Boron (B) alleviates aluminum (Al) toxicity in higher plants; however, the underlying mechanisms behind this phenomenon remain unknown. Here, we used bromocresol green pH indicator, noninvasive microtest, and microelectrode ion flux estimation techniques to demonstrate that B promotes root surface pH gradients in pea () roots, leading to alkalization in the root transition zone and acidification in the elongation zone, while Al inhibits these pH gradients. B significantly decreased Al accumulation in the transition zone (∼1.0-2.5 mm from the apex) of lateral roots, thereby alleviating Al-induced inhibition of root elongation. Net indole acetic acid (IAA) efflux detected by an IAA-sensitive platinum microelectrode showed that polar auxin transport, which peaked in the root transition zone, was inhibited by Al toxicity, while it was partially recovered by B. Electrophysiological experiments using the Arabidopsis () auxin transporter mutants (; []) and the specific polar auxin transporter inhibitor1-naphthylphthalamic acid showed that PIN2-based polar auxin transport is involved in root surface alkalization in the transition zone. Our results suggest that B promotes polar auxin transport driven by the auxin efflux transporter PIN2 and leads to the downstream regulation of the plasma membrane-H-ATPase, resulting in elevated root surface pH, which is essential to decrease Al accumulation in this Al-targeted apical root zone. These findings provide a mechanistic explanation for the role of exogenous B in alleviation of Al accumulation and toxicity in plants.
Many bermudagrass (Cynodon sp.) and zoysiagrass (Zoysia sp.) cultivars are not available as seed and are commonly planted vegetatively using sprigs, especially for sod production or in sand-based systems. Sprig planting is typically done in late spring or early summer, but this can result in an extended grow-in period and delay the use of the turf in the first growing season. The objective of this study was to determine if sprigs of bermudagrass and zoysiagrass could be planted earlier in the year, during the dormancy phase, to hasten establishment. A field study was carried out in Fayetteville, AR, in 2014 and 2016 using ‘Tifway’ hybrid bermudagrass (Cynodon dactylon × Cynodon transvaalensis) and ‘Meyer’ zoysiagrass (Zoysia japonica), and in Guangzhou, China, in 2015, using ‘Tifway’ hybrid bermudagrass and ‘Lanyin III’ zoysiagrass (Z. japonica). Sprigs were planted in March (dormant), May (spring) and July (summer) in Fayetteville, and in January (dormant), March (spring) and May (summer) in Guangzhou. Sprigging rates of 30, 60, and 90 m3·ha−1 were tested at both locations and across all planting dates. Bermudagrass was less affected by planting date, with dormant, spring or summer plantings effectively establishing full cover in the first growing season. Zoysiagrass that was sprigged in the dormant season was successfully established by the end of the first growing season while a full zoysiagrass cover was not achieved with either spring or summer plantings in Arkansas. Dormant sprigging reached full coverage as fast or faster than traditional spring or summer planting dates at both locations, indicating that bermudagrass and zoysiagrass establishment can be achieved earlier in the growing season using dormant sprigging methods.
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