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versión impresa ISSN 0001-3765
An. Acad. Bras. Ciênc. vol.84 no.3 Rio de Janeiro set. 2012 Epub 24-Jul-2012
Bruno F. Sant'Anna-SantosI; Aristéa A. AzevedoII; Luzimar C. SilvaII; Marco A. OlivaII
IUniversidade Federal de Minas Gerais, Campus Regional Montes Claros, Av. Universitária, 1000, Caixa Postal 135, Bairro Universitário, 39404-547 Montes Claros, MG, Brasil
IIUniversidade Federal de Viçosa, Departamento de Biologia Vegetal, Av. PH Rolfs, s/n, Centro, 36570-000 Viçosa, MG, Brasil
The goal of this study was to determine the symptoms and microscopic damage caused by fluoride on Spondias dulcis, a fluoride-sensitive species. The plants were exposed to simulated fog with fluoride (0, 5, 10, 15 and 20 mg L-1) for 20 min daily during four consecutive days. Samples from leaflets without any apparent fluoride injury were collected to microscopic analysis. The percentage of necrosed leaf area was measured, and the level of pollutant in the dry matter from the basal and apical portions of the plant was determined. The necroses began 24 h after the first simulation mainly from the base of the leaflets. A higher level of necrosis was observed at the apical portion of the plants, a region of higher fluoride accumulation. The damage on the surface of the leaflets was characterized as plasmolysis, erosion of the epicuticular waxes and epidermal rupture. Structurally, the noticeable accumulation of granules and droplets green stained by toluidine blue in the spongy parenchima and the boundaries of ending veinlets was observed. The limb thickness reduction occurred due to plasmolysis in the mesophyll, showing an apparent correlation with the damage observed on the surface. The parameters observed in the laboratory are promising for field biomonitoring studies.
Key words: Leaf anatomy, bioindicator, necrosis, pollution, symptomatology.
O objetivo deste estudo foi determinar os sintomas e danos microscópicos causadas pelo flúor em Spondias dulcis, espécie sensível a essa substância. As plantas foram expostas a nevoeiros simulados com flúor (0, 5, 10, 15 e 20 mg L-1) por 20 minutos diários, durante quatro dias consecutivos. Amostras de folíolos sem qualquer lesão aparente ao flúor foram coletadas para análise microscópica. Mensurou-se a percentagem de área foliar necrosada e o teor do poluente na matéria seca das porções basal e apical da planta. As necroses surgiram 24 horas após a primeira simulação e tiveram início, principalmente, a partir da base dos folíolos. As necroses foram mais severas na porção apical das plantas, região com maior acúmulo de flúor. O dano na superfície dos folíolos foi caracterizado como plasmólise, erosão das ceras epicuticulares e ruptura da epiderme. Estruturalmente, observou-se considerável acúmulo de grânulos e gotas coradas de verde pelo azul de toluidina no parênquima lacunoso e nas proximidades das terminações xilemáticas. Houve redução da espessura do limbo devido a plasmólise no mesofilo, havendo aparente correlação com os danos observados na superfície. Os parâmetros observados em laboratório são promissores para estudos de biomonitoramento em campo.
Palavras-chave: Anatomia foliar, bioindicador, necrose, poluição, sintomatologia.
Fluoride, an extremely phytotoxic atmospheric pollutant (Smith and Hodge 1979), can be released into the atmosphere during the production of aluminium, bricks, glass, and steel (Fornasiero 2001). In Brazil there is little data regarding the concentration of fluoride in the atmosphere, most of them restricted to Cubatão city, São Paulo State (Klumpp et al. 1996a, b, 1998, Domingos et al. 2003). However, the aluminium industry has been blamed for the emission of this pollutant, for instance, at the metallurgical zone in Minas Gerais State (Divan Junior et al. 2007, 2008).
Some plant species, such as Panicum maximum cv. Colonião and Chloris gayana, have been used in Brazil as bioindicators for detecting the presence of fluoride in the atmosphere (Divan Junior et al. 2007). When carrying out field studies, it is essential to have a prior knowledge on plant-specific morphoanatomical, physiological and biochemical responses to fluoride. Information from prior experiments in laboratory makes it possible to precisely diagnose plant injuries (Silva et al. 2000, Fornasiero 2001, Chaves et al. 2002, Oliva and Figueiredo 2005).
The symptomatology, the most used parameter for assessing the sensitivity of a plant species to several stress factors, frequently requires additional validation using microscopy (Vollenweider et al. 2003, Reig-Arminaña et al. 2004). Non-specific symptoms such as chlorosis and necrosis, in addition to not being useful in determining the nature of the stressing agent involved (Günthardt-Goerg and Vollenweider 2007), also elicit statements such as the following: "all environmental stresses lead to chlorophyll degradation" (Munné-Bosch and Alegre 2004) or "if no pathogen is found, an abiotic cause for the disease must be considered". However, according to Günthardt-Goerg and Vollenweider (2007), if supported by microscopy, the symptomatology may be used in the precise diagnosis of stress. The macroscopic and microscopic studies, in most cases, must therefore be integrated to assure an accurate diagnosis.
The symptomatology and the microscopic characterization of the injury have been used as biomarkers in several studies aimed at determining the sensitivity of a species to fluoride (Silva et al. 2000, Fornasiero 2001, Chaves et al. 2002, Oliva and Figueiredo 2005, Peixoto et al. 2005). However, there has been little focus on the prognostic value of microscopic parameters.
In several countries, a standardized method has been employed to monitor areas polluted with fluoride (VDI 1982). This method uses Lolium multiflorum ssp. italicum, a grass species that accumulates fluoride (Ruthsatz and Wey 1991). However, Ellenberg (1991) questioned the universal use of this species, since changes in the eco-physiological properties of L. multiflorum can mask the fluoride-specific symptomatology. The scarcity of data addressing the sensitivity of this tropical species to pollution limits the possible biomonitoring programs and the assessment of the environmental impacts, reinforcing the need for more studies concerning this species (Silva et al. 2000).
Spondias dulcis Forst. F. (Anacardiaceae), commonly known as cajá-mirim, is a perennial species from Polynesia that is distributed throughout Brazil (Souza et al. 1998), mainly in south and southeast of the country (Lorenzi et al. 2003). S. dulcis, has pinnately compound leaves with 7-11 pairs of membranaceous leaflets ranges from 10 to 15 mm in height (Lorenzi et al. 2003). Due to its high sensitivity to fluoride in comparison to other tropical tree species, Silva et al. (2000) highlighted the potential use of S. dulcis as a bioindicator and proposed depth studies to precisely diagnose the injuries caused by fluoride. The aim of this study is to determine the damage caused by fluoride on the leaf blades of S. dulcis under laboratory conditions.
MATERIALS AND METHODS
S. dulcis, a tropical tree species sensitive to fluoride (Silva et al. 2000), was supplied by the Nursery of Parque Estadual do Rio Doce-MG (NPERD). The plants were obtained from seminiferous propagation from a unique adult individual located at an altitude of 280 m, at the coordinates Lat 19º57'04'' S and Long 42º50'27'' W, mapped through the global positioning system (GPSII plus, Garmin Ltd., Hampshire, UK) at the boundaries of NPERD. The voucher specimen was stored at VIC Herbarium under the number 29607.
Sowing was performed in plastic bags that were 100 mm in diameter and 220 mm in length, and containing soil from NPERD (Tab. I). Two months after sowing the plants were transferred to a greenhouse for acclimation. The greenhouse was located at Department of Plant Biology, Federal University of Viçosa, at an altitude of 649 m and at the coordinates Lat 20º45'20" S and Long 42º52'40" W. After being transferred to 2.6 dm3 pots, the plants received Hoagland 0.25-strength nutritive solution (Hoagland and Arnon 1950) at every five days during the acclimation period (two months) and until the end of the experiment.
The simulation experiment was adapted from the method proposed by Silva et al. (2000). S. dulcis plants average 380 mm in height and have an average of 8 knots presenting compound leaves with seven leaflets. The plants were exposed daily for 20 min, totalling 5.22 mm day-1 of precipitation, in a simulation chamber with a spray system adapted from the model proposed by Evans et al. (1977). Treatments were applied in a completely randomized design with five treatments (0, 5, 10, 15 and 20 mg L-1) and five plants per treatment. The treatments with fluoride (pH=6.0) were prepared by adding potassium fluoride to deionised water. The fog applied in the control treatment contained only deionised water at pH 6.0. Before and after each fog, the plants were placed under a luminous panel for 15 min, under an irradiance of 95 W m-2 provided by eight incandescent high-pressure mercury lamps (E-27, 220-230 V, 250 W). The plants remained under ambient light conditions (24.8/17.5/11.9ºC average of the maximum/middle/low temperatures, relative humidity 83.6%) the rest of the time. The beginning of leaf abscission in the plants exposed to fluoride (after the fourth fog) determined the end of the experiment.
During the simulation period all leaflets of plants in the five different treatments were photographed daily with the aim of recording the beginning of symptoms and the evolution of the necroses caused by the pollutant. The photographs were taken using a digital camera. At the end of the experiment, all leaves from the basal portion (5th knot from the apical bud to the 8th knot) and apical portion (1st knot from the apical bud to the 4th knot) of each S. dulcis plant were digitalized and analyzed using Image Pro-Plus, version 4.1 for Windows® (Media Cybernetics, Silver Spring, MD, USA) to calculate the percentage of necrosed leaf area.
All leaves (n=5) from the basal and apical portion of plants from all treatments were dried in a stove at 70 ºC and reduced to particles with dimensions of less than 1 mm using a Wiley grinder. Then, 0.5 g aliquots of each sample were extracted in 0.1 M perchloric acid (Garcia-Ciudad et al. 1985) using an ionic strength adjustment buffer (Larsen and Widdowson 1971) for the potentiometric determination of the fluoride content. The analyses were carried out in duplicate and repeated twice.
Only the leaflets without any apparent fluoride injury were collected to microscopic analysis. Samples were collected from leaves from the 3rd or 4th knots (from the apical bud) at the end of the experiment. The samples were collected from the middle portion of one representative leaflet of each plant (n=5) and fixed in Karnovsky's solution (glutaraldehyde solution (2.5%) and paraformaldehyde (4%), with sodium cacodylate buffering - pH 7.2 - and the addition of calcium chloride 5 mM (Karnovsky 1965).
For the scanning electron microscopy analysis, the samples fixed in Karnovsky's solution were post-fixed in osmium tetroxide (1%), dehydrated in ethylic series and dried until the critical point (model CPD 020, Bal-Tec, Balzers, Liechtenstein). The leaflets were covered with gold using the cathodic spray process in a Sputter Coater (model FDU010, Bal-Tec, Balzers, Liechtenstein). The analyses were made using SEM LEO 1430 VP, Zeiss (Cambridge, England).
With regard to the anatomical studies, after fixation in Karnosvsky's solution and dehydration in the ethylic series, the samples were placed in methacrylate (Historesin, Leica Instruments, Heidelberg, Germany). Transversal and paradermal sections (8 and 3 µm thick, respectively) were obtained using a rotary microtome (model RM2155, Leica Microsystems Inc., Deerfield, USA) and stained with toluidine blue (pH=4.0) (O'Brien and McCully 1981), and the slides were mounted in Permount. The images were obtained using a light microscope with a digital camera (model Olympus AX70TRF, Olympus Optical, Tokyo, Japan).
For the micromorphometric evaluations we measured the percentage of intercellular spaces in the spongy parenchyma in the paradermal sections. In the transversal sections we measured the thickness of the limb, palisade parenchyma and spongy parenchyma, and the height of the adaxial and abaxial epidermis at the leaf mid-region. We performed 27 measures/repetitions/parameters totalling 162 records per repetition. The Image Pro-Plus, version 4.1 for Windows® (Media Cybernetics, Silver Spring, MD, USA) was used.
The experimental delineation was completely randomized with five treatments (0, 5, 10, 15, and 20 mg L-1) and five plants per treatment. The data were submitted to analysis of variance (ANOVA) employing SAEG software (Euclydes 1983), and the measurements from the treatments were compared using Tukey's test at 5 % probability.
In the control treatment the leaflets of S. dulcis showed a uniform color (Fig. 1A), typically brilliant green without injuries. In the leaflets of plants exposed to 10, 15 and 20 mg L-1 fluoride fog (Fig. 1B-E and 2A-F), the symptoms occurred 24 h after the first fluoride fog simulation. There were noticeably more severe necroses on plants subjected to fog at concentrations of 15 (Fig. 2A-C) and 20 mg L-1 (Fig. 2D-F). Necrosis was not observed in plants exposed to 5 mg L-1 until after the end of the experiment. The leaf abscission began 96 h after the first fluoride simulated fog at concentrations of 15 and 20 mg L-1.
In the plants exposed to fluoride, necrosis occurred in all leaflets in marginal areas, as well as in interveinal areas, mainly at the base of the leaflets (92.5% of the leaflets showed necrosis) (Fig. 1B-E). Necrosis was characterized by the presence of three distinct color zones: blackened, greyish and brown (Fig. 1D and E).
The apical portion (1st knot from the apical bud to the 4th knot) of the plants exposed to the pollutant showed a higher percentage of necrosed leaf areas than the basal portion (5th knot from the apical bud to the 8th knot). In the leaflets from the apical portion of the plants exposed to 20 mg L-1, 45% of the leaf area showed necrosis, while only 6% of the leaf area of leaflets from the basal portion presented injuries at the end of the experiment (Fig. 3).
The leaflets from the basal portion of the plants exposed to 5, 10, 15 and 20 mg L-1 fluoride showed 28.7, 51.1, 75.4 and 182.7%, respectively, more fluoride content than the control (Fig. 4). At the basal portion of the plants, the pollutant contents were 46.6, 72.5, 106.5 and 219.4%, respectively. This was higher than in the control treatment (Fig. 4).
The correlation between the degree of leaf injury and the fluoride content in the leaves was significant (p<0.01) and high on both the basal and apical portions of the plants (0.86 and 0.88, respectively).
The leaflets of S. dulcis are glabrous (Fig. 5A; 6A-B; 7A-B) and hypostomatic (Fig. 5A and 6A), with a unisseriate epidermis where the cells show a well-defined shape in the adaxial and abaxial faces. One layer of compact cells forms the palisade parenchima (Fig. 7A-B), while four to six layers of armed cells form the spongy parenchima (Fig. 7A and E).
All fluoride treatments caused micromorphological damage to both the adaxial and abaxial epidermis (Fig. 5 and 6). The adaxial epidermis presented turgor loss and flattening of the outer periclinal wall (Fig. 5B), showed changes in the relief of the cell groups (Fig. 5C) and demonstrated the formation of concavities in some regions of the leaf blade (Fig. 5D). Besides the relief alteration, which gives the abaxial epidermis an irregular aspect (Fig. 6B), epicuticular wax erosion areas (Fig. 6C) and the presence of fungal hyphae were observed (Fig. 6D and E). The rupture of some epidermal regions exposed the inner tissues to the pollutant (Fig. 6D and F).
All concentrations of fluoride (5, 10, 15 and 20 mg L-1) led to a significant effect on the quantitative parameters assessed in the leaflets without any apparent fluoride injury, except on the height of abaxial epidermal cells (Tab. II). The plants exposed to 20 mg L-1 showed a decrease of 13.3 % in the thickness of the limb (Tab. II and Fig. 7B). The mesophyll and the epidermis represent 85 and 15 %, respectively, of the total thickness of the leaflet of S. dulcis in the control, and 83 and 17 % in the plants exposed to 20 mg L-1. The correlation between the thickness of the limb and the height of the cells of the palisade and spongy parenchyma was high (0.86 and 0.89, respectively) and significant (p<0.01). However, a significant alteration in the proportion of the palisade to spongy parenchyma was not observed. In the plants exposed to 20 mg L-1 there was a noticeable increase in the size of the chloroplasts (Fig. 7C-D).
The plants exposed to 10, 15 and 20 mg L-1 showed a significant increase (p<0.05) in the percentage of intercellular spaces in comparison with the control (Tab. II). They also had an accumulation of granules that were strongly stained (green) by toluidine blue (Fig. 7B and F) and droplets surrounding the ending veinlets (Fig. 7G) at the interface between the palisade and the spongy parenchyma.
According to the literature, the symptoms of the exposure to fluoride are described as marginal necrosis and apical necrosis. In the majority of studies, a more accurate description of the differences in color in the necrosis is not presented (Silva et al. 2000, Chaves et al. 2002, Oliva and Figueiredo 2005).
In the present work, the brownish color observed in the necrosis likely indicates the oxidation of phenolic compounds that accumulated in response to the high concentration of fluoride in regions where the drops of the fog settled. This is consistent with the observations of Pita-Barbosa et al. (2009) in leaves of Brachiaria brizantha and B. decumbens that were exposed to fluoride. In leaves of Salvinia auriculata, Peixoto et al. (2005) highlighted the round shape and dark brown color of the necroses caused by fluoride. Fornasiero (2001) described the leaf necroses in plants of Hypericum perforatum in response to fluoride as red-brownish, indicating possible differences among plant species.
S. dulcis plants reacted rapidly to the pollutant, corroborating the Silva et al. (2000) report, which discovered the high sensitivity of this species to fluoride. Silva et al. (2000) also observed necroses 24 h after the first exposure to the simulated rain containing 30 mg L-1 of fluoride without the appearance of chlorosis. In Hypericum perforatum plants exposed to the pollutant (Fornasiero 2001), chloroses preceded the necrosis of the leaf tissue, a finding also reported by Silva et al. (2000) in Gallesia gorazema. The high sensitivity of S. dulcis to fluoride leads to rapid tissue death and does not allow enough time for the formation of chlorosis. Nevertheless, the rapid outbreak of necrosis may be related to the exposure of the plants to high pollutant concentrations (Weinstein and Davison 2003). The symptoms observed in S. dulcis plants exposed to the fluoride fog in the present experiment were identical to those observed in previous experiments using a fluoride rain simulation (Sant'Anna-Santos and Azevedo 2007). This highlights the reliability of the use of the symptomatology in the diagnosis of the stress caused by the pollutant.
In S. dulcis the data measuring the accumulation of the pollutant suggest a higher capacity of accumulation by the leaves under expansion, as the dry matter from the apical portion showed a higher content of fluoride than the matter from the basal portion. The amount of fluoride accumulated and the degree of injury in the tissues may vary with the age of the leaf (Silva et al. 2000).
In S. dulcis, the leaves from the apical portion of the plant accumulated more fluoride than the basal leaves and showed a higher percentage of necrosed leaf areas. This was also observed in Magnolia ovata plants exposed to the pollutant (Sant'Anna-Santos et al. 2007). In some plant species there is a correlation between the degree of injury and the high rates of accumulation of the pollutant (Klumpp et al. 1995, Silva et al. 2000, Fornasiero 2001).
Fluoride, provided to a plant through simulated rain or fog, reaches the internal part of a leaf mainly throughout the cuticle. The fluoride may then be absorbed by the cells of the mesophyll, reaching the symplast, or the fluoride may be dragged by the transpiration stream to the ending veinlets where it is accumulated (Oliva and Figueiredo 2005). The fluoride distribution pattern in most grass species suggests that it is accumulated in tissues with high metabolic activity (Oliva and Figueiredo 2005). The entrance of the anion throughout the apoplast in the young tissues of plants is facilitated by the small amount of cutin and epicuticular waxes in the epidermal cells, and by the high amount of pectins (Kannan 1986) in comparison to expanded leaves.
Because attributing a symptom to a specific stress factor is difficult, the symptomatology requires other parameters, such as microscopic analysis, to ensure a precise diagnosis (Vollenweider et al. 2003, Reig-Arminaña et al. 2004). In this work the treatment with fluoride caused alterations in both surfaces of the epidermis at all assessed concentrations (5, 10, 15 and 20 mg L-1). The samples were taken from leaves without any apparent fluoride injury. The micromorphological alterations observed in the leaf blades of S. dulcis are most likely related to fluoride-induced changes in the cuticle and epicuticular wax structure, which would facilitate the entrance of fluoride into the epidermis and would allow, secondarily, the invasion of pathogens (Heredia et al. 1998). Similar results for this species were observed by Sant'Anna-Santos et al. (2006) in response to acid rain.
There are few reports on the effects of fluoride on leaf micromorphology (Chaves et al. 2002, Sant'Anna-Santos and Azevedo 2007, Sant'Anna-Santos et al. 2007), and little attention is given to this parameter as a prognostic biomarker. The presence of damage in samples from leaflets without apparent fluoride injury indicates the usefulness of micromorphology for field biomonitoring studies and as a biomarker for the presence of the pollutant in the atmosphere.
The green color given by toluidine blue indicates the phenolic nature of the granules and droplets observed through the light microscope, according to Briggs et al. (2005). According to Oliva and Figueiredo (2005), fluoride is accumulated in the boundaries of the ending veinlets, which explains the accumulation of phenolic compounds in this region. The accumulation of phenols has been interpreted as a defence mechanism of plants (Vaughn and Duke 1984, Changlian et al. 2006) and has been reported in other plant species exposed to fluoride (Chaves et al. 2002, Sant'Anna-Santos et al. 2007). The reduction in the thickness of leaflets that did not show symptoms of exposure to the pollutant reflects the alterations in leaf relief observed through scanning electron microscopy. Therefore, the use of light microscopy, among other techniques, is necessary for optimizing the characterization of fluoride phytotoxicity.
Most concentrations of fluoride used in the fog experiments caused a rapid development of necroses and induced leaf abscission, with the exception of the 5 mg L-1 one. Thus, this concentration can be used in further experiments to assess the chlorosis that precedes tissue necroses, as it would induce injuries more slowly. The symptoms observed in S. dulcis in response to fluoride are not plant-specific. S. dulcis shows color injuries, the beginning of necrosis at the basal portion of the leaflet and the highest percentage of the leaf area damaged by necrosis at the apical part of the plant. Therefore, in active biomonitoring studies, the assessment of specific patterns in the precise diagnosis of injuries caused by fluoride is strongly advised. The alterations in the structure and micromorphology were evident in the leaflet samples without any apparent fluoride injury, demonstrating that these tools are potentially useful in the prognosis of fluoride injury. The use of such techniques in future experiments, in addition to physiological and ultra-structural analyses, will be essential for elucidating the phytoxicity caused by pollutants.
The authors thank Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) for a scholarship, the Nursery of Parque Estadual do Rio Doce-MG (NPERD) for supplying the plants and the Núcleo de Microscopia e Microanálise (Universidade Federal de Viçosa-UFV) for helping with the elaboration of the electron microscopy part of this work.
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Bruno F. Sant'Anna-Santos
Manuscript received on August 23, 2010
accepted for publication on November 16, 2010