Literature DB >> 33854170

Intensifying cropping systems through doubled-up legumes in Eastern Zambia.

Mulundu Mwila1, Blessing Mhlanga2, Christian Thierfelder3.   

Abstract

Declining soil fertility and negative impacts of climate effects threaten the food security of millions in Africa. Conservation Agriculture (CA) is a promising strategy to address these challenges. However, lack of viable economic entry points and short-term benen class="Disease">fits for smallholders limit its adoptionpan>. Legume inpan>tenpan>sificationpan> canpan> possibly inpan>crease the output per unpan>it area, thus makinpan>g the system more attractive. Rotationpan>s of pan> class="Species">maize with intensified legume systems were tested for three consecutive years under ridge and furrow (RF) tillage and CA to investigate: (a) increases in productivity of legumes and the subsequent maize crop; (b) changes in land equivalent ratios (LERs) and; (c) improved total system productivity. Results showed an increase in legume yields when growing two legumes simultaneously, leading to greater LERs (ranging between 1.13 and 1.29). However, there was only a significant season and not a main treatment effect as CA did not outperform RF in both phases of the rotation. Full populations of companion legumes improved overall system productivity, yielding 76.8 GJ ha-1 in a more conducive season while sole cropping of pigeonpea yielded only 4.4 GJ ha-1. We conclude that the doubled-up legumes systems have great potential to improve household food security when integrated into current smallholder farming.

Entities:  

Year:  2021        PMID: 33854170      PMCID: PMC8047045          DOI: 10.1038/s41598-021-87594-0

Source DB:  PubMed          Journal:  Sci Rep        ISSN: 2045-2322            Impact factor:   4.379


Introduction

Food and nutrition security in southern Africa are a major concern for millions of smallholder farmers. This has become particularly important in recent years as climate variability and change are increasingly affecting smallholder farming systems[1,2]. In addition, declining soil fertility is critical for farmers[3] due to limited use of mineral fertilizers and their ability to cope with crop demands of their main staple food crop, n class="Species">maize (pan> class="Species">Zea mays L.)[4,5]. During the last two decades, efforts have been made to sustainably increase current farming systems using Conservation Agriculture (CA) with improved n class="Species">maize-legume systems as inpan>tervenpan>tionpan> strategies[6-11]. CA is a crop manpan>agemenpan>t system based onpan> three mainpan> prinpan>ciples: minimum soil disturbanpan>ce, crop residue retenpan>tionpan> anpan>d crop diversificationpan> through rotationpan> anpan>d/or inpan>tercroppinpan>g[12,13]. However, research has shown that the simultanpan>eous applicationpan> of these three mainpan> prinpan>ciples is oftenpan> not enpan>ough to have anpan> impact onpan> soil quality anpan>d productivity inpan>crease. Complemenpan>tary practices are needed to augmenpan>t CA systems unpan>der the conpan>ditionpan>s of southern Africa[14]. Such complemenpan>tary practices may inpan>clude adequate fertilizer applicationpan>, timely weedinpan>g inpan>cludinpan>g improved weed conpan>trol with herbicides, use of pan> class="Disease">stress-tolerant varieties, and integration of shrubs or tree-based components, among others. CA systems are currently adopted on approximately 180 M ha around the world, with the bulk being adopted in South and n class="Chemical">North America, Canpan>ada anpan>d Australia, mostly onpan> large commercial farms[15]. The extenpan>t of adoptionpan> is signclass="Chemical">pan>ificanpan>tly smaller for smallholder farmers inpan> Africa with approximately 1.5 M ha unpan>der CA to date[15]. One of the key constraints hindering successful application of CA systems is the lack of adoption of the principle of crop diversification through rotations and intercropping in southern Africa[16,17]. n class="Species">Maize monpan>ocroppinpan>g, especially inpan> lanpan>d conpan>strainpan>ed enpan>vironpan>menpan>ts, is very commonpan> anpan>d has led to nutrienpan>t minpan>ing, soil pan> class="Chemical">carbon depletion, increased exposure to new invasive pests and diseases and soil erosion[18]. One way to make CA systems more attractive and financially viable is to diversify and increase the output per unit area, which is a key principle of sustainable intensification[19]. Companion legume systems, also known as “doubled-up legumes systems”, have been promoted in Malawi in the last two decades in an effort to increase productivity from the same area of land[20,21]. The systems combine two legumes in the field, which are less competitive in their growth habit. Usually, groundnut (Arachis hypogaea L.), a grain legume and pigeonpea (Cajanus cajan Millsp.), a woody perennial legume which contributes significant quantities of nitrogen (N) through the production of biomass (leaves and stems), while producing edible grain, are commonly used as companion crops in maize-based systems[22]. Research by Turner and Taylor[23] shows that growing n class="Species">maize inpan> rotationpan> with doubled-up legumes is more productive thanpan> continpan>uous pan> class="Species">maize monocropping and maize-pigeon pea intercropping especially under low fertility and limited mineral fertilizer use. For southern Africa, the lack of available vegetative biomass in rotational systems is an impediment to sustained soil fertility improvement. Rotations with soybean (Glycine max L.) or groundnut mean that there is very little decomposable biomass left once the crop is harvested, but this can be provided by the pigeonpea in the case of a doubled-up legumes system. This added advantage needs to be quantified to understand how much each crop and their combination would add to the total system yield. Previous research from southern Africa has shown that soil organic n class="Chemical">carbon (SOC) inpan>crease inpan> CA systems is closely linpan>ked to the level of crop diversification[24] anpan>d its absenpan>ce canpan> oftenpan> lead to no SOC inpan>crease[25]. The inpan>clusionpan> of pan> class="Species">pigeonpea in a rotational system, especially if the fibrous parts of the residues are retained on the soil surface, is therefore seen as very beneficial in maintaining enough ground cover and adding organic carbon to the soil. In pursuance of the integration of the concept of doubled-up legumes in CA systems, a research study was designed for Eastern Zambia. The objective of this study was to assess the pen class="Chemical">rformanpan>ce of doubled-up legumes systems unpan>der CA as compared to conpan>venpan>tionpan>al tillage-based ridge anpan>d furrow (pan> class="Chemical">RF) practices with significant interest in the rotational effects of the crop management system on maize productivity. Our hypotheses were: (a) the rainfall season in target areas affects crop management systems more than soil treatment; (b) doubled-up legumes systems yield more per unit area in a rotational system than sole legumes; (c) doubled-up legumes systems under CA have a greater actual and residual benefit on legumes, and n class="Species">maize planpan>ted after the legumes; (d) doubled-up legumes systems lead to greater total system yield thanpan> sole croppinpan>g.

Results

Rainfall

Rainfall records from the trial sites showed different patterns in the three cropping seasons (Figure S2). However, the across site variability was almost the same for all the seasons with coefficient of variances (CV) ranging from 20.1 to 21.9% (Figure S2). Average rainfall in the cropping season 2015/2016 ranged between 402 and 655 mm, which coincided with one of the strongest El n class="Chemical">Niño seasonpan>s onpan> record (Figure S2a). Croppinpan>g seasonpan> 2016/2017 had higher rainpan>fall of 717–1202 mm, coinpan>cidinpan>g with a medium La Niña season (Figure S2b). Finally, cropping season 2017/2018 was characterized by a rainfall range of 495–800 mm (Figure S2c). The rainfall variation across the seasons was high with a CV of 34.5%. Cropping season 2015/2016 and 2017/2018 were further characterized by long dry spells (up to 13 days) and early tailing-off of rainfall at the end of March of each season.

Effect of crop management systems, doubled-up legumes systems, and seasons on legume productivity

The interaction of crop management systems and years significantly affected grain yield of legumes (p < 0.0001, Table 1). The CA system in the 2016/2017 season had the highest grain yield averaging 2.0 t ha−1 (Fig. 1a). The least grain yield was observed in both the CA and the n class="Chemical">RF systems inpan> the 2015/2016 seasonpan> with anpan> average of 0.73 t ha−1. Inpan> additionpan>, there was a clear groupinpan>g of pepan> class="Chemical">rformance of the crop management systems based on the year with the crop management systems performing best in 2016/2017, followed by 2017/2018 and lastly 2015/2016. Additionally, legume grain yield was significantly affected by the interaction of the different legumes and their populations with seasons (p < 0.0001, Table 1). Sole groundnut in 2016/2017 had the highest grain yield of 3.1 t ha−1 (Fig. 1b). The least legume grain yield was observed in 2015/2016 for the fullGN/halfPP, solePp and fullGN/fullPP sub-treatments which averaged 0.5 t ha−1.
Table 1

Significance of fixed effects on legume and maize grain and biomass yield across the years.

SourceDegrees of freedomGrainBiomass
Sum of squaresWald statisticp value¶Sum of squaresWald statisticp value¶
Legumes
(Intercept)1113.89324.152.20 e−16***443.81219.892.20 e−16***
Treatment (Treat)10.8072.30.12959ns0.530.266.09 e−01ns
Subtreatment (Subtreat)3139.192396.162.20 e−16***670.93332.432.20 e−16***
Season2172.551491.112.20 e−16***115.7757.363.50 e−13***
Treat × subtreat30.170.480.92236ns26.0412.94.86 e−03***
Treat × season25.46915.570.00042***33.4716.580.00025**
Subtreat × season632.56892.72.20 e−16***66.5132.961.07 e−05***
Treat × subtreat × season60.2160.620.99613ns15.397.630.26684ns
Residual (MS)0.3512.02
Maize
(Intercept)172.19860.6486.77 e−15***154.853137.162.20 e−16***
Treatment (Treat)11.1050.9280.3354ns0.7680.680.40945ns
Subtreatment (Subtreat)33.9323.3030.3473ns7.9487.040.07064. ns
Season171.8660.3647.88 e−15***39.43434.9283.42 e−09***
Treat × subtreat30.8370.7030.8725ns0.7940.7030.8724ns
Treat × season11.2481.0480.3059ns0.0410.0370.84817ns
Subtreat × season30.2570.2160.975ns2.031.7980.61531ns
Treat × subtreat × season31.4131.1870.7561ns5.3014.6950.19555ns
Residual (MS)1.191.129

¶ns, not significant.

*p < 0.05; **p < 0.01; ***p < 0.001.

Figure 1

Interactive effects of different crop management systems and legume combinations and populations with seasons on (a), (b) legume grain yield and (c), (d) legume biomass yield over the seasons of implementation: RF = ridge and furrow; CA = conservation agriculture; soleGn = sole groundnuts; solePp = sole pigeonpea; fullGN/halfPP = legume intercropping with full population of groundnut and half population of pigeon pea; and fullGN/fullPP = legume intercropping with full population of groundnut and full population of pigeon pea. Boxplots with different letters above them are significantly different from each other. The error bars represent the standard error of mean (SEM). The jittered dots represent the individual observations from each plot over the seasons.

Significance of fixed effects on legume and n class="Species">maize grainpan> and biomass yield across the years. ns, not significant. *p < 0.05; **p < 0.01; ***p < 0.001. For biomass yield, the interaction of crop management systems and seasons significantly affected legume biomass yield (p < 0.001, Table 1). The highest biomass yield was observed in the CA system in the 2016/2017 season and the same CA system yielded the least in the 2015/2016 season (Fig. 1c). The different legumes and their different populations significantly interacted with the seasons (p < 0.001, Table 1) and n class="Chemical">solePp had the highest yield of 6.5 t ha−1 observed inpan> 2017 (Fig. 1d). The combinpan>ationpan>s of the legumes with full populationpan>s yielded the least inpan> the 2015/2016 anpan>d 2017/2018 seasonpan>s with a meanpan> yield of 2.8 t ha−1. Both legume grainpan> anpan>d biomass yield differed across the years anpan>d across their differenpan>t populationpan>s anpan>d combinpan>ationpan>s (p < 0.001 for both) (Table 1). n class="Chemical">SolePp in n class="Chemical">RF systems resulted in highest yield of 5.6 t ha−1 but this was not significantly different from solePp under CA with a mean yield of 5.0 t ha−1 (Fig. 2). All the combinations of legumes and their populations yielded the least regardless of the crop management system in which they were combined and these averaged 3.0 t ha−1.
Figure 2

Interactive effect of crop management systems and legume combinations and their different populations on legume biomass yield over the seasons of implementation: RF = ridge and furrow; CA = conservation agriculture; soleGn = sole groundnuts; solePp = sole pigeonpea; fullGN/halfPP = legume intercropping with full population of groundnut and half population of pigeon pea; and fullGN/fullPP = legume intercropping with full population of groundnut and full population of pigeon pea. Boxplots with different letters above them are significantly different from each other. The error bars represent the standard error of mean (SEM). The jittered dots represent the individual observations from each plot over the seasons.

Effects of crop management systems, doubled-up legumes systems, and seasons on maize productivity

n class="Species">Maize grain yields differed signpan>ificanpan>tly onpan>ly amonpan>g the 2 years inpan> which pan> class="Species">maize was planted (p < 0.0001, Table 1). Greater maize grain yield was observed in the 2016/2017 season and this had a mean of 5.2 t ha−1 while the 2017/2018 had a grain yield of 4.3 t ha−1 (Fig. 3a). Maize biomass yields also significantly differed among the years (p < 0.0001, Table 1). The 2016/2017 season had a greater yield of 3.8 t ha−1 while the 2017/2018 season had a yield of 3.1 t ha−1 (Fig. 3b).
Figure 3

Effect of different seasons on (a) maize grain and (b) biomass yield averaged across all sites. Boxplots with different letters above them are significantly different from each other. The error bars represent the standard error of mean (SEM). The jittered dots represent the individual observations from each plot over the seasons.

Interactive effects of different crop management systems and legume combinations and populations with seasons on (a), (b) legume grain yield and (c), (d) legume biomass yield over the seasons of implementation: n class="Chemical">RF = ridge anpan>d furrow; CA = conpan>servationpan> agriculture; soleGn = sole grounpan>dnuts; pan> class="Chemical">solePp = sole pigeonpea; fullGN/halfPP = legume intercropping with full population of groundnut and half population of pigeon pea; and fullGN/fullPP = legume intercropping with full population of groundnut and full population of pigeon pea. Boxplots with different letters above them are significantly different from each other. The error bars represent the standard error of mean (SEM). The jittered dots represent the individual observations from each plot over the seasons. Interactive effect of crop management systems and legume combinations and their different populations on legume biomass yield over the seasons of implementation: n class="Chemical">RF = ridge anpan>d furrow; CA = conpan>servationpan> agriculture; soleGn = sole grounpan>dnuts; pan> class="Chemical">solePp = sole pigeonpea; fullGN/halfPP = legume intercropping with full population of groundnut and half population of pigeon pea; and fullGN/fullPP = legume intercropping with full population of groundnut and full population of pigeon pea. Boxplots with different letters above them are significantly different from each other. The error bars represent the standard error of mean (SEM). The jittered dots represent the individual observations from each plot over the seasons. Effect of different seasons on (a) n class="Species">maize grainpan> anpan>d (b) biomass yield averaged across all sites. Boxplots with differenclass="Chemical">pan>t letters above them are significanpan>tly differenpan>t from each other. The error bars represenpan>t the stanpan>dard error of meanpan> (SEM). The jittered dots represenpan>t the inpan>dividual observationpan>s from each plot over the seasonpan>s. Planting n class="Species">maize after the differenpan>t legumes anpan>d their differenclass="Chemical">pan>t population combinpan>ationpan>s was of marginpan>al signpan>ificanpan>ce to pan> class="Species">maize biomass yield (p < 0.100, Table 1). Although the effect of these legumes was not significant, this marginality could reflect potential of significant effects with soleGn showing its high potential.

Effects of different legume combinations and populations on total system grain, total system biomass and overall total system yield

In a two-phase rotation, both crops are grown within the same season although on half of the piece of land. Here, we assessed the contribution of all crops involved in a rotation as a measure of total system productivity in terms of energy expressed in GJ ha−1. However, we assessed total grain energy and biomass energy separately since these usually have different uses within a household and added them to get the overall system productivity. Overall total system yield was significantly affected by the interaction of crop management system and the seasons (p < 0.01, Table 2). The CA system in 2016/2017 season had the highest total yield averaging 99.8 GJ ha−1 and this was comparable to the n class="Chemical">RF system of the same seasonpan> which averaged 95.5 GJ ha−1 (Fig. 4a). The least yield was obtainpan>ed inpan> the CA anpan>d pan> class="Chemical">RF systems both in the 2015/2016 season with an average of 46.2 GJ ha−1 (Fig. 4a). On the other hand, there was a clear grouping of performance based on the season as also observed for the individual crop performance. The legumes combinations affected total system yields differently (p < 0.05, Table 2). The highest total system yield was observed in 2017 for the fullGN/halfPP, soleGn and fullGN/fullPP subtreatments which averaged 102.8 GJ ha−1 (Fig. 4b). All different combinations of legumes and their populations in 2015/2016 resulted in the least total system yield ranging from 40.1 to 49.3 GJ ha−1.
Table 2

Significance of fixed effects on total system grain yield, total system biomass yield and overall total system yield across the years.

SourceDegrees of freedomSum of squaresWald statisticp-value¶
Overall total system yield
(Intercept)173,851367.032.20e−16***
Treatment (Treat)1313.50.729655ns
Subtreatment (Subtreat)317,395225.631.35e−14***
Season2264,631735.022.20e−16***
Treat × subtreat35080.750.57751ns
Treat × season2263326.280.005974**
Subtreat × season6374772.370.02384*
Treat × subtreat × season67083.310.839173ns
Residual (MS)257
Total system grain yield
(Intercept)131,484198.042.20e−16***
Treat1560.350.554526ns
Subtreat335,1352212.20e−16***
Season2208,2131309.682.20e−16***
Treat × subtreat31440.910.824183ns
Treat × season23612.270.321296ns
Subtreat × season6344121.640.001405**
Treat × subtreat × season63632.290.891634ns
Residual (MS)159
Total system biomass yield
(Intercept)116,939.5267.852.20e−16***
Treat1168.82.6690.1023ns
Subtreat37932.6125.4322.20e−16***
Season25374.684.9842.20e−16***
Treat × subtreat3232.83.6820.57751ns
Treat × season21999.831.6210.005974***
Subtreat × season63683.558.2440.02384***
Treat × subtreat × season6395.56.2540.839173ns
Residual (MS)63.2

¶ns, not significant.

*p < 0.05; **p < 0.01; ***p < 0.001.

Figure 4

Interactive effects of (a) different crop management systems and (b) legume combinations and populations with the seasons on total system grain yield, total system biomass yield and overall total system yield (grain plus biomass) over the seasons of implementation: RF = ridge and furrow; CA = conservation agriculture; soleGn = sole groundnuts; solePp = sole pigeonpea; fullGN/halfPP = legume intercropping with full population of groundnut and half population of pigeon pea; and fullGN/fullPP = legume intercropping with full population of groundnut and full population of pigeon pea. The letters within each segment of the stacked columns denote significance for that segment for grain and biomass and the letters above the columns denote significance for overall total system yield. Stack segments and columns with different letters are significantly different from each other.

Significance of fixed effects on total system grain yield, total system biomass yield and overall total system yield across the years. ns, not significant. *p < 0.05; **p < 0.01; ***p < 0.001. Interactive effects of (a) different crop management systems and (b) legume combinations and populations with the seasons on total system grain yield, total system biomass yield and overall total system yield (n class="Disease">grain plus biomass) over the seasonpan>s of implemenpan>tationpan>: pan> class="Chemical">RF = ridge and furrow; CA = conservation agriculture; soleGn = sole groundnuts; solePp = sole pigeonpea; fullGN/halfPP = legume intercropping with full population of groundnut and half population of pigeon pea; and fullGN/fullPP = legume intercropping with full population of groundnut and full population of pigeon pea. The letters within each segment of the stacked columns denote significance for that segment for grain and biomass and the letters above the columns denote significance for overall total system yield. Stack segments and columns with different letters are significantly different from each other. Total system grain yield was significantly affected by the legume combinations, the seasons, and the interaction of legume combinations and seasons (p < 0.01, Table 2). Thus, we present in detail, the interactive effect of the legume combinations and seasons. Growing n class="Species">pigeonpea alonpan>e inpan> the 2016/17 seasonpan> resulted inpan> the highest total system grainpan> yield of 76.8 GJ ha−1 anpan>d this was comparable to growinpan>g grounpan>dnut inpan> full populationpan> anpan>d pan> class="Species">pigeonpea in half population within the same year (Fig. 4b). Planting sole n class="Species">pigeonpea resulted inpan> the least total grainpan> yield of 4.4 GJ ha−1. For total system biomass yield, the interaction of seasonpan> anpan>d system (p < 0.001) anpan>d legume combinpan>ationpan>s (p < 0.001) signpan>ificanpan>tly affected total system biomass (Table 2). The CA system inpan> 2016/17 resulted inpan> the highest total system biomass yield of 33.5 GJ ha−1 while the same system yielded the least inpan> the 2016 seasonpan> (23.3 GJ ha−1) (Fig. 4a). Planpan>tinpan>g pan> class="Species">pigeonpea and groundnut in their full populations in 2016/17, sole pigeon in 2016/2017 and sole pigeon pea in 2015/16 yielded highest total biomass with 37.3 GJ ha−1, 34.8 GJ ha−1 and 35.7 GJ ha−1, respectively (Fig. 4b). Sole groundnut in the 2015/2016 season resulted in the least total biomass yield.

Land equivalent ratio

All doubled-up legumes systems had greater LERs than 1 indicating a yield advantage when growing two legumes simultaneously as opposed to growing one legume. When comparing monocropping to the legume configuration with both groundnut and n class="Species">pigeonpea at their full populationpan>s (fullGpan> class="Chemical">N/fullPP), LER significantly differed among the seasons (p < 0.01) (Table 3). The 2016/2017 and 2017/2018 seasons had the highest values of 1.3 compared to the 2015/2016 with an LER value of 1.1 (Table 4). There was no significant difference with the other population system (fullGN/halfPP) in terms of LER. When comparing monocropping system to fullGN/halfPP, LER values did not differ significantly among the systems, the seasons or their interaction (Table 3).
Table 3

Significance of fixed effects on land equivalent ratio (LER) of total system yield across the years.

SourceDegrees of freedomSum of squaresWald statisticp-value¶
LER (FullGn/fullPp)
(Intercept)1104.0742394.52 < 2.20e−16***
Treatment (Treat)10.0410.950.329709ns
Season20.5211.960.002524**
Treat × season20.0030.060.971593ns
Residual (MS)0.043
LER (FullGn/halfPp)
(Intercept)1111.7181542.15 < 2.00e−16***
Treatment (Treat)10.020.270.6013ns
Season20.3124.310.1159ns
Treat × season20.212.90.235ns
Residual (MS)0.072

¶ns, not significant.

*p < 0.05; **p < 0.01; ***p < 0.001.

Table 4

Land equivalent ratios for the different legume configurations for total system yield averaged across locations in different seasons.

SeasonLand equivalent ratio
FullGN/fullPPFullGN/halfPP
2015/161.13 b1.29 a
2016/171.28 a1.22 a
2017/181.25 a1.16 a

Means followed by different letters are significantly different from each other.

Significance of fixed effects on land equivalent ratio (LER) of total system yield across the years. ns, not significant. *p < 0.05; **p < 0.01; ***p < 0.001. Land equivalent ratios for the different legume configurations for total system yield averaged across locations in different seasons. Means followed by different letters are significantly different from each other.

Discussion

Declining soil fertility and increased threats of climate variability and change will require that crop management systems are sustainably intensified or the number of hungry n class="Species">people arounpan>d the world will inpan>crease[1,19,26]. We presenpan>t onpan>e strategy of sustainpan>able inpan>tenpan>sificationpan> of currenpan>t pan> class="Species">maize-based cropping systems through incorporation of doubled-up legumes systems. The results of the trial are consistent with those of Snapp et al. (2002) in showing that combining two legumes in maize-legume rotations enhance crop yields on limited landholding[17]. Nutritional benefits from the inclusion of more legumes in the diet can be anticipated[27]. It can further support cash-constrained farmers who cannot buy large quantities of mineral fertilizers to maintain soil fertility through biological N fixation[28,29]. The study focussed on answering four hypotheses which will be discussed here. The relatively high CV in the rainfall observed over the study seasons shows how variable the rainfall patterns have become because of climate change and the asson class="Disease">ciated risks that farmers face[30]. The lonpan>g dry spells anpan>d early tailinpan>g-off of the rainpan>fall seasonpan>s signpan>ificanpan>tly affected crop production inpan> the trial areas as it coinpan>cided with critical growth stages (pod formationpan> onpan> legumes anpan>d/or cob formationpan> anpan>d grainpan> fillinpan>g onpan> pan> class="Species">maize). From the statistical analysis (Table 1), the seasonal rainfall effect was stronger than the crop management systems effect. Our first hypothesis can therefore be accepted. The results call for crop management systems that are more adapted and more resilient to an increasingly variable climate[31]. Overcoming the downside effects of in-season dry-spells has previously been researched upon[32] and CA holds promise to be climate-resilient[33]. Previous research from Eastern Zambia also showed that CA systems can maintain or increase their productivity despite these climate conditions[8,34]. Combinations of improved doubled-up legumes systems and CA therefore seem logical as this would reduce the impact of climate on the crop management systems. All doubled-up legumes systems led to higher LERs which indicates advantages of growing several crops over monocropping grain legumes. In the 2015/2016 season, lower grain yields were recorded in fullGn class="Chemical">N/fullPP whenpan> compared to the 2016/2017 anpan>d 2017/2018 seasonpan>s as reflected inpan> the lower LERs (Table 4). The lower yield of pan> class="Species">pigeonpea in the first season affected the crop management system in that season. The reasons were lack of control of pests and crop competition for soil moisture in the very dry El Niño year. Pigeonpea is frequently affected by insect pests and requires control as often the pests affect the reproductive parts (flowers, pods) as previously found out by[35,36]. As per the LERs, there was a clear advantage of growing crops in combination in a doubled-up legumes system thus supporting our second hypothesis. Interestingly, the other population (fullGN/halfPP) had the opposite trend of yielding more in the driest year (although not significant), whereas in other years it was not as productive. It appears that moisture stress and crop competition between the species was less pronounced in this population in the very dry years as compared with (fullGN/fullPP), where both factors could have been mitigated by higher rainfall in the other two seasons. The lack of significant main treatment effect in the 3 years of study was surprising and unexpected. Possible reasons for the lack of a consistent response to the main crop management systems considering a variable climate may include the following: (a) the same plant population of groundnut was used in both CA and non-CA treatments to reduce the bias due to plant population. Traditionally, farmers in Eastern Zambia just plant a single row of groundnut on top of the ridge while double rows is a new cropping practice researched and promoted by the International Centre for Research in the Semi-Arid Tropics (ICRISAT) and its partners in the region[37]. The comparison with the traditional farmer spacing would have probably yielded significant effects of the crop management system as has been previously shown in Malawi[38]; (b) a relatively short-term conversion period (3 years) from n class="Chemical">RF to CA as researched inpan> these trials did not lead to immediate yield benpan>epan> class="Disease">fits. This lag time until benefits accrue has been highlighted as a major disadvantage of the promotion of CA systems[10]. It normally requires 2–5 cropping seasons in a maize-based system until the yield benefits become apparent[39,40]. Our third hypothesis, that doubled-up legumes systems under CA increase the maize and legume yields was therefore partially rejected. However, the interaction of the crop management system and the season showed superior performance of CA in some seasons under a variable climate. Labour requirements to plant crops on the flat and on ridges were not measured. We therefore suggest that even in the absence of a conclusive yield advantage over n class="Chemical">RF, CA would conpan>fer reduced labour for planpan>tinpan>g anpan>d weedinpan>g uponpan> practitionpan>ers of the crop combinpan>ationpan>s studied. Producinpan>g a crop with less labour on planpan>tinpan>g, as no manpan>ual ridginpan>g is required unpan>der CA, would meanpan> anpan> immediate econpan>omic benpan>efit for smallholders while waitinpan>g for the lonpan>ger-term yield inpan>crease. However, as these benpan>epan> class="Disease">fits were not quantified in these trials we can only refer to other literature on economic benefits of manual CA systems in the region[8,41,42]. The reduced legume grain yield for the fullGn class="Chemical">N/halfPP, class="Chemical">pan> class="Chemical">solePp and fullGN/fullPP subtreatments in the 2015/2016 season, considering the legume combinations and seasons interactions may have been due to moisture stress experienced as a result of the low rainfall. This was the year of an unprecedented El Niño, which significantly affected the whole region and its farmers[43]. Competition for moisture in more intensified crop management systems with several crops in a doubled-up legumes system is expected and may have led to reduced productivity of the constituents[44,45]. The reduced biomass yields in the doubled-up legumes systems in two years was attributed to lower rainfall received in the 2015/2016 and 2017/2018 agricultural seasons and asson class="Disease">ciated crop competitionpan> for soil moisture. Less pan> class="Chemical">water stress and crop competition on the other hand was experienced in the higher rainfall season of 2016/2017 emphasizing again the strong influence of rainfall season on crop yields. We can therefore conclude that doubled-up legumes systems and their individual components are affected more seriously in drier seasons as a result of the competition from the constituent crops. Legume intensification with n class="Species">pigeonpea anpan>d grounpan>dnut is therefore not overcominpan>g climate related challenpan>ges, despite the drought-toleranpan>t nature of both grounpan>dnut anpan>d pan> class="Species">pigeonpea. This is in contrast to results from Rusinamhodzi, et al.[46] who concluded that this was the case for central Mozambique. The n class="Species">maize grain anpan>d biomass yield differenpan>ces betweenpan> the seasonpan>s are also reflective of the differenpan>t rainpan>fall amounpan>ts received durinpan>g the study period. There was no effect of precedinpan>g legume combinpan>ationpan>s onpan> pan> class="Species">maize yields in subsequent seasons. The lack of response could be explained by (a) the duration of the trial as an accumulation of soil fertility (especially residual N and SOC) is a slow process and would require additional years to become apparent; (b) the current management of pigeonpea biomass in the system is critical. Traditional management of pigeonpea leaves and stems means cutting the pigeonpea stalks at harvest (in July/August) and replanting pigeonpea in the following cropping season. If this practice is continued, the green leaf of pigeonpea, the plant part where most of the nitrogen is accumulated[47] will not be used and most of the N in the leaves will volatilize during the long dry period between harvest and planting maize losing the benefit to the atmosphere. Ratooning of pigeonpea at maize planting time and using the green leaves at seeding of maize would be a better strategy[48]; (c) the retention of fibrous biomass from pigeonpea may have led to negative effects on N mobilization. Although pigeonpea residue has a low C:N ratio as compared to many cereals, the high lignin content negatively influences its decomposition. This is further exacerbated by the retention of residues of the succeeding maize crop. Retention of crop residues with a wide C:N ratio can lead to nitrogen lock-up, depending on the soil type and rainfall regime[49,50] which negatively affects the maize crop in subsequent years. Nitrogen lock-up has been associated with an increase in biological activity (macro- and meso-fauna) and proliferation of these organisms which limits available N for use by the plants[49,51]. Possibly as a result of these reasons, the residual effect of growing two legumes was not significant on individual maize yield in post-planted crops and confirms the rejection of our third hypothesis. Total system grain yield was much influenced by the seasons. In 2016/2017, overall total system grain yield under both CA and n class="Chemical">RF out-yielded the pepan> class="Chemical">rformance of these systems in the other seasons (Fig. 4a). The effects of the treatments were masked by the seasonal effects. The 2015/16 season also showed the least overall yield, explained by the low rainfall received in this El Niño season. The greatest benefits on overall total system yield were observed in 2016/17 season where both pigeonpea and groundnut were grown (Fig. 4b). The favourable conditions of 2016/2017 favoured the systems with both legumes in various populations, which yielded highest. In the same year, the sub-treatment involving groundnut as a sole crop was comparable. Groundnut are known to be more drought-tolerant[52] and are therefore a very important component in these systems. In all other years, the doubled-up legumes systems out-yielded sole legume systems. These results confirm that doubled-up legumes systems can provide farmers with additional calories to feed their families as well as their soil and livestock. Increased levels of biomass as a result of doubling-up legumes or n class="Species">pigeonpea alonpan>e may be benclass="Chemical">pan>eficial for CA systems in the lonpan>ger term as retainpan>inpan>g enpan>ough amounpan>ts of crop residues has beenpan> a major challenpan>ge inpan> implemenpan>tinpan>g CA systems inpan> the regionpan>. Grounpan>dnut kernel yields were always higher inpan> the trials as compared to pan> class="Species">pigeonpea grain yields, which indicates how important the crop is in this combination from a grain yield perspective. However, a greater proportion of biomass was produced by the pigeonpea even in 2015/2016 despite it being an El Niño year, confirming its drought-tolerance. Soil fertility benefits over time in the pigeonpea intercrop management systems have been reported and could reduce soil fertility decline as has been shown by various scholars[53-55]. Pigeonpea grain provides nutritional benefits and a potential cash income from the export markets. Stalks can be used as firewood or left standing and used as mulch at the onset of the cropping season while the leaves can be browsed by goats or cattle providing supplementary feed which is scarce during the dry season[20,21,36,56]. The results of our study show that with ideal moisture levels and adequate pest management, doubled-up legumes systems may lead to yield advantage. The combined results of both legumes show that doubling-up legumes offers farmers a range of benen class="Disease">fits anpan>d advanpan>tages over sole croppinpan>g[57]. Inpan> the study donpan>e by de Graaff anpan>d Kessler[29] across districts of Malawi, pan> class="Species">pigeonpea-groundnut doubled-up legumes systems generated the greatest amount of biologically fixed N (82.8 kg N ha−1) as compared to sole cropping of pigeonpea (54.1 kg N ha−1) or groundnut (55.8 kg N ha−1). For CA systems to become more attractive in the short term, doubled-up legumes systems may offer an additional entry point as they provide a diversity of marketable grain from legumes with different growth habits and sequence. In fact, groundnut is widely known and consumed by farmers in southern Africa, whereas n class="Species">pigeonpea has a good export market inpan> Inpan>dia but is, to-date, less conpan>sumed by farmers. There is need to develop a local market anpan>d socialize the crop with farmers, so it is locally conpan>sumed. Due to lack of funding and functional laboratory facilities on-site, the specific effects of doubled-up legumes systems under CA on soil fertility and biological n class="Chemical">nitrogen fixationpan>, as well as econpan>omic benpan>epan> class="Disease">fits of the different systems could not be explored further. These remain future areas of research in the quest to find sustainable systems for smallholder farmers in Southern Africa.

Conclusion

The research on doubled-up legumes systems under the conditions of eastern Zambia showed that there is a benefit of growing doubled-up legumes systems as compared to single crop rotations. We conclude from this research that: (a) the level of trial pen class="Chemical">rformanpan>ce was stronpan>gly determinpan>ed by the rainpan>fall anpan>d croppinpan>g seasonpan> anpan>d was not consistenpan>t; (b) there was no detectable residual benpan>efit of doubled-up legumes systems onpan> post-planpan>ted pan> class="Species">maize yield, which means that the contribution of preceding legumes to maize in the second cropping season is too small and this may be attributed to the short cycle annual rotation effect and/or the short experimental duration of 3 years which limited significant increase in soil fertility. Residual benefit of legumes on succeeding maize which is usually through soil fertility build-up depends on organic matter turnover and carbon sequestration which takes time; (c) Overall, total systems yield as well as total system grain and biomass yield can be improved by doubling-up the legumes and rotating with maize. This will provide not only additional grain yields but an improved nutritional supplementation for smallholders who are usually faced with low calorie intake; (d) supplementary biomass is produced by doubling-up legumes hence improving the levels of biomass in the system for surface crop residue retention as well as feed for livestock, which are an important component of smallholder farming systems; (e) growing doubled-up legumes systems under CA would potentially lead to reductions in labour for planting as CA systems can be flat planted without manual labour for ridging whereas the conventionally tilled system requires extensive labour on tilling and ridging the soil. This can potentially brighten prospects for CA. Further research should focus on the specific effects of doubled-up legumes systems under CA on soil fertility and biological nitrogen fixation, as well as on economic benefits.

Materials and methods

Study site description

The study was carried out in five on-farm communities of eastern Zambia (Table S1). Eastern Zambia lies between latitude − 10° to 15° S and longitude 30°–33° E[58] and all farming systems practiced in this area are n class="Species">maize-mixed farminpan>g systems[59]. The sites lie inpan> the Zambianpan> agro-ecological zonpan>e IIa, which receives anpan>nual rainpan>fall betweenpan> 800 anpan>d 1000 mm[60]. The rainpan>fall season is unimodal, usually startinpan>g inpan> pan> class="Chemical">November and ending in April. The soils are relatively fertile Acrisols and Luvisols[61].

Experimental design

In establishing the doubled-up legumes systems trial, only combinations of legumes were planted to plots in the first season (the legumes phase). In the second season, the legumes phase plots were superimposed with a uniform n class="Species">maize crop (the pan> class="Species">maize phase) and a new legumes phase was equally added. In the third season, the plots hosting the legumes combinations were once again super-imposed with a uniform maize crop while a second legume phase was initiated on plots hosting the uniform maize crop in the previous season. In summary, plots planted to legumes combinations were planted to a uniform maize crop in the subsequent season and alternated thereafter. However, the trial could not proceed beyond the third season due to funding constraints. The trial was set up in a split plot design with five replications at each site. The main treatments were based on crop management systems: Conservation Agriculture (CA)—no-tillage with residue retention; and Conventional tillage-based ridge and furrow tillage (n class="Chemical">RF)—with residue removal The main plots were split into sub-plots with four sub-treatments based on different legumes with different populations: Groundnut planted as sole crop (soleGn) n class="Species">Pigeonpea planted as sole crop (n class="Chemical">solePp) Groundnut planted in full population plus half population of n class="Species">pigeonpea (fullGn class="Chemical">N/halfPP) Groundnut planted in full population plus full population of n class="Species">pigeonpea (fullGn class="Chemical">N/fullPP) The plot size was 6 m × 6 m and a net plot of four rows by 5 m in length was harvested. Land preparation for the n class="Chemical">RF treatmenpan>t was inpan> manpan>ually dug ridges, prepared inpan> October before the onpan>set of the cropping season. The ridges were spaced at 75 cm anpan>d had a height of approximately 25–30 cm. Sowinpan>g unpan>der CA was donpan>e inpan> riplinpan>es of approximately 10 cm depth created by anpan> ox-drawn Magoye ripper without further soil disturbanpan>ce.

Crop management

Crops were sown after the first effective rains at each site which was in mid-December of each season. In the first season, the groundnut variety MGV 4 and n class="Species">pigeonpea variety Chitedze 1 were sown. Inpan> pan> class="Chemical">RF, groundnut was sown in a double row spaced at 10 cm apart on top of ridges spaced at 75 cm and with an in-row spacing of 20 cm (target population of 133,333 plants ha−1). In CA systems, groundnuts were sown in rows spaced at 37.5 cm on the flat with an in-row spacing of 20 cm (133,333 plants ha−1). Although farmers are currently only sowing one row of groundnut on top of the ridge in the RF system, we used double rows to avoid higher plant populations in the CA system as the plant population would double and possibly bias the results in favour of CA. Pigeonpea in full population (sub-treatments 2 and 4) was sown at a spacing of 75 cm × 60 cm with 2 plants per station (44,444 plants ha−1) whereas in its half population (sub-treatment 3), it was sown with only one plant per station (22,222 plants ha−1). Pigeonpea was sown either on top of the ridge between the groundnut rows (RF) or planted in every second groundnut row when planted on the flat (CA). Maize sowing in the season following the legumes phase was done at a plant spacing of 75 cm × 25 cm (53,000 plants ha−1) for all treatments. The commercial, medium maturing maize variety KKS501 was sown in both cropping seasons. Fertilization was uniform across all treatments at a rate of 10 kg ha−1 n class="Chemical">N:20 kg ha−1 pan> class="Chemical">P2O5:10 kg ha−1 K2O applied as basal dressing at sowing to both legumes and maize in each season. This is half the Zambian Government recommended rate. Maize further received a top dressing of 46 kg ha-1 N in the form of urea which is again half of the recommended rate. Legumes also received gypsum at a rate of 500 kg ha−1 (147 kg ha−1 Ca and 118 kg ha−1 S) to enhance pod formation. Weed control at all sites was achieved with an initial spray of glyphosate [N-(phosphono-methyl) glycine] at a rate of 3 l ha−1 followed by hoe weeding whenever weeds reached 10 cm in height or circumference for weeds with a stoloniferous growth habit. An initial application of 2.5–3 t ha−1 (dry-weight) of maize stalk residues was done to the first-season legume plots and at the beginning of each season thereafter. Pest control was minor in the first season but pests such as the blister beetle (Mylabris oculata MYLBPU) and cotton bollworm (Helicoverpa amigra Hb.) heavily attacked the pigeonpea which led to a significant yield penalty on the crop in the first season (See Figure S1). We therefore resorted to spraying the pigeonpea with DDVP (Dichlorvos; active ingredient 2,2-dichlorovinyl dimethyl phosphate) at recommended rates to control these insects from the second season onwards. Relevant institutional, national, and international laws guiding studies on plants were adhered to in the conduct of this study.

Data collection

Rainfall collected in rain gauges installed at each site was recorded daily by farmers who hosted the trial after every rainfall event (usually before 9:00 a.m.). Yields were determined from the net plots by weighing all the plants including the pods or cobs, removing the pods or cobs and weighing them separately. Subsample of pods (approximately 500 g) or 10 cobs and biomass (approximately 500 g) were taken to determine the dry weight. After shelling the subsamples and weighing the grains, a moisture reading was taken (using a mini GAC moisture tester from Dickey – John, USA) to determine the yield at 12.5% and 9% moisture content for n class="Species">maize anpan>d legumes, respectively. Biomass weight was determinpan>ed at a pan> class="Disease">dry-weight basis. Both yields were then reported in t ha-1.

Calculations and statistical analyses

Legume and maize productivity and total grain, total biomass and overall total system yield

To assess the effects of crop management systems and different legumes and their different population combinations on yield of n class="Species">maize, yield of legumes, anpan>d total system yield; mixed models were used for the split plot designpan>. Inpan> these models, crop manpan>agemenpan>t systems had the mainpan> effects while the differenpan>t legumes anpan>d their differenpan>t populations had the sub-effects, anpan>d these were inpan>cluded as fixed effects together with seasonpan>s (years). Sites anpan>d plots withinpan> blocks withinpan> sites were inpan>cluded as ranpan>dom effects to accounpan>t for groupinpan>g factors anpan>d repeated measures across the seasonpan>s. The signpan>ificanpan>ce of the fixed effects was tested usinpan>g the Wald chi-square test inpan> Asreml-R package[62] as well as usinpan>g the 'lme4’ package[63] anpan>d meanpan> conpan>trasts were donpan>e usinpan>g the multiple comparisonpan> procedure with multiplicity adjustmenpan>t usinpan>g the 'emmeanpan>s' package[64] inpan> R statistical enpan>vironpan>menpan>t[65]. Overall total system yield was calculated as a sum of both grainpan> yield anpan>d biomass yield of all crops inpan>volved inpan> each crop manpan>agemenpan>t system conpan>verted to enpan>ergy inpan> GJ ha−1. For the conpan>versionpan> of grainpan> yield to enpan>ergy, grainpan> enpan>ergy values were obtainpan>ed from the GEpan> class="Chemical">NuS database where energy values of the unprocessed grain are reported. Maize, pigeonpea and groundnut are indicated to contain 353 kcal 100 g−1, 301 kcal 100 g−1 and 578 kcal 100 g−1, respectively. For the energy values of above ground biomass, we referred to various sources such as the Feedipedia (https://www.feedipedia.org/) where energy values of biomass were reported for livestock feeding. Maize, pigeonpea and groundnut biomass were reported to contain 125 kcal 100 g−1, 186 kcal 100 g−1 and 155 kcal 100 g−1 of energy in their biomass, respectively. Energy values of each system were calculated using either Eq. (1) or (2) as follows:where TS and TS2 are the total system yield of crops in the system, with respect to their energy value (GJ ha−1) for systems without rotation and with rotation, respectively, that involved crops i and j. Yc and Yc are yields of crops in each phase of the system (kg ha−1; Ec and Ec represent energy contents of crops i and j involved in the intercrop (kcal 100 g−1) and GJ is a conversion factor that converts kcal to GJ, where 1 GJ is 238,845.9 kcal. Equation (1) was used for calculation of total system yield in season 2015/16 since only the legume phase of the rotation was planted and Eq. (2) was used for seasons 2016/17 and 2017/18 since both the maize and legume phases of the rotation were present and yield was based on half of each system in each phase. Data was further presented in terms of land equivalent ratio (LER) to better understand the ratio of the area under legume sole cropping to the area under companion legumes systems that would be needed to produce the same total system yield[66]. The LER was used to assess the total system yield advantage of the different legume intercropping configurations based on crop management system and season as compared to the monocropping system. Since two intercropping systems were involved based on different populations of the legumes, LER was assessed separately for these i.e., (a) ratio of sole cropping to intercropping with full populations of groundnut and n class="Species">pigeon pea anpan>d, (b) ratio of sole croppinpan>g to inpan>tercroppinpan>g with full grounpan>dnut populationpan> plus half populationpan> pan> class="Species">pigeonpea. Land equivalent ratio was calculated using Eq. (3): where LGn and LPp are partial LERs for groundnut and pigeonpea, respectively; Y and Y are the energy values of groundnut and pigeonpea in the companion system, respectively (GJ ha−1); Y and Y are energy values of sole groundnut and pigeonpea, respectively (GJ ha−1). If the LER is greater than 1, it means that there is an advantage of the companion legumes system over sole planting and if it is below then there is a yield penalty in using the companion legumes system as compared to sole cropping. Effects of crop management systems and seasons on LER were analysed using the same models as used for yield in the previous section. Supplementary Information.
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1.  Insect pests of pigeonpea and their management.

Authors:  T G Shanower; J Romeis; E M Minja
Journal:  Annu Rev Entomol       Date:  1999       Impact factor: 19.686

Review 2.  Food security: the challenge of feeding 9 billion people.

Authors:  H Charles J Godfray; John R Beddington; Ian R Crute; Lawrence Haddad; David Lawrence; James F Muir; Jules Pretty; Sherman Robinson; Sandy M Thomas; Camilla Toulmin
Journal:  Science       Date:  2010-01-28       Impact factor: 47.728

3.  Biodiversity can support a greener revolution in Africa.

Authors:  Sieglinde S Snapp; Malcolm J Blackie; Robert A Gilbert; Rachel Bezner-Kerr; George Y Kanyama-Phiri
Journal:  Proc Natl Acad Sci U S A       Date:  2010-11-22       Impact factor: 11.205

4.  Prioritizing climate change adaptation needs for food security in 2030.

Authors:  David B Lobell; Marshall B Burke; Claudia Tebaldi; Michael D Mastrandrea; Walter P Falcon; Rosamond L Naylor
Journal:  Science       Date:  2008-02-01       Impact factor: 47.728

Review 5.  Climate change impacts on global food security.

Authors:  Tim Wheeler; Joachim von Braun
Journal:  Science       Date:  2013-08-02       Impact factor: 47.728

6.  Agriculture: Plant perennials to save Africa's soils.

Authors:  Jerry D Glover; John P Reganold; Cindy M Cox
Journal:  Nature       Date:  2012-09-20       Impact factor: 49.962

Review 7.  Beyond conservation agriculture.

Authors:  Ken E Giller; Jens A Andersson; Marc Corbeels; John Kirkegaard; David Mortensen; Olaf Erenstein; Bernard Vanlauwe
Journal:  Front Plant Sci       Date:  2015-10-28       Impact factor: 5.753

  7 in total

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