Soil quality of first rotation Eucalyptus stands growing on an Andisol using soil microbial indicators

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Journal of Soil Science and Plant Nutrition, 2012, 12 (3) 599-603 Soil quality of first rotation Eucalyptus stands growing on an Andisol using soil microbial indicators C. Córdova 1*, M. Barrandeguy 2 and E. Navarrete 2 1 Departamento de Suelos y Recursos Naturales. Facultad de Agronomía. Universidad de Concepción. Campus Chillán. Av. Vicente Méndez 595. Chillán. Chile. Telephone: +56 42 208853 - +56 42 208886. 2 Escuela de Ciencias y Tecnologías. Universidad de Concepción. Campus Los Ángeles. Juan Antonio Coloma 0201. Los Ángeles. Chile. * Corresponding author: cacordov@udec.cl Abstract The potential soil biological change due to the establishment of Eucalyptus plantations in volcanic soils has not been reported. The objective of this research was to assess the soil quality of Eucalyptus stands growing on a volcanic ash derived soil, compared with a natural forest (Nat-forest, control) and a Pinus radiata stand, previously established to the Eucalyptus stand. A complete randomised design was established (n=4) within Nat-forest and commercial plantations. Soil samples (10 cm) were taken in autumn, to measure soil microbial biomass (C biom ) by soil fumigationextraction, and CO 2 -C respiration (C min ) from soil microorganisms by soil incubation. Metabolic quotient (q met ) was calculated to compare (p < 0.05) the microbial efficiency of the soil biomass between treatments. As expected, Nat- forest showed the largest C biom and C min (p < 0.05). However, no differences were found between E. globulus, E. nitens and P. radiata (p < 0.05). The low C biom and C mic in Eucalyptus stands might be attributed to the effect of recalcitrant inputs of C from the previous pine plantation, although the efficiency of the soil microbial population (q met ) was not affected (p < 0.05) by the C quality of the plantations. Thus, it seems that Eucalyptus stands are not entirely detrimental to the soil quality of volcanic soils of temperate forest ecosystems. Keywords: Soil organic matter, carbon mineralization, forest soil, andisol. 599

600 Cordova et al. 1. Introduction Eucalyptus nitens and Eucalyptus globulus are the main plant Eucalyptus species planted in Chile due to their high production capability associated with tolerance to low temperatures. E. nitens in particular shows volumetric increments of 30 to 45 m 3 ha -1 y -1, and is better adapted to low temperatures than E. globulus. On the other hand, volume growth rate of E. globulus is in the range of 20 to 25 m 3 ha -1 y -1, and naturally losses part of its branches during its growing cycle (Muñoz et al., 2005). Aiming to improve stand yield, forest management is similar for both species, which consists of soil tillage, N applications, and control of invasive vegetation (Guerra and Puentes, 2002). However, there is no information about how these practices affect soil quality in the South of Chile. Soil microbial biomass has been used to assess soil quality under Eucalyptus stands under different conditions in both tropical and subtropical regions, i.e., evaluating the impact of machinery on soil tillage (Ilstedt et al., 2006), assessing land use from grassland to E. grandis (Sicardi et al, 2004), and assessing the effect of native forest, regenerated native and Eucalyptus forest (Behera and Sahani, 2003). However, as far as we know, potential soil change due to the establishment of Eucalyptus plantations in volcanic soils has not been reported. The piedmont region between 36 o S and 38 o S has a large potential to sustain Eucalyptus plantations (more than 250000 ha planted, INFOR, 2008), but the volcanic soils where Eucalyptus is being planted is in several cases susceptible to being degraded, particularly if soil C stock is depleted (Dube et al., 2009). Despite progress on management of Eucalyptus stands, the role of soil in vulnerable pre-mountain ecosystems of South America has not received enough attention. Therefore, in order to evaluate the soil quality of Andisols, this research assessed an active fraction of the organic matter -the soil microbial biomass, under Eucalyptus plantations located at the piedmont of the Andes mountains (South of Chile). 2. Materials and methods The study area was located at the piedmont of the Andes mountains of Chile (460 m.a.s.l., latitude 37º 32 S, longitude 71º 55 W). The top 10 cm of Santa Bárbara soil (Typic Haploxerands) showed characteristics of Andisols (Shoji et al., 1993) such as, high organic matter content (6 to 17%) and low bulk density (0.7 to 1.0 g cm -3 ), low ph (5.4 to 5.9), and low available P (6.2 ppm). The climate of this region is temperate-mediterranean (Novoa and Villaseca, 1989). The native forest in hydromorphic conditions of this region has been progressively replaced by Pinus and Eucalyptus plantations, as well as by arable crops. Therefore, we assessed soil microbial biomass within natural forest, Pinus radiata, Eucalyptus nitens and Eucalyptus globulus plantations. The native forest (26 ha) is a renewal of transitional evergreen-sclerophyll forest, occasionally affected by human interventions. The E. nitens (3 ha) and E. globulus (3 ha) stands in site were planted on a square grid design at a density of 1600 stems ha -1 (1996), over interspaced rows left by the previous Pinus radiata plantation. After six years of plantation, the growing parameters of the stands of E. nitens and E. globulus were similar, as shown in Table 1.

Soil quality of first rotation eucalyptus stands growing on an Andisol using soil microbial indicators 601 Table 1. Growing parameters of Eucalyptus stands planted on a volcanic soil at the South-central piedmont of Chile. Dasometric index Eucalyptus nitens Eucalyptus globulus Diameter breast height (cm) Total height (m) Canopy diameter (m) Canopy length (m) Dominant height (m) Volume (m 3 stem -1 ) 8.18 12.85 0.45 12.25 24.13 0.14 8.70 10.50 0.60 13.57 21.54 0.14 Lowercase letters across the rows correspond to statistical differences between treatments using Tuckey test (p 0.05). Soil samples were taken at 10 cm depth of the topsoil in autumn (2004) from experimental plots (25m x 10m) arranged in a complete random design, with four replicates (n=4). After collection, soil samples were stored at 4 o C until analysis. Prior to soil microbial analysis, soils were thoroughly mixed and sieved at 2 mm, and roots and gross plant/tree residues were removed from the samples. Soil microbial biomass (C biom ) was measured using the fumigation-extraction method with N-ninhydrine reagent (Joergensen and Brookes, 1990). Samples were adjusted to 25% of water capacity and 25 g of soil were fumigated (in three replicates) whilst another portion of the same weight was used as a control (non-fumigated, three replicates). The fumigation was carried out applying ethanol-free CHCl 3 on the samples for 24 hours at 25ºC. The fumigant was removed, and soil samples were extracted with 100 ml of 0.5 M K 2 SO 4, shaken for 30 min and centrifuged at 2000 g for 5 min. Soil extracts were filtered (2.5 µm), and aliquots of 2 ml were transferred to 50 ml test tubes and 1 ml of ninhydrin reagent was added and mixed, to be placed afterwards on a boiling water bath for 25 min. Samples were cooled and 20 ml of 50% ethanol was added. Absorbance (570 nm) of the samples and blanks (0.5 M K 2 SO 4 ) were measured in a spectrophotometer (Perkin Elmer, Junior Model 35). A standard solution of L-leucine at different concentrations (0, 2.5, 5, 7.5, 10, and 15 g µg N ml -1 ) was used to plot a calibration curve against the measured absorbance values to obtain ninhydrin reactive N. C biom was calculated as C biom = 31 x ninhydrin-n (Ocio and Brookes, 1990). Microbial activity was measured as CO 2 -C evolved (C min ) after the soil was incubated at 22 o C for 10 days (Alef and Nannipieri, 1995) and three sub-samples (25 g) from each field repetition were individually incubated in a sealed glass container (capacity of 1 L) including an alkaline solution (0.5 M NaOH). At the end of the incubation period, CO 2 -C was measured by removing the alkaline trap, adding BaCl 2 and titrating with 0.1 N HCl. The metabolic efficiency of the soil microbial biomass (q met ) was evaluated as the ratio between soil microbial respiration and the microbial biomass (Xu et al., 2006). Analysis of variance (F test) for complete randomised design was applied to assess soil microbial variables. 3. Results and discussion C biom showed its largest value (p 0.05) under Natforest soil and no differences between pine plantation and species of Eucalyptus were recorded (Table 2). Similar values have been found for temperate natural forests elsewhere (Saviozzi et al., 2001), whilst C biom from Eucalyptus soil was in the range of reported values for non volcanic soils (Mendham et al., 2002).

602 Cordova et al. Soil respiration followed a similar trend, Nat-forest > E. nitens > E. globulus > P. radiata, whilst the q met showed no statistical differences between the stands and the Nat-forest (Table 2). Table 2. Soil microbial and metabolic activity in natural forest and Pinus and Eucalyptus stands in the study area. Parameters Natural forest Pinus radiata Eucalyptus nitens Soil microbial biomass (µg C g soil -1 ) Soil microbial respiration (µg CO 2 -C g soil -1 ) Metabolic quotient -1 (µg CO 2 -C mg C biom ) Eucalyptus globulus 1333.60 a 391.55 b 498.7 b 504.07 b 216.47 a 83.02 b 102.61 b 86.23 b 16.66 a 23.81 a 20.81 a 16.74 a The large C biom and soil microbial activity at Nat-forest is likely due to the diversity of organic inputs from the understory vegetation that improves litter quality (Jia et al., 2005). In contrast, C biom in soils under plantation might be decreased by the effect of pine tree residues that have a detrimental effect on the microbial activity. Pine litter contains more recalcitrant compounds as the stand becomes older (waxes, lipids, cutins and resins), and difficult to be metabolised by soil microorganisms (Gartzia et al., 2011). Despite no significant differences (p < 0.05) in C biom and C min between Eucalyptus and Pinus stands, these indicators showed some increase under Eucalyptus stands. The Nat-forest showed the smaller q met indicator. The trend was Nat-forest < E. globulus < E. nitens < P. radiata, but there were no differences between treatments (p < 0.05) (Table 2). Despite statistical differences, the soil under E. globulus showed the same q met coefficient as Nat-forest, which indicates an efficient microbial biomass community, capable of incorporating and maintaining larger C substrates into their metabolic processes against losses through respiration, better than E. nitens and P. radiata stands. Pine residues might influence an input of low metabolisable C compounds (Dube et al., 2009) to this first rotation of Eucalyptus, but the microbial activity seems to recover with time. Perhaps at the end of the first rotation of Eucalyptus, the organic matter provided by the above biomass and root exudates might better define the quality of Eucalyptus litter, and the growth of the microbial biomass component. 4. Conclusions The biological quality of the pre-mountains Andisols was affected by E. nitens and E. globulus stands, as shown by the small size of the microbial biomass pool and its respiration activity when compared with a natural forest. However, the biological indicator q met between the plantations and the natural forest did not show differences (p < 0.05). Thus, it seems that Eucalyptus stands have at some extend, a detrimental effect on the soil quality of Andisols of temperate forest ecosystems. Acknowledgements The authors thank the support of The University of Concepción that funded this research (DIUC 203415.004-1.0).

Soil quality of first rotation eucalyptus stands growing on an Andisol using soil microbial indicators 603 References Alef, K., Nannipieri, P., 1995. Estimation of microbial activities, In: Kassem Alef and Paolo Nannipieri, Editor(s), Methods in Applied Soil Microbiology and Biochemistry, Academic Press, London, p. 193-270. Behera N., Sahani, U., 2003. Soil microbial biomass and activity in response to Eucalyptus plantation and natural regeneration on tropical soil. For. Ecol. Manage. 174. 1-11. Dube, F., Zagal, E., Stolpe, N., Espinosa, M., 2009. The influence of land-use change on the organic carbon distribution and microbial respiration in a volcanic soil of the Chilean Patagonia. For. Ecol. Manage. 257, 1695-1704. Gartzia-Bengoetxea, N., Camps Arbestain, M., Mandiola E., Martínez de Arano, I., 2011. Physical protection of soil organic matter following mechanized forest operations in Pinus radiata D.Don plantations. Soil Biol. Biochem. 43, 141-149. Guerra, E., Puentes, G., 2002. Aumento de la productividad de plantaciones de Eucalipto por medio de técnicas racionales del sistema suelo- agua- planta: resultados finales. Primer Congreso Chileno de Ciencias Forestales- Libro de Resúmenes. Santiago- Chile, p. 174. Ilstedt, U., Nordgren, A., Malmer, A., 2006. Soil chemical and microbial properties after disturbance by crawler tractors in a Malaysian forest plantation. For. Ecol. Manage. 225, 313 319. INFOR, Instituto Forestal, 2008. Anuario Forestal 2008. Boletín estadístico 121. Álvarez, V., Pardo, E., Soto, D., Ávila, A. (Eds.), Santiago, Chile, p. 161, ISB 956-318. Jia, G-M., Cao, J., Wang, C., Wang, G., 2005. Microbal biomass and nutrients in soil at the different stages of secondary forest succession in Ziwulin, northwest China. For. Ecol. Manage. 217, 117-125. Joergensen, R.G., Brookes, P.C., 1990. Ninhydrinreactive nitrogen measurements of microbial biomass in 0.5 M K 2 SO 4 soil extracts. Soil Biol. Biochem. 22, 1023-1027. Medham, D.S., Sankaran, K.V., O Connell, A.M., Grove, T.S., 2002. Eucalyptus globulus harvest residue management effects on soil carbon and microbial biomass at 1 and 5 years after plantation establishment. Soil Biol. Biochem. 34, 1903-1912. Muñoz, F., Espinosa, M., Herrera, M.A., Cancino, J., 2005. Características del crecimiento en diámetro y volumen de una plantación de Eucalyptus nitens sometida a tratamientos silvícolas de poda y raleo. Bosque 26, 93-99. Novoa, R., Villaseca, S., 1989. Mapa agroclimático de Chile. Santiago, Instituto Nacional de Investigación Agropecuaria (INIA), p. 221. Saviozzi, A., Levi-Minzi, R., Cardelli, R., Riffaldi, R., 2001. A comparison of soil quality in adjacent cultivated, forest and native grassland soils. Plant Soil 233, 251-259. Shoji, S., Nanzyo, M., Dahlgren, R.A., 1993. Volcanic ash soils - Genesis, properties and utilization. Developments in Soil Science 21, Elsevier, Amsterdam, p. 288. Sicardi M., García-Préchac, F., Frioni, L., 2004. Soil microbial indicators sensitive to land use conversion from pastures to comercial Eucalyptus grandis (Hill ex maiden) plantations in Uruguay. Appl. Soil Ecol. 27, 125-133. Xu, X., Inubushi, K., Sakamoto, K., 2006. Effect of vegetations and temperature on microbial biomass carbon and metabolic quotients of temperate volcanic forest soils. Geoderma 136, 310-319.