Grain Legumes and Green Manures for Soil Fertility in ... - cimmyt
Grain Legumes and Green Manures for Soil Fertility in ... - cimmyt
Grain Legumes and Green Manures for Soil Fertility in ... - cimmyt
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to amount of biomass, quality of biomass <strong>in</strong> terms<br />
of L+P: N ratio, litter fall, <strong>and</strong> preseason <strong>in</strong>organic<br />
N. These results were <strong>in</strong> agreement with those reported<br />
by Mafongoya et al. 1999).<br />
Based on these results we can safely conclude that<br />
the ma<strong>in</strong> predictors of fallow per<strong>for</strong>mance are quantity<br />
of biomass, quality of the biomass, preseason<br />
<strong>in</strong>organic N <strong>and</strong> texture on the soil. The relevance of<br />
these predictors needs to be tested over a wide<br />
range of conditions <strong>and</strong> with different fallov: species.<br />
<strong>Soil</strong> Chemical Properties<br />
The major soil chemical changes that take place under<br />
tree fallows are <strong>in</strong>creases <strong>in</strong> labile pools of SaM,<br />
N stocks, exchangeable cations <strong>and</strong> extractable P<br />
(Rao et al. 1998). Details of the mechanisms of soil<br />
improvement by tree fallows were reviewed by<br />
(Buresh <strong>and</strong> Tian, 1998). In theory, planted tree fallows<br />
are expected to improve soils faster than natural<br />
fallows s<strong>in</strong>ce the l<strong>and</strong> is completely covered by<br />
fast grow<strong>in</strong>g legum<strong>in</strong>ous trees <strong>for</strong> 2 to 3 years.<br />
However the magnitude of these soil improvements<br />
depends on tree species, length of fallow, soil <strong>and</strong><br />
climatic conditions. In this section, we will concentra<br />
te on these changes as measured from experiments<br />
<strong>in</strong> southern Africa.<br />
Biological nitrogen fixation <strong>and</strong> N cycles<br />
The contribution of legum<strong>in</strong>ous trees through N2<br />
fixation is well recognized, although not all legumes<br />
fix N2. Nitrogen fixation <strong>in</strong> the humid <strong>and</strong> subhumid<br />
zones of Africa has been reviewed by Sang<strong>in</strong>ga<br />
(1995). There has been little work on quantification<br />
of N2 fixation by trees <strong>in</strong> southern Africa. This work<br />
has proved to be difficult due to constra<strong>in</strong>ts <strong>in</strong> the<br />
methodologies <strong>for</strong> measur<strong>in</strong>s N2 fixed. A series of<br />
multi-location trials have been set to measure the<br />
amount of N2 fixed by different tree genera <strong>and</strong><br />
provenances (Table 3) us<strong>in</strong>g the 15N natural abundance<br />
method. The data on percent Ndfa shows<br />
high variability among provenances of the same<br />
species <strong>for</strong> N derived from atmospheric N2 fixation.<br />
Sang<strong>in</strong>ga et al. (1990) found that percent Ndfa<br />
ranged from 37 to 74% <strong>for</strong> provenances of Leucaena<br />
leucocephala. The data shown <strong>in</strong> Table 3 falls with<strong>in</strong><br />
the range reported by Sang<strong>in</strong>ga et al. (1990). These<br />
prelim<strong>in</strong>ary data show the huge potential of trees to<br />
fix N2 <strong>and</strong> <strong>in</strong>crease N <strong>in</strong>puts <strong>in</strong> N deficient soils.<br />
Our future analysis will focus on factors responsible<br />
<strong>for</strong> this variability <strong>in</strong> N2 fixation across s~tes <strong>and</strong><br />
how to optimize N2 fixation under field conditions.<br />
Barrios et al (1997) m~asured availability of soil N<br />
follow<strong>in</strong>g 2- <strong>and</strong> 3-year fallows a N- deficient soils<br />
<strong>in</strong> eastern Zambia. His results confirmed that tree<br />
fallows <strong>in</strong>crease N availability compared to cont<strong>in</strong>uous<br />
cropp<strong>in</strong>g without fertilization. Subsequent N<br />
measurements down to 200 cm <strong>in</strong> the soil profile<br />
showed significant N <strong>in</strong>organic accumulation at<br />
depth dur<strong>in</strong>g the cropp<strong>in</strong>g phase (Figure 2).<br />
These results show that improved fallows can create<br />
a very "leaky" N cycle after fallow clearance. Most<br />
of the N is leached beyond the root<strong>in</strong>g depth of<br />
maize <strong>and</strong> this N is released from organic <strong>in</strong>puts<br />
be<strong>for</strong>e peak N dem<strong>and</strong> by maize. Hence there will<br />
be asynchrony between N release <strong>and</strong> N dem<strong>and</strong> by<br />
maize. Consequently there is need to design systems<br />
which try to m<strong>in</strong>imize N losses <strong>and</strong> <strong>in</strong>crease N<br />
use efficiency, <strong>and</strong> cycl<strong>in</strong>g.<br />
Based on those results we designed mixed fallows<br />
of coppic<strong>in</strong>g species <strong>and</strong> noncoppic<strong>in</strong>g species. The<br />
hypothesis is that the coppic<strong>in</strong>g species will act as a<br />
permanent "safety net" <strong>for</strong> N when the noncoppic<strong>in</strong>g<br />
fallows are cut due to resprout growth <strong>and</strong> deep<br />
root system <strong>in</strong> the soil. Results of gliricidia <strong>and</strong> sesbania<br />
mixed fallows have shown higher maize prcr<br />
ductivity <strong>and</strong> efficient N cycl<strong>in</strong>g compared to s<strong>in</strong>gle<br />
species fallows (Figure 3).<br />
<strong>Soil</strong> acidification <strong>and</strong> cations<br />
There are several reports on soil pH <strong>and</strong> improved<br />
fallows. Topsoil pH decreased under fallows of<br />
Acacia auriculi<strong>for</strong>mis (Drechsel et al. 1996). However<br />
Oonsson et al. 1996) found no changes <strong>in</strong> soil pH<br />
after fallows. Our results over a 10-year period<br />
showed significant decrease <strong>in</strong> topsoil soil pH, 0-60<br />
cm <strong>and</strong> an <strong>in</strong>crease <strong>in</strong> soil pH with depth (Figure 5).<br />
This decrease <strong>in</strong> topsoil pH <strong>and</strong> <strong>in</strong>crease <strong>in</strong> soil pH<br />
is attributed to leach<strong>in</strong>g of N03 <strong>and</strong> cations such as<br />
magnesium as shown <strong>in</strong> Figure 6. The movements<br />
of cations from the topsoil were also confirmed by<br />
low CEC <strong>in</strong> 0-20 cm (6.25 compared with 9.50) <strong>in</strong><br />
the 20-100 cm soil profile. These pH changes, which<br />
will take place after fallows, may have little effect<br />
Table 3. Biological nitrogen fixation (%BNF) of coppic<strong>in</strong>g species/<br />
provenances across three sites <strong>in</strong> eastern Zambia after 1 year of<br />
growth<br />
Kalichero Kalunga Masumba<br />
Treatment %BNF Nkg/ha %BNF Nkg/ha %BNF N kg/ha<br />
A. angustisma 52.1 210.4 61.8 201.4 54.8 260.8<br />
C. calothyrsus 48.4 81.4 44.1 214.4 48.7 193.<br />
G. sepium 79.2 212.4 71.4 408.4 70.8 297.5<br />
l. coll<strong>in</strong>sii 74.7 303.2 57.2 236.7 102.1 475.9<br />
l. diversif(Jlia 35/88 77.5 196.8 33.8 88.6 50.0 161.1<br />
l. diversifolia 53/88 58.4 121.5 14.0 40.5 46.9 112.6<br />
l. esculenta 52/87 70.9 99.3 . 46.6 110.1 46.7 274.5<br />
l. esculenta·Machakos 84.7 223.6 35.2 120.2 69.0 538.0<br />
l. pallida 58.6 87.8 33.7 125.2 44.7 168.1<br />
146<br />
<strong>Gra<strong>in</strong></strong> legumes <strong>and</strong> <strong>Green</strong> <strong>Manures</strong> <strong>for</strong> <strong>Soil</strong> <strong>Fertility</strong> <strong>in</strong> Southern Africa