Abstract

Summary.‘Kensington’ mango fruit harvested at the mature green stage were partial pressure (vacuum) infiltrated with calcium (4 g Ca 2+/L as CaCl2) at 3 reduced pressure levels (–33, –66 and –99 kPa). Concentrations of Ca2+ in unripened calcium-treated fruit were about 1-, 2- and 3-fold higher, respectively, than Ca2+ concentrations in the skin and flesh of control (untreated; i.e. not vacuum infiltrated) fruit. For example, skin tissue Ca2+ concentrations of control fruit and of those treated at –33, –66 and –99 kPa were 1.51, 1.93, 3.42 and 5.01 mg Ca2+/g dry weight, respectively. Concentrations of Ca2+ in the skin of both control fruit and of Ca2+ -treated fruit were consistently higher, by about 2-fold, than those in the fruit flesh. Compared with the –33 kPa infiltration treatment, Ca2+ levels in the fruit flesh were increased by only about 2-fold by further reductions in the partial pressure infiltration levels to –66 or –99 kPa. Infiltration of Ca2+ into mango fruit was apparently via lenticels and along xylem conduits open at the cut pedicel. These infiltration pathways were revealed by inclusion of Brilliant Blue dye in the Ca2+ solution. Undyed and dyed lenticels were separately excised for Ca2+ analysis. Dark (dyed) lenticels had higher Ca2+ concentrations (1.86 ± 0.11 mg Ca2+/g dry weight) than light (undyed) lenticels (0.83 ± 0.19 mg Ca2+/g dry weight). Partial pressure infiltration of Ca2+ at any of the 3 subatmospheric pressure levels did not result in shelf life extension. Fruit infiltrated at –66 and –99 kPa exhibited injuries, which included exacerbated lenticel blackening and anaerobic off-odour and taste evident at the end of shelf life. In comparison, both control (untreated) mango fruit and those infiltrated with Ca2+ at –33 kPa ripened normally.

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