Nitrate fertilization may delay autumn leaf senescence, while amino acid treatments do not

Fertilization with nitrogen (N)-rich compounds leads to increased growth, but may compromise phenology and winter survival of trees in boreal regions. During autumn, N is remobilized from senescing leaves and stored in other parts of the tree to be used in the next growing season. However, the mechanism behind the N fertilization effect on winter survival is not well understood and it is unclear how N levels or forms modulate autumn senescence. We performed fertilization experiments and showed that treating Populus saplings with high or low levels of inorganic nitrogen resulted in a delay in senescence. In addition, by using precise delivery of solutes into the xylem stream of Populus trees in their natural environment, we found that delay of autumn senescence was dependent on the form of N administered: inorganic N (NO3-1) delayed senescence but amino acids (Arg, Glu, Gln, and Leu) did not. Metabolite profiling of leaves showed that the levels of tricarboxylic acids (TCA), arginine catabolites (ammonium, ornithine), glycine, glycine-serine ratio and overall carbon-to-nitrogen (C/N) ratio were affected differently by the way of applying NO3-1 and Arg treatments. In addition, the onset of senescence did not coincide with soluble sugar accumulation in any of the treatments. Taken together, metabolomic rearrangement under different N forms or experimental setups could modulate senescence process, but not initiation and progression in Populus. We propose that the different regulation of C and N status through direct molecular signaling of NO3-1 could account for the contrasting effects of NO3-1 and Arg on senescence.

Onset of autumn senescence in High Arctic plants shows similar patterns in natural and experimental snow depth gradients

Predicted changes in snow cover and temperature raise uncertainties about how the beginning and the end of the growing season will shift for Arctic plants. Snowmelt timing and temperature are known to affect the timing of bud burst, but their effects on autumn senescence are less clear. To address this, researchers have examined senescence under natural and experimental environmental gradients. However, these approaches address different aspects of plant responses and the extent to which they can be compared is poorly understood. In this study, we show that the effect of snowmelt timing on the timing of autumn senescence in High Arctic plants is the same between a natural and an experimental gradient in three out of four studied species. While the two approaches mostly produce comparable results, they give in combination greater insight into the phenological responses to predicted climate changes. We also showed that a short warming treatment in autumn delayed senescence by 3.5 days in D. octopetala, which is a 10 % extension of the growing season end for this species. Warming treatments have commonly been applied to the whole growing season, but here we show that even isolated autumn warming can be sufficient to affect plant senescence.

Singlet oxygen, flavonols and photoinhibition in green and senescing silver birch leaves

Key message Decreased absorptance and increased singlet oxygen production may cause photoinhibition of both PSII and PSI in birch leaves during autumn senescence; however, photosynthetic electron transfer stays functional until late senescence. Abstract During autumn senescence, deciduous trees degrade chlorophyll and may synthesize flavonols. We measured photosynthetic parameters, epidermal flavonols, singlet oxygen production in vivo and photoinhibition of the photosystems (PSII and PSI) from green and senescing silver birch (Betula pendula) leaves. Chlorophyll a fluorescence and P700 absorbance measurements showed that the amounts of both photosystems decreased throughout autumn senescence, but the remaining PSII units stayed functional until ~ 90% of leaf chlorophyll was degraded. An increase in the chlorophyll a to b ratio, a decrease in > 700 nm absorbance and a blue shift of the PSI fluorescence peak at 77 K suggest that light-harvesting complex I was first degraded during senescence, followed by light-harvesting complex II and finally the photosystems. Senescing leaves produced more singlet oxygen than green leaves, possibly because low light absorption by senescing leaves allows high flux of incident light per photosystem. Senescing leaves also induced less non-photochemical quenching, which may contribute to increased singlet oxygen production. Faster photoinhibition of both photosystems in senescing than in green leaves, under high light, was most probably caused by low absorption of light and rapid singlet oxygen production. However, senescing leaves maintained the capacity to recover from photoinhibition of PSII. Amounts of epidermal flavonols and singlet oxygen correlated neither in green nor in senescing leaves of silver birch. Moreover, Arabidopsis thaliana mutants, incapable of synthesizing flavonols, were not more susceptible to photoinhibition of PSII or PSI than wild type plants; screening of chlorophyll absorption by flavonols was, however, small in A. thaliana. These results suggest that flavonols do not protect against photoinhibition or singlet oxygen production in chloroplasts.

Response to Comment on “Increased growing-season productivity drives earlier autumn leaf senescence in temperate trees”

Our study showed that increases in seasonal productivity drive earlier autumn senescence of temperate trees. Norby argues that this finding is contradicted by observations from free-air CO2 enrichment (FACE) experiments, where elevated CO2 has been found to delay senescence in some cases. We provide a detailed answer showing that the results from FACE studies are in agreement with our conclusions.

Spring temperatures affect senescence and N uptake in autumn and N storage for winter in Rhynchospora alba (Cyperaceae)

Environmental and physiological factors underlying variation in timing of autumn senescence are not well known. We investigated how the time of the onset of the growth in spring affects senescence and its functional consequences for nitrogen (N) uptake in autumn and storage of N for the winter, in a species that each year develops its bulbils for storage and overwintering anew. Rhynchospora alba was grown outdoors with two treatments, identical except for a 3 week difference in the start of growth in May. Leaf and root growth and senescence, and N uptake were recorded from August to November. By August, late-starting plants had caught up in size and total N content, but had smaller bulbils. They had a higher δ 13C, indicating a higher stomatal conductance during growth. Leaf and root senescence were delayed, extending 15N tracer uptake by 4 weeks. Nevertheless, after senescence, plants with an early start had 55% more N in their overwintering bulbils, due to earlier and more efficient remobilization. We conclude that timing of senescence in R. alba is a result of an interplay between the status of winter storage and cold temperatures, constrained by a trade-off between prolonged nutrient uptake and efficient remobilization of nutrients.