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The importance of different forest management systems for people’s dietary quality in Tanzania

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Context A large body of literature has shown that forests provide nutritious foods in many low- and middle-income countries. Yet, there is limited evidence on the contributions from different types of forest and tree systems. Objectives Here, we focus on individual trees and smaller forest patches outside established forest reserves as well as different forest management systems. Methods We do so by combining novel high-resolution data on tree cover with 24-h dietary recall surveys from 465 women in Tanzania. Results We show that people with more unclassified tree cover (i.e., individual trees and small forest patches) in their nearby surroundings have more adequate protein, iron, zinc, and vitamin A intakes. We also find that having a nearby forest under Participatory Forest Management (PFM) system is associated with higher adequacy levels of energy, iron, zinc and vitamin A. By contrast, tree cover within other types of forest (e.g., Government Forest Reserves and Government Forest Plantations) is not positively associated with people’s dietary quality. Conclusions Our key finding is that having individual trees, smaller forest patches and/or forest under PFM in close proximity is more beneficial for people’s diets than other types of established forests. Our results highlight the nutritional importance of trees outside established forests and question the often-assumed benefits of forests if these are made inaccessible by social barriers (e.g., legislation). Finally, our results emphasize the need to distinguish between different forest management systems when studying forest-diet linkages.
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Landsc Ecol (2024) 39:176
https://doi.org/10.1007/s10980-024-01961-6
RESEARCH ARTICLE
The importance ofdifferent forest management systems
forpeople’s dietary quality inTanzania
R.S.Olesen · F.Reiner· B.denBraber·
C.Hall· C.J.Kilawe· J.Kinabo· J.Msuya·
L.V.Rasmussen
Received: 24 January 2024 / Accepted: 11 August 2024 / Published online: 11 September 2024
© The Author(s) 2024
Abstract
Context A large body of literature has shown that
forests provide nutritious foods in many low- and
middle-income countries. Yet, there is limited evi-
dence on the contributions from different types of for-
est and tree systems.
Objectives Here, we focus on individual trees
and smaller forest patches outside established for-
est reserves as well as different forest management
systems.
Methods We do so by combining novel high-reso-
lution data on tree cover with 24-h dietary recall sur-
veys from 465 women in Tanzania.
Results We show that people with more unclassi-
fied tree cover (i.e., individual trees and small forest
patches) in their nearby surroundings have more ade-
quate protein, iron, zinc, and vitamin A intakes. We
also find that havinga nearby forest under Participa-
tory Forest Management (PFM) systemis associated
with higher adequacy levels of energy, iron, zinc and
vitamin A. By contrast, tree cover within other types
of forest (e.g., Government Forest Reserves and Gov-
ernment Forest Plantations) is not positively associ-
ated with people’s dietary quality.
Conclusions Our key finding is that having indi-
vidual trees, smaller forest patches and/or forest
underPFM in close proximity is more beneficial for
people’s diets than other types of established for-
ests. Our results highlight the nutritional importance
of trees outside established forests and question the
often-assumed benefits of forests if these are made
inaccessible by social barriers (e.g., legislation).
Finally, our results emphasize the need to distinguish
between different forest management systems when
studying forest-diet linkages.
Keywords Food and nutrition security· Nutrient
adequacy· Dietary quality· Forest management·
Tree cover· Multi-functional landscape
Supplementary Information The online version
contains supplementary material available at https:// doi.
org/ 10. 1007/ s10980- 024- 01961-6.
R.S.Olesen(*)· F.Reiner· B.denBraber· C.Hall·
L.V.Rasmussen
Department ofGeosciences andNatural Resource
Management, University ofCopenhagen, Øster Voldgade
10, 1350Copenhagen, Denmark
e-mail: rso@ign.ku.dk
C.Hall
Biological andEnvironmental Sciences, University
ofStirling, StirlingFK94LA, UK
C.J.Kilawe
Department ofEcosystems andConservation, Sokoine
University ofAgriculture, Morogoro, Tanzania
J.Kinabo· J.Msuya
Department ofHuman Nutrition andConsumer Sciences,
Sokoine University ofAgriculture, Morogoro, Tanzania
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Introduction
Recent literature has established positive linkages
between forests and food and nutrition security in
low- and middle-income countries, both based on
large-scale datasets (Ickowitz et al. 2014; Galway
etal. 2018; Rasolofoson etal. 2018; DenBraber etal.
2024) as well as site-specific case studies (Baudron
etal. 2017; Cheek etal. 2022). There are four over-
arching pathways by which forests and trees can
positively affect people’s food and nutrition security
(Baudron etal. 2019b; Gergel et al. 2020): (1) The
direct provision of food as forests often host numer-
ous and nutrient-rich wild plants and animals that are
consumed by local communities (Powell etal. 2013;
Asprilla-Perea and Díaz-Puente 2019), (2) the pro-
vision of ecosystem services (e.g., soil protection,
water provision, pollination, access to manure and
biomass), which can improve the productivity of sur-
rounding agricultural lands (Baudron et al. 2019a;
Yang 2020), (3) the provision of fuelwood, which is
vital for cooking and boiling water in many countries
(Karki etal. 2018), and (4) income generation from
sale of forest and tree products, which can facilitate
the purchase of nutritious foods from markets (Miller
etal. 2020).
Despite the well-established positive linkages
between forests and people’s diets, little is known
about (1) the potential contribution of trees outside
of established forest reserves beyond agroforestry
systems, which are well-studied (Babu and Rhoe
2002; Bostedt etal. 2016; Afentina etal. 2021), and
(2) different types of forest management systems. We
note that trees outside of established forest reserves
differ from agroforestry as they are not limited to
being located in or around farmland but include trees
growing across all types of non-forest landscapes
(e.g., urban settlements, roads, lakes). One poten-
tial reason behind the limited knowledge on the role
of trees outside forests is that large-scale landscape
studies tend to apply binary forest/non-forest classi-
fications based on either moderate spatial resolution
data (Johnson etal. 2013; Rasmussen etal. 2019) or
larger political forest units (Kumeh etal. 2021). Con-
sequently, most knowledge on tree-diet relationships
comes from local case studies that examine the effects
of agroforestry systems on people’s diets (Ghosh-
Jerath et al. 2021; Jemal et al. 2021; Zahoor et al.
2021; Kulsum and Susandarini 2023). Such studies
tend to find positive linkages between agroforestry
and dietary quality (Jamnadass etal. 2013; Montag-
nini 2017; Dagar etal. 2020). For example, a cross-
sectional study among 170 farmers in India estimated
that a 1% increase in tree density and tree diversity
on farms would increase people’s food consumption
score (mean level: 28) by 0.2% point and 0.1% point,
respectively (Singh etal. 2023). A recent review cov-
ering 36 publications on the linkages between tree-
based farming systems and food and nutrition secu-
rity in low- and middle-income countries found that
trees located around farmland had generally positive
effects on people’s diets, directly through provision
of wild and cultivated foods, and indirectly through
improved income opportunities (Vansant et al.
2022). Another review assessing 207 case studies
from sub-Saharan Africa found that 68% of the stud-
ies indicated an increase in food availability due to
the presence of trees on farms (Kuyah etal. 2016).
Yet, a study among 399 farmers in six agroecologi-
cal zones in Rwanda found that trees on farms mainly
represented a safety net for the poorest households
rather than an important contributor to overall food
security (Ndoli etal. 2021). Also, there is mixed evi-
dence on the effects of agroforestry on crop produc-
tion with some studies pointing to the positive effects
on yields (Baier etal. 2023) and soil quality (Kuyah
etal. 2019), whereas other studies indicate that trees
on farms may also be associated with lower yields of
crops such as wheat (Khan etal. 2023).
Even though more than one quarter of Africa’s tree
cover is found outside areas previously classified as
forest (Reiner etal. 2023), the role of individual trees
outside forests (beyond agroforestry) has long been
overlooked due to a lack of high-resolution satellite
imagery (Schnell et al. 2015). However, in the past
few years progress has been made through the com-
bination of new high-resolution satellite imagery and
deep learning methods, which has enabled large-scale
mapping of non-forest trees at the individual tree
level. This includes the detection of 1.8 billion trees
in West African Sahara and Sahel covering areas that
had previously been perceived and categorized as
bare dry lands or deserts (Brandt etal. 2020). There-
fore, it is now possible—and needed—to examine
more closely how trees outside of forests are related
to people’s food and nutrition security in low- and
middle-income countries.
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The second knowledge gap that we aim to address
is how different forest management systems can
contribute to people’s diets, as management sys-
tems around forests can influence how people use
forests and trees as a food source (Adhikari et al.
2016; Andrieu et al. 2019). For example, enforce-
ment of environmental policies in Nepal combined
with increased timber extraction has caused reduc-
tions in local livestock holdings due to lack of fod-
der resources, resulting in a worsening of people’s
food security (Dhakal et al. 2011). The authors of
this study suggested that policies could alternatively
promote agroforestry systems combined with com-
munity-based forest management to gain both forest
protection and better food security for local commu-
nities. This suggestion was later supported by another
Nepalese study which, based on national survey data
from 3064 rural households, found that households
who used resources from community-based forests
experienced higher levels of calorie adequacy com-
pared to households using government-owned forests
(Paudel 2018). Furthermore, a study from Tanzania
assessed the effects of community-based forestry
on wealth, food security and child health, and found
improvements in household food security (measured
by meals/day and fish and meat consumption) in areas
with community-based forest management compared
to areas without (Pailler etal. 2015). Also, a study in
Cameroon reported that more than half of the com-
munity forest users were highly dependent on the for-
est resources, as these resources provided 61–100% of
their income, food, energy and material needs (Ngang
etal. 2018).
While these case studies from Nepal, Tanzania and
Cameroon go beyond broad-scale studies that treat
forests as a homogenous landscape feature, they tend
to use broad food security metrics as opposed to more
detailed measures of dietary quality. This absence of
detailed dietary quality metrics was highlighted by a
recent review of 30 publications on linkages between
social forestry (the term was used by the authors to
describe initiatives linking communities with sustain-
able forest management) and food security in Asia.
The authors found that none of the publications exam-
ined how different forest management systems affect
the dietary quality of local communities (Yahya etal.
2022). When examining the forest-diet relationship, it
is important to move beyond crude measures of food
security in favour of more detailed dietary quality
metrics (where the data allows), as these measures
provide more insight into the mechanisms driving the
observed positive relationships.
In this study, we examined the effects of (1)
unclassified tree cover (i.e., individual trees and small
forest patches outside established forests) and (2)
different types of forest management systems (e.g.,
Government Forest Reserve, Government Forest
Plantation, Private Forest, Participatory Forest Man-
agement (PFM)) on people’s dietary quality, meas-
ured by macro- and micronutrient adequacy levels.
By doing so, we demonstrate how different tree and
forest systems can have varying effects on diets—and
we thereby contribute to a more nuanced understand-
ing of forest-tree-diet linkages.
Material andmethods
Study sites
Tanzania is an appropriate country for studying the
linkages between forests, trees, and people’s diets
for a number of reasons. First, the country hosts sev-
eral large bio-diverse forests (Capitani et al. 2019;
Kacholi etal. 2015) and around 30% of the popula-
tion live within 5km of a forest (Newton etal. 2020).
Second, casestudies from different parts of the coun-
try have shown how communities rely on forest-based
resources in their diet (Murray etal. 2001; Ceppi and
Nielsen 2014; Kaya and Lyana 2014; Pollom et al.
2020). For example, a study in the North Uluguru
and the West Usambara Mountains revealed that local
communities consumed 114 different indigenous for-
est plant foods (Msuya etal. 2010). Another study
among women living in close proximity to forests in
the East Usambara Mountains identified 92 wild food
species and found these wild foods to be an impor-
tant source of vitamin A (31% of intake), vitamin C
(20%), and iron (19%) for both women and children
(Powell et al. 2013). Furthermore, deforestation in
rural areas of Tanzania has been shown to reduce peo-
ple’s fruit and vegetable consumption, with negative
effects on vitamin A adequacy (Hall etal. 2022). Tan-
zania’s forests are also under increasing pressure from
agricultural expansion and logging activities (Dog-
gart etal. 2020). Finally, despite more than 20years
of sustained economic growth, culminating in its
transition from low-income to lower middle-income
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status in 2020, the proportion of people suffering
from severe food insecurity has increased from 21 to
26% between 2016 and 2022 (FAO et al. 2022). In
addition, the number of people not able to afford a
healthy diet increased from 49 to 52 million between
2017 and 2020, corresponding to 88% of the coun-
try’s population (FAO etal. 2022).
In this study, we collected data from eight villages
in East Usambara Mountains and Uluguru Mountains
in Tanzania from October to December 2021 (Fig.1).
The villages were selected to represent different for-
est management systems, while being relatively simi-
lar in terms of people’s living standards, agricultural
practices, and climatic conditions.
Within each of the eight villages, we surveyed
women with at least one child under the age of five
years, since this group is particularly vulnerable to
nutritional deficiencies (Lartey 2008). We selected
60 women from each village using a random stratified
sampling technique. That is, every village consisted
of four to eight hamlets, and we selected respondents
from each hamlet proportional to its relative popu-
lation size. For example, when 25% of the village’s
total population lived in one hamlet, we would ran-
domly select 25% (or 15 women) of our respondents
from that hamlet.
Forest management classification
We base our forest categories on Tanzania’s official
forest classifications (United Republic of Tanzania,
1998, 2002). The country’s forests are grouped into
the following categories of ownership: (1) Central
Government Forest Reserve—owned and managed by
East Usambara Mountains
Uluguru Mountains
Kiwanda
Lat: -5.05511, Long: 38.71170
Elevation: 229 m
MPI: 0.74
Chalagule
Lat: -6.87596, Long: 38.68114
Elevation: 1080 m
MPI: 0.62
Shambangeda
Lat: -5.06322, Long: 38.628376
Elevation: 948 m
MPI: 0.62
Kilemela
Lat: -5.11557, Long: 38.71277
Elevation: 326 m
MPI: 0.71
Vinele
Lat: -7.03603, Long: 37.63597
Elevation: 1384 m
MPI: 0.69
Tchenzema
Lat: -7.10713, Long: 38.58642
Elevation: 1704 m
MPI: 0.67
Tongwe
Lat: -5.11557, Long: 38.71277
Elevation: 258 m
MPI: 0.48
Bombani
Lat: -5.13315, Long: 38.70266
Elevation: 193 m
MPI: 0.43
Government Forest Reserve
Government Plantation
Private Forest
Participatory Forest
Management
East Usambara Mountains
Uluguru Mountains
Fig. 1 Forest management systems, position coordinates,
elevation and mean Multidimensional Poverty Index (MPI)
Living Standarddimension across the eight villages included
in the study. The red dots represent the survey respondents’
homes and show variation in vitamin A adequacy levels within
and across sites. The locations have been randomly displaced
up to 300m for confidentiality purposes
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the central government, including both forest reserves
and forest plantations), (2) Local Authority Forest
Reserve—owned and managed by district authorities,
(3) Village Forest Reserve—owned and managed by
a village government, (4) Private Forest owned and
managed by private companies, and (5) forest patches
in non-reserved forest land—covering small tree plots
less than 10 hectares, sometimes owned by the Cen-
tral Government but most often with open access.
In addition, Community Based Forest Manage-
ment (CBFM) takes place on village land. Villagers
take full ownership and management responsibilities
for the forest, and they also collect forest royalties
from the sales of forest products and services. Finally,
Joint Forest Management is based on a partnership
between communities and the government and has
typically been introduced in Central Government For-
est Reserves that were previously under the manage-
ment of the central government (United Republic of
Tanzania 2008). The partnership means that commu-
nities are given more responsibilities in terms of man-
aging the use of forest resources, while the central
government continues to hold ownership (Mbwambo
etal. 2012).
We regrouped these categories based on the actors
managing the forest. Village Forest Reserve, CBFM
and Joint Forest Management were combined into
one category named Participatory Forest Manage-
ment (PFM). This regrouping is reasonable because
(1) forest access was similar across these three types,
and (2) forest management is given to local commu-
nities—yet with some differences in forest ownership
(Khatun etal. 2015; Luswaga and Nuppenau 2020).
Also, PFM is formally used as an umbrella term in
Tanzania to cover the above-mentioned categories
(United Republic of Tanzania 1998). Using QGIS and
shapefiles showing official forest boundaries provided
by the Central Government of Tanzania, we renamed
and divided Central Government Forest Reserves into
two groups: Government Forest Reserves and Govern-
ment Forest Plantations. We renamed forest patches
in non-reserved forest land to unclassified tree cover
and expanded the category to include all trees outside
of the above-mentioned forest categories, regardless
of the plot size to also capture scattered trees in the
landscape. Private Forest was maintained as a sepa-
rate category. We did not include Local Authority
Forest Reserve since this type of ownership was not
present in any of our study sites.
Forest and tree data
We collected GPS coordinates of the respondents
homes, allowing us to measure the amount of tree
cover in each respondent’s nearby surroundings. In
this study, a tree is defined as a plant with a more or
less permanent shoot system that is supported by a
single trunk of wood (Mbuya etal. 1994). We used
a Very High Resolution (VHR) map of African tree
cover in 2019 (Reiner etal. 2023), which was created
using a deep learning model to segment tree cover
at the individual tree level, based on 3-m resolution
PlanetScope. We spatially aggregated the binary tree
cover data to extract the percentage tree cover in
2000-m radius buffer circles around each respond-
ent’s house. We used a radius of 2000m since this is
the distance most wild foods are collected from peo-
ple’s homes (Layton etal. 1991; Powell etal. 2011).
We then overlaid this with shapefiles provided by the
Tanzanian government on polygons of Government
Forest Reserves, Government Forest Plantations,
Private Forests, and PFMs. For each respondent, we
thus obtained the percentage tree cover within each
of the five forest/tree categories: Government Forest
Reserve, Government Forest Plantation, Private For-
est, PFM, and unclassified tree cover.
Outcome variables
Most studies on forest-tree-diet linkages use food
security metrics such as days without food, the house-
hold food insecurity access scale (Donn etal. 2016;
Tata Ngome etal. 2019), or dietary diversity scores
(Galway etal. 2018; Rasolofoson etal. 2018). Here,
we go beyond these metrics by estimating people’s
macro- and micronutrient intake,with our main out-
come variables being people’s energy, protein, iron,
zinc, and vitamin A adequacy. Nutrient adequacy
ratios (NAR) were calculated from detailed dietary
recall surveys, which aim to record every food item
that the respondent has consumed within the past
24 hours. The 24-h dietary recalls were carried out
twice within a week on two non-consecutive days to
account for unusual dietary intakes (Gibson 2005).
Quantities of each food item were estimated using
local serving size aids (e.g., cups, plates, spoons) and
photo aids.
We then estimated macro- and micronutrient
contents of all reported food items using nutritional
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information from food composition tables (FCTs). A
number of FCTs were used due to missing or incom-
plete nutrient information. We used data from the
Tanzanian tables (Lukmanji and Hertzmark 2008)
as much as possible. When data were missing, we
sourced data from the FCTs for Kenya (FAO 2018a),
Malawi (MAFOODS 2019), Zambia (NFNC 2009)
and West Africa (Vincent etal. 2020)—in that order.
Since all of our respondents were interviewed
twice within one week, we were able to calculate the
usual intake with a Multiple Source Method (MSM)
(Tooze 2020). The methodology consists of three
sequential steps: Initially, the probability of consum-
ing a particular food on a given day is estimated for
each individual. Subsequently, the usual amount
of food intake on days when consumption occurs is
estimated individually. Finally, the overall usual food
intake across all days is computed by multiplying
the probability of food consumption with the usual
amount of food intake on consumption days (Hart-
tig et al. 2011). We then calculated mean NAR by
comparing the estimated nutrient intakes with aver-
age recommended nutrient intakes for energy (FAO
etal. 2002), protein (WHO 2007), iron, zinc and vita-
min A (WHO and FAO 2004). The adequacy ratios
accounted for whether women were pregnant or
breastfeeding. We note that our final adequacy ratios
might be underestimated due to known issues with
underreporting of certain food items, for example in
cases where respondents eat from a shared bowl (Gib-
son 2005). Therefore, we interpret the calculated ade-
quacy levels as relative values between respondents
rather than total values to be compared with national
or international averages.
We calculated dietary diversity scores (DDS)
given that more diverse diets are a good proxy for
micronutrient intake and overall dietary quality (Ken-
nedy etal. 2007; Verger etal. 2019). To measure die-
tary diversity, we used the Minimum Dietary Diver-
sity Score for Women (MDD-W), which categorizes
foods into ten groups: (1) Grains, white roots and
tubers, and plantains, (2) pulses (beans, peas and len-
tils), (3) nuts and seeds, (4) dairy, (5) meat, poultry
and fish, (6) eggs, (7) dark green leafy vegetables, (8)
other vitamin A-rich fruits and vegetables, (9) other
vegetables, and (10) other fruits (FAO 2021; FAO
and FHI 360 2016).
In addition to calculating DDS, we focused spe-
cifically on the consumption of each of the six most
nutritionally important food groups (‘grains, white
roots and tubers, and plantains’, ‘pulses’, ‘meat, poul-
try and fish’, ‘dark green leafy vegetables’, ‘other
vitamin A-rich fruits and vegetables’, and ‘other
fruits’). Together, these six groups represent 99% of
respondents’ nutrient intake (i.e., for protein, iron,
zinc, and vitamin A) (Fig.S2).
Covariates
We controlled for a number of variables known to
affect people’s diets and thus confound the rela-
tionship between forests, trees, and diets. We con-
trolled for agricultural practices (i.e., total crop
count, homegarden presence, tropical livestock units
(TLU))—as more diverse crop and/or livestock pro-
duction can lead to better overall dietary quality (Ali
and Khan 2013; Jones 2017; Headey etal. 2018; Sib-
hatu and Qaim 2018; Christian etal. 2019). We cal-
culated TLU using conversion factors for each live-
stock owned by the household according to FAO’s
guidelines (FAO 2018b). We also controlled for indi-
vidual and household characteristics known to affect
diets, including age (Malapit etal. 2015), education
level measured as years of schooling (Torheim etal.
2004), living standards, region, and household size
(Workicho etal. 2016; Powell etal. 2017). To assess
living standards, we used the Multidimensional Pov-
erty Index (MPI) Living Standard dimension, ranging
from 1 (deprived) to 0 (not deprived) and based on six
indicators; cooking fuel, sanitation, drinking water,
electricity, housing, and assets (Alkire etal. 2021).
We used the distance to the nearest road from the
household (based on respondents’ estimated walking
time) as a proxy for market access, which is known
to influence people’s consumption of specific foods
(Ickowitz etal. 2019). We used distance to the near-
est road rather than other variables such as distance
to the nearest market as local people had different
perceptions of market definitions (e.g., minor stand
by the road, permanent market, travelling market).
Finally, when using one of the five tree or forest cat-
egories as the ‘treatment’ variable (e.g., unclassified
tree cover), we controlled for the other four catego-
ries (e.g., Government Forest Reserve, Government
Forest Plantation, Private Forest, and PFM). TableS1
provides an overview of all covariates.
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Statistical approach
We tested whether tree cover (%) within our five tree
and forest categories was associated with people’s
dietary adequacy and dietary diversity. We employed
Covariate Balancing Generalized Propensity Score
(CBGPS) matching, which is a quasi-experimental
technique. CBGPS was chosen because it is robust to
model misspecifications and applicable in the case of
a continuous treatment (Imai and Ratkovic 2014). The
weights produced by CBGPS minimize the correla-
tion between treatment and observable pre-treatment
covariates when included in the subsequent regres-
sion models. This reduces the dependence (endogene-
ity) between treatment assignment and outcome given
covariates. If not addressed, this dependence may
lead to biased estimates of the effects of tree cover on
people’s dietary quality. CBGPS extends traditional
propensity score methods used for binary treatments
by creating inverse propensity score weights (Fong
etal. 2018). To calculate CBGPS weights, we used
the control variables mentioned earlier as pre-treat-
ment variables: Crop count, homegarden presence,
TLU, age and educational level of the respondent,
MPI living standards, household size, region, dis-
tance to nearest road and the remaining four forest
and tree categories not acting as the treatment. We
used the CBPS package (Fong etal. 2022) in R (ver-
sion 4.3.2) to perform the matching analyses. Corre-
lations between treatment (tree cover inside Govern-
ment Forest Reserve, Government Forest Plantation,
Private Forest, and PFM and unclassified tree cover
included one by one controlling for the other types)
and covariates were sufficiently reduced after match-
ing (Fig.S1). When using NAR as the outcome vari-
able (i.e., adequacy levels for energy, protein, iron,
zinc and vitamin A), we fitted a linear model using
the CBGPS weights, with tree cover within the five
different types of tree and forest systems as the key
predictor of interest. When using the consumption of
the six focus food groups (grams of unique food items
consumed within each food group), we used the same
model specification. When using DDS as the out-
come, we applied a quasipoisson generalized linear
model to account for the non-continuous categorical
outcome variable (Warton etal. 2016). We checked
for overdispersion using the ‘dispersiontest’ function
in the AER package in R, but found no overdispersion
in our models and therefore did not use the negative
binomial distribution (Kleiber et al. 2020). Finally,
we used the sandwich package to compute cluster-
robust standard errors at the village level to adjust for
the lack of independence of households within the
same village (Zeileis etal. 2020).
We used both a pairwise correlation matrix as
well as the variance inflation factor (VIF) to assess
potential collinearity among independent vari-
ables included in our models. All correlation coeffi-
cients were < 0.5 and VIF did not exceed a value of
5. Lastly, to check the robustness of our results, we
re-ran all models using a 1000-m radius instead of
2000-m radius (TableS2).
Results
Our study has two main findings: (1) People living
in areas with more unclassified tree cover (covering
individual trees and forest patches) appear to have
higher adequacy levels of protein, iron, zinc, and vita-
min A. (2) People living in areas with greater tree
cover within PFM appear to have higher adequacy
levels of energy, iron, zinc, and vitamin A (Fig. 2;
TableS1).
Positive associations betweenunclassified tree
cover anddietary quality
We found that the amount of unclassified tree cover
is positively associated with people’s adequacy lev-
els of protein and all three micronutrients. That is, a
1% increase in unclassified tree cover translates into
higher adequacy levels of 0.6% for protein (p < 0.001),
0.2% for iron (p < 0.05), 0.3% for zinc (p < 0.05), and
0.5% for vitamin A (p < 0.001) (Fig.2A).
With the mean unclassified tree cover being
28.9%, an increase from no tree cover to this level
would translate into 16.4%, 4.7%, 9.8%, and 14%
higher adequacy levels of protein, iron, zinc, and vita-
min A, respectively. Although such increases may
not appear substantial, they are notable given that
dietary adequacy is very low in our study area. For
example, only 22% of our respondents meet protein
requirements, no respondents meet iron requirements,
4% meet zinc requirements, and 14% meet vitamin A
requirements.
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However, such translation should be considered
with caution since it assumes a continuous linear
effect between increases in unclassified tree cover
and people’s nutrient adequacy. Recent studies have
shown how forests and trees can be linked to diets in
non-linear ways (Friant etal. 2019; Rasmussen etal.
2019; Kumeh et al. 2022). Likewise, the potential
underestimation of our respondents’ nutrient ade-
quacy levels merits caution when interpreting these
estimates.
Along with effects on nutrient adequacy levels, we
also examined the effects of unclassified tree cover
on people’s intake of six key food groups. We found
a positive association with the intake of three food
groups: ‘meat, poultry and fish’ (p < 0.05), ‘other
vitamin A-rich fruits and vegetables’ (p < 0.001) and
‘other fruits’ (p < 0.001) (Fig.2B). Respondents with
above median levels of unclassified tree cover on
average consumed 111g per day of ‘meat, poultry
and fish’ compared to only 40g for those respond-
ents with below median tree cover (Table1; Fig.3).
Fig. 2 Post-matching
results for how tree cover
within five different types
of tree and forest manage-
ment systems is associated
with people’s A macro- and
micronutrient adequacy,
and B intake of four key
food groups. Results are
not shown for the two
food groups ‘grains, white
roots and tubers, and
plantains’ and ‘pulses’ as
no significant results were
found. P-values: * < 0.05,
** < 0.01, *** < 0.001.
N = 465
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Given that 91% of the total amount of ‘meat, poultry
and fish’ consumed was fish (Fig.S2), it is likely that
this was the main driver of higher protein, iron and
zinc intakes for those respondents living in areas with
higher unclassified tree cover. This is in line with
other studies that have documented the importance
of fish consumption for dietary quality in East Africa
(Wessels etal. 2023). Furthermore, it is likely that
higher intakes of ‘other vitaminA-rich fruits and veg-
etables’ (especially mangos and papayas (Fig. S2))
explain the observed positive associations between
unclassified tree cover and the higher adequacy levels
of vitamin A.
Positive associations betweenparticipatory forest
management anddietary quality
We also found that the extent of tree cover classified
as PFM is positively associated with higher adequacy
levels of energy, iron, zinc, and vitamin A as well
as higher dietary diversity scores (Fig.S3). That is,
a 1% increase in tree cover within PFM translates
into increases of nutrient adequacy levels of 0.7% for
energy (p < 0.05), 0.4% for iron (p < 0.001), 0.8% for
zinc (p < 0.01), and 1.3% for vitamin A (p < 0.001)
(Fig. 2A). This is likely driven by higher consump-
tion of fish, other vitamin A-rich fruits and vegeta-
bles, and other fruits, as the consumption of these
food groups was also significantly positively associ-
ated with tree cover within PFM (Fig.2B).
By contrast, tree cover within Government For-
est Plantations was negatively associated with ade-
quacy levels of zinc (−1.3%, p < 0.05) and vitamin
A (−1.9%, p < 0.001). Similarly, we found negative
associations between tree cover within Government
Forest Reserves and vitamin A (−0.4%, p < 0.05) and
Private Forests and people’s adequacy level of zinc
(−5.1%, p < 0.05). These results might be explained
by lower consumption of vitamin A-rich fruits and
vegetables and dark green leafy vegetables by people
living in areas with more tree cover within Govern-
ment Forest Plantation (− 5.9%, p < 0.01, − 1.6%,
p < 0.05, respectively). Likewise, people living in
areas with more tree cover within Government Forest
Reserves had lower consumption of vitaminA-rich
fruits and vegetables (−3.1%, p < 0.05).
Discussion
Trees and forest patches outside forests are beneficial
for dietary quality
Our findings suggest that trees and small forest
patches outside of established forest reserves can
improve people’s nutrient adequacy. These findings
demonstrate the importance of moving beyond forest/
non-forest dichotomies,which have been a common
approach in the forest-diet literature (e.g. Johnson
et al. 2013; Galway et al. 2018). Also, the existing
bulk of research on relationships between tree-based
farming systems and food and nutrition security
(Vansant etal. 2022) tends to focus on trees in crop-
lands and thereby dismisses the potential contribu-
tions from individual trees in fallows, pasture, around
settlements or along roads, lakes and rivers. By using
VHR satellite data, we were able to include trees that
would not be accounted for otherwise—both on farms
and scattered trees outside of forests. While existing
studies attending to on-farm trees often rely on self-
reported counts or time-consuming field measure-
ments, our method can be extrapolated and poten-
tially up-scaled to cover even greater areas.
However, we were not able to distinguish between
different types of trees (e.g., timber trees vs fruit
trees), which limits the ability to tease apart causal
mechanisms between tree cover and dietary quality.
For example, we found a positive significant rela-
tionship between unclassified tree cover and people’s
vitamin A adequacy levels as well as their consump-
tion of vitamin A-rich fruits and vegetables (Fig. 2
and TableS1). These relationships indicate that peo-
ple living in areas with higher tree cover might be
consuming more vitamin A-rich fruits harvested from
trees, such as mango and papaya. When looking at
where people source their vitamin A-rich fruits and
vegetables, we observe that people living in areas with
above median tree cover source a higher proportion of
this food group from the wild (4.5% as compared to
0% for people living in areas with below median tree
cover) as well as from cultivated fields (61% as com-
pared to 52%) (Table2). Such explanation would be
in line with other studies that have established a posi-
tive role of fruit trees for diets (Jamnadass etal. 2011;
Bostedt etal. 2016; Mathewos etal. 2018; Omotayo
and Aremu 2020; Kulsum and Susandarini 2023). For
example, a study from Ethiopia found that growing
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fruit trees was positively associated with higher die-
tary diversity among women and young children in
the households (Desalegn and Jagiso 2020).
We also found a positive association between
unclassified tree cover and adequacy levels of protein,
iron, and zinc. This may be explained by higher fish
consumption among people living in areas with high
tree cover. Positive associations between tree cover
and fish consumption have also been documented in
both Indonesia (Ickowitz etal. 2023) and Nigeria (Lo
etal. 2019), suggesting that trees provide ecosystem
services that enhance the availability of fish stocks.
While we do observe a marginal higher proportion of
fish being sourced from the wild among people living
in areas with higher tree cover (1.8% as compared to
1.4% among people living in areas with below median
tree cover), most of the consumed fish is purchased
from the market rather than caught in local rivers and
lakes (Table2). Nevertheless, the nutritional impor-
tance of fish in East Africa is notable (Béné et al.
2016). It has been estimated that utilizing the entire
amount of the potential sustainable catch of Silver
cyprinid (small pelagic fish) in Lake Victoria would
provide a sufficient daily source of vitamin B12, cal-
cium, zinc and iron to approximately 33 million peo-
ple in the region (Wessels etal. 2023). Twenty-five
percent of our respondents consumed less than 100g
of fish relish per day. Thus, a relatively small increase
in fish consumption may be a promising avenue to
increase nutrient adequacy levels.
Linkages betweenforest management systems
anddietary quality
It is well established that the type of forest manage-
ment system in place matters for the type and quantity
of products that people can harvest from the forest—
and thereby influencethe potential of forests to allevi-
ate poverty (Miller etal. 2020). Yet, the role of forest
management systems in relation to dietary quality has
been somewhat overlooked,especially in quantitative
Table 1 Mean values of covariates for respondents living in areas with above vs below median levels of unclassified tree cover and
in areas with vs without PFM within a 2000-m radius
N = 465
Mean (SD)
Variables Unclassified tree cover Participatory forest management
(PFM)
Above median Below median With Without
Age 30.19 (7.44) 29.16 (8.11) 29.06 (7.79) 30.06 (7.78)
Household size 5.24 (1.84) 5.13 (2) 5.21 (2.07) 5.17 (1.82)
Number of crops cultivated 5.07 (2.78) 4.6 (2.63) 4.87 (2.73) 4.81 (2.71)
Tropical livestock unit (TLU) 0.26 (0.85) 0.26 (0.5) 0.29 (0.8) 0.24 (0.63)
Distance to nearest road (minutes walking) 95.7 (163.63) 68.84 (88.92) 122.44 (180.44) 57.24 (81.01)
Multidimensional poverty index (MPI) 0.63 (0.2) 0.62 (0.16) 0.62 (0.18) 0.63 (0.18)
Energy adequacy ratio (%) 0.77 (0.17) 0.65 (0.22) 0.71 (0.19) 0.71 (0.21)
Protein adequacy ratio (%) 0.72 (0.26) 0.53 (0.31) 0.60 (0.28) 0.64 (0.31)
Iron adequacy ratio (%) 0.44 (0.12) 0.39 (0.14) 0.42 (0.13) 0.41 (0.13)
Zinc adequacy ratio (%) 0.6 (0.2) 0.48 (0.22) 0.54 (0.22) 0.54 (0.22)
Vitamin A adequacy ratio (%) 0.62 (0.25) 0.56 (0.25) 0.63 (0.26) 0.56 (0.24)
DDS 3.69 (1.45) 3.97 (1.36) 4.1 (1.5) 3.67 (1.36)
Grains, white roots and tubers, and plantains (mean g/day) 1044.8 (406.25) 908.9 (432) 997.06 (427.27) 964.46 (422.76)
Pulses (mean g/day) 54.43 (70.56) 55.33 (78.37) 50.75 (70.76) 57.46 (76.72)
Meat, poultry and fish (mean g/day) 110.71 (115.5) 40.12 (68.5) 73.36 (97.25) 76.82 (103.84)
Dark green leafy vegetables (mean g/day) 48.89 (56.5) 57.29 (76.21) 43.23 (48.52) 59.23 (75.91)
Other vitamin A-rich fruits and vegetables (mean g/day) 101.81 (197.07) 23.31 (81.97) 99.45 (182.17) 39.66 (132.21)
Other fruits (mean g/day) 45.81 (148.78) 51.76 (199.27) 55.65 (199.2) 44.49 (159.37)
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Fig. 3 Share of energy, protein and micronutrients com-
ing from the different MDD-W food groups, broken down
into respondents living in areas with above vs below median
unclassified tree cover. We have merged ‘nuts and seeds’,
‘dairy’, ‘eggs’ and ‘other vegetables’ into ‘other’ because
these food groups contributed less than 1% of total nutrient
intake. The category ‘sugar sweetened beverages’ was added
to the figure as it contributed 4.5% and 3.5% of energy intake
for respondents living in areas with above and below median
unclassified tree cover, respectively. N = 465
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studies. Here, we find substantial variations across
different forest management systems, with positive
effects seen in PFM systems and negative effects of
other forest management systems (Government Forest
Reserves and Government Forest Plantations).
These negative effects on people’s diets exemplify
how forest conservation initiatives and profit-oriented
forestry might have unintended consequences for food
and nutrition security when people’s access to these
forests is restricted. For example, the respondents in
our study sites were only allowed to enter the Govern-
ment Forest Reserves and Government Forest Planta-
tions once a week to collect fuelwood and wild plants.
When entering the Government Forest Reserves, they
were not allowed to bring a machete, which made
the dense part of the forests impenetrable. Also, the
Government Forest Plantations were dominated by
one exotic teak tree species (Tectona grandis) with
low levels of biodiversity and relatively few wild
foods to find. Multiple studies from various parts of
the world have described how forest conservation
can lead to negative social outcomes if local people
are not appropriately compensated or included in the
management regimes (Blaney etal. 2009; Ibarra etal.
2011; Sylvester etal. 2016; Nakamura and Hanazaki
2017; Campbell etal. 2021). For example, Hall etal.
(2014) assessed both ecological and livelihood con-
sequences of the newly established Derema Forest,
a large protected forest corridor in East Usambara
Mountains. Two years after establishment, the area
appeared to succeed in terms of functioning as an
ecologically important corridor but failed to mitigate
livelihood losses especially for the poorest people
(Hall et al. 2014). Likewise, forest conservation in
Oaxaca, Mexico was perceived to make indigenous
communities more food insecure as local community
members found a decrease in subsistence crop yields,
land available for agriculture and shortened fallow
cycles to be a result of implemented conservation pol-
icies (Ibarra etal. 2011). More recently, a study from
Southwestern Ghana suggested that forest conserva-
tion initiatives should be combined with so-called
‘food security corridors’ in degraded forest-fringes to
ensure that local populations benefit from both forests
and cultivated resources—which in turn can reduce
exploitation of the inner forest reserve (Kumeh etal.
2022). Yet, we note that previous studies have also
shown how mixed plantations and private forests can
provide a variety of beneficial ecosystem services,
including local food provision (Liu etal. 2018). For
example, a study from the Congo Basin examined
land use competition between timber concessions and
fruit trees harvested by local communities and found
that both interests could co-exist as long as timber
harvesting only targeted the largest trees and allowed
appropriate minimum distances between the remain-
ing trees to ensure gene flow for future forest regen-
eration (Snook etal. 2015).
It is also important to emphasize that PFM is an
umbrella term that covers different sub-management
systems (e.g., Joint Forest Management, Commu-
nity Forest Management and Village Forest Man-
agement). Although we found it reasonable to group
these into one category based on similarities in terms
Table 2 The share of six focus food groups coming from different sources (cultivated, purchased or wild) among respondents living
with above vs below median unclassified tree cover within a 2000-m radius
N = 465
Source (% of food items)
Food group Cultivated Purchased Wild
Above median Below median Above median Below median Above median Below median
Grains, white roots and tubers,
and plantains
33.5 30.2 65.8 68.4 0.6 1.4
Pulses 9.8 19.9 89.9 79.5 0.3 0.6
Meat, poultry and fish 0.2 0.7 97.9 97.9 1.8 1.4
Dark green leafy vegetables 30.9 35.4 51.3 45.6 17.8 19.0
Other vitamin A-rich fruits and
vegetables
60.9 52.4 34.5 47.6 4.5 0.0
Other fruits 45.1 29.4 51.0 64.7 3.9 5.9
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of access to resources, these sub-systems may differ
in other aspects that may affect dietary quality. For
example, a study from Tanzania comparing Commu-
nity Forest Management and Joint Forest Manage-
ment found that the level of participation was higher
among communities with Joint Forest management
(Luswaga and Nuppenau 2020), yet the study did not
measure differences in resource use. Also, PFM is not
always found to have the anticipated positive effects
on local livelihoods, and potential co-benefits are
most often dependent on site-specific contextual fac-
tors (Duguma etal. 2018; Hajjar and Oldekop 2018).
For example, participatory forest initiatives in Nepal
have been centred around timber extraction and bio-
diversity conservation, while disregarding food secu-
rity outcomes for local people (Khatri etal. 2017). In
other words, while the results of this study suggest
that the inclusion of local communities in forest man-
agement systems is more likely to produce dietary
benefits, as compared to more exclusive and inacces-
sible forests management systems, PFM should not
be perceived as a panacea to improve food and nutri-
tion security.
Policy implications andfuture research directions
Our findings have policy relevance in terms of
future strategies for improving local people’s food
and nutrition security, particularly in rural areas of
low- and middle-income countries. In particular,
our findings have two key policy implications:
1. Decision-makers should support initiatives
towards multi-functional and nutrition-rich land-
scapes through the promotion of trees and forest
patches outside established forest reserves and in
near surroundings of the targeted populations.
2. Because we show positive effects of PFM sys-
tems on local people’s diets, but negative effects
of other forest management systems, decision-
makers should attend to sustainable food extrac-
tion from community-based forests (e.g., api-
culture and foraging of wild foods and medical
plants).
Moreover, our study allows us to point to a num-
ber of directions for future research. Firstly, future
research on linkages between forests, trees and
dietary quality should move beyond dichotomies
of forest versus non-forest. Trees grow not only in
established forest blocks or on farmlands but are
scattered across the landscape and are present along
roads, rivers, and lakes. Secondly, while we have
shown the potential importance of these scattered
trees (not constituting a forest) in Tanzania, more
work is needed to examine whether these relation-
ships hold in other countries and contexts. Thirdly,
our approach does not allow us to tease apart the
dietary contributions from different tree species.
Future research efforts would benefit from identifi-
cation of and distinction between different tree spe-
cies and their effect on people’s diets.
Acknowledgements We like to thank our research assistants
Anna Peter Tesha, Hope Masanja, Kudra Ally, Maria Machilu,
Mercy Mtaita, Monica Chande and Naamani Mwaisenye.
Author contributions R.S.O. conceived the idea. R.S.O.,
C.J.K., J.K., J.M. and L.V.R designed the data collection pro-
cess. R.S.O. carried out data collection. R.S.O., F.R. and
C.J.K. conducted the spatial forest and tree classifications.
R.S.O., L.V.R., C.H. and B.d.B. designed the analysis. R.S.O.
conducted the analysis. F.R., L.V.R., B.d.B., C.H. and C.J.K.
contributed with interpretations of results. All authors con-
tributed to the writing of the paper. All authors reviewed the
manuscript.
Funding Open access funding provided by Copenhagen Uni-
versity. The research for this paper was funded by the European
Research Council (ERC) under the European Union’s Horizon
2020 Research and Innovation Programme (Grant Agreement
No. 853222 FORESTDIET).
Data availability The data are available from the authors
upon reasonable request and with the permission of University
of Copenhagen.
Declarations
Competing interest The authors have no relevant financial or
non-financial interests to disclose.
Open Access This article is licensed under a Creative Com-
mons Attribution 4.0 International License, which permits
use, sharing, adaptation, distribution and reproduction in any
medium or format, as long as you give appropriate credit to the
original author(s) and the source, provide a link to the Crea-
tive Commons licence, and indicate if changes were made. The
images or other third party material in this article are included
in the article’s Creative Commons licence, unless indicated
otherwise in a credit line to the material. If material is not
included in the article’s Creative Commons licence and your
intended use is not permitted by statutory regulation or exceeds
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from the copyright holder. To view a copy of this licence, visit
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Forests are attracting attention as a promising avenue to provide nutritious and ‘free’ food without damaging the environment. Yet, we lack knowledge on the extent to which this holds in areas with sparse tree cover, such as in West Africa. This is largely due to existing methods being poorly designed to quantify tree cover in drylands. Here, we estimate how various levels of tree cover across West Africa affect children’s (aged 12-59 months) consumption of vitamin A-rich foods. We do so by combining detailed tree cover estimates based on PlanetScope imagery (3 m resolution) with Demographic Health Survey data from more than 15,000 households. We find that the probability of consuming vitamin A-rich foods increases from 0.45 to 0.53 with an increase in tree cover from the median value of 8.8% to 16.8% (which is the tree cover level at which the predicted probability of consuming vitamin A-rich foods is highest). Moreover, we observe that the effects of tree cover vary across poverty levels and ecoregions: The poor are more likely than the non-poor to consume vitamin A-rich foods at low levels of tree cover in the lowland forest-savanna ecoregions, whereas the difference between poor and non-poor is less pronounced in the Sahel-Sudan. These results highlight the importance of trees and forests in sustainable food system transformation, even in areas with sparse tree cover.
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