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Investigation and Prevention of Cork Spot Disorder in ‘Akizuki’ Pear (Pyrus pyrifolia Nakai)

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Yan-xin DuanCollege of Horticulture, Qingdao Agricultural University, Qingdao 266109, China

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Ying XuCollege of Horticulture, Qingdao Agricultural University, Qingdao 266109, China

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Ran WangCollege of Horticulture, Qingdao Agricultural University, Qingdao 266109, China

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Chun-hui MaCollege of Horticulture, Qingdao Agricultural University, Qingdao 266109, China

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Abstract

‘Akizuki’ (Pyrus pyrifolia Nakai) is a dominant Asian pear cultivar with gradually increasing cultivation area in Shandong province. However, this cultivar is found susceptible to cork spot disorder in recent years. In this study, we explored the physiological-biochemical mechanism of cork spot disorder in pear fruit, and investigated the effectiveness of spraying calcium (Ca), boron (B) solution or prohexadione calcium (P-Ca) on cork spot incidence. Cork spotted fruit had the characteristics of significantly larger fruit size with shorter fruit pedicels. Compared with normal fruit, cork spotted fruit had lower content of total soluble solids, soluble and reducing sugar, and vitamin C. In addition, cork spotted fruit accumulated much higher levels of N and Mg, and lower levels of K and P. However, Ca deficiency was not observed in cork spotted fruit, on the contrary, we determined high concentrations of Ca and free Ca2+ in disordered fruit. At the same time, the ratios of K/Ca, Mg/Ca, and (K+Mg)/Ca were significantly lower in cork spotted fruit as compared with normal fruit. Among all treatments, spraying with 3500 times dilution of P-Ca at 15-day intervals from 30 to 90 days after full bloom showed promise for reducing cork spot incidence in ‘Akizuki’ pear without affecting fruit quality attributes. This research herein reveals the physiological-biochemical characteristic of cork spot disorder, and implicates P-Ca as a potential tool to reduce cork spot incidence in Asian pear cultivar Akizuki.

‘Akizuki’ (Pyrus pyrifolia Nakai), a Japanese pear, plays an important role in pear production in China because of its good quality characteristics such as large fruit, pretty shape, delicate pulp. and high soluble solid content. However, with the cultivation area increasing, a physiological disorder that appears to be cork spot in this cultivar has occurred in several pear orchards in Shandong province of China, and become a serious problem over the years.

Cork spot, bitter pit, and corky core, the most typical physiological disorders that develop in apple fruit skin, are commonly called cork spot-like physiological disorder (CSPD) (Faust and Shear, 1968; Ferguson and Watkins, 2011). In pear fruits, cork spot is also the most common physiological disorder except for hard end, corky core, and water core (Inomata et al., 1993; Lu et al., 2014). Except for ‘Akizuki’, this disorder is also frequently found in other pear varieties such as ‘Anjou’, ‘Alexander Lucas’, and ‘Oushuu’ pear (Hayama et al., 2017; Raese and Drake, 1993; Richardson and Lombard, 1979; Tomala and Trzak, 1994). Cork spot-like disorder involves the suberization of cells in pear flesh (Tamura, 2017). A recent report indicated that cork spot symptoms were observed more markedly in the late maturing fruit in ‘Akizuki’ pear (Hayama et al., 2017). In addition, the severity of the cork spot disorder showed an association with the fruit fresh weights: more cork spots appeared on larger fruit (Hayama et al., 2017). Moreover, more cork spots were observed in the middle of the fruit, with few at the stem end (Hayama et al., 2017).

Many physiological disorders are closely related to Ca deficiency in fruit, and control of these physiological disorders requires maintenance of adequate levels of Ca (Dong et al., 2015; Lee et al., 2007; Miqueloto et al., 2014; Raese, 1988; Raese and Drake 1995). Cork spot presented symptoms similar to those of bitter pit, was induced by Ca deficiency, and, thus, Ca spraying was a useful alleviating measure (Faust and Shear, 1969; Raese and Drake, 1993, 1995, 2006; Richardson and Lombard, 1979). Besides Ca, the levels of other mineral nutrients could also influence fruit susceptibility to calcium deficiency disorders (Lee et al., 2007). For example, K and Mg can antagonize the uptake or the function of Ca at the membrane or compete with Ca at active site on membranes (Schönherr and Bukovac, 1973; Yermiyahu et al., 1994). High levels of N in the fruit have been reported to aggravate the development of Ca deficiency symptoms in apple (Bangerth, 1974; Shear, 1971). However, there are also some conflicts, for example, Mason and Welsh (1970) showed that fruits with bitter pit or cork spot had higher Mg concentration than normal fruits, whereas Woodbridge (1971) found no significant differences between them. Therefore, the nutrient concentration ratios such as K/Ca, Mg/Ca, and (K+Mg)/Mg are more meaningful to predict Ca deficiency disorders than total fruit Ca concentration alone (Dris et al., 1998; Freitas et al., 2010; Lanauskas and Kviklienė, 2006; Schumacher and Fankhauser, 1970). Although the association between cork spot and mineral concentrations in European pear has been frequently reported, little has been done on Asian pear cultivars.

Prohexadione calcium (P-Ca) inhibits the biosynthesis of gibberellin (Evans et al., 1999; Rademacher et al., 2004). Compared with other three triazole growth inhibitors, P-Ca has low toxicity and limited persistence in the environment, being metabolized or decomposed 6 to 7 weeks after application (Evans et al., 1999; Owens and Stover, 1999; Rademacher et al., 2004). Previous studies have demonstrated significant control of shoot growth by P-Ca on a range of pear varieties (Asín et al., 2007; Costa et al., 2001; Einhorn et al., 2014; Elfving et al., 2003; Hawerroth et al., 2012), and P-Ca has little effect on fruit quality attributes in pear (Costa et al., 2004; Einhorn et al., 2014; Elfving et al., 2003). Moreover, P-Ca was reported to induce resistance to apple scab and fire blight (Costa et al., 2001; Römmelt et al., 1999). However, whether P-Ca has potential to reduce cork spot incidence in ‘Akizuki’ pear has not been studied.

The goals of our study were to elucidate the difference of fruit characteristics and content of mineral elements between cork spotted and normal fruits in ‘Akizuki’ pear, and to determine an effective spray material for reducing the incidence of cork spot without affecting fruit quality attributes.

Materials and Methods

Plant materials.

Six-year-old ‘Akizuki’ pear trees grown on Pyrus betulaefolia Bunge pear rootstocks were selected for the experiment. The orchard, trained to a trellis cultivation system, with spacing of 4 × 3 m, was located in Qingdao City, Shandong Province, People’s Republic of China. Cork spotted and normal fruits in this same orchard were collected at maturity, 140 d after full bloom (DAFB) in 2014–16. Whole fruit flesh tissues were divided into three parts (the calyx end, the middle part, and the stem end) with the core and seeds excluded, and then were sliced and immediately frozen in liquid nitrogen and maintained at −70 °C for further study.

Performance of exogenous Ca, B, and P-Ca treatments.

Ca, B, P-Ca (Kumiai Chemical Industry Co., Ltd, Tokyo, Japan), or unsprayed control were used in this experiment. Each treatment was randomly allocated to three trees selected by uniformity and size (canopy volume), making five replications for each. All treatments were conducted every 15 d, with a total of five replications from beginning at 30 DAFB. When spraying, H3BO3 and Ca(NO3)2 were diluted 600 times with water, and P-Ca was diluted 1500, 2500, and 3500 times with water, respectively. Fruit samples from the treated and control trees were harvested at commercial maturity (140 DAFB) and subsequently transported to the laboratory within a period of 2 h, and then used for fruit quality evaluation. Effects on cork spot incidence were assessed on fruits, and data were expressed as percentage of the number of disordered fruit divided by the total number of fruit.

Fruit quality analysis.

Fruit firmness was determined by removing fruit skin on four sides of each fruit, using a texture analyzer (CT3; Brookfield, Middleboro, MA) with a 2-mm-diameter probe, 10-mm penetration depth, and 0.5-mm·s−1 penetration rate, expressed in kg·cm−2.

Average fruit weight was determined by sampling and individually weighing 200 fruits randomly chosen from all trees per treatment. The vertical and horizontal diameter of fruit, the length and diameter of fruit pedicel, and the calyx concave depth were measured by vernier caliper.

To measure the total soluble solids, the sample of the stem end, the middle part, and the calyx end of fruit was juiced, respectively, placed on the prism of a digital handheld Abbe-type refractometer and expressed as °Brix. Titratable acidity of different fruit parts was measured using titration with 0.1 N sodium hydroxide (NaOH) and calculated as a malic acid equivalent. The content of vitamin C, soluble sugar and starch, and reducing sugars was determined by colorimetry by molybdenum blue method, anthrone reagent method, and a 3, 5-dinitrosalicylic acid colorimetric method, respectively.

Measurement of the mineral nutrient content.

Fruit flesh tissues were dried in an oven at 105 °C for 30 min, and then at 75 °C until a constant weight was achieved; 0.5 g of flesh tissues was mixed with 2 mL perchloric and 10 mL nitric acids. After digestion and dissolution, the total contents of Ca, Mg, K, Fe, Zn, and P were analyzed by using an ICP-OES optima 8000 (PerkinElmer Inc., Waltham, MA).

For the determination of total N content, 1 g of dried flesh samples was mixed with 0.3 g CuSO4, 3 g anhydrous Na2SO4, and 10 to 12 mL concentrated H2SO4. After digestion and dissolution, the N content was assayed using a Kjeldahl nitrogen apparatus (K9860; Hanon instruments Co., Ltd., Jinan, China).

Observation of Ca2+ localization.

The localization of free Ca2+ was observed by fluorescence imaging as previously described by Qu et al. (2012), with some modifications. Thin slices of flesh were collected from the same region under the peel tissue of normal and cork spot fruit by using a razor blade. The flesh tissues were initially washed twice with HEPES buffer solution, which were loaded with fluo-4/AM supplemented with 25% Pluronic F-127 and then subsequently washed three times with HEPES buffer solution. After maintaining the tissue in the dark at 37 °C for 1 h, we visualized fluo-4 fluorescence (488-nm excitation laser light and 516-nm long-pass emission filter) using a laser scanning confocal microscope (TCS SP5 II; Leica, Wetzlar, Germany). The fluorescence results were analyzed using Image-Pro Plus software (Media Cybernetics, Rockville, MD).

Statistical analysis.

The statistical analysis was performed using SPSS 17.0 software (IBM-SPSS, Armonk, NY). Data expressed as percentage were transformed by arcsine [square root (n + 1)] analysis. Sample means were compared using analysis of variance. Mean separation was determined by Duncan’s multiple range test, and significance was tested at 5% or 1%. Figures were composed using Microsoft Excel software (Redmond, WA).

Results and Discussion

Symptoms of cork spotted pear fruit.

The symptoms of cork spot were observed more markedly in the late maturing fruit in ‘Akizuki’ pear, which is consistent with previous reports (Hayama et al., 2017; Mason and Welsh, 1970). At harvest stage, one or more small dark green or brown round dimpled spots of 0.3 to 1.0 cm in diameter were observed on the skin of disordered fruits, and below them was the affected brown spot (Fig. 1A and B). Much larger bumpy surface with necrotic flesh tissue under the affected area were observed with severe cork spotted fruits (Fig. 1C and D). Consistent with the report of Hayama et al. (2017), more cork spots were observed in the middle of the fruit (Fig. 1B and D). The brown spot could be anywhere between the skin and the core, but in most cases, it was close to the surface of the fruit just beneath the skin, which was similar to the report of Faust and Shear (1968). A depression developed above the internal spots as the fruit enlarged, due to the reduced growth in the affected tissues. With longitudinal cutting of the fruit, a localized desiccated tissue resembling cork was observed in the flesh of the fruit, which was brown and necrotic with dry and water-deficiency in vascular bundle tissue (Fig. 1E and F).

Fig. 1.
Fig. 1.

Symptoms of ‘Akizuki’ pear fruit with cork spot. (A) Fruit with light cork spot. (B) Longitudinal section of fruit with light cork spot. (C) Fruit with severe cork spot. (D) Longitudinal section of fruit with severe cork spot. (E, F) Endogenic type or subcutaneous of suberized tissue in pear fruit flesh, respectively.

Citation: HortScience horts 54, 3; 10.21273/HORTSCI13775-18

Comparison of fruit quality attributes between normal and cork spotted fruit.

The average fruit weight of disordered fruit was significantly higher than that of normal fruit (Table 1), which is similar to the report of Hayama et al. (2017). The diameter of fruit pedicels and the calyx concave depth in disordered fruit were also significantly greater than that of normal ones (Table 1); however, total soluble solids in each part of disordered fruit was significantly lower than that in the same part of normal ones (Table 2). In addition, there was no significant difference in titratable acidity and fruit firmness with the exception of that in the calyx end (Table 2).

Table 1.

Fruit characteristic of cork spotted and normal ‘Akizuki’ fruits.

Table 1.
Table 2.

Fruit quality of cork spotted and normal ‘Akizuki’ fruits.

Table 2.

We also determined the contents of vitamin C and carbohydrates, including soluble sugar, reducing sugar, and starch of different fruits. From the calyx end to the stem end, the content of soluble and reducing sugar, and vitamin C in normal fruit were significantly higher than those of disordered fruit (Fig. 2). Inconsistent with the report of Li et al. (1999), the starch content in our research was much higher in cork spotted fruits than normal fruit, but the difference was not significant. All the results presented previously indicated that cork spotted pear fruit had larger fruit size and decreased the contents of total soluble solids, soluble and reducing sugar, and vitamin C, which resulted in fruit quality deterioration.

Fig. 2.
Fig. 2.

Comparison of carbohydrate content of fruit flesh between cork spotted and normal ‘Akizuki’ pear. Error bars with different lowercase letters represent a statistical difference by Duncan’s multiple range test (P < 0.05).

Citation: HortScience horts 54, 3; 10.21273/HORTSCI13775-18

Analysis of mineral nutrient content in normal and cork spotted pear fruit.

Cork spot has been linked to fruit nutritional imbalance (Facteau et al., 2010; Richardson and Al-Ani, 1982; Tomala and Trzak, 1994). Mineral nutrient contents in the stem end, middle part, and calyx end of normal and disordered pear fruit were determined in this research. At the same time, the ratios of K/Ca, Mg/Ca, and (K+Mg)/Ca were also evaluated. Compared with normal fruit, ‘Akizuki’ pear with cork spot showed much higher N, significantly higher Mg, and lower P content (Table 3). The results herein were not quite consistent with previous results, which showed significantly higher Mg and P in the spotted fruit (Faust and Shear, 1969; Tomala and Trzak, 1994). This conflict with P was probably due to the different cultivar or the cultivation conditions. The K content in the stem end and the middle part of normal fruit was significantly higher than those showing cork spot, which was in agreement with Al-Ani (1978), who found that low K in the fruit maybe related to the incidence of cork spot. Previous studies suggested that a high level of N reduces the movement of Ca toward the fruit (Ho et al., 1999) and triggers rapid fruit and cell expansion, which can potentially result in further dilution of the limited Ca content that moves into the fruit (Bar-Tal et al., 2001; Saure, 2001), and thus results in the occurrence of cork spot (Raese and Staiff, 1990). In our study, high levels of N correlated with cork spot in ‘Akizuki’ pear, but did not lead to Ca deficiency. Zn and Fe content seemed irrelevant to this disorder.

Table 3.

Total mineral element content of cork spotted and normal ‘Akizuki’ fruits from the calyx to stem end.

Table 3.

In some research, adequate Ca in fruit is necessary for controlling cork spot disorder in pears (Raese, 1989; Raese and Drake, 1995; Tomala and Trzak, 1994), but there is a report that indicated that cork spotted pear fruit had higher Ca concentrations than normal fruit (Mason and Welsh, 1970). However, our results showed that Ca concentration in all three parts of disordered ‘Akizuki’ pear fruit was much higher than those of normal fruit, especially for the middle and calyx end where the differences of Ca content were significant, suggesting that the occurrence of cork spot in this cultivar might not be due to a deficiency of total Ca (Fig. 3). Mg2+ and K+ could compete with Ca2+ for binding sites at the plasma membrane; therefore, high levels of them reduced Ca absorption (Schönherr and Bukovac, 1973; Yermiyahu et al., 1994) and increased the susceptibility to Ca deficiency disorders (Askew et al., 1960). Therefore, it was more precise to use the ratios of N/Ca, K/Ca, and Mg/Ca to predict Ca deficiency disorders than fruit total Ca concentration alone (Dris et al., 1998; Freitas et al., 2010; Lanauskas and Kviklienė, 2006). In our study, cork spot in ‘Akizuki’ pear was correlated with lower ratios of K/Ca, (K+Mg)/Ca, and Mg/Ca (Fig. 3). In addition, the most susceptible fruit part to cork spot (the middle part) not only accumulated significantly higher levels of Mg but also Ca, whereas it had significantly lower K content. These conflicts may have resulted from the fruit development difference between Asian and European pears, because ‘Akizuki’ and ‘Anjou’ pears belong to Asian and European pear cultivars, respectively.

Fig. 3.
Fig. 3.

The ratio of K/Ca, Mg/Ca, (K+Mg)/Ca, and Ca content in normal and cork spotted ‘Akizuki’ pear fruit. Error bars indicate se from three replicates. Error bars with different letters represent a statistical difference by Duncan’s multiple range test (P < 0.05).

Citation: HortScience horts 54, 3; 10.21273/HORTSCI13775-18

Analysis of the free Ca2+ localization in the flesh of cork spotted and normal pear fruit.

At harvest, the free Ca2+ localization was detected in the flesh cells loaded with fluo-4/AM. High levels of free Ca2+ were observed in the cell wall and intercellular space of cork spotted fruit flesh; however, lower free Ca2+ spread over all of the flesh cells of normal fruit (Fig. 4). This cellular distribution difference of free Ca2+ between cork spotted and normal fruit may be a reason for cork spot. In addition, the free Ca2+ in the cork spotted fruit was much greater than normal fruit, which was in accordance with the results of total Ca content (Fig. 3), and partially consistent with the results of Wang et al. (2018), who suggested that the free Ca2+ localization in the flesh cells of hard end fruit was greater than that of normal fruit at harvest (120 DAFB), whereas it showed an opposite tendency during ‘Whangkeumbae’ pear fruit development (75–105 DAFB) (Wang et al., 2018).

Fig. 4.
Fig. 4.

Localization of free Ca2 + fluorescence signals in the flesh cells of normal and cork spotted ‘Akizuki’ pear. (AC) Free Ca2+ fluorescence signals in normal fruits by Argon ion laser excitation (A), light field (B), and merge field (C). (DF) Free Ca2+ fluorescence signals in cork spotted fruits by Argon ion laser excitation (D), light field (E), and merge field (F). Scale bar is 250 µm for (AC), and 100 µm for (DF), respectively.

Citation: HortScience horts 54, 3; 10.21273/HORTSCI13775-18

Effect of exogenous treatments on the incidence of cork spot in ‘Akizuki’ pear.

CSPD symptoms are reported to be induced by Ca or B deficiency, and the exogenous application of supplemental sprays containing these mineral nutrients improves the symptoms (Faust and Shear, 1968; Raese and Drake, 1995; Richardson and Lombard, 1979; Vang-Petersen, 1980). To prevent the incidence of cork spot in ‘Akizuki’ pear, five sprays at 30, 45, 60, 75, and 90 DAFB with different treatments [H3BO3, Ca(NO3)2, and P-Ca] were adopted in this research. As expected, Ca, B, and P-Ca treatments helped in controlling the cork spot in fruits from both axillary and spur bud (Fig. 5), which agreed with previous reports (Faust and Shear, 1968; Raese and Drake, 1993, 1995; Richardson and Lombard, 1979). However, the research of Matsumoto et al. (2018) indicated that none of Ca or B solutions decreased the CSPD incidence in ‘Kurenainoyume’ apple. In our research, we also observed higher levels of Ca and free Ca2+ in cork spotted fruit, indicating that deficiency of total Ca was not the major cause of this disorder in ‘Akizuki’ pear. But one consideration is why cork spot incidence could be inhibited by exogenous Ca solutions, because this disorder was not caused by lack of Ca? It may be more meaningful to consider factors such as the existing state of Ca (soluble or insoluble) or the balance between Ca and other elements besides the hereditary factor, soil pH, cultivation conditions, tree vigor, and the climate condition, which will affect the incidence of cork spot (Richardson and Lombard, 1979; Tamura, 2017).

Fig. 5.
Fig. 5.

Effect of exogenous treatments on cork spot incidence of fruit from axillary and spur bud in ‘Akizuki’ pear. Error bars with different letters represent a statistical difference by Duncan’s multiple range test (P < 0.05).

Citation: HortScience horts 54, 3; 10.21273/HORTSCI13775-18

There were significant differences in cork spot incidence of fruits from axillary bud between treatments and control, with the exception of H3BO3 (Fig. 5). The inhibitory effect of Ca(NO3)2 on cork spot was better than that of H3BO3, but there was no significant difference between them. Among the exogenous treatments, the most effective one was P-Ca sprayed with 3500 times dilution, which reduced the incidence of cork spot from 16.39% to 8% and from 15.87% to 6% in fruits from axillary and spur bud, respectively (Fig. 5). As is known, P-Ca has been widely used in the control of vegetative growth of several pear cultivars (Asín et al., 2007; Hawerroth et al., 2012; Pasa and Einhorn, 2014). ‘Akizuki’ pear shows a strong growth habit, from which new shoots stop growth 20 d later than other Asian pear cultivars, which may be correlated with its susceptibility to cork spot. Application of P-Ca alleviates the nutrition competition between fruit development and new shoot growth, which may have resulted in the prevention of cork spot incidence. In a word, P-Ca efficiently helped to reduce cork spot incidence in ‘Akizuki’ pear, thus providing a new control approach for cork spot in pear.

Effect of exogenous treatments on fruit quality in ‘Akizuki’ pear.

To further test the effects of exogenous treatments on fruit quality in ‘Akizuki’ pear, we investigated the fruit characteristics of treated fruit and unsprayed control. The results showed that all exogenous treatments had no negative effects on fruit quality attributes, especially for fruit size (Table 4). Fruit quality attributes were unaffected by P-Ca, similar to that found for ‘Anjou’ (Einhorn et al., 2014), ‘Bartlett’ (Elfving, et al., 2003), ‘Abate Fetel’ (Costa et al., 2004), and ‘Le Conte’ (Carra et al., 2016); however, it was not in agreement with the results in which P-Ca sprayed fruits were much larger than control fruits (Costa et al., 2001), or reports in which P-Ca has been reported to be associated with reduction of fruit size (Smit et al., 2005; Sugar et al., 2004). This may be due to the application time and concentration of P-Ca.

Table 4.

Effects of exogenous treatments on fruit characters of ‘Akizuki’ pear.

Table 4.

Furthermore, exogenous treatments helped to improve the development of fruit pedicels and the calyx concave: Ca(NO3)2 significantly increased the diameter and shortened the fruit pedicels, H3BO3 promoted the diameter increment of fruit pedicels, and P-Ca at different rates decreased the calyx concave depth (Table 5). Moreover, spraying of Ca(NO3)2 and H3BO3 solutions significantly reduced the titratable acidity, resulting in improved fruit flavor. For soluble solids, P-Ca with 1500 or 3500 times dilution did not differ from control (Table 5), which agrees with those found for ‘Rosemarie’, ‘Forelle’, ‘Packham’s Triumph’, and ‘Le Conte’ pear (Carra et al., 2016; Smit et al., 2005). P-Ca with 2500 times dilution significantly decreased fruit firmness and improved total soluble solids in the middle and the calyx of fruit (Table 5). To sum up, five sprays of P-Ca with 3500 times dilution was promise for inhibiting the incidence of cork spot without affecting fruit quality attributes, and could be used widely in ‘Akizuki’ pear cultivation.

Table 5.

Effects of exogenous treatments on fruit quality.

Table 5.

Conclusions

Compared with normal ‘Akizuki’ pear fruit, cork spotted fruit had significantly larger fruit size with shorter fruit pedicels. Furthermore, higher levels of N, Ca, and Mg, and lower ratios of K/Ca, Mg/Ca, and (K+Mg)/Ca were correlated with cork spot in ‘Akizuki’ pear fruit. Moreover, localization of free Ca2+ mainly in the cell wall and intercellular space may be strongly correlated with cork spot. Five sprays of P-Ca with 3500 times dilution at 15-d intervals from 30 to 90 DAFB showed promise for reducing cork spot incidence in ‘Akizuki’ pear without affecting fruit quality attributes. However, the mechanism of cork spot is complex and there are still many unclear details; therefore, further studies are needed focus on the relationship between cork spot and influence factors such as cultivar, climatic and soil conditions, and cultural practices including orchard fertilizer practices, excessive pruning, and poor rootstocks.

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  • Li, S.J., Facteau, T.J., Chen, P.M. & Mielke, E.A. 1999 Comparison of amylase activity and starch content in normal and cork spotted ‘d ’anjou’ pears J. Food Biochem. 23 5 509 518

    • Search Google Scholar
    • Export Citation
  • Lu, G., Li, Z., Zhang, X., Wang, R. & Yang, S. 2014 Expression analysis of lignin-associated genes in hard end pear (Pyrus pyrifolia Whangkeumbae) and its response to calcium chloride treatment conditions J. Plant Growth Regulat. 34 2 251 262

    • Search Google Scholar
    • Export Citation
  • Mason, J.L. & Welsh, M.F. 1970 Cork spot (pit) of ‘Anjou’ pear related to calcium concentration in fruit HortScience 5 447

  • Matsumoto, K., Kobayashi, T., Kougo, T., Fujita, T., Sato, S. & Moriguchi, T. 2018 Prevention of new cork spot-like physiological disorder in ‘Kurenainoyume’ apples by pre-harvest fruit bagging Hort. J. 87 2 174 183

    • Search Google Scholar
    • Export Citation
  • Miqueloto, A., Steffens, C.A., Santos, A.D. & Mitcham, E. 2014 Relationship between xylem functionality, calcium content and the incidence of bitter pit in apple fruit Scientia Hort. 165 319 323

    • Search Google Scholar
    • Export Citation
  • Owens, C.L. & Stover, E. 1999 Vegetative growth and flowering of young apple trees in response to prohexadione-calcium HortScience 34 1997 1999

  • Pasa, M.S. & Einhorn, T.C. 2014 Heading cuts and prohexadione-calcium affect the growth and development of ‘d’Anjou’ pear shoots in a high-density orchard Scientia Hort. 168 267 271

    • Search Google Scholar
    • Export Citation
  • Qu, H.Y., Jiang, X., Shi, Z., Liu, L. & Zhang, S. 2012 Fast loading ester fluorescent Ca2+ and pH indicators into pollen of Pyrus pyrifolia J. Plant Res. 125 185 195

    • Search Google Scholar
    • Export Citation
  • Rademacher, W., Saarloos, K., Van Porte, J.A.G., Forcades, F.R., Senechal, Y., Andreotti, C., Spinelli, F., Sabatini, E. & Costa, G. 2004 Impact of prohexadione-ca on the vegetative and reproductive performance of apple and pear trees Eur. J. Hort. Sci. 69 221 228

    • Search Google Scholar
    • Export Citation
  • Raese, J.T. 1988 Calcium sprays and fertilizers found effective against ‘d’Anjou’ pears disorders Good Fruit Grower 39 35 39

  • Raese, J.T. 1989 Physiological disorders and maladies of pear fruit Hort. Rev. 11 357 411

  • Raese, J.T. & Drake, S.R. 1993 Effects of preharvest calcium sprays on apple and pear quality J. Plant Nutr. 16 9 1807 1819

  • Raese, J.T. & Drake, S.R. 1995 Calcium sprays and timing affect fruit calcium concentrations, yield, fruit weight, and cork spot of ‘Anjou’ pears HortScience 30 5 1037 1039

    • Search Google Scholar
    • Export Citation
  • Raese, J.T. & Drake, S.R. 2006 Calcium foliar sprays for control of alfalfa greening, cork spot, and hard end in ‘Anjou’ pears J. Plant Nutr. 29 3 543 552

    • Search Google Scholar
    • Export Citation
  • Raese, J.T. & Staiff, D.C. 1990 Fruit calcium, quality and disorders of apples (Malus domestica) and pears (Pyrus communis) influenced by fertilizers, p. 619–624. In: M.L. Van Beusichem (ed.). Plant nutrition-physiology applications. Kluwer, Dordrecht, The Netherlands

  • Richardson, D.G. & Al-Ani, A.M. 1982 Cork spot of d'Anjou pear fruit relative to critical calcium concentration and other minerals. Acta Hort. 124:895–905

  • Richardson, D.G. & Lombard, P.B. 1979 Cork spot of anjou pear: Control by calcium sprays Commun. Soil Sci. Plan. 10 1-2 383 389

  • Römmelt, S., Treutter, D., Rademacher, W. & Speakman, J.B. 1999 Effects of prohexadione-Ca on the flavonoid metabolism of apple with respect to plant resistance against fire blight Acta Hort. 489 359 365

    • Search Google Scholar
    • Export Citation
  • Saure, M.C. 2001 Blossom-end rot of tomato (Lycopersicon esculentum Mill.): A calcium- or a stress-related disorder Scientia Hort. 90 193 208

  • Schönherr, J. & Bukovac, M.J. 1973 Ion exchange properties of isolated tomato fruit cuticular membrane: Exchange capacity, nature of fixed charges and cation selectivity Planta 109 73 93

    • Search Google Scholar
    • Export Citation
  • Schumacher, R. & Fankhauser, F. 1970 Stippe und ihre Bekampfung Schweiz Z Obst–Weinbau 106 264 268

  • Shear, C.B. 1971 Symptoms of calcium deficiency on leaves and fruits of ‘York Imperial’ apple J. Amer. Soc. Hort. Sci. 96 415 417

  • Smit, M., Meintjes, J.J., Jacobs, G., Stassen, P.J.C. & Theron, K.I. 2005 Shoot growth control of pear trees (Pyrus communis L.) with prohexadione-calcium Scientia Hort. 106 515 529

    • Search Google Scholar
    • Export Citation
  • Sugar, D., Elfving, D.C. & Mielke, E.A. 2004 Effects of prohexadione-calcium on fruit size and return bloom in pear HortScience 39 1305 1308

  • Tamura, F. 2017 Occurrence of physiological disorders in Japanese pear fruit and advances in research on these disorders Hortic. Res. (Japan) 16 4 373 381

    • Search Google Scholar
    • Export Citation
  • Tomala, K. & Trzak, M. 1994 Occurrence of cork spot (pit) in ‘Alexander Lucas’ pears depends on fruit mineral element content Acta Hort. 368 570 577

    • Search Google Scholar
    • Export Citation
  • Vang-Petersen, O. 1980 Calcium nutrition of apple trees: A review Scientia Hort. 12 1 9

  • Wang, Y.L., Zhang, X.F., Wang, Y.Z., Yang, S.L. & Qu, H.Y. 2018 The changes of intracellular calcium concentration and distribution in the hard end pear (Pyrus pyrifolia cv. ‘Whangkeumbae’) fruit Cell Calcium 71 15 23

    • Search Google Scholar
    • Export Citation
  • Woodbridge, C.G. 1971 Calcium level of pear tissues affected with cork and black end HortScience 6 451 453

  • Yermiyahu, U., Nir, S., Ben-Hayyim, G. & Kafkafi, U. 1994 Quantitative competition of calcium with sodium or magnesium for sorption sites on plasma membrane vesicles of melon (Cucumis melo L.) root cells J. Membr. Biol. 138 55 63

    • Search Google Scholar
    • Export Citation
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    Symptoms of ‘Akizuki’ pear fruit with cork spot. (A) Fruit with light cork spot. (B) Longitudinal section of fruit with light cork spot. (C) Fruit with severe cork spot. (D) Longitudinal section of fruit with severe cork spot. (E, F) Endogenic type or subcutaneous of suberized tissue in pear fruit flesh, respectively.

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    Comparison of carbohydrate content of fruit flesh between cork spotted and normal ‘Akizuki’ pear. Error bars with different lowercase letters represent a statistical difference by Duncan’s multiple range test (P < 0.05).

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    The ratio of K/Ca, Mg/Ca, (K+Mg)/Ca, and Ca content in normal and cork spotted ‘Akizuki’ pear fruit. Error bars indicate se from three replicates. Error bars with different letters represent a statistical difference by Duncan’s multiple range test (P < 0.05).

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    Localization of free Ca2 + fluorescence signals in the flesh cells of normal and cork spotted ‘Akizuki’ pear. (AC) Free Ca2+ fluorescence signals in normal fruits by Argon ion laser excitation (A), light field (B), and merge field (C). (DF) Free Ca2+ fluorescence signals in cork spotted fruits by Argon ion laser excitation (D), light field (E), and merge field (F). Scale bar is 250 µm for (AC), and 100 µm for (DF), respectively.

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    Effect of exogenous treatments on cork spot incidence of fruit from axillary and spur bud in ‘Akizuki’ pear. Error bars with different letters represent a statistical difference by Duncan’s multiple range test (P < 0.05).

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  • Li, S.J., Facteau, T.J., Chen, P.M. & Mielke, E.A. 1999 Comparison of amylase activity and starch content in normal and cork spotted ‘d ’anjou’ pears J. Food Biochem. 23 5 509 518

    • Search Google Scholar
    • Export Citation
  • Lu, G., Li, Z., Zhang, X., Wang, R. & Yang, S. 2014 Expression analysis of lignin-associated genes in hard end pear (Pyrus pyrifolia Whangkeumbae) and its response to calcium chloride treatment conditions J. Plant Growth Regulat. 34 2 251 262

    • Search Google Scholar
    • Export Citation
  • Mason, J.L. & Welsh, M.F. 1970 Cork spot (pit) of ‘Anjou’ pear related to calcium concentration in fruit HortScience 5 447

  • Matsumoto, K., Kobayashi, T., Kougo, T., Fujita, T., Sato, S. & Moriguchi, T. 2018 Prevention of new cork spot-like physiological disorder in ‘Kurenainoyume’ apples by pre-harvest fruit bagging Hort. J. 87 2 174 183

    • Search Google Scholar
    • Export Citation
  • Miqueloto, A., Steffens, C.A., Santos, A.D. & Mitcham, E. 2014 Relationship between xylem functionality, calcium content and the incidence of bitter pit in apple fruit Scientia Hort. 165 319 323

    • Search Google Scholar
    • Export Citation
  • Owens, C.L. & Stover, E. 1999 Vegetative growth and flowering of young apple trees in response to prohexadione-calcium HortScience 34 1997 1999

  • Pasa, M.S. & Einhorn, T.C. 2014 Heading cuts and prohexadione-calcium affect the growth and development of ‘d’Anjou’ pear shoots in a high-density orchard Scientia Hort. 168 267 271

    • Search Google Scholar
    • Export Citation
  • Qu, H.Y., Jiang, X., Shi, Z., Liu, L. & Zhang, S. 2012 Fast loading ester fluorescent Ca2+ and pH indicators into pollen of Pyrus pyrifolia J. Plant Res. 125 185 195

    • Search Google Scholar
    • Export Citation
  • Rademacher, W., Saarloos, K., Van Porte, J.A.G., Forcades, F.R., Senechal, Y., Andreotti, C., Spinelli, F., Sabatini, E. & Costa, G. 2004 Impact of prohexadione-ca on the vegetative and reproductive performance of apple and pear trees Eur. J. Hort. Sci. 69 221 228

    • Search Google Scholar
    • Export Citation
  • Raese, J.T. 1988 Calcium sprays and fertilizers found effective against ‘d’Anjou’ pears disorders Good Fruit Grower 39 35 39

  • Raese, J.T. 1989 Physiological disorders and maladies of pear fruit Hort. Rev. 11 357 411

  • Raese, J.T. & Drake, S.R. 1993 Effects of preharvest calcium sprays on apple and pear quality J. Plant Nutr. 16 9 1807 1819

  • Raese, J.T. & Drake, S.R. 1995 Calcium sprays and timing affect fruit calcium concentrations, yield, fruit weight, and cork spot of ‘Anjou’ pears HortScience 30 5 1037 1039

    • Search Google Scholar
    • Export Citation
  • Raese, J.T. & Drake, S.R. 2006 Calcium foliar sprays for control of alfalfa greening, cork spot, and hard end in ‘Anjou’ pears J. Plant Nutr. 29 3 543 552

    • Search Google Scholar
    • Export Citation
  • Raese, J.T. & Staiff, D.C. 1990 Fruit calcium, quality and disorders of apples (Malus domestica) and pears (Pyrus communis) influenced by fertilizers, p. 619–624. In: M.L. Van Beusichem (ed.). Plant nutrition-physiology applications. Kluwer, Dordrecht, The Netherlands

  • Richardson, D.G. & Al-Ani, A.M. 1982 Cork spot of d'Anjou pear fruit relative to critical calcium concentration and other minerals. Acta Hort. 124:895–905

  • Richardson, D.G. & Lombard, P.B. 1979 Cork spot of anjou pear: Control by calcium sprays Commun. Soil Sci. Plan. 10 1-2 383 389

  • Römmelt, S., Treutter, D., Rademacher, W. & Speakman, J.B. 1999 Effects of prohexadione-Ca on the flavonoid metabolism of apple with respect to plant resistance against fire blight Acta Hort. 489 359 365

    • Search Google Scholar
    • Export Citation
  • Saure, M.C. 2001 Blossom-end rot of tomato (Lycopersicon esculentum Mill.): A calcium- or a stress-related disorder Scientia Hort. 90 193 208

  • Schönherr, J. & Bukovac, M.J. 1973 Ion exchange properties of isolated tomato fruit cuticular membrane: Exchange capacity, nature of fixed charges and cation selectivity Planta 109 73 93

    • Search Google Scholar
    • Export Citation
  • Schumacher, R. & Fankhauser, F. 1970 Stippe und ihre Bekampfung Schweiz Z Obst–Weinbau 106 264 268

  • Shear, C.B. 1971 Symptoms of calcium deficiency on leaves and fruits of ‘York Imperial’ apple J. Amer. Soc. Hort. Sci. 96 415 417

  • Smit, M., Meintjes, J.J., Jacobs, G., Stassen, P.J.C. & Theron, K.I. 2005 Shoot growth control of pear trees (Pyrus communis L.) with prohexadione-calcium Scientia Hort. 106 515 529

    • Search Google Scholar
    • Export Citation
  • Sugar, D., Elfving, D.C. & Mielke, E.A. 2004 Effects of prohexadione-calcium on fruit size and return bloom in pear HortScience 39 1305 1308

  • Tamura, F. 2017 Occurrence of physiological disorders in Japanese pear fruit and advances in research on these disorders Hortic. Res. (Japan) 16 4 373 381

    • Search Google Scholar
    • Export Citation
  • Tomala, K. & Trzak, M. 1994 Occurrence of cork spot (pit) in ‘Alexander Lucas’ pears depends on fruit mineral element content Acta Hort. 368 570 577

    • Search Google Scholar
    • Export Citation
  • Vang-Petersen, O. 1980 Calcium nutrition of apple trees: A review Scientia Hort. 12 1 9

  • Wang, Y.L., Zhang, X.F., Wang, Y.Z., Yang, S.L. & Qu, H.Y. 2018 The changes of intracellular calcium concentration and distribution in the hard end pear (Pyrus pyrifolia cv. ‘Whangkeumbae’) fruit Cell Calcium 71 15 23

    • Search Google Scholar
    • Export Citation
  • Woodbridge, C.G. 1971 Calcium level of pear tissues affected with cork and black end HortScience 6 451 453

  • Yermiyahu, U., Nir, S., Ben-Hayyim, G. & Kafkafi, U. 1994 Quantitative competition of calcium with sodium or magnesium for sorption sites on plasma membrane vesicles of melon (Cucumis melo L.) root cells J. Membr. Biol. 138 55 63

    • Search Google Scholar
    • Export Citation
Yan-xin DuanCollege of Horticulture, Qingdao Agricultural University, Qingdao 266109, China

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Ying XuCollege of Horticulture, Qingdao Agricultural University, Qingdao 266109, China

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Ran WangCollege of Horticulture, Qingdao Agricultural University, Qingdao 266109, China

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Chun-hui MaCollege of Horticulture, Qingdao Agricultural University, Qingdao 266109, China

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Contributor Notes

This work was funded by the Key Research and Development Program of Shandong Province (2017CXGC0209), the China Agricultural Research System (CARS-29-07), and the subproject of Key National R&D Programs (2018YFD1000204).

Corresponding author. E-mail: machunhui2000@163.com.

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