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Eficiencia fotoquimica del fotosistema II y crecimiento en plantas de curuba (Passiflora tripartita (Juss.) var. mollissima (Kunth)) bajo estres salino.

Photochemical efficiency of photosystem II and growth in banana passionfruit plants (Passiflora tripartita (Juss.) var. mollissima (Kunt) L.H. Bailey under salt stress


In 2009, banana passionfruit was cultivated on 1326 ha in Colombia, of which 52.6% was in the department of Boyaca (Agronet 2011). In Boyaca non-irrigated plantations have increased because farmers lack the economic resources to install irrigation systems. Non-irrigated production systems suffer plant osmotic stress due to high soil solute concentration in the dry season. Osmotic stress is a major hindrance to crop production. Salt stress has negative effects on plant growth, ion balance, and water relations (Munns, 2002).

However, there exists little information on the response of banana passionfruit plants to salinity. On the other hand, studies carried out using yellow passion fruit, Passiflora edulis, may be useful to understanding the behavior of banana passionfruit plants exposed to salt stress, since both species belong to the same genus. Soares et al. (2002) found that yellow passion fruit may be considered as moderately tolerant to salinity during the initial growth phase. On the other hand, Nyagah and Musyimi (2009) categorized passion fruit seeds as very sensitive to salt stress. Their results showed that sodium chloride solution treatment notably reduced germination percentage of passion fruit seeds, as well as radicle and plumule growth. Presumably, higher salinity reduced the absorption of water and nutrients into yellow passion fruit seedlings. A possible explanation is that salinity stress causes seedling stomata to close in order to minimize water loss, which reduces production of new leaves, and thus significantly affects dry matter (DM) production (Soares et al., 2002).

Photosynthesis is one of the most important metabolic processes in plants and its performance is greatly affected under stress conditions. Photosynthesis may be directly affected by salt stress interference on photosynthetic electron transport. Chlorophyll a fluorescence analysis is useful for measuring induced changes in the photosynthetic apparatus.

Because there is limited information regarding salinity's effect on banana passionfruit plants (Passiflora tripartita (Juss.) Poir. var. mollissima (Kunth) Holm-Niesen & P.M. J0rg.), the present study aimed to evaluate the growth and photochemical efficiency of photosystem II (PSII) in banana passionfruit seedlings under saline stress.

Materials and methods

The study was conducted in a greenhouse at the Pedagogical and Technological University of Colombia (UPTC), Tunja, Colombia (5[grados] 33' 16.25" N, 73[grados] 21'9.14" W) at 2790 m. a. s. l. Average growth conditions inside the greenhouse were: photosynthetic photon flux of 341.71 [micro]mol [m.sup.-2] [s.sup.-1], 15.8 [grados]C temperature and 72% relative humidity.

The Castilla cultivar of banana passionfruit was used for the experiment. Seeds were allowed to germinate in one-pound plastic bags containing a 1:1 mixture of soil and peat. Eight weeks after germination at the six-leaf stage, single seedlings were transplanted to 4 kg plastic bags filled with medium. Plantlets were daily watered with tap water and were grown up to the 8-10 leaf stage (18 days after transplanting), after which NaCl treatments were administered to the planting medium at concentrations of 20, 40, 60, and 80 mmol NaCl [kg.sup.-1]. These corresponded to electrical conductivities of 2.20, 3.39, 5.47, and 8.12 dS.[m.sup.-1], respectively. Control plants were not treated with salt (electrical conductivity 0.97 dS.m-1). To avoid osmotic shock to plants, treatments were imposed incrementally, increasing the concentration weekly until the final concentration was reached.

One hundred and twenty eight days after transplanting, chlorophyll fluorescence measurements were conducted on a fully expanded leaf of each plant, located in the middle third of the plant, using a Junior-Pam Chlorophyll Fluorometer with an actinic light pulse of 25 [micro]mol [m.sup.-2] [s.sup.-1] (H. Walz, Effeltrich, Germany). Before measuring chlorophyll (Chl) fluorescence parameters (FPs), leaves were put in a dark-adapted state for 30 min using light exclusion clips. The following chlorophyll fluorescence yields (FYs) were measured: minimum Chl FY in the dark adapted state ([F.sup.o]), maximum Chl FY in the dark-adapted state ([F.sup.m]). Using these parameters, were calculated the following ratios: maximum PSII photochemical efficiency [F.sup.v]/ [F.sup.m] = ([F.sup.m] - [F.sup.o])/Fm; maximal variable fluorescence [F.sup.v] = [F.sup.m] - [F.sup.o]. Plants were harvested 138 days after transplanting. Then they were dried to determine total dry weight and dry weight of each plant organ (roots, petioles + stem + shoots and leaves), by drying in an oven at 70 [grados]C for 48 h. The leaf area was measured using an analyzer LI-3000-A (LI-COR, Lincoln, USA). Soil salinity of all treatments was measured by determining the electrical conductivity (EC) of vacuum-pumped extracts from saturated soil.

Chlorophyll fluorescence measurements were taken on three plants for each treatment, with one leaf per plant analyzed. The plants exposed to the saline levels were arranged in a complete randomized design, with three replications and four plants per plot. All data were subjected to one-way Anova and significant differences between means were determined by Tukey's multiple-range test. Tendency curves for averages of treatments were calculated by a regression analysis, using the PASW statistics 18 program, version 18.0.0. Unless otherwise stated, differences were considered statistically significant when P < 0.05.

Results and discussion Plant growth

The plant growth response of banana passionfruit plants to salinity produced statistically significant differences (P < 0.05) in terms of leaf area, total stem length, and total dry weight per plant. In comparison with control plants, plants exposed to 20, 40, 60, and 80 mmol NaCl reduced leaf area by 20.89, 42.91, 58.37, and 76.40%, respectively. In the same order, total stem length showed a reduction of 9.97, 27.28, 42.79, and 55.77% with relation to control plants. Total dry weight per plant was reduced by 23.89, 31.49, 39.60, and 61.26% (Table 1).

Leaf growth inhibition is seen as an adaptive response to salinity and water deficiency. Plants with lower leaf area can cut water losses by slowing transpiration, and thus delay the onset of more severe stress (Casierra-Posada et al., 2006). Increased dead leaves are another contributing factor to leaf area reduction. In fact, the leaf death rate increased in plants experiencing saline stress when compared with control plants. Increased leaf death under saline stress is generally attributed to toxic levels of salt accumulation (Munns, 2002).

Casierra-Posada y Roa (2006) exposed P. ligularis plants to water stress, and found that stressed plants presented a 35.8% reduction in total stem length compared to control plants watered with a normal regime. This result can be compared to the behavior of P. tripartita plants in the present study, as both are rapidly-growing plants of the same genus, and both water and osmotic stress have similar effects on plant growth (Munns, 2002).

Dry matter distribution in different plant organs is another factor that is strongly influenced by saline conditions. While DM accumulation in leaves was inversely proportional to NaCl concentration in the substrate, a higher proportion of DM was allocated to roots with increasing soil salinity, with statistically significant differences (P < 0.05) for both parameters. DM allocation to stems and branches showed no statistically significant difference (Figure 1).

The results in this study agree with Awang et al. (1993) who reported a reduction in total dry weight of leaves as salinity lowered plant growth parameters. CasierraPosada and Garcia (2005) mention that salinity negatively affects leaf growth and induces an increase in relative root weight, as roots tend to grow in order to reduce toxic ion concentration in tissues through dilution, and in order to explore the soil to find areas of lower toxic concentration.


Chlorophyll fluorescence measurement

[F.sub.v]/[F.sub.m] represents the maximum quantum yield of photosystem II, which in turn is highly correlated with the quantum yield of net photosynthesis. The present study found highly significant differences (P < 0.01) for this variable between treatments. Compared to the control plants, [F.sub.v]/[F.sub.m] was reduced by 11.29, 14.23, 38.89, and 92.25%, respectively, in treatments with 20, 40, 60, and 80 mmol NaCl (Figure 2). Up to 40 mmol NaCl the reduction can be considered moderate, but beyond this value, the ratio [F.sub.v]/[F.sub.m] found in plant leaves is drastically reduced, especially with a concentration of 80 mmol NaCl in the substrate.

Elevated salinity can further reduce photosynthesis by lowering stomatal conductance and thus depressing carbon uptake, and/or by inhibiting photochemical capacity (Dubey, 1997). Salinity has been shown to affect reaction centers of PSII either directly or through accelerated senescence (Kura-Hotta et al., 1987). Maximal quantum yield of PSII (Fv/Fm) was reduced with increasing salt concentration in the present study, especially at very high concentrations. Electron flow was severely affected with 80 mmol NaCl.



* Saline conditions drastically reduced a number of growth factors in banana passionfruit. Leaf area, stem length, and DM weight all went down strongly with increasing salt concentration. PSII quantum yield also suffered an extreme reduction with increasing salinity.

* Data from the current experiment clearly support the general correlation between photosynthetic capacity and leaf area. Furthermore, the reduction of leaf area, PSII quantum yield, and the other factors measured in salt-affected banana passionfruit induced a reduction in DM production. This dry matter reduction closely follows the trend in PSII maximum quantum yield ([F.sub.v]/[F.sub.m]), which suggests that the major impact of salinity on the passionfruit plants was due to negative effects on photosynthesis.


The team gratefully acknowledges the generous support of the Research Directorate (Direccion de Investigaciones-DIN) of the Pedagogical and Technological University of Colombia (UPTC) for providing us with the funding and opportunity to conduct this research project. We also gratefully acknowledge matching support from the members of the Research Group in Plant Ecophysiology (Grupo Ecofisiologia Vegetal) of the Faculty of Agricultural Sciences of the UPTC.


Agronet. 2011. Analisis-Estadisticas. Ministerio de Agricultura y Desarrollo Rural. (Available online at: AnalisisEstadisticas/tabid/73/Default.aspx; accessed May 2011).

Awang, Y. B.; Atherton, J. G.; y Taylor, A. J. 1993. Salinity effects on strawberry plants grown in rockwool. I. Growth and leaf relations. J. Hort. Sci. 68:783-790.

Casierra-Posada, F.; Garcia, N. 2005. Crecimiento y distribucion de materia seca en cultivares de fresa (Fragaria sp.) bajo estres salino. Rev. Agron. Col. 23 (1): 83-89.

Casierra-Posada, F. y Roa, H. A. 2006. Efecto del deficit hidrico moderado en el suelo sobre el crecimiento y distribucion de materia seca en granadilla (Passiflora ligularis Juss). Rev. U.D.C.A. Actualidad y Divulgacion Cientifica 9(2):169-180.

Casierra-Posada, F.; Dotor, B. A.; y Gonzalez L. A. 2006. Efecto de la salinidad en la eficiencia en el uso del agua y la produccion de materia seca en guayabo. Acta Agron. 55(3):23-32.

Dubey, R. S. 1997. Photosynthesis in plants under stressful conditions. En: Pessarakli, M. (ed.). Handbook of photosynthesis. Marcel Dekker, Nueva York. p. 859-875.

Kura-Hotta, M.; Satoh, K.; y Katoh, S. 1987. Relationship between photosynthesis and chlorophyll content during leaf senescence of rice seedlings. Plant Cell Physiol. 28:1321-1329.

Munns, R. 2002. Comparative physiology of salt and water stress. Plant Cell Environ. 25:239-250.

Nyagah, A. W. y Musyimi, D. M. 2009. Effects of sodium chloride solution stress on germination and growth of passion fruits seedlings. ARPN J. Agric. Biol. Sci. 4:49-53.

Soares, F. A.; Gheyi, H. R.; Viana, S. B.; Uyeda, C. A.; y Fernandes, P. D. 2002. Water salinity and initial development of yellow passion fruit. Scientia Agricola 59(3):491-497.

(1) Fanor Casierra-Posada, (1) Jaime E. Pena-Olmos, (2) Gregory Vaughan

(1) Grupo de investigacion Ecofisiologia Vegetal, Facultad de Ciencias Agropecuarias, Universidad Pedagogica y Tecnologica de Colombia (UPTC). Avenida Central del Norte, Tunja, Boyaca, Colombia. (2) Grupo Interdisciplinario de Investigaciones Arqueologicas e Historicas, Museo Arqueologico de Tunja, Universidad Pedagogica y Tecnologica de Colombia. Avenida Central del Norte, Tunja, Boyaca, Colombia. 'Corresponding author:

Rec.: 13.10.11 Acep.: 31.07.13
Table 1. Growth in banana passion fruit (Passiflora tripartita
(Juss.) Poir. var. mollissima (Kunth) Holm- Niesen and P.M. J0rg.)
exposed to different levels of NaCl salinity.

NaCl     Electrical conduc-   Leaf area      Total stem length
(mmol)   tivity               ([cm.sup.2])   (cm)
         (dS [m.sup.-1])

0        0.97                 938.61 e *     897.20 c
20       2.20                 742.45 d       807.70 c
40       3.39                 535.81 c       652.40 b
60       5.47                 390.71 b       513.25 a
80       8.12                 221.49 a       396.78 a

NaCl     DM per plant
(mmol)   (g)

0        30.47 d
20       23.19 c
40       20.87 bc
60       18.40 b
80       11.80 a

* Means followed by the same letter are not statistical different
according to Tukey's adjustment for multiple comparison test (P <
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Title Annotation:articulo en ingles
Author:Casierra-Posada, Fanor; Pena-Olmos, Jaime E.; Vaughan, Gregory
Publication:Acta Agronomica
Date:Mar 1, 2013
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