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Article

Available Nitrogen and Responses to Nitrogen Fertilizer in Brazilian Eucalypt Plantations on Soils of Contrasting Texture

by
Ana Paula Pulito
1,
José Leonardo de Moraes Gonçalves
2,*,
Philip J. Smethurst
3,
José Carlos Arthur Junior
4,
Clayton Alcarde Alvares
5,
José Henrique Tertulino Rocha
2,
Ayeska Hübner
2,
Luiz Fabiano de Moraes
6,
Aline Cristina Miranda
7,
Marcos Yassuo Kamogawa
8,
José Luiz Gava
6,
Raul Chaves
9 and
Claudio Roberto Silva
1
1
Fibria S.A., Aracruz CEP: 29197-900, Brazil
2
Department of Forest Science, Luiz de Queiroz College of Agriculture (ESALQ), University of São Paulo (USP), Piracicaba CEP:13418-900, Brazil
3
CSIRO, Private Bag 12, Hobart TAS 7001, Australia
4
Forest Science and Research Institute (IPEF), Piracicaba, CEP: 13400-970, Brazil
5
Department of Forestry and Environmental Resources, North Carolina State University, Raleigh, NC 27695, USA
6
Suzano, Itapetininga CEP: 18207-780, Brazil
7
Department of Forest Science, "Julio de Mesquita Filho" Universidade Estadual Paulista, Botucatu CEP: 18603-970, Brazil
8
Mathematics, Statistics and Chemistry Department, Luiz de Queiroz College of Agriculture (ESALQ), University of São Paulo (USP), Piracicaba CEP:13418-900, Brazil
9
Duratex, Agudos CEP: 17120-000, Brazil
*
Author to whom correspondence should be addressed.
Forests 2015, 6(4), 973-991; https://doi.org/10.3390/f6040973
Submission received: 22 December 2014 / Revised: 11 March 2015 / Accepted: 19 March 2015 / Published: 2 April 2015

Abstract

:
Eucalyptus plantations have seldom responded to N fertilization in tropical and subtropical regions of Brazil. This implies that rates of N mineralization have been adequate to supply tree needs. However, subsequent crop rotations with low N fertilization may result in declining concentrations of organic and potentially mineralizable N (N0), and consequent loss of wood productivity. This study investigated (a) in situ N mineralization and N0 in soils of eucalypt plantations in São Paulo state, Brazil; (b) tree growth responses to N fertilizer applied 6–18 months after planting; and (c) the relationships between N0, other soil attributes and tree growth. We established eleven N fertilizer trials (maximum 240 kg ha−1 of N) in E. grandis and E. grandis x urophylla plantations. The soil types at most sites were Oxisols and Quartzipsamments, with a range of organic matter (18 to 55 g kg−1) and clay contents (8% to 67%) in the 0–20 cm layer. Concentrations of N0 were measured using anaerobic incubation on soil samples collected every three months (different seasons). The samples collected in spring and summer had N0 140–400 kg ha−1 (10%–19% total soil N), which were best correlated with soil texture and organic matter content. Rates of in situ net N mineralization (0–20 cm) ranged from 100 to 200 kg ha−1 year−1 and were not correlated with clay, total N, or N0. These high N mineralization rates resulted in a low response to N fertilizer application during the early ages of stand growth, which were highest on sandy soils. At the end of the crop rotation, the response to N fertilizer was negligible and non-significant at all sites.

1. Introduction

Establishment of a forest plantation using the Eucalyptus genus for pulp and paper production and other products is justified by their high productivity across different soils and climates. However, sustainable wood production might be compromised in the short- or long-term when plantations are established on soils of low fertility, such as Oxisols and Quartzipsamments [1,2]. Productive plantations with high capacity for nutrient extraction can greatly impact N pools in the soil. Adequate management practices, including fertilizer application, are required to sustain tree growth rates and ensure soil quality over successive rotations [3].
Although trees require large amounts of N, some researchers found that eucalypts did not respond to N fertilizer application under tropical and subtropical climate conditions [1,4,5]. Commonly, N fertilizer application enhances the early growth of a eucalypt stand, but the response is not continued through the entire rotation [3,4,5]. The lack of response possibly occurs due to significant mineralization rates of organic N [3,6] and to atmospheric N deposition [7,8,9,10]. Mineralization of organic N is the main natural N source for plantations and appears to be sufficient to meet tree demand [3,11], which in southeast Brazil ranges from 20 to 50 kg ha−1 year−1 [3,6]. However, intensively managed eucalypt plantations are expected to respond to N fertilizer application following several crop rotations because of high N outputs via harvesting [3,6,12], low N fertilizer rates applied [1,13], and depletion of organic N pools in soil [3]. Some studies carried out at sites with low soil organic matter (SOM) and N status showed that eucalypt stands might respond to N application under this condition [14,15]. Hence, the need for N fertilization in Brazilian plantations should be examined each rotation across a range of soil types.
The complexity of determining N fertilizer recommendations is attributed to the difficulty in accurately predicting the supply of available N (N mineralization). Gonçalves et al. [2] described a recommendation index for N fertilizer application to eucalypt plantations in Brazil based on SOM content. Although SOM is the main source of N, such an indicator does not consider the effect of SOM quality, climate and forest management [16,17].
The definition of a useful index of N availability is one that is practical, and chemical analyses can be faster than biological assays [18,19]. Several laboratory methods have been proposed to estimate potentially mineralizable N (N0) in soils, and the anaerobic incubation method appears promising [11,20,21].
To better understand the interactions of N supply and tree growth at this stage of eucalypt plantation development in southeast Brazil,, this study investigated (a) in situ N mineralization and N0 in soils of eucalypt plantations in São Paulo state, Brazil, (b) tree growth responses to N fertilizer applied 6–18 months after planting, and (c) the relationships between N0, other soil attributes and tree growth.

2. Material and Methods

2.1. Site Description

We selected eleven Eucalyptus grandis and Eucalyptus grandis × urophylla sites in São Paulo state, Brazil, ranging from 1 to 11.4 years old. The sites belong to industrial companies and to the Itatinga Experimental Station of Forest Sciences, University of São Paulo and are representative of the majority of soils, climates and plantation management in this state (Figure 1). The climate is Cwa, according to Köppen classification at Altinópolis site; Cfa at Agudos, Angatuba, Capão Bonito, São Miguel Arcanjo and Votorantim sites; and Cfb at Botucatu, Itatinga and Paraibuna sites [22]. Cwa is a humid subtropical climate with a dry winter and a hot summer. Cfa is a humid subtropical climate without a dry season and with a hot summer. Cfb is a humid subtropical climate without a dry season and with a temperate summer. C climate types have an average annual temperature below 18 °C. Cw climates have rainfall of the driest month (RDRY) more than 40 mm, while the Cf climates have RDRY less than 40 mm. Average annual rainfall at the studied sites ranges from 1170 to 1517 mm (Table 1). Soils in the municipalities of Itatinga, São Miguel Arcanjo and Paraibuna are Typic Hapludox (Red-Yellow Latosol); at Altinópolis, Angatuba and Botucatu, Typic Quartzipsamment (Quartzarenic Neosol); at Agudos and Capão Bonito 2, Typic Hapludox (Red Latosol); at Capão Bonito 1, Typic Hapludox (Yellow Latosol); at Votorantim, Typic Paleudult (Red-Yellow Argisol); and at Capão Bonito 3, Typic Dystropept (Dystrophic Cambisol) [23]. These are the main soils used in forest plantations in São Paulo State [2]. Further soil details of Itatinga and Capão Bonito can be found in Gonçalves et al. [24] and Alvares et al. [25], respectively. The contents of SOM ranged from 18 to 55 g kg−1 and clay contents from 8% to 68% in the 0–20 cm layer (Table 2). They are also quite acidic with pH 3.9–4.9.
Figure 1. Map of São Paulo state showing locations of the experimental sites: 1—Agudos; 2—Altinópilis; 3—Angatuba; 4—Botucatu; 5, 6, 7—Capão Bonito; 8—Itatinga; 9—São Miguel Arcanjo; 10—Paraibuna; and 11—Votorantim.
Figure 1. Map of São Paulo state showing locations of the experimental sites: 1—Agudos; 2—Altinópilis; 3—Angatuba; 4—Botucatu; 5, 6, 7—Capão Bonito; 8—Itatinga; 9—São Miguel Arcanjo; 10—Paraibuna; and 11—Votorantim.
Forests 06 00973 g001
At each site, we used a randomized block experimental design with three replicates. Measured plots were 10 m by 10 m, with 36 trees per plot, surrounded by a two-tree border. The treatments were: (i) control (low N dose of fertilizer application, sufficient to provide good establishment of plants; c. 15 kg ha−1); (ii) usual dose (N dose used by the companies; c. 100 kg ha−1); and (iii) increased dose (100% higher than commercial doses; c. 200 kg ha−1). The N fertilizer application schedule was 25% of total dose at planting, and the rest applied equitably at 6, 12 and 18 months after planting. The fertilizer application after planting was placed in a continuous line under canopy projection. Additional to N fertilization, all treatments received 30 kg ha−1 of P, 130 kg ha−1 of K, 230 kg ha−1 of Ca, 100 kg ha−1 of Mg, 3 kg ha−1 of B, 60 kg ha−1 of S, 1.5 kg ha−1 of Zn and 0.5 kg ha−1 of Cu. Calcium and Mg were supplied through lime application. Throughout the experiment, the stands were kept free of weed competition by herbicide application.
Table 1. Latitude (Lat), longitude (Long), altitude (Alt), mean annual temperature (T), mean annual pluviometric precipitation (PP), topography, planted genotype, tree spacing and planting date of each experiment.
Table 1. Latitude (Lat), longitude (Long), altitude (Alt), mean annual temperature (T), mean annual pluviometric precipitation (PP), topography, planted genotype, tree spacing and planting date of each experiment.
MunicipalitySite CodeLatLongAltT 3PPGeology 4GenotypeTree SpacingPlanting
Formation or GroupLithotype
SWm°Cmm m
AgudosAGU22°28′48°59′58020.61170MaríliaSandstone, sandy argillite and limestoneE.grandis 13.0 × 2.0Aug-2005
AltinópolisALT21°01′47°22′88919.41517BotucatuQuartz-sandstoneE.grandis × urophylla 23.0 × 2.5May-2002
AngatubaANG23°17′48°28′64919.71262PirambóiaShale, thin sandstone and silty-clayey sandstoneE.grandis × urophylla 23.0 × 2.0Apr-2006
BotucatuBOT22°53′48°26′80419.11302MaríliaSandstone, sandy argillite and limestoneE.grandis13.0 × 2.0Nov-2005
Capão Bonito 1CB124°00′48°20′70518.91210ItararéSandstone, diamictite and shaleE.grandis × urophylla 23.0 × 3.0Jun-1999
Capão Bonito 2CB224°00′48°20′70518.91210E.grandis × urophylla 23.0 × 2.0Feb-2007
Capão Bonito 3CB324°00′48°20′70518.91210E.grandis × urophylla 23.0 × 2.0Dec-2006
ItatingaITA23°06′48°36′84518.81308MaríliaSandstone, sandy argillite and limestoneE.grandis13.0 × 2.0Apr-2002
São M. ArcanjoSMA23°51′47°51′71518.91174ItararéSandstone, diamictite and shaleE.grandis × urophylla 23.0 × 2.0Aug-2006
ParaibunaPAR23°23′45°39′63419.21249Natividade da SerraMonzogranite, biotite and graniteE.grandis13.0 × 2.5Mar-1997
VotorantimVOT23°32′47°26′57019.81287Granite SorocabaGranite, Granodiorite, monzogranite and syenograniteE.grandis × urophylla 23.0 × 2.0Oct-2006
1 Seedling plantations; 2 Clonal plantations; 3 Alvares et al. [26]; 4 IPT [27].
Table 2. Soil physical and chemical attributes (0–20 cm layer) at the eleven sites.
Table 2. Soil physical and chemical attributes (0–20 cm layer) at the eleven sites.
SiteClay 1Silt 1Sand 1OM 2pH 3P-resin 4Cation Exchange 4
CoarseFineKCaMgAl
%g kg−1 mg kg−1mmolc kg−1
AGU16.72.730.749.9153.92.30.61.00.68.3
ALT6.71.338.753.3134.34.40.84.81.93.7
ANG10.01.029.359.7164.08.50.55.31.57.6
BOT10.03.032.055.0114.04.80.33.03.74.1
CB147.810.48.733.1233.92.20.81.00.812.8
CB265.315.35.314.1294.43.61.64.44.813.7
CB327.223.41.048.4164.13.71.82.72.619.1
ITA19.32.237.541.0184,02.30.61.61.89.7
SMA65.117.32.914.7454.946.95.348.613.61.3
PAR36.55.543.914.1154.13.62.029.010.30.9
VOT67.011.115.36.6464.04.21.61.81.014.7
1 Pipette method [28]; 2 Organic matter determined by potassium dichromate and sulfuric acid extraction; 3 CaCl2 0.01mol L−1 soil to solution ratio 1:2.5; 4 Ion Exchange resin [29].

2.2. Growth Assessment

In all plots, we measured diameter at breast height (DBH), total height and tree survival, and estimated the mean annual increment (MAI) of solid wood volume (SV) with bark. The SV was estimated by allometric equations using DBH and height developed by companies specifically for the genetic material used in each plantation. To compare eucalypt response to N fertilizer application in all sites, regardless of the growth increment, relative productivity (RP) increase was calculated as follows (Equation (1)).
RP ( % )   =   SV SVmax   × 100
where: “SV” is solid wood volume with bark of a given treatment and “SVmax” is the solid wood volume with bark of the highest dose treatment.

2.3. Soil Analysis

Soil chemical and physical properties were determined for the 0–20 cm layer at all sites. Ten soil samples were collected from each plot, in a diagonal transect across the inner part of the plot between planting lines. The samples were used to make one mixed sample per plot, which was air dried and homogenized. Next, the samples were sieved through a 2 mm mesh and mixed up again.
Particle size analysis (pipette method) of soil was performed according to Embrapa [28]. We determined the pH in CaCl2 0.01 mol L−1, available phosphorus and exchangeable calcium, magnesium, potassium extracted by ion-exchange resins and aluminum extracted by KCl 1 M, according to Raij et al. [29]. We assessed soil total carbon (Ct) at all sites in the control treatment (0–20 cm layer) using the South Dakota method with modifications by Raij et al. [29]. This method consists of organic matter oxidation by dichromate (K2Cr2O7 + H2SO4), and quantification by colorimetry. Total N (Nt) was determined by the micro-Kjeldahl method [30].

2.4. Assessment of N Mineralization

At all sites, soil samples from the 0–20 cm layer were collected to evaluate potential N mineralization under anaerobic conditions in the laboratory (N0). The samples were collected in April (fall), July (winter), November (spring), 2007, and in January (summer), 2008. We performed anaerobic incubations (40 °C for 7 days) using chemical methods according to those proposed by Keeney and Bremner [20]. Prior to incubation, 30 mL of nutritional solution, consisting of: MgSO4 (0.002 mol L−1) and Ca (H2PO4)2 (0.005 mol L−1), was added. Jars were manually shaken until soil dispersion, and then covered with polyethylene film to avoid water loss by evaporation and algal growth [11]. N was extracted again 7 days after incubation by adding 4.47 g of KCl to each jar, which provide a concentration of 2 mol L−1 of KCl. Jars were then shaken manually for about 60 s, placed to rest 24 h and then filtered and analyzed for NH4 as described above. To calculate potentially mineralizable N we subtracted the initial concentrations of mineral N.
To measure net N mineralization, the in situ method of Raison et al. [31] was used to in the 0–20 cm soil layer of control plots. Five pairs of steel tubes 30 cm long and 5 cm diameter were placed between tree rows in a diagonal transect across the inner part of the plot. The principle of the method is that inserting a sharpened corer severs roots, and adding capping during in situ incubation excludes rainfall. Net N mineralization thereby proceeds without leaching or uptake. By measuring mineral N initially (in additional representative soil samples) and again after incubation, net ammonification and nitrification can be calculated. For this study, one tube of each pair was immediately removed to assess initial mineral N concentrations (t0) for all plots, and the remaining tubes were covered to avoid leaching of N, remaining in soil for 30 days on average. The amount of mineral N at t0 was subtracted from the mineral N content after incubation to calculate in situ net N mineralization for each 30 day period. The same rate was assumed for other periods of the same season. Soil from each set of five tubes per plot was mixed to obtain a composite sample. The in situ method was used at all sites for January–December 2008.
For each collection, samples at all sites were collected within 8 days of each other to minimize time-related climatic variations between sites. The tubes were transported vertically to the lab, to minimize disturbance, and they were kept in thermal boxes (2–5 °C), individually wrapped in plastic bags. Refrigeration was used to minimize microbial activity, reducing mineralization that could occur prior to mineral N extraction [32]. Soil samples remained refrigerated until extraction, which was performed within two days of each collection.
For initial N (t0) extraction, 10 g of soil were placed in 110 mL jars and 100 mL of KCl 2 mol L−1 added. Jars were manually shaken for c. 60 seconds for soil dispersion, and placed to rest for 24 h. Afterwards, the suspension was filtered through Whatman No. 42 filter paper, and the filtrate was analyzed to for NH4+ and NO3, following the addition of 0.1 mL of microbial inhibitor (mercury acetate phenyl 0.5 mg L−1).
For both N0 and in situ N mineralization, NH4+ and NO3 concentrations were determined using the Analyze System of Injection in Automatic flow—ASIA (Ismatec, Glattbrugg, Switzerland) [33] and detected by colorimetry at 605 nm, which has a detection limit of 0.01 µg mL−1.

2.5. Data Analysis

Data were checked for normality (Shapiro-Wilk) and homoscedasticity (Box-Cox). ANOVA was used to assess the significance of differences between means. Where there was a significant (p < 0.05) F test, a Tukey test (5% probability) was used for contrasting means. The relationship between dependent and independent variables was assessed by Pearson correlation and linear regression.

3. Results

Net N mineralization in situ rates ranged from 4.8 to 11.5 kg ha−1 month−1 (fall and winter) and from 10.6 to 15.0 kg ha−1 month−1 (spring and summer) for sandy soils, from 7.4 to 15.2 kg ha−1 month−1 (fall and winter) and from 11.0 to 17.6 kg ha−1 month−1 (spring and summer) for loamy soils, and from 3.6 to 19.1 kg ha−1 month−1 (fall and winter) and from 9.4 to 24.3 kg ha−1 month−1 (spring and summer) for clayey soils (Table 3). The average rates of N mineralization were highest in clayey soils, ranging from 110 to 207 kg ha−1 year−1, and the lowest to sandy soils, ranging from 107 to 140 kg ha−1 year−1. The average ratio of N-NH4+/N-NO3 was 1.6 for sand soils, 1.7 for loamy soils and 1.9 for clayey soils.
Values of N0 during summer ranged from 60 to 154 mg kg−1 of soil (190 and 398 kg ha−1), with an average of 97 ± 11 mg kg−1 of soil (241 ± 18 kg ha−1) (Table 4). Values of N0 in sandy soils during summer were on average 168 kg ha−1 of N0, 212 kg ha−1 in loamy soils, and 303 kg ha−1 in clayey soil. During winter, these values ranged from 20 to 91 mg kg−1 of soil (63 and 178 kg ha−1). In sandy soils, N0 corresponded to 19% of Nt, 14% in loamy soil, and 13% in clayey soils.
At all sites, tree survival was higher than 95%. On average, nitrogen fertilizer application resulted in an increase in MAI of 14% at early age, 6% at intermediate age and 0% at the end of the crop rotation (Table 5). Relative production (RP) at early age of control treatment ranged from 74% to 98% (average of 87% ± 2%), and from 90% to 98% (average of 95% ± 1%) at intermediate age. In the treatment that received commercial fertilizer application, RP ranged from 88% to 111% (average of 100% ± 2%) at early age, and from 98% to 107% (average of 100% ± 1%) at intermediate age. After five years of age (approximate harvesting age), RP ranged from 99% to 103% (average of 102% ± 1%).
The relative wood volume response to N application was greater in sandy soils, and, in absolute terms, at soils with higher clay content (Table 5 and Figure 2). During the first two years of age, RP of the control was about 16% lower than in the treatments that received commercial fertilizer application at sandy soils, and 9% to 10% at soils with higher clay content. Greater relative response to N application at early age occurred in soils with lower Nt, N0 and clay contents (Figure 2). At the end of the rotation, regardless of soil texture, no significant responses to N application were found.

4. Discussion

4.1. N mineralization

Higher rates of N mineralization in clayey soils are attributed to higher stocks of organic N, due to the greater net primary productivity of the ecosystem, and to higher amounts of soil organic-mineral complexes (Table 3 and Table 4). Under this condition, microbial activity increases due to higher amounts of substrate [34,35] and water availability. Eaton [36] reported that after two days of intensive rains, clayey soils in subtropical forests showed a significant increase in microbial C and N-NH4+ mineralization rates, compared to sandier soils. The author speculated that part of the active organic matter pool became detached from soil clay particles, and thereby became available to microorganisms.
Low rates of nitrification (Table 3) might be caused by high acidity and low fertility in these soils, and high NH4+ uptake under high growth rate stands could restrict substrate availability for nitrifying bacteria [3,37,38,39]. Under high acidity and low soil fertility, nitrifying bacteria (Nitrobacter and Nitrosomonas) have impaired active. Higher NH4+ than NO3 availability is usually not a limitation for eucalypt nutrition [40,41]. Gonçalves and Carlyle [39] studying N mineralization in Pinus radiata plantation soils under laboratory conditions reported that, despite the increased rate of nitrification during incubation, it was not proportional to the reduction of NH4+ concentration, showing the possibility of NH4+ immobilization and/or denitrification caused by soil moisture variations.
Figure 2. Relative productivity (RP) of the control treatments in relation to the usual and increased N rate treatments. (a) at young ages (less than two years) and (b) later ages (more than five years) at all sites, grouped according to soil texture. See Table 1 for x-axis site codes.
Figure 2. Relative productivity (RP) of the control treatments in relation to the usual and increased N rate treatments. (a) at young ages (less than two years) and (b) later ages (more than five years) at all sites, grouped according to soil texture. See Table 1 for x-axis site codes.
Forests 06 00973 g002
Table 3. Rates of net ammonification and net nitrification in situ and N-NH4+/N-NO3 ratio at each site (0–20 cm layer).
Table 3. Rates of net ammonification and net nitrification in situ and N-NH4+/N-NO3 ratio at each site (0–20 cm layer).
SiteSummerFallWinterSpringYearly Total
N-NH4+N-NO3N-totalNH4+/NO3N-NH4+N-NO3N-totalNH4+/NO3N-NH4+N-NO3N-totalNH4+/NO3N-NH4+N-NO3N-totalNH4+/NO3N-NH4+N-NO3N-totalNH4+/NO3
kg ha−1 month−1 kg ha−1 month−1 kg ha−1 month−1 kg ha−1 month−1 kg ha−1 yr−1
Sandy Soils
ALT5.78.013.70.74.64.18.71.16.62.69.22.610.14.815.02.181.258.6139.81.4
ANG8.63.812.42.33.31.64.82.14.31.35.53.48.05.113.11.672.435.2107.62.1
BOT5.67.613.20.76.94.511.51.54.13.77.81.19.11.510.66.177.052.0129.01.5
Mean6.66.513.11.24.93.48.31.65.02.57.52.49.13.812.93.376.948.6125.51.6
s 11.72.30.70.91.81.63.40.51.41.21.91.21.12.02.22.54.412.116.40.4
Loamy Soils
AGU11.26.517.61.79.04.213.22.26.13.29.31.911.33.214.53.5113.051.1164.02.2
CB36.97.514.40.93.95.99.80.76.84.911.71.48.03.011.02.776.863.7140.51.2
ITA8.54.412.92.03.34.17.40.89.26.115.21.59.63.012.63.291.752.6144.31.7
Mean8.96.115.01.55.44.710.11.27.44.712.11.69.63.112.73.193.855.8149.61.7
s2.21.62.40.63.11.02.90.81.61.53.00.31.70.11.80.418.26.912.60.5
Clayey Soils
CB17.01.98.93.78.96.715.61.34.08.612.60.513.06.819.81.998.772.2170.91.4
CB211.24.916.02.33.62.35.91.53.87.010.90.511.85.317.12.291.158.7149.81.6
SMA6.03.49.41.86.51.27.75.43.41.95.21.89.74.714.42.176.933.5110.42.3
PAR14.37.822.11.812.76.519.11.91.12.63.60.417.76.624.32.7137.270.2207.42.0
VOT13.46.920.41.96.42.69.02.57.51.99.43.910.23.513.82.9112.545.0157.52.5
Mean10.45.015.42.37.63.911.52.53.94.48.31.412.55.417.92.4103.355.9159.21.9
s3.72.46.10.83.42.65.61.72.33.23.81.53.21.44.30.422.916.635.10.5
1 Mean standard deviation.
Table 4. Seasonal values of potentially mineralizable N (N0), total C (Ct), total N (Nt), C/N ratio and N0/Nt ratio at each site grouped by texture class.
Table 4. Seasonal values of potentially mineralizable N (N0), total C (Ct), total N (Nt), C/N ratio and N0/Nt ratio at each site grouped by texture class.
Site 1N0Ct 2Nt 3N0 4N0/NtC/N
FallWinterSpringSummerFallWinterSpringSummer
mg kg−1kg ha−1mg kg−1%
Sandy Soils
ALT2620476082631491907723387601520
ANG2846396163103881377025323611922
BOT53315666142831501777090301662224
Mean3632476296831291687279337621922
s 515.013.18.53.241.220.035.527.6385.644.73.23.52.0
Loamy Soils
AGU30427360841182051699233387601624
CB3104_ 695115279_25530993428101151412
ITA71437375149901531587850589751313
Mean684380831711042052128808595831416
s37.10.712.728.499.319.851.084.2831.7211.628.41.56.7
Clayey Soils
CB156699111113917122627513,4037741111417
CB2114_112107276_27125918,8149811071119
SMA3491981256717819224524,49812671251019
PAR1258310813836124031239810,8378931381512
VOT158_134154344_29233629,72412761541223
Mean978110912723719625830319,45510381271318
s51.111.116.419.4129.338.049.063.67781.3225.319.42.14.0
1 Described in Table 1; 2 Determined by humid oxidation; 3 Bremmer [30] method; 4 adaptation of Keeney and Bremner [20] method; 5 Mean standard deviation; 6 Data not collected.
Gonçalves et al. [11] found similar values of N0 in eucalypt stands ranging from 50 to 249 mg kg−1 of soil (average of 111 ± 23 mg kg−1 of soil). Variations in N mineralization rates under laboratory conditions due to season of sampling were also found by Adams and Attiwill [42], Khanna [43], Smethurst and Nambiar [38], and Theodorou and Bowen [44]. Those authors also found higher N mineralization rates during temperate summers coinciding with warm, moist soils. For Theodorou and Bowen [44,45], seasonal fluctuations in mineral N availability were related to microbial activities in the soil, which are mostly affected by temperature and soil moisture [39]. When incubating a soil sample collected during summer, a higher microbial population is also incubated, leading to a higher mineralization rate.
N0 contents were highly correlated with Nt (r = 0.92; p < 0.0001), but less so with SOM (r = 0.69; p = 0,0192) and clay contents (r = 0.83; p = 0,0015) (Figure 3). This confirms that soil total N is a good indicator of potential N mineralization, as also found by Pottker and Tedesco [46] and Noble and Herbert [47]. However, N0 was only weakly correlated with annual N mineralization in situ (r = 0.35), and the latter was not correlated with Nt, SOM, or clay content.
The N0/Nt percentage varied mostly between 10 and 22% (Table 4), signifying the proportional amount of mineralizable organic N. Gonçalves et al. [11] found N0/Nt percentages between 5% and 15%. The Nt in this study accounted for 3%–5% of SOM. That ratio decreased with increased clay content (Figure 4). Therefore, there may be greater proportional N availability in soils with lower clay content. High N mineralization in sandy soils is related to better soil aeration and less clay protection of SOM. In absolute terms though, soils with higher clay content have more potential availability of N, because Nt stocks are higher.
Table 5. Solid wood volume with bark (SV) and mean annual increment (MAI) in the different treatments and ages at each site.
Table 5. Solid wood volume with bark (SV) and mean annual increment (MAI) in the different treatments and ages at each site.
SiteTreatmentSVMAI
m3 ha−1m3 ha−1year−1
Sandy Soils
Age (year)1.84.05.71.84.05.7
ALTControl45b 1192a285a25b48a50a
Usual dose55a198a285a31a50a50a
Increased dose55a198a275a30a49a48a
2.03.05.52.03.05.5
ANGControl96a175a352a48a58a64a
Usual dose109a181a351a55a60a64a
Increased dose108a183a356a54a61a65a
2.03.04.05.02.03.04.05.0
BOTControl40a172a209a267a20a57a52a53a
Usual dose47a187a211a266a23a62a53a53a
Increased dose42a176a197a260a21a59a49a52a
Loamy soils
Age (year)2.03.04.05.06.02.03.04.05.06.0
AGUControl52a132a186a257a313a26a44a47a51a52a
Usual dose52a133a190a274a323a26a44a47a55a54a
Increased dose53a135a183a249a312a27a45a46a50a52a
1.12.01.12.0
CB3Control14a88b13a44b
Usual dose16a109a14a54a
Increased dose16a111a14a55a
2.04.02.04.0
ITAControl50b159a25b40b
Usual dose60a174a30a43a
Increased dose61a174a30a44a
Clayey Soils
Age (year)2.04.09.02.04.09.0
CB1Control28b168b452a14b42b50a
Usual dose33ab184ab460a17ab46a51a
Increased dose38a187a455a19a47a51a
1.02.04.71.02.04.7
CB2Control10a80b330a10a40b70a
Usual dose11a92a332a11a46a71a
Increased dose12a96a333a12a48a71a
1.52.51.52.5
SMAControl68a187a45a75a
Usual dose73a185a49a74a
Increased dose71a200a47a80a
2.24.011.42.24.011.4
PARControl33a146a439a15a36a39a
Usual dose39a153a430a18a38a38a
Increased dose42a153a430a19a38a38a
1.23.11.23.1
VOTControl21b177a18a57a
Usual dose25a194a21a62a
Increased dose23b184a19a59a
1 Values in the same column and site followed by the same letter do not differ statistically by Tukey mean test (p = 0.05).
The C/N ratio ranged from 12 to 24 (average of 19 ± 4) (Table 4). Maquere et al. [48], Montero [49] and Lima et al. [50] found higher ratios in eucalypt stands compared to other native vegetation. This explains in part the larger recalcitrance of SOM in eucalypt stands. N release slows as N mineralization proceeds, since reserves of labile N decrease along with microbial activity. This effect is unfavorable to plant nutrition in the short-term, but beneficial for N conservation in the long-term because it decreases N losses by leaching and volatilization [37,51,52]. The C/N ratio across sites was inversely correlated with N0 (r = 0.66, p = 0.036), confirming that the more recalcitrant SOM has lower potential N availability. Although not quantified in the current study, temporal changes in C/N ratios at each site can be expected [53], whereby these ratios decrease during the early age of a rotation along with specific rates of mineralization (i.e., rates of N mineralization per unit of carbon). In sandy surface soils (0–15 cm depth) supporting Pinus radiata stands in southeast Australia, the specific rates of N mineralization decreased by more than 50% (from 207 to 93 g N month−1 t−1 C) during the first four years after planting as C/N ratios also decreased in both the <2 mm and >2 mm soil fractions [53]. For unsieved soil, the C/N ratio decreased from 38 to 31 during this period. This slow down in specific rate of N mineralization might reflect a decrease in the labile pool of organic N and organic matter quality. Such changes can be expected in any stand prior to replenishment of this labile pool as organic matter and nutrient cycling is restored by above- and below-ground litter production later in the crop rotation. Hence, the relationship C/N ratio and N mineralization depends on poorly understood temporal and spatial factors of SOM quality.
Figure 3. Correlations between soil organic matter (SOM), clay content, total N (Nt) and potentially mineralizable N (N0).
Figure 3. Correlations between soil organic matter (SOM), clay content, total N (Nt) and potentially mineralizable N (N0).
Forests 06 00973 g003
Figure 4. Correlation between clay content and N0/Nt ratio across all sites.
Figure 4. Correlation between clay content and N0/Nt ratio across all sites.
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4.2. Nitrogen Fertilizer Application Response

The response to N fertilizer application only occurred at an early stage of tree growth, when the canopy was in formation. For eucalypt stands in Brazil, around 70%–80% of N accumulates in aboveground components during the first two or three years of growth [1,54]. At this stage, N relative buildup is higher than biomass accumulation, due to formation of N-rich components (mainly, leaf and fine root), and N released from SOM by mineralization might not be enough to meet the N demand of trees [2]. After three years of age, competition among trees for water and light intensifies [55] and tree growth rates decline, leading to reduced N demand that is mostly supplied by N released through litter decomposition (biogeochemical cycling) and internal transfers (biochemical cycling) [1,54]. Gonçalves et al. [3] found a biochemical cycling of 54 kg N ha−1 year−1 and biogeochemical cycling 42 kg N ha−1 year−1 in E. grandis stands at seven years old, which are higher than the amounts required by trees (50 kg N ha−1 year−1). Therefore, during early growth, N fertilizer application may accelerate tree growth rates by increasing N availability when N mineralization rates in soil and litter do not supply enough N to highly demanding trees. However, these responses disappear in subsequent years under the conditions examined here.
The mineral fertilizer requirements of any plantation depend on the nutrient demand required to reach an expected productivity, and the ability of the soil to supply this demand. When plant demand is greater than soil supply, fertilizers must be added. Thus, the criteria for N fertilizer application should involve only situations where response to N fertilizer exists, because fertilizer application aims to fill the deficit of N not released by soils. Fertilizer application practices must be linked with conservative methods of management to minimize N losses from the system, and thereby increasing sustainability [3].

Acknowledgments

The authors wish to thank Duratex S.A., Fibria Celulose S.A., International Paper of Brazil and Suzano Papel e Celulose S.A. for the financial support and making their areas available for the project. We also thank the Silviculture and Management Thematic Program (PTSM) of IPEF for financial support and assistance with for fieldwork. We also thank Antonio Bianchi for the revision of the English.

Author Contributions

Ana Paula Pulito, José Leonardo de Moraes Gonçalves, Luiz Fabiano de Moraes, José Luiz Gava, Raul Chaves and Claudio Roberto Silva designed the study and conducted of field trial. Ana Paula Pulito, José Carlos Arthur Junior, Aline Cristina Miranda and Marcos Yassuo Kamogawa were responsible for the samples collection and laboratory analysis. Ana Paula Pulito, José Carlos Arthur Junior, Clayton Alcarde Alvares and José Henrique Tertulino Rocha, were responsible for the statistical analyses, with contribution from José Leonardo de Moraes Gonçalves. Ana Paula Pulito, José Leonardo de Moraes Gonçalves, Philip J. Smethurst, Clayton Alcarde Alvares, José Henrique Tertulino Rocha and Ayeska Hübner wrote the paper.

Conflicts of Interest

The authors declare no conflict of interest.

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MDPI and ACS Style

Pulito, A.P.; Leonardo de Moraes Gonçalves, J.; Smethurst, P.J.; Junior, J.C.A.; Alcarde Alvares, C.; Henrique Tertulino Rocha, J.; Hübner, A.; Fabiano de Moraes, L.; Miranda, A.C.; Kamogawa, M.Y.; et al. Available Nitrogen and Responses to Nitrogen Fertilizer in Brazilian Eucalypt Plantations on Soils of Contrasting Texture. Forests 2015, 6, 973-991. https://doi.org/10.3390/f6040973

AMA Style

Pulito AP, Leonardo de Moraes Gonçalves J, Smethurst PJ, Junior JCA, Alcarde Alvares C, Henrique Tertulino Rocha J, Hübner A, Fabiano de Moraes L, Miranda AC, Kamogawa MY, et al. Available Nitrogen and Responses to Nitrogen Fertilizer in Brazilian Eucalypt Plantations on Soils of Contrasting Texture. Forests. 2015; 6(4):973-991. https://doi.org/10.3390/f6040973

Chicago/Turabian Style

Pulito, Ana Paula, José Leonardo de Moraes Gonçalves, Philip J. Smethurst, José Carlos Arthur Junior, Clayton Alcarde Alvares, José Henrique Tertulino Rocha, Ayeska Hübner, Luiz Fabiano de Moraes, Aline Cristina Miranda, Marcos Yassuo Kamogawa, and et al. 2015. "Available Nitrogen and Responses to Nitrogen Fertilizer in Brazilian Eucalypt Plantations on Soils of Contrasting Texture" Forests 6, no. 4: 973-991. https://doi.org/10.3390/f6040973

APA Style

Pulito, A. P., Leonardo de Moraes Gonçalves, J., Smethurst, P. J., Junior, J. C. A., Alcarde Alvares, C., Henrique Tertulino Rocha, J., Hübner, A., Fabiano de Moraes, L., Miranda, A. C., Kamogawa, M. Y., Gava, J. L., Chaves, R., & Silva, C. R. (2015). Available Nitrogen and Responses to Nitrogen Fertilizer in Brazilian Eucalypt Plantations on Soils of Contrasting Texture. Forests, 6(4), 973-991. https://doi.org/10.3390/f6040973

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