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Book of Abstracts - Geyseco

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P - Posters<br />

nez, M.S. 4 - Morales, D. 4 - Olano, J.M. 5 - García-Plazaola, J.I. 1<br />

1<br />

University Of Basque Country<br />

2<br />

Universidad de Sevilla<br />

3<br />

UNAM-León<br />

4<br />

Universidad de La Laguna<br />

5<br />

Universidad de Valladolid<br />

*Corresponding author, e-mail: raquel.esteban@ehu.es<br />

Mangrove forests are worldwide distributed in tropical and subtropical<br />

shores. Several tree species co-exist in this environment<br />

displaying different strategies to cope with salinity. One <strong>of</strong> them,<br />

the black mangrove (Avicennia germinans L), excretes salt taken<br />

up by roots through specialised glands located in leaves. As a<br />

consequence, at noon when relative humidity is low, leaves become<br />

whitish because <strong>of</strong> the deposition <strong>of</strong> salt crystals that liquate<br />

again at the end <strong>of</strong> the day. As mangrove ecosystems are exposed<br />

to strong light the reversible formation <strong>of</strong> crystals during periods<br />

<strong>of</strong> strong photoprotective demand could have a photoprotective<br />

role for leaves, as light intensity intercepted by photosynthetic<br />

tissues is attenuated.<br />

It was therefore the objective <strong>of</strong> this study to verify this hypothesis.<br />

Experiments were performed in Juan Venado Island<br />

Nature Reserve (Nicaragua) in both dry (November) and rainy<br />

seasons (August). Salt was removed from one half <strong>of</strong> the leaves<br />

and both parts were compared. In August no differences were<br />

observed in any <strong>of</strong> the physiological parameters analysed, but<br />

in the dry season, when crystal deposition is more conspicuous,<br />

leaves with salt showed higher photochemical efficiency during<br />

the afternoon, indicating higher photodamage in exposed leaves.<br />

Furthermore, salty leaves showed a tendency to have higher values<br />

<strong>of</strong> Photochemical Reflectance Index, which indicates that<br />

more photons are used photosynthetically. Thus, the ability<br />

<strong>of</strong> A. germinans leaves to excrete the absorbed salt, apart from<br />

contributing to osmoregulation, may represent a photoprotective<br />

mechanism that generates dynamic changes in leaf reflectance,<br />

making it more tolerant to extreme conditions <strong>of</strong> the mangrove<br />

ecosystem.<br />

P01-067: EFFECT OF PHENOLIC COMPOUNDS IN PI-<br />

SUM SATIVUM AND LUPINUS LUTEUS PLANTS UN-<br />

DER SOIL DROUGHT<br />

Skrzypek, E. 1 * - Czyczylo-Mysza, I. 1 - Marcinska, I. 1 - Waligorski,<br />

P. 1 - Dziurka, K. 1 - Dziurka, M. 1 - Stawicka, A. 1 - Dubert, F. 1 -<br />

Plazek, A. 2 - Koscielniak, J. 2<br />

1<br />

The F. Gorski Institute <strong>of</strong> Plant Physiology, Polish Academy <strong>of</strong><br />

Sciences<br />

2<br />

Department <strong>of</strong> Plant Physiology, University <strong>of</strong> Agriculture<br />

*Corresponding author, e-mail: skrzypek@ifr-pan.krakow.pl<br />

Increase in phenolic compounds biosynthesis have been observed<br />

in a variety <strong>of</strong> biotic and abiotic stresses. Legume species<br />

showed high ability to endure intense dehydratation and return to<br />

normal turgor after soil rehydratation.<br />

The aim <strong>of</strong> the investigation was to determine the drought resistance<br />

diversity in chosen genotypes <strong>of</strong> yellow lupine and pea<br />

cultivated in Poland.<br />

Influence <strong>of</strong> soil drought on changes <strong>of</strong> plants growth, leaf water<br />

content, endogenous level <strong>of</strong> phenolics in pea and lupine genotypes<br />

were compared. Plants were grown in 4.5 l pots with soil<br />

(70% <strong>of</strong> soil field water capacity, FWC) during the late spring<br />

and early summer time in the open-air shelter. Drought stress<br />

(25% FWC) was subjected to the plants for 14 days, when the<br />

plants were after flowering phase. After stress treatment plants<br />

were well watered and recovery <strong>of</strong> their vitality was observed.<br />

Drought differentiated, dependently on the genotype, seedlings<br />

growth and leaves injury.<br />

Leaf water content (lower under drought stress than in control)<br />

and endogenous level <strong>of</strong> phenolics (higher under stressed plants)<br />

allowed to select tolerant and susceptible pea and lupine genotypes.<br />

Research funded by grant 621/N-COST/09/2010/0<br />

P01-068: COLD-INDUCED CHANGES OF CELL WALL<br />

STRUCTURE AND COMPOSITION IN TRITICALE LI-<br />

NES THAT ARE SENSITIVE OR RESISTANT TO FUN-<br />

GAL PATHOGEN MICRODOCHIUM NIVALE<br />

Szechynska-Hebda, M. 1 * - Hebda, M. 2 - Wedzony, M. 1<br />

1<br />

Institute <strong>of</strong> Plant Physiology PAS<br />

2<br />

Institute <strong>of</strong> Material Engineering CUT<br />

*Corresponding author, e-mail: szechynska@wp.pl<br />

The work was based on the observation that exposure <strong>of</strong> triticale<br />

seedlings to cold promotes their resistance to infection with the<br />

fungal pathogen Microdochium nivale. Since, the expression <strong>of</strong><br />

resistance is dependent on the plant genotype, two lines, namely<br />

Hewo (pathogen-tolerant) and Magnat (pathogen-sensitive) were<br />

used in the study <strong>of</strong> the cell wall properties during cold harvesting.<br />

Two types <strong>of</strong> plant resistance are suggested: resistance to<br />

the establishment <strong>of</strong> the initial infection and resistance to hyphal<br />

invasion through the plant tissue. The physiological and chemical<br />

state <strong>of</strong> the cell wall, brought by their exposure to cold determined<br />

the resistance efficiency <strong>of</strong> both types.<br />

The first type <strong>of</strong> resistance we studied using coupling techniques:<br />

TG, DSC and QMS. We showed that the expression <strong>of</strong> plant resistance<br />

strongly depend on the cell wall structure and composition.<br />

The signal was assigned using model substances. In this<br />

way we showed that pectin was degraded first, then hemicellulose,<br />

cellulose and finally lignin. Different thermal behavior was<br />

found between the cell wall components <strong>of</strong> Hewo and Magnat<br />

treated with cold. The peaks, assigned to the cellulose and lignin<br />

thermal decomposition, occurred at a different temperature and<br />

had remarkably differences in the shape <strong>of</strong> the curves. It can be<br />

explained by the different amount <strong>of</strong> cellulose and lignin and its<br />

different thermal stability.<br />

The second type <strong>of</strong> resistance was confirmed by physiological<br />

tests. Resistant plant responded defensively to hyphae invasion<br />

with the events at the place <strong>of</strong> the first contact: callose deposition<br />

for surrounding the necks <strong>of</strong> invasion hyphae and generation <strong>of</strong><br />

H 2<br />

O 2<br />

by cell wall peroxidases.<br />

The research was supported by a projects: 595/N-COST/2009/0<br />

and MERG-CT-2007-207350.<br />

P01-069: TOLERANCE OF ARABIDOPSIS THALIANA<br />

PLANTS TO THE ALLELOCHEMICAL PROTOCATE-<br />

CHUALDEHYDE (PCA)<br />

Reigosa, M.* - Martínez-Peñalver, A. - Sánchez-Moreiras, A.M.<br />

University <strong>of</strong> Vigo<br />

*Corresponding author, e-mail: mreigosa@uvigo.es<br />

Protocatechualdehyde (PCA), is a phenolic compound found in<br />

many plant organs <strong>of</strong> different species (stems <strong>of</strong> Ilex litseaefolia,<br />

roots <strong>of</strong> Salvia miltiorrhiza, leaves <strong>of</strong> Vitis vinifera, etc). This<br />

plant secondary metabolite has many beneficial effects for human<br />

health as anticarcinogenic, anticoagulant, etc (Zhou et al.,<br />

2005). However, there are very few studies evaluating its role<br />

as allelochemical. Reigosa and Pazos-Malvido (2007) showed<br />

the phytotoxic capacity <strong>of</strong> PCA during root growth and germination,<br />

but we have found no experiments in the literature, either<br />

short or long term, with information about PCA phytotoxicity on<br />

adult plants. Therefore we studied the phytotoxicity <strong>of</strong> PCA on<br />

Arabidopsis plants, monitoring the effect by imaging chlorophyll<br />

a fluorescence, pigment content, concentration <strong>of</strong> free radicals<br />

(O 2<br />

- and H 2<br />

O 2<br />

), lipid peroxidation, total protein and glutathione<br />

transferase at various times during 8 days treatment. Photosynthetic<br />

efficiency and fluorescence emission values <strong>of</strong> PCA treated<br />

plants remained broadly in values close to control suggesting a<br />

non-phytotoxic effect <strong>of</strong> PCA. However, just minutes after the<br />

addition <strong>of</strong> the allelochemical oxidative burst was observed with<br />

increased values <strong>of</strong> O 2<br />

- and H 2<br />

O 2<br />

. This burst was followed by a<br />

very significant increase <strong>of</strong> lipid peroxidation in the early hours<br />

<strong>of</strong> measurement. But plants were able to cope with PCA toxicity<br />

showing very low values <strong>of</strong> MDA content after 48 h treatment, as<br />

P

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