Guide To Monitoring Carbon Storage in Agroforestry Projects
Guide To Monitoring Carbon Storage in Agroforestry Projects
Guide To Monitoring Carbon Storage in Agroforestry Projects
WhSh / Ch
h=1
L
where n = sample size (i.e., total number of sample plots required)
t = tabular value of Students t
h = stratum number
L = the number of strata
W
h
= N
h
/N
Nh = number of sample units in stratum h
N = total number of sample units
S = stratum standard deviation
A = allowable error expressed in units of the mean
Ch = the cost of selecting a sample plot in stratum h
Allocation of these sample plots among strata is calculated as: n
h
= np
h
where: n
h
= number of sample plots for stratum h
n = total number of sample plots
and
Ph = WhSh / Ch ( )/ WhSh / Ch
h=1
L
24 For a more detailed description of this approach see Forestry handbook (2nd edition), ed. K.F. Wenger (New
York: John Wiley and Sons, 1984) and Sampling techniques (3rd edition), by W.G. Cochran (New York: John
Wiley and Sons, 1977).
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2. Optimum allocation of plots with fixed costs
If costs for sampling are fixed before sample size or plot allocations are determined, plot allocations
can be assigned to minimize the inventory cost. The second portion of the spreadsheet performs these
calculations using the following formula:
Vc = n ChPh
h =1
L
where: V
c
= variable costs for sampling
The user inputs include site name, measured parameter (e.g. woody biomass), number of preliminary
sample plots used to calculate plot-to-plot variances, desired level of probability (p), allowable error
(in % of the mean), sampling budget (if variable costs for sampling are set before sample size is
calculated), sample plot size, costs for the establishment and measurement of sample plots, and the
proposed number of times measurements will be made after plot establishment and baseline
measurement. The minimum value for planned number of samplings is one (final measurement).
When using the formula, the following conventions must be used:
If the mean and standard deviation values are not calculated from sample plot data in the
spreadsheet, they must also be entered for each stratum.
Cost values must be entered into the column labeled "Cost per plot" near the bottom of the
sheet. Calculate cost per plot using the input values in the box at the top of the sheet, but enter
these manually in the cost per plot cells to allow separate cost values for each stratum.
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Appendix 3: Inputs for Carbon Modelling with SCUAF
The data required for carbon modelling using the Soil Changes Under Agroforestry (SCUAF)
software are listed in the table below. Data on soil organic carbon, tree growth rates, biomass
partitioning, and site descriptions must be entered before running models. All inputs, including
defaults, must be listed in the form. If data other than the default values are used, the source of this
data should be listed in the "Source" column.
The following are inputs required to use SCUAF:25
Input Value Source
1 CYCLE
Cycle selected for modelling
If carbon cycle only is selected, it is not necessary to input
data on nitrogen.
1 Carbon
Cycle
2 Carbon
and Nitrogen
Cycles
2 DOCUMENTATION
File name
Title
Source
Location
Date
Notes
25The source references indicate values that are different from the SCUAF default data set.
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3 PHYSICAL ENVIRONMENT
Climate:
Soil texture:
Drainage:
Soil reaction:
Slope class:
1 Lowland
humid
2 Lowland
subhumid
3 Lowland
semi-arid
4 Highland
humid
5 Highland
subhumid
6 Highland
semi-arid
1 Medium
textured
2 Sandy
3 Clayey
1 Free
2 Imperfect
3 Poor
1 Strongly
acid
2 Acid
3 Neutral
4 Alkaline
1 Flat
2 Gentle
3 Moderate
4 Steep
4 AGROFORESTRY SYSTEM
Length (years)
Fraction of land under trees
Fraction of land under crop
Is it a cut year? (Yes/No)
What fraction of tree is N-fixing?
What fraction of crop is N-fixing?
Period
1 2 3 4 5 6
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5 INITIAL SOIL CONDITIONS
DEPTH
Topsoil depth (cm)
Soil depth considered (cm)
Total depth of soil (cm)
CARBON
Initial Carbon, Topsoil (percent)
Initial Carbon, Subsoil (percent)
Bulk density, Topsoil (g/cc)
Bulk density, Subsoil (g/cc)
Initial soil Carbon (kg/ha)
NITROGEN
Initial Nitrogen, Topsoil (percent)
Initial soil Nitrogen (kg/ha)
6 EROSION
Soil Erosion (kg/ha/yr) = Climate Factor * Soil Erodibility Factor
* Slope Factor * Cover Factor * 1000
Enter best estimate for each factor:
Climate factor
Soil erodibility factor
Slope factor
Cover factor under tree
Cover factor under crop
Soil erosion under tree (kg/ha/yr)
Soil erosion under crop (kg/ha/yr)
Tree proportionality factor
Measured soil erosion in Year 1 (kg/ha/yr)
Carbon enrichment factor
Nitrogen enrichment factor
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7 INITIAL PLANT GROWTH
Tree, Net Primary Production, above-ground (kg DM/ha/yr)
Crop, Net Primary Production, above-ground (kg DM/ha/yr)
Roots as a fraction of above-ground NPP, tree
Roots as a fraction of above-ground NPP, crop
NPP in parts of tree (kg/ha/yr):
Leaf
Fruit
Wood
Root
NPP in parts of crop (kg/ha/yr):
Leaf
Fruit
Wood
Root
Fractions of Tree retained as growth annually:
Leaf
Fruit
Wood
Root
Fractions of Crop retained as growth annually:
Leaf
Fruit
Wood
Root
Proportion of tree roots that are coarse roots
Proportion of crop roots that are coarse roots
Is any part of tree or crop retained as growth in cut year (Yes/No)
If Yes:
Fractions of Tree retained as growth during cut year:
Leaf
Fruit
Wood
Root
Fractions of Crop retained as growth during cut year:
Leaf
Fruit
Wood
Root
Fraction of roots growing below soil depth considered:
Tree roots
Crop roots
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CARBON
Carbon Fraction in dry mass, Tree
Carbon Fraction in dry mass, Crop
NITROGEN
Nitrogen % in:
or
Carbon:Nitrogen ratio of:
Tree Leaf
Tree Fruit
Tree Wood
Tree Root
Crop Leaf
Crop Fruit
Crop Wood
Tree Root or Crop Root
8 ADDITIONS
Organic (kg DM/ha/yr)
Carbon fraction in organic additions
Nitrogen percent in organic additions
or Carbon:Nitrogen ratio in organic additions
Fertilizer (kg/ha/yr)
Nitrogen fraction in fertilizer
Period
1 2 3 4 5 6
Period
1 2 3 4 5 6
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9 REMOVALS
A: HARVEST
Fraction of Tree harvested annually:
Leaf
Fruit
Wood
Root
Fraction of Crop harvested annually:
Leaf
Fruit
Wood
Root
Additional fraction of Tree harvested in cut year:
Leaf
Fruit
Wood
Root
Additional fraction of Crop harvested in cut year:
Leaf
Fruit
Wood
Root
B: OTHER LOSSES FROM SYSTEM
Are there any losses of plant material from the system
other than harvest (e.g. burning)? (Yes/No) If Yes:
Fraction of Tree lost annually:
Leaf
Fruit
Wood
Root
Fraction of Crop lost annually:
Leaf
Fruit
Wood
Root
Additional fraction of Tree lost in cut year:
Leaf
Fruit
Wood
Root
Additional fraction of Crop lost in cut year:
Leaf
Fruit
Wood
Root
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10 SOIL PROCESSES
CONVERSION LOSSES (Litter to Humus)
Fraction of above-ground parts lost through oxidation
Fraction of roots lost through oxidation
Fraction of organic additions lost through oxidation
Fraction of coarse tree roots decaying at least 1 year later
Fraction of coarse crop roots decaying at least 1 year later
Fraction of remaining coarse tree roots decaying 2 years later
Fraction of remaining coarse crop roots decaying 2 years later
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HUMUS DECOMPOSITION CONSTANTS
Number of humus fractions considered (1 or 2)
LABILE HUMUS
K for the tree
K for the crop
For 2-fraction humus only:
STABLE HUMUS
K for the tree
K for the crop
Fraction of humified litter becoming labile humus
Fraction of labile humus transformed annually to stable
NITROGEN CYCLE
NITROGEN GAINS
Symbiotic Fixation per unit area of N-fixing Tree (kg/ha/yr)
Symbiotic Fixation per unit of N- fixing Crop (kg/ha/yr)
Fraction of symbiotic fixed N entering soil humus
Non-Symbiotic Fixation (kg/ha/yr)
Throughfall and stemflow (kg/ha/yr)
NITROGEN LOSSES
A. Mineral N of organic origin:
Fraction of mineral N leached under tree
Fraction of mineral N leached under crop
Fraction of mineral N lost
- by gaseous losses (dentrification + volatilization)
- by fixation onto clay minerals
(net)
B. Fertilizer N:
Fraction of fertilizer N leached under tree
Fraction of fertilizer N leached under crop
Fraction of fertilizer N lost:
- by gaseous losses
(denitrification+volatilization)
- by fixation onto clay minerations (ncl)
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11 SOIL/PLANT FEEDBACK FACTORS
CARBON
Rise or fall in soil carbon, relative to initial state, of 1
percent causes increase or decrease in rate of plant growth by x
percent:
For Tree
For Crop
NITROGEN
Rise or fall in soil nitrogen, relative to initial state, of 1 percent
causes increase or decrease in rate of plant growth by x percent:
For Tree
For Crop
SOIL DEPTH
Rise or fall in soil depth, relative to initial state, of 1 percent
causes increase or decrease in rate of plant growth by x percent:
For Tree
For Crop
NOTES
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Appendix 4: Measuring Woody Biomass
Woody biomass will nearly always be the largest and most easily manipulated carbon pool in carbon
storage forestry projects. The inventory approaches for woody biomass are:
1. Measure the woody biomass of trees larger than a minimum diameter (e.g. >5 cm dbh) in
project and non-project areas using timber cruises of permanent, continuous inventory sample
plots. At the same time, sample the herbaceous biomass, standing litter crop and soil carbon
vegetation, using the methods described in Appendix 5.
2. If permanent plots are not desirable or practical (due to frequent wildfire or grazing, for
example), use the plotless quarter point vegetation survey to evaluate biomass and carbon
content of vegetation on non-project sites. In plantation projects, the quarter-point method
(which uses the distance between a systematic sampling point and the nearest tree or shrub)
can be used to monitor lands left under natural vegetation. For preservation projects, this
method can be used to monitor changes in lands converted to agriculture or other land uses
with low tree population densities.
A. Timber cruising
Use permanent, inventory plots to measure timber on project and non-project sites, following a
stratified random sampling design. In general, most carbon sequestered by project activities will occur
in the largest diameter classes, so the timber cruise part of the inventory requires particular care.
Size and shape of fixed plots
Circular plots established using a well-identified plot center and a digital distance measure are
recommended (Table 4). Optimal plot size can also be calculated using the following formula26:
Size = P
1
t
2
m
where: P
1
= size of plot used in preliminary sample to assess time and variation in any unit of area; t =
average travel time between neighboring plots in minutes; m=average plot measurement time for plot
size P
1
in minutes
To calculate optimal plot size, measure a minimum of three plots of size P1. Plots should be separated
by the same distances anticipated in an actual inventory. Travel speed between plots and the plot
measurement time (m) should be recorded. Calculate t by dividing the distance between neighboring
plots by the travel speed or measure and average travel time between plots. Calculate P using the
formula above.
26 Zeide, B. 1980. Plot size optimization. Forest Science 26:251-257.
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Table 4. Plot radii for carbon inventory plots
Plot size (m
2
) Plot radius (m) Area per tree (m
2
tree-1) Application
100 5.64 0 - 15 Very dense vegetation, stands
with large number of small
diameter stems, uniform
distribution of larger stems
250 8.92 15 - 40 Moderately dense woody
vegetation
500 12.62 40 - 70 Moderately sparse woody
vegetation
666.7 14.56 70 - 100 Sparse woody vegetation
1,000
or use quarter
point method
17.84 > 100 Very sparse woody vegetation
Relating diameter to biomass
Biomass tables or equations are needed to relate dbh and the number of plants per ha to total biomass.
Biomass tables should therefore be sought for important species of native vegetation. Where these
tables are not available, there are three alternatives:
1. Develop biomass tables for each important tree species using the method described in
section C of this appendix. This is the most precise (and most costly) approach.
2. Develop biomass tables for groups of tree or shrub species. The most useful groupings may
be by morphology class (e.g., single-stemmed trees, multiple-stemmed trees, shrubs).
3. Use one of the general biomass equations found in section C. This is the least precise
approach, but also the least expensive. Given the wide range of species included in these
equations, they should not be used except where the alternatives above are not possible.
B. Non-project woody vegetation
This method should be used to measure natural vegetation prior to project establishment at the same
interval set for the measurement of the permanent inventory plots in the project. To save time in
laying out plots in measuring woody savannah vegetation, use the quarter point method,27 which
uses the distance between a systematic sampling point and the nearest tree or shrub.
The steps for this method are:
1. Establish a series of parallel sample lines 100 m apart. Locate sample points every 10 m
along each line.
27 For a more detailed description of this approach see Methods of sampling lesser vegetation, pp. 58-59 in Forestry
handbook (2nd edition), ed. K.F. Wenger (New York: John Wiley and Sons, 1984).
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2. At each sample point, divide the immediate area into quarters using the sample line plus a
second line that crosses the sample point perpendicularly to the sample line. Figure 3
demonstrates placement of line and sample point, along with quarter numbers for each sample
point.
3. Collect species and diameter data using the data collection form. For shrubs and small trees
with low branching, measure diameter at 30 cm above the ground; for trees with better tree
form, use dbh at 1.3 m. Also record the distance from each tree or shrub to the sample point.
A minimum of 100 distance measurements are required per stratum.
4. Calculate average distances as follows:
Average the four distances at each point, then average the distances for the entire
sample area. Use this number to calculate the mean area per tree as: M = d
2
, where M
= mean area per tree in m2 and d = average distance over the entire sample area.
For the total sample area, calculate density using the formula: D = 10,000 / M,
where D = trees per hectare.28
Construct a stand table, with appropriate size diameter classes, and estimate biomass
based on a biomass table.
28 If only a few species predominate, then accuracy is probably increased by determining biomass and carbon
content by individual species. The method outlined in this section presumes relatively high species diversity and
relatively low return to the additional investment needed to estimate non-project biomass by species.
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C. Developing biomass tables29Tree biomass weight tables show the average weight of
individual trees for one or more dimensions, usually stem diameter alone (for local tables) or stem
diameter along with height or length. The tables employ data obtained in destructive sampling.
Through regression analysis, wood or foliage weight can be related to dbh, diameter at 0.3 m, and
height. This appendix describes the process for developing standard biomass weight tables.
Developing local weight tables is not recommended in view of their limited application and the great
deal of effort they require, as well as the duplication of effort they involve.
Planning a weight table
Critical decisions must be made before beginning to develop a weight table, including:
Defining the range of tree or shrub dimensions to be covered by the table.
Defining the type(s) of biomass to be included in the table(s); this may include stem wood,
stem and branch wood, or foliage; a table will need to be developed for each biomass type.
Determining what measurements to use in relating biomass to a practical field measurement
(e.g., d, dbh, or h).
Defining size classes throughout the range of tree sizes.
Field sampling
A key issue is the number of trees necessary to develop a weight table for a given species. Estimates
from many recent biomass studies suggest that 30-100 trees are enough for a regional table using
stratified sampling of the population. Sufficient evidence supports the case that if sample trees are
selected in equal or near-equal numbers for each size class, 30 trees for an individual tree biomass
table are adequate. At least 30 well-selected trees should be used per species for individual tree
biomass tables, unless the tables are to be used only for a specific site. For such purposes, as few as
12 trees may be adequate.
For calculating foliar nutrient content, more samples may be needed for foliage and branches than for
stem wood. If scarce funds prevent the measurement of more than 30 sample trees for foliage,
consider reducing the number of samples for stem wood in order to make resources available for
foliage and branch sampling.
Partitioning and weighing
Each individual tree or shrub should be harvested; measured for diameter, length, and height30; and
divided into the major components defined during the planning stage. Length measurements are
recommended, but if vertical height is to be included as an independent variable, the measurement
must be taken before the tree is harvested. Individual components (stem, branches, leaves, etc.)
should be divided into several size classes for convenient handling and sub-sampling. Sub-samples
should be taken to determine moisture content and specific gravity.
Techniques for weighing tree components depend largely on tree size and the availability of
equipment. Take care to keep each tree and its parts separate from other trees. The best way to ensure
29This section is taken largely from Standard research methods for multipurpose trees and shrubs, eds. K.G.
MacDicken, G.V. Wolf and C.B. Briscoe (Arlington, Virginia: Winrock International, 1991).
30Length is the measured distance of a tree or specified portion of a tree following the lean or curvature, not
necessarily vertical or straight; height is the vertical distance between a standing trees apical bud and ground level.
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this is to partition and weigh only one tree at a time. Measure green weight in the field. To calculate
moisture content, sub-samples should be taken, dried at 80 C and re-veighed.
Although harvesting is the preferred way to develop weight tables, it is not always possible due to
conservation or regeneration considerations. For biomass tables from non-destructive samples,
calculate stemwood volumes and convert them to biomass using specific gravity for wood and
expansion factors for canopy biomass. This requires a device for measuring diameter, such as a
Wheeler pentaprism caliper, Spiegel Relaskop or laser measuring device. A sample form for
recording data to construct biomass tables or volume tables using a metric Relaskop follows.
Analysis
Regression analysis should be performed for each biomass type defined during the planning process.
To make the tables useful for the widest possible range of environments, at least one complete set of
equations and weight tables should include both diameter and height terms.
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The most common equations for biomass types include:
____________________________________________________________________________
Biomass Type Most Common Equation(s)*
____________________________________________________________________________
Whole Tree B = b
0
+ b
1
D
2
H
B = b
0
+ b
1
D
Woody Biomass B = b
0
+ b
1
D
2
H
Branch, Foliage, B = b
0
+ b
1
D
2
or Crown Weight B = b
0
+ b
1
D
____________________________________________________________________________
*B = predicted total or above-ground biomass, D = diameter (cm) at breast height (1.3 m), H = total
height (m), b
0
and b
1
= regression parameters estimated from the data.
Results should be represented as both regression equation and table to allow the widest possible
application of the work. When tables are unavailable and it is not practical to develop species-specific
biomass tables, the following general equations can be used:
Climate type based on
annual rainfall
Equation R
2
adjusted
Dry (<1500 mm) y = 34.4703 - 8.0671 D + 0.6589 D
2
.67
Moist (1500-4000 mm) y = 38.4908 - 11.7883 D + 1.1926 D
2
y = exp[-3.1141 + 0.9719 ln( D
2
H)]
y = exp[-2.4090 + 0.9522 ln( D
2
HS)]
H = exp[1.0710 + 0.5677 ln D)]
.78
.97
.99
.61
Wet (>4000 mm) y = 13.2579 - 4.8945 D
y = exp[-3.3012 + 0.9439 ln( D
2
H)]
H = exp[1.2017 + 0.5627 ln D]
.90
.90
.74
SOURCE: Brown, S., A.J.R. Gillespie and A.E. Lugo. 1989. Biomass estimation methods for tropical
forests with applications to forest inventory data. Forest Science 35:881-902.
where: exp [...] means " raised to the power of [...]"
y = above-ground biomass in kg
H = height in m
D = diameter at breast height (1.3 m)
S = wood density in units of tons/m3
NOTE: These equations are valid only for stems with dbh >5 cm.
The mean tree technique for biomass estimation
Allometry is an effective method for accurately estimating biomass of trees, tree components and
stands. However, the labor and expense of constructing and validating the necessary equations limit
the application of the allometric approach in biomass sampling. Many of the allometric equations
developed in the past were published in obscure journals, and furthermore have restricted applicability
outside the area of their development.
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The mean tree technique can be a cost-effective alternative to more time-consuming allometric
methods. The mean tree technique was developed by several investigators during the 1960s and 70s
(Baskerville 1963; Attiwill and Ovington 1968; Crow 1971; Madgwick 1970; Madgwick and Satoo
1975; Madgwick 1981; Satoo and Madgwick 1982). The concept behind the method is that an
average-sized tree will also have an average amount of biomass. The usual approach is to select a
tree or trees of mean basal area. Basal area tends to be a good predictor of total biomass, since
diameter, basal area, and sapwood area all have a similar functional relationship to the quantity of live
foliage and branches in the crown. The selected trees are then destructively sampled to determine
their biomass. Subsampling may be used in the case of large trees (see Satoo and Madgwick 1982 for
detailed applications of subsampling tree components). The mean tree weight is then multiplied by
the number of trees in the stand to obtain an estimate for the total stand biomass. This basic technique
can be modified by including stratified random sampling, the basal area ratio method, or by using
weighted average values (Madgwick and Satoo 1975; Satoo and Madgwick 1982).
Properly used, the mean tree technique has several significant advantages: it is fast, it can be accurate,
and it does not require elaborate computations. It is most appropriately applied in homogenous, even-
aged, and well-spaced stands. The accuracy of this technique declines in diverse stands with a wide
array of bole diameters and tree sizes. Most agroforestry plantings, with their systematically spaced
trees of near-uniform age and size, are well-suited to the mean tree technique. Biomass estimates
within 2-10% of the true value appear realistic based on literature.
The precision of stand biomass estimates obtained by the mean tree technique can be improved by
using the basal area ratio method, and by stratified random sampling. Stratified random sampling
should be considered if the range of stem sizes is large. In stratified designs, approximately five trees
over several diameter classes are sampled. The biomass of each diameter class is calculated
separately, and then the class estimates are combined to derive a biomass estimate for the stand. This
is a less intensive sampling effort than would be required for the development of allometric equations,
but more effort than is needed for stands in which a single mean tree is adequate. If substantially more
than five trees per size class need to sampled, the mean tree technique loses any advantage over
standard allometric approaches.
The main disadvantage of the mean tree technique is that there is no estimate of the error. This leads
to two problems. First, without replication, there is no way to detect a poor estimate. Secondly, there
is no statistical method to compare sequential samples. Another shortcoming is that almost all
applications of the mean tree technique have been on coniferous species, which tend to be more
uniform in shape than deciduous species. Finally, since tree size is related exponentially to diameter,
the mean tree technique tends to be biased towards an underestimation of the actual stand biomass.
This bias becomes more pronounced as the range of tree sizes in the stand increases.
The largest challenge in using the mean tree technique in the field is to select trees for biomass
determination that are truly of average size. This requires careful measurement of stand diameters and
simple (yet crucial) math computations that could be a source of error by inexperienced technicians.
Second, if subsampling or stand stratification are required, the math and technical problems increase,
and more highly-trained field crews are required. However, it should be noted that these problems
apply to any method biomass determination used on trees in the field. Biomass measurement is a
tedious process. If the trees of a stand have a uniform size and structure and reliable allometric
equations for biomass are not available, the mean tree technique may provide rapid estimates of the
biomass of the stand.
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References
Attiwill, P.M. and J.D. Ovington. 1968. Determination of forest biomass. Forest Science 14: 13-15.
Baskerville, G.L. 1965. Estimation of dry weight of tree components and total standing crop in
conifer stands. Ecology 46: 867-869.
Crow, T.R. 1971. Estimation of biomass in an even-aged: regression and mean tree techniques.
University of Minnesota Agricultural Experiment Station Science Journal Paper Series Paper no.
7487.
Crow, T.R. 1978. Common regressions to estimate tree biomass in tropical stands. Forest Science
24: 110-114.
Crow, T.R. and P.R. Laidly. 1980. Alternative models for estimating woody plant biomass.
Canadian Journal of Forest Resources 10: 367-370.
Madgwick, H.A.I. and T. Satoo. 1975. On estimating the aboveground weights of tree stands.
Ecology 56: 1446-1450.
Madgwick, H.A.I. 1981. Estimating the above-ground weight of forest plots using the basal area ratio
method. New Zealand Journal of Forest Science 11(3): 278-286.
Satoo, T. and H.A.I. Madgwick. 1982. Forest biomass. The Hague: Martinus Nijhoff / Dr. W. Junk,
Publishers.
Snell, J.A.K. and J.K. Brown. 1978. Comparison of tree biomass estimators: DBH and sapwood area.
Forest Science 24(4): 455-457.
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Biomass table data collection form
Cruiser ________________ Project ________________ Date ___/___/___
Country________________ Tree species:________________ Biomass or volume (circle one)
Volume
Volume
segment no.
Stump
Diameter (cm) or Metric Relaskop
(Circle one)
Length
(m)
Bark
thickness
(cm)
Tree
no.
or biomass
component
diameter
(cm)
DBH
(1.3 m)
D1 D2 D3 Weight (kg) Comments
Metric relaskop diameter measurements
Distance to tree (m) Wide strip value(cm) Narrow strip value (cm) Distance to tree (m) Wide strip value (cm) Narrow strip value (cm)
15 30 7.5 25 50 12.5
20 40 10 30 60 15
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D. Plot procedures
1. Navigate to plot center coordinates provided from database, map, map table or Form E.
2. Establish plot center by setting a plot center post (preferably PVC pipe painted with fluorescent
paint and marked with the plot number). Flag plot center area to increase visibility.
3. Set DGPS unit up near plot center and collect data for a minimum of 10 minutes (this assumes the
base station is already set and is collecting data simultaneously with the same receiver settings).
4. Set digital distance measurer on tripod over the plot center.
5. If the slope is greater than 10%, use a clinometer, Abney hand level or relaskop to determine slope.
Correct for slope using the following formula:
L
s
= L / cos S
where L
s
is the corrected plot radius, S is the slope angle in degrees, cos is the cosine decimal taken
from the back of the clinometer or from a table, and L is the plot radius.
Note plot dimension corrections on the plot card.
6. The crew chief begins by measuring the distance to the plot edge, flagging the beginning point and
directing a technician to begin taking dbh measurements. Each tree should be marked with bright,
durable paint at 1.3 m. The top edge of the painted mark should be at 1.3 m. Figure 4 shows the
proper placement of the dbh tape. The technician should read out the measurement, which the crew
chief should record and check visually.
7. When all of the trees in the plot have been measured, the crew chief must check to see that all of the
trees have been measured and painted.
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Figure 4 continued.
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Appendix 5: Field Procedures for Herbaceous
Vegetation, Soils and Standing Litter Crop
The carbon content of soil and litter can be measured and analyzed at relatively low cost if the data is
collected at the same time the inventory is conducted. This appendix describes sampling and analysis
of carbon in herbaceous vegetation, soil and standing litter crop.
In general, data should be collected in the following order:
1. Herbaceous vegetation
2. Standing litter
3. Soil
A. Procedure overview
1. Go to the northern edge of the plot and select a point 1 m inside the outside edge of the permanent
sample plot. This will be the first sampling location for herbaceous vegetation, litter and soils.
2. Lay the quadrat or circular sampling frame on the ground with the outer edge 1 m from the plot
boundary. Include in the sample only the vegetation that originates inside the sampling frame.
Exclude vegetation over-hanging inside the frame if the plant originates outside the frame, but include
vegetation over-hanging outside the frame if the plant originates inside the frame.
3. Clip herbaceous vegetation and small woody vegetation of less than 2 cm dbh, place in the sample
weighing bag, weigh, and record the weight. Select a small random sub-sample (e.g., a handful) of
this vegetation and place in a numbered sample bag for moisture content determination.
4. Before moving on, collect standing litter from the same sample site, place in the sample-weighing
bag, weigh, and record the weight. Mix the sample well and select a small random sub-sample (e.g., a
handful) of this litter and place in a numbered sample bag for moisture content determination.
5. Collect a soil core or slice for soil carbon analysis, place this on a plastic tarp, screen with 5-mm
mesh, mix well with other cores or slices, randomly select a sample, and place in a numbered sample
bag for carbon content analysis.
6. Proceed in a clockwise direction to the next sampling site within the sample plot. From the first
sampling location (i.e., North) this will be East, the next will be South and the last sampling location
will be West.
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B. How many samples to collect
An inventory effort should calculate the number of samples required for a specified level of precision
before plot measurements begin. However, if data can be analyzed during the inventory (i.e., using
data collected from the previous days collections), fewer samples may be needed. Use Form C to
describe the sampling design for soil organic carbon.
C. Herbaceous vegetation
In permanent sample plots, herbaceous understory vegetation can be sampled using four to six
quadrats or circular sample frames per plot. Figure 5 shows three types of sampling frames useful for
this type of sampling, although many alternatives exist. The main criterion is that the frames be
durable and retain their size and shape over long periods of use. All frames used in a project must be
of the same size. Frames with at least one hinge allow the user to wrap the frame around broad
canopied plants when necessary. Experience suggests that round aluminum frames with hinges on
two sides are more durable than welded square frames, and are also more easily transported.
In plotless quarter-point surveys, one quadrat should be collected at random in each quarter (see
Figure 3).
Cut all vegetation inside each quadrat/circular sampling frame at ground level. Take care to cut at the
same height for each sample. Clip herbs within the sampling frame in a vertical column extending
from inside the sampling frame, so that samples represent the biomass within the frames area. Weigh
biomass for each quadrat and take and weigh a sub-sample for moisture content, and possibly for
determining nutrient concentration.
D. Standing litter crop31
Changes in standing litter crop can be important, particularly when forest soils are converted to land
uses that oxidize organic matter (e.g., crops that require intensive cultivation). It is easy to measure
the standing litter crop, but it requires consistent adherence to pre-defined standards.
Measure the standing litter crop by collecting all litter on the soil surface in each of the sampling
frames used for measuring herbaceous vegetation. Samples can be bulked by plot. Make sure to
record the number of sample frames collected in each plot. Samples should be weighed and sub-
samples collected in the same way as for herbaceous vegetation.
31Standing litter crop is the total weight per unit area of litter on the soil surface at the time of sampling. Litter is
organic debris on the soil surface, and is usually freshly fallen or slightly decomposed vegetation. Measurement of
the standing litter crop does NOT require monitoring of litterfall.
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E. Soil sampling In general, soil samples should be taken when the permanent plots are
established and measured. Use either a soil corer of 30 cm in length or hand-dug pits of 30 cm in
depth. A soil corer may provide greater efficiency where soils are not excessively stony, although a
folding entrenching shovel (military type) is usually lighter and more versatile. Due to charcoals
high carbon content, it is important to take special care to remove bits of charcoal from samples at any
sites that have been burned prior to sampling.
Soil samples should be collected from the 0-30 cm horizon unless otherwise specified.32 To collect
soil samples, remove all vegetation and litter from the soil surface prior to sampling. Place the soil
core or slice on the plastic tarp and remove coarse fragments using a 5-mm screen. If multiple
subsamples are to be taken per plot, screen all samples on the plastic tarp and mix thoroughly to a
uniform color and consistency. Place a sample in a clearly labeled sample bag (preferably a cloth or
Tyvek oil sand bag). The quantity of soil required may depend upon the laboratory and analysis to be
used; discuss sample needs thoroughly with laboratory technicians beforehand, to ensure that samples
are properly prepared and labelled in the field.
To convert total or organic carbon concentrations into total quantities, bulk density of soils is required.
32 The greatest changes in soil organic carbon in non-humic tropical soils are often found between the 0-30 cm and
>30 cm horizons. For a summary of organic C contents in a wide range of tropical soils, see Table 5.2 in Properties
and management of soils in the tropics, by P. Sanchez (New York: John Wiley and Sons, 1976).
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Bulk density is considered to have relatively low spatial variability,33 with coefficients of variability
of less than 10%. For a uniform soil type, four samples should be sufficient to estimate mean bulk
density to within 10% of the true value 95% of the time. The following procedure can be used to
determine bulk density with a Modified Uhland soil corer:
1. Identify tin sample boxes and tops, weigh and record as W1 (g).
3. Prepare a smooth surface at a sampling depth of 5 cm.
4. Drive sampler into the soil to fill inner core without compression (use mineral oil if soil-metal
adhesion occurs).
5. Trim ends, remove core. If core does not completely fill the cylinder, use glass bead adjustment. If
it does fill the cylinder, push contents into sample tin, close tin, mark and record tin number.
6. Place samples in an oven set to 100
o
C for about 72 hours. After drying, record the weight of the
tin + dry soil as W2 (g).
7. Calculate bulk density as: BD (g cm
-3
) = (W2-W1)/344.77
Soil C content (t ha-1 for the 0-30 cm soil depth) = BD * 300 kg m-2 * C concentration (%) * 10
F. Deciding what type of soil carbon analysis to do
Soils can contain two types of carbon: organic and inorganic (carbonate). All agricultural soils
contain some organic carbon, but not all soils contain inorganic carbon. In most cases, soil organic
carbon will be the most important source of soil carbon, although this is not true in arid soils
(Aridisols) and several other soil types. Most changes in soil carbon due to project activities are
assumed to be in organic matter34, and not in inorganic carbonate.
Many laboratories routinely use the Walkley-Black procedure for determining soil organic carbon,
although it is known to have a number of important limitations. However, because it is commonly
used, rapid, and simple, this method is recommended for analysis of soil organic carbon where total
carbon analysis is not required. Table 5 compares methodologies for determining soil organic carbon,
including Walkley-Black.
If soils are known to contain substantial quantities of inorganic carbonate and the inorganic carbonate
fraction is likely to change (e.g., if an arid soil is irrigated), then total carbon methods are necessary.
Table 6 provides a summary of the relative quantities of organic and carbonate soil carbon in soils, by
suborder, using Soil Taxonomy. Table 7 summarizes methodologies used for determining total soil
carbon.
33 Warrick, A.W. and D.R. Neilson. 1980. Spatial variability of soil physical properties in the field. In D. Hillel,
ed., Applications of soil physics. New York: Academic Press.
34 The average C content of soil organic matter ranges from 48 to 58%.
69
Table 5 Comparison of methodologies for determining organic C in soils.
Method Principle Advantages Disadvantages
Difference between total
C and inorganic C
Total C and inorganic C are determined on
separate samples: Organic C = Total C -
inorganic C.
Useful if total C and inorganic C
are routinely determined
Two separate analyses are required.
Total C determination requires special
equipment. Organic C calculated by
difference has some inherent error.
Determined as total C
after removal of
inorganic C
Total C is determined in soil sample after
removal of inorganic C with an acid
pretreatment:
Organic C = Total C
Accurate if dolomite is absent
from soil
Not all dolomite in soil may be removed
by acid treatment. Specialized equipment
needed.
Dichromate oxidation
without external heat
Dichromate oxidizes organic C to CO
2
in acid
medium. Amounts of Cr
2
O
7
2-
reduced is
quantitatively related to organic C present.
Not all organic C in samples is oxidized when
external heat is omitted, and a correction
factor is required.
Very rapid and simple. No
special equipment required
Incomplete oxidation of organic C
necessitates use of correction factors,
which often results in erroneous values.
Chloride, Fe
2+
and MnO
4
interfere with
method. It assumes soil organic C has an
average valence of 0.
Dichromate oxidation
with external heat
This is the same as the dichromate method
above except that all organic C in the sample
is oxidized, and no correction factor is
required.
Rapid and simple. Complete
oxidation of organic C occurs
Chloride, Fe
2+
, and MnO
2
interfere with
method. Some specialized equipment is
needed. It assumes soil organic C has an
average valence of 0>
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Table 6. Organic and carbonate carbon mass in soils of the world35
Organic Carbon Carbonate Carbon Total Carbon
Suborder/Order
---------------- Gigatons of carbon (Petagrams or 1 x 10
15
g) ----------------
Folists 1 0 1
Fibrists 250 0 250
Hemists 68 0 68
Saprists 71 0 71
Histosols 390 0 390
Aquands 1 0 1
Cyrands 18 0 18
Torrands 1 1 2
Xerands 2 0 2
Vitrands 1 0 1
Ustands 13 0 13
Udands 33 0 33
Andisols 69 1 70
Aquods 4 0 4
Ferrods 0 0 0
Humods 41 0 41
Orthods 53 0 53
Spodosols 98 0 98
Aquox 1 0 1
Torrox 0 0 0
Ustox 41 0 41
Perox 16 0 16
Udox 92 0 92
Oxisols 150 0 150
Aquerts 1 1 1
Xerets 5 1 6
Torrets 12 14 26
Uderts 5 0 5
Usterts 15 9 24
35 Source: Eswaran, H., E. Van den Berg, P. Reich and J. Kimble.1995. Global soil carbon resources in R. Lal, J.
Kimble, E. Levine and B.A. Stewart (Eds.). Soils and Global Change, CRC Lewis Publishers, Boca Raton, FL.
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Table 6 continued.
Suborder/Order Organic Carbon Carbonate Carbon Total Carbon
Vertisols
Salids 5 113 118
Gypsids 3 12 15
Calcids 17 407 424
Durids 0 1 1
Argids 38 112 150
Cambids 47 399 446
Aridisols 110 1044 1154
Aquults 5 0 5
Humults 4 0 4
Udults 50 0 50
Ustults 40 0 40
Xerults 2 0 2
Ultisols 101 0 101
Albolls 2 0 2
Aquolls 1 1 2
Rendolls 0 1 1
Xerolls 13 23 36
Borolls 15 29 54
Ustolls 17 32 49
Udolls 24 53 49
Mollisols 72 139 139
Aqualfs 6 0 6
Boralfs 35 0 35
Ustalfs 45 71 116
Xeralfs 14 0 14
Udalfs 36 56 92
Alfisols 136 127 236
Aquepts 67 12 79
Plaggepts 0 0 0
Tropepts 20 26 46
Ochrepts 135 247 382
Umbrepts 45 0 45
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Table 6 continued.
Suborder/Order Organic Carbon Carbonate Carbon Total Carbon
Inceptisols 267 285 552
Aquents 20 0 20
Arents 0 0 0
Psamments 21 30 51
Fluvents 3 6 9
Orthents 62 81 143
Entisols 106 117 223
Rocky land 13 0 13
Shifting sand 5 0 5
Misc land 18 0 18
TOTAL 1555 1738 3293
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Table 7. Comparison of methods used for determining total C in soils.
Method Principles CO
2
Determination
Advantages Disadvantages
Dry
combustion
(resistance
furnace)
Sample is mixed with CuO and
heated to 1000 C in a stream of O
2
to
convert all C in sample to CO
2
.
Gravimetric
Titrimetric
Reference method widely used
in other disciplines Variable
sample size
Time-consuming; leakfree O2
sweep train is required. Slow
release of CO
2
from alkaline
earth carbonates
Dry
combustion
(induction
furnace)
Sample is mixed with Fe or
accelerators and rapidly heated to
>1,650 C in a stream of O
2
to convert
all C in sample to CO
2
Gravimetric Rapid combustion
High temperature ensures
conversion of C to CO
2
Leakfree O
2
sweep train
required, induction furnace is
expensive
Dry
combustion
(automated
methods)
Sample is mixed with catalysts or
accelerators and heated with
resistance or induction furnaces in a
stream of O
2
to convert all C in
sample to CO
2
Gas
chromatography
Gravimetric
Conductrimetric
Rapid and simple, good
precision
Expensive equipment. Slow
release of CO
2
from alkaline
earth carbonates with
resistance furnace
Wet
combustion
(combustion
train)
Sample is heated with K
2
Cr
2
O
7
-
H
2
SO
4
-H
3
PO
4
mixture in a CO
2
-free
air stream to convert all C in sample
to CO
2
Gravimetric,
Titrimetric
Equipment readily available,
good accuracy, easily adapted
to analysis of solutions,
titrimetric analysis of CO
2
less
subject to operator error
Time-consuming; gravimetric
determination of CO
2
requires
careful analytical techniques,
titrimetric determination of
CO
2
is less precise
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G. Sample preparation
This section describes procedures for preparing samples of soil, litter and vegetation for analysis after
they have been collected in the field.
Soils
Soils should be air-dried, but not exposed to direct sunlight. Check with the laboratory for detailed
arrangements.
Litter and vegetation
After weighing the samples, take sub-samples of litter and vegetation to determine moisture content
and nutrient concentration. The following guidelines are suggested:
Moisture content: Mix the sample and collect one random sub-sample of approximately one handful
of litter of vegetation per quadrat/circular sample plot. Bulk these subsamples by permanent plot or
transect when using the plotless method. For moisture content, collect at least five sub-samples for
each vegetation type. Sub-samples should be weighed in the field then returned to the laboratory for
oven-drying at 70-80
o
C to a constant weight and reweighed to determine dry-matter.
Nutrient concentration: This is necessary only if the decision is made to use actual C concentration
data for vegetation, or if actual data are to be used to predict carbon pool changes using a computer
model. A minimum of five samples for each partition is suggested for C (for carbon calculations
only) or C and N analysis (for modelling purposes). This means five core samples of wood (collected
at dbh), five foliage and litter samples.
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Appendix 6: Measuring Carbon in Agroforestry
These methods are designed for use in agroforestry and farm forestry plantings as described in Section
3. They have been only preliinarily field tested, and should be used or cited with caution (see Field
Tests of Methods for Monitoring Carbon in Forestry Projects).
Map the project area.
1) Using current aerial photos, determine the number, size, and location of agroforestry plantings in
the project area. If aerial photos are not available, obtain a list of farmers who have associated
agroforestry plantings in association with the project and plot the locations of their farms to the
extent possible on a topographical map.
2) Use a soils map to stratify the plantings into groups if soil types vary significantly within the
project area. If a soils map is not available for the area, consider stratification if there are major
differences in topography, drainage, or parent material which affect the suitability of soil for crops
or trees. Avoid establishing more than three strata, if possible.
3) Assign a number to each planting within the project area.
Select a preliminary sample of plantings for the determination of required sample size.
1) Using the assigned numbers, randomly select three farms from each stratum. Measure
accumulated above- and below ground-biomass in the agroforestry plantings using the methods
outlined below. Calculate the variance in the data, and use this value to estimate the number of
farms in each stratum that must be sampled to estimate carbon accumulation at the desired level of
precision (see Appendix 2).
2) If aerial photos are not available for the region and a preliminary estimate of average
agroforestry plantation size was not calculated, then at least six farms must be selected per stratum.
The size of agroforestry plantings will be measured on each of these six farms, while three will be
selected at random for the measurement of accumulated biomass. As with biomass, the variance in
planting size will be calculated to determine the number of farms that must be sampled to estimate
the average area of agroforestry plantings at the desired level of accuracy.
Select a sample of plantings for the determination of accumulated biomass.
1) Using the numbers assigned to each farm and the desired sample size calculated in the preceding
step, randomly select a sample of farms from each stratum. Make the sample list large enough so
that it includes several alternates.
2) The sampling scheme must be nested if aerial photos were not used to provide a preliminary
estimate of farm size. First, establish a random list of farms in each stratum that will be sampled
for agroforestry planting size. Next, from this list randomly select a sub-sample. Agroforestry
plantations on these farms will be sampled for both size and accumulated biomass.
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3) Circle the location of the farms to be sampled on an aerial photo or topographic map. Use this
map to efficiently organize the sampling effort. Include the names of each farmer on both the map
and list of sample farms, if available.
Farmer contact
1) Before initiating field measurements, first make contact with local community leaders and
officials. Be prepared to present identification, official letters, or other forms of authorization.
2) Contact a farmer on the sample list. Formally introduce the carbon inventory crew: the names of
each crew member, where they come from, their professional titles, and the names of their
respective organizations.
3) Describe clearly the purpose of the carbon inventory. Do not avoid explaining why carbon
sequestration is important, if asked. Describe the types of measurements that will be conducted.
4) Ask permission to inventory the accumulated biomass of the farmers agroforestry planting. If
permission is not granted, thank the family for their time, and move on to the next farm. Replace
the sample from the list of alternates.
Conduct farmer interview (see interview form, this Appendix).
Plot reference point location
1) Prepare a sketch map of the farms agroforestry plantings on the reference point location form.
2) Walk around the perimeter of the agroforestry planting to determine the location of each corner
of the planting with the GPS unit. Record these values on the sketch map.
3) Estimate the approximate length and width of the agroforestry planting. Record the values on
the reference point location form.
4) Divide the estimated length and width of the agroforestry planting by two. Record the values on
the reference point location form.
5) Locate the southeast corner of the agroforestry planting. Label the location of the southeast
corner on the sketch map.
6) Starting at the southeast corner and proceeding along the long side of the agroforestry plantation,
measure out a line exactly equal to one half the value of the previously estimated length of the
plantation (Figure 6). Use a 100 meter tape to measure this distance precisely. Record the exact
distance and bearing of the line on the reference point location form. The endpoint of this line shall
be referred to as the turn point.
7) Paint a blue ring at DBH on a tree located along the perimeter of the plantation proximal to the
turn point.
8) At the turn point, turn exactly 90 relative to the direction of travel and towards the interior of the
planting. Proceed a distance exactly equal to one half of the previously estimated width of the
agroforestry planting. Use the 100 meter tape to measure out this distance precisely. The endpoint
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of the line shall be referred to as the plot reference point. Record the exact distance and bearing of
the line on the reference point location form.
9) Mark the plot reference point with a 40cm section of rebar. The bar shall be driven 30cm into
the soil, and the last ten cm of the rebar above the soil surface shall be painted blue.
10) Measure the exact distance and bearing to the plot reference point from two reference trees.
Record these values on the reference point location form. The difference between the bearings
from the two reference trees should be approximately 90 . Paint a blue ring around each reference
tree at DBH, and record the species and DBH of each reference tree on the reference point location
form.
11) Determine the coordinates of the plot reference point with the GPS. Record the coordinates on
the reference point location form.
12) Once a plot size has been selected, employ the same plot size on all plots throughout the
duration of the biomass inventory, regardless of the tree spacing encountered on a particular
agroforestry planting.
Plot location
1) Refer to Figure 7. If the inventory plot size is 1/20th ha or greater, the following distances and
bearings shall be used to locate four plots in relation to the plot reference point (RP):
plot 1 is located 60.0 m from the RP at a bearing of 45 NE
plot 2 is located 20.0 m from the RP at a bearing of 135 SE
plot 3 is located 60.0 m from the RP at a bearing of 225 SW
plot 4 is located 20.0 m from the RP at a bearing of 315 NW
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2) If the inventory plot size is 1/40th ha or less, use the following distances and bearings to locate
four plots in relation to the plot reference point (RP):
plot 1 is located 45.0 m from the RP at a bearing of 45 NE
plot 2 is located 15.0 m from the RP at a bearing of 135 SE
plot 3 is located 45.0 m from the RP at a bearing of 225 SW
plot 4 is located 15.0 m from the RP at a bearing of 315 NW
3) If either the plot center or more than 25% of the plot area is located outside the perimeter of the
agroforestry planting, do not establish a plot at that point. Instead, attempt to install a plot at an
alternate location. The first alternate is plot 5, falls outside of the agroforestry planting, then the
next alternate is plot 6, then plot 7, and finally plot 8.
4) Install the plot rope stake firmly at the center of the plot.
5) Mark the plot center with a wire flag labeled with the plot number.
Conduct an inventory of woody stems >5.0 cm DBH
1) Starting at north and moving clockwise, record the total height, DBH, and species of all woody
stems > 5.0 cm DBH that fall within the plot. Record that data on the large stem biomass form.
2) For borderline trees, if more than half the stem falls within the plot, the tree is in; if more than
half the stem falls outside the plot, the tree is out. If the plot boundary coincides exactly with the
center point of the tree, flip a coin. If heads, the tree is in; if tails, the tree is out.
3) The corrected slope distance should be calculated for borderline trees or for trees just outside the
plot if the slope is greater than ~20%. To do this, determine the slope angle from the plot center to
the tree in question with a clinometer. Next, multiply the cosine of the angle (provided by the table
printed on the side of the clinometer) by the apparent distance. The resulting value is the true
horizontal distance. Use this value to determine if the tree is in or out of the plot.
Conduct inventory of herbs, litter, soil and woody stems < 5.0 cm DBH (See Appendix 5)
Limitations
The methods outlined here should be adequate for a wide array of agroforestry system configurations,
but they are not appropriate for all types of plantings that may be encountered. These methods are
intended for agroforestry systems which: are predominantly square, rectangular, or round in shape; at
least 0.25 hectares in size; and have trees as the predominant cover type. Narrow strips of trees, such
as windbreaks, would require a different inventory method; so would silvopastural systems in which
the trees are widely scattered over a dominant matrix of grass. However, for most situations in which
an objective of the agroforestry project is to sequester carbon, this inventory scheme should prove
adequate.
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Woody stem inventory form
mo / day / year
Crew:____________________________________________ date:___/_____/____
Farm number:_______________ Stratum number:________________________________
Plot number: _______________ Plot radius: _________________
Woody stems >5.0 cm DBH
tree
number
species
code
height DBH tree
number
species
code
height DBH
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Farmer interview
Crew:____________________________________________ date:___/___/___
Farmers name: ________________________________________________________________
Farm number:_______________ Stratum number:________________________________
Farm location:_________________________________________________________________
Approximate date when agroforestry planting was established:__________________________
Land use of the plot before the planting was established:
_ fallow___ years _ pasture___ years _ crop___ years _ forest
Approximate size of agroforestry planting:___________________________________________
Reasons for establishing the agroforestry planting:_____________________________________
_____________________________________________________________________________
Tree component of the agroforestry planting:
species spacing number
planted
growth rate problems products/ yield
Crop component of the agroforestry planting:
species spacing planting date harvest date problems products/ yield
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Reference point location form
mo / day / year
Crew:____________________________________________ date:___/_____/____
Farm number:_______________ Stratum number:_________________________________
Agroforestry plantation sketch map
est. length of agroforestry plantation = ______ 2 = ______ bearing to turn pt. = _______
est. width of agroforestry plantation = ______ 2 = ______ bearing to reference pt. = _______
species DBH distance to
reference pt.
bearing to
reference pt.
1st reference tree
2nd reference tree
GPS coordinates of the plot reference point = ________________
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Appendix 7: Estimating Root Biomass36
Estimating root biomass is expensive. Yet, root biomass is an important carbon pool because
it often represents 10 to 40% of total biomass. Two general approaches for claiming carbon
credit for root biomass are possible: 1) use conservative, non-controversial estimates of root
biomass based on literature values for similar vegetation types, and; 2) measure root biomass.
The only advantage to measuring biomass for carbon credit is that in most cases, actual root
biomass will likely be substantially greater than the conservative estimates. The decision of
whether or not to measure should be based on the price of carbon compared to the cost of
collecting the additional data required to claim credit.
A. Estimating root biomass using the literature
The data available on root biomass are limited due to the high costs of sampling and
measuring roots. However, the literature does contain root biomass values for a wide range of
vegetation types. Unfortunately, the methods used vary greatly and the very limited
information on vegetation type by site class does not allow high confidence in using actual
literature values in most cases. For example, limited root biomass data from tropical forests
suggest that the root:shoot ratio varies from 0.03 to 0.49, with below-ground biomass ranging
from 11 to over 130 t/ha. The fact that some root biomass exists below living above-ground
biomass is undisputable, but the question is, How much? How conservative should estimates
using literature values be? In a literature-based approach, the key is to use estimates that are
conservative enough so that they are not easily refuted. In the example of the root:shoot ratio
in tropical forests, a value of 0.10 or 0.15 would generally suit this purpose.
The level of conservatism required to pass minimum criteria for carbon credit is still
undefined. A reasonable approach might be to use the lowest above-ground:below-ground
biomass ratios to estimate below-ground biomass, based on actual inventory data of above-
ground biomass.
B. Measuring root biomass
If such data are not available, root biomass can be estimated by sampling and measurement
using the methods described in the following paragraphs. In measuring root biomass, note the
following points:
Samples should be taken from representative volumes of soil usually 0-30 cm soil depth
unless otherwise specified.
36 Portions of this appendix come from Appendix D: Roots: Length, biomass, production and mortality, by
M. Van Noordwijk, in Tropical soil biology and fertility: A handbook of methods, eds. J.M. Anderson and
J.S. Ingram (London: CAB International, 1992) and Methods of studying root systems, by W. Bohm
(Berlin: Springer-Verlag, 1979).
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Samples should be taken during the time when expected standing root biomass is highest
(e.g., avoid the late part of the growing season).
The methods for sampling, storing, and washing samples will always lead to some loss of
dry weight and nutrients. A correction factor of 1.25 - 2.0 should be applied to the final
data, with the correction factor based on the estimated losses due to sampling and
processing.
Two types of sampling may be required: 1) core sampling to determine root biomass in the 0-
30-cm soil depth; 2) monolith sampling to determine relative root distribution beyond 30 cm
soil depth. Decisions about the types of sampling required must be site specific and include
consideration of precision needs, the availability of data on root distributions for the species
being inventoried, soil depth, texture and stoniness.
Core sampling
A soil corer removes a known volume of soil from a known depth in the profile, without the
need for digging a soil pit. A core of 50 - 80 mm diameter is satisfactory, and the corer can be
inserted either manually or mechanically. Manual coring is difficult at depths greater than 50
cm and in clay or stony soil. In dry sandy soil a smaller core diameter may be needed to
reduce losses of soil when extracting the core. In very stony soil, or where there are many
woody tree roots, coring may not be possible. In these cases, regular, known volumes of soil
(monoliths) can be taken from the face of a pit and treated in the same way as cores.
A commercially available split-core corer, such as the AMS split core sampler kit with core
tip, is recommended.
Ideally the profile should be sampled to the limits of rooting depth. At that depth, however,
rooting intensity is low and spatial variability high. A meaningful lower limit can be set based
on initial observations of the profile wall. In some cases a linear relationship of the log of root
mass versus depth (a negative exponential root distribution) may help to extrapolate root
densities in the soil beyond sampling depth. All soils must be sampled to a minimum depth of
30 cm.
Root extraction
The best approach to root extraction is to wash roots from the cores immediately upon return
from the field. Core samples can be stored in sealed polyethylene bags in a refrigerator for a
few days or deep freeze until processed. If deep freeze facilities are not available, samples can
be stored air-dried and re-wetted before washing. Losses of dry weight due to the methods
used for storage should be checked.
Soil texture, structure, degree of compaction and organic matter content greatly influence the
precision and time required to extract roots from cores. The simplest method involves gently
washing a presoaked sample over a large diameter sieve of 0.3 - 0.5 mm mesh. The work can
be simplified by washing over a combination of sieves: one with 1.1 and one with 0.3 mm
mesh. The first sieve will contain mostly roots, the second mostly debris. The material
removed from the sieve(s) can then be mixed in water and the suspended material decanted
(live roots of most species have a specific gravity of about 1.0). This residue should then be
hand sorted in shallow dishes under water to remove fragments of organic matter and dead
roots; normally it is better to pick live roots from the sample and leave debris behind in the
dish.
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Presoaking samples overnight in 5% sodium hexametaphosphate expedites the process of
washing roots from clay soils, but the chemical discolors the roots (particularly in soils with
high organic matter content) and may disrupt the tissue, making subsequent identification of
live roots more difficult. Such pretreatment will also interfere with chemical analyses. Any
lengthy washing procedure may alter the element content of root tissue; only a subsample
hand sorted with a minimum of water and processed on the day of sampling should be used
for analysis.
Classifying the roots
Fine roots are the most important part of the root system for water and nutrient uptake, as they
form the largest part of total root length or root surface area. For woody perennial vegetation
there is a fairly obvious distinction between the more or less permanent, secondarily thickened
roots and the ephemeral, unthickened roots. This functional distinction usually falls
somewhere between 1 and 3 mm root diameter. Roots above 10 mm diameter are not
adequately sampled by coring. For herbaceous perennial and short-lived vegetation, roots
should be separated into <2 mm and > 2 mm classes. In mixed vegetation, separation of roots
of different species is difficult and is not necessary.
Sampling intensity
Even in the most homogeneous soils, spatial variability of root density will be high, with
coefficients of variation in root weight commonly in excess of 40%. On heterogeneous soils
the C.V. may be much higher. This variability implies that many replicate samples are needed
if estimates of root weight need to be precise.
It is advisable to obtain reliable information at one or two well chosen situations, rather than
non-reliable data on many. Within each treatment plot take at least 3 cores. Within each plot
the samples can be pooled. In natural vegetation where there is no obvious strategy for sample
stratification, take the cores on random coordinates. Where patterns are likely to occur (e.g,.
row crops, alley cropping) stratification should use within row vs. between-row strata.
Monolith sampling
Monolith samples can be obtained with pinboards made by inserting U-shaped, stainless steel
pins or bolts in plywood. The size of the pinboard is determined by the vegetation type, based
on previous observations, such as rooting depth and distribution and practical considerations.
Soil collected with a pinboard is heavy (a sample of 100 x 60 x 10 cm of soil will weigh about
100 kg), so pinboard size should be matched to the means of supporting and moving a full
pinboard. Washing away the soil exposes the roots for observation. If a coarse mesh screen is
put on the pins before the board is pushed into the soil, this screen can help to keep the roots in
their original location while washing the sample. Washing the sample can be facilitated by
soaking overnight in water, deep freezing (for clay soils), soaking in oxalic acid (for soils with
free calcium carbonate) or soaking in hexametaphosphate, preferably under vacuum.
Whatever the pretreatment used, gentle washing must follow.
After washing away the soil: lift the root system on the mesh screen; photograph it (on a black
cloth as background); and/or cut it according to soil layers (indicated by string between the
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pins while washing the sample), depth zones and/or distance to the plant, in order to obtain
root biomass and/or root length (see below for root length). To estimate total biomass per
plant, root weight density per zone and depth has to be integrated over the relevant volume.
Although the pinboard method is more time-consuming than other methods, it gives more
information per unit of effort spent. The methods major weakness is that roots may break or
be displaced during washing. It is easier to distinguish between live and dead roots via
pinboard sampling than in methods where the root system is not sampled in its entirety.
Assessment of root mass
Washed root samples can be stored in sealed polyethylene bags for a short time in a
refrigerator, but deep-freeze storage is preferable. Oven-dry the roots and weigh. Next the
dried samples should be combusted for 5 hr. in a muffle furnace in 550
C and the residue
weighed. Results should be expressed as ash-free oven-dry mass per unit volume of soil.