Growth, Mineral Nutrients, Photosynthesis and Related Physiological Parameters of Citrus in Response to Nitrogen Deﬁciency

: Limited data are available on the physiological responses of Citrus to nitrogen (N) deﬁciency. ‘Xuegan’ ( Citrus sinensis (L.) Osbeck) and ‘Shantian pummelo’ ( Citrus grandis (L.) Osbeck) seedlings were fertilized with nutrient solution at a N concentration of 0, 5, 10, 15 or 20 mM for 10 weeks. N deﬁciency decreased N uptake and N concentration in leaves, stems and roots and disturbed nutrient balance and homeostasis in plants, thus inhibiting plant growth, as well as reducing photosynthetic pigment levels and impairing thylakoid structure and photosynthetic electron transport chain (PETC) in leaves, hence lowering CO 2 assimilation. The imbalance of nutrients intensiﬁed N deﬁciency’s adverse impacts on biomass, PETC, CO 2 assimilation and biosynthesis of photosynthetic pigments. Citrus displayed adaptive responses to N deﬁciency, including (a) elevating the distributions of N and other elements in roots, as well as root dry weight (DW)/shoot DW ratio and root-surface-per-unit volume and (b) improving photosynthetic N use efﬁciency (PNUE). In general, N deﬁciency had less impact on biomass and photosynthetic pigment levels in C. grandis than in C. sinensis seedlings, demonstrating that the tolerance of C. grandis seedlings to N deﬁciency was slightly higher than that of C. sinensis seedlings, which might be related to the higher PNUE of the former. Our ﬁndings showed that N deﬁciency decreased maximum primary yield of photochemistry of PSII (F v /F o ), total electron carriers per reaction center (RC; S m or EC o /RC), F v /F m (TR o /ABS), quantum yield for electron transport ( ϕ Eo or ET o /ABS), efﬁciency with which an electron can move from the reduced intersystem electron acceptors to the photosystem I (PSI) end electron acceptors ( δ Ro or RE o /ET o ), quantum yield for the reduction in end acceptors of PSI per photon absorbed ( ϕ Ro or RE o /ABS), probability that a trapped exciton moves an electron into the electron transport chain beyond Q A − ( ψ Eo or ET o /TR o ), efﬁciency with which a trapped exciton can move an electron into the electron transport chain from Q A − to the PSI end electron acceptors ( ρ Ro or RE o /TR o ), electron transport ﬂux per RC (ET o /RC), reduction in end acceptors at PSI electron acceptor side per RC (RE o /RC), reduction in end acceptors at PSI electron acceptor side per cross section (CS; RE o /CS o ), maximum amplitude of IP phase, and total performance index (PI abs,total ) by 26%, 49%, 6%, 48%, 23%, 60%, 45%, 58%, 14%, 34%, 48%, 65% and 90%, respectively, in C. grandis leaves and by 26%, 45%, 5%, 47%, 22%, 58%, 44%, 56%, 9%, 29%, 44%, 64% and 90%, respectively, in C. sinensis leaves, and increased minimum ﬂuorescence (F o ), approximated initial slope (in ms − 1 ) of the ﬂuorescence transient V = f(t) (M o ), relative variable ﬂuorescence at the J- (2 ms, V J) and I- (30 ms, V I ) steps, absorption ﬂux per RC (ABS/RC), quantum yield for energy dissipation (DI o /ABS),


Introduction
After carbon, nitrogen (N) is an essential element required in larger amounts by plants than any other elements. N, as a component of chlorophyll (Chl), nucleic acids, amino acids, proteins, plant hormones, coenzymes and secondary metabolites, accounts for 1-5% of the total plant dry matter. Therefore, N plays a key role in various metabolic processes of plants such as Chl biosynthesis and photosynthesis [1,2]. N is one of the main elements limiting crop productivity, especially in the agricultural system with aerobic soil, in which nitrate is easily leached under the condition of high rainfall [3]. The common N deficiency symptoms of crops include arrested vegetative growth, leaf yellowing, narrow leaves and reduced yields [2,4,5]. To meet the required high crop yields, N fertilizers have been widely applied [3,6]. The amounts of N fertilizers applied in the world from 11.4 Tg fertilizer N year −1 in 1961 to 107.7 Tg fertilizer N year -1 in 2019 [7]. Therefore, it is becoming increasingly imperative to find a widely applicable method to lower the amount of N fertilizer used without reducing yields [8]. Understanding the physiological responses of crops to N deficiency is key for the improvement of N use efficiency and the reduction in N fertilization.
Leaf CO 2 assimilation (A CO2 ) relies heavily on the functions of photosynthetic pigments and proteins (enzymes), which occupy the majority of N in leaves [9][10][11][12]. Therefore, N deficiency causes a decrease in A CO2 , which is often accompanied by decreases in the concentrations of photosynthetic pigments such as Chl and carotenoids (Car) and the activities of photosynthetic enzymes such as ribulose-1,5-bisphosphate carboxylase/oxygenase (Rubisco) [3,[9][10][11][12][13][14]. N is highly related to stomatal conductance (g s ) and/or stomatal movement [9]. In a study, Zhao et al. [15] suggested that the reduction in A CO2 in N deficiency sorghum leaves was mainly caused by lower g s , because its reduction was accompanied by decreases in both g s and intercellular CO 2 concentration (C i ). However, growing evidence is showing that N-deficiency-induced reduction in leaf A CO2 is primarily caused by non-stomatal factors, because the reduction is accompanied by increased C i and/or the ratio of intercellular to ambient CO 2 concentration (C i /C a ), despite the reduced g s [10][11][12]14,[16][17][18][19].
Scientific reports on N deficiency's effects on primary photochemistry and electron transport of photosystem II (PSII) are inconsistent. Using Chl a fluorescence techniques, a lot of researches have shown that the reduction in leaf A CO2 was associated with a reduced electron transport rate and raised thermal dissipation of absorbed light energy [9,14,16,[20][21][22][23][24]. However, Cruz et al. [17] indicated that N deficiency induced a decrease in A CO2 in cassava leaves, which was mainly caused by a decline in biochemical capacity for carboxylation, rather than electron transport, in which the maximum PSII efficiency of dark-adapted leaves (F v /F m ) was not significantly altered by N deficiency. Unchanged F v /F m also have been obtained in the N-deficient leaves of sorghum [18], maize and wheat [25]. Polyphasic Chl a fluorescence (OJIP) transients and related fluorescence (OJIP test) parameters have been widely used to reveal the alterations of PSII photochemistry caused by various nutrients deficiencies, such as phosphorus (P), potassium (K), calcium (Ca), sulfur (S), iron (Fe), boron (B), magnesium (Mg), manganese (Mn), copper (Cu) and zinc (Zn) in leaves [26][27][28][29][30][31][32][33][34]. However, limited information is available on N-deficiency-induced alterations of OJIP transients and OJIP test parameters in leaves. So far, all of these studies have focused on herbs (i.e., maize, tomato, radish and wheat) and shrubs (i.e., tea) [14,20,25,28,29].
There were several studies investigating N deficiency's effects on the uptake of nutrients and their concentrations in leaves, stems and/or roots, but the results were not unanimous [3,[35][36][37][38][39][40][41]. For example, the concentrations of P, K, Ca, Mg, Mn, Cu and Fe in roots and shoots of barley decreased significantly in response to N deficiency, with a few exceptions that only displayed a decreased trend; but the decreased extent depended on elements, plant tissues and genotypes [38]. N deficiency increased the concentrations of P and K in Parthenocissus tricuspidata (Sieb. & Zucc.) Planch. roots, stems and leaves (mg g −1 DW), but decreased their accumulation in roots, stems and leaves (mg plant −1 ) [39]. In sugar cane, N deficiency lowered the concentration of N in stems and leaves, increased the concentrations of P, K and Mg in leaves and P, Mg and S in roots, decreased the concentration of Ca in roots, but had little influence on the concentrations of Ca and S in leaves and K in roots. In leaves, N deficiency led to an increase in the ratio of P, K, Mg, Ca or S concentration to N concentration, while in stems, N deficiency caused a decrease in the ratio of N-, K-, Ca-, Mg-or S-to-P concentration [41]. The absence of N lowered the accumulation of N, P, K, Mg, S and Ca in snap bean shoots [35]. In Spathiphyllum leaves, N deficiency increased the concentrations of P and Ca, but it decreased the concentrations of N and K [40]. Nasr Esfahani et al. [42] found that nitrate or phosphate (Pi) imbalance (deficiency) caused stronger molecular responses than combined deficiencies of nitrate and Pi in chickpea roots and leaves. N deficiency, therefore, may disturb other nutrient balance and homeostasis, and thus intensify its adverse impacts on growth, biosynthesis of photosynthetic pigments, photosynthetic electron transport chain (PETC) and A CO2 . To date, such data are very rare.
To deal with N deficiency, plants have evolved various adaptive mechanisms [6,8,[43][44][45][46]. Many studies have shown that N deficiency can increase the partitioning of photosynthetic dry matter to roots, thus increasing the root/shoot ratio. The increase may be related to the preferential allocation of limited N-to-N-deficient roots [3,6,14,36,39,[47][48][49][50][51][52][53]. Wang et al. [39] observed that, in addition to increasing N distribution in P. tricuspidata roots, N deficiency led to an increase in the distributions of P and K in roots. In general, N-deficiency-induced decreases in P, K, Mg, Cu, Ca, Fe and Mn concentrations were less in barley roots than in shoots [38]. Under N deficiency, the increased distributions of the other nutrient elements in roots might contribute to the higher root/shoot ratio. Increasing evidence shows that the alteration of root architecture in response to N deficiency plays a key role in enhancing N acquisition of plants [6,8,44,45,54].
N is a major factor limiting yield for many crops including Citrus [5,8,44]. The optimum range of N concentration in Citrus leaves is 23-28 g kg −1 DW [55]. Yellow leaves may show when foliar N concentration ranges from 12.5 to 17.5 g kg −1 DW [5]. Chen et al. [56] indicated that Citrus plants were ammonium sensitive. In China, N deficiency often occurs in Citrus orchards, which is one of the main causes of yield loss and fruit quality decline [57][58][59][60][61]. Limited data are available on the physiological responses of Citrus to N deficiency [10,44,45]. Using Citrus sinensis (L.) Osbeck and Citrus grandis (L.) Osbeck seedlings as materials, we investigated N deficiency impacts on growth, root architecture (i.e., root length, root surface area, root average diameter and root volume), nutrient elements in leaves, stems and roots, and photosynthetic pigments, gas exchange, OJIP transients and related parameters in leaves. The objectives of this study were (a) to test the hypothesis whether nutritional imbalance aggravates the symptoms of N deficiency, (b) to understand the possible physiological mechanisms of Citrus adaptation to N deficiency, and (c) the causes of leaf A CO2 decline in response to N deficiency.

Seedling Culture and N Treatments
Seedling culture and N treatments were carried out according to Yang et al. [32] with some modifications. Six-week-old uniform 'Xuegan' (Citrus sinensis (L.) Osbeck) and 'Shantian pummelo' (Citrus grandis (L.) Osbeck) seedlings were planted to 6 L pots (two plants pot −1 ) filled with sand and cultivated in a greenhouse under natural conditions at Fujian Agriculture and Forestry University, Fuzhou (26 • 5 N, 119 • 14 E) with annual average sunshine hours, temperature and relative humidity of~1600 h, 20 • C and 76%, respectively [62]. Seven weeks after transporting, each pot was fertilized thrice weekly with nutrient solution at a N concentration of 0, 5 10, 15 or 20 mM (i.e., macronutrients (Table 1) and micronutrients: 20 µM Fe-EDTA, 10 µM H 3 BO 3 , 2 µM ZnSO 4 , 2 µM MnCl 2 , 0.5 µM CuSO 4 and 0.065 µM (NH 4 ) 6 Mo 7 O 24 ) until part of the nutrient solution started to leak out of the hole at the bottom of the pot (~500 mL pot −1 ). Ten weeks after N treatments, the recent, fully expanded (approximately 7-week-old) leaves were used for all measurements. Firstly, both leaf gas exchange and OJIP transients were measured. Then, 6 mm-diameter leaf discs from the same seedlings used for the above measurements were harvested at a sunny noon and immediately frozen in liquid N 2 , then stored at −80 • C until assay of photosynthetic pigments. These plants unused for disc collection were used for the measurements of biomass and elements. Leaf, stem and root DW was weighted after being dried to a constant weight at 70 • C. The image of clean root was captured using digital scanner (Epson Expression 10000XL, Epson America, San Jose, CA, USA) at 600-dpi resolution. Total root length, root surface area, root average diameter and root volume were analyzed using WinRHIZO software (Version 2009b, Regent Instruments, Montreal, QC, Canada) [56].

Elements in Leaves, Stems and Roots
Recent fully expanded mature leaves, the middle parts of stems and fibrous roots were collected for element analysis. N, K, P, Mg, Ca, S, Mn, Zn, B, Cu and Fe were extracted and measured as described by Cai et al. [64] and Long et al. [65].
Element uptake per plant (plant total element content) was the sum of element content (element concentration × tissue DW) in leaves, stems and roots. Element uptake per root DW was calculated as plant total element content/root DW. Element distribution in leaves, stems or roots (%) was calculated as element content in leaves, stems or roots/plant total element × 100, respectively [64,65].

Gas Exchange, OJIP Transients and Related Fluorescence Parameters in Leaves
Gas exchange was made with a CIRAS-2 portable photosynthesis system (PP Systems, Herts, UK) between 9:00 and 11:00 a.m. on a sunny day [26]. Water use efficiency (WUE) and photosynthetic N use efficiency (PNUE) were calculated as A CO2 /transpiration rate (Tr) [62] and A CO2 /leaf N concentration [66], respectively. Leaf OJIP transients were measured after plants had been stored in the dark for 3 h at room temperature using the Handy PEA (Hansatech Instruments Limited, Norfolk, UK). Fluorescence parameters were calculated according to Kalaji et al. [29] and Jiang et al. [67].

Statistical Analysis
The results were the means ± SE of 3-12 replicates. Except for the mean OJIP transients (only means), a plant in different pots was a repeat. Data were analyzed by two-way ANOVA (five (N levels) × two (species)) followed by the least significant difference (LSD) at p < 0.05 level. Calculation of Pearson correlation coefficients (PCCs) were performed with the SPSS statistical software (version 17.0, IBM Corp., Armonk, NY, USA) [26,68].

Effects of N Supply on Seedling Growth
As shown in Figure 1, 0 mM N treatment significantly reduced root length, root surface area, root average diameter, root volume, root DW, stem DW, leaf DW, shoot DW and whole plant DW by 30%, 44%, 20%, 55%, 23%, 46%, 49%, 48% and 41%, respectively, in C. grandis seedlings and 29%, 36%, 25%, 53%, 41%, 67%, 65%, 66% and 58%, respectively, in C. sinensis seedlings, and significantly increased the ratio of root/shoot DW by 48% and 74% in C. grandis and C. sinensis seedlings, respectively, relative to 20 mM N treatment, while other N treatments had no significant effect on these ten parameters, with only a few exceptions. The root DW/shoot DW ratio was higher in C. sinensis seedlings than in C. grandis seedlings or similar between the two depending on N supply, while the reverse was the case for the other nine parameters. As shown in Figure S1, N deficiency symptoms such as vein chlorosis or yellow vein in older leaves and weak, yellowish and small new leaves were observed in 0 mM N-treated seedlings, but not in 5-20 mM N-treated seedlings [4,5]. Therefore, seedlings treated with 0 mM N were considered N deficient, and those treated with 5-20 mM N were considered N sufficient.

Effects of N Supply on Element Concentrations in Roots, Stems and Leaves
N concentration in leaves and roots increased with increasing N supply, and N concentration in stems increased as N supply increased from 0 to 5 mM, after which it remained relatively stable with the elevating N supply. P concentration in C. grandis and C. sinensis leaves, C. sinensis stems and C. grandis roots decreased as N supply increased from 0 to 5 mM, but it then remained unchanged with increasing N supply; P concentration in C. grandis stems decreased as N supply increased from 0 to 5 mM, but it then rose with increasing N supply; P concentration in C. sinensis roots decreased or remained stable as N supply increased from 0 to 15 mM, and then increased at 20 mM N. The concentrations of K, Ca, Mg and S in leaves, stems and roots decreased or remained stable with increasing N supply. The concentrations of N, K, Ca and Mg in leaves, and P, K, Ca, Mg and S in roots, were higher in C. sinensis seedlings than those in C. grandis seedlings or similar between the two at each given N supply, while the concentrations of N, P, K, Ca, Mg and S in roots, N in stems, and P and S in leaves were higher in C. grandis seedlings than those in C. sinensis seedlings or similar between the two at each given N supply, with the exceptions that the concentrations of P and S in 0 mM N-treated leaves and P in 0 and 20 mM N-treated roots were higher in C. sinensis seedlings than those in C. grandis seedlings ( Figure 2). Fe concentration in C. grandis and C. sinensis roots and leaves, and C. grandis stems decreased or remained stable with increasing N supply with the only exception that Fe concentration in C. grandis leaves was higher at 15 mM N than at 10 and 20 mM N, while its concentration in C. sinensis stems increased or remained unchanged with increasing N supply. The concentrations of Mn and Zn in C. sinensis roots, stems and leaves, Zn in C. grandis leaves, and Cu in C. grandis and C. sinensis leaves increased as N supply increased from 0 to 10 mM, but they then decreased or remained unchanged with further increasing N supply. The concentrations of Mn in C. grandis leaves, stems and roots, Zn in C. grandis stems and roots, and Cu in C. grandis roots increased as N supply increased from 0 to 5 mM, and then decreased or remained relatively stable with further increasing N supply with the only exception that Mn concentration in stems was higher at 20 mM N than that at 0-15 mM N. B concentration in leaves was higher at 0 mM N than that at 5-20 mM N, while its concentration in stems and roots did not significantly alter in response to N supply. Cu concentration in stems increased or remained stable with increasing N supply. The concentrations of Fe in leaves and stems, Mn and Zn in leaves, stems and roots, and Cu in stems were higher in C. sinensis seedlings than those in C. grandis seedlings or similar between the two at each given N supply with the only exception that Fe concentration in 0 mM N-treated stems was higher in C. grandis than in C. sinensis seedlings, while the concentrations of Fe in roots, and Cu in leaves and roots were higher in C. grandis than those in C. sinensis seedlings or similar between the two at each given N supply with the exception that Cu concentration in 20 mM N-treated leaves and roots was higher in C. sinensis seedlings than that in C. grandis seedlings ( Figure 3). Compared with 20 mM N treatment, N deficiency significantly increased the ratios of P/N, K/N, Ca/N, Mg/N, S/N, Fe/N, B/N and Cu/N by 423%, 333%, 436%, 280%, 182%, 214%, 331% and 154%, respectively, in C. grandis leaves and by 1022%, 336%, 420%, 279%, 290%, 199%, 270% and 62%, respectively, in C. sinensis leaves, by 97%, 171%, 371%, 142%, 128%, 520%, 158% and 42%, respectively, in C. grandis stems and by 192%, 151%, 310%, 151%, 1713%, 15% (the only exception without significant difference), 121% and 24%, respectively, in C. sinensis stems, and by 250%, 184%, 463%, 159%, 146%, 427%, 150% and 573%, respectively, in C. grandis roots and 212%, 157%, 187%, 216%, 99%, 334%, 131% and 275%, respectively, in C. sinensis roots. The absence of N, therefore, led to an increase in all the eight elements in roots, stems and leaves relative to N. N deficiency lowered Mn/N ratio in C. sinensis leaves, stems and roots by 23%, 53% and 65%, respectively, relative to 20 mM N treatment, but it was similar in C. grandis roots, stems and leaves between 0 and 20 mM treatments. Zn/N ratio in C. sinensis leaves and C. grandis roots and leaves was higher at 0 mM N than that at 20 mM N, but the reverse was the case for Zn/N ratio in C. sinensis stems. Zn/N ratio in C. grandis stems and C. sinensis roots was similar between 0 and 20 mM N treatments ( Figures S2 and S3).
In leaves, the ratios of K/N, Ca/N, Mg/N, S/N, Fe/N, B/N and Cu/N were not significantly lower at C. grandis than those at C. sinensis at each given N supply with the exceptions that the ratios of Ca/N and Mg/N were higher in the latter at 5 mM N; the ratio of P/N was higher (lower) in C. sinensis than in C. grandis at 0 mM (5-20 mM) N; the ratios of Mn/N and Zn/N were not significantly lower in C. sinensis than in C. grandis ( Figures S2 and S3).
In stems, the ratios of all the ten elements to N were higher in C. sinensis than those in C. grandis at given N supply with a few of exceptions ( Figures S2 and S3).
In roots, the ratios of P/K, S/N, Mn/N, B/N and Zn/B were not significantly lower in C. sinensis than those in C. grandis at each given N supply with the only exception that the ratio of Mn/N was significantly lower in the former at 0 mM N, but the ratios of K/N, Ca/N, Mg/N, Fe/N and Cu/N were not significantly lower in C. grandis than those in C. sinensis with the only exception that the ratio of K/N was significantly lower in the former at 10 mM N ( Figures S2 and S3).

Effects of N Supply on Nutrient Uptake
For C. grandis seedlings, N uptake per plant (root DW) increased with increasing N supply, and Fe uptake per plant (root DW) decreased with increasing N supply. P uptake per plant (root DW) decreased as N supply increased from 0 to 5 mM, but it then increased or remained relatively stable with further increasing N supply. K, Ca, Mg, S, Cu, B, Mn and Zn uptake per plant (root DW) increased significantly as N supply increased from 0 to 5 mM, after which they decreased or remained relatively stable with further increasing N supply with the exceptions that Ca and B uptake per root DW did not significantly alter at the range of 0-5 mM N and that S uptake per root DW was higher at 15 mM than at 10 mM. For C. sinensis seedlings, N uptake per plant (root DW) increased with the increase in N supply. P uptake per plant (root DW) decreased or remained stable as N supply rose from 0 to 15 mM, and then reduced at 20 mM N. K, Ca, Mg, S and B uptake per plant (root DW) significantly increased as N supply rose from 0 to 5 mM, but they then decreased or remained relatively stable with the increase in N supply with the only exception that Fe uptake per root DW did not significantly differ between 0 and 5 mM N treatments. Cu, Mn and Zn uptake per plant (root DW) significantly rose as N supply rose from 0 to 10 mM, and then decreased or did not significantly alter with further increasing N supply ( Figure 4). As shown in Figure 4, N, P, K, Ca, Mg, Cu, B and Fe uptake per plant (root DW) were higher in C. grandis seedlings than those in C. sinensis seedlings or similar between the two at each given N supply with the exceptions that P uptake per root DW at 0 mM N, K uptake per root DW at 10 mM N, Ca uptake per root DW at 5 and 10 mM N, and Mg uptake per root DW at 5 mM N were higher in C. sinensis than those in C. grandis seedlings, while Mn and Zn uptake per plant (root DW) were higher in C. sinensis than those in C. grandis seedlings or similar between the two at each given N supply with the exception that Mn uptake per plant was higher in C. grandis than in C. sinensis seedlings at 0 mM N.
Generally viewed, the ratios of P, K, Ca, Mg, S, Fe, B and Cu uptake per plant to N uptake per plant increased with the decrease in N supply, while plant total Mn/N and Zn/N ratios for C. grandis (C. sinensis) increased significantly as N supply increased from 0 to 5 (10) mM, then decreased with further increasing N supply. It is noteworthy that both plant total Mn/N and Zn/N ratios in C. grandis seedlings were 33% and 80% higher at 0 mM N than those at 20 mM, respectively. The absence of N, thus, caused an increase in the uptake of the 10 elements per plant in C. sinensis and C. grandis seedlings relative to N uptake per plant with the exceptions of B and Zn uptake per plant in C. sinensis seedlings. Plant total P/N, Ca/N, Mn/N and Zn/N ratios were not significantly lower in C. sinensis than those in C. grandis seedlings with the exceptions that plant total Ca/N and Mn/N ratios were significantly lower in the former at 0 mM N, while plant total S/N, Fe/N, B/N and Cu/N ratios were not significantly lower in C. grandis than those in C. sinensis seedlings at each given N supply. The plants' total K/N ratio at 0-5 mM N and Mg/N ratio at 0 and 20 mM N were significantly higher in C. grandis than those in C. sinensis seedlings, while plant total K/N ratio at 10-15 mM N and Mg/N ratio at 5-10 mM N were significantly higher in the latter ( Figure 5). PCCs were calculated for whole plant DW, plant total element content (element uptake per plant) and the ratios of plant total element content to total N content ( Figure S4). Wholeplant DW was significantly and positively related to plant total N, B, S, Mg or K content (r > 0.8866), and displayed an upward trend with increasing plant total Cu, Mn, Ca, Zn or P content; but it was significantly and negatively related to plant total P/N, Mg/N, Ca/N, K/N, S/N or B/N ratio (r < −0.7809), and displayed a downward trend with increasing plant total Fe/N, Cu/N or Zn/N ratio. A positive and significant relationship existed between any two parameters of plant total N, B, S, Mg and K contents (r > 0.6366) or plant total P/N, Mg/N, Ca/N, K/N, S/N and B/N ratios (r > 0.8728).

Effects of N Supply on Element Distributions in Roots, Stems and Leaves
As shown in Figure S5, N distribution in roots significantly decreased as N supply increased from 0 to 5 mM, and then increased or remained relatively stable with increasing N supply, while N distribution in stems and leaves significantly rose as N supply increased from 0 to 5 mM, and then decreased or remained unchanged with further increase in N supply. P distribution in roots and leaves decreased or remained stable with the increase in N supply with the only exception that P distribution in C. sinensis roots was higher at 20 mM N than at 5-15 mM N, while P distribution in stems increased with the increase in N supply with the only exception that P distribution in C. sinensis stems was lower at 20 mM N than at 10 mM N. K distribution in roots and leaves did not significantly alter in response to N supply except for an increase in K distribution in roots at 0 mM N, while K distribution in stems increased or remained stable with the increase in N supply. Ca distribution in roots decreased or remained unchanged as N supply decreased from 20 to 5 mM N, and then increased at 0 mM N; Ca distribution in leaves significantly increased as N supply increased from 0 to 5 mM, and then decreased or remained stable with further increase in N supply; Ca distribution in stems did not significantly alter in response to N supply except for an increase in 10 mM N-treated C. grandis and 20 mM N-treated C. sinensis seedlings. Mg distribution in roots decreased or remained unchanged with the increase in N supply, while the reverse was the case for Mg distribution in stems and leaves with the only exception that Mg distribution in leaves was lower in 20 mM N-treated C. sinensis than in 10 mM N-treated C. sinensis seedlings. N supply had little influence on S distribution in roots, stems and leaves except for an increase in S distribution in C. grandis and C. sinensis roots and a decrease in S distribution in C. grandis leaves. As shown in Figure S6, Cu, Fe, Mn and Zn distributions in roots decreased or remained unchanged with the increase in N supply with the exceptions that Mn distribution in C. grandis roots was significantly lower at 0 mM N than at 5 mM N, and that Mn distribution in C. sinensis roots was significantly lower at 0 mM N than at 10 mM N, while their distributions in stems and leaves increased or remained unchanged with the increase in N supply except that Fe distribution in C. grandis stems was significantly higher at 0 mM N than at 5 mM N, and that Cu distribution in C. grandis leaves was significantly higher at 15  As shown in Figures S5 and S6, the distributions of N, P, K, Ca, Mg, Cu, Fe and Mn in roots, N and Ca in stems, and P, S and Zn in leaves were higher in C. grandis than those in C. sinensis seedlings or similar between the two at each given N supply except that C. sinensis seedlings had higher distributions of P and Mn in 20 mM N-treated roots and P in 0 mM N-treated leaves relative to C. grandis seedlings, while the reverse was the case for the distributions of S and Zn in roots, P, K, Mg, S, Cu, Fe, Mn and Zn in stems and N, Ca, Mg, Cu, Fe and Mn in leaves except that C. grandis seedlings had higher distributions of Cu and Mn in 20 mM N-treated stems and Cu in 15 mM N-treated leaves relative to C. sinensis seedlings.

Effects of N Supply on Gas Exchange and Photosynthetic Pigments in Leaves
N deficiency decreased A CO2 , g s , Tr, WUE by 48%, 21%, 18% and 36%, respectively, in C. grandis leaves and by 46%, 28%, 30% and 24%, respectively, in C. sinensis leaves, but increased C i and C i /C a by 20% and 21%, respectively, in C. grandis leaves and by 21% and 20%, respectively, in C. sinensis leaves. The six parameters did not significantly alter over the range of 5-20 mM N supply. All the six parameters were similar between C. grandis and C. sinensis leaves at each given N supply with the only exception that Tr was significantly lower in C. sinensis than in C. grandis leaves at 0 mM N. PNUE, which decreased with the increase in N supply, was significantly lower in C. sinensis than that in C. grandis leaves at each given N supply. N deficiency increased A CO2 /Chl by 22% in C. sinensis leaves relative to 20 mM N, but not in C. grandis leaves. A CO2 /Chl was lower in C. grandis leaves than that in C. sinensis leaves at 0 mM N, but it was lower in the latter at 5 and 15 mM N ( Figure 6).  (PNUE, (B)), A CO2 /chlorophyll (Chl, (C)), stomatal conductance (g s , (D)), transpiration rate (Tr, (E)), water use efficiency (WUE, (F)), intercellular CO 2 concentration (C i , (G)) and ratio of intercellular to ambient CO 2 concentration (C i /C a , (H)) in leaves. N deficiency significantly reduced Chl a, Chl b, Chl a + b and Car concentrations and Chl a/b ratio by 45%, 42%, 44%, 35% and 5%, respectively, in C. grandis leaves and by 57%, 55%, 56%, 48% and 4% (the only exception without significant difference), respectively, in C. sinensis leaves, but significantly increased Car/Chl, Chl/N and Car/N ratios by 14%, 78% and 102%, respectively, in C. grandis leaves and by 17%, 31% and 54%, respectively, in C. sinensis leaves relative to 20 mM N. The concentrations of Chl a, Chl b, Chl a + b and Car were higher in C. grandis than in C. sinensis leaves at 0 mM N, but were not lower in the latter at 5-20 mM N. However, the ratios of Chl a/b, Car/Chl, Chl/N and Car/N were not lower in C. grandis leaves than those in C. sinensis leaves at each given N supply (Figure 7).

Effects of N Supply on OJIP Transients and Related Parameters in Dark-Adapted Leaves
We observed that the heterogeneity of samples (leaves) was greater at 0 mM N than at 5-20 mM N, and that OJIP transients from N deficiency C. grandis and C. sinensis leaves had greatly increased O-step, slightly increased (C. sinensis) or unaltered (C. grandis) P-step, positive ∆L-, ∆K-, ∆J-, and ∆I-bands, positive ∆ O-K , ∆ O-J and ∆ J-I bands, but negative ∆ I-P bands compared with OJIP transients from 20 mM N-treated leaves, with greater alterations of ∆L-bands, ∆K-bands and ∆ I-P bands and less alterations of ∆ J-I bands in N deficiency C. sinensis than in N deficiency C. grandis leaves. Few, if any, differences existed among the OJIP transients from the 5, 10, 15 and 20 N-treated leaves (Figures 8 and S7). Our findings showed that N deficiency decreased maximum primary yield of photochemistry of PSII (F v /F o ), total electron carriers per reaction center (RC; S m or EC o /RC), F v /F m (TR o /ABS), quantum yield for electron transport (ϕ Eo or ET o /ABS), efficiency with which an electron can move from the reduced intersystem electron acceptors to the photosystem I (PSI) end electron acceptors (δ Ro or RE o /ET o ), quantum yield for the reduction in end acceptors of PSI per photon absorbed (ϕ Ro or RE o /ABS), probability that a trapped exciton moves an electron into the electron transport chain beyond Q A − (ψ Eo or ET o /TR o ), efficiency with which a trapped exciton can move an electron into the electron transport chain from Q A − to the PSI end electron acceptors (ρ Ro or RE o /TR o ), electron transport flux per RC (ET o /RC), reduction in end acceptors at PSI electron acceptor side per RC (RE o /RC), reduction in end acceptors at PSI electron acceptor side per cross section (CS; RE o /CS o ), maximum amplitude of IP phase, and total performance index (PI abs,total ) by 26%, 49%, 6%, 48%, 23%, 60%, 45%, 58%, 14%, 34%, 48%, 65% and 90%, respectively, in C. grandis leaves and by 26%, 45%, 5%, 47%, 22%, 58%, 44%, 56%, 9%, 29%, 44%, 64% and 90%, respectively, in C. sinensis leaves, and increased minimum fluorescence ( ) by 31%, 167%, 68%, 21%, 68%, 28%, 114%, 58% and 67%, respectively, in C. grandis leaves and by 35%, 179%, 70%, 22%, 73%, 28%, 123%, 64% and 74%, respectively, in C. sinensis leaves relative to 20 mM N. Interestingly, N deficiency increased maximum fluorescence (F m ) by 6% in C. sinensis leaves and decreased maximum variable fluorescence (F v ) by 4% in C. grandis leaves relative to 20 mM N, but had no significant impact on both F m in C. grandis leaves and F v in C. sinensis leaves. There were relatively little differences in all 24 parameters among 5, 10, 15 and 20 mM N-treated leaves. and PI abs,total were higher in C. sinensis than in C. grandis leaves or similar between the two at each given N supply. DI o /ABS and DI o /CS o were higher in C. grandis than in C. sinensis leaves or similar between the two at each given N supply (Figure 9).

Correlation Coefficient Matrices of Gas Exchange, Photosynthetic Pigments, Element Concentrations and Fluorescence Parameters in Leaves
PCCs were calculated using the means of gas exchange, photosynthetic pigments, element levels and fluorescence parameters in leaves in order to understand the relationships between them ( Figure 10). There was a significant negative or positive relationship (r > 0.6349 or <−0.6447) between any two parameters of the 11 parameters for gas exchange and photosynthetic pigments (C i/ C a , Tr, WUE, A CO2 , PNUE, g s , C i , Chl a, Chl b, Chl and Car) with a few exceptions including the relationships between C i /C a and g s (r = −0.4153),

The Tolerance of C. grandis Seedlings to N Deficiency Was Slightly Higher than That of C. sinensis Seedlings
Plants need adequate amount of N for normal growth, development and reproduction. The availability of N to roots plays a key role in plant growth and photosynthetic pigment biosynthesis [2,13,35]. Regressive analysis showed that whole plant DW was positively related to N uptake per plant, but negatively related to the ratio of P, Mg, Ca, K, S or B uptake per plant to N uptake per plant ( Figure S4), and that leaf Chl a, Chl b, Chl a + b or Car concentration was positively related to leaf N, but negatively related to leaf P/N, K/N, Ca/N. Mg/N, S/N, Fe/N or B/N ratio (Figure 10), suggesting that the imbalance of plant (leaf) nutrients might aggravate the N-deficiency-induced decrease in plant growth (leaf photosynthetic pigment biosynthesis). Here, N deficiency affected root, stem, leaf, shoot and whole plant DW (Figure 1), and leaf concentrations of Chl a, Chl b, Chl a + b and Car (Figure 7) more in C. sinensis than those in C. grandis seedlings. In addition, N-deficiency-induced alterations of OJIP transients were slightly greater in C. sinensis than those in C. grandis leaves, as indicated by the more pronounced positive ∆V O-K and ∆V O-J bands, and negative ∆V I-P band with the exception that the positive ∆V J-I band was more pronounced in C. grandis leaves than that in C. sinensis leaves (Figure 8). These results indicated that C. grandis seedlings had slightly higher tolerance to N deficiency than that of C. sinensis seedlings. PNUE increases in response to N deficiency. A higher PNUE can make plants use N effectively for biomass production and improve N use efficiency. There were genotypic differences in PNUE of maize and olives, and PNUE in N-efficient genotypes was higher than that of N-inefficient genotype. A genotypic difference in PNUE has in fact been observed in maize, and PNUE of N-efficient genotypes was higher than that of N-inefficient genotype [69,70]. Boussadia et al. [66] found that PNUE increased in N deficiency 'Meski' olive leaves, but remained unchanged in 'Koroneiki' olive leaves, concluding that 'Meski' had an improvement of N budget in its leaves than 'Koroneiki', and hence might be better adapted to N deficiency. The higher tolerance of C. grandis to N deficiency could be explained in this way, because N-deficiency-induced increase in PNUE was greater in C. grandis than that in C. sinensis leaves and PNUE was higher in the former than in the latter at each given N supply ( Figure 6).

N Deficiency Disturbed Nutrient Balance and Homeostasis, and Altered Nutrient Distributions in Roots, Stems and Leaves
N has both antagonism and synergism on other elements, affecting the uptake and distributions of other elements, and ultimately determining the contents of other elements in different organs of plants [3,37]. Here, N deficiency increased or did not affect P, K, Ca, Mg, S, Fe and B concentrations in roots, stems and leaves and Cu concentration in roots with the exceptions that N deficiency lowered the concentrations of P in C. grandis stems and Fe in C. sinensis stems (Figures 2 and 3). N deficiency led to an increase in the ratios of P, K, Ca, Mg, S, Fe, B and Cu concentrations to N concentration in roots, stems and leaves ( Figures S2 and S3), and the ratios of P, K, Ca, Mg, S, Fe, B and Cu uptake per plant to N uptake per plant ( Figure 5) in C. sinensis and C. grandis seedlings relative to 20 mM N treatments with the exception that the ratio of stem Fe/N in C. sinensis seedlings did not significantly differ between 0 mM and 20 mM N treatments. Therefore, N had antagonistic effect on the uptake of these elements. In maize, Schlüter et al. [71] observed that N-starvation led to a strong accumulation of Pi in leaves accompanied by the downregulation of genes involved in Pi-starvation response, demonstrating the importance of Pi homeostasis in stress adaption. Excessive N supply was considered as a cause of Citrus Cu deficiency in Florida [5]. There was report showing that N absorption could lower the uptake of P and K in plants [37]. Additionally, N deficiency affected Mn and Zn concentrations and the ratios of Mn/N and Zn/N in roots, stems and leaves, as well as the ratios of Mn (Zn) uptake per plant to N uptake per plant in C. grandis and C. sinensis seedlings with the exceptions that Zn concentration and Mn/N in C. grandis roots, Zn/N in C. sinensis roots and Zn uptake per plant/N uptake per plant in C. sinensis seedlings did not differ significantly between 0 and 20 mM N treatments (Figures 3, 5 and S3). Lack of N, therefore, altered nutrient uptake per plant to N uptake per plant, thus distributed nutrient balance and homeostasis in leaves, stems and roots. N-deficiency-induced imbalance of nutrients has been obtained in peace lily leaves [40], sugar cane leaves and stems [41], barley [49], grapevine [72], pear [3], Cyclocarya paliurus (Batal.) Iljinskaja [37], snap bean [35] and sorghum [36].
The distributions of 11 elements in roots were not significantly lower at 0 mM N than those at 20 mM, while the reverse was the case for their distributions in leaves and stems with the exceptions that P distributions in leaves was significantly higher at 0 mM N than that at 20 mM N (Figures S4 and S5). On the whole, lack of N, therefore, increased the distributions of nutrients in roots, but decreased their distributions in shoots. N-deficiencyinduced increase in N, P, K distributions in roots has been obtained in P. tricuspidata [39] and maize [6] plants.

Citrus Displayed Adaptive Responses to N Deficiency
In addition to suppressing plant growth, N deficiency also affects dry matter allocation [15,50]. According to the classical theory of 'functional equilibrium' between shoots and roots, under N deficiency, both the relative deficiency of N and the relative surplus of carbohydrates in plants will have less influence on root development than on shoot development [52]. Here, root DW decreased to a less extent than shoot DW in response to N deficiency, and the ratio of root DW/shoot DW increased (Figure 1). Similar reports for increased partitioning of photosynthetic dry matter to the roots and the increase in the ratio of root DW/shoot DW are well recorded for other N deficiency plants including Betula pendula Roth. [51], maize [6,52], lettuce [73], peace lily [40], wheat [48,74,75], sorghum [15], swithgrass [76], pear [3], P. tricuspidata [39], soybean [53], snap bean [35], rice [47], sweet potato [77], chickpea [42] and pumpkin [50]. Our results demonstrated that among the four parameters (root length, root surface area, root average diameter and root volume) for root architecture, root volume had the greatest decrease under N deficiency, thus leading to increased root-surface-per-unit volume (Figure 1). Plasticity of root architecture plays a role in the acclimation to N deficiency [6]. Yang et al. [48] observed that low N-induced increase in the ratio of root DW/shoot DW was greater in a newly formed hexaploid wheat with stronger tolerance to N deficiency than its parents, which might be an adaptive growth strategy for the hexaploid because relative more roots fed relative less shoots with N, thereby causing higher N accumulation in the shoots. Active elongation of thin roots to search for N has also been considered as the survival strategy for plants [50]. Thus, N-deficiency-induced increases in the root-surface-per-unit volume due to reduced root diameter and the ratio of root DW/shoot DW might facilitate N uptake and acquisition, thus improving Citrus tolerance to N deficiency. However, the difference in N deficiency tolerance between C. sinensis and C. grandis could not be explained in this way, because N-deficiency-induced increase in the ratio was greater in the former than in the latter ( Figure 1). Under low-N stress, N rather than carbon should be the most limited resource for root growth [46]. Here, we observed that N concentration reduced to a less extent in N deficiency roots than that in N deficiency stems and leaves, and N deficiency increased N distribution in roots (Figures 2 and S2), indicating that the limited N in N deficiency seedlings was preferentially allocated to the roots to maintain their growth. To conclude, N deficiency Citrus seedlings enhanced their ability to acquire N by increasing N distribution in roots and altering their dry matter partitioning to favor root growth and by optimizing root architecture. In addition, the preferential allocation of the other elements (K, Ca, Mg, Cu, B, Mn and Zn in N deficiency roots ( Figures S5 and S6) might contribute to higher ratio of root DW/shoot DW (Figure 1).

Possible Causes for N-Deficiency-Induced Decrease in A CO2 in Leaves
Regressive analysis showed that leaf A CO2 (PNUE) was positively (negatively) related to leaf N concentration, but negatively (positively) related to leaf P/N, K/N, Ca/N, Mg/N, S/N, Fe/N, B/N or Cu (Figure 10), implying that the imbalance of leaf nutrients might intensify N-deficiency-induced decrease in A CO2 . The higher C i and C i /C a in N-deficient leaves ( Figure 6) and negative relationships between A CO2 and C i as well as A CO2 and C i /C a ( Figure 10) indicated that N-deficiency-induced decrease in A CO2 was mainly caused by non-stomatal factors, as obtained in 'Cleopatra mandarin' (Citrus reticulata L.) [10], apple [12], grape [78], rice [47] and soybean [79]. However, Zhao et al. [15] suggested that N-deficiency-induced decrease in sorghum leaf A CO2 was firstly caused by stomatal closure, because both C i and g s decreased with the decrease in A CO2 .
Both Chl and Car, the important photosynthetic pigments, were lowered in N deficiency Citrus leaves (Figure 7). Chl is a key component of photosynthesis, responsible for the absorption, transportation and transformation of light energy. Many studies have shown that leaf A CO2 decrease with the decrease in Chl level [9,14,22]. Apart from general non-photochemical quenching (NPQ), Car can effectively quench the excited triplet state of Chl and 1 O 2 and protect thylakoid membranes, PSI and PSII from reactive oxygen species (ROS) damage [79,80]. We found that leaf A CO2 significantly decreased with the decrease in Chl, Chl a, Chl b or Car level (Figure 10), that under N deficiency stress, the decrease in Chl in C. sinensis leaves was greater than that of A CO2 , while the decrease in Chl and A CO2 in C. grandis leaves was not significantly different, and that Car declined less in C. grandis leaves relative to A CO2 in response to N deficiency, while the decrease in Car and A CO2 in C. sinensis leaves did not significantly differ (Figures 6 and 7). N-deficiency-induced decrease in photosynthetic pigments might play a role in A CO2 decline, at least in C. sinensis leaves. Zhao et al. [15] observed increased A CO2 /Chl ratio in N-limited sorghum leaves, concluding that the higher A CO2 /Chl ratio might partially alleviate negative effects of N deficiency on A CO2 . N-deficiency-induced an increase in A CO2 /Chl ratio has been obtained in maize [81]. The ratio of Chl a/b was significantly lowered in N deficiency C. grandis leaves due to the more reduction in Chl a relative to Chl b, but not in N deficiency C. sinensis leaves (Figure 7). There were mixed reports on N deficiency's effects on Chl a/b ratio; N deficiency decreased the ratio in apple [12] and Citrus medica L. [22], increased it in 'Cleopatra mandarin' [10] and maize [23,69], but had no influence on it in soybean, Populus and rice [9]. Under N deficiency, Car decreased less relative to Chl in leaves, and the ratio of Car/Chl increased ( Figure 6). Similar results have been obtained on B. pendula and B. pubescens [82], C. medica [22], and sweetpotato [77]. A higher ratio of Car/Chl (Figure 7) might be an adaptation mechanism of photosynthetic function to N deficiency by protecting thylakoid membranes, PSI and PSII from photo-oxidative damage [78,82]. Nutrient deficiencies, including N deficiency, can cause photoinhibition of PSII, thereby lowering leaf photosynthetic rate [14,20,26,29,33,34]. As expected, photoinhibition of PSII was observed in N-deficient leaves [83], as indicated by lower F v /F m and ET o /ABS, and higher DI o /RC, DI o /CS o and DI o /ABS, as well as markedly altered OJIP transients relative to 20 mM N-treated leaves (Figures 8 and 9). The decline of F v /F m in response to N deficiency was caused by an increase in F o , because F m increased in N deficiency C. sinensis leaves and did not significantly alter in N deficiency C. grandis leaves relative to 20 mM N-treated leaves. A higher F o usually occurs in the damaged antennal complex, which cannot effectively transfer energy to the RC [29]. The increase in F o has been suggested to results from the decoupling of PSII light-harvesting complex (LHCII) from PSII rather than the degradation of LHCII [20].
The decrease in F v /F o indicated that the thylakoid structure of N-deficient leaves was damaged [84]. N-deficiency-induced damage of chloroplast (thylakoid) ultrastructure has been observed by confocal laser scanning and/or transmission electron microscopy in radish [28] and 'Cleopatra mandarin' [10] leaves. There was report suggesting that the reduction in Citrus leaf A CO2 in response to N deficiency was the direct consequence of the destruction of thylakoid assembly [10]. Regressive analysis showed that F v /F o was significantly and positively to leaf A CO2 , Chl, Chl a, Chl b or Car (r > 0.9251) ( Figure 10). Lack of N, therefore, damaged the structure of thylakoids, thus lowering leaf photosynthetic pigment levels and A CO2 .
The positive O-K (∆L-) band in N-deficient leaves corresponded to less connected antennae complexes with lower energy transfer and absorption efficiency due to improper membrane organization [29] and more fragile PSII units with less stability [85], as indicated by the increase in leaf heterogeneity ( Figure S7). The positive O-J (∆K-) band in N-deficient leaves resulted from the inhibition of electron donation from the oxygen-evolving complex (OEC) to P680 + due to the inactivation of OEC [86]. The positive O-K (∆L-) and O-J (∆K-) bands have been obtained in N-deficient tea [14], maize, tomato [28] and radish [20] and various higher plants submitted to other nutrient deficiencies [26,[28][29][30]33,34].
Imbalance in the energetic connectivity between PSII units led to an increase in the inactivation of RCs, as confirmed by the increase in ABS/RC (Figure 8). The inactivation of RCs might protect N-deficient leaves from photooxidative damage by dissipating excessive absorbed light energy [28,29]. This agreed with our findings that N deficiency had higher Car/Chl ratio ( Figure 7) and energy dissipation, as confirmed by increased DI o /RC, DI o /CS o and DI o /ABS (Figure 9).
The positive ∆J-band (increased V J ), ∆I-band (increased V I ) and negative I-P band (decreased maximum amplitude of IP phase) indicated that N deficiency had more reductive PSII acceptor side, but more oxidative PSI acceptor side. In other word, PSII acceptor side was more sensitive site to N deficiency than PSII donor side; and PSI was less impaired by N deficiency than that of PSII [26,87]. This was also supported by our findings that N-deficient leaves had higher F o and lower F v relative to 20 mM N-treated leaves, which were the characteristic of photoinhibitory damage at PSII acceptor side [88]. Similar results have been reported in N-deficient tea [14] and rapeseed [29]. Unfortunately, IP phase and I-P normalized curves were not investigated in the reports of Kalaji et al. [29] and Lin et al. [14], respectively.
The decreases in RE o /ET o , RE o /ABS, RE o /TR o , RE o /RC, RE o /CS o and PI abs,total indicated that N deficiency lowered both the efficiency of electron transport to the PSI end electron acceptors and the reduction in PSI end-electron acceptors. This was confirmed by the more oxidize PSI acceptor side, as confirmed by the decrease in maximum amplitude of IP phase (Figure 9). Similar results have been obtained in N-deficient tea [14], radish [28] and rapeseed [29].
Except for F v and F m , each other fluorescence parameter had a significant positive or negative correlation with leaf N concentration, leaf P/N, K/N, Ca/N, Mg/N, S/N, Fe/N, or B/N ratio, but the relationships between fluorescence parameters and leaf N were opposite to those between fluorescence parameters and these ratios ( Figure 10). Imbalance of leaf nutrients, therefore, intensified N-deficiency-induced impairment of PETC from the donor side of PSII to the reduction in PSI end-electron acceptors (i.e., photon absorption in LHCII, structural damage of thylakoids, electron supply from OEC, stability of PSII units, Q A and plastoquinone reduction at PSII acceptor site, and reductions of PSI end-electron acceptors  (Figure 10). These results of this study indicated that the impairment of PETC in N-deficient leaves might contribute to the decrease in A CO2 .

Conclusions
The results of this study clearly demonstrated that N deficiency decreased N uptake and N concentration in roots, stems and leaves and disturbed nutrient balance and homeostasis in plants, thus reducing plant growth, as well as lowering photosynthetic pigment levels, impairing thylakoid structure and whole PETC in leaves, and thereby decreasing A CO2 (Figure 11). The imbalance of nutrients intensified N deficiency adverse impacts on biomass, photosynthetic pigment biosynthesis, PETC and A CO2 . Citrus seedlings displayed adaptive responses to N deficiency, including (a) increasing the distributions of N and other elements in roots, as well as root DW/shoot DW ratio and root-surface-per-unit volume and (b) enhancing PNUE ( Figure 11). The tolerance of C. grandis seedlings to N deficiency was slightly higher than that of C. sinensis seedlings, which might be related to the higher PNUE of the former. This study provided some novel information on the physiological adaption of Citrus to N-deficiency. Figure 11. A diagram for the physiological response of C. grandis and C. sinensis seedlings to N deficiency. A CO2 , CO 2 assimilation; Car, Carotenoids; Chl, chlorophyll; N, nitrogen; PETC, photosynthetic electron transport chain; PNUE, photosynthetic N use efficiency; R/S, root DW/shoot DW; RSPV, root-surface-per-unit volume.

Supplementary Materials:
The following are available online at https://www.mdpi.com/article/10 .3390/agronomy11091859/s1, Figure S1: Effects of nitrogen (N) supply on growth of Citrus sinensis (A,B) and Citrus grandis (C,D) seedlings, Figure S2: Effects of N supply on mean (±SE, n = 4) ratios of P, K, Ca, Mg or S concentration to N concentration in leaves (A-E), stems (F-J) and roots (K-O) of Citrus grandis and Citrus sinensis seedlings, Figure S3: Effects of N supply on mean (±SE, n = 4) ratios of Fe, Mn, B, Zn or Cu concentration to N concentration in leaves (A-E), stems (F-J) and roots (K-O) of Citrus grandis and Citrus sinensis seedlings, Figure S4: Matrices of Pearson correlation coefficients (PCCs) for the mean whole plant DW (n = 12), element uptake per plant (plant total element content) and the ratio of element uptake per plant to N uptake per plant (n = 4) in C. grandis and C. sinensis seedlings, Figure S5