Phenotypic differences in the seasonal pattern of net photosynthesis in Cladonia stellaris

1983 ◽  
Vol 61 (8) ◽  
pp. 2169-2180 ◽  
Author(s):  
K. A. Kershaw ◽  
J. D. MacFarlane ◽  
M. R. Webber ◽  
A. Fovargue

Despite the contrasting thermal and light environment of sun and shade ecotypes of Cladonia stellaris, analysis of the pattern of net photosynthesis throughout the year as well as enzyme polymorphism in each morphotype has found little genotypic difference. The large disparity between photosynthetic capacity in the sun and shade replicates is shown to be due to a difference in chlorophyll content. There is a significant decline in photosynthetic capacity in November and this is shown to be reversible uncoupling of energy transduction in some photosynthetic units during the winter period. The control of coupling and uncoupling of photosynthetic units is found to be mediated by both day length and thallus temperature and a double environmental signal in June and July of short days coupled to low temperature will initiate and finalize the event within 12 h. This response pattern is discussed in relation to identical capacity changes in other lichen species. Apart from a single isoenzyme difference in esterase polymorphism, no differences in the zymograms of leucine aminopeptidase, phosphoglucoisomerase, or acid phosphatase were detected and this overall genetic homogeneity was equally evident in a general protein gel. This unexpected degree of homogeneity is discussed in terms of the difficulties in assessing enzyme polymorphisms in different plant populations, without maximum refinement of protein preparation methods and electrophoretic techniques. It is concluded that the two quite distinct sun and shade morphotypes only reflect phenotypic differences. In contrast, however, significant differences are reported in the distribution of specific enzymes between the tops and bases of the podetia.

Ecology ◽  
1973 ◽  
Vol 54 (2) ◽  
pp. 413-419 ◽  
Author(s):  
Martin J. Lechowicz ◽  
Michael S. Adams

2013 ◽  
Vol 25 (1) ◽  
pp. 62-69 ◽  
Author(s):  
Samuel Cordeiro Vitor Martins ◽  
Kelly Coutinho Detmann ◽  
Josimar Vieira dos Reis ◽  
Lucas Felisberto Pereira ◽  
Lílian Maria Vincis Pereira Sanglard ◽  
...  

1973 ◽  
Vol 60 (5) ◽  
pp. 426-435 ◽  
Author(s):  
Edward J. DePuit ◽  
Martyn M. Caldwell

2020 ◽  
Vol 71 (20) ◽  
pp. 6460-6470
Author(s):  
Alicia V Perera-Castro ◽  
Miquel Nadal ◽  
Jaume Flexas

Abstract In vascular plants, more rigid leaves have been linked to lower photosynthetic capacity, associated with low CO2 diffusion across the mesophyll, indirectly resulting in a trade-off between photosynthetic capacity (An) and bulk modulus of elasticity (ε). However, we evaluated mosses, liverworts, and Chara sp., plus some lycophytes and ferns, and found that they behaved as clear outliers of the An–ε relationship. Despite this finding, when vascular and non-vascular plants were plotted together, ε still linearly determined the cessation of net photosynthesis during desiccation both in species with stomata (either actively or hydro-passively regulated) and in species lacking stomata, and regardless of their leaf structure. The latter result challenges our current view of photosynthetic responses to desiccation and/or water stress. Structural features and hydric strategy are discussed as possible explanations for the deviation of these species from the An–ε trade-off, as well as for the general linear dependency between ε and the full cessation of An during desiccation.


2012 ◽  
Vol 110 (3) ◽  
pp. 731-741 ◽  
Author(s):  
Juan M. Posada ◽  
Risto Sievänen ◽  
Christian Messier ◽  
Jari Perttunen ◽  
Eero Nikinmaa ◽  
...  

1976 ◽  
Vol 87 (3) ◽  
pp. 649-660 ◽  
Author(s):  
J. L. Hammerton

SummaryTwo dwarf pigeon pea cultivars, each at two spacings, were planted at 4-weekly intervals over a year. Differences in height and number of branches between cultivars and spacings were generally small but planting date had much greater effects. Heights at reaping were > 2 m in plantings made in March or April, but decreased with later planting to ca. 1 m in November–February plantings. Time from planting to reaping varied from ca. 120 days in September-February plantings to > 225 days in March or April plantings. Four of the 13 plantings showed loss of mainstem dominance. Defoliation by rust disease showed no seasonal pattern, nor any association with yield. March plantings showed a ‘preliminary’ flowering in which only some wide-spaced and perimeter plants flowered in late July. Yields varied from 0–5 to 10 t/ha as green pods, but one cultivar at a spacing of 0·45 × 0·45 m (49385/ha) gave a mean yield of ca. 5 ±0·57 t/ha. Late-May planting appeared the most efficient, giving a large number of pods per day, per flowering branch and per metre of height, but plants exceeded 2 m in height and took 200 days from planting to reaping. December or January planting gave smaller plants, taking ca. 125 days from planting to reaping. Day-length was a dominant factor influencing growth and yield, but part of this may have been a response to radiation rather than to photoperiod.


2012 ◽  
Vol 109 (22) ◽  
pp. 8612-8617 ◽  
Author(s):  
W. L. Bauerle ◽  
R. Oren ◽  
D. A. Way ◽  
S. S. Qian ◽  
P. C. Stoy ◽  
...  

Author(s):  
Martijn Slot ◽  
Sami Rifai ◽  
Klaus Winter

Atmospheric and climate change will expose tropical forests to conditions they have not experienced in millions of years. To better understand the consequences of this change we studied photosynthetic acclimation of the neotropical tree species Tabebuia rosea to combined 4°C warming and twice-ambient (800 ppm) CO. We measured temperature responses of the maximum rates of ribulose 1,5-bisphosphate carboxylation (V), photosynthetic electron transport (J), net photosynthesis (P), and stomatal conductance (gs), and fitted the data using a probabilistic Bayesian approach. To evaluate short-term acclimation plants were then switched between treatment and control conditions and re-measured after 1–2 weeks. Consistent with acclimation, the optimum temperatures (T) for V, J and P were 1–5°C higher in treatment than in control plants, while photosynthetic capacity (V, J, and P at T) was 8–25% lower. Likewise, moving control plants to treatment conditions moderately increased temperature optima and decreased photosynthetic capacity. Stomatal density and sensitivity to leaf-to-air vapor pressure deficit were not affected by growth conditions, and treatment plants did not exhibit stronger stomatal limitations. Collectively, these results illustrate the strong photosynthetic plasticity of this tropical tree species as even fully-developed leaves of saplings transferred to extreme conditions partially acclimated.


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