Factors Affecting Mechanical Properties of the Skin of Sweet Cherry Fruit

IF 1.1 4区 农林科学 Q3 HORTICULTURE
M. Brüggenwirth, M. Knoche
{"title":"Factors Affecting Mechanical Properties of the Skin of Sweet Cherry Fruit","authors":"M. Brüggenwirth, M. Knoche","doi":"10.21273/JASHS.141.1.45","DOIUrl":null,"url":null,"abstract":"The skins of all fruit types are subject to sustained biaxial strain during the entire period of their growth. In sweet cherry (Prunus avium L.), failure of the skin greatly affects fruit quality. Mechanical properties were determined using a biaxial bulging test. The factors considered were the following: ripening, fruit water relations (including turgor, transpiration, and water uptake), and temperature. Excised discs of fruit skin were mounted in a custom elastometer and pressurized from their anatomically inner surfaces. This caused the skin disc to bulge outwards, stretching it biaxially, and increasing its surface area. Pressure (p) and biaxial strain (e) due to bulging were quantified and the modulus of elasticity [E (synonyms elastic modulus, Young’s modulus)] was calculated. In a typical test, e increased linearly with p until the skin fractured at pfracture and efracture. Stiffness of the skin decreased in ripening late stage III fruit as indicated by a decrease inE. The value of pfracture also decreased, whereas that of efracture remained about constant. Destroying cell turgor decreased E and pfracture relative to the turgescent control. The E value also decreased with increasing transpiration, while pfracture and (especially) efracture increased. Water uptake had little effect on E, whereas efracture and pfracture decreased slightly. Increasing temperature decreased E and pfracture, but had no effect on efracture. Only the instantaneous elastic strain and the creep strain increased significantly at the highest temperatures. A decrease inE indicates decreasing skin stiffness that is probably the result of enzymatic softening of the cell walls of the skin in the ripening fruit, of relaxation of the cell walls on eliminating or decreasing turgor by transpiration and, possibly, of a decreasing viscosity of the pectin middle lamellae at higher temperatures. The effects are consistent with the conclusion that the epidermal and hypodermal cell layers represent the structural ‘‘backbone’’ of the sweet cherry fruit skin. Rain cracking is a limitation in sweet cherry production almost wherever this high-value crop is grown (Christensen, 1996). Fruit cracking in many species, including grape (Vitis vinifera L.) and sweet cherry, is thought to be related to water uptake by the fruit. Thus, any net water uptake necessarily increases fruit volume and subjects the skin to additional strain (Considine and Brown, 1981). If the limit of extensibility of the fruit skin is exceeded, the fruit cracks. On the basis of this concept, the following two categories of factors will affect cracking susceptibility: 1) the fruit’s water uptake/loss characteristics— these determine the rate and total amount of water accumulated by the fruit, and 2) the fruit’s mechanical characteristics, particularly those of the principle load-bearing layer of the fruit—its skin (Br€uggenwirth et al., 2014). Water uptake by sweet cherries has been investigated in some detail, including that through the fruit surface (Beyer et al., 2002, 2005; Beyer and Knoche, 2002; Weichert and Knoche, 2006) and that through the pedicel vasculature (Hovland and Sekse, 2004; Measham et al., 2010). In contrast, there have been only a few studies that have addressed the mechanical properties of the sweet cherry skin (Bargel et al., 2004; Br€uggenwirth et al., 2014; Knoche and Peschel, 2006). Investigating the mechanical properties of the fruit skin is challenging. First, the sweet cherry is about spherical and hence, any strain of its skin during growth and water uptake is biaxial. Thus, a biaxial laboratory test is essential, if the in vivo strain in the skin is to be mimicked with any degree of accuracy. Second, uniaxial tests of skin strips result in marked narrowing of the sample as tension is applied. This is indexed by a high Poisson ratio and a gross overestimation of fracture strain and extensibility, and a gross underestimation of the E (Br€uggenwirth et al., 2014). Third, the sweet cherry skin is already markedly strained in vivo and these elastic and viscoelastic strains are reversible (Grimm et al., 2012). Thus, on excision the skin relaxes almost instantaneously and special care has to be taken to prevent this relaxation (Br€uggenwirth et al., 2014). The first biaxial tensile test for sweet cherry fruit skin was described by Bargel et al. (2004). Excised fruit skin segments were pressurized from the inner side and the extent of bulging for each pressure increment was quantified. Br€uggenwirth et al. (2014) modified the test to prevent relaxation of the fruit skin after excision, thereby maintaining the in vivo strain in the fruit surface. Furthermore, the skin segments were pressurized using silicone oil rather than water thereby eliminating any uncontrolled water uptake and bursting of cells on the inner side (Simon, 1977). This test protocol offers a standardized test for identifying mechanical properties of sweet cherry fruit skins. Among the factors known to affect mechanical properties of fruit is the degree of ripening, especially during the later stages of development (Brummell, 2006; Christensen, 1996). Also, the fruit’s turgescence is expected to be affected by the balance between transpiration and water uptake (Considine and Brown, 1981). Furthermore, many fleshy fruits, including sweet cherries, are soft to the touch when warm, but firmer at low temperatures (M. Br€uggenwirth and M. Knoche, unpublished Received for publication 17 Sept. 2015. Accepted for publication 27 Oct. 2015. This researchwas funded in part by a grant from theDeutsche Forschungsgemeinschaft. We thank Dieter Reese and Christoph Knake for constructing, engineering, and programming the elastometer, Friederike Schroeder andSimonSitzenstock for technical support, Bishnu P. Khanal and Sandy Lang for helpful discussion and useful comments on an earlier version of this manuscript. Corresponding author. E-mail: moritz.knoche@obst.uni-hannover.de. J. AMER. SOC. HORT. SCI. 141(1):45–53. 2016. 45 data). Also, increasing temperature markedly increased cracking (for review, see Christensen, 1996). As with all materials, one would expect the mechanical properties of a fruit skin to be affected by temperature. The objectives of this study were to quantify the effects of 1) ripeness stage; 2) turgor, transpiration, and water uptake; and 3) temperature on the mechanical properties of sweet cherry fruit skin using a biaxial tensile test. Materials and Methods PLANT MATERIAL. Fruit of sweet cherry cultivars Adriana, Kordia, Sam, and Sweetheart were harvested at commercial maturity from field-grown or glasshouse-grown trees at the Horticultural Research Station of the Leibniz University in Ruthe, Germany (lat. 52 14#N, long. 9 49#E) in the 2012, 2013, and 2015 growing seasons. Trees were grafted on ‘Gisela 5’ rootstocks (Prunus cerasus L. · Prunus canescens Bois). Fruit were selected for freedom from visual defects and for uniformity of development based on size and color. In a preliminary experiment, the effect of storing sweet cherry at 2 C and at water vapor concentrations close to saturation for up to 30 d on mechanical properties of the fruit skin was investigated. During the first 4 d of storage, stiffness of the skin increased as indexed by a 81% increase in the E. The pressure at fracture slightly increased (+10%) and the strain at fracture decreased [–26% (M. Br€uggenwirth, unpublished data)]. There was no further change in mechanical properties between 4 and 30 d of storage. To avoid potential artifacts resulting from storage, all fruit were harvested in the mornings, covered by a damp paper towel, brought to the laboratory, and used in experiments within 2 h. GENERAL EXPERIMENTAL PROCEDURE. Biaxial tensile tests were performed using the elastometer described in detail by Br€uggenwirth et al. (2014). Briefly, a brass washer (12 mm i.d.) was mounted on one of the two shoulders of a sweet cherry fruit using cyanoacrylate adhesive (Loctite 406; Henkel/Loctite Deutschland, Munich, Germany). Next, an exocarp segment [ES (synonym fruit skin segment)] comprising the exocarp and some adhering mesocarp [thickness (mean ± SE) 2.5 ± 0.0 mm] was excised by cutting horizontally beneath the washer using a razor blade. This procedure preserved the in vivo strain of the skin after excision (Br€uggenwirth et al., 2014; Grimm et al., 2012; Knoche and Peschel, 2006). The brass washer with the ES was mounted in the elastometer, whose chamber was then filled with silicone oil (AK10; Wacker Chemie, Munich, Germany) and any visible air bubbles were carefully removed. The chamber was pressurized by driving a motorized piston into the oil. This displaced the oil, reduced the chamber volume, and caused the ES to bulge outward. Pressure in the chamber was recorded using a pressure transducer (Typ 40PC100G; Honeywell International, Morristown, NJ) and the deflection of the bulging ES was recorded by the displacement transducer (KAP-S/5N; AST Angewandte System Technik, Wolnzach, Germany) of a universal material testing machine (BXCFR2.5TN; Zwick Roell, Ulm, Germany). Unless specified otherwise, pressure was increased continually until the ES fractured. The pressure at the moment of failure is referred to as the fracture pressure [pfracture (kilopascals)] and the area (i.e., biaxial) strain at failure as the fracture strain [efracture (square millimeters per square millimeter)]. The strain (e) was calculated as the fractional increase in surface area; i.e., the increase in area [DA (square millimeters)] due to the bulging of the ES, relative to the initial area [A0 (square millimeters)] before bulging:","PeriodicalId":17226,"journal":{"name":"Journal of the American Society for Horticultural Science","volume":"141 1","pages":"45-53"},"PeriodicalIF":1.1000,"publicationDate":"2016-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"19","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of the American Society for Horticultural Science","FirstCategoryId":"97","ListUrlMain":"https://doi.org/10.21273/JASHS.141.1.45","RegionNum":4,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"HORTICULTURE","Score":null,"Total":0}
引用次数: 19

Abstract

The skins of all fruit types are subject to sustained biaxial strain during the entire period of their growth. In sweet cherry (Prunus avium L.), failure of the skin greatly affects fruit quality. Mechanical properties were determined using a biaxial bulging test. The factors considered were the following: ripening, fruit water relations (including turgor, transpiration, and water uptake), and temperature. Excised discs of fruit skin were mounted in a custom elastometer and pressurized from their anatomically inner surfaces. This caused the skin disc to bulge outwards, stretching it biaxially, and increasing its surface area. Pressure (p) and biaxial strain (e) due to bulging were quantified and the modulus of elasticity [E (synonyms elastic modulus, Young’s modulus)] was calculated. In a typical test, e increased linearly with p until the skin fractured at pfracture and efracture. Stiffness of the skin decreased in ripening late stage III fruit as indicated by a decrease inE. The value of pfracture also decreased, whereas that of efracture remained about constant. Destroying cell turgor decreased E and pfracture relative to the turgescent control. The E value also decreased with increasing transpiration, while pfracture and (especially) efracture increased. Water uptake had little effect on E, whereas efracture and pfracture decreased slightly. Increasing temperature decreased E and pfracture, but had no effect on efracture. Only the instantaneous elastic strain and the creep strain increased significantly at the highest temperatures. A decrease inE indicates decreasing skin stiffness that is probably the result of enzymatic softening of the cell walls of the skin in the ripening fruit, of relaxation of the cell walls on eliminating or decreasing turgor by transpiration and, possibly, of a decreasing viscosity of the pectin middle lamellae at higher temperatures. The effects are consistent with the conclusion that the epidermal and hypodermal cell layers represent the structural ‘‘backbone’’ of the sweet cherry fruit skin. Rain cracking is a limitation in sweet cherry production almost wherever this high-value crop is grown (Christensen, 1996). Fruit cracking in many species, including grape (Vitis vinifera L.) and sweet cherry, is thought to be related to water uptake by the fruit. Thus, any net water uptake necessarily increases fruit volume and subjects the skin to additional strain (Considine and Brown, 1981). If the limit of extensibility of the fruit skin is exceeded, the fruit cracks. On the basis of this concept, the following two categories of factors will affect cracking susceptibility: 1) the fruit’s water uptake/loss characteristics— these determine the rate and total amount of water accumulated by the fruit, and 2) the fruit’s mechanical characteristics, particularly those of the principle load-bearing layer of the fruit—its skin (Br€uggenwirth et al., 2014). Water uptake by sweet cherries has been investigated in some detail, including that through the fruit surface (Beyer et al., 2002, 2005; Beyer and Knoche, 2002; Weichert and Knoche, 2006) and that through the pedicel vasculature (Hovland and Sekse, 2004; Measham et al., 2010). In contrast, there have been only a few studies that have addressed the mechanical properties of the sweet cherry skin (Bargel et al., 2004; Br€uggenwirth et al., 2014; Knoche and Peschel, 2006). Investigating the mechanical properties of the fruit skin is challenging. First, the sweet cherry is about spherical and hence, any strain of its skin during growth and water uptake is biaxial. Thus, a biaxial laboratory test is essential, if the in vivo strain in the skin is to be mimicked with any degree of accuracy. Second, uniaxial tests of skin strips result in marked narrowing of the sample as tension is applied. This is indexed by a high Poisson ratio and a gross overestimation of fracture strain and extensibility, and a gross underestimation of the E (Br€uggenwirth et al., 2014). Third, the sweet cherry skin is already markedly strained in vivo and these elastic and viscoelastic strains are reversible (Grimm et al., 2012). Thus, on excision the skin relaxes almost instantaneously and special care has to be taken to prevent this relaxation (Br€uggenwirth et al., 2014). The first biaxial tensile test for sweet cherry fruit skin was described by Bargel et al. (2004). Excised fruit skin segments were pressurized from the inner side and the extent of bulging for each pressure increment was quantified. Br€uggenwirth et al. (2014) modified the test to prevent relaxation of the fruit skin after excision, thereby maintaining the in vivo strain in the fruit surface. Furthermore, the skin segments were pressurized using silicone oil rather than water thereby eliminating any uncontrolled water uptake and bursting of cells on the inner side (Simon, 1977). This test protocol offers a standardized test for identifying mechanical properties of sweet cherry fruit skins. Among the factors known to affect mechanical properties of fruit is the degree of ripening, especially during the later stages of development (Brummell, 2006; Christensen, 1996). Also, the fruit’s turgescence is expected to be affected by the balance between transpiration and water uptake (Considine and Brown, 1981). Furthermore, many fleshy fruits, including sweet cherries, are soft to the touch when warm, but firmer at low temperatures (M. Br€uggenwirth and M. Knoche, unpublished Received for publication 17 Sept. 2015. Accepted for publication 27 Oct. 2015. This researchwas funded in part by a grant from theDeutsche Forschungsgemeinschaft. We thank Dieter Reese and Christoph Knake for constructing, engineering, and programming the elastometer, Friederike Schroeder andSimonSitzenstock for technical support, Bishnu P. Khanal and Sandy Lang for helpful discussion and useful comments on an earlier version of this manuscript. Corresponding author. E-mail: moritz.knoche@obst.uni-hannover.de. J. AMER. SOC. HORT. SCI. 141(1):45–53. 2016. 45 data). Also, increasing temperature markedly increased cracking (for review, see Christensen, 1996). As with all materials, one would expect the mechanical properties of a fruit skin to be affected by temperature. The objectives of this study were to quantify the effects of 1) ripeness stage; 2) turgor, transpiration, and water uptake; and 3) temperature on the mechanical properties of sweet cherry fruit skin using a biaxial tensile test. Materials and Methods PLANT MATERIAL. Fruit of sweet cherry cultivars Adriana, Kordia, Sam, and Sweetheart were harvested at commercial maturity from field-grown or glasshouse-grown trees at the Horticultural Research Station of the Leibniz University in Ruthe, Germany (lat. 52 14#N, long. 9 49#E) in the 2012, 2013, and 2015 growing seasons. Trees were grafted on ‘Gisela 5’ rootstocks (Prunus cerasus L. · Prunus canescens Bois). Fruit were selected for freedom from visual defects and for uniformity of development based on size and color. In a preliminary experiment, the effect of storing sweet cherry at 2 C and at water vapor concentrations close to saturation for up to 30 d on mechanical properties of the fruit skin was investigated. During the first 4 d of storage, stiffness of the skin increased as indexed by a 81% increase in the E. The pressure at fracture slightly increased (+10%) and the strain at fracture decreased [–26% (M. Br€uggenwirth, unpublished data)]. There was no further change in mechanical properties between 4 and 30 d of storage. To avoid potential artifacts resulting from storage, all fruit were harvested in the mornings, covered by a damp paper towel, brought to the laboratory, and used in experiments within 2 h. GENERAL EXPERIMENTAL PROCEDURE. Biaxial tensile tests were performed using the elastometer described in detail by Br€uggenwirth et al. (2014). Briefly, a brass washer (12 mm i.d.) was mounted on one of the two shoulders of a sweet cherry fruit using cyanoacrylate adhesive (Loctite 406; Henkel/Loctite Deutschland, Munich, Germany). Next, an exocarp segment [ES (synonym fruit skin segment)] comprising the exocarp and some adhering mesocarp [thickness (mean ± SE) 2.5 ± 0.0 mm] was excised by cutting horizontally beneath the washer using a razor blade. This procedure preserved the in vivo strain of the skin after excision (Br€uggenwirth et al., 2014; Grimm et al., 2012; Knoche and Peschel, 2006). The brass washer with the ES was mounted in the elastometer, whose chamber was then filled with silicone oil (AK10; Wacker Chemie, Munich, Germany) and any visible air bubbles were carefully removed. The chamber was pressurized by driving a motorized piston into the oil. This displaced the oil, reduced the chamber volume, and caused the ES to bulge outward. Pressure in the chamber was recorded using a pressure transducer (Typ 40PC100G; Honeywell International, Morristown, NJ) and the deflection of the bulging ES was recorded by the displacement transducer (KAP-S/5N; AST Angewandte System Technik, Wolnzach, Germany) of a universal material testing machine (BXCFR2.5TN; Zwick Roell, Ulm, Germany). Unless specified otherwise, pressure was increased continually until the ES fractured. The pressure at the moment of failure is referred to as the fracture pressure [pfracture (kilopascals)] and the area (i.e., biaxial) strain at failure as the fracture strain [efracture (square millimeters per square millimeter)]. The strain (e) was calculated as the fractional increase in surface area; i.e., the increase in area [DA (square millimeters)] due to the bulging of the ES, relative to the initial area [A0 (square millimeters)] before bulging:
影响甜樱桃果皮力学特性的因素
所有水果类型的果皮在其整个生长期间都受到持续的双轴应变。在甜樱桃(Prunus avium L.)中,果皮的失效极大地影响了果实的品质。采用双轴胀形试验确定了材料的力学性能。考虑的因素如下:成熟、果实水分关系(包括膨胀、蒸腾和水分吸收)和温度。切除的水果皮盘安装在定制的弹性计中,并从其解剖内部表面加压。这导致皮肤椎间盘向外凸起,双轴拉伸,并增加其表面积。量化胀形引起的压力(p)和双轴应变(e),计算弹性模量[e(同义词弹性模量,杨氏模量)]。在一个典型的试验中,e随p线性增加,直到皮肤在骨折前和骨折后破裂。果皮的硬度在成熟的第三阶段果实中下降,这是由inE的下降所表明的。pfracture的值也有所下降,而efracture的值基本保持不变。与肿胀对照组相比,破坏细胞肿胀使E和pfracture降低。E值也随蒸腾量的增加而降低,而pfracture和(尤其是)efracture则增加。水分吸收对E的影响不大,而efracture和pfracture略有下降。升高温度可降低E值和断裂速率,但对断裂速率无影响。在最高温度下,只有瞬时弹性应变和蠕变应变显著增加。inE的降低表明果皮硬度的降低,这可能是由于果实成熟过程中果皮细胞壁的酶软化、通过蒸腾作用消除或减少膨胀时细胞壁的松弛,也可能是由于果胶中间薄片在较高温度下粘度的降低。这与表皮和下皮细胞层构成甜樱桃果皮结构“骨干”的结论是一致的。几乎在任何种植这种高价值作物的地方,雨裂都是甜樱桃生产的一个限制(Christensen, 1996)。包括葡萄(Vitis vinifera L.)和甜樱桃在内的许多物种的果实开裂被认为与果实的水分吸收有关。因此,任何净水分的吸收都必然会增加果实的体积,并使表皮承受额外的压力(Considine and Brown, 1981)。如果超过果皮的拉伸极限,水果就会开裂。根据这一概念,以下两类因素会影响开裂敏感性:1)水果的吸水/失水特性——这些决定了水果积累水分的速率和总量;2)水果的机械特性,特别是水果的主要承受力层——果皮的力学特性(Br€uggenwirth et al., 2014)。甜樱桃的水分吸收已经进行了一些详细的研究,包括通过果实表面的水分吸收(Beyer等人,2002,2005;Beyer and Knoche, 2002;Weichert and Knoche, 2006)以及通过花梗血管系统(Hovland and Sekse, 2004;Measham et al., 2010)。相比之下,只有少数研究解决了甜樱桃皮的机械特性(Bargel等人,2004;Br uggenwirth等人,2014;Knoche and Peschel, 2006)。研究果皮的机械特性是很有挑战性的。首先,甜樱桃大约是球形的,因此,在生长和吸水过程中,它的表皮的任何拉伸都是双轴的。因此,如果要以任何程度的准确性模拟皮肤中的体内应变,则必须进行双轴实验室测试。其次,皮条的单轴试验导致试样在施加张力时明显变窄。这可以通过高泊松比和对断裂应变和拉伸的严重高估以及对E的严重低估来表示(Br€uggenwirth等人,2014)。第三,甜樱桃皮在体内已经有明显的应变,这些弹性和粘弹性应变是可逆的(Grimm et al., 2012)。因此,在切除时,皮肤几乎是瞬间松弛的,必须特别注意防止这种松弛(Br€uggenwirth et al., 2014)。Bargel等人(2004)首次对甜樱桃果皮进行了双轴拉伸试验。从内侧对切除的果皮段加压,并对每次加压后的膨胀程度进行量化。Br uggenwirth et al.(2014)对试验进行了修改,以防止果皮在切除后松弛,从而维持果表面的体内应变。此外,皮肤部分使用硅油而不是水加压,从而消除了任何不受控制的水分摄取和内部细胞的破裂(Simon, 1977)。本测试协议提供了一个标准的测试,以确定甜樱桃果皮的机械性能。 所有水果类型的果皮在其整个生长期间都受到持续的双轴应变。在甜樱桃(Prunus avium L.)中,果皮的失效极大地影响了果实的品质。采用双轴胀形试验确定了材料的力学性能。考虑的因素如下:成熟、果实水分关系(包括膨胀、蒸腾和水分吸收)和温度。切除的水果皮盘安装在定制的弹性计中,并从其解剖内部表面加压。这导致皮肤椎间盘向外凸起,双轴拉伸,并增加其表面积。量化胀形引起的压力(p)和双轴应变(e),计算弹性模量[e(同义词弹性模量,杨氏模量)]。在一个典型的试验中,e随p线性增加,直到皮肤在骨折前和骨折后破裂。果皮的硬度在成熟的第三阶段果实中下降,这是由inE的下降所表明的。pfracture的值也有所下降,而efracture的值基本保持不变。与肿胀对照组相比,破坏细胞肿胀使E和pfracture降低。E值也随蒸腾量的增加而降低,而pfracture和(尤其是)efracture则增加。水分吸收对E的影响不大,而efracture和pfracture略有下降。升高温度可降低E值和断裂速率,但对断裂速率无影响。在最高温度下,只有瞬时弹性应变和蠕变应变显著增加。inE的降低表明果皮硬度的降低,这可能是由于果实成熟过程中果皮细胞壁的酶软化、通过蒸腾作用消除或减少膨胀时细胞壁的松弛,也可能是由于果胶中间薄片在较高温度下粘度的降低。这与表皮和下皮细胞层构成甜樱桃果皮结构“骨干”的结论是一致的。几乎在任何种植这种高价值作物的地方,雨裂都是甜樱桃生产的一个限制(Christensen, 1996)。包括葡萄(Vitis vinifera L.)和甜樱桃在内的许多物种的果实开裂被认为与果实的水分吸收有关。因此,任何净水分的吸收都必然会增加果实的体积,并使表皮承受额外的压力(Considine and Brown, 1981)。如果超过果皮的拉伸极限,水果就会开裂。根据这一概念,以下两类因素会影响开裂敏感性:1)水果的吸水/失水特性——这些决定了水果积累水分的速率和总量;2)水果的机械特性,特别是水果的主要承受力层——果皮的力学特性(Br€uggenwirth et al., 2014)。甜樱桃的水分吸收已经进行了一些详细的研究,包括通过果实表面的水分吸收(Beyer等人,2002,2005;Beyer and Knoche, 2002;Weichert and Knoche, 2006)以及通过花梗血管系统(Hovland and Sekse, 2004;Measham et al., 2010)。相比之下,只有少数研究解决了甜樱桃皮的机械特性(Bargel等人,2004;Br uggenwirth等人,2014;Knoche and Peschel, 2006)。研究果皮的机械特性是很有挑战性的。首先,甜樱桃大约是球形的,因此,在生长和吸水过程中,它的表皮的任何拉伸都是双轴的。因此,如果要以任何程度的准确性模拟皮肤中的体内应变,则必须进行双轴实验室测试。其次,皮条的单轴试验导致试样在施加张力时明显变窄。这可以通过高泊松比和对断裂应变和拉伸的严重高估以及对E的严重低估来表示(Br€uggenwirth等人,2014)。第三,甜樱桃皮在体内已经有明显的应变,这些弹性和粘弹性应变是可逆的(Grimm et al., 2012)。因此,在切除时,皮肤几乎是瞬间松弛的,必须特别注意防止这种松弛(Br€uggenwirth et al., 2014)。Bargel等人(2004)首次对甜樱桃果皮进行了双轴拉伸试验。从内侧对切除的果皮段加压,并对每次加压后的膨胀程度进行量化。Br uggenwirth et al.(2014)对试验进行了修改,以防止果皮在切除后松弛,从而维持果表面的体内应变。此外,皮肤部分使用硅油而不是水加压,从而消除了任何不受控制的水分摄取和内部细胞的破裂(Simon, 1977)。本测试协议提供了一个标准的测试,以确定甜樱桃果皮的机械性能。 已知影响水果机械特性的因素之一是成熟程度,特别是在发育的后期阶段(Brummell, 2006;克里斯坦森,1996)。此外,预计果实的膨润会受到蒸腾和水分吸收之间平衡的影响(Considine和Brown, 1981)。此外,许多肉质水果,包括甜樱桃,在温暖时摸起来很软,但在低温下更紧实(M. Br€uggenwirth和M. Knoche,未发表)。接受于2015年10月27日发表。这项研究的部分资金来自德国研究协会。我们感谢Dieter Reese和Christoph Knake构建、设计和编程弹性计,感谢Friederike Schroeder和simonsitzenstock的技术支持,感谢Bishnu P. Khanal和Sandy Lang对本文早期版本的有益讨论和有用评论。相应的作者。电子邮件:moritz.knoche@obst.uni-hannover.de。j·阿。SOC。长的矮。科学。141(1): 45-53。2016. 45数据)。此外,温度升高会显著增加裂缝(回顾,见Christensen, 1996)。和所有材料一样,果皮的机械性能会受到温度的影响。本研究的目的是量化1)成熟期的影响;2)膨润、蒸腾和吸水;3)温度对甜樱桃果皮力学性能的影响采用双轴拉伸试验。材料和方法植物材料。在德国吕特的莱布尼茨大学园艺研究站,甜樱桃品种Adriana, Kordia, Sam和甜心的果实在商业成熟时从田间种植或温室种植的树上收获。52 14#N,长。9 49#E)在2012年、2013年和2015年生长季节。树木嫁接在‘Gisela 5’砧木(Prunus cerasus L.·Prunus canescens Bois)上。选择的水果没有视觉缺陷,并且根据大小和颜色发育均匀。在初步实验中,研究了甜樱桃在2℃和接近饱和的水汽浓度下贮藏30 d对果皮力学性能的影响。在储存的前4天,表皮的刚度增加,e增加81%,骨折处的压力略有增加(+10%),骨折处的应变下降[-26% (M. Br€uggenwirth,未发表的数据)]。贮藏4 ~ 30 d后,其力学性能无进一步变化。为了避免由于储存而产生的潜在伪影,所有的水果都在早晨收获,用湿纸巾盖住,带到实验室,并在2小时内用于实验。一般实验程序。使用Br€uggenwirth等人(2014年)详细描述的弹性计进行双轴拉伸试验。简单地说,一个黄铜垫圈(12毫米直径)安装在一个甜樱桃果实的两个肩膀之一使用氰基丙烯酸酯粘合剂(乐泰406;汉高/乐泰德国,慕尼黑,德国)。接下来,用剃须刀片在洗衣机下面水平切割,切除由外果皮和一些粘附的中果皮组成的外果皮段[ES(同义果皮段)][厚度(平均值±SE) 2.5±0.0 mm]。该方法保存了切除后皮肤的体内应变(Br€uggenwirth et al., 2014;Grimm等人,2012;Knoche and Peschel, 2006)。将带有ES的黄铜垫圈安装在弹性计中,弹性计腔内填充硅油(AK10;瓦克化学,慕尼黑,德国)和任何可见的气泡被小心地去除。这个腔室通过驱动一个电动活塞进入油中而加压。这样就取代了油,减少了腔体体积,使ES向外膨胀。使用压力传感器(type 40PC100G;Honeywell International, Morristown, NJ),并通过位移传感器(KAP-S/5N;AST Angewandte System Technik, Wolnzach, Germany)的万能材料试验机(BXCFR2.5TN;Zwick Roell,乌尔姆,德国)。除非另有说明,否则持续增加压力直到ES断裂。破坏时刻的压力称为断裂压力[pfracture(千帕斯卡)],破坏时的面积(即双轴)应变称为断裂应变[efracture(平方毫米/平方毫米)]。应变(e)计算为表面积增加的分数;即ES胀形后相对于胀形前初始面积[A0(平方毫米)]增加的面积[DA(平方毫米)]: 已知影响水果机械特性的因素之一是成熟程度,特别是在发育的后期阶段(Brummell, 2006;克里斯坦森,1996)。此外,预计果实的膨润会受到蒸腾和水分吸收之间平衡的影响(Considine和Brown, 1981)。此外,许多肉质水果,包括甜樱桃,在温暖时摸起来很软,但在低温下更紧实(M. Br€uggenwirth和M. Knoche,未发表)。接受于2015年10月27日发表。这项研究的部分资金来自德国研究协会。我们感谢Dieter Reese和Christoph Knake构建、设计和编程弹性计,感谢Friederike Schroeder和simonsitzenstock的技术支持,感谢Bishnu P. Khanal和Sandy Lang对本文早期版本的有益讨论和有用评论。相应的作者。电子邮件:moritz.knoche@obst.uni-hannover.de。j·阿。SOC。长的矮。科学。141(1): 45-53。2016. 45数据)。此外,温度升高会显著增加裂缝(回顾,见Christensen, 1996)。和所有材料一样,果皮的机械性能会受到温度的影响。本研究的目的是量化1)成熟期的影响;2)膨润、蒸腾和吸水;3)温度对甜樱桃果皮力学性能的影响采用双轴拉伸试验。材料和方法植物材料。在德国吕特的莱布尼茨大学园艺研究站,甜樱桃品种Adriana, Kordia, Sam和甜心的果实在商业成熟时从田间种植或温室种植的树上收获。52 14#N,长。9 49#E)在2012年、2013年和2015年生长季节。树木嫁接在‘Gisela 5’砧木(Prunus cerasus L.·Prunus canescens Bois)上。选择的水果没有视觉缺陷,并且根据大小和颜色发育均匀。在初步实验中,研究了甜樱桃在2℃和接近饱和的水汽浓度下贮藏30 d对果皮力学性能的影响。在储存的前4天,表皮的刚度增加,e增加81%,骨折处的压力略有增加(+10%),骨折处的应变下降[-26% (M. Br€uggenwirth,未发表的数据)]。贮藏4 ~ 30 d后,其力学性能无进一步变化。为了避免由于储存而产生的潜在伪影,所有的水果都在早晨收获,用湿纸巾盖住,带到实验室,并在2小时内用于实验。一般实验程序。使用Br€uggenwirth等人(2014年)详细描述的弹性计进行双轴拉伸试验。简单地说,一个黄铜垫圈(12毫米直径)安装在一个甜樱桃果实的两个肩膀之一使用氰基丙烯酸酯粘合剂(乐泰406;汉高/乐泰德国,慕尼黑,德国)。接下来,用剃须刀片在洗衣机下面水平切割,切除由外果皮和一些粘附的中果皮组成的外果皮段[ES(同义果皮段)][厚度(平均值±SE) 2.5±0.0 mm]。该方法保存了切除后皮肤的体内应变(Br€uggenwirth et al., 2014;Grimm等人,2012;Knoche and Peschel, 2006)。将带有ES的黄铜垫圈安装在弹性计中,弹性计腔内填充硅油(AK10;瓦克化学,慕尼黑,德国)和任何可见的气泡被小心地去除。这个腔室通过驱动一个电动活塞进入油中而加压。这样就取代了油,减少了腔体体积,使ES向外膨胀。使用压力传感器(type 40PC100G;Honeywell International, Morristown, NJ),并通过位移传感器(KAP-S/5N;AST Angewandte System Technik, Wolnzach, Germany)的万能材料试验机(BXCFR2.5TN;Zwick Roell,乌尔姆,德国)。除非另有说明,否则持续增加压力直到ES断裂。破坏时刻的压力称为断裂压力[pfracture(千帕斯卡)],破坏时的面积(即双轴)应变称为断裂应变[efracture(平方毫米/平方毫米)]。应变(e)计算为表面积增加的分数;即ES胀形后相对于胀形前初始面积[A0(平方毫米)]增加的面积[DA(平方毫米)]:
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来源期刊
CiteScore
3.80
自引率
0.00%
发文量
31
审稿时长
2 months
期刊介绍: The Journal of the American Society for Horticultural Science publishes papers on the results of original research on horticultural plants and their products or directly related research areas. Its prime function is to communicate mission-oriented, fundamental research to other researchers. The journal includes detailed reports of original research results on various aspects of horticultural science and directly related subjects such as: - Biotechnology - Developmental Physiology - Environmental Stress Physiology - Genetics and Breeding - Photosynthesis, Sources-Sink Physiology - Postharvest Biology - Seed Physiology - Postharvest Biology - Seed Physiology - Soil-Plant-Water Relationships - Statistics
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