Abstracts
Abstract
Aim: The measurement of the caloric content evidences the amount of energy that remains in the leaf and that can be released to the aquatic trophic chain. We assessed the energy content of leaves from five riparian tree species of a forest fragment in south Brazil and analyzed whether leaf caloric content varied between leaf species and between seasons (dry and wet). The studied sites are located in Northwest of Paraná State, inside a Semi-Deciduous Forest fragment beside two headwater streams.
Methods
Sampling sites were located along the riparian vegetation of these two water bodies, and due to its proximity and absence of statistical differences of caloric values, analyzed as one compartment.
Results
Caloric content varied significantly among species and among all pairs of species, with exception of Nectandra cuspidata Ness and Calophyllum brasiliensis Cambess. Two species presented significant differences between seasons, Sloanea guianensis (Aubl.) Ben and Calophyllum brasiliensis Cambess.
Conclusions
The absence of significant seasonal differences of energy content for some species may be due to the characteristics of the tropical forest, in which temperature did not varied dramatically between seasons. However, the energy differed between species and seasons for some species, emphasizing the necessity of a preliminary inspection of energy content, before tracing energy fluxes instead of using a single value to all species from riparian vegetation.
Keywords:
leaf litter; energy; allochthonous organic matter; headwater stream; Atlantic Forest
Resumo
Objetivo: O conteúdo calórico evidencia a quantidade de energia que permanece na folha e que pode ser libertado para a cadeia trófica aquática. O presente estudo teve como objetivo investigar o conteúdo calórico de folhas de cinco espécies de árvores de vegetação ripária e avaliar sua variação interespecífica e sazonal (seca e chuva).
Métodos
As coletas foram realizadas trimestralmente durante um ano, na área de vegetação ripária de um fragmento florestal no sul do Brasil. Os locais de amostragem foram localizados ao longo da vegetação ripária desses dois corpos de água, e devido à sua proximidade e ausência de diferenças estatísticas significativas do conteúdo calórico, analisados em conjunto.
Resultados
O conteúdo calórico variou significativamente entre as espécies e entre todos os pares de espécies, com exceção de Nectandra cuspidata Ness e Calophyllum brasiliensis Cambess. Duas espécies apresentaram diferenças significativas entre estações, Sloanea guianensis (Aubl.) Ben e Calophyllum brasiliensis Cambess.
Conclusões
A ausência de diferenças significativas sazonais no teor energético de algumas espécies pode ser devido às características da floresta tropical, em que a temperatura não variou significativamente entre as estações do ano. No entanto, a diferença de energia entre as espécies e de sazonalidade para algumas espécies, enfatiza a necessidade de uma inspeção preliminar no teor energético, antes de traçar fluxos de energia, em detrimento do uso de um único valor para toda a vegetação ripária.
Palavras-chave:
serapilheira; energia; matéria orgânica alóctone; riacho de cabeceira; Mata Atlântica
1 Introduction
Food webs of small streams in forested watersheds are based almost entirely on detritus (Trevisan & Hepp, 2007Trevisan, A. and Hepp, L.U. Dinâmica de componentes químicos vegetais e fauna associada ao processo de decomposição de espécies arbóreas em um riacho do norte do Rio Grande do Sul, Brasil. Neotropical Biology and Conservation, 2007, 2(1), 54-60.; Sánchez-Carmona et al., 2012Sánchez-Carmona, R., Encina, L., Rodríguez-Ruiz, A., RODRÍGUES-SÁNCHEZ, M.V. and GRANADO-LORENCIO, C. Food web structure in Mediterranean streams: exploring stabilizing forces in these ecosystems. Aquatic Ecology, 2012, 46(3), 311-324. http://dx.doi.org/10.1007/s10452-012-9400-5.
http://dx.doi.org/10.1007/s10452-012-940...
) and detritus can be any form of non-living organic matter, including different types of plant tissues, such as leaves (Moore et al., 2004Moore, J.C., Berlow, E.L., Coleman, D.C., Ruiter, P.C., Dong, Q., HASTINGS, A., JOHNSON, N.C., MCCANN, K.S., MELVILLE, K., MORIN, P.J., NADELHOFFER, K., ROSEMOND, A.D., POST, D.M., SABO, J.L., SCOW, K.M., VANNI, M.J. and WALL, D.H. Detritus, trophic dynamics and biodiversity. Ecology Letters, 2004, 7(7), 584-600. http://dx.doi.org/10.1111/j.1461-0248.2004.00606.x.
http://dx.doi.org/10.1111/j.1461-0248.20...
). Leaves represents up to 70% of the allochthonous organic matter biomass provided by riparian vegetation to streams (Gonçalves Junior & Callisto, 2013Gonçalves JUNIOR, J.F. and Callisto, M. Organic-matter dynamics in the riparian zone of a tropical headwater stream in Southern Brasil. Aquatic Botany, 2013, 109, 8-13. http://dx.doi.org/10.1016/j.aquabot.2013.03.005.
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) and litter fall dynamics on the tropics is composed of a few species that contribute with high values of leaf biomass (Gonçalves Junior et al., 2014Gonçalves jUNIOR, J.F., Rezende, R.S., Gregório, R.S. and Valentin, G.C. Relationship between dynamics of litterfall and riparian plant species in a tropical stream. Limnologica, 2014, 44, 40-48. http://dx.doi.org/10.1016/j.limno.2013.05.010.
http://dx.doi.org/10.1016/j.limno.2013.0...
). These leaves are accumulated, processed and transported downstream, providing energy supply to the aquatic system (Moore et al., 2004Moore, J.C., Berlow, E.L., Coleman, D.C., Ruiter, P.C., Dong, Q., HASTINGS, A., JOHNSON, N.C., MCCANN, K.S., MELVILLE, K., MORIN, P.J., NADELHOFFER, K., ROSEMOND, A.D., POST, D.M., SABO, J.L., SCOW, K.M., VANNI, M.J. and WALL, D.H. Detritus, trophic dynamics and biodiversity. Ecology Letters, 2004, 7(7), 584-600. http://dx.doi.org/10.1111/j.1461-0248.2004.00606.x.
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).
The energy supplied by leaves can be expressed by their caloric content, which measure the combustion heat of specific dry mass and can describe energy patterns in ecological process (Lindeman, 1942Lindeman, R.L. The trophic dynamic aspect of ecology. Ecology, 1942, 23(4), 399-418. http://dx.doi.org/10.2307/1930126.
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). Caloric value can be used as a coefficient index when biomass is converted into equivalent energy and it is the primary energy storage available to high trophic levels, constituting a helpful tool to study energy transfer (Yajing et al., 2007Yajing, B., Zhenghai, L., Xingguo, H., Guodong, H. and Yankai, Z. Caloric content of plant species and its role in a community of Inner Mongolia, China. Leymus chinensis steppeActa Ecologica Sinica, 2007, 27(11), 4443-4451. http://dx.doi.org/10.1016/S1872-2032(08)60002-5.
http://dx.doi.org/10.1016/S1872-2032(08)...
; Lin & Cao, 2008Lin, H. and Cao, M. Plant energy storage strategy and caloric value. Ecological Modelling, 2008, 217(1-2), 132-138. http://dx.doi.org/10.1016/j.ecolmodel.2008.06.012.
http://dx.doi.org/10.1016/j.ecolmodel.20...
). It is directly related to leaves biodegradability, which is influenced by the presence of low energetic inorganic compounds (Costa, 1982Costa, A.F. Farmacognosia. Lisboa: Fundação Calouste Gulbenkian, 1982.), or dependent on the presence of high energetic and organic compounds such as sugar and fatty acids (Francisco & Pinotti, 2000Francisco, I.A. and Pinotti, M.H.P. Cyanogenic glycosides in Plants. Brazilian Archives of Biology and Technology, 2000, 43(5), 487-492. http://dx.doi.org/10.1590/S1516-89132000000500007.
http://dx.doi.org/10.1590/S1516-89132000...
). Such energetic content of leaves may be detected by grazers, which enhance the consumption rates of high quality plants (Prado & Heck, 2011Prado, P. and Heck, K.L. Seagrass selection by omnivorous and herbivorousconsumers: Determining factors. Marine Ecology Progress Series, 2011, 429, 45-55. http://dx.doi.org/10.3354/meps09076.
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).
The effective amount of caloric content provided by leaves can change according to the species, climatic conditions, water supply and dissolved mineral salt concentration (Dourado et al., 2004Dourado, E.C.S., Peretti, D. and Benedito-CECILIO, E. Variability in the caloric content of vascular plants in two Paraná State reservoirs. Acta Scientiarum. Biological Sciences, 2004, 26(2), 137-142.). High light intensity can improve caloric gain in plants growthand season variability changes energy transfer and storage of plant parts (Meletiou-Christou et al., 1994Meletiou-Christou, M.S., Rhizopoulou, S. and Diamantoglou, S. Seasonal changes of carbohydrates, lipids and nitrogen content in sun and shade leaves from four mediterranean evergreen sclerophylls. Environmental and Experimental Botany, 1994, 34(2), 129-140. http://dx.doi.org/10.1016/0098-8472(94)90032-9.
http://dx.doi.org/10.1016/0098-8472(94)9...
; Núnez-Regueira et al., 2004Núñez-Regueira, L., Proupín-Castiñeiras, J. and Rodríguez-Añón, J.A. Energy evaluation of forest residues originated from shrub species in Galicia. Bioresource Technology, 2004, 91(2), 215-221. http://dx.doi.org/10.1016/S0960-8524(03)00169-X. PMid:14592753.
http://dx.doi.org/10.1016/S0960-8524(03)...
). Caloric content can be a function of the plants’ nutritive status and life history (Yajing et al., 2007Yajing, B., Zhenghai, L., Xingguo, H., Guodong, H. and Yankai, Z. Caloric content of plant species and its role in a community of Inner Mongolia, China. Leymus chinensis steppeActa Ecologica Sinica, 2007, 27(11), 4443-4451. http://dx.doi.org/10.1016/S1872-2032(08)60002-5.
http://dx.doi.org/10.1016/S1872-2032(08)...
). For mangrove plant species such as Avicennia marina and Aegiceras corniculatum, authors recorded values of 19.25 kJ g–1 and 21 kJ g–1, respectively (Lin et al., 2007Lin, Y.M., Liu, J.W., Xiang, P., Lin, P., Ding, Z.H. and Sternberg, L.S.L. Tannins and nitrogen dynamics in mangrove leaves at different age and decay stages (Jiulong River Estuary, China). Hydrobiologia, 2007, 583(1), 285-295. http://dx.doi.org/10.1007/s10750-006-0568-3.
http://dx.doi.org/10.1007/s10750-006-056...
; Zhou et al., 2010Zhou, H.C., Wei, S.D., Zeng, Q., Zhang, L.H., Tam, N.F. and Lin, Y.M. Nutrient and caloric dynamics in Avicennia marina leaves at different development and decay stages in Zhangjiang River Estuary, China. Estuarine, Coastal and Shelf Science, 2010, 87(1), 21-26. http://dx.doi.org/10.1016/j.ecss.2009.12.005.
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), while for freshwater systems, riparian vegetation and macrophytes leaves reached up to 19.5 kJ g–1 (Dourado et al., 2004Dourado, E.C.S., Peretti, D. and Benedito-CECILIO, E. Variability in the caloric content of vascular plants in two Paraná State reservoirs. Acta Scientiarum. Biological Sciences, 2004, 26(2), 137-142.).
The measurement of the caloric content as a surrogate for energy content evidences the amount of energy that remains in the leaf and that can be released to the aquatic trophic chain. We assessed the energy content of leaves from five riparian tree species of a forest fragment in south Brazil and analyzed whether leaf energy content varied between leaf species and between seasons (dry and wet).
2 Material and Methods
2.1 Study area
The studied sites are located in Northwest of Paraná State (Figure 1), inside a Semi deciduous forest fragment from Atlantic Forest called Caiuá Ecological Station (CES). Inside CES drains two headwater streams, 900 meters apart, named Conceição and Scherer. Sampling sites were located along the riparian vegetation of these two water bodies, and due to its proximity, analyzed as one compartment – CES riparian areas. Statistical analyzes were performed prior to grouping these areas, no differences were detected between species along both riparian areas. CES has an area of 1.427,30 ha, with high variety of native species in the riparian vegetation areas, along with rare and endangered species. Families with high richness are Leguminosae, Myrtaceae e Lauraceae.
Sampling stations in Caiuá Ecological Station riparian areas along Conceição and Scherer streams, Northwest Paraná State.
Conceição stream (22°35’15.0”S 052°53’29.0”W) banks are well protected by a dense riparian cover, with a diversity of vegetation layers such as herbaceous, shrubs and trees with different heights and thickness. Leaf litter accumulates on the banks and margins, protecting the soil and are promptly available to reach the stream channel, which catches up to 450 m length. Scherer stream (22°36’06,7” S 052°53’02,0” W) banks presents dense riparian cover along with clear-cut areas for tracks, along a 1600 m longitudinal length. There are high accumulation leaf litter over the banks and immediate margin, some can readily reach stream’ channel, while other are frequently buried by bank displacement due to erosion.
2.2 Sampling
Leaves were sampled in July 2008, October 2008, January 2009 and April 2009 (which are representative of annual seasons: July and April – dry season; October and January – wet season) with the help of twelve nets (1 m2, 5 mm mesh size). The nets were displayed randomly six at each margin of the streams – riparian vegetation areas, which represents the potential stock that can be transported to the stream. All nets were kept in the field for a month before sampling. The species with high and constant biomass input through all the sampling period were chosen for identification and caloric content analysis. Leaf samples were dried up in a lamp greenhouse, at approximately 60ºC and weighted repeatedly until reaching a constant weight. Species were: Nectandra cuspidata Ness (Lauraceae), Calophyllum brasiliensis Cambess (Clusiaceae), Alchornea triplinervia (Spreng.) Müll.Arg. (Euphorbiaceae) and Sloanea guianensis (Aubl.) Ben (Elaeocarpaceae). The fifth specie belong to the Bignoniaceae family and it was not possible to identify to species level. Due to its high biomass input through the months, it was considered for analyzes and called sp. B.
Sub-sampling was conducted after leaf retrieval from the field. One sub-sample consisted of four randomly peaked leafs of a specific species (Table 1). Each sub-sample was dried and macerated to powder material which was combusted using a calorimeter PARR 1620 (Automatic Isoperibol Bomb Calorimeter - Parr Instrument Company) for caloric content determination, expressed as KJ.g–1 of dry weight. Leaves were selected in similar decomposition stages, avoiding extreme ones (young green leaves, or in an advanced decomposition stage), searching for similar sizes and coloration.
Number of sub-samples (N) and mean ± standard deviation (Mean ± SD) of caloric content (KJ.g–1 ) of each species and months from CES riparian areas.
2.3 Data analysis
There were no significant differences in the caloric content between leaf samples of the same species, which occurred in both riparian areas (Conceição and Scherer), so we analyzed the caloric content of leaves from CES riparian areas as one. In order to verify differences in the average caloric content between species it was applied a one-way ANOVA test. To investigate for seasonal differences in the caloric content of species, a one-way ANOVA was applied separately for each species. For significant differences, post-hoc Tukey HSD test was used to determine which pair of observations differed from each other. Analyses were conducted in the software Statistica 7.1® (Statsoft, 2005STATSOFTStatistica (data analysis software system)Version 7.1 for WindowsTulsaStatsoft2005) with a level of significance of 5%.
3 Results
Caloric content varied significantly among species (F4, 157= 157.52; p < 0.050) and among all pairs of species (Post-hoc Tukey HSD test, p < 0.050), with exception of N. cuspidata and C. brasiliensis (Post-hoc Tukey HSD test, p = 0.685) (Figure 2).
Mean (box) and standard deviation (line) in caloric content of leaves from tree species from CES riparian areas. Sg = Sloanea guianensis; Nc = Nectandra cuspidata; Cb = Calophyllum brasiliensis; At = Alchornea triplinervia; sp. B = specie of the Bignoniaceae family.
The largest caloric content was observed for Nectandra cuspidata, varying from 17.84 to 23.68KJ.g–1,and lower caloric content for sp. B. varying from 9.27 to 18.52KJ.g–1. Two species presented significant differences between seasons (Table 2), S. guianensis and C. brasiliensis (F3,40= 4.612; p < 0.050 and F3,15=5.15; p=0.020, respectively). Especially between January and April for S. guianensis (Post-hoc Tukey HSD test, p < 0.050), and October and April for C. brasiliensis (Post-hoc Tukey HSD test, p = 0.030). For all other species no seasonal differences were detected (Figure 3).
ANOVA test for seasonal variation of caloric content (KJ.g–1 ) for each species of CES riparian area.
Temporal variationin the caloric content of tree leaves from CES riparian area. Mean (box) and standard deviation (line). Please note that graphics have different Y-axis scales, in order to better visualize the results. sp. B = specie of the Bignoniaceae family.
4 Discussion
Caloric content of the most dominant leaf species in the riparian area of CES vegetation ranged from 9.3 to 23.7 KJ.g–1 dry weight. Semi deciduous leaf species presents highenergetic amplitude and are available to aquatic ecosystems once it reaches the water bodies. The reported species presented higher amplitude than the 11.7 to 19.2 KJ.g–1 reported for riparian vegetation specimens from the upper Paraná river basin (Dourado et al., 2004Dourado, E.C.S., Peretti, D. and Benedito-CECILIO, E. Variability in the caloric content of vascular plants in two Paraná State reservoirs. Acta Scientiarum. Biological Sciences, 2004, 26(2), 137-142.), and aquatic macrophytes from the same basin (7.9 to 19.5 KJ.g–1) (Lopes et al., 2006Lopes, C.A., Faria, A.C.E.A., Manetta, G.I. and Benedito-CECILIO, E. Caloric density of aquatic macrophytes in different environments of the Baía River Subsystem, Upper Paraná River Floodplain, Brazil. Brazilian Archives of Biology and Technology, 2006, 49(5), 835-842. http://dx.doi.org/10.1590/S1516-89132006000600018.
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). The caloric content of vascular plants from Semi deciduous forest vary greatly and highlights the importance of leaf diversity as energy input to aquatic systems. Caloric content amplitude varied less for herbaceous species on a grassland ecosystem ranging from 13.2 to 18.1 KJ.g-1 (Yajing et al., 2007Yajing, B., Zhenghai, L., Xingguo, H., Guodong, H. and Yankai, Z. Caloric content of plant species and its role in a community of Inner Mongolia, China. Leymus chinensis steppeActa Ecologica Sinica, 2007, 27(11), 4443-4451. http://dx.doi.org/10.1016/S1872-2032(08)60002-5.
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), much lower than those reported for tree leafs in our study.
Caloric content differed between pairs of species with exception of N. cuspidata and C. brasiliensis. Yang et al. (2003)Yang, J., Weske, B., Jie, C. and Nin, J. Quantitative caloric energy distributionand variations in two rice varieties related to different nitrogen application levels in paddy field. Journal of Plant Nutrition, 2003, 26(4), 709-729. http://dx.doi.org/10.1081/PLN-120018560.
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reported that caloric values varies among plant species and within species in different environments, due to chemical composition of the organic substances (Lin et al., 2007Lin, Y.M., Liu, J.W., Xiang, P., Lin, P., Ding, Z.H. and Sternberg, L.S.L. Tannins and nitrogen dynamics in mangrove leaves at different age and decay stages (Jiulong River Estuary, China). Hydrobiologia, 2007, 583(1), 285-295. http://dx.doi.org/10.1007/s10750-006-0568-3.
http://dx.doi.org/10.1007/s10750-006-056...
). It is noteworthy that plants that grow better and can achieve higher biomass presents higher caloric content (Yajing et al., 2007Yajing, B., Zhenghai, L., Xingguo, H., Guodong, H. and Yankai, Z. Caloric content of plant species and its role in a community of Inner Mongolia, China. Leymus chinensis steppeActa Ecologica Sinica, 2007, 27(11), 4443-4451. http://dx.doi.org/10.1016/S1872-2032(08)60002-5.
http://dx.doi.org/10.1016/S1872-2032(08)...
).Major caloric content was recorded for Nectandra cuspidata (17.8 KJ.g–1 to 23.7 KJ.g–1 dry weight). Some studies registered the presence of cyanogenic glycosides to species of the genus Nectandra (Francisco & Pinotti, 2000Francisco, I.A. and Pinotti, M.H.P. Cyanogenic glycosides in Plants. Brazilian Archives of Biology and Technology, 2000, 43(5), 487-492. http://dx.doi.org/10.1590/S1516-89132000000500007.
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), that when hydrolyzed by enzymes, produce sugar, fatty acids, aldehyde or ketone and hydrocyanic acid (Buhrmester et al., 2000Buhrmester, R.A., Ebinger, J.E. and Seigler, D.S. Sambunigrin and cyanogenic variability in populations of Sambucus canadensis L. (Caprifoliaceae). Biochemical Systematics and Ecology, 2000, 28(7), 689-695. http://dx.doi.org/10.1016/S0305-1978(99)00105-2. PMid:10854744.
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) that contribute directly to the energetic potential of the species. Yajing et al. (2007)Yajing, B., Zhenghai, L., Xingguo, H., Guodong, H. and Yankai, Z. Caloric content of plant species and its role in a community of Inner Mongolia, China. Leymus chinensis steppeActa Ecologica Sinica, 2007, 27(11), 4443-4451. http://dx.doi.org/10.1016/S1872-2032(08)60002-5.
http://dx.doi.org/10.1016/S1872-2032(08)...
reported that plants with high caloric values are better competitors than those with low caloric content. Minor caloric content was observed for sp. B (9.3 KJ.g–1), which had high inorganic compounds concentration after combustion on the calorimeter. Inorganic compounds can consist in carbonate, chloride and other oxides that have been found in other Bignoniaceae species (Costa, 1982Costa, A.F. Farmacognosia. Lisboa: Fundação Calouste Gulbenkian, 1982.; Alves et al., 2010Alves, M.S.M., Mendes, P.C., Vieira, J.G.P., Ozela, E.F., Barbosa, W.L.R. and Silva Junior, J.O.C. Análise farmacognóstica das folhas de Arrabidaea chica (Humb. & Bonpl.) b. Verlot. Bignoniaceae. Revista Brasileira de Farmacognosia, 2010, 20(2), 215-221. http://dx.doi.org/10.1590/S0102-695X2010000200013.
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).
The caloric content of S. guianensis and C. brasiliensis varied seasonally with higher caloric values in the dry month (April). Some studies found strong seasonality of litter fall in the driest months (Selva et al., 2007Selva, E.C., Couto, E.G., Johnson, M.S. and Lehmann, J. Litter fall production and fluvial export in headwater catchments of the southern Amazon. Journal of Tropical Ecology, 2007, 23(03), 329-335. http://dx.doi.org/10.1017/S0266467406003956.
http://dx.doi.org/10.1017/S0266467406003...
) with low temperatures (Lin & Cao, 2008Lin, H. and Cao, M. Plant energy storage strategy and caloric value. Ecological Modelling, 2008, 217(1-2), 132-138. http://dx.doi.org/10.1016/j.ecolmodel.2008.06.012.
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). During our study the temperature did not varied dramatically between seasons, however, the driest months corresponded tocolder ones. During colder seasons plants accumulate more energy to reduce heat lose, energy is condensed and the caloric content increase (Lin & Cao, 2008Lin, H. and Cao, M. Plant energy storage strategy and caloric value. Ecological Modelling, 2008, 217(1-2), 132-138. http://dx.doi.org/10.1016/j.ecolmodel.2008.06.012.
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). Caloric difference between species and seasons, for some species, emphasize the necessity of a preliminary inspection of energy content before tracing energy fluxes instead of using a single value to each species.
The amount of energy provided by leaves from CES riparian vegetation to aquatic ecosystems are highly variable and reaches high amplitude, due to species specific characteristics and seasonality. Knowledge about energetic content of leaves can help elucidating fish trophic behavior, since they depend on food resources derived from the adjacent vegetation (Uieda & Kikuchi, 1995Uieda, V.S. and Kikuchi, R.M. Entrada de material alóctone (detritos vegetais e invertebrados terrestres) num pequeno curso de água corrente na costa de Botucatu, São Paulo. Acta Limnologica Brasiliensia, 1995, 2, 105-114.). Higher caloric content valueshave been registered for detritivorous fishes from aquatic environments with preserved vegetation (Pazianoto et al., 2013Pazianoto, L.H.R., Souza, M.L.S., Veronezzi, A.L. and Benedito-CECILIO, E. Influência do ambiente no conteúdo calórico e na condição fisiológica de duas espécies migradoras de peixes neotropicais. Iheringia. Série Zoologia, 2013, 103(3), 206-213. http://dx.doi.org/10.1590/S0073-47212013000300001.
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), since allochthonous source availability inside water bodies are proportional to vegetation coverage (Sarragiotto et al., 2014Sarragiotto, M.C., Souza Filho, E.E., Couto, E.V., MANETTA, G.I. and BENEDITO-ceciliO, E. The influence of vegetal cover on carbon assimilation by (Characiformes: Prochilodontidae) in the upper Paraná river floodplain. ProchiloduslineatusActa Scientiarum. Biological Sciences, 2014, 36(3), 293-298. http://dx.doi.org/10.4025/actascibiolsci.v36i3.19820.
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). Overall, the maintenance of riparian vegetation represents one of the most important features for headwaters equilibrium since it propitiates sources of energy for different organisms.
Acknowledgements
The authors would like to thank all those who helped in the field/lab work: José Nelson Campanha e Doraci de Oliveira in behalf of Instituto Ambiental do Paraná (IAP) for providing accommodation and support for all the field work; CNPq and CAPES, by financial support; PEA/Nupélia-UEM by logistic support; and Jaime Luiz Lopes Pereira and Celso Pereira dos Santos, by technician support to this work.
References
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Publication Dates
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Publication in this collection
Jul-Sep 2015
History
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Received
20 Nov 2014 -
Accepted
30 June 2015