Plant Biology (PLANT BIOLOGY)

Publisher: Deutsche Botanische Gesellschaft; Koninklijke Nederlandse Botanische Vereniging, Wiley

Journal description

Plant Biology is an international journal of the broadest scope bringing together the different subdisciplines of plant science, such as physiology, molecular biology, cell biology, development, genetics, systematics, ecology, evolution, ecophysiology, plant-microbe interactions and mycology. To this end, the members of the board of section editors represent all major areas of plant science giving the journal an international base.

Current impact factor: 2.63

Impact Factor Rankings

2015 Impact Factor Available summer 2016
2014 Impact Factor 2.633
2013 Impact Factor 2.405
2012 Impact Factor 2.32
2011 Impact Factor 2.395
2010 Impact Factor 2.409
2009 Impact Factor 2.223
2008 Impact Factor 1.944
2007 Impact Factor 2.012
2006 Impact Factor 2.059
2005 Impact Factor 1.91
2004 Impact Factor 1.582
2003 Impact Factor 1.42
2002 Impact Factor 1.352
2001 Impact Factor 1.828
2000 Impact Factor 1.215
1999 Impact Factor

Impact factor over time

Impact factor

Additional details

5-year impact 2.70
Cited half-life 6.00
Immediacy index 1.02
Eigenfactor 0.01
Article influence 0.74
Website Plant Biology website
Other titles Plant biology (Stuttgart, Germany: Online)
ISSN 1435-8603
OCLC 45967059
Material type Document, Periodical, Internet resource
Document type Internet Resource, Computer File, Journal / Magazine / Newspaper

Publisher details


  • Pre-print
    • Author can archive a pre-print version
  • Post-print
    • Author cannot archive a post-print version
  • Restrictions
    • 12 months embargo
  • Conditions
    • Some journals have separate policies, please check with each journal directly
    • On author's personal website, institutional repositories, arXiv, AgEcon, PhilPapers, PubMed Central, RePEc or Social Science Research Network
    • Author's pre-print may not be updated with Publisher's Version/PDF
    • Author's pre-print must acknowledge acceptance for publication
    • Non-Commercial
    • Publisher's version/PDF cannot be used
    • Publisher source must be acknowledged with citation
    • Must link to publisher version with set statement (see policy)
    • If OnlineOpen is available, BBSRC, EPSRC, MRC, NERC and STFC authors, may self-archive after 12 months
    • If OnlineOpen is available, AHRC and ESRC authors, may self-archive after 24 months
    • Publisher last contacted on 07/08/2014
    • This policy is an exception to the default policies of 'Wiley'
  • Classification

Publications in this journal

  • G Tang · X Li · L Lin · H Guo ·
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    ABSTRACT: Plant senescence is largely influenced by carbohydrate content. In order to investigate the impact of carbohydrate content on leaf senescence and photosystem II (PSII) during the senescence process, phloem girdling (PG), leaf removal (LR), and a combination of phloem girdling and leaf removal (GR) were performed on Alhagi Sparsifolia at the end of the growing season. The results showed that during senescence, leaf soluble sugar content, starch content, the energy absorbed by the unit reaction center (ABS/RC) increased; whereas, leaf photosynthetic rate, photosynthetic pigment content, maximum photochemical efficiency (φPo ), and energy used by the acceptor site in electron transfer (ETo /RC) decreased. The degree of change was PG> GR> CK (control)> LR. The result of the present work implied that phloem girdling (PG) significantly accelerated leaf senescence and single leaf removal (LR) slightly delayed leaf senescence; whereas, leaf removal significantly delayed the senescence process on girdled leaf (GR). Natural or delayed senescence only slightly inhibited the acceptor site of PSII and did not damage the donor site of PSII. On the other hand, induced senescence not only damaged the donor site of PSII (e.g., oxygen-evolving complex), but also significantly inhibited the acceptor site of PSII. In addition, leaf senescence led to an increase in the energy absorbed by the unit reaction center (ABS/RC), which subsequently resulted in an increasing excitation pressure in the reaction center (DIo /RC), as well as additional saved Car for absorbing residual light energy and quenching reactive oxygen species during senescence. This article is protected by copyright. All rights reserved. This article is protected by copyright. All rights reserved.
    Plant Biology 02/2015; 17(5). DOI:10.1111/plb.12309
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    ABSTRACT: The germination ecology of Sideritis serrata was investigated in order to improve ex-situ propagation techniques and management of their habitat. Specifically, we analysed: (i) influence of temperature, light conditions and seed age on germination patterns; (ii) phenology of germination; (iii) germinative response of buried seeds to seasonal temperature changes; (iv) temperature requirements for induction and breaking of secondary dormancy; (v) ability to form persistent soil seed banks; and (vi) seed bank dynamics. Freshly matured seeds showed conditional physiological dormancy, germinating at low and cool temperatures but not at high ones (28/14 and 32/18 °C). Germination ability increased with time of dry storage, suggesting the existence of non-deep physiological dormancy. Under unheated shade-house conditions, germination was concentrated in the first autumn. S. serrata seeds buried and exposed to natural seasonal temperature variations in the shade-house, exhibited an annual conditional dormancy/non-dormancy cycle, coming out of conditional dormancy in summer and re-entering it in winter. Non-dormant seeds were clearly induced into dormancy when stratified at 5 or 15/4 °C for 8 weeks. Dormant seeds, stratified at 28/14 or 32/18 °C for 16 weeks, became non-dormant if they were subsequently incubated over a temperature range from 15/4 to 32/18 °C. S. serrata is able to form small persistent soil seed banks. The maximum seed life span in the soil was 4 years, decreasing with burial depth. This is the second report of an annual conditional dormancy/non-dormancy cycle in seeds of shrub species. This article is protected by copyright. All rights reserved. This article is protected by copyright. All rights reserved.
    Plant Biology 01/2015; 17(4). DOI:10.1111/plb.12306
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    ABSTRACT: Trehalose and the trehalose biosynthetic pathway are important contributors and regulators of stress responses in plants. Among recent findings for trehalose and its metabolism, the role of signalling in the regulation of growth and development and its potential for use as a storage energy source can be listed. The xerophytic plant Capparis ovata (caper) is well adapted to drought and high temperature stress in arid and semi-arid regions of the Mediterranean. The contribution of trehalose and the trehalose biosynthetic pathway to drought stress responses and tolerance in C. ovata are not known. We investigated the effects of PEG-mediated drought stress in caper plants and analysed physiological parameters and trehalose biosynthetic pathway components, trehalose-6-phosphate synthase (TPS), trehalose-6-phosphate phosphatase (TPP), trehalase activity, trehalose and proline content in drought stress-treated and untreated plants. Our results indicated that trehalose and the trehalose biosynthetic pathway contributed to drought stress tolerance of C. ovata. Overall growth and leaf water status were not dramatically affected by drought, as both high relative growth rate and relative water content were recorded even after 14 days of drought stress. Trehalose accumulation increased in parallel to induced TPS and TPP activities and decreased trehalase activity in caper plants on day 14. Constitutive trehalose levels were 28.75 to 74.75 μg·g·FW−1, and drought stress significantly induced trehalose accumulation (385.25 μg·g·FW−1 on day 14) in leaves of caper. On day 14 of drought, proline levels were lower than on day 7. Under drought stress the discrepancy between trehalose and proline accumulation trends might result from the mode of action of these osmoprotectant molecules in C. ovata.
    Plant Biology 01/2015; 17(2):402-407.
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    ABSTRACT: Measuring biomarkers from plant tissue samples is challenging and expensive when the desire is to integrate transcriptomics, fluxomics, metabolomics, lipidomics, proteomics, physiomics and phenomics. We present a computational biology method where only the transcriptome needs to be measured and is used to derive a set of parameters for deterministic kinetic models of metabolic pathways. The technology is called Transcriptome-To-Metabolome™ (TTM™ ) biosimulations, currently under commercial development, but available for non-commercial use by researchers. The simulated results on metabolites of 30 primary and secondary metabolic pathways in rice (Oryza sativa) were used as the biomarkers to predict whether the transcriptome was from a plant that had been under drought conditions. The rice transcriptomes were accessed from public archives and each individual plant was simulated. This unique quality of the TTM™ technology allows standard analyses on biomarker assessments, i.e. sensitivity, specificity, positive and negative predictive values, accuracy, receiver operator characteristics (ROC) curve and area under the ROC curve (AUC). Two validation methods were also used, the holdout and 10-fold cross validations. Initially 17 metabolites were identified as candidate biomarkers based on either statistical significance on binary phenotype when compared with control samples or recognition from the literature. The top three biomarkers based on AUC were gibberellic acid 12 (0.89), trehalose (0.80) and sn1-palmitate-sn2-oleic-phosphatidylglycerol (0.70). Neither heat map analyses of transcriptomes nor all 300 metabolites clustered the stressed and control groups effectively. The TTM™ technology allows the emergent properties of the integrated system to generate unique and useful 'Omics' information.
    Plant Biology 07/2014; DOI:10.1111/plb.12221.