Photosynthetic capability and Fe，Mn，Cu，and Zn contents in two Moraceae species under different phosphorus levels

Deke Xing·Yanyou Wu·Rui Yu·Yansheng Wu·Chuan Zhang· Zheng Liang

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Photosynthetic capability and Fe，Mn，Cu，and Zn contents in two Moraceae species under different phosphorus levels

Deke Xing1·Yanyou Wu2·Rui Yu1·Yansheng Wu1·Chuan Zhang1· Zheng Liang1

?Science Press，Institute of Geochemistry，CAS and Springer-Verlag Berlin Heidelberg 2016

ThestrongadaptabilityofBroussonetia papyrifera（L.）Vent.to low phosphorus（P）conditions can be attributed to the large amount of root-exuded organic acids and the high efficiency of P extraction.However，microelement contents are influenced by low-P stress，and their effects on the photosynthetic capability of B.papyrifera remain unknown.In this study，we investigated the effects of low-P treatment on net photosynthetic rate（PN）；chlorophyll a fluorescence（ChlF）characteristics；and Fe，Mn，Cu，and Zn contents of B.papyrifera and Morus alba L.seedlings.Results show that B.papyrifera exhibited better photosynthetic capability under moderate P deficiency（0.125，0.063，and 0.031 mmol/L P treatments），whereas the photosynthetic capability of M.alba decreased under moderate and severe P deficiency（0.016 and 0 mmol/L P treatments）.Under moderate P deficiency，the decrease in Cu and Zn contents in B.papyrifera was lower than that in M.alba.Under severe P deficiency，a considerable decrease of photosynthetic capability in B.papyrifera and M.alba was associated with low Cu and Zn contents.The PNof the two Moraceae species exhibited a better correlation with Cu and Zn contents than with Fe or Mn content.P deficiency could not only decrease cyclic photophorylation and photosynthetic efficiency，but could also affect the stability of thylakoid membrane structure and electron transport efficiency by influencing the contents of Cu or Zn，thereby affecting photosynthesis.

Adaptability·Chlorophyll a fluorescence· Microelement·Organic acids·Sensitive

Abbreviations

ΦPSIIActual photochemical quantum efficiency of PSII

B.papyriferaBroussonetia papyrifera（L.）Vent

ChlFChlorophyll a fluorescence

FsFluorescence in stable state

FoInitial fluorescence

LSDLeast significant difference

FmMaximum fluorescence

F′mMaximumfluorescenceinthelightadapted state

Fv/FmMaximum quantum yield of PSII

M.albaMorus alba L

PNNet photosynthetic rate

P Phosphorus

PSIIPhotosystem II

SEStandard errors

FvVariable fluorescence

1 Introduction

Broussonetia papyrifera（L.）Vent.and Morus alba L.are perennial tree species belonging to the family Moraceae and are characterized by higher growth rate and greater adaptability to adverse environments than other species in this family（Zhao et al.2005）.B.papyrifera is moretolerant to a low-phosphorus（P）environment（Liu et al. 2010）.Unlike M.alba，B.papyrifera can acclimate to karst soil and resist alien invasion（Wu et al.2009）.A higher amount of organic acids is found in root exudates of B.papyrifera than in M.alba in low-P environments （Shahbaz et al.2006）.Root-exuded organic acids sometimes form organometallic complexes with insoluble phosphoric compounds in soil，releasing available P（Jones and Darrah 1994）；the strong adaptability of B.papyrifera to low-P environments can be attributed to the high efficiency of P extraction（Zhao and Wu 2014）.However，the root-exudedorganicacidsmightalsoimprovethe bioavailability of microelements（Hoffland et al.1992）.The concentration and uptake of plant microelements increase when smaller amounts of P are applied（Racz and Haluschak 1974；Rutkowska et al.2014）.Nonetheless，the relationship between the increase in concentration of plant microelements and the adaptability of B.papyrifera remains unknown.

Inorganic P is one of the least available nutrients in the soils of several terrestrial ecosystems（Alloush et al.2003；Li et al.2006）.P deficiency leads to a considerable decrease in cyclic photophorylation and photosynthetic efficiency（Watanabe and Yoshida 1970）.Some studies have demonstrated that P deficiency induces possible photoinhibition and damage to photosystem II（PSII）（Li et al.2004）.Moreover，the uptake of microelements-such as Fe，Mn，Cu，and Zn-in plants is also related to photosynthesis.Fe is an essential micronutrient for plants（Hao et al.2007）.Bertamini et al.（2002）proved that a low photosyntheticelectrontransportrateinFe-deficient grapevine leaves is mainly due to the loss of PSII activity. Mn plays an important role in the water-splitting reaction leading to oxygen evolution in photosynthesis（Sauer 1980）.The most important role of Cu is associated with blocking of photosynthetic electron transport，leading to production of radicals which start peroxidative chain reactions involving membrane lipids（Fernandes and Henriques 1991）.Finally，Zn deficiency causes reduction of electron use in dark reactions and decreases heat dissipation（Hajiboland et al.2010）.

A certain amount of supplemental P increases the uptake of some micronutrients，while decreasing the uptake of Zn in some plant organs（Nyoki and Ndakidemi 2014）.The total amounts of Fe，Mn，Cu，and Zn absorbed by aboveground plant tissue decrease in treatments in which nutrient deficiencies are observed，but the micronutrient concentrations in tissues do not decrease（Choi and Lee 2012）. Root-exuded organic acids might increase the uptake of microelements in plants，compensate for the loss of microelements under a low-P environment，and slow the decrease of microelement contents.As a result，the lower rate of decrease in microelement contents could alleviate the damage caused by microelement deficiency to plants in a low-P environment，thereby enhancing photosynthesis. Given that microelements play important roles in photosynthesis，the variations in microelement contents could be a photosynthetic adaptive mechanism of B.papyrifera to low-P stress.

Non-invasive methods such as chlorophyll a fluorescence（ChlF）have been used to observe various types of stress affecting the photosynthetic machinery（Huang et al. 2004）.ChlF has been widely used to evaluate plant tolerance to environmental stresses（Gray et al.2006）.The present study examined net photosynthetic rate（PN）；ChlF parameters；and Fe，Mn，Cu，and Zn contents in two Moraceae species.The influence of Fe，Mn，Cu，and Zn contents on the photosynthetic capability of B.papyrifera and M.alba was analyzed.Results of this study provide deeper understanding of the photosynthetic adaptive mechanism of B.papyrifera in a low-P environment，which can be used as a guide for selecting appropriate plant species for reforestation efforts in a heterogeneous environment.

2 Materials and methods

2.1Plant growth and low-P treatment

Seedlings of B.papyrifera and M.alba were cultivated and treated according to Xing and Wu（2014）.After 90 days of growth，the nutrient solution was replaced by a modified Hoagland solution（Hoagland and Arnon 1950）containing 6 mmol/L KNO3，4 mmol/LCa（NO3）2，2 mmol/L MgSO4，2 mmol/L Fe（Na）EDTA，2 μmol/LKCl，50 μmol/L H3BO3，4 μmol/L MnSO4，4 μmol/L ZnSO4，0.2 μmol/L CuSO4，and 0.2 μmol/L（NH4）6MO7O24.Five low-P treatments of 0.125，0.063，0.031，0.016，and 0 mmol/L were simulated by varying concentration combinations of NH4H2PO4and NH4Cl；0.250 mmol/L P was used as the control.Determination was conducted on day 45 from the onset of treatment.Five recently-matured leaves from each of the treated seedlings were measured.

2.2Measurement of net photosynthetic rate

Net photosynthetic rate was determined using the method in Xing and Wu（2012）.

2.3Measurement of chlorophyll a fluorescence

ChlF was determined according to the method described by Xing and Wu（2012）.The maximum quantum yield of PSII（Fv/Fm）was calculated as（Fm-Fo）/Fm，where Fv=Fm-Fo.The actual photochemical quantum efficiency of PSII（ΦPSII）was calculated as（F′m-Fs）/F′m.

2.4Contents of Fe，Mn，Cu，and Zn

Five plants from each treatment group were selected and dried in an oven at 80°C.Approximately 0.3-0.5 g of dried plant tissue was digested using the H2SO4-H2O2digestion method（Xu 2000）.The Fe，Mn，Cu，and Zn contents were determined using atomic absorption spectroscopy（PE-5100-PC，PerkinElmer，USA）.

2.5Statistical analysis

All experimental measurements consisted of five replicates. Data were analyzed using SPSS software（version 13.0，SPSS Inc）.The differences between low-P treatments were assessed using the least significant difference（LSD）post hoc test at a 5%significance level（p≤0.05）.Data were shown as the means±standard errors（SE），which were determined using one-sample T test（confidence interval was 95%）.The correlation between PNand content of Fe，Mn，Cu，or Zn was analyzed using bivariate correlations.

3 Results

3.1Effect of low-P on net photosynthetic rate

M.alba showed a significant decrease in PNfrom the onset oflow-Ptreatment（Table 1）.Whilethesignificant decrease of PNof B.papyrifera appeared at 0.063 mmol/L. The PNof M.alba exhibited a more significant decrease than that of B.papyrifera from 0.031 to 0.016 mmol/L. The values of PNof B.papyrifera at 0.016 and 0 mmol/L were 49%and 41%，respectively，of the value of the control，while the values of PNof M.alba at 0.016 and 0 mmol/L were only 38%and 13%，respectively，of the value of the control.The value of PNof B.papyrifera was higher than M.alba at each low-P stress level.

3.2Effects of low-P on ChlF parameters

The values of initial fluorescence（Fo）of B.papyrifera subjected to 0.016 and 0 mmol/L P treatments were higher than those in 0.250，0.125，0.063，and 0.031 mmol/L P treatments；the Fovalues of B.papyrifera in treatments with P nutrient levels ranging from 0.250 to 0.031 mmol/L showed no significant difference（Fig.1a）.The Fovalue of M.alba of the control was lower than that at other P nutrient levels；the Fovalues of M.alba in treatments with P nutrient levels ranging from 0.125 to 0.016 mmol/L showed no significant difference.

The maximum quantum yields of PSII（Fv/Fm）of B.papyrifera at 0.016 and 0 mmol/L P treatments were lower than those of higher P treatments；the Fv/Fmvalues of B.papyrifera in treatments with P nutrient levels ranging from 0.250 to 0.031 mmol/L showed no significant difference（Fig.1b）.The Fv/Fmof M.alba of the control was higher than that of other P nutrient levels；the Fv/Fmvalues of M.alba in treatments with P nutrient levels ranging from 0.125 to 0.016 mmol/L showed no significant difference.

The actual photochemical quantum efficiencies of PSII （ΦPSII）closely mimicked the pattern observed in maximum quantum yields.ΦPSIIvalues of B.papyrifera at 0.016 and 0 mmol/L were lower than those with higher P treatments；the ΦPSIIvalues of B.papyrifera in treatments with P nutrient levels ranging from 0.250 to 0.031 mmol/L showed no significantdifference（Fig.1c）.TheΦPSIIofM.albaofthecontrol was higher than of those subjected to P deficiency；the ΦPSIIvalues of M.alba in treatments with P nutrient levels ranging from0.125to0.031 mmol/Lshowednosignificantdifference.

Table 1 Effect of low-P on net photosynthetic rate

3.3Effects of low-P on contents of Fe，Mn，Cu，and Zn

Fe，Mn，Cu，and Zn contents varied between plant species and P levels（Table 2）.Low-P treatment was associatedwith lower contents of Fe and Mn at all P-deficient treatment levels in B.papyrifera，whereas the Fe and Mn contents in M.alba in treatments with P nutrient levels ranging from 0.250 to 0.031 mmol/L showed no significant difference.The micronutrient contents in M.alba in 0.016 and 0 mmol/L P treatments were lower than in higher P treatments.

Low-P treatment was consistently associated with lower contents of Cu in both B.papyrifera and M.alba（Table 2）.

The contents of Zn in B.papyrifera in treatments with P nutrient levels ranging from 0.250 to 0.031 mmol/L showed no significant difference.The Zn contents of B.papyrifera at 0.016 and 0 mmol/L P treatments were lower than those higher-P treatments（Table 2）.

Fig.1 Effects of low-P on initial fluorescence（Fo），maximum quantum yields of PSII（Fv/Fm）and the actual photochemical quantum efficiencies of PSII（ΦPSII）.a Fo；b Fv/Fm；c ΦPSII.Different letters appear above the error bars of the same parameter of the same plantspecies　when　subsequentvalues　differsignificantly-at P≤0.05，according to one-way ANOVA and t tests

3.4Relationship between net photosynthetic rate and content of Fe，Mn，Cu，or Zn

The relationships between PNand the content of Cu or Zn displayed good positive correlations（Fig.2c，d），in which the determination coefficient（R2）ranged from 0.245 to 0.865；the R2of Cu or Zn was greater than that of Fe or Mn （Fig.2a，b）.In other words，an increase in Cu and Zn contents correlated with an increase of PNin both B.papyrifera and M.alba.

4 Discussion

Photosynthetic activity represents the growth potential of a plant（Walters et al.1993）.B.papyrifera exhibited better photosynthetic capability than M.alba under moderate P deficiency，whereas the photosynthetic capability of M. alba decreased significantly under moderate and severe P deficiency；the influence of low-P on photosynthesis was more severe in M.alba than in B.papyrifera.In addition，the resistances of B.papyrifera and M.alba to a low-P environment were different；the photochemical apparatus of B.papyrifera was not damaged under moderate P deficiency，whereas the increase of Fo in B.papyrifera under severe P deficiency indicated that the activity of PSII reaction centers had decreased.The response to decreased P of Fv/Fm and ΦPSIIin B.papyrifera also indicated little damage to the PSII reaction centers under moderate P deficiency.However，the activity of PSII reaction centers in M.alba decreased in low-P treatments；that is，the PSII reaction centers of M.alba were damaged under low-P stress conditions.When the P concentration of nutrient solution was higher than 0.031 mmol/L，the B.papyrifera exhibited good tolerance.However，the tolerance of M.alba decreased under even moderate P deficiency.

Under moderate P deficiency，the amount of root-exuded organic acids in B.papyrifera increased more significantly than in M.alba（Wu and Zhao 2013），and according to Hofflandetal.（1992），thebioavailabilityofmicroelementsaround the rootof B.papyrifera couldbeimproved as a result.Dueto the increase in root-exuded acids，the Cu content in B.papyrifera washigher thanthat inM.alba，andthe Zn content in B.papyrifera exhibited a lower rate of decrease than that in M.alba.SincethemostimportantroleofCuisassociatedwith blocking of peroxidative chain reactions involving membrane lipids（Fernandes and Henriques 1991），higher Cu content in B.papyrifera could maintain the stability of thylakoid membrane structure more efficiently.Moreover，Zn could improve electron use in dark reactions（Hajiboland et al.2010）；therefore，the lower rate of decrease in Zn in B.papyrifera could maintain the stability of dark reactions more efficiently.Bycontrast，the damage caused by the decrease in Cu and Zn contents to M.alba could not be alleviated efficiently，and the photosynthesisofM.albacouldnotbemeliorated.Theresults in the present study also indicate that the photosynthetic capability of B.papyrifera was relatively unaffected，whereas the photosynthetic capability of M.alba is sensitive to moderate P deficiency.Under severe P deficiency，the amount of root-exuded organic acids in M.alba increased more significantly than in B.papyrifera（Wu and Zhao 2013）.Although the Cu content in M.alba exhibited a lower rate of decrease，the decrease in Zn content was significant.Under severe P deficiency，the increase in the amount of root-exuded organic acids in B.papyrifera and M.alba could not alleviate the loss of microelements.Moreover，a considerable decrease of photosynthetic capability in B.papyrifera and M.alba was associated with the lower Cu and Zn contents.

Table 2 Effects of low-P on Fe，Mn，Cu，and Zn contents （mg/g）

Given that the availability of Fe and Mn are higher than that of Cu or Zn in the soils of several terrestrial ecosystems（Chen et al.2013），plant growth is more easily affected by Cu or Zn content in soil.In the present study，the applied amounts of Fe and Mn were probably enough for the growth of the two Moraceae species in low-P environments.P deficiency could not only bring about a decrease in cyclic photophorylation and photosynthetic efficiency（Watanabe and Yoshida 1970），but could also affect the stability of thylakoid membrane structure and electron transport efficiency by influencing the content of Cu or Zn，thereby affecting photosynthesis.Moreover，the PNof the two Moraceae species exhibited a better correlation with Cu and Zn contents，rather than with Fe or Mn content.P deficiency had almost no effect on PSII activity or on the water-splitting reaction in either plant species.

Fig.2 Relationships between the net photosynthetic rate（PN，μmol/m2s）and content of Fe，Mn，Cu，or Zn（mg/g）.Note：Y is the PN；X is the content of Fe，Mn，Cu or Zn.a Fe；b Mn；c Cu；d Zn

5 Conclusion

The responses of B.papyrifera and M.alba to low-P treatment with different Fe，Mn，Cu，and Zn contents varied in terms of photosynthetic capability.B.papyrifera exhibited better photosynthetic capability under moderate P deficiency，whereas the photosynthetic capability of M.alba decreased under moderate and severe P deficiency. Under moderate P deficiency，the decreases in Cu and Zn contents in B.papyrifera were lower than those in M.alba. Under severe P deficiency，a significant decrease of photosynthetic capability in B.papyrifera and M.alba was associated with lower Cu and Zn contents.The PNof the two Moraceae species exhibited a better correlation with Cu and Zn contents than with Fe or Mn content.Furthermore，P deficiency could not only decrease the cyclic photophorylation and photosynthetic efficiency，but also affect the stability of thylakoid membrane structure and electron transport efficiency by influencing the content of Cu or Zn，thereby affecting photosynthesis.Nevertheless，P deficiency had almost no effect on PSII activity or watersplitting.

AcknowledgmentsThis study was supported by the project of the National Natural Science Foundation of China（No.31301243），a project funded by the Priority Academic Program Development of Jiangsu higher education institutions（PAPD），the research foundation for introduce talents of Jiangsu university（13JDG030），the brainstorm project on social development of Guizhou Province（SY［2010］3043）.

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8 December 2015/Revised：16 January 2016/Accepted：21 February 2016/Published online：27 February 2016

? Yanyou Wu wuyanyou@mail.gyig.ac.cn
1Key Laboratory of Modern Agricultural Equipment and Technology，Ministry of Education，Institute of Agricultural Engineering，Jiangsu University，Zhenjiang 212013，China2Research Center for Environmental Bio-Science and Technology，State Key Laboratory of Environmental Geochemistry，Institute of Geochemistry，Chinese Academy of Sciences，Guiyang 550081，China