Tropical Grasslands-Forrajes Tropicales (2018) Vol. 6(1):15–25 15

DOI: 10.17138/TGFT(6)15-25

Research Paper

Soil attributes of a silvopastoral system in Pernambuco Forest Zone

Atributos del suelo en un sistema silvopastoril en la “Zona da Mata”,

Pernambuco, Brasil

HUGO N.B. LIMA1, JOSÉ C.B. DUBEUX JR.2, MÉRCIA V.F. SANTOS1, ALEXANDRE C.L. MELLO1, MÁRIO

A. LIRA2,3 AND MÁRCIO V. CUNHA1

1 Departamento de Zootecnia, Universidade Federal Rural de Pernambuco, Recife, PE, Brazil. www.ufrpe.br

2 University of Florida, North Florida Research and Education Center, Marianna, FL, USA. nfrec.ifas.ufl.edu

3 Instituto Agrônomico de Pernambuco, Recife, PE, Brazil. www.ipa.br

Abstract

This research evaluated soil properties in a silvopastoral system using double rows of tree legumes. Treatments were signalgrass ( Brachiaria decumbens) in monoculture or in consortium with sabiá ( Mimosa caesalpiniifolia) or gliricidia ( Gliricidia sepium). Treatments were arranged in a complete randomized block design, with 4 replications. Response variables included chemical characteristics and physical attributes of the soil. Silvopastoral systems had greater (P<0.001) soil exchangeable Ca (gliricidia = 3.2 and sabiá = 3.0 mmolc/dm3) than signalgrass monoculture (2.0

mmolc/dm3). Water infiltration rate was greater within the tree legume double rows (366 mm/h) than in signalgrass (162

mm/h) (P = 0.02). However, soil moisture was greater in signalgrass pastures (15.9%) (P = 0.0020) than in silvopastures (14.9 and 14.8%), where soil moisture levels increased as distance from the tree rows increased. Conversely, the light fraction of soil organic matter was greater within the tree legume double rows than in the grassed area (P = 0.0019).

Long-term studies are needed to determine if these benefits accumulate further and the productivity benefits which result.

Keywords : Fertility, legumes, soil physics, trees.

Resumen

Entre enero 2012 y diciembre 2013 en Itambé, Pernambuco, Brasil, se evaluaron algunas propiedades físicas y químicas del suelo en un sistema silvopastoril, utilizando filas dobles de leguminosas arbóreas. Los tratamientos consistieron en Brachiaria decumbens sola o en asociación con sabiá ( Mimosa caesalpiniifolia) o gliricidia ( Gliricidia sepium) en un diseño de bloques completos al azar, con 4 repeticiones. Los sistemas silvopastoriles presentaron mayor contenido (P<0.001) de calcio intercambiable (gliricidia = 3.2 y sabiá = 3.0 mmolc/dm3) comparados con la gramínea sola (2.0

mmolc/dm3). La tasa de infiltración de agua fue mayor en el suelo dentro de las filas dobles de los árboles leguminosos (366 mm/h) en comparación con la gramínea sola (162 mm/h) (P = 0.02). No obstante, la humedad fue más alta en el suelo con gramínea (15.9%) (P = 0.0020) comparada con los sistemas silvopastoriles (14.9 y 14.8%, respectivamente para sabiá y gliricidia). La humedad en el suelo aumentó con la distancia a partir de la línea de árboles. Por el contrario, la fracción ligera de la materia orgánica del suelo fue mayor (P = 0.0019) dentro de las filas dobles de árboles (0.071

mg/kg) comparada con el suelo fuera de la línea de árboles. Se requieren estudios a largo plazo para determinar si estos beneficios continuan acumulándose y si resultan en mayor productividad.

Palabras clave: Árboles, fertilidad, física del suelo, leguminosas.

___________

Correspondence: J.C. Batista Dubeux Jr., University of Florida, North

Florida Research and Education Center, 3925 Highway 71, Marianna,

FL 32446, USA.

Email: dubeux@ufl.edu

Tropical Grasslands-Forrajes Tropicales (ISSN: 2346-3775)

16 H.N.B. Lima, J.C.B. Dubeux Jr., M.V.F. Santos, A.C.L. Mello, M.A. Lira and M.V. Cunha Introduction

Given the economic and environmental importance of

these systems, this study aimed to evaluate the chemical

Good soil physical characteristics are essential to ensure

composition and physical properties of soils in

satisfactory crop and pasture productivity. Pasture soils tend

signalgrass pastures [ Brachiaria decumbens Stapf; now:

to have greater soil density than preserved vegetation soil,

Urochloa decumbens (Stapf) R.D. Webster], in associa-

presumably due to trampling by animals (Vitorino 1986),

tion with tree legumes in the coastal region (“Zona da

which can also have an impact on the water infiltration rate

Mata”) of Pernambuco State, Brazil.

and soil moisture holding capacity, both of which have

significant effects on pasture productivity. The amount of

Materials and Methods

water that infiltrates and flows over the ground is directly

related to soil physical properties such as density, and the

The research was conducted at the Experimental Station

existing vegetative cover (Lanzanova et al. 2007).

of the Agronomic Institute of Pernambuco (IPA), located

Soil organic matter (SOM) has a major influence on

in Itambé, Pernambuco, Brazil. Average annual rainfall is

ecosystem productivity because it affects chemical and

1,300 mm, and average annual temperature is 25 °C

physical characteristics of soils. Since SOM is the net

(CPRH 2003). The climate is sub-humid, the topography

result of soil processes occurring in the long term, it is

is undulating and the soil of the study area is classified as

difficult to detect early changes if analyzing total SOM

Ultisol (red-yellow dystrophic Argissol according to the

(Haggerty and Gorelick 1998). The light fraction of the

Brazilian Soil Classification or Paleudult or Ferric

SOM is formed by plant and animal residues in the early

Luvisol according to FAO World Reference Base)

stages of decomposition. It represents recent changes in

(Jacomine et al. 1972; Embrapa 2006). Initial soil

chemical characteristics of the experimental area were:

land management and can detect early changes in SOM

pH in water (1:2.5) 5.5; P (Mehlich-I) 2.2 mg/dm3; K 1.3

dynamics (Jinbo et al. 2007; Rangel and Silva 2007).

mmolc/dm3; Ca 27 mmolc/dm3; Mg 20 mmolc/dm3; Na

Increases in ecosystem primary productivity lead to

1.4 mmolc/dm3; Al 2.7 mmolc/dm3; H+Al 61.7 mmolc/

increasing residue deposition, both above- and below-

dm3; and SOM 44.2 g/kg. Average monthly rainfall for

ground.

the experimental years is shown in Figure 1.

Silvopastoral systems improve soil physical attributes

Three treatments were tested in a complete

such as soil aggregates, soil density and water infiltration

randomized block design with 4 replications. Treatments

rates (Carvalho et al. 2004). Litter deposition from tree

included: 1) sabiá with signalgrass; 2) gliricidia with

foliage is a major pathway for recycling of nutrients in a

signalgrass; and 3) signalgrass monoculture. Each

silvopastoral system (Apolinário et al. 2016). Limited

experimental unit measured 660 m2 (33 x 20 m). Tree

nitrogen (N) availability in warm-climate grasslands is

legumes (sabiá and gliricidia) were established in 2008 in

one of the major limiting factors to increases in

double rows spaced at 10.0 m (between double rows) x

productivity (Vendramini et al. 2014), and N addition via

1.0 m (between rows) x 0.5 m (within rows). Each plot

litter represents a significant input and might result in

contained 3 double rows. The signalgrass was growing

greater ecosystem primary productivity. Tree legumes

throughout the area of each plot, but reduced growth

such as sabiá ( Mimosa caesalpiniifolia Benth.) and

occurred between the individual tree legume rows that

gliricidia [ Gliricidia sepium (Jacq.) Kunth] can be used in

formed the double rows (“within tree legume double

silvopastoral systems (Souza and Espíndola 2000; Vieira

rows” from here on), especially under sabiá trees.

et al. 2005; Apolinário et al. 2016; Costa et al. 2016).

Livestock were introduced to the paddocks when the

Besides biological N2 fixation, litter deposition and

sward height reached 60 cm, and remained until the

decomposition are important sources of nutrients to be

stubble height of the grass was reduced to 10‒15 cm.

reused by the system (Apolinário et al. 2016).

Soils from tree legume paddocks were sampled in

Tree legumes can provide extra alternative income

September 2012 in order to determine the chemical

through the sale of fencing posts and firewood

composition. Samples were collected in 2 transect lines

(Apolinário et al. 2015). Incorporating tree legumes in

perpendicular to the tree rows. Along each transect, 5

silvopastoral systems can also provide other ecosystem

different points were sampled (0, 1, 2, 3 and 4 m distance

services including the maintenance of biodiversity,

from each tree double row) giving 30 samples per plot

improvement of water and nutrient flow, enhancement of

(Figure 2). Paddocks with signalgrass monoculture were

soil quality, reduction of soil erosion, improvement of C

sampled randomly at 5 sites. All soil samples were taken

storage and provision of green areas for urban society

from the 0‒20 cm soil layer. Soil samples to determine

(Kemp and Michalk 2005).

bulk density and soil gravimetric moisture were collected

Tropical Grasslands-Forrajes Tropicales (ISSN: 2346-3775)

Soils in a silvopastoral system 17

300

250

200

150

mm

100

50

0

Month / Year

Figure 1. Rainfall (monthly averages) in the experimental area during the research period. Source: Meteorological data collected at the experimental site.

in May 2013, using the same sampling protocol (per-

were macerated and sieved through a 0.5 mm sieve, and

pendicular transects) described to collect the soil fertility

then put into a 0.053 mm sieve and washed in running

samples, and the same soil depth. Undisturbed soil cores

water. The retained material was then transferred to

were collected using volumetric rings. Samples were

containers filled with water, where it remained undisturbed

dried in an oven at 105 °C for 24 hours, following

for 24 h for density separation (heavy and light fraction).

methodology described by Embrapa (1979).

The supernatant (floating) material was retrieved in 0.053

Light fraction of SOM was determined by weighing

mm mesh, dried at 65 °C for 72 h, and weighed on a

50 g of soil (samples collected for fertility analyses), which

precision scale (Correia et al. 2015).

Figure 2. Location of soil sampling points relative to tree legume rows in the silvopasture treatments.

Tropical Grasslands-Forrajes Tropicales (ISSN: 2346-3775)

18 H.N.B. Lima, J.C.B. Dubeux Jr., M.V.F. Santos, A.C.L. Mello, M.A. Lira and M.V. Cunha Water infiltration rate (WIR) was determined in

and soil exchangeable Na was greater in the signalgrass-

January 2013. Infiltrometers made of concentric rings

sabiá pasture than in the other pastures (Table 1). When

(Bouwer 1986) were placed at 2 specific points in each

com-paring the sampling points in relation to the distance

tree legume paddock: 1) within tree legume double rows

from the rows of legumes, there was no significant effect

(sampling point 1); 2) in the middle of the grassed area

for the response variables evaluated, except for pH (Figure

(sampling point 5). A total of 48 samples were collected

3), where values increased exponentially as distance from

(2 replicates for each sample location within each

the legume rows increased, with a peak at 3 m.

silvopastoral system, and 4 samples for each signal-grass

plot). Water infiltration rate was determined when the rate

Water infiltration rate

was constant, using the following equation:

Water infiltration rate was higher within the tree legume

WIR (mm/min) = L2 - L1 (mm) / time (min)

double rows of gliricidia and sabiá (356 and 366 mm/h,

where: L2 is water at the beginning of the measurement

respectively; Figure 4) than in the signalgrass mono-

and L1 is the remaining water in the tube after the time

culture (162 mm/h) and in the grassed area of the signal-

spent measuring.

grass-sabiá (128 mm/h) treatment.

Soil attributes were analyzed using PROC MIXED

(SAS 2007). A complete randomized block design was

Gravimetric moisture

used to compare signalgrass monoculture with the

silvopastoral systems. When transects were analyzed, the

Soil moisture (Table 2) levels were higher (P<0.05) in the

transect points were considered split-plot and the main

signalgrass monoculture than in the mixed pastures; in the

plot the vegetation cover, with both being fixed effects. In

mixed pastures soil moisture increased as distance from

all analyses, blocks were considered a random effect.

the tree rows increased (P<0.05; Table 3).

Significance was declared at 5% probability. LSMEANS

Soil density was not affected by type of pasture

were compared using the PDIFF procedure and adjusted

(P = 0.58) (Table 2), but in the mixed pastures soil density

Tukey test.

increased as distance from the tree rows increased

(P<0.05; Table 3).

Results

Light fraction of soil organic matter

Soil fertility

Light fraction of SOM was unaffected by pasture type

While soil chemical composition was affected by

(P = 0.22), but within the silvopastoral treatments, light

vegetation cover (Table 1), levels of most nutrients were

fraction of SOM was greater in the sabiá treatment than

similar in all treatments (P>0.05). Soil pH was greater in

under gliricidia (64 vs.45 mg/kg, respectively; P = 0.002)

the signalgrass monoculture than in the 2 grass-legume

(Table 4). The light fraction of SOM was greater under

tree pastures. Soil exchangeable Ca was greater in the

the trees than in the grass area (71 vs. 50 mg/kg,

grass-legume tree pastures than in the grass-only pasture,

respectively; Table 3).

Table 1. Soil chemical analyses (0‒20 cm layer) in signalgrass, signalgrass-gliricidia and signalgrass-sabiá pastures.

Treatment

pH

P

K

Mg

Ca

Na

Al

H + Al

C

OM

(water – 1:2.5)

(mg/dm³)

(mmolc/dm³)

(g/kg)

Signalgrass

5.8 a

1.6 a

1.4 a

2.0 a

2.0 b

0.1 b

0.3 a

5.6 a

22.0 a

48.5 a

Gliricidia

5.4 b

2.5 a

1.7 a

2.0 a

3.2 a

0.1 b

0.3 a

6.5 a

29.3 a

43.4 a

Sabiá

5.4 b

2.5 a

1.7 a

1.9 a

3.0 a

0.3 a

0.3 a

6.4 a

23.6 a

40.7 a

Probability

0.02

0.26

0.17

0.87

0.001

0.02

0.91

0.15

0.23

0.71

CV (%)

3

38

85

14

12

67

51

10

23

30

Values followed by the same letter within columns do not differ by Duncan’s test (P>0.05). OM = organic matter.

Tropical Grasslands-Forrajes Tropicales (ISSN: 2346-3775)

Soils in a silvopastoral system 19

5.5

Table 2. Soil moisture and density (0‒20 cm layer) in signal-

) 5.45

grass monoculture, signalgrass-gliricidia and signalgrass-sabiá

5.:2 5.4

pastures.

1

y = -0.0264x2 + 0.1667x + 5.2071

r 5.35

tea 5.3

Treatment

Moisture (%)

Density (g/cm3)

(w 5.25

Signalgrass

15.9 a

1.21 a

Hp 5.2

Gliricidia

14.9 b

1.22 a

5.15

Sabiá

14.8 b

1.19 a

0

1

2

3

4

Probability

0.002

0.74

Distance (m) from tree legume rows

CV (%)

3.19

4.7

Figure 3. Soil pH relative to the distance from tree legume rows

Values followed by the same letter within columns do not differ

in signalgrass-gliricidia and signalgrass-sabiá pastures.

by Duncan’s test (P<0.05).

Grassed area in signalgrass-sabiá pasture (sampling point 5)

Signalgrass monoculture

Grassed area in signalgrass-gliricidia pasture (sampling point 5)

WIR (mm/h)

Within gliricidia double rows (sampling point 1)

Within sabiá double rows (sampling point 1)

0

100

200

300

400

500

Figure 4. Water infiltration rate (mm/h) in signalgrass monoculture and grassed areas in signalgrass-gliricidia and signalgrass-sabiá pastures, and within gliricidia and sabiá double rows in the mixed pastures. The bars represent the standard error.

Table 3. Effect of distance from tree legume rows on soil moisture, soil density and soil organic matter (SOM) light fraction (0‒20

cm layer) in signalgrass-gliricidia and signalgrass-sabiá pastures.

Distance (m) from tree rows

Soil moisture (%)

Soil density (g/cm3)

SOM light fraction (g/kg)

0

14.5 b

1.18 b

0.071 a

1

14.1 b

1.19 b

0.051 b

2

15.2 ab

1.19 b

0.056 b

3

14.8 ab

1.22 ab

0.052 b

4

15.5 a

1.24 a

0.042 b

Probability

0.04

0.07

0.02

CV (%)

9.6

4.0

32.5

Values followed by the same letter within columns do not differ by Duncan’s test (P>0.05).

Tropical Grasslands-Forrajes Tropicales (ISSN: 2346-3775)

20 H.N.B. Lima, J.C.B. Dubeux Jr., M.V.F. Santos, A.C.L. Mello, M.A. Lira and M.V. Cunha Table 4. Soil organic matter (SOM) light fraction (0‒20 cm

development of the trees, increase in litter deposition and

layer) in signalgrass-gliricidia and signalgrass-sabiá pastures.

accumulation of animal waste, provided that the system is

appropriately managed (Balbino et al. 2012; Padovan and

Treatment

SOM light fraction (g/kg)

Pereira 2012; Loss et al. 2014).

Gliricidia

0.045 b

Sabiá

0.064 a

Water infiltration rate

Probability

0.002

CV (%)

32.4

Greater WIR in the signalgrass area in consortium with

Values followed by the same letter within columns do not differ

by Duncan’s test (P>0.05).

gliricidia might be due to the fact that this legume has a

deeper root system, providing advantages such as

increased water absorption and greater efficiency in the

Discussion

search for nutrients, resulting in its high performance as

fodder for livestock (Abdulrazak et al. 1997; Ondiek et al.

This study has provided some interesting results on

1999; Juma et al. 2006). A more specific study of the root changes in soil parameters when tree legumes are

systems of gliricidia and sabiá is necessary to better

introduced into a pure grass pasture. They contribute to

understand the influence of root properties (length, depth

our knowledge of how the legumes alter the soils in

and density) on WIR.

conjunction with an associated grass.

Silvopastoral systems allow increases in SOM because

of greater litter deposition from trees, and Bell et al.

Soil fertility

(2011) indicated that greater litter deposition increases

soil macroporosity, contributing to improved water

As in our study, Carvalho et al. (2003) reported increased

infiltration and aeration. Moisture, biological activity and

soil exchangeable Ca in silvopastoral systems 5 years after

vegetation cover can also influence soil responses, such

establishment, and attributed this increase to the greater

as the WIR (Carduro and Dorfman 1988). Dunger et al.

accumulation of litter produced by the trees. Similarly,

(2005) reported that silvopastoral systems provide a

Camarão et al. (1990) suggested that the increase in soil

favorable microclimate to increase soil microfauna,

exchangeable Ca in silvopastoral systems might be

which tend to seek shaded and humid habitats. An

explained by the increased above- and below-ground litter

increase of Coleoptera beetles in association with the

deposition. Xavier et al. (2003) also observed an increase

introduction of legumes from the genus Mimosa in

in soil exchangeable Ca in signalgrass- Acacia mangium

pastures has been reported by Dias et al. (2007). These

pasture compared with pure signalgrass.

beetles dig underground galleries in order to nest, thus

The reduction in soil pH in the mixed pastures recorded

providing the opportunity for greater water infiltration

in our study is in contrast with the findings of Oliveira et

(Miranda et al. 1998).

al. (2000), Andrade et al. (2002), Xavier et al. (2003) and Increased height and density of tree legumes in the

Dias et al. (2006), where soil pH was not affected by the

experimental area reduced the transit of grazing cattle

introduction of trees. Dias et al. (2006) also studied soil

through the rows, which might explain the lower soil

chemical composition of grass-tree legume pastures in

density at these points (Table 3). The WIR was greater

relation to the distance from the tree trunk and found

along tree legume rows as compared with the grazed area

variations in soil pH and levels of P, K, Ca and Mg tending

under the effects of treading by animals, as indicated with

to increase or decrease, depending on the legume species,

changes in soil density. These data corroborate those of

planting density and biomass production.

Lanzanova et al. (2007), who studied the effects of

In silvopastoral systems, most litter deposition occurs

grazing on water infiltration rates in soils, finding greater

near the tree trunks (Silva et al. 2013), which might

WIR values in ungrazed areas and decreasing values as

influence the reduction of soil pH. Greater litter

grazing became more intense. In our research, the

accumulation leads to greater amounts of litter nutrients

increases in soil density as distance from tree legumes

being mineralized. As a result, more leaching of ex-

increased (Table 3) was reflected in decreases in WIR.

changeable bases due to release of anions from OM might

Bertol et al. (2001) showed that heavy clay soils have a

occur (Balbinot et al. 2010). However, Pavan et al. (1986)

low percentage of the pore volume occupied by air, which

obtained an increase in soil pH in an area with greater

leads to greater rates of runoff water, lower retention of

litter deposition. Several studies on silvopastoral systems

water and consequently lower infiltration capacity.

indicated that the benefits brought by the trees to soil

Prevedello (1996) also pointed out that the reduction in

fertility of the pastures tend to increase over time with

WIR with time can be influenced by factors that operate

Tropical Grasslands-Forrajes Tropicales (ISSN: 2346-3775)

Soils in a silvopastoral system 21

on the soil surface, such as surface sealing due to the

agrosilvopasture (combination of trees, crops and

impact of raindrops, which may be reduced by the canopy

livestock, grown on a particular site) and intensive

of tree legumes. Roots of tree legumes in the silvopastoral

cultivation. Perin et al. (2000) also observed greater soil

systems used in this experiment might favor soil physical

moisture when soil was covered with a thick litter layer of

aspects, maintaining and improving soil structure and

herbaceous legumes.

increasing WIR (Hernández 1998).

The increase in soil moisture as distance from the tree

Excretion of organic acids and inorganic compounds

legume rows increased meant that grasses growing in the

(e.g. P and K) by roots can influence soil characteristics,

middle of the grass strips suffered reduced competition

as they allow for increased dissolution of mineral

for soil moisture from the trees, while still having some

substances and contribute to the development of

shade to assist retention of soil moisture (Table 3). Near

rhizosphere microorganisms (Cintra et al. 1999). Roots

tree rows, there was reduced soil cover because of greater

can also favor SOM accumulation, as Lehmann and Zech

competition for resources between herbaceous and woody

(1998) found that the litter produced by the renewal of

vegetation.

roots adds about 20‒50% of the total root biomass to the

SOM pool, while only 10‒20% of litter arising from the

Soil density

aerial parts is transformed into SOM (Schroth et al. 1999).

Since roots are more recalcitrant than leaves and stems, a

Average soil density was 1.2 g/cm3, which is adequate for

greater proportion of original root biomass ends up in the

root development (Alvarenga et al. 1996; Corsini and

SOM pool than leaves and stems.

Ferraudo 1999). According to Argenton et al. (2005),

characterization of soil density depends on its textural

Gravimetric moisture

class and Rosenberg (1964) and Cintra and Mielniczuk

(1983) suggest that each soil type has a critical density,

The greater soil moisture in signalgrass monoculture was

which can reduce or even prevent root development.

probably due to the competition by different species for

Reichert et al. (2003) showed that 1.4 g/cm3 is considered

water. Legumes are less efficient in water usage than C4

the critical soil density for satisfactory growth of the root

grasses. On average, legumes use 800 kg of water to

system of plants in clay soils, but Reinert et al. (2008)

produce 1 kg of dry matter, while C4 plants use 300 kg of

indicated a greater soil density (1.85 g/cm3) as critical for

water to produce the same amount of DM (Taiz and

legumes and other vegetables in clayey soils.

Zeiger 2004; Marenco and Lopes 2009). Plant species

The lower soil density near the trees (Table 3) can be

have a marked influence on water availability in

attributed to the existence of microfauna near the trees

silvopastoral systems and Vanzela and Santos (2013)

(Miranda et al. 1998; Dunger et al. 2005; Dias et al. 2007)

highlighted that the use of eucalypts in silvopastoral

as well as a greater SOM accumulation between trees,

systems increased competition for water and nutrients

increasing the amount of soil aggregates. Iori et al. (2012)

between the trees and the associated grass.

studied soil density and soil moisture in degraded

Andrade and Valentim (1999) showed that shading is

pastures, banana cultivation, a silvopastoral system and

a positive factor in maintaining soil moisture, resulting in

preserved forest. They found greater soil moisture in less

satisfactory forage development in silvopastoral systems.

dense soil, which can be correlated with the shading

In natural shading conditions, however, trees also

potential and greater SOM in these areas. Beltrame et al.

compete with one another and the grass for light, water

(1981) stated that soil moisture affects the cohesion

and nutrients. Therefore, the water requirements of the

between soil particles, with increases in aggregation when

tree legumes might have contributed to reduced soil

soil moisture is limited, which hinders their separation by

moisture near the trees in the current research.

external forces (Silveira et al. 2010).

Another aspect that should be highlighted is the fact

that, during the collection period, the grass monoculture

Light fraction of soil organic matter

was approximately 60 cm tall, which provided 100%

ground cover, helping to maintain soil moisture. In the

While vegetation cover did not affect the light fraction of

silvopastoral systems, tall trees with dense canopies might

SOM (P = 0.22), in the mixed pastures sabiá presented

have compromised production of signalgrass, which has

greater values of SOM than gliricidia (Table 4). Chan et

only moderate shade tolerance and might suffer

al. (2002) and Zinn et al. (2005) observed that SOM

production loss due to shading (Schreiner 1987). In

stocks are directly related to residue inputs, their rate of

contrast to this, Aguiar et al. (2006) recorded greater soil

decomposition and SOM fractionation. They pointed out

moisture in silvopastoral systems compared with

that the replacement of conventional farming systems

Tropical Grasslands-Forrajes Tropicales (ISSN: 2346-3775)

22 H.N.B. Lima, J.C.B. Dubeux Jr., M.V.F. Santos, A.C.L. Mello, M.A. Lira and M.V. Cunha with improved systems, such as silvopastures, changes

sistemas agroflorestais no município de Sobral, CE. Revista

the dynamics of litter accumulation and litter

Ciência Agronômica 37:270–278. goo.gl/1MSAV5

decomposition rate, and consequently generates greater

Alvarenga RC; Costa LM; Moura Filho W; Regazzi AJ. 1996.

increases in the light fraction of SOM. Similarly, Maia et

Crescimento de raízes de leguminosas em camadas de solo

al. (2008) showed greater amounts of light fraction of

compactadas artificialmente. Revista Brasileira de Ciência

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persistência de Arachis pintoi submetido a diferentes níveis

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445. DOI: 10.1590/S1516-35981999000300001

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matter in intermediate stages of decomposition (Souza et

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DOI: 10.1590/S1516-35982002000300006

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Apolinário VXO; Dubeux Jr. JCB; Lira MA; Ferreira RLC;

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Mello ACL; Santos MVF; Sampaio EVSB; Muir JP. 2015.

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Apolinário VXO; Dubeux Jr. JCB; Lira MA; Sampaio EVSB;

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Amorim SO; Silva NGM; Muir JP. 2016. Arboreal legume

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Agronomy Journal 108:2478–2484. DOI: 10.2134/

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agronj2016.02.0120

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Argenton J; Albuquerque JA; Bayer C; Wildner LP. 2005.

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Comportamento de atributos relacionados com a forma da

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plantas de cobertura. Revista Brasileira de Ciência do Solo

29:425–435. DOI: 10.1590/S0100-06832005000300013

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Balbino LC; Cordeiro LAM; Oliveira P; Kluthcouski J;

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solo em plantios puros e consorciados de Mimosa

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10.1016/s0377-8401(98)00210-7

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Tropical Grasslands-Forrajes Tropicales (ISSN: 2346-3775)