environmental, social, and management drivers of soil nutrient mass balances in an extensive andean...
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Environmental, Social,and Management Drivers of Soil
Nutrient Mass Balances in anExtensive Andean Cropping System
S. J. Vanek1* and L. E. Drinkwater2
1Department of Crop and Soil Sciences, Cornell University, Ithaca, NY 14853, USA; 2Department of Horticulture, Cornell University,
Ithaca, New York 14853, USA
ABSTRACT
Sustainable nutrient cycling in agroecosystems com-
bining grazing and crops has global ramifications for
protecting these ecosystems and for the livelihoods
they support. We sought to understand environ-
mental, management, and social drivers of nutrient
management and sustainability in Andean grazing/
crop systems. We assessed the impact of farmer
wealth, fields’ proximity to villages, topography, and
rangeland net primary productivity (NPP) on mass
balances for nitrogen (N), phosphorus (P), and
potassium (K) of 43 fields. Wealthier farmers applied
greater total amounts (kg) of manure nutrients.
However, higher manure application rates (kg ha-1)
were associated with field proximity and NPP rather
than wealth. Manure P inputs in far fields (> 500-m
distant) were half those in near fields. Harvest exports
increased with manure inputs (P < 0.001) so that
balances varied less than either of these flows. Erosion
nutrient losses in steeper far fields matched crop
exports, and yields declined with increasing field
slope (P < 0.001), suggesting that erosion reduces
productivity. Balances for P were slightly positive in
near and far fields (+2.2 kg P ha-1 y-1, combined
mean) when calculated without erosion, but zero in
near fields and negative in far fields with erosion in-
cluded (-6.1 kg P ha-1 y-1 in far fields). Near/far
differences in both inputs and erosion thus drove P
limitation. Crop K exports dominated K balances,
which were negative even without accounting for
erosion. Modeled intensification scenarios showed
that remediating far field deficits would require P
addition and erosion reduction. Management nested
within environmental constraints (NPP, erosion)
rather than socioeconomic status drives soil nutrient
sustainability in these agroecosystems. Time-lags
between management and long-term degradation are
a principal sustainability challenge to farming in these
montane grazing/crop agroecosystems.
Key words: nutrient mass balances; Andes; soil
erosion; rangeland; mixed cropping systems; time-
lags; Bolivia; manure; phosphorus; potassium.
INTRODUCTION
In smallholder systems with a mix of grazing and
cropland, traditional methods used by low-intensity
smallholders have been characterized as sustainable,
relying on primary productivity in grazing areas and
transformation of soil nutrients into useable form by
fallow vegetation and animals (Powell and others
Received 19 February 2013; accepted 23 July 2013;
published online 21 August 2013
Electronic supplementary material: The online version of this article
(doi:10.1007/s10021-013-9699-3) contains supplementary material,
which is available to authorized users.
Author Contributions: SJV and LED conceived the study and wrote the
paper. SJV conducted research and analyzed data.
*Corresponding author; e-mail: [email protected]
Ecosystems (2013) 16: 1517–1535DOI: 10.1007/s10021-013-9699-3
� 2013 Springer Science+Business Media New York
1517
1996; Pestalozzi 2000). However, traditional systems
face pressure from increasing human and animal
populations, breakdown of communal management
systems, and external market incentives (Mayer
1979; Lightfoot and Noble 2001; Pendleton and
Howe 2002; Baijukya and others 2005; Pacheco
2009). Frequently, intensification of these systems
increases erosion and truncates the regeneration of
soil fertility,1 so that fallows and grazing-derived
manure fail to replenish nutrient deficits. Degrada-
tion and declining productivity create a downward
spiral that undermines food security for smallhold-
ers. However, other research suggests that innova-
tion often averts degradation within smallholder
systems via practices such as agroforestry, fertilizer
and manure additions, efficient residue recycling,
and sustainable-grazing management, often sup-
ported by markets, regional policies, and local
knowledge and governance (Mortimore and Harris
2005; Schechambo and others 1999; Scherr 2000).
Mixed cropping systems utilizing rangelands are
an important setting in which to analyze potential
degradation by smallholders. The strategy of sup-
porting intensively managed crops by integrating
rangeland and animals is found worldwide from
uplands in Mexico and India to wide swaths of
African savanna and mountain regions (Powell and
others 1996; Saberwal 1996; Elias and others 1998;
Aganga and Mosimanyana 2001; Schlecht and
others 2004; Arriaga-Jordan and others 2005; Ruf-
ino and others 2011). Rangelands with significant
human habitation cover over 20% of the earth’s
non-wild land area (Ellis and others 2010). These
form an important grazing–cropping ‘‘anthrome’’
on marginal landscapes that are not suited for
intensive agriculture due to poor soils, steep
topography, or limited rainfall. Such systems con-
trast markedly with densely populated, intensive
smallholder systems that were the focus of the
Green Revolution, where confined livestock do not
interact with rangelands (Thorne and Tanner 2002).
Nutrient mass balances can be used to understand
the potential drivers of nutrient depletion in these
systems. Mass balances are an important tool of
ecosystem ecology whose use has expanded to study
managed ecosystems (Smaling and others 1996;
Baker and others 2001). As applied to agricultural
management, balances quantify net gain or loss of
nutrients over time for fields and other land units
and can identify which nutrients (for example, N, P)
or processes (for example, manure inputs, crop
export) most limit agroecosystem productivity,
suggesting leverage for innovations in practices
(Berry and others 2003; Baijukya and others 2005).
Mass balances have also identified crop rotations,
land uses, or spatial components of systems that are
most vulnerable to nutrient depletion (Elias and
others 1998; Wortmann and Kaizzi 1998; Lesschen
and others 2007), or suggested that relative wealth
or poverty drive degradation (Elias and others 1998;
Nkonya and others 2005; Yirga and Hassan 2006;
Cobo and others 2009).
In this study, we used nutrient balances to
evaluate the relative importance of environmental,
social, and management drivers on the sustainability
of soil nutrient stocks in Andean agroecosystems.
These are extensive, mixed crop–livestock systems
managed by smallholders with a shared land base
for grazing, combined with some degree of social
stratification. Households rely mainly on forage
production in extensive rangelands and food pro-
duction in crop fields dispersed within mountain
terrain at varying distances from a central village.
We hypothesized that the NPP of community
territories and soil erodibility from varying slopes of
fields would be environmental drivers of these bal-
ances. We predicted that NPP (kg ha-1) within a
community’s boundary would correlate positively
to manure nutrient inputs to fields because animals
graze freely on surrounding non-cropped lands.
Because of the steep topography we also expected
that soil erosion related to differing field slopes
would influence mass balances, with flatter fields
in areas near communities suffering smaller erosion
losses. As a social driver, we expected that farmer
wealth level indicated by land and animal owner-
ship would affect field nutrient balances, because
livestock is a means of capturing manure nutrients
from rangeland for application to cropland. We
expected that wealthier farmers with more animals
would apply both a greater total amount and at a
higher per-hectare rate on farmed fields. The cor-
responding lower manuring rates among poorer
farmers would create more negative balances and
thus greater degradation potential. Manuring rate
was expected to be the important management dri-
ver governing soil nutrient stocks, expressing social
factors of differential access to rangeland manure
nutrients, and also knowledge and management
strategies particular to each farm. We expected that
higher manuring rates on near versus far fields
would create gradients in soil nutrients and pro-
ductive capacity by creating more positive nutrient
1 We use ‘‘soil fertility’’ to refer broadly to soil produc-tive capacity which reflects not only nutrient availabilitybut also soil physical and chemical characteristics such aspore structure, water holding capacity, cation exchangecapacity, and pH which all impact plant productivity.
1518 S. J. Vanek and L. E. Drinkwater
balances on near fields. We also expected mass
balances to show whether N, P, or K most con-
strains crop productivity in these systems. Lastly,
we used our data to create scenarios that model
management alternatives into the future. We
compared a status quo rotation scenario to balances
resulting from management changes that would be
expected to slow or accelerate degradation.
MATERIALS AND METHODS
Research Area
Field-scale nutrient balances were constructed for
43 farms in northern Potosi, Bolivia, an isolated
region with rainfed potato-cereal-pulse rotations
set within areas of rangeland and fallows (Fig-
ure 1). Livestock are a versatile economic asset and
a manure source for these farms (McCorkle 1990).
Sheep predominate at higher elevations and goats
at lower elevations, with some llamas at higher
elevations and bullocks throughout for traction.
Animals are grazed on rangeland year-round
(predominantly C3 grasses at high elevations and
shrubs at lower elevations; CIF-UMSS 2013), with
seasonal feeding of crop stubble and cultivated
forage oats. Average annual precipitation of
650 mm occurs between October and March (FAO
2010). Mean temperatures during this cropping
season range from 9.5 to 18.0�C varying by field
elevation (between 2,700 and 4,200 m asl). Agri-
cultural management regimes differ based on
proximity to villages: far fields in contiguous blocks
under community sectoral fallows undergo syn-
chronized crop rotations (Pestalozzi 2000). Erosion
prevention measures include stone retention walls
and shrub live barriers that reduce but do not
eliminate substantial field slopes, in contrast to
other areas in the central Andes where crops are
grown on terraces. Nearer to households, field
rotations are determined by each household with-
out synchronization. The dominant soil nutrient
input is manure derived from rangeland grazing
and feeding of crop residues. Crop rotations gen-
erally begin with potato, which receives the bulk of
manure in the rotation. A 2nd year with maize,
wheat, barley, fava beans, peas, or oca (Oxalis tu-
berosum) receives sporadic manuring. A final rota-
tion year without manure follows, usually a cereal,
forage oats, or Andean lupine (tarwi locally, Lupinus
mutabilis Sweet). On average, legumes occur once
per 25 years in far fields and once per 7 years in
near fields (unpublished survey data). Maize is
grown below 3,600 m elevation, sometimes in
continuous cropping alternating with wheat.
Wealth Ranking and Land and AnimalAssets of Farmers
Data on household asset levels were drawn from a
local project baseline study (Neighbors 2006).
Community members anonymously ranked peers
into three groups as those with ‘‘most’’, ‘‘less’’, and
‘‘very little’’ and estimated typical asset levels of
these groups in animal numbers and cropland area.
Farmers with fields sampled for nutrient balances
provided the number of animals they owned and
kg of seed planted for each crop. Total cropped area
for the farm was calculated by dividing these seed
amounts by local crop seeding rates (kg ha-1) given
by experienced farmers and project staff.
Remotely-Sensed NPP and SlopeGradient Data Within CommunityBoundaries
Annual NPP (g C m-2) on a 1,000-m grid, averaged
over the years 2000–2006 was downloaded from an
online database (MODIS, Zhao and others 2008).
Community boundaries were geo-referenced and
transferred to the NPP layer. Mean NPP was cal-
culated for the five to ten 1-km2 pixels covering
each community. To examine how village and field
locations influenced soil erosion potential, a digital
elevation model (DEM) at 30-m resolution (ASTER,
Figure 1. Study location, with latitude/longitude coor-
dinates.
Drivers of Andean Soil Nutrient Mass Balances 1519
ERSDAC 2007) was used to create a histogram of
slope gradient (degrees slope, binned at 2-degree
intervals) for the entire community and also for
pixels in a 500-m radius of villages. The proportion
of highly erodible land in each community area was
calculated as the percentage of pixels with slope
greater than 21% (12� slope gradient). This slope
threshold represents highly erodible land in the
Revised Universal Soil Loss Equation (RUSLE; Re-
nard and others 1997) and was also chosen to create
the widest separation between communities with
flat and steep topography in a 45-community survey
dataset from another study (Jones 2011).
Field Selection and Overall BalanceApproach
One field per farm was identified in collaboration
with a random sample of farmers, stratified by
anonymous wealth ranking so that fields from all
three wealth levels in all communities were sam-
pled. The final sample contained ten each of
highest and lowest grouped-farmers, and 23 of the
middle group. Balances were calculated as inputs
minus outputs for an entire rotation divided by the
rotation length (giving kg ha-1 y-1). Rotations of
2 years were measured for near fields in the lowest
community, where continuous cropping of maize
and wheat takes place. Six-year rotations with
three cropped and three fallow years occurred in
most other fields, whereas some near fields at
higher elevations had 3-year crop sequences
without fallows. We used 3 years as the fallow
length for far fields based on farmers’ projections of
likely future fallows, and the median fallow length
(3.2 years) from a parallel survey of 297 house-
holds (Jones 2011).
Sampling during two sequential years was stag-
gered to capture 3 years of cropping reflecting
common local crop sequences. Manuring rates and
two sequential-cropped years were measured on
the 43 designated fields, during which all manuring
and most of the crop exports occur. Then, we
estimated cereal and lupine nutrient exports of a
3rd year by sampling a similar set of fields in their
3rd year of production following potatoes and a
2nd-year crop. These cereal fields were in the same
communities, near/far locations, and elevations as
those sampled for 2-year sequences. We fit P
exports from these fields to a random normal dis-
tribution and used draws from this distribution to
estimate P exports for the 3rd year, for fields in
which farmers later reported growing cereals in the
3rd year. To find N and K exports for these fields,
we multiplied these P exports by a similar draw
from N:P and K:P distributions of harvest nutrient
content ratios based on the sampled cereal fields.
When lupine occurred in the 3rd year, qualitative
yield estimates from farmers were converted to
exports of N, P, and K, and fixed N inputs using
local field experiment data (Vanek 2011).
Manure Inputs to Fields
Manure inputs of N, P, and K were measured in
two manuring systems used by farmers. At lower
elevations (2,500–3,400 masl), fields receive two to
four nights of manuring when animals are corralled
at night in fields prior to cropping (‘‘field-corral’’).
At elevations generally above 3,500 masl a second
‘‘fixed-corral’’ system is used: manure accumulates
over an entire year in fixed sleeping pens, and then
is transported to fields for direct application to crops
at seeding.
For the field-corral system, manure was gathered
from three stratified, randomly selected quadrats of
0.25 m2 within the corral after at least two nights of
corralling. Small amounts of soil (< 2%) adhering
to manure was included to maximize capture of
manure and urine nutrients. Manure was weighed
and subsampled for dry matter (DM) calculation
and nutrient analysis (below). Mean DM per
0.25 m2 for three quadrats gave a field-level
nutrient application rate. The nightly rate was
multiplied by the intended number of nights of
manuring to give a total manure input rate.
Our manure rate measurements are most accu-
rate for P inputs, which remain in a particulate
form in manure without gaseous losses. Our field-
corral N measurements may slightly underestimate
manure N inputs: samples were air-dried before
analysis from a moist field state, and ammonia-N in
urine may have entered the soil without being in-
cluded in the sample. Typical ammonia-N fractions
of about 25% of total N for ruminant manure are
an upper bound on this uncertainty (Antil and
others 2009). Urine K may likewise not be captured
by our measurements. We adjusted field-corral
manure K concentrations upward by a factor of
1.96, the ratio of fixed-corral to field-corral K
content of manure in a community that used both
manuring practices (that is, based on the same
animals and rangeland forages and likely to create
similar levels of K excretion in livestock urine). We
conducted a simple sensitivity analysis to test the
impact of imprecision in manure K content (see
results).
Fixed-corral manuring using manure from
household pens was measured late in the dry sea-
son and did not suffer N and K leaching, because
1520 S. J. Vanek and L. E. Drinkwater
corral manure DM content was always greater than
50%. Small, regularly spaced piles of manure are
placed on fields at planting, so that manuring could
be measured by estimating the weight of 15–20
piles within rectangular control areas. Manure
weight in each rectangle was estimated by weigh-
ing two piles with a calibrated spring scale. Manure
bulk density was then calculated as mean weight
divided by mean volume of the piles (modeled as
cones with rounded tops, using their heights and
average diameters). The weight of remaining piles
in the field area was then found by multiplying the
volume of each pile (measured as for the weighed
piles) by the manure bulk density. Manuring rate
was computed as the total DM of the piles divided
by the rectangle area. A bulked sample was taken
from all piles in the field for nutrient analysis.
Seed Nutrient Inputs
Seeding rates (kg ha-1) were given by local farmers
and field staff: potatoes, 1,700; maize, 80; wheat
and barley, 100; oats, 120; fava beans, 120; and
lupine, 60. Seed nutrient inputs were the product
of these rates by mean crop nutrient contents (be-
low). For oat seed a literature value was used
(NRCS 2010).
Fixed N and Nutrient Deposition
N additions by legume crops (fava beans, lupine)
were estimated as net zero; local experiments with
lupine indicated that the mean shoot N fraction
(69%) equaled the fraction of N fixed (%Ndfa;
Vanek 2011) so that grain and straw N exports
cancelled the N-fixation input (Ndfa). This is con-
servative given higher estimates of %Ndfa for fava
(75%; Ross and others 2008), and higher lupine
%Ndfa for the most P-fertile sites in the area (80%;
Vanek 2011). Field experiments have shown a
16 kg N ha-1 input from lupine residues (Villarroel
and others 1986). Mean Ndfa inputs would however
be small on an annualized basis because legumes
are infrequently grown.
Three-year fallows in sampled fields were as-
signed an N-fixation credit of 4 kg N ha-1 y-1. This
was determined by sampling three fallow fields of
age 2–5 years for which shoot + root N equaled
24 kg ha-1, with %Ndfa of 50% calculated for
endemic range legumes (for example, Trifolium
amabile, unpublished data). We did not account for
additional fixed N left as manure during grazing on
wild legumes in fallows. This flow was likely much
smaller than manure N inputs during cropping.
Deposition was minor and was not included in our
balance calculations (< 0.2 kg ha-1 of N and K per
year; Duncan Fairlie and others 2007; Lesschen and
others 2007).
Crop and Residue Exports
Crops and residues were weighed from three ran-
dom, stratified quadrats in each field (1 m2 for
cereals, 3 m2 for other crops). Harvested weight
was divided by the quadrat area, giving yield
(kg ha-1), and the mean of the three quadrat DM
yields was calculated. For maize, stalks and ears
with grain were weighed separately, and subsam-
ples of two ears and two stalks were taken to
measure DM and nutrient content. Dry subsample
grain and stalk weight allowed calculation of yields
from total ear and stalk weight. Maize stalk biomass
was added to cob and husk DM to calculate residue
export for each quadrat. For broadcast forage oats,
wheat, and barley, mature whole shoots from three
1-m2 quadrats per field were weighed. A random
subsample of 25 stems was dried and threshed to
calculate grain and straw DM yields per quadrat.
Maize and cereal residues were treated as exports
reflecting local practices of threshing and feeding
residues off-field. Crops and weeds were cut at
3-cm height to reflect post-harvest grazing of fields.
Moisture Content and Nutrient Analyses
Crop and manure samples were dried in paper bags
on pavement in strong sunlight (45�C), followed by
oven-drying at 58�C. Tubers were frozen before
drying. Dry weight over field fresh weight gave DM
content. N content was measured in ground sample
DM by combustion (LECO St. Joseph, MI). Total P
and K in crops and manures was determined using
nitric acid digestion followed by P and K analysis by
ICP-AES (Kalra 1998). Nitrogen, P and K flows
were then calculated as crop or manure DM stocks
(kg ha-1) multiplied by their nutrient concentra-
tions.
Soil Erosion, Gaseous, and LeachingLosses
To estimate erosion losses from fields, we calibrated
RUSLE (Renard and others 1997) for 1 year on six
fields growing cereal crops and five fields recently
placed in fallow. Fallow fields contained a mix of
crop residues and vegetation grazed by animals.
Measured erosion rates were regressed to RUSLE’s
topographic factor LS, representing slope length (L)
and gradient (S) from the soil loss equation:
Drivers of Andean Soil Nutrient Mass Balances 1521
Erosion Mg soil ha�1y�1� �
¼ R K LSð ÞC Pr:
Here R represents rainfall erosivity, K is soil
erodibility, C and Pr incorporate the effects of soil
cover and management practices, respectively. We
measured L (m) and S (% slope) on calibration
fields and those used for balances so that soil ero-
sion could be estimated as
Erosionmodeled ¼MlocalLS
with Mlocal the fitted slope of measured erosion rates
against LS (that is, equal to R K C Pr). We measured
erosion on the 11 calibration fields by modifying the
erosion pins method (Haigh 1977; Hudson 1993),
which measures the elevation change of the soil
surface compared to a datum to quantify erosion or
deposition. At each of four field replicates we
measured 15–20 microelevation changes over
1 year. We then multiplied this elevation change by
soil bulk density, corrected for stone content dif-
ferences in the initial and final bulk density sam-
pling cores. On the six calibration fields with cereal
crops, we also corrected for the elevation change of
soil resulting from settling and compaction of soil in
a tilled crop field in addition to that from soil ero-
sion. The detailed methods are given in the online
supplementary information (SI).
To determine N, P, and K erosion losses, the
erosion rate was multiplied by total soil N (com-
bustion) and P (perchloric acid digest), and 10.1
times the exchangeable soil K content (Kexch,
ammonium acetate method), a factor that repre-
sents long-term plant-available K and its relation to
Kexch in published data on 20 soils with similar
climate and mineralogy to those sampled here
(Andrist-Rangel and others 2007; Ogaard and
others 2004; Simonsson and others 2007; see SI for
details).
Nitrogen and K gaseous and leaching losses
were estimated with transfer functions in Less-
chen and others (2007) using N and K inputs, and
area-wide climate and soil data (see SI for detailed
functions).
Scenarios of Alternative Management
To model future impacts of management alterna-
tives, four scenarios of intensification in a far field
were compared (Table 6): (1) A status quo rotation;
(2) shortened fallows with no other changes; (3) a
‘‘legume/P’’ strategy in which shortened fallows
were compensated for by P addition and greater le-
gume use (Kihara and others 2010); (4) ‘‘integrated
intensification’’ combining P addition, legumes, and
erosion reduction (for example, live barriers, erosion
catch ditches). We modeled erosion in these sce-
narios using our RUSLE calibration with L = 15 m
and S = 10% slope. Mean far field manuring inputs
of N, P, and K from the field balances were used. Crop
yields were estimated using Monte Carlo simulation
in which random draws were taken from a 95%
confidence interval of our yield data modeled as a
normal distribution. We assumed that P addition to
forages and green manures would reduce erosion by
10% by enhancing soil cover (Vanek 2011). Under
‘‘integrated intensification’’ we assumed a 50%
reduction in soil erosion. Balances of N, P, and K for
scenarios were composed in an Excel spreadsheet
and replicated 200 times with random draws for crop
yields, with mean and standard deviation calculated
for each scenario.
Statistical Analyses
For data linking wealth ranking to land and animal
tenure, analysis of variance (JMP, SAS Institute,
Cary, NC) tested farmer wealth differences. Anal-
ysis of covariance was used to test categorical and
continuous predictors of manure and crop flows
and nutrient concentrations as well as whole bal-
ances for N, P, and K. Linear regression was used to
test the association between field slope and grain or
tuber yield standardized to the mean yield of each
crop. Pairwise comparisons were made using two-
sided t tests.
RESULTS
Nutrient Input Rates
The relation between farmer wealth and manure
inputs showed several trends. First, farmers ranked
by peers as those with ‘‘very little’’ had fewer
animals and less cropped land than those ranked in
wealthier groups (Table 1). However, manure
application rates (kg ha-1) for N and P did not
differ significantly among any wealth groups or in
proportion to animals owned. Relative poverty may
therefore not drive nutrient depletion of cropland
in this system. Both the number of animals and
cropped acreage increased with wealth level, so
that farmers with fewer animals also had less land
to manure, which would explain similar manuring
rates. However, the ratio of animals:land area also
increased with land area, and it was puzzling that
the wealthiest farmers with the highest ratios of
animals:land did not manure at higher rates. In
fact, none of the balance terms or whole balances
differed with wealth, so we combined wealth
groups in all other analyses. However, similar
1522 S. J. Vanek and L. E. Drinkwater
manuring rates across wealth levels implied that
wealthier farmers with more land applied greater
total amounts of manure nutrients than the poorest
farmers.
Meanwhile, communities situated in environ-
ments with greater NPP had larger application rates
of N and P via manure (Figure 2). The highest-NPP
community had greater amounts of tree and shrub
browse for livestock, whereas the lowest NPP
community presented obvious rangeland degrada-
tion, corroborating the relation between lower re-
motely-sensed NPP and reduced access to animal
forage and manure. Manure N and P concentra-
tions were also greater in manures from higher-
NPP communities (Figure 2; Table 2).
Nitrogen inputs derived directly from biologically
fixed N (Ndfa) through legume crops was dwarfed
by manure N. Legume Ndfa did not differ between
near and far fields, and was approximately five
times smaller than manure N in far fields, and 20
times smaller in near fields due to the large differ-
ences in near/far manuring rates (Table 3).
Uncertainties in our estimates of Ndfa would be
unlikely to alter this comparison given these large
differences. However, Ndfa from rangeland forages
grazed by livestock is likely an important source of
N that is aggregated into the manure N flows.
Crop Yields and Nutrient Exports: FieldProximity and Rotation SequenceImpacts
Crop yields in sampled fields were highly variable
due to a variety of factors including soil nutrient
availability. Fresh potato yields varied tenfold, from
3 to over 30 Mg ha-1, and maize grain varied
100-fold, from less than 100 kg ha-1 to 5 Mg ha-1.
Biotic and abiotic stresses certainly played a role in
this yield variation, as indicated by collaborating
farmers. However, both nutrient concentrations
and total nutrient flows in exported crops suggested
that differences in soil nutrient levels between near
and far fields contributed to the trend for lower
yields in far fields as well as the steep drop in cereal
yields grown 3 years after manure was applied.
Averaged across potato, cereal, and maize crop
fields and rotation year, yields were 40% higher in
near than far fields (P = 0.0012, n = 111)
Crop nutrient contents also indicate that soil
nutrient availability was greater in near than far
fields. Potato tuber P and K and cereal grain N
concentrations were all higher in near than far
fields (Table 4), and when averaged across all
crops, P and K concentrations in crops were higher
in near than in far fields (P < 0.05, n = 151). Tab
le1.
Com
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130
32
52a
12a
Less
56a
1.3
0b
0.4
6a
119
28
47a
11a
Very
litt
le23b
0.6
9c
0.2
3b
123
28
23b
5b
Sig
nifi
can
ceP
<0.0
01**
*P
<0.0
01**
*P
<0.0
01**
*n
sn
sP
<0.0
1**
P<
0.0
1**
Tot
al
Nan
dP
appli
edare
calc
ula
ted
ona
farm
basi
sm
ult
iply
ing
man
ure
appli
cati
onra
teby
the
repor
ted
are
ain
maiz
ean
dpot
ato
esth
at
are
pot
enti
al
crop
sfo
rm
an
ure
appli
cati
on.
Soc
ial
ran
kin
gdata
wer
epart
ofa
pro
ject
base
lin
eev
alu
ati
onpro
vided
by
alo
cal
non
-gov
ern
men
tal
orga
niz
ati
on.
Drivers of Andean Soil Nutrient Mass Balances 1523
Taken together, differences in yields and nutri-
ent concentrations resulted in larger nutrient ex-
port amounts from near fields compared to far
fields; reflecting the greater nutrient additions
through manure applications (Tables 3, 5). Maize
P and cereal N, P, and K exports declined as the
time since manure was added lengthened from
two to 3 years and nutrients derived from manure
were removed by crop harvests and lost through
erosion (Table 5). Contrasts in P nutrient exports
between near and far fields and over the rotation
sequence were especially notable suggesting that
manure additions were a crucial source of P in
these agroecosystems.
Erosion Losses: Strong Driver of Near/FarField Differences
Erosion rates measured on six cereal and six fallow
fields ranged from 35 to 169 and 3 to 121 Mg ha-1,
respectively (Figure 3). Mean erosion on crop fields
was roughly three times that on fallow fields,
controlling for the effect of slope. Erosion flows of
N, P, and 10.1 Kexch were respectively 12.4, 8.0,
and 11.4 times the RUSLE LS factor on cropped
cereal fields and 3.9, 2.0, and 4.3 times the LS
factor on fallow fields, which represent regression
slopes fit to the erosion data in Figure 3.
Slope data from DEMs showed that areas near
villages were flatter on average than areas far from
the village (> 500-m distant): only 25% of far
areas versus 42% of near areas had slopes less than
12% (paired t test, P < 0.05, n = 6; based on his-
tograms of slope data for 30-m elevation pixels).
This was likely the basis for near/far differences in
sampled fields’ slopes. The range of soil slopes was
similar in near and far fields (0–33 and 3–34%,
respectively) but the distribution of near field
slopes was skewed towards flatness: 75% of near
fields, but only 41% of far fields, had slopes less
than 13%. As a result, far fields were steeper on
average than near fields (mean slopes of far vs.
near, 17.1� vs. 9.3�, t test P < 0.01, n = 43), and
modeled soil nutrient losses were greater in far
fields (Table 3). Yields of crops were negatively
correlated to field slope (Figure 4) consistent with
erosion nutrient exports on steeper fields limiting
crop productivity.
Mass Balances: Near versus Far FieldDifferences and Pervasive K Deficits
Manuring rates combined with erosion differences
created dramatic near versus far field differences in
nutrient balances. Manuring rates annualized
across the rotation were about twice as large in
near fields (< 500 m to dwellings) as in more
distant fields (Table 3). These annualized rates in
far fields are lower partly because they divide
manuring by more years of fallow in far fields.
However, even when we calculated manuring rates
on a cropped-year basis, rates were lower in far
compared to near fields (39 vs. 24 kg P ha1 y-1,
respectively, t = 13.8, P < 0.001, n = 43).
Meanwhile, higher erosion rates in far fields
meant that soil erosion matched crop harvest
exports in far field balances, accentuating the N and
P deficits (Table 3). Erosion and manuring rates
rather than distance from the community per se
drove these negative balances. Thus the steepest far
Figure 2. Dependence on remotely sensed community
NPP of: A manure N and P concentrations and B phos-
phorus application rate in manure.
1524 S. J. Vanek and L. E. Drinkwater
fields had the most negative P balances, whereas
flatter far fields had lower erosion rates and P
balances intermediate between steep far fields and
flat, well-manured near fields. Balances for N and P
calculated without erosion were positive in near
fields, suggesting that erosion reduction in these fields
would ease N and P constraints to crop productivity.
Crop yield exports were positively correlated to
manure inputs, reinforcing this finding (Table 3).
Meanwhile, negative K balances, even without
erosion, resulted from substantial K exports in
potatoes and maize and cereal residues (Table 3).
In these balances uncertainties were larger for K
than for P inputs due to uncertainty regarding K
content of manure from corralling on fields. How-
ever, K deficits persisted when field-corral fields
were removed from the analysis, and even when
both manuring strategies were assigned the higher
K content from fixed corral manure (data not
shown). Crop exports therefore tend to produce K
deficits in these rotations regardless of uncertainties
in K inputs.
Scenarios for Reversing the Declineof Soil Nutrient Stocks
Modeled scenarios for intensification in nutrient
management demonstrated that increased pressure
on grazed rangelands would result from shortened
fallow lengths, and showed benefits from erosion
reduction and a legume/P strategy. The status quo
scenario used crop sequences and manuring rates
from this study, so that the resulting N and P def-
icits matched those in sampled far fields (Table 3).
By comparison, the shortened fallows scenario re-
tained these deficits but required 33% more man-
ure (Table 6), threatening rangeland forage
production and the ability to sustain present man-
ure input rates, as suggested by the correlation
between rangeland NPP and manure inputs (Fig-
ure 2). The legume/P and ‘‘integrated intensifica-
tion’’ scenario increased both N and P stocks
through erosion reduction, P from rock phosphate
(RP) addition and N through increased legume
cultivation (Table 6). In the legume/P scenario,
legume N from green manures prior to potatoes
allowed for the reduction by half of manure
applications, so that manure use did not exceed the
status quo. Oat/vetch forages in this scenario also
spared N from soil export, and substantial RP
additions in this scenario were intended to reha-
bilitate soil P in depleted outfields. In the ‘‘inte-
grated intensification’’ scenario, erosion reduction
doubled the positive impacts of the legume/P
strategy on soil N and P. Interestingly, addition of
RP and legume N in these latter two scenarios
exacerbated K deficits because manure K was re-
duced relative to crop K export.
DISCUSSION
Our results demonstrate that social and manage-
ment factors are nested within environmental
constraints in this Andean mixed rangeland/crop-
ping system, so that management and environment
together are the strongest determinants of soil
nutrient sustainability. Negative balances in far
fields are indicative of an unsustainable trajectory,
Table 2. Regression Slopes of N and P Concentration and Application Rate on MODIS Remotely-sensed NPPand Mean N and P Concentrations of Manure from Two Different Manuring Strategies
Regression coefficients of nutrient content and application rates to mean NPP (2000–2006)
Nutrient in manure N P K Units of coefficient
Coefficient and significance
Nutrient content of manure 4.1*** 0.04** 12.6*** g kg-1 nutrient content per
Mg C ha-1 y-1 NPP
Nutrient application rate
(in application year)
63.8* 14.0* 137*** kg ha-1 nutrient per
Mg C ha-1 y-1 NPP
Nutrient concentrations in manure from different manuring strategies
N content (g N kg-1) P content (g P kg-1) K content (g K kg-1)
Fixed household pen (fixed-corral; n = 44) 16.9ns (0.4) 4.4ns (0.4) 16.9* (0.8)
Animals corralled on field (field-corral; n = 18) 16.5ns (0.6) 3.9ns (0.6) 9.2* (1.2)
Significance of differences by two-sided t test: *P < 0.05; **P < 0.01; ***P < 0.001.
Drivers of Andean Soil Nutrient Mass Balances 1525
Tab
le3.
Nu
trie
nt
Bala
nce
Term
san
dB
ala
nce
sfo
rN
,P,
an
dK
inN
ear
an
dFar
Fie
lds
Bala
nce
term
sN
(kg
Nh
a-
1y
-1)
P(k
gP
ha
-1
y-
1)
K(k
gK
ha
-1
y-
1)
Near
(n=
21)
Far
(n=
22)
Sig
.N
ear
(n=
21)
Far
(n=
22)
Sig
.N
ear
(n=
21)
Far
(n=
22)
Sig
.
Man
ure
in36.3
(4.3
)17.3
(2.0
)**
*10.6
(1.3
)4.2
(0.7
)**
*31.0
(5.1
)10.6
(1.5
)**
*
Nfi
xati
on
in1.3
(0.7
)3.2
(1.0
)n
s–
––
–
Cro
pexport
ou
t30.8
(2.7
)12.4
(1.3
)**
*7.6
(0.6
)2.6
(0.4
)**
*53.0
(5.6
)23.1
(2.9
)**
*
Ero
sion
ou
t3.2
(0.9
)9.0
(1.7
)**
2.0
(0.9
)5.5
(1.7
)**
3.0
(0.8
)8.8
(1.7
)**
Leach
ing
an
dgase
ou
slo
sses
ou
t112.0
(1.6
)6.3
(0.8
)**
*–
–5.4
(0.9
)1.6
(0.8
)**
*
Corr
ela
tion
of
crop
export
sto
man
ure
inpu
ts(n
ear,
far
com
bin
ed)
R=
0.3
2,
n=
43
*R
=0.4
2,
n=
43
**R
=0.4
1,
n=
43
**
Wh
ole
bala
nce
san
dst
ati
stic
al
com
pari
son
toze
ro
Bala
nce
wit
hle
ach
ing/g
ase
ou
slo
sses,
wit
hou
tero
sion
-4.5
(2.8
)0
-1.4
(2.7
)0
ns
3.0
(1.1
)>
01.5
(1.1
)>
0n
s-
23.1
(4.9
)<
0-
9.4
(3.6
)<
0n
s
Bala
nce
wit
hero
sion
,n
ole
ach
ing/
gase
ou
slo
sses
8.3
(3.8
)>
0-
3.8
(3.3
)0
*-
0.3
(1.8
)0
-6.1
(1.4
)<
0*
-27.7
(6.3
)<
0-
22.7
(6.2
)<
0n
s
Bala
nce
wit
hlo
sses
an
dero
sion
-5.8
(3.8
)0
-10.3
(3.6
)<
0n
s-
0.3
(1.8
)0
-6.1
(1.4
)<
0*
-32.7
(6.0
)<
0-
24.3
(5.9
)<
0n
s
1E
stim
ate
du
sin
gtr
an
sfer
fun
ctio
ns
(Les
sch
enan
dot
her
s2007).
All
figu
res
are
an
nu
ali
zed
acr
oss
the
len
gth
ofa
rota
tion
oftw
o,th
ree,
or6
years
.N
ear
fiel
ds
are
loca
ted
less
than
500-m
dis
tan
tfr
omfa
rmer
dw
elli
ngs
,w
her
eas
far
fiel
ds
are
grea
ter
than
500-m
dis
tan
t.T
oil
lust
rate
the
impact
sof
dif
fere
nt
loss
path
ways
,bala
nce
sare
give
nw
ith
out
eros
ion
an
dw
ith
Nan
dK
leach
ing
an
dga
slo
sses
,w
ith
eros
ion
an
dw
ith
out
thes
elo
sses
,an
dw
ith
all
loss
esan
der
osio
n.
Bala
nce
dif
fere
nce
sfr
omze
row
ere
ass
esse
dw
ith
atw
o-si
ded
tte
stat
P=
0.0
5co
nfiden
ce.
Sig
nifi
can
ceis
als
osh
own
for
the
dif
fere
nce
bet
wee
nn
ear
an
dfa
rfiel
ds:
*P
<0.0
5;
**P
<0.0
1;
***P
<0.0
01.
1526 S. J. Vanek and L. E. Drinkwater
Tab
le4.
Nu
trie
nt
Con
cen
trati
on
sof
Cro
ps
an
dR
esi
du
es
inR
ota
tion
al
Sequ
en
ces
an
dN
ear
vers
us
Far
Fie
lds
Cro
pan
dfr
act
ion
Year
of
rota
tion
Pvalu
efo
r
dif
fere
nce
Pro
xim
ity
tovil
lage
Pvalu
efo
r
dif
fere
nce
N(fi
eld
s)
On
e
(man
ure
ap
pli
ed
)
Tw
oT
hre
eN
ear
Far
Nco
nce
ntr
ati
on
gN
kg
-1
Pota
totu
bers
9.8
(0.2
)–
––
10.1
(0.4
)9.8
(0.3
)n
s63
Maiz
egra
in13.1
(1.0
)10.9
(0.9
)–
0.0
9n
s11.0
(0.7
)13.1
(1.4
)n
s21
Maiz
est
over
3.9
(0.3
)3.6
(0.2
)–
ns
3.8
(0.2
)3.7
(0.4
)n
s21
Cere
als
gra
in–
16.2
(0.4
)16.6
(0.9
)n
s17.7
(0.7
)15.1
(0.5
)0.0
03**
23
Cere
als
stra
w–
2.9
(0.2
)2.7
(0.3
)n
s3.1
(0.3
)2.5
(0.2
)0.0
8n
s23
Fora
ge
oats
–4.5
(0.6
)6.3
(0.8
)0.0
8n
s6.1
(1.0
)4.8
(0.5
)n
s7
Pco
nce
ntr
ati
on
gP
kg
-1
Pota
totu
bers
1.7
(0.0
4)
––
–1.8
(0.1
)1.6
(0.1
)0.0
08**
63
Maiz
egra
in3.7
(0.2
)3.0
(0.2
)–
0.0
02**
3.4
(0.1
)3.2
(0.2
)n
s21
Maiz
est
over
1.6
(0.3
)1.1
(0.2
)–
ns
1.6
(0.2
)1.1
(0.4
)n
s21
Cere
als
gra
in–
3.5
(0.2
)3.4
(0.4
)n
s3.5
(0.3
)3.3
(0.2
)n
s23
Cere
als
stra
w–
0.7
(0.1
)0.4
(0.1
)0.1
0n
s0.6
(0.2
)0.4
(0.3
)n
s23
Fora
ge
oats
–1.8
(0.3
)2.0
(0.4
)n
s2.5
(0.5
)1.3
(0.3
)0.0
4*
7
Kco
nce
ntr
ati
on
gK
kg
-1
Pota
totu
bers
18.0
(0.3
)–
––
19.2
(0.4
)17.4
(0.3
)0.0
08**
63
Maiz
egra
in6.5
(0.4
)5.0
(0.3
)–
0.0
1**
5.7
(0.3
)5.6
(0.6
)n
s21
Maiz
est
over
14.8
(0.8
)15.9
(0.6
)–
ns
15.9
(0.5
)14.8
(0.9
)n
s21
Cere
als
gra
in–
4.9
(0.2
)4.6
(0.4
)n
s4.9
(0.2
)4.7
(0.3
)n
s23
Cere
als
stra
w–
9.5
(0.3
)7.7
(0.5
)0.1
1n
s9.9
(0.5
)7.4
(0.3
)0.0
2*
23
Fora
ge
oats
–14.9
(0.5
)14.4
(0.8
)n
s16.6
(0.9
)12.8
(0.5
)n
s7
Nea
rfiel
ds
are
loca
ted
less
than
500-m
dis
tan
tfr
omfa
rmer
dw
elli
ngs
an
dfa
rare
grea
ter
than
500-m
dis
tan
t.Sig
nifi
can
cep
valu
efo
rdif
fere
nce
sby
two-
sided
tte
stis
als
osh
own
:*P
<0.0
5;
**P
<0.0
1;
***P
<0.0
01.
Drivers of Andean Soil Nutrient Mass Balances 1527
Tab
le5.
Yie
ldan
dN
utr
ien
tE
xport
sof
Cro
ps
inR
ota
tion
al
Sequ
en
ces
an
din
Near
vers
us
Far
Fie
lds
Cro
pan
dfr
act
ion
Year
of
rota
tion
Pvalu
efo
r
dif
fere
nce
Pro
xim
ity
tovil
lage
Pvalu
efo
r
dif
fere
nce
N(fi
eld
s)
On
e(m
an
ure
ap
pli
ed
)T
wo
Th
ree
Near
Far
Yie
ld(M
gh
a-
1)
Pota
to13
(1.0
)–
––
17
(1.5
)11
(1.2
)<
0.0
01**
*63
Maiz
e2.0
(0.3
)2.1
(0.3
)–
Ns
2.6
(0.3
)2.1
(0.4
)0.0
6n
s21
Cere
als
(wh
eat,
barl
ey)
–2.5
(0.2
)1.2
(0.2
)<
0.0
01**
*1.7
(0.2
)1.8
(0.2
)n
s30
NE
xport
(kg
Nh
a-
1)
Pota
to34
(2.6
)–
––
41
(4.3
)26
(2.2
)<
0.0
1**
63
Maiz
e46
(7.3
)34
(7.3
)–
Ns
49
(5.6
)30
(9.4
)0.1
0n
s21
Cere
als
(wh
eat,
barl
ey,
fora
ge
oats
)–
56
(5.0
)24
(3.5
)<
0.0
01**
*41
(6.0
)32
(2.9
)0.1
4n
s30
PE
xport
(kg
Ph
a-
1)
Pota
to6
(0.5
)–
––
7(0
.7)
4(0
.3)
<0.0
01**
*63
Maiz
e16
(2.2
)10
(2.2
)–
0.0
5*
18
(1.7
)8
(2.8
)0.0
1**
21
Cere
als
(wh
eat,
barl
ey,
fora
ge
oats
)–
11
(1.9
)5
(1.4
)<
0.0
01**
*9
(2.4
)6
(1.2
)0.0
5*
30
KE
xport
(kg
Kh
a-
1)
Pota
to60
(4.2
)–
––
78
(6.0
)48
(4.6
)<
0.0
01**
*63
Maiz
e91
(13.0
)71
(13.0
)–
0.0
6n
s101
(10.0
)61
(16.8
)0.0
6n
s21
Cere
als
(wh
eat,
barl
ey,
fora
ge
oats
)–
56
(8.7
)27
(6.4
)0.0
2*
43
(9.4
)35
(6.1
)n
s30
Nea
rfiel
ds
are
thos
ele
ssth
an
500-m
dis
tan
tfr
omfa
rmer
dw
elli
ngs
an
dfa
rare
grea
ter
than
500-m
dis
tan
t.Sig
nifi
can
ceP
valu
efo
rdif
fere
nce
sby
two-
sided
tte
stis
als
osh
own
:*P
<0.0
5;
**P
<0.0
1;
***P
<0.0
01.
1528 S. J. Vanek and L. E. Drinkwater
a feature of subsistence farming in developing
regions where soil nutrient deficits are common
(Vitousek and others 2009). Within this panorama
of overall deficits, we provide a counterexample to
the linkage often purported between relative pov-
erty and soil degradation. We also suggest that time
lags between the year-to-year focus of farmers on
production goals and the decadal consequences of
erosion and rangeland degradation define the
central challenge to agroecosystem sustainability
for extensive, montane smallholder systems.
Erosion and Rangeland NPP:Environmental Constraintson Management
Erosion is a complex process driven by climate, soil,
topographic, and management factors that has long
been recognized as a major vulnerability for agri-
culture, because soil losses under annual tillage
tend to exceed soil formation rates (Lal 1990;
Montgomery 2007). This is especially true in
mountainous regions where soil erosion from
agriculture on slopes is a central threat to sustain-
ing food production (Lal 1998; Kaihura and others
1999). The erosion rates measured in our study
(29–134 Mg ha-1 in cereal crops, 3–122 Mg ha-1
in fallows) are very high and are comparable to
other Andean erosion data (Alegre and others
1990; Zimmerer 1993; Romero-Leon 2005). The
range of erosion rates within each management
class, crops versus fallow, reflects the impact of
slope, and contributed to drastically different N and
P balances among fields depending on their prox-
imity to flatter village areas. Compared to most
subsistence systems, erosion poses a greater threat
to crop production and food security in these
Andean systems. The rates we measured are several
times those from Sahelian-mixed crop/livestock
systems with flatter topography (5–21 Mg ha-1; Pieri
1989) and also exceed the median rate reported for a
large agricultural data set (� 18 Mg ha-1; Mont-
gomery 2007). A similar pattern of very high erosion
was seen in an Ethiopian montane system, where
erosion comprised 80% of P losses and resulted
Figure 4. Regression of standardized yield data from
114 harvest samplings over 2 years against field slope.
Yields were standardized to the mean and standard
deviation of each crop. Summary statistics for dry grain
or tuber yield (kg ha-1) of each crop is shown in legend:
number of fields sampled (n); mean yield (l) and stan-
dard deviation (s).
Figure 3. Measured soil erosion rates of N, P, and K regressed against RUSLE LS factor, for (A) six cereal fields and
(B) five fallow fields in the study area. Linear regressions shown were used to estimate erosion losses of total N, total P, and
10.1 Kexch for nutrient balances, based on the LS factors of balance fields. ANOVA table (inset) gives significance of RUSLE
LS factor as a linear predictor and of field type (fallow vs. cereal) as a categorical predictor.
Drivers of Andean Soil Nutrient Mass Balances 1529
Tab
le6.
Sce
nari
os
for
Net
An
nu
alize
dN
utr
ien
tB
ala
nce
sover
18
Years
of
Rota
tion
on
aFie
ldw
ith
10%
Slo
pe
Sce
nari
oA
nn
uali
zed
bala
nce
,k
gh
a-
1y
1
Mean
(SD
),200
run
s
Cro
pro
tati
on
an
dfe
rtil
ity
inp
uts
Fall
ow
an
dgre
en
man
ure
ssh
ow
nin
bol
d
NP
K
1.
Sta
tus
qu
oro
tati
on
0.2
(2.5
)-
4.5
(0.6
)-
6.6
(4.1
)R
ota
tion
:P–W
–Fo-T
-ff-
P-M
-Fo-f
ff-P
-Fb-W
-fff
Man
ure
:410-8
5-3
90
kg
ha
-1
N–P-K
over
18
years
2.
Sh
ort
en
ed
fall
ow
s0.5
(3.4
)-
4.6
(0.8
)-
5.5
(4.7
)R
ota
tion
:P–W
–Fo-f
-P-M
-Fo-f
f-P-F
b-F
o-f
f-P–W
-T-f
Man
ure
:520-1
15-5
10
kg
ha
-1
N–P-K
over
18
years
3.
Legu
me/P
stra
tegy
4.8
(2.2
)2.7
(0.8
)-
14.1
(4.8
)R
ota
tion
:P–W
-F/V
rp-G
m-P
-M-T
rp-f
f-P-F
b-F
/V-f
-Gm
-
P–W
-T-f
Man
ure
:410-8
5-3
90
kg
ha
-1
N–P-K
over
18
years
Rock
ph
osp
hate
:160
kg
ha
-1
Pas
RP
iny
3,4
,7,
an
d13
4.
‘‘In
tegra
ted
inte
nsi
fica
tion
’’
(Legu
me/P
plu
sero
sion
redu
ctio
n)
9.8
(2.2
)5.8
(0.8
)-
12.9
(4.8
)R
ota
tion
:P–W
-F/V
rp-G
m-P
-M-T
rp-f
f-P-F
b-F
/V-f
-Gm
-P–W
-T-f
Man
ure
:410-8
5-3
90
kg
ha
-1
N–P-K
over
18
years
Rock
ph
osp
hate
:160
kg
ha
-1
Pas
RP
iny
3,4
,7,
an
d13
Ero
sion
man
agem
en
t:re
du
cest
atu
squ
oero
sion
by
50%
Cro
ps
inro
tati
on:
P,
pot
ato
;W
,w
hea
t;F
o,fo
rage
oat;
T,
tarw
i;M
;m
aiz
e;F
b,
fava
bea
n;
F/V
,fo
rage
oat
wit
hve
tch
;G
m,
tarw
igr
een
man
ure
;f,
fall
ow.
Res
ult
ssh
own
are
mea
ns
an
dst
an
dard
dev
iati
onof
200
run
sof
rota
tion
wit
hra
ndom
dra
ws
for
crop
yiel
ds.
Th
est
atu
squ
oro
tati
onre
pea
tsin
6-y
ear
cycl
es,
wit
h3
years
ofcr
oppin
gan
d3
years
offa
llow
,an
dm
an
ure
once
per
cycl
e.In
ten
sifica
tion
via
‘‘sh
orte
ned
fall
ows’
’gr
ows
pot
ato
esfo
ur
tim
esin
18
years
inst
ead
ofth
ree,
wit
ha
33%
incr
ease
inm
an
ure
appli
cati
on.
Th
e‘‘
legu
me/
P’’
stra
tegy
use
sa
year
ofgr
een
man
ure
bef
ore
pot
ato
,an
dro
ckph
osph
ate
(RP
)addit
ion
tofo
ur
legu
me
crop
sin
the
rota
tion
.‘‘
Inte
grate
din
ten
sifica
tion
’’u
ses
legu
mes
,R
Paddit
ion
,an
der
osio
nre
du
ctio
nw
ith
grass
con
tou
rbarr
iers
an
dse
dim
ent
captu
retr
ench
esso
that
eros
ion
ish
alv
ed.
1530 S. J. Vanek and L. E. Drinkwater
in large cropland P deficits (Haileslassie and others
2005).
After erosion, rangeland NPP was a second
important environmental driver and point of vul-
nerability for these cropping systems. The positive
correlation of rangeland NPP to both application
rates and nutrient content of manure illustrates its
importance as the primary source of manure-
derived nutrients. This NPP-manure linkage has
been observed in other subsistence farming sys-
tems: one Sahelian rangeland/cropping system
with low, rainfall-limited NPP had manuring rates
only one tenth of those we measured here (Powell
and others 1996), suggesting that NPP of range-
lands globally places constraints on farmer nutrient
management. To understand these constraints,
systemic nutrient balances at the community and
rangeland level are needed to quantify the forage
and manure nutrient flows that rangelands can
sustainably provide based on N fixation, mineral
weathering, and nutrient deposition.
Manure Impacts on Soil NutrientBalances: Field Proximityand Management
In these Andean systems, community decisions
about village siting affect the location of fields for
crop production, creating a complex landscape of
intensively managed fields within a matrix of
communal rangelands that sets the stage for near/
far soil nutrient gradients that correspond with
differences in soil productive capacity due to
steepness and soil depth. Villages occupy flatter
land, suggesting that their locations evolve toward
the best soils, as demonstrated in other managed
landscapes (Imhoff and others 1997). Farmers’
agronomic management practices are nested with-
in the landscape and rely heavily on the steepest
lands which serve as nutrient reservoirs that are
tapped via manure from grazing.
Within this landscape, higher manuring rates in
near fields reinforced near/far erosion differences
and accentuated N and P deficits in far fields, mir-
roring near/far soil P contrasts in other smallholder
systems (Rowe and others 2006; Phiri and others
2010). Landscape factors explain these near/far
gradients. Most simply, far fields are less accessible
in difficult terrain. Farmers in our study hauled
manure up to 1.2 km, perhaps dissuading high
manuring rates. Also, fallows are longer in far than
near fields so that farmers reduce manuring rates to
account for the nutrients from fallow vegetation
(Pestalozzi 2000). Smallholders also achieve greater
returns to their manure from higher crop yields in
flatter near fields (Figure 4). Farmers tend to favor
these fields with manure, whereas far fields are
used to diversify climate and pest risks to crops
(Goland 1993).
Over time, management nested within landscape
gradients is likely to reinforce contrasts in soil
productive potential, a trend also seen in African
systems with near/far management gradients (Gil-
ler and others 2006). Strengthened soil nutrient
gradients in rangeland/cropping systems enable
farmers to produce higher yields in the best soils.
However, as management intensifies in these sys-
tems, reduced manuring rates combined with high
erosion will accelerate soil nutrient depletion in far
fields causing yields to decline.
Examining the stoichiometry of different flows in
the balance also helps to explain patterns of
depletion in nutrients: if inputs and outputs have
unmatched stoichiometries then depletion or sur-
plus can occur. The N:P stoichiometry of manure
inputs was approximately 3:1 (Table 3), which is
slightly less than that of crop exports (�4:1) and
more than that of erosion (�2:1). This shows how
far fields could become P-limited because erosion
accounts for a greater share of nutrient exports,
whereas flatter near fields where harvest exports
dominate the balances retain proportionately
greater P, a conclusion that is substantiated by
lower available P in more marginal fields (Vanek
2011). Nevertheless, these differences in N:P ratios
are not enormous, so that the large erosion N losses
in far fields and minimal direct inputs of N via N
fixation in cropped fields also result in negative N
balances in far fields.
In contrast to these small differences in N:P ra-
tios, K exports from tuber crops and cereal residues
dominated the K balances. This can be attributed to
the high K:P ratio of crop exports, which at
approximately 7:1 greatly exceeded the K:P ratio of
manure or erosion (� 3:1 and 1.5:1, respectively,
Table 3). Potassium balances were so dominated by
crop harvests that they did not vary with erosion
and field proximity. In spite of these K deficits,
the stronger contrasts in P than K crop exports
(Table 5) suggest that P is currently more limiting
than K in these systems, which is reinforced by the
unresponsiveness of Bolivian highland soils to K
addition (Valente and Oliver 1993). However, we
also observed insufficient levels of exchangeable K
(< 125 mg K kg-1) in 12 of 17 fields during soil
sampling in the project area, suggesting that K
limitation may be anticipated in the future
(unpublished data).
Drivers of Andean Soil Nutrient Mass Balances 1531
The Weak Impact of Relative Wealthon Manuring Rates: Do Poorer FarmersCause Degradation?
Compared to other subsistence farming systems
that have been studied, manuring rates in these
Andean communities were surprisingly consistent
across farms that varied in wealth, even as the ratio
of animals:land increased with wealth. For example
in Ethiopia and Zimbabwe, wealthier farmers ap-
plied greater rates of fertilizer and manure (Elias
and others 1998; Cobo and others 2009), a trend
that was generally true across Africa (Cobo and
others 2010). Compared to Sahelian rangeland–
cropping systems, a far greater proportion of
farmers in our study had access to animal manure
(Harris 1999; Augustine 2003). In one Sahelian
community, Achard and Banoin (2003) found that
32% of farmers had no livestock, and among
farmers with animals only 37% owned enough to
apply appreciable rates of manure. These wealthier
farmers applied 5.5 kg P ha-1 y-1 as manure,
similar to the mean rate we report (Table 3).
However, fully a third of farmers in these com-
munities lacked animals and thus were without
any means to replenish nutrients in their fields, so
that in this region, poorer farmers may degrade
cropland soil fertility by mining soil nutrient stocks
and accelerating soil loss. In the communities we
studied, social mechanisms allow farmers without
herds to pursue a shared standard of soil nutrient
management by exchanging their labor for man-
ure. This transfer of manure to poorer families may
account for the relatively consistent rates of man-
ure application across wealth classes, although we
are not sure based only on this sample of farmers
whether such social mechanisms and equal
manuring rates are prevalent across the region.
Nevertheless, due to similar application rates,
wealthier farmers gather and apply greater total
amounts of manure across their larger holdings,
and may in fact cause greater rangeland degrada-
tion than poor farmers. This would be especially
true if larger total manure harvests reinforce
wealth differences and inequality in herd sizes over
time (Giller and others 2006). Examining the
depletion rates of nutrients from rangeland by
wealthier farmers might contrast with common
assumptions about the impact of poorer farmers on
nutrients in cropland. Mass balances of whole
communities utilizing common-pool resources are
challenging to calculate. They could however
clarify the role of wealth in driving degradation and
also point to sustainable grazing and manure yields
of rangelands as we suggest above.
Lastly, similar manuring rates across wealth
levels and pulses of manure nutrients coordinated
with crop rotations suggest a community knowl-
edge system regarding soil nutrient management.
Andean farmers’ knowledge of soil fertility regen-
eration in fallows (Pestalozzi 2000) and manage-
ment systems of African smallholders (Boesen and
Friis-Hansen 2001) also exemplify this complex
and widely held management knowledge. Ironi-
cally, widely held strategies may insulate farmers
from perceiving range and cropland degradation,
exacerbating the time lag effects considered next.
Time Lags: Modeling as a Learning Toolto Forecast Agroecosystem Trajectories
It is likely that the tendency of farmers in these
systems to overlook soil-degradation stems from
time lags between management and the impact on
the environment. Degradation arising from the
delayed consequences of management on ecosys-
tem services occurs in other managed ecosystems
such as fisheries (Devine and Haedrich 2011) and
grazing management (Zhou and others 2011). In
these Andean systems soil management is oriented
towards food production on a yearly timescale,
whereas soil erosion and rangeland degradation
accrues over decadal timescales to eventually im-
pact production. Manure application is sufficient at
present to mitigate erosion impacts on crop yields.
As a result, soil degradation is not as swiftly
apparent and cannot be factored into the short-
term decisions. Lower yields on steeper slopes
related to erosion deficits represent a signal to
managers who might respond by reversing erosion.
However, crop yields vary around this trend
because of many other biotic and abiotic factors
(Terrazas and others 1998), and above-average
production occurs even on steep slopes where
erosion deficits will accrue in the long run, espe-
cially if crops receive manure (Figure 3). The ero-
sion signal may not be sufficiently perceived for
decades. Farmers may also ignore degradation if
yields decline slowly enough that they redefine
yield benchmarks, as examples from managed
fisheries indicate (Bunce and others 2008). Beyond
these issues of perception is the farmers’ ability to
respond. If farmers respond by increasing manur-
ing rates or expanding cropped area rather than
erosion reduction, rangeland degradation will
accelerate. The current response subsidizes crop
production at shorter time scales and smaller spatial
scales by sacrificing the longer-term resilience
of rangeland, a pattern identified by Carpenter
and others (2001). Zimmerer (1993) also described
1532 S. J. Vanek and L. E. Drinkwater
labor shortages driven by national-scale policies
that constrain Andean farmers’ response to erosion.
The modeled scenarios we present clarify the
likely outcomes of long-term processes. Shortened
fallows without compensatory changes in man-
agement will result in severe degradation (Table 6).
The legume/P strategy would slow the decline in
soil nutrient stocks by replacing some manure with
legumes and RP. Improved legume forages and
management that access greater soil P might also
improve forage quality and animal-based liveli-
hoods, and also boost soil and manure nutrient
stocks, and soil cover in marginal crop fields and
rangeland, helping to reverse negative soil N and P
balances (for example, Meneses 1998). However,
only erosion reduction along with inputs to redress
past depletion will improve the long-term P and K
balances of these systems. Farmers’ short-term fo-
cus on crop production set within widely-held
knowledge systems may impede the promotion of
soil rehabilitation. In response, short-term positive
outcomes could incentivize changes in practices:
green manures would reduce the effort for manure
transport and the aggregate manure requirement;
live barriers with appropriate species could improve
forage resources; RP would improve legume yields
and enhance fixed N inputs. Nutrient balance
models can support farmer learning about long-
term processes so that the influence of important
drivers like erosion and rangeland NPP is amplified
in local knowledge systems. Removing barriers to
long-term investments in soil fertility by farmers
may also be needed, in the form of community
credit schemes, access to markets that incentivize
soil rehabilitation, or community or regional gov-
ernment assistance.
ACKNOWLEDGMENTS
We acknowledge MODIS 17A3 NPP data from
National Aeronautics and Space administration
(NASA) and the University of Montana Numerical
Terradynamic Simulation Group, and ASTER DEM
data (a product of NASA and the Japanese Ministry
of Economy, Trade, and Industry- METI). We
received invaluable support from Fulbright and
Fulbright-Hays fellowships and the McKnight
Foundation Collaborative Crop Research Program.
We thank World Neighbors Bolivia and collabo-
rating farmers for focal group data and sampling
assistance, and Ann Piombino and Keith Jenkins
for invaluable lab and GIS assistance respectively.
We also thank Marissa Weiss, Jennifer Blesh, Sean
Berthong and anonymous reviewers for sugges-
tions that greatly improved the manuscript.
REFERENCES
Achard F, Banoin M. 2003. Fallows, forage production and
nutrient transfers by livestock in Niger. Nutr Cycl Agroecosyst
65:183–9.
Aganga AA, Mosimanyana N. 2001. Gender impact on sheep
and goat production in Botswana. A case of Gaborone region.
J Agric Tropics Subtrop 102:15–18.
Alegre JC, Felipe-Morales C, LaTorre B. 1990. Soil erosion
studied in Peru. J Soil Water Conserv 45:417–20.
Antil RS, Janssen BH, Lantinga EA. 2009. Laboratory and
greenhouse assessment of plant availability of organic N in
animal manure. Nutr Cycl Agroecosyst 85:95–106.
Arriaga-Jordan CM, Pedraza-Fuentes AM, Nava-Bernal EG,
Chavez-Mejia MC, Castelan-Ortega OA. 2005. Livestock ag-
rodiversity of Mazahua smallholder Campesino systems in the
highlands of Central Mexico. Hum Ecol 33:821–45.
Augustine DJ. 2003. Long-term, livestock-mediated redistribu-
tion of nitrogen and phosphorus in an East African savanna.
J Appl Ecol 40:137–49.
Baijukya F-P, de-Ridder N, Masuki K-F, Giller K-E. 2005.
Dynamics of banana-based farming systems in Bukoba dis-
trict, Tanzania: changes in land use, cropping and cattle
keeping. Agric Ecosyst Environ 106:395–406.
Baker LA, Hope D, Xu Y, Edmonds J, Lauver L. 2001. Nitrogen
balance for the central Arizona–Phoenix (CAP) ecosystem.
Ecosystems 4:582–602.
Berry P-M, Stockdale E-A, Sylvester-Bradley R, Philipps L, Smith
K-A, Lord E-I, Watson C-A, Fortune S. 2003. N, P and K
budgets for crop rotations on nine organic farms in the UK.
Soil Use Manage 19:112–18.
Boesen J, Friis-Hansen E. 2001. Soil fertility management in
semi-arid agriculture in Tanzania: farmers’ perceptions and
management practices. CDR Working Papers, 31 p.
Bunce M, Rodwell LD, Gibb R, Mee L. 2008. Shifting baselines in
fishers’ perceptions of island reef fishery degradation. Ocean
Coast Manage 51:285–302.
Carpenter S, Walker B, Anderies JM, Abel N. 2001. From met-
aphor to measurement: resilience of what to what? Ecosys-
tems 4:765–81.
CIF-UMSS (Centro de Investigacion en Forrajes: Universidad
San Simon). 2013. Guıa ilustrada de especies forrajeras nativas
de la zona andina en Bolivia. Cochabamba: Universidad
Mayor San Simon. p 191.
Cobo JG, Dercon G, Monje C, Mahembe P, Gotosa T, Nya-
mangara J, Delve RJ, Cadisch G. 2009. Cropping strategies,
soil fertility investment and land management practices by
smallholder farmers in communal and resettlement areas in
Zimbabwe. Land Degrad Dev 20:492–508.
Cobo JG, Dercon G, Cadisch G. 2010. Nutrient balances in
African land use systems across different spatial scales: a re-
view of approaches, challenges and progress. Agric Ecosyst
Environ 136:1–15.
Devine JA, Haedrich RL. 2011. The role of environmental conditions
and exploitation in determining dynamics of redfish (Sebastes
species) in the Northwest Atlantic. Fish Oceanogr 20:66–81.
Duncan Fairlie T, Jacob DJ, Park RJ. 2007. The impact of
transpacific transport of mineral dust in the United States.
Atmospheric Environ 41:1251–66.
Elias E, Morse S, Belshaw D-G-R. 1998. Nitrogen and phos-
phorus balances of Kindo Koisha farms in southern Ethiopia.
Agric Ecosyst Environ 71:93–113.
Drivers of Andean Soil Nutrient Mass Balances 1533
Ellis EC, Klein Goldewijk K, Siebert S, Lightman D, Ramankutty
N. 2010. Anthropogenic transformation of the biomes, 1700 to
2000. Glob Ecol Biogeogr 19:589–606.
ERSDAC. 2007. ASTER Global Digital Elevation Model. http.://
www.ersdac.or.jp/GDEM/E/index.html.
FAO. 2010. SD Dimensions Special: Global Climate Maps. SD
Dimensions. FAO Sustainable Development Department.
http://www.fao.org/sd/EIdirect/climate/EIsp0002.htm.
Giller KE, Rowe EC, de Ridder N, van Keulen H. 2006. Resource
use dynamics and interactions in the tropics: scaling up in
space and time. Agric Syst 88:8–27.
Goland C. 1993. Field Scattering as agricultural risk manage-
ment: a case study from Cuyo Cuyo, Department of Puno,
Peru. Mountain Res Dev 13:317–38.
Haigh MJ. 1977. The use of erosion pins in the study of slope
evolution. In: Finlayson B, Ed. British Geomorphological Re-
search Group, Technical Bulletin 18. Norwich, England: Geo
Books. p 31–49.
Haileslassie A, Priess J, Veldkamp E, Teketay D, Lesschen JP.
2005. Assessment of soil nutrient depletion and its spatial
variability on smallholders’ mixed farming systems in Ethiopia
using partial versus full nutrient balances. Agric Ecosys
Environ 108:1–16.
Harris F. 1999. Nutrient management strategies of small-holder
farmers in a short-fallow farming system in north-east Nigeria.
Geogr J 165:275–85.
Hudson NW. 1993. Field measurement of soil erosion and run-
off. Food and Agriculture Organization of the United Nations,
Rome. 139 p
Imhoff ML, Lawrence WT, Elvidge CD, Paul T, Levine E, Pri-
valsky MV. 1997. Using nighttime DMSP/OLS images of city
lights to estimate the impact of urban land use on soil re-
sources in the United States. Remote Sens Environ 59:105–17.
Jones A. 2011. Overcoming barriers to improving infant and
young child feeding practices in the Bolivian Andes: the role
of agriculture and rural livelihoods. Doctoral dissertation,
Cornell University, Ithaca, NY
Kaihura FBS, Kullaya IK, Kilasara M, Aune JB, Singh BR, Lal R.
1999. Soil quality effects of accelerated erosion and manage-
ment systems in three eco-regions of Tanzania. Soil Tillage Res
53:59–70.
Kalra YP. 1998. Handbook of reference methods for plant anal-
ysis. CRC Press, Boca Raton, FL. 300 p
Kihara J, Vanlauwe B, Waswa B, Kimetu JM, Chianu J, Bationo
A. 2010. Strategic phosphorus application in legume-cereal
rotations increases land productivity and profitability in wes-
tern Kenya. Exp Agric 46:35–52.
Lal R. 1990. Soil erosion in the tropics: principles and manage-
ment. New York: McGraw-Hill. 580 p
Lal R. 1998. Soil erosion impact on agronomic productivity and
environment quality. Crit Rev Plant Sci 17:319–464.
Lesschen JP, Stoorvogel JJ, Smaling EMA, Heuvelink GBM,
Veldkamp A. 2007. A spatially explicit methodology to
quantify soil nutrient balances and their uncertainties at the
national level. Nutr Cycl Agroecosyst 78:111–31.
Lightfoot C, Noble R. 2001. Tracking the ecological soundness of
farming systems: instruments and indicators. J Sustain Agric
19:9–29.
Mayer E. 1979. Land-use in the Andes: ecology and agriculture
in the Mantaro Valley of Peru with special reference to
potatoes. Lima, Peru: International Potato Center. 115 p
McCorkle CM, Ed. 1990. Improving Andean sheep and Alpaca
production: recommendations from a decade of research in
Peru. Columbia, Missouri: University of Missouri-Columbia.
Meneses R. 1998. Asociacion de cereales menores con legumi-
nosas y momentos de corte para produccion de forraje.
Compendio de trabajos presentandos por el Proyecto Rhizo-
biologıa (Cochabamba) en eventos y publicaciones de otras
instituciones.
Montgomery DR. 2007. Soil erosion and agricultural sustain-
ability. Proc Nat Acad Sci 104:13268–72.
Mortimore M, Harris F. 2005. Do small farmers’ achievements
contradict nutrient depletion scenarios for Africa? Land Use
Policy 22:43–56.
Neighbors World. 2006. Linea de base, proyecto Heifer de se-
guridad alimentaria Norte de Potosı. Cochabamba, Bolivia:
Vecinos mundiales. 28 pp
Nkonya E, Kaizzi C, Pender J. 2005. Determinants of nutrient
balances in a maize farming system in eastern Uganda. Agric
Syst 85:155–82.
NRCS. 2010. Crop Nutrient Tool. Natural Resources Conserva-
tion Service, U.S. Department of Agriculture, Beltsville. http://
plants.usda.gov/npk/main.
Pacheco P. 2009. Smallholder livelihoods, wealth and defores-
tation in the Eastern Amazon. Hum Ecol 37:27–41.
Pendleton LH, Howe EL. 2002. Market integration, develop-
ment, and smallholder forest clearance. Land Econ 78:1–19.
Pestalozzi H. 2000. Sectoral fallow systems and the management
of soil fertility: the rationality of indigenous knowledge in the
high Andes of Bolivia. Mt Res Dev 20:64–71.
Phiri AT, Njoloma JP, Kanyama-Phiri GY, Snapp S, Lowole MW.
2010. Maize yield response to the combined application of
Tundulu rock phosphate and Pigeon Pea residues in Kasungu,
Central Malawi. Afr J Agric Res 5:1235–42.
Pieri CJ. 1989. Fertility of soils: a future for farming in the West
African Savanna. Berlin: Springer. 348 p
Powell JM, FernandezRivera S, Hiernaux P, Turner MD. 1996.
Nutrient cycling in integrated rangeland/cropland systems of
the Sahel. Agric Syst 52:143–70.
Renard KG, Foster GR, Weesies GA, McCool DK, Yoder DC.
1997. Predicting soil erosion by water: a guide to conservation
planning with the Revised Universal Soil Loss Equation
(RUSLE), Agriculture Handbook 703. Beltsville, MD: USDA
Agricultural Research Service. 384 p
Romero-Leon C. 2005. A multi-scale approach for erosion
assessment in the Andes. The Hague: Wageningen University.
147 p
Ross SM, Izaurralde RC, Janzen HH, Robertson JA, McGill WB.
2008. The nitrogen balance of three long-term agroecosystems
on a boreal soil in western Canada. Agric Ecosyst Environ
127:241–50.
Rowe E, Vanwijk M, Deridder N, Giller K. 2006. Nutrient allo-
cation strategies across a simplified heterogeneous African
smallholder farm. Agric Ecosyst Environ 116:60–71.
Rufino MC, Dury J, Tittonell P, van Wijk MT, Herrero M,
Zingore S, Mapfumo P, Giller KE. 2011. Competing use of
organic resources, village-level interactions between farm
types and climate variability in a communal area of NE Zim-
babwe. Agric Syst 104:175–90.
Saberwal VK. 1996. Pastoral politics: Gaddi grazing, degradation,
and biodiversity conservation in Himachal Pradesh, India.
Conserv Biol 10:741–9.
1534 S. J. Vanek and L. E. Drinkwater
Schechambo F, Sosoveli H, Kisanga D. 1999. Rethinking natural
resource degradation in semi-arid sub-Saharan Africa: the
case of semi-arid Tanzania. Dar Es Salaam, Tanzania: Overseas
Development Institute. 58 p.
Scherr SJ. 2000. A downward spiral? Research evidence on the
relationship between poverty and natural resource degrada-
tion. Food Policy 25:479–98.
Schlecht E, Hiernaux P, Achard F, Turner MD. 2004. Livestock
related nutrient budgets within village territories in western
Niger. Nutr Cycl Agroecosyst 68:199–211.
Smaling E-M-A, Fresco L-O, De-Jager A. 1996. Classifying,
monitoring and improving soil nutrient stocks and flows in
African agriculture. AMBIO 25:492–6.
Terrazas F, Suarez V, Gardner G, Thiele G, Devaux A, Walker T.
1998. Diagnosing potato productivity in farmers’ fields in
Bolivia, Working paper 1998-5. Social Science Department,
International Potato Center (CIP), Lima, Peru
Thorne PJ, Tanner JC. 2002. Livestock and nutrient cycling in
crop–animal systems in Asia. Agric Syst 71:111–26.
Valente JF, Oliver R. 1993. Fertisuelos: evaluacion de la fertili-
dad de los suelos del antiplano, valle central y los llanos de
Bolivia. Rome: FAO. 123 p
Vanek S. 2011. Legume-phosphorus synergies in mountain
agroecosystems: field nutrient balances, soil fertility gradients,
and effects on legume attributes and nutrient cycling in the
Bolivian Andes. Doctoral dissertation, Cornell University.
Villarroel J, Augstburger F, Meneses R. 1986. Fixation and
contribution of nitrogen to the soil by Lupinus mutabilis, and
its effects on following barley. Proceedings of the Fourth
International Lupin Conference. p 308.
Vitousek PM, Naylor R, Crews T, David MB, Drinkwater LE,
Holland E, Johnes PJ, Katzenberger J, Martinelli LA, Matson
PA, Nziguheba G, Ojima D, Palm CA, Robertson GP, Sanchez
PA, Townsend AR, Zhang FS. 2009. Nutrient imbalances in
agricultural development. Science 324:1519–20.
Wortmann CS, Kaizzi CK. 1998. Nutrient balances and expected
effects of alternative practices in farming systems of Uganda.
Agric Ecosyst Environ 71:115–29.
Yirga C, Hassan RM. 2006. Poverty soil conservation efforts
among smallholder farmers in the central highlands of Ethi-
opia. South Afr J Econ Manage Sci 9:244–61.
Zhao M, Nemani R, Running S. 2008. ftp://ftp.ntsg.umt.edu/
pub/MODIS/Mirror/MOD17A3.LATEST/Improved_MOD17A3_
C5.1_GEOTIFF_1km/,fileNpp_QC_1km_C5.1_mean_00_to_
06.tif. University of Montana Numerical Terradynamic
Simulation Group, Bozeman, MT.
Zhou ZY, Li FR, Chen SK, Zhang HR, Li GD. 2011. Dynamics of
vegetation and soil carbon and nitrogen accumulation over
26 years under controlled grazing in a desert shrubland. Plant
and Soil 341:257–68.
Zimmerer KS. 1993. Soil-erosion and labor shortages in the
Andes with special reference to Bolivia, 1953–1991: implica-
tions for conservation-with-development. World Dev
21:1659–75.
Drivers of Andean Soil Nutrient Mass Balances 1535