RESUMO
As part of the plant water-use process, plant nocturnal sap flow (Q n) has been demonstrated to have important ecophysiological significance to compensate for water loss. The purpose of this study was to explore nocturnal water-use strategies to fill the knowledge gap in mangroves, by measuring three species co-occurring in a subtropical estuary. Sap flow was monitored over an entire year using thermal diffusive probes. Stem diameter and leaf-level gas exchange were measured in summer. The data were used to explore the different nocturnal water balance maintaining mechanisms among species. The Q n existed persistently and contributed markedly over 5.5%~24.0% of the daily sap flow (Q) across species, which was associated with two processes, nocturnal transpiration (E n) and nocturnal stem water refilling (R n). We found that the stem recharge of the Kandelia obovata and Aegiceras corniculatum occurred mainly after sunset and that the high salinity environment drove higher Q n while stem recharge of the Avicennia marina mainly occurred in the daytime and the high salinity environment inhibited the Q n. The diversity of stem recharge patterns and response to sap flow to high salinity conditions were the main reasons for the differences in Q n/Q among species. For Kandelia obovata and Aegiceras corniculatum, R n was the main contributor to Q n, which was driven by the demands of stem water refilling after diurnal water depletion and high salt environment. Both of the species have a strict control over the stomata to reduce water loss at night. In contrast, Avicennia marina maintained a low Q n, driven by vapor pressure deficit, and the Q n mainly used for E n, which adapts to high salinity conditions by limiting water dissipation at night. We conclude that the diverse ways Q n properties act as water-compensating strategies among the co-occurring mangrove species might help the trees to overcoming water scarcity.
RESUMO
Stem cells serve as the source of new cells for plant development. A group of stem cells form a stem cell niche (SCN) at the root tip and in the center of the SCN are slowly dividing cells called the quiescent center (QC). QC is thought to function as a signaling hub that inhibits differentiation of surrounding stem cells. Although it has been generally assumed that cell-to-cell communication provides positional information for QC and SCN maintenance, the tools for testing this hypothesis have long been lacking. Here we exploit a system that effectively blocks plasmodesmata (PD)-mediated signaling to explore how cell-to-cell communication functions in the SCN. We showed that the symplastic signaling between the QC and adjacent cells directs the formation of local auxin maxima and establishment of AP2-domain transcription factors, PLETHORA gradients. Interestingly we found symplastic signaling is essential for local auxin biosynthesis, which acts together with auxin polar transport to provide the guidance for local auxin enrichment. Therefore, we demonstrate the crucial role of cell-to-cell communication in the SCN maintenance and further uncover a mechanism by which symplastic signaling initiates and reinforces the positional information during stem cell maintenance via auxin regulation.
