Skip to main content
Log in

Are the fluorescence parameters of German chamomile leaves the first indicators of the anthodia yield in drought conditions?

  • Original Papers
  • Published:
Photosynthetica

Abstract

7-day soil drought followed by 7-day rehydration was applied to potted German chamomile (Chamomilla recutita) plants at the beginning of their generative stage. Plants of a wild type (WT), plus two diploid (2n) and two tetraploid (4n) genotypes were studied, in order to examine the alterations in chlorophyll (Chl) and carotenoids (Car) contents, and chlorophyll fluorescence (CF) parameters during water shortage and rehydration. The fresh mass of the anthodia after the recovery was also studied.

WT plants adjust better to water stress than modern breeding genotypes, because drought resulted in the low fall in leaf water content of WT, the lowest decrease in the fresh mass of its anthodia (a 41% decrease from the control), and the most elastic response of the photosynthetic apparatus. 4n C11/2 strain plants suffered from the highest reduction in anthodia yield (87%), and had the lowest constitutive pigment contents. It was also the only genotype which revealed nontypical alterations in various CF parameters obtained on a dark- and light-adapted leaf. During drought, a big increase was noticed in minimal, maximal, and variable fluorescence of PSII reaction centres in the dark- adapted (F0, Fm and Fv, respectively), and in the light-adapted state (F0′, Fm′ and Fv′). It was accompanied by the biggest decline in linear electron transport rate (ETR), quantum efficiency of PSII electron transport (ΦPSII) and photochemical quenching coefficient (qP). These alterations were prolonged to the stage when the normal leaf water content was retained. On the contrary, C6/2 strain plants had the highest constitutive Chl and Car contents, which additionally increased after rehydration, similarly to the values of F0, Fm and Fv, which reflects the high photosynthetic potential of this genotype. It was accompanied by the relatively high yield of its anthodia after drought. Considering the drop in the yield triggered by drought, it seems to be the only parameter which may be linked with the ploidy level.

Although the yield formation of chamomile strains cannot simply be estimated by CF assay, this technique may serve as an additional tool in the selection of plants to drought. The following circumstances should be submitted; namely: measurement at the proper developmental stage of plants, in different water regimes, and an analysis of various CF parameters. The increase in F0 and F0′, and the reduction in ETR, Fv′/Fm′, ΦPSII and qP values in response to water deficit should be an indicator of the impairment of the photosynthetic apparatus through drought.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

Abbreviations

Car:

carotenoid

CF:

chlorophyll fluorescence

Chl:

chlorophyll

F0, Fm :

minimal and maximal fluorescence in the dark-adapted state, respectively

Fv :

variable fluorescence in the dark-adapted state

Fv/Fm :

photochemical efficiency of PSII in the dark-adapted state

F0′, Fm′:

minimal and maximal fluorescence in the light-adapted state, respectively

Fv′:

variable fluorescence in the light-adapted state

Fv′/Fm′:

PSII maximum efficiency

ETR:

linear electron transport rate

ΦPSII :

quantum efficiency of PSII electron transport

NPQ:

nonphotochemical quenching of maximal CF

PSII:

photosystem II

qP :

photochemical quenching coefficient

References

  • Baker, N.R., Rosenqvist, E.: Applications of chlorophyll fluorescence can improve crop production strategies: an examination of future possibilities. — J. Exp. Bot. 55: 1607–1621, 2004.

    Article  PubMed  CAS  Google Scholar 

  • Bączek-Kwinta, R., Adamska, A., Seidler-Łożykowska, K., Tokarz, K.: Does the rate of German chamomile growth and development influence the response of plants to soil drought? — Biologia 65: 837–842, 2010.

    Article  Google Scholar 

  • Bączek-Kwinta, R., Adamska, A., Seidler-Łożykowska, K.: [Growth patterns of aerial part sof some German chamomile genotypes as influenced by soil drought.] — Folia Hortic. 1: 54–60, 2006a. [In Polish.]

    Google Scholar 

  • Bączek-Kwinta, R., Filek, W., Grzesiak, S., Hura, T. The effect of severe soil drought and rehydration on growth and antioxidative activity in flag leaves of winter triticale. — Biol. Plant.- 50: 55–60, 2006b.

    Article  Google Scholar 

  • Bączek-Kwinta, R., Seidler-Łożykowska, K.: Cultivars of German chamomile (Chamomilla recutita (L.) Rausch.) and their resistance to water stress. — Acta Physiol. Plant. 26: 142–143, 2004.

    Google Scholar 

  • Bączek-Kwinta R., Kozieł A. [Reaction of photosynthetic apparatus of leaves and the field of heads of German chamomile subjected to drought.] — Advances Agr. Sci. 545: 103–116, 2010. [In Pol.]

    Google Scholar 

  • Bernier, G., Havelange, A., Houssa, C., Petitjean, A., Lejeune, P.: Physiological signals that induce flowering. — Plant Cell 5: 1147–1155, 1993.

    Article  PubMed  CAS  Google Scholar 

  • Bradford, K.J., Hsiao T.C.: Physiological responses to moderate water stress. — In: Lange, O.L., Nobel, P.S., Osmond, C.B., Ziegler, H. (ed).: Physiological Plant Ecology II. Water Relations and Carbon Assimilation. Pp. 263–324. Springer-Verlag Berlin — Heidelberg — New York 1982.

    Google Scholar 

  • Bertamini, M., Nedunchezhian, N.: Photoinhibition of photosynthesis in mature and young leaves of grapevine (Vitis vinifera L.). — Plant Sci. 164: 635–644, 2003.

    Article  CAS  Google Scholar 

  • Cornic, G.: Drought stress inhibits photosynthesis by decreasing stomatal aperture, not by affecting ATP synthesis. — Trends Plant Sci. 5: 187–188, 2000.

    Article  Google Scholar 

  • Cornic, G., Le Gouallec, J.L., Briantais, J.M., Hodges, M.: Effect of dehydration and high light on photosynthesis of two C3 plants (Phaseolus vulgaris L. and Elatostema repens (Lour.) Hall f.). — Planta 177: 84–90, 1989.

    Article  CAS  Google Scholar 

  • Critchley, C.: Photoinhibition. — In: Raghavendra, A.S. (ed.): Photosynthesis: a Comprehensive Treatise. Pp. 264–272. Cambridge University Press, Cambridge 2000.

    Google Scholar 

  • Demmig-Adams, B., Adams, W.W., III: The role of xanthophyll cycle carotenoids in the protection of photosynthesis. — Trends Plant Sci. 1: 21–26, 1996.

    Article  Google Scholar 

  • Demmig, B., Björkmann, O.: Comparison of the effect of excessive light on chlorophyll fluorescence (77K) and photon yield of O2 evolution in leaves of higher plants. — Planta 171: 171–184, 1987.

    Article  CAS  Google Scholar 

  • Ebbs, S., Uchil, S.: Cadmium and zinc induced chlorosis in Indian mustard [Brassica juncea (L.) Czern] involves preferential loss of chlorophyll b. — Photosynthetica 46: 49–55, 2008.

    Article  CAS  Google Scholar 

  • Genty, B., Briantais J.-M., Baker, N.R.: The relationship between the quantum yield of photosynthetic electron transport and quenching of chlorophyll fluorescence. — Biochim. Biophys. Acta 990: 87–92, 1989.

    CAS  Google Scholar 

  • Huner, N.P.A., Öquist, G., Hurry, V.M., Krol, M., Falk, S., Griffith, M.: Photosynthesis, photoinhibition and low temperature acclimation in cold tolerant plants. — Photosynth. Res. 37: 19–39, 1993.

    Article  CAS  Google Scholar 

  • Jin, E., Yokthongwattana, K., Polle, J.E.W., Melis, A.: Role of the reversible xanthophyll cycle in the photosystem II damage and repair cycle in Dunaliella salina. — Plant Physiol. 132: 352–364, 2003.

    Article  PubMed  CAS  Google Scholar 

  • Johnston, J.A., Grise, D.J., Donovan, L.A., Arnold, M.L: Environment-dependent performance and fitness of Iris brevicaulis, I. fulva (Iridaceae), and hybrids. — Am. J. Bot. 88: 933–938, 2001.

    Article  PubMed  Google Scholar 

  • Kovačik, J., Repčak, M., Kron, I.: Nitrogen deficiency induced changes of free amino acids and coumarin contents in the leaves of Matricaria chamomilla. — Acta Physiol. Plant. 28: 159–164, 2006.

    Article  Google Scholar 

  • Kouřil, R., Lazár, D. Lee, H., Jo, J., Nauš, J.: Moderately elevated temperature eliminates resistance of rice plants with enhanced expression of glutathione reductase to intensive photooxidative stress. — Photosynthetica 41: 571–578, 2003.

    Article  Google Scholar 

  • Kováčik, J., Klejdus, B., Hedbavny, J., Štork, F. Bačkor, M.: Comparison of cadmium and copper effect on phenolic metabolism, mineral nutrients and stress-related parameters in Matricaria chamomilla plants. — Plant Soil 320: 231–242, 2009.

    Article  Google Scholar 

  • Kráľová, K., Masarovičová, E., Ondrejkovičová, I., Bujdoš, M.: Effect of selenium oxidation state on cadmium translocation in chamomile plants. — Chem. Papers 61: 171–175. 2007.

    Article  Google Scholar 

  • Krause, G.H., Weis, E.: Chlorophyll fluorescence and photosynthesis. The basics. — Annu. Rev. Plant Physiol. 42: 313–349, 1991.

    Article  CAS  Google Scholar 

  • Kubát, K., Hrouda, L., Chrtek, J.,Jr., Kaplan, Z., Kirschner, Štěpánek, J. (ed.): [Key to the Flora of the Czech Republic]. — Akademia, Praha 2002. [In Czech.]

    Google Scholar 

  • Lavaud, J., Kroth, P.G.: In diatoms, the transthylakoid proton gradient regulates the photoprotective non-photochemical fluorescence quenching beyond its control on the xanthophyll cycle. — Plant Cell Physiol. 47: 1010–1016, 2006.

    Article  PubMed  CAS  Google Scholar 

  • Lichtenthaler, H.K., Wellburn, A.R.: Determination of total carotenoids and chlorophyll a and b of leaf extracts in different solvents. — Biochem. Soc. Trans. 11: 591–592, 1983.

    CAS  Google Scholar 

  • Lichtenthaler, H.K., Ač, A., Marek, M.V., Kalina, J., Urban, O.: Differences in pigment composition, photosynthetic rates and chlorophyll fluorescence images of sun and shade leaves of four tree species. — Plant Physiol. Biochem. 45: 577–588, 2006.

    Article  Google Scholar 

  • Lu, C.M., Lu, Q.T., Zhang, J.H., Zhang, Q., Kuang, T.Y.: Xantophyll cycle, light energy dissipation and photosystem II down-regulation in senescent leaves of wheat plants grown in the field. — Aust. J. Plant Physiol. 28: 1023–1030, 2001.

    CAS  Google Scholar 

  • Montanaro, G., Dichio, B., Xiloyannis, C.: Response of photosynthetic machinery of field-grown kiwifruit under Mediterranean condition during drought and re-watering. — Photosynthetica 45: 533–540, 2007.

    Article  CAS  Google Scholar 

  • Maxwell, K., Johnson, G.N.: Chlorophyll fluorescence — a practical guide. — J. Exp. Bot. 51: 659–668, 2000.

    Article  PubMed  CAS  Google Scholar 

  • Ohtsuka, T., Ito, H., Tanaka, A.: Conversion of chlorophyll b to chlorophyll a and the assembly of chlorophyll with apoproteins by isolated chloroplasts. — Plant Physiol. 113: 137–147. 1997.

    PubMed  CAS  Google Scholar 

  • Öquist, G., Hurry, V.M., Huner, N.P.A.: The temperature dependence of the redox state of QA and the susceptibility of photosynthesis to photoinhibition. — Plant Physiol. Biochem. 31: 683–691, 1993.

    Google Scholar 

  • Ort, D.R: When there is too much light. — Plant Physiol. 125: 29–32, 2001.

    Article  PubMed  CAS  Google Scholar 

  • Papadakis, I.E., Giannakoula A., Antonopoulou, C.P., Moustakas, M., Avramaki, E., Therios, I.N. Photosystem 2 activity of Citrus volkameriana (L.) leaves as affected by Mn nutrition and irradiance. — Photosynthetica 45: 208–213, 2007.

    Article  CAS  Google Scholar 

  • Pavlovič, A., Masarovičová, E., Kráľová, K., Kubová, J.: Response of chamomile plants (Matricaria recutita L.) to cadmium treatment. — Bull. Environ. Contamin. Toxic. 77: 763–771, 2006.

    Article  Google Scholar 

  • Proctor, M.C.F., Tuba, Z.: Poikilohydry and homoihydry: antithesis or spectrum of possibilities? — New Phytol. 156: 327–349, 2002.

    Article  Google Scholar 

  • Ramírez, D.A., Valladares, F., Domingo, F., Bellot, J.: Seasonal water-use efficiency and chlorophyll fluorescence response in alpha grass (Stipa tenacissima L.) is affected by tussock size. — Photosynthetica 46: 222–231, 2008.

    Article  Google Scholar 

  • Razmjoo, K., Heydarizadeh, P. Sabzalian, M.R.: Effect of salinity and drought stresses on growth parameters and essential oil content of Matricaria chamomila. — Int. J. Agr. Biol. 10: 451–454, 2008.

    Google Scholar 

  • Rutkowski, L. [Key to the Recognition of Vascular Plants of Lowland Poland.] PWN, Warsaw 1998. [In Pol.]

    Google Scholar 

  • Šalamon, I.: The Slovak gene pool of German chamomile (Matricaria recutita L.) and comparison in its parameters. — HortSci. 2: 70–75, 2004.

    Google Scholar 

  • Šalamon, I., Kráľová, K. Masarovičová, E.: Accumulation of cadmium in chamomile plants cultivated in Eastern Slovakia regions. — Acta Hort. 749: 217–222. 2007.

    Google Scholar 

  • Schreiber, U., Bilger, W.: Progress in chlorophyll fluorescence research: major developments during the past years in retrospect. — Progr. Bot. 54: 151–173, 1993.

    CAS  Google Scholar 

  • Schreiber, U., Schliwa, U., Bilger, W.: Continuous recording of photochemical and non-photochemical chlorophyll fluorescence with a new type of modulation fluorometer. — Photosynth Res. 10: 51–62, 1986.

    Article  CAS  Google Scholar 

  • Seidler-Łożykowska, K.: Chamomile cultivars and their cultivation in Poland. — Acta Hortic. 749: 111–114. 2007.

    Google Scholar 

  • Seidler-Łożykowska, K.: [Comparison of some traits of chamomile strains and varieties with high content of alfabisabolol. Part II.] — Herba Pol. 1: 5–11, 2000. [In Pol.]

    Google Scholar 

  • Sofo A., Dichio B., Montanaro G., Xiloyannis C.: Photosynthetic performance and light response of two olive cultivars under different water and light regimes. — Photosynthetica 47: 602–608, 2009.

    Article  CAS  Google Scholar 

  • Verhoeven, A.S., Demmig-Adams, B., Adams, W.W.: Enhanced employment of the xanthophylls cycle and thermal energy dissipation in spinach exposed to high light and N stress. — Plant Physiol. 113: 817–824, 1997.

    PubMed  CAS  Google Scholar 

  • Wentworth, M., Murchle, E.H., Gray, J.E., Villegas, D., Pastenes, C., Pinto, M., Horton, P.: Differential adaptation of two varieties of common bean to abiotic stress. II. Acclimation of photosynthesis. — J. Exp. Bot. 57: 699–709, 2006.

    Article  PubMed  CAS  Google Scholar 

  • Xu, D.H., Li J.H., Fang, X.W., Wang, G., Su, P.X.: Photosynthetic activity of poikilochlorophyllous desiccation tolerant plant Reaumuria soongorica during dehydration and re-hydration. — Photosynthetica 46: 547–551, 2008.

    Article  CAS  Google Scholar 

  • Yamane, Y., Shikanai, T., Kashino, Y., Koike, H., Satoh, K.: Reduction of QA in the dark: another cause of fluorescence F0 increases by high temperatures in higher plants. — Photosynth. Res. 63: 23–34, 2000.

    Article  PubMed  CAS  Google Scholar 

  • Zhang, Q., Chen, J.-W., Li, B.-G., Cao, K.-F.: The effect of drought on photosynthesis in two epiphytic and two terrestrial tropical fern species. — Photosynthetica 47: 128–132, 2009.

    Article  Google Scholar 

Download references

Acknowledgement

The authors thank to Ms Ewa Piechocka and Ms Ewa Przydanek (Institute of Natural Fibres and Medicinal Plants, Poznań) for excellent technical support. RBK will also to thank to the two anonymous reviewers for the comments which allowed to improve the final version of the manuscript.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to R. Bączek-Kwinta.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Bączek-Kwinta, R., Kozieł, A. & Seidler-Łożykowska, K. Are the fluorescence parameters of German chamomile leaves the first indicators of the anthodia yield in drought conditions?. Photosynthetica 49, 87–97 (2011). https://doi.org/10.1007/s11099-011-0013-3

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s11099-011-0013-3

Additional key words

Navigation