Iron deficiency in peach trees: effects on leaf chlorophyll and nutrient concentrations in flowers and leaves

The effects of iron deficiency on the leaf chlorophyll concentrations and on the macro- (N, P, K, Ca and Mg) and micro-nutrient (Fe, Mn, Zn and Cu) composition of flowers (at full bloom) and leaves (60 and 120 days after full bloom) of field-grown peach (Prunus persica L. Batsch) trees were investigated. Flowers and leaves were taken and analysed from fifty individual trees. Our data indicate that large decreases in leaf chlorophyll concentration were found at the beginning of the season in control trees, possibly associated to a dilution effect by leaf growth, that were later followed by leaf chlorophyll concentration increases. Leaf Fe chlorosis apparently results from two different processes, the dilution of leaf Chl caused by growth and the subsequent inability to produce and/or stabilize new Chl molecules in the thylakoid membrane. Iron chlorosis did not change the seasonal change patterns of any of the nutrients studied. In Fe-deficient trees the K concentration and the K/Ca ratio were high not only in leaves but also in flowers, indicating that this is a characteristic of Fe-deficient plant tissue in the whole fruit tree growing season. Flower Fe concentrations were well correlated with the degree of chlorosis developed later in the season by the trees, suggesting that flower analysis could be used for the prognosis of Fe deficiency in peach.     

Iron deficiency causes changes in chlorophyll fluorescence due to the reduction in the dark of the Photosystem II acceptor side

Iron deficiency was found to affect the redox state of the Photosystem II acceptor side in dark-adapted, attached leaves of sugar beet (Beta vulgaris L.). Dark-adapted iron-deficient leaves exhibited relatively high F_o and F_pl levels in the Kautsky chlorophyll fluorescence induction curve when compared to the iron-sufficient controls. However, far-red illumination led to marked decreases in the apparent F_o and F_pl levels. Modulated fluorescence showed that far-red light decreased the fluorescence yield to the true F_o levels by increasing photochemical quenching, without inducing changes in the level of non-photochemical quenching. In dark-adapted, iron-deficient leaves, far-red illumination induced a faster fluorescence decay in the µs-ms time domain, indicating an improvement in the electron transport after the primary quinone acceptor in the reducing side of Photosystem II. All these data indicate that in iron-deficient leaves the plastoquinone pool was reduced in the dark. The extent of the plastoquinone reduction in sugar beet depended on the chlorophyll concentration of the leaf, on the time of preillumination and on the duration of dark adaptation. The dark reduction of plastoquinone was observed not only in sugar beet but also in other plant species affected by iron deficiency both in controlled conditions and in the field.     

Chlorophyll Fluorescence as a Possible Tool for Salinity Tolerance Screening in Barley (Hordeum vulgare L.)

The application of chlorophyll fluorescence measurements to screening barley (Hordeum vulgare L.) genotypes for salinity tolerance has been investigated. Excised barley leaves were cut under water and incubated with the cut end immersed in water or in a 100-mM NaCl solution, either in the dark or in high light. Changes in rapid fluorescence kinetics occurred in excised barley leaves exposed to the saline solution only when the incubation was carried out in the presence of high light. Fluorescence changes consisted of decreases in the variable to maximum fluorescence ratio and in increases in the relative proportion of variable fluorescence leading to point I in the Kautsky fluorescence induction curve. These relative increases in fluorescence at point I appeared to arise from a delayed plastoquinone reoxidation in the dark, since they disappeared after short, far-red illumination, which is known to excite photosystem I preferentially. We show that a significant correlation existed between some fluorescence parameters, measured after a combined salt and high-light treatment, and other independent measurements of salinity tolerance. These results suggest that chlorophyll fluorescence, and especially the relative fluorescence at point I in the Kautsky fluorescence induction curve, could be used for the screening of barley genotypes for salinity tolerance.     

Photosystem II efficiency and mechanisms of energy dissipation in iron-deficient,field-grown pear trees (Pyrus communis L.)

The dark-adapted Photosystem II efficiency of field-grown pear leaves, estimated by the variable to maximum chlorophyll fluorescence ratio, was little affected by moderate and severe iron deficiency. Only extremely iron-deficient leaves showed a decreased Photosystem II efficiency after dark adaptation. Midday depressions in Photosystem II efficiency were still found after short-term dark-adaptation in iron-deficient leaves, indicating that Photosystem II down-regulation occurred when the leaves were illuminated by excessive irradiance. The actual Photosystem II efficiency at steady-state photosynthesis was decreased by iron deficiency both early in the morning and at midday, due to closure of Photosystem II reaction centers and decreases of the intrinsic Photosystem II efficiency. Iron deficiency decreased the amount of light in excess of that which can be used in photosynthesis not only by decreasing absorptance, but also by increasing the relative amount of light dissipated thermally by the Photosystem II antenna. When compared to the controls, iron-deficient pear leaves dissipated thermally up to 20% more of the light absorbed by the Photosystem II, both early in the morning and at midday. At low light iron-deficient leaves with high violaxanthin cycle pigments to chlorophyll ratios had increases in pigment de-epoxidation, non-photochemical quenching and thermal dissipation. Our data suggest that pH could be the major factor controlling thermal energy dissipation, and that large (more than 10-fold) changes in the zeaxanthin plus antheraxanthin to chlorophyll molar ratio caused by iron deficiency were associated only to moderate increases in the extent of photoprotection.This revised version was published online in October 2005 with corrections to the Cover Date.     

La transgression thanétienne (Paléocène supérieur) dans l’Aurès occidental (Algérie), d’après les associations de Foraminifères de la coupe d’El Kantara

In the W-Aures (Algeria), the El Kantara pass displays about 50 m of Red Marls overlying the Maastrichtian limestones with Laffitteina. The Red Marls are, in their turn, overlain by the Thanetian marly limestones of the river El Haï. The micropaleontological inventory of these Red Marls establishes the co-occurrence of subaerian (Microcodium = Paronipora), fresh-water (Charophyta) and marine microfossils (Foraminifers). The stratigraphical significance of these microfossils is discussed. The upper part of the Red Marls, yielding abundant Valvulina and scarce Glomalveolina, is of Thanetian age. The age of the lower part is less established, but the occurrence of Microcodium suggests a Thanetian age too. Located at the margin of the northern opening of the trans-Saharan epeiric sea, the El Kantara section establishes a Thanetian age for the beginning of the Paleocene transgression. Danian deposits are missing, in spite of the absence of an obvious hiatus on the field. After general emersion during the early Paleocene, the Thanetian transgression starts with the set up of lakes at the depositional area of the Red Marls. Marine influences, limited at first, become gradually prevailing, and end with the deposition of neritic marly limestones of river El Haï.     

Effects of Salinity on Chlorophyll Fluorescence and Photosynthesis of Barley (Hordeum Vulgare L.) Grown Under a Triple-Line-Source Sprinkler System in the Field

In flag leaves of four cultivars of barley (Hordeum vulgare L.) grown in the field under a triple-line-source sprinkler system, that produces a linear soil salinity gradient, a decrease in net carbon dioxide assimilation rate (P_N) and stomatal conductance for water vapour (gs) was found. These changes were related to salinity tolerance at moderate salinity. With increasing salinity, P_N was saturated at low irradiances and stomatal frequencies increased. A decrease in photosystem 2 (PS2) efficiency was not found in the field after dark adaptation even at high salinity. Salinity induced only small decreases in the actual PS2 efficiency at midday steady-state photosynthesis, indicating that the photosynthetic electron transport was little affected by salinity. Therefore, using PS2 efficiency estimates in attached leaves is probably not a useful tool to screen barley genotypes grown under saline conditions in the field for salinity tolerance. In contrast, excised flag leaves from high salinity plots, once in the laboratory, exhibited a decrease in the variable to maximum chlorophyll fluorescence ratio as compared to excised leaves from control plants. On the other hand, the PN rate might allow for a good discrimination between tolerant and non-tolerant cultivars. This revised version was published online in June 2006 with corrections to the Cover Date.