more slowly and is the major limiting step in current breeding programmes to enable further increases in plant productivity. Faster progress requires a substantial increase in capacity (both technical and conceptual) of the plant science community to analyse quantitatively the existing genetic resources for their interaction with the environment. Advances in phenotyping are, therefore, the key factor for success in modern breeding, as well as for basic plant research, and this requires a multidisciplinary effort which includes the integration of sensor networks, environment simulation facilities, specialized platforms for mechanistic, medium- and high-throughput platforms, field phenotyping systems, and modelling (Fiorani and Schurr, 2013).
Despite the fact that our understanding about the link between the genotype and the phenotype is advancing and new species and traits can be addressed, we will never be able experimentally to explore the entire genotype–environment matrix for individual factors and their interactions (see, for example, Mittler and Blumwald, 2010). Therefore, modelling platforms are needed to test the existing or virtual combinations of alleles in a variety of climatic scenarios or management practices to make relevant predictions about phenotypes. This requires collection, storage, and access to phenotypic data, based on standards which allow interoperability among data providers, and to link specific phenotypes with the associated genomic sequence information. This is particularly challenging because of the large variability of phenotyping protocols, the multitude of phenotypic traits which can be measured, and their dependence on the environment. Establishing standardized procedures such as experimental protocols and environmental monitoring, as well as data managements that allow comparability between measurements, is the next important challenge which requires an effort beyond the plant science community and extended interaction between different stakeholders.
In addition, close co-operation and interaction between scientists establishing plant phenotyping platforms, technology developers, as well as other diverse users, is of great importance to foster a discussion about the needs and requirements of plant phenotyping. There is a number of national and international networks (e.g. APPF, http://www.plantphenomics.org.au/; DPPN, www.dppn.de; FPPN, https://www.phenome-fppn.fr/; UK-PPN, http://www.ukppn.org.uk/) as well as projects (e.g. EPPN, http://www.plant-phenotyping-network.eu/; COST action, http://costfa1306.eu/) or initiatives focusing on specific crops (G20, http://www.wheatinitiative.org/activities/expert-working-groups), which aim to foster the discussion between the various stakeholders. In particular, the International Plant Phenotyping Network (IPPN, http://www.plant-phenotyping.org/) focuses on wide international interaction by organizing bi-annual symposia and promoting discussion and interaction between scientists and industry (http://www.plant-phenotyping.org/previous_events). The first two symposia in Canberra in 2009 and Jülich in 2011 had a strong focus on encouraging the development and spread of new techniques and algorithms for the automation of analyses as well as data management frameworks enabling modelling as depicted in the resulting special issues (Furbank, 2009; Pieruschka and Poorter, 2012). The latest symposium in Chennai in 2014 indicated that plant phenotyping is becoming a tool to be used to address complex traits such as yield, plant biomass, and plant productivity in response to biotic and abiotic stress. Thus, plant phenotyping as a research field is developing towards phenotyping for the diverse needs of users, which is accompanied by the development and implementation of novel technology to effectively address the phenotyping bottleneck. This special issue on plant phenotyping initiated by the Symposium in Chennai underlines this development with publications about phenotyping for biotic and abiotic stress resistance of different crops accompanied by a descriptions of methods, quantitative approaches, and platforms for phenotyping of specific traits.
Content of this special issue
Phenotyping root traits is of particular importance for improved uptake of resources such as water and nutrients. Kuijken et al. (2015) discuss the heritability of root traits in relation to relevant breeding targets. Niederbacher et al. (2015) present an approach to define disease resistance and stress tolerance by measuring volatile organic compounds. Detailed physiological phenotyping across different scales is proposed to integrate the precise characterization of metabolic processes into high-throughput phenotyping of whole-plants and canopies (Großkinsky et al., 2015). The importance of standardization is discussed by Krajewski et al. (2015) who highlight the problems and shortcomings as well as the benefits. A number of contributions deal with plant properties under different stress conditions. Soil moisture affects root and shoot properties, in particular, under different irradiances that plants are exposed to (Nagel et al., 2015). Water availability was studied with respect to different lentil genotypes in combination with salinity stress indicating different biochemical markers (Muscolo et al., 2015); remote sensing approaches used to screen apple populations revealed different QTLs (Virlet et al 2015); and Parent et al. (2015) showed a possible common genetic basis linking greenhouse and field measurements. York and Lynch (2015) found different root architecture under varying nitrogen availability which affects plant growth. The effect of domestication on root and shoot properties under different nutrient availability was investigated by Gioia et al. (2015) showing a significantly reduced diversity; In ‘t Zandt et al. (2015) designed different nutrient supply treatments using a rhizoslide system. Jammer et al. (2015) studied the key carbohydrate metabolic enzyme dynamics of crops exposed to different environmental conditions such as elevated CO2 or heat stress. Infection of sugar beets with Cercospora significantly affects the growth and morphological dynamics of taproots (Schmittgen et al., 2015). Genetic components of early vigour in rice (Rebolledo et al., 2015) or growth dynamics in Arabidopsis (Bac-Molenaar et al., 2015) were studied with dedicated mapping populations. In addition, different methods and approaches are discussed, such as methods for phenotyping photosynthetic performance using the sun-induced fluorescence approach (Tubuxin et al., 2015) or evaluation of vegetation indices for remote chlorophyll measurement when measured on ad- and abaxial surfaces of poplar leaves (Lu et al., 2015). Yang et al. (2015) presents a leaf scorer which is implemented into a phenotyping platform and validated in a genome-wide association study in rice. A new platform for 3-D imaging and lysimetry was specifically developed for the phenotyping of drought stress by Vadez et al. (2015). Hatzig et al. (2015) use a neural network approach to quantify root architecture which was tested under drought stress. In summary, this special issue deals with very diverse topics relevant for plant phenotyping such as an understanding of basic plant processes, the identification of genetic regions related to different physiological processes, the development and implementation of novel methods to identify novel traits etc. Thus, within the last few years, plant phenotyping has become a more and more important tool to quantify the link between the genotype and the environment that is highly relevant to address future grand challenges.
Acknowledgements
This special issue was supported by the International Plant Phenotyping Network (IPPN), the European Plant Phenotyping network (EPPN, Grant Agreement No. 284443) and the German Plant Phenotyping Network (DPPN, Förderkennzeichen: 031A053A/B/C).
References
- Bac-Molenaar JA, Vreugdenhil D, Granier C, Keurentjes JJB. 2015. Genome wide association mapping of growth dynamics detects time-specific and general QTLs. Journal of Experimental Botany 66, 5567–5580. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ehrhardt DW, Frommer WB. 2012. New technologies for 21st century plant science. The Plant Cell 24, 374–394. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Fiorani F, Schurr U. 2013. Future scenarios for plant phenotyping. Annual Review of Plant Biology 64, 267–291. [DOI] [PubMed] [Google Scholar]
- Furbank RT. 2009. Plant phenomics: from gene to form and function. Functional Plant Biology 36. [DOI] [PubMed] [Google Scholar]
- Gioia T, Nagel KA, Beleggia R, Fragasso M, Ficco DBM, Pieruschka R, De Vita P, Fiorani F, Papa R. 2015. The impact of domestication on the phenotypic architecture of durum wheat under contrasting nitrogen fertilisation. Journal of Experimental Botany 66, 5519–5530. [DOI] [PubMed] [Google Scholar]
- Großkinsky DK, Svensgaard J, Christensen S, Roitsch T. 2015. Plant phenomics and the need for physiological phenotyping across scales to narrow the genotype-to-phenotype knowledge gap. Journal of Experimental Botany 66, 5429–5440. [DOI] [PubMed] [Google Scholar]
- Hatzig SV, Schießl SV, Stahl A, Snowdon RJ. 2015. Plant breeding meets neuroscience: characterizing root response phenotypes by neural network analysis. Journal of Experimental Botany 66, 5617–5624. [DOI] [PMC free article] [PubMed] [Google Scholar]
- in ‘t Zandt D, Le Marié C, Kirchgessner N, Visser EJW, Hund A. 2015. High-resolution quantification of root dynamics in split-nutrient rhizoslides reveals rapid and strong proliferation of maize roots in response to local high nitrogen. Journal of Experimental Botany 66, 5507–5517. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Jammer A, Gasperl A, Luschin-Ebengreuth N, et al. 2015. Simple and robust determination of the activity signature of key carbohydrate metabolism enzymes for physiological phenotyping in model and crop plants: application to monitor differential impacts of elevated atmospheric CO2 concentration in oilseed rape leaves and cold treatment in ryegrass inflorescences. Journal of Experimental Botany 66, 5531–5542. [DOI] [PubMed] [Google Scholar]
- Krajewski P, Chen D, Cwiek H, et al. 2015. Towards recommendations for metadata and data handling in plant phenotyping. Journal of Experimental Botany 66, 5417–5427. [DOI] [PubMed] [Google Scholar]
- Kuijken RCP, van Eeuwijk FA, Marcelis LFM, Bouwmeester HJ. 2015. Root phenotyping: from component trait in the lab to breeding. Journal of Experimental Botany 66, 5389–5401. [DOI] [PubMed] [Google Scholar]
- Lu S, Lu X, Zhao W, Liu Y, Wang Z, Omasa K. 2015. Comparing vegetation indices for remote chlorophyll measurement of white poplar and Chinese elm leaves with different adaxial and abaxial surfaces. Journal of Experimental Botany 66, 5625–5637. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Mittler R, Blumwald E. 2010. Genetic engineering for modern agriculture: challenges and perspectives. Annual Review of Plant Biology 61, 443–462. [DOI] [PubMed] [Google Scholar]
- Muscolo A, Junker A, Klukas C, Weigelt-Fische K, Riewe D, Altman T. 2015. Phenotypic and metabolic responses to drought and salinity of four contrasting lentil genotypes. Journal of Experimental Botany 66, 5467–5480. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Nagel KA, Bonnett D, Furbank R, Walter A, Schurr U, Watt M. 2015. Simultaneous effects of leaf irradiance and soil moisture on growth and root system architecture of novel wheat genotypes: implications for phenotyping. Journal of Experimental Botany 66, 5441–5452. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Niederbacher B, Winkler JB, Schnitzler JP. 2015. Volatile organic compounds as non-invasive markers for plant phenotyping. Journal of Experimental Botany 66, 5403–5416. [DOI] [PubMed] [Google Scholar]
- Parent B, Shahinnia F, Maphosa L, Berger B, Rabie H, Chalmers K, Kovalchuk A, Langridge P, Fleury D. 2015. Combining field performance with controlled environment plant imaging to identify the genetic control of growth and transpiration underlying yield response to water deficit stress in wheat. Journal of Experimental Botany 66, 5481–5492. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Pieruschka R, Poorter H. 2012. Phenotyping plants: genes, phenes and machines. Functional Plant Biology 39, 813–820. [DOI] [PubMed] [Google Scholar]
- Poland JA, Rife TW. 2012. Genotyping-by-sequencing for plant breeding and genetics. The Plant Genome 5, 92–102. [Google Scholar]
- Ray DK, Mueller ND, West PC, Foley JA. 2013. Yield trends are insufficient to double global crop production by 2050. PLoS ONE 8, e66428. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Rebolledo MC, Dingkuhn M, Courtois B, Clément-Vidal A, Cruz D, Duitama J, Lorieux M, Gibon Y, Luque D. 2015. Phenotypic and genetic dissection of component traits for early vigour in rice using plant growth modelling, sugar content analyses, and association mapping. Journal of Experimental Botany 66, 5555–5566. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Schmittgen S, Metzner R, Van Dusschoten D, Jansen M, Fiorani F, Jahnke S, Rascher U, Schurr U. 2015. Magnetic Resonance Imaging of sugar beet taproots in soil reveals growth reduction and morphological changes during foliar Cercospora beticola infestation. Journal of Experimental Botany 66, 5543–5553. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Tubuxin B, Rahimzadeh-Bajgiran P, Ginnan Y, Hosoi F, Omasa K. 2015. Estimating chlorophyll content and photochemical yield of photosystem II (φPSII) using solar-induced chlorophyll fluorescence measurements at different growing stages of attached leaves. Journal of Experimental Botany 66, 5595–5603. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Vadez V, Kholová J, Hummel G, Zhokhavets U, Gupta SK, Hash CT. 2015. LeasyScan: a novel concept combining 3-D imaging and lysimetry for HT phenotyping of traits controlling plant water budget. Journal of Experimental Botany 66, 5581–5593. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Virlet N, Costes E, Martinez S, Kelner JJ, Regnard JL. 2015. Multispectral airborne imagery in the field reveals genetic determinisms of morphological and transpiration traits of an apple tree hybrid population in response to water deficit. Journal of Experimental Botany 66, 5453–5465. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Yang W, Guo Z, Huang C, Wang K, Jiang N, Feng H, Chen G, Liu Q, Xiong L. 2015. Genome-wide association study of rice leaf traits with a high-throughput leaf scorer. Journal of Experimental Botany 66, 5605–5615. [DOI] [PMC free article] [PubMed] [Google Scholar]
- York LM, Lynch JP. 2015. Intensive phenotyping of maize (Zea mays L.) root crowns reveals phenes and phene interactions associated with plant growth and N capture. Journal of Experimental Botany 66, 5493–5505. [DOI] [PMC free article] [PubMed] [Google Scholar]