Course name: Microcomputers;
Mini-projects, experimental design, biometrics
Course period and place: July 28 to
List of protocols for Mini-projects
Measuring
fertility of soils by the bio-test method
Effect
of method of offering tree foliages to goats on intake and eating/ruminating
time
Effect
of method of offering tree foliages to goats on digestibility and N retention
Manure
or biodigester effluent as fertilizer for duckweed
Manure
or Biodigester effluent as fertilizer for Water Spinach
Effect
of the urea level on biomass production of
water spinach (WS) grown on soil or in water
Increasing
the germination capacity of tree cuttings
Scavenging
characteristic of local and exotic chickens.
Teaching
exotic chickens to scavenge
Evaluating
vegetative protein source for monogastric animals
Water
spinach and broken rice as low cost feed resources for growing rabbits
Effects
of different substrates and levels of seeding on reproductive rate of
earthworms
Effect
of age of leaves from forage trees on nutritive value
Mini-project 1
The fertility of soils is important in agriculture particularly in making decisions on planting of crops. The plants will grow well and be more productive when planting in fertile and suitable soils. The different kinds of soils and different locations is likely to influence fertility also. Therefore measuring fertility of soils is necessary to know which will give information concerning fertility of soils or suitable plants for cultivating. There are many ways to measure fertility of soils. Planting some indicator plants in that soil and measuring growth and production is one way to do this in a simple and low cost procedure. It is believed that growth of maize will be the best indicator of N status while the development of tillers by the rice plant will indicate P status.
Plants such as maize and rice will be good indicators of the fertility of soil
Samples of soil will be taken from different locations and ranked according to the growth rate of maize and rice plants.
There are two sets of treatments (types of soil and indicator plants), arranged as a 8*2 factorial with 3 replications in a Complete Randomized block design Design ( CRBD) (Table 1).
Type of soil
There are 8 types of soil;
Nc = sand (negative control)
Cl = Clay (0-20 cm. Depth)
Lo = Loam (0-20 cm. Depth)
Rs = Rock soil (0-20 cm. Depth)
Sl =
Sm = Sub soil under Loam (more than 20 cm. Depth)
Ss = Sub soil under sandy loam (more than 20 cm. Depth)
Pc = More fertility soil with (possitive control)
R = Rice
M = Maize
|
Table 1: Arrangement of treatments |
||||||||
|
Blocks |
1 |
2 |
3 |
4 |
5 |
6 |
7 |
8 |
|
Rice |
NcR1 |
ClR1 |
LoR1 |
RsR1 |
SlR1 |
SmR1 |
SsR1 |
PcR1 |
|
NcR2 |
ClR2 |
LoR2 |
RsR2 |
SlR2 |
SmR2 |
SsR2 |
PcR2 |
|
|
NcR3 |
ClR3 |
LoR3 |
RsR3 |
SlR3 |
SmR3 |
SsR3 |
PcR3 |
|
|
Maize |
NcM1 |
ClM1 |
LoM1 |
RsM1 |
SlM1 |
SmM1 |
SsM1 |
PcM1 |
|
NcM2 |
ClM2 |
LoM2 |
RsM2 |
SlM2 |
SmM2 |
SsM2 |
PcM2 |
|
|
NcM3 |
ClM3 |
LoM3 |
RsM3 |
SlM3 |
SmM3 |
SsM3 |
PcM3 |
|
The following are required:
48 plastic bags
72 maize seeds
72 rice seeds
1 hoe
1 water bucket
1 ruler to measure height
1 weigh scale (200 g)
8 different kinds of soil
The soils will be taken at 0-10cm depth from different places around the An Giang University and put into plastic bags (2 litre capacity). 3 seeds or maize or rice will be put in each bag according to the experimental layout in Table 1. A hole is put in the bottomof eacg bag so the excess water can drain away. Water is applied uniformly to all bags each morning and observations made of germination and growth of the plants. When the seeds have germinated 1 or two plants will be removed to leave only one seedling in each bag.
The height of the plants will be measured every 5 days
After 28 days, the plants and roots will be removed, washed free of soil, and weighed 30 minutes later, the green parts and the roots separately.
The linear regression of height on days will be calculated to determine growth rate in height. The ANOVA GLM option of the Minitab software will be used to analyse the data. The sources of variation will be: soils, blocks and error. When the F-test is significant at P<0.05, the Tukey test in the Minitab software will b used to separate mean values that differ at P<0.05
***********************
Mini-project 2
Goats have been raised many years by farmers. They traditionally hang the foliages from the sides of the pen, or on some raised structure (Kouch et al 2003a). It has recently been shown that this method results in higher intake and digestibility compared with putting the foliage in a feed trough (Kouch et al 2003b). It is proposed to test this idea with some foliages commonly available in villages in the An Giang area.
Goats will eat more dry matter when the foliage of a tree is hanging in the pen compared with putting it in the feed trough.
To improve the feed intake of animals and also to compare both methods, putting the foliage in the feed trough and hanging in the pen.
Four growing 6-8 kg live weight local weaned goats are
confined in cages made frorm bamboo fitted with plastic sheet to collect the faeces
and urine separately. Foliages from Kra Kop trees (Cambodian name) (Trung Ca in
A changeover will be applied to 4 local weaned goats with 3 treatments and 4 replicates.
The treatments are two kinds foliage and two ways of offering them to the goats:
Source of foliage:
Method of feeding:
The design is a changeover 2*3 factorial arrangement of the 6 treatments (Table 1) which are:
CH: Cassava foliage hanging
CT: Cassava foliage in the feed trough
CL: Cassava leaves in the feed trough
MH: Muntingia foliage hanging
MT: Muntingia foliage in the feed trough
ML: Muntingia leaves in the feed trough
|
Table 1: Layout of the treatments |
||||
|
|
Goat number |
|||
|
Period (days) |
1 |
2 |
3 |
4 |
|
0-8 |
CL |
CT |
ML |
MT |
|
9-16 |
CH |
CL |
MH |
ML |
|
17-24 |
CT |
CH |
MT |
M H |
Muntingia will be collected within the An Giang University and Cassava will be bought from farmers. Feeds will be offered 2 times in the morning and in the afternoon and will be ad libitum (about 20% more than observed intake).
Weight of feed offered and refused will be recorded and samples analysed for DM and N. Samples of the feed components will be analysed for water extractable DM and N. Time spent eating and ruminating during 24 hour period will be monitored on the last day of each period.
Statistical analysis
The data will be analyzed with the GLM option of the ANOVA software of Minitab Version 13.31. Sources of variation are animals, feeding system, foliages and interaction feeding system*foliages and error
Mini -project 3
An
The major cause of low
productivity of livestock, especially in the tropical regions, is the
inadequate and poor quality of feeds. The main feed resources for animal are
permanent pastures, crop residues and other agroindustrial by-products. Goat
production in
Hypothesis
That the digestibility of the foliage from Muntingia calabura by goats will be higher when it is suspended in the pen compared with offering it in the feed trough.
Objectives
4 goats will be used to study the effect on digestibility and N retention when offered the foliage of Muntingia calabura by hanging it in the pen compared with putting it in the feed trough.
Materials and Methods:
Treatments and design:
There are two factors:
Source of foliage:
Method of feeding:
The design is a changeover 2*3 factorial arrangement of the 6 treatments (Table 1) which are:
MH: Cassava foliage hanging
MT: Cassava foliage in the feed trough
ML: Cassava leaves in the feed trough
CH: Muntingia foliage hanging
CT: Muntingia foliage in the feed trough
CL: Muntingia leaves in the feed trough
|
Table 1: Layout of the treatments |
||||
|
|
Goat number |
|||
|
Period (days) |
1 |
2 |
3 |
4 |
|
0-8 |
CL |
CB |
ML |
MB |
|
9-16 |
CH |
CL |
MH |
ML |
|
17-24 |
CB |
CH |
MB |
M H |
Feeding system
Foliage of muntingia is collected as whole branches. Cassava is purchased from farmers as leaves plus petiole (so as not to affect the production of roots). For MH and CH, the branches of muntingia and the leaves plus petioles of the cassava are hung from a bamboo stick above the pen. For MT and CT these feeds are placed in the feed trough. For ML and CL the leaves are separated and put in the feed trough. In all cases feeding is ad libitum at an estimated level of about 20% above actual intake. Days 1 to 4 of each period are for adaptation to the new treatment; on days 5 to 8 faeces and urine are collected; on day 9, samples of rumen fluid are taken by stomach tube 2 hours after offering the feed in the morning. The time table of activities is in Table 2.
|
Table 2: Time table of activities |
|||||||||
|
Days |
1-4 |
5-8 |
9 |
10-13 |
14-17 |
18 |
19-22 |
23-26 |
27 |
|
Adaptation |
**** |
|
|
**** |
|
|
**** |
|
|
|
Collect faces & urine |
|
**** |
|
|
**** |
|
|
**** |
|
|
Collect rumen fluid |
|
|
* |
|
|
* |
|
|
* |
Faeces are collected twice daily and stored at -20 ºC until analysed. Urine is collected in a bucket with 50 ml of 25% sulphuric acid to maintain the pH below 4 so as to prevent escape of ammonia.
Measurements:
The foliage of Muntingia is separated into stem, petiole and leaf; the foliage of cassava is separated into petiole and leaf. In each case the proportions are recorded and analysed for DM and N and water soluble DM. Weights of feeds offered and refused are recorded. During the collection period samples of feed offered and the refusals, and faeces, are collected and stored at -20ºC until the end of the collection period when samples are bulked and analysed for DM and N. Urine is collected daily stored in a bucket and at the end of the collection period is weighed and analysed for N. Rumen fluid is analysed for pH immediately after collection, 5 ml is acidified with sulphuric acid and 5 ml fixed with formal saline for later counting of the protozoa (this sample should not be frozen but kept at room temperature).
The goats are weighed at the beginning of each adaptation period in the morning before offering feed.
DM is determined by micro-wave radiation (Undersander et al
19??) and N by the kjeldahl method (AOAC 1990). Rumen ph is measured with a
digital electronic meter and ammonia by distillation (AOAC 1990). Samples for
protozoa are counted according to the method described by Nguyen Thi
References
Mini-project 4
Cassava (Manihot
esculenta Crantz) is an annual root crop grown widely in tropical and
sub-tropical regions. In
The
hypothesis
Objectives
Materials
and methods
Treatments and design
The two treatments will be :
The experimental design will be a single changeover arrangement (Table 1) with 4 replicates (pigs).
|
Tab le 1: Layout of the
experiment |
||||
Pig No
Period\
|
1 |
2 |
3 |
4 |
|
1 |
CH |
CHW |
CH |
CHW |
|
2 |
CHW |
CH |
CHW |
CH |
Animals and housing
Four local pigs (Bauxin breed) with weight
about 10 kg and age of 3 months will be used.
The pigs will be housed in bamboo metabolism cages that
allow the separate collection of urine and faeces. The size of the metabolism cage
is 1m x1.5m
The experimental period will be 10 days: five days for adaptation
period to allow the pigs to become familiarized with the new diet and a five
days period for collection of faeces and urine.
Feed and feeding system
Cassava root meal will be fed at
the rate of 2% (DM basis) of live weight. The cassava leaves will be offered on
free choice basis.
Measurements
Urine and faeces of each pig will
be collected separately and weighed twice daily and stored at –20 0C. Urine
will be collect in a bucket via a plastic
sheet and funnel placed below the cage .
To prevent nitrogen losses by
evaporation of ammonia, the pH will be kept below pH 4 by collecting the
urine in 50ml of 25% sulphuric acid.
The urine and faeces from each
animal will be collected for five days and at the end of the period, the faeces
will be mixed, ground and representative sample taken for analysis.
Dry matter of feed offered and refused and DM in faeces will be done by micro-wave radiatikon (Undersander et al 19??). Nitrogen in faeces and nitrogen in urine will be determined according to the Kjeldahl method (AOAC 1990).
Statistical analysis
The data will be analysed using the GLM option of the
Minitab (version 13.31) ANOVA software. Sources of variation are: source of
cassava leaves, pigs, and source of cassava*pigs interaction, and error.
Mini project 5
Duckweed (Lemna minor)
is rich in protein of high biological value, and has been fed to pigs (Du Thanh
Hang …), ducks (Bui Xuan Men ….; Le Duc Anh….) and chickens (Du Thanh Hang
…..). The protein content and the yield
increases when it is fertilized with biodigester effluent (Rodríguez and
An experiment will be conducted to compare the growth response of duckweed to increasing concentration of N from two resources (cow manure and effluent from a biodigester charged with the same cow manure).
Two factors will be studied:
Source of fertilizer: Cow manure (M) or effluent (E) from a biodigester charged with cow
manure
Level of fertilizer: Five
levels of fertilizer N equivalent to 0, 50, 100, 150 and 200 kg N/ha.
The design is a
split-plot arrangement with level of fertilizer as main plot and the source as
split-plot, according to the randomized block arrangement in Table 1.
|
Table 1: Arrangement of the treatments |
|||||
|
Replicate |
Level of N |
||||
|
50 kg/ha |
150 kg/ha |
200 kg/ha |
100 kg/ha |
0 kg/ha |
|
|
1 |
M |
M |
M |
M |
M |
|
1 |
E |
E |
E |
E |
E |
|
2 |
M |
M |
M |
M |
M |
|
2 |
E |
E |
E |
E |
E |
Cow manure and biodigester effluent will be analyzed for DM and N, to determine the quantities to be applied according to the treatment and design. Baskets lined with polyethylene film will be used to carry out the experiment. The volume of each is about 50 litres. The experiment will last 20 days and the fertilizers will be applied in 5 equal quantities every 4 days.
The baskets will be seeded with duckweed at the rate of 50g/m2 (about 30 g per basket). The total production will be measured 24 h after seeding and 30 g replaced for the next growth period.
The harvested duckweed will be weighed and a sample taken for analysis of DM (every day). Samples of the dried duckweed will be bulked over 5 days for analysis of N and water extractable DM and N.
Samples of the water in the baskets will be taken every 5 days for analysis of N, NH3 and pH. Samples of manure and effluent will be analysed for DM and N every 5 days.
The data will be analysed by the GLM option of the ANOVA software of Minitab version 13.31. Sources of variation in the model will be: source of fertilizer, level of fertilizer, interaction source*level and error
Mini-project: 6
Heifer
International,
Malnutrition is widely identified as a main problem for both
human well-being and also animal production in the world, especially developing
countries. Because of lack of understanding of the people, especially the poor
farmers at the rural areas in Cambodia who run their production with a
traditional way, about how to develop their land use as integrated farming
system for improving their food security as well as income-generation. Anyway,
lack of information of technical system relating to appropriate skills on
agriculture makes the farmers with a small land feel less confident or have
less attention on their production causing a problem of loss of land among the
poor farmer families. Using water spinach as vegetable and animal feeding
resource is very common in
Water spinach will have higher
yields when grown from seed than from cuttings
To study growth of water
spinach planted as seed or stems and with fertilizer from biodigester effluent.
Treatments
There are 2 methods of planting
S Seed ; P Plant material
And 5 levels of N (0, 50, 100, 150, 200 kg N/ha),
arranged as a split-plot design with main plots being level of N and split plots the seed vs plant material.
|
Block |
Replicate |
200kg/ha |
0kg/ha |
100kg/ha |
150kg/ha |
50kg/ha |
|
1 |
1 |
S |
P |
S |
P |
S |
|
2 |
P |
S |
P |
S |
P |
|
|
2 |
1 |
P |
P |
S |
S |
S |
|
2 |
S |
S |
P |
P |
P |
Materials
·
Biodigester as source of effluent
·
Materials for land/row preparation
·
20 PVC baskets lined with
polyethylene film
·
Water spinach (0.5 kg of seed and
5 kg of stem)
·
Watering container/sprayer
·
Laboratory raw materials
Procedure
The plants will be grown in soil in PVC baskets, lined with polyethylene film and watered 2 times a day. The biodigester effluent will be applied every 4 days added to the soil at the rate of one sixth of the total application.
The growth rates of the plants will be measured as the height every 4 days. Measurements will be made before applying the fertilizer. The biomass will be separated into stems and leves and each analysed for DM, N, water extractable DM and N.
The data will be analysed using the GLM option of the ANOVA
software of Minitab, version 13.31. Sources of variation are: plant material,
level of N fertilizer, the interaction of plant material*N level and error.
Benefits
This field research study will be used as a resource base of
“learning by doing” to help the poor farmer families with a small plot
of land can develop their indigenous knowledge and practical skills as well as
improving their land use for integrated farming system and other agricultural
productivity. Based on their limited resources, but strong commitment and best
practice, the inputs will become more productive to assist them in order for
improving and sustaining their living condition through a small scale of
agriculture production which is ecologically and economically sound.
(Mini-project No 7)
Water spinach has a very high biomass yield. It is a vegetable resource in tropical regions for humans and animals, such as pigs, rabbits, poultry and fish. It is very easy to grow by the farmer. The traditional practice is to use urea as the fertilizer for water spinach but there is no information on the optimum level to use.
Biomass yield will be higher when water spinach is grown on soil rather than in the water. There will be a linear response in yield up to the application of 150 kg N/ha
Water spinach will be grown on soil and in the water in plots/ponds made from baskets lined with polyethylene, and with increasing levels of urea up to 150 kg/ha.
The experiment will be done in the An Giang University during a 4 week growing period.
The experiment has two sets of treatments:
Design of experiment
The treatments will be arranged in a split-plot design in which the mainplots are the levels of fertilizer and the spilt plots are the planting medium. There will be two replications, arranged as blocks, of each of the treatment combinations (see the table for thelayout)
Layout of experiment (S = soil; W = water)
|
|
|
El of urea-N, kg/ha |
||||
|
Block |
Replicate |
150 |
0 |
50 |
100 |
25 |
|
1 |
1 |
S |
W |
S |
W |
S |
|
1 |
W |
S |
W |
S |
W |
|
|
2 |
2 |
W |
W |
S |
S |
S |
|
2 |
S |
S |
W |
W |
W |
|
Baskets lined with polyethylene (capacity about 50 litres) will be used. baskets are use in experiment. A layer of soil (5 cm) is placed in the baskets for the water treatment. Water will then be added to a depth of 25cm. For the soil treatment the depth of soil will be 25cm. Holes will be made in the polyethylene in this treatment so that excess water can drain away. The soil will be obtained close to the experiment area.
In both soil and water treatments the urea will be applied at 4 day intervals over a period of 28 days.
Measurements
· The height of the water spinach will be measured every 4 days
· Total biomass will be harvested at the end of 28 days and separated into leaves and stems
· Analysis of DM and N, and
of water extractable DM and N will be made on the samples of stems and leaves,
using the micro-wave radiation method (Undersander et al 19??) N will be deternmined by the kjeldahl
techniqe and CP calculated as N*6.25 . Water extractable DM and N will be
determined by the method described by Ly
et al (19??).
The data from the experiment will be analysedusing the GLM option of the AN OVA software of Minitab (verfsjion 13.31). Sources of variation are plantiong medium, level of N, interaction medium*N level and error. The treatment means which show significant differences at the probability level of P<0.05 will be compared using the Tukey comparison in Minitab software.
Mini-project 8
Background
The human
population continues to increase in developing countries, creating increasing demand
for animal products. Thus the animal production in developing countries has also
increased very quickly, and as a result
more manure is produced. Biological water pollution by waste water from the
animal excreta is an emergency problem in rural parts of the
To solve the
problem of pollution from the animal excreta, there are some ways that can be
applied at present. The plastic biodigester is one of the most efficient
technologies for small scale animal farms because of its low investment, fast
payback, simplicity and positive effect on pollution (
The plastic
biogas digester is a means of generating biogas and organic fertilizer from
human and livestock excreta through anaerobic fermentation (Vo lam and Takesi Watanabe 2002).
However, retention time, the dimensions of the plastic biodigester, kinds of
manure all have an effect on gas production and composition of the effluent. Most
fermentation tubes are about 1m in diameter and 10m long, which is a length :
diameter ratio of 10:1. Recent research has shown that gas yields are higher in
small biodigesters with a length : diameter ratio of 3:1 (San thy et al 2003).
It is therefore
planned to carry out an experiment comparing three ratios of 3:1, 5:1, 8:1,
using experimental biodigesters of 60cm diameter. These will be 2m, 3m, and 5m
long each 60cm diameter.
Hypothesis
Gas yields as a
function of digester volume will be higher, and there will be greater
conversion of organic to ammonia-N, when the length: diameter ratio is
decreased.
Objectives:
·
To identify the suitable ratio of
length and diameter, which can produce higher gas production
·
To determine total nitrogen,
ammonia nitrogen, pH of the effluent from biodigesters with different length :
diameter ratios
Materials and methods
The experiment has three treatments consisting of different
dimensions of plastic biodigester:
B2: plastic biodigester is about 2 meters long and 60 cm
diameter
B3: plastic biodigester is about 3 meters long and 60 cm
diameter
B5: plastic biodigester is about 5 meters long and 60 cm diameter
Procedure:
Three biodigesters are made from tubular polyethylene film (internal diameter 0.637m), enclosed in brick walls, with internal measurements about 64cm wide and 60cm high to ensure the correct dimensions of the digesters, and to provide a liquid volume in the proportion of 75% of biodigester capacity volume.
They will be inoculated with
effluent from a working biodigester and then charged with cow manure at a rate
of 5 kg dry matter per 1 cubic meter liquid capacity. The manure is charged to
each biodigester at exactly the same
time. The manure is put into the biodigester when fresh and mixed with water in
quantities that will result in a retention time of 20 days. The quantities of
manure and water to be added daily to the biodigester are shown in Table 1.
|
Table 1: The ratio between fresh manure and water |
||||
|
Constants |
|
|
|
|
|
Plastic width (m) |
1 |
|
|
|
|
Circumference (m) |
2 |
|
|
|
|
Internal diameter (m) |
0.637 |
|
|
|
|
Loading rate, kg/m3 |
5 |
|
|
|
|
DM of Manure, % |
20% |
|
|
|
|
|
B2 |
B3 |
B5 |
|
|
Biodigester length (m) |
2 |
3 |
5 |
|
|
Volume (lit) |
6367 |
955 |
1592 |
|
|
Liquid volum (%) |
75 |
75 |
75 |
|
|
Liquid vol (lit) |
477 |
716 |
1194 |
|
|
Retention time (day) |
20 |
20 |
20 |
|
|
Daily input (lit) |
23.9 |
35.8 |
59.7 |
|
|
Manure DM (kg/day) |
2.4 |
3.6 |
6.0 |
|
|
Manure FM (kg/day) |
11.9 |
17.9 |
29.9 |
|
|
Water (lit/day) |
11.9 |
17.9 |
29.9 |
|
Gas production is measured daily by
collecting the gas using inverted plastic tubes of 50 diameter permanently
connected to the gas outlet, supported inside with a bamboo frame, and
suspended in drums filled with water (Santhy et al 2003). Measurements are made
three times per day. Samples of fresh cow manure and effluent will be taken daily
on days 21 to 30 and analyzed for dry matter, total N, ammonia-N, and pH. The
first 20 days of the experiment is for adaptation. Total N and ammonia are
determined by Kjeldahl procedures (AOAC 1990). DM content is determined by
micro-wave radiation (Undersander et al 1993).
Statistical analysis
There is one replicate of each
treatment as this is a pilot observation to find out if the configuration is a
factor determining the performance of the biodigester.
AOAC 1990 Official Method of Analysis. Association of Official
Analytical Chemical .15th edition (K Helrick editor)
San Thy,
Tran
Thi Phan and Takesi Watanabe 2002 Development of the new technologies and
their practice for sustainable farming systems in the Mekong Delta. Proceeding
of the 2002 annual workshop of JICAS Mekong Delta Project.
Undersander D, Mertens D R and Thiex N
1993 Forage analysis procedures.
National Forage Testing Association.
Vo lam and Takesi Watanabe 2002 Development of the new technologies and their practice
for sustainable farming systems in the Mekong Delta. Proceeding of the 2002
annual workshop of JICAS Mekong Delta Project.
Mini-project 9
There are many kinds of plant species that can be used for
animal feed that are derived from local resources. Use of these plants will
make farming systems more sustainable for poor farmers in the developing
countries around the world especially in the tropics. However, many farmers
don’t know or neglect some useful plants that can be used for animals feed. On
the other hand, we don’t always know the nutritional value of these plants so
this study will help us to recognize the differences in nutritive value among
some plants, in the local area.
The dry matter and water extraction indices will be
different among different plants species and will be related to literature
values for digestibility of DM and N.
Measuring the dry matter and nitrogen losses when plant
samples are suspended in nylon bags in a washing machine during a 90 minutes
cycle have been shown to be closely correlated with in vitro and vivo
digestibility indices.
Materials
and Methods:
These are a range of plant species including trees, shrubs, water plants and grasses
Samples of foliage from trees, shrubs, water plants and grasses will be collected and separated into stem, petiole and leaf, all of which will be weighed in the fresh state to determine the proportions of each of the components. Samples of each component will analysed for DM by the micro-wave radiation method (Undersander et al 19??) and for N (AOAC 1990). Dried samples will be ground and evaluated by the water extraction technique to determine the water extractable DM and N method (Ly et al ???). Where possible values for digestibility of DM and of N will be obtained from the literature (Göhl 19??) and compared with the values obtained by the water extraction method.
Fodder trees are
important in farming systems as besides being a source of animal feed, they
also act as “sinks” for storing carbon dioxide, help to prevent erosion and in
many instances help to restore or improve soil fertility. A constraint to more
widespread use of fodder trees is that to establish them often takes a long
time.
Recently it has been
demonstrated in
It is believed that peeling the bark from the lower 2-3 cm of tree cuttings will accelerate the time taken for the cutting to germinate and form a root system.
There are two factors:
Effect of peeling
Tree species:
The individual treatments are:
There are 8 replications of each treatment arranged in a split-plot design with effect of peeling being the sub-plot and the tree species the main plots.
The layout is shown in Table 1.
|
Table 1: Layout of experiment |
||||||||
|
Replicate |
1 |
2 |
3 |
4 |
5 |
6 |
7 |
8 |
|
TG |
TGNP |
TGP |
TGNP |
TGP |
TGP |
TGNP |
TGP |
TGNP |
|
TG |
TGP |
TGNP |
TGP |
TGNP |
TGNP |
TGP |
TGNP |
TGP |
|
|
|
|
|
|
|
|
|
|
|
CP |
CPP |
CPP |
CPNP |
CPNP |
CPP |
CPP |
CPP |
CPNP |
|
CP |
CPNP |
CPNP |
CPP |
CPP |
CPNP |
CPNP |
CPNP |
CPP |
|
|
|
|
|
|
|
|
|
|
|
SB |
SBP |
SBNP |
SBP |
SBP |
SBNP |
SBP |
SBNP |
SBP |
|
SB |
SBNP |
SBP |
SBNP |
SBNP |
SBP |
SBNP |
SBP |
SBNP |
|
|
|
|
|
|
|
|
|
|
|
MC |
MCNP |
MCP |
MCNP |
MCNP |
MCP |
MCNP |
MCNP |
MCP |
|
MC |
MCP |
MCNP |
MCP |
MCP |
MCNP |
MCP |
MCP |
MCNP |
The tree cuttings (about 30cm long) are planted in plastic bags (2 litre capacity) filled with a mixture of soil and composted organic matter. Peeling is done by removing with a knife the bark from the lower 2-3 cm of the cutting.
Records are kept of the day the first green shoot appears on the stems, and when the first leaves are formed. At the start of the experiment the length above ground of the cuttings and the diameter at the mid-point are measured. At the end of 28 days, the cuttings are removed from the bags and the number and mean length of the roots is measured.
The data will be analysed by the GLM option of the Minitab AN OVA software, version 13.31. Sources of variation in the model are: peeling, species peeling*species interaction and error.
MINI-PROJECT 11
NAFRI, Lao
Background:
Nowadays, the population growth in
the region is so fast that protein becomes a limiting resource. Poultry
production plays very important role to solve this problem in the world. To
reduce the high cost product of animal feed, however, it is necessary to
develop appropriate technologies for non-ruminant feeding. Duckweed is a water
plant with high protein content that can be produced by the farmer, so an experiment will be conducted on “scavenging
characteristics of local and exotic chickens when they have access to duckweed
as a protein source.”.
Hypothesis:
Local birds will begin to eat the duckweed sooner than the exotic birds. Exotic chicken will prefer to eat soya beans and broken rice rather than the duckweed
Objective:
Materials and methods
Treatments
There are two treatments each with two replications:
Design of experiment
The experiment will be a randomized block design (CRBD). The pens of local and exotic birds will be allocated at random within each block.
|
Block 1 |
Pen with 4 local birds |
Pen with 4 exotic birds |
|
Block 2 |
Pen with 4 exotic birds |
Pen with 4 local birds |
Feeding
systems
Three kinds of feed will be
offered in separate feeders: Broken rice, soyabean meal and fresh duckweed. Fresh feed is provided twice a day morning (
Measurements
Feed intake record every morning and afternoon for each ingredient.
The birds will be weighed every 5 days in the morning before feeding
At the end of the trial the birds will be slaughtered to observe the contents of the crop
Analysis will be made of DM, N
and the water extractable DM of each of the feeds
Statistical analysis
The data will be analysed using the GLM option of the Minitab (version 13.31) ANOVA software. Sources of variation are: bird ecotype and error
Mini-project 12
NAFRI,
Background
Mostly, exotic breeds of chicken are raised in confinement and fed on concentrated feeds. However, for poor farmers this system is too expensive and use of local birds in scavenging systems is generally preferred. Exotic breeds have the potential for higher rates of production but it is generally believed that they have lost the capacity to scavenge for their feed. It is possible that given the opportunity to learn (from peers in the same pen) they may be able to scavenge effectively.
The hypothesis
The exotic birds can learn to scavenge when they are raised with the local birds in the same pen
Objective
To study the capacity of exotic birds to select local feeds when raised with local birds.
Materials and methods
Treatment
There are two treatments:
E: Exotic birds raised in the pen
EL: Exotic birds raised with local birds in the same
pen
Experiment layout
Two treatments with two replicates in a CBRD arrangement as in the table
|
Replicate 1 |
Replicate 2 |
||
|
EL |
E |
E |
EL |
Animals
18 exotic and six local birds of about six weeks of age will be used in the experiment
Procedure
There will be two periods each of 10 days. In period 1, the birds in treatment “E” and “EL” will have access to broken rice, soybean meal and duckweed. In period 2, the local birds will be removed from treatment “EL” and the feeds on offer will only be broken rice and duckweed for birds in both treatments.
At the end of the experiment the birds will be slaughtered to measure the contents of the crop.
Measurements
Daily intake of each feed and composition (DM and N)
Contents of the crop and the different components
Body weights of the birds taken every 5 days
Statistical analysis
The data will be analysed using the GLM option of the ANOVA softare in the Minitab (version 13.31) programme. Sources of variation are: treatment and error
Mini-project 13
Usually, soybean meal and fish meal have been used as sources of protein in diets for monogastric animals for example pigs, ducks, chicken, but the prices are high, which results in high costs of production. Thus use of local feed resources can help to reduce costs of production and improve the income to small holder farmers. Many researchers (Bui Xuan Men 19??; Du Thanh Hang 19??; Le Thi Men 19??) reported that water spinach and duckweed have potential as protein sources when combined with energy rich feeds which are low in fiber (e.g. cassava root meal, sugar cane juice, broken rice). However, both water spinach and duckweed are low in methionine.
1. On basal diets of cassava root meal, a mixture of both water spinach and duckweed will increase growth rate of ducklings more than either water spinach or duckweed as the only supplement.
2. The ducklings will grow more when they are fed diets with added synthetic DL-methionine than on a diet without synthetic methionine.
1. To study use of either water spinach or duckweed and mixture of both as protein sources in diets of cassava root meal for growing ducklings.
2. To study of use of synthetic methionine as a supplement in diets of cassava root meal supplemented with duckweed and/or water spinach
A 3x2 factorial arrangement with two replicates in a Completely Randomized Design will be used.
There are two factors and two replicates as follows:
Factor 1 is source of protein
Factor 2 is supplementation of synthetic methionine
Lay out of experiment (1, 2 are replicates)
|
WM1 |
WD1 |
D2 |
WM2 |
|
WDM1 |
W1 |
W2 |
DM2 |
|
DM1 |
D1 |
WD2 |
WDM2 |
Experimental animals
Animals will be 48 duckling(about 1 week of age)
Diets will be prepared with 50% of dry matter from cassava root meal and 50% of dry matter from water spinach or duckweed or mixture (60:40 on fresh basis) of both. The water spinach is chopped finely before mixing with the cassava root meal. Duckweed will be mixed with cassava root meal without chopping. Three similar diets are prepared with 0.3% (on dry matter basis) DL-methionine.
The ducklings will be fed ad libitum on each of the
treatments according to the layout of the experiment, feeds being offered twice
daily at
Water will be available all the time.
These are:
Feed offered and refused (fresh and dry basis)
Live weights at 5 days interval
Feed composition (DM and crude protein)
Statistical analysis
The data will be analysed using the GLM option of the Minitab (version 13.31) software. Sources of variation are: protein sources, methionine, methioine*protein sources interaction and error.
Mini-project 14
The water
spinach is a creeping water plant and easy to plant with a very high biomass
yield which is a good source of protein. It is a vegetable very suitable for
animal production in
It has been
reported by Miech Phalla (personal communication) that rabbits can grow on
eater spinach as the sole feed but the growth rate was faster when 20 g/day of
broken rice was also given.
The
hypothesis to be tested is that there will
be benefits in animal
performance from adding broken rice to a
basal diet of water spinach and that the optimum economic level will be in the
range of 10 to 20 g/day, and that the economic optimum will not be the
biological optimum.
The aim of the study is to determine the effect
of different levels of broken rice(BR)
as a supplement to fresh water spinach for growing rabbits
The experiment
will be carried out from 1 August to
Treatments, animals and design
The treatments are five levels of broken rice (0 , 15, 10, 15 and 20 g/day) with two replications. Individual treatments are:
T0: BR 0 g /d
+ WS offered ad libitum 2 Rep
T5: BR 5
g/d + WS offered ad libitum 2 Rep
T10: BR
10 g/d + WS offered ad libitum 2 Rep
T15: BR
15 g/d + WS offered ad libitum 2 Rep
T20:BR
20 g/d + WS offered ad libitum 2 Rep
The experimental animals are ten recently weaned rabbits.
The design is a randomized random block with blocks being the replications (see Table 1).
|
Table 1:
Layout of experiment |
|||||
|
|
Level of broken
rice, g/day |
||||
|
|
0 |
5 |
10 |
15 |
20 |
|
Block 1 (cages 1 to 5) |
1 |
4 |
5 |
2 |
3 |
|
Block 2 (cages 6 to 10) |
10 |
6 |
7 |
8 |
9 |
The rabbits are allocated to the cages on a stratified weight basis (see example below). The rabbits are weighed and arranged in order of ascending weight, and allocated to the cages as per the following example
|
Cage no |
1 |
2 |
3 |
4 |
5 |
|
Rabbit LW, g |
10 |
12 |
13 |
15 |
16 |
|
Cage no |
6 |
7 |
8 |
9 |
10 |
|
Rabbit LW, g |
17 |
17 |
17 |
19 |
20 |
Feeding system
Leaves attached to stems of water spinach will be hung in the cage, by tying them to a bamboo stick over the cage. The broken rice will be given in a bowl which is tied to the cage. The rabbits will be adapted to confinement in individual cages during a preliminary period of one day after which the experiment will start.
Digestibility of the diets
Faeces will be collected on days 10 to 15 to determine digestibility of DM and of N.
Materials needed
The water spinach that is offered and refused will be separated into leaves and stems to determine the proportions. The leaves and stems that are offered are analysed for DM (micro-wave radiation according to Undersander et al 19--), N (AOAC 1990) and water extractable DM and N by the methods of Ly et al (19--). Faeces are analysed on fresh basis for DM and N by the previously defined methods..
Statistical analysis
The data will be analysed using the GLM option of the ANOVA software of Minitab (version ??). Sources of variation in the model are: levels of broken rice, blocks and error.
Mini-project 15
NIAH,
Background:
Recently, the use of the California Red worm (Eisenia
foetida) as an agent for recycling live stock manure has received
increasing attention (
The hypothesis:
There are two
hypotheses:
Objectives:
The objectives are to determine the effect of different
substrates (cow and poultry manure) and the initial proportion of worms in the
substrate on the rate of growth and
reproduction of earth worms and rate of breakdown of the substrate.
Materials and design
Location
The experiment will be conducted in An Giang University.
Experimental design
The treatments are five seeding rates of adult California
Red worms (Eisenia foetida) and two sources of substrate (manure derived
from cattle and poultry). The
proportions of earth worms are 0.5, 1.0, 1.5, 2.0 and 2.5% of earth worms in
the fresh manure (Table 1).
The experimental layout is a completely randomized block
design with two replicates . The experiment will last for 28 days.
|
Table 1: The experimental layout |
|||||
|
Treatments |
0.5 |
1.0 |
1.5 |
2.0 |
2.5 |
|
Seeding earth worm, (g) |
500 |
1000 |
1500 |
2000 |
2500 |
|
Cow manure, (g) |
9500 |
9000 |
8500 |
8000 |
7500 |
|
Poultry manure, (g) |
9500 |
9000 |
8500 |
8000 |
7500 |
Sampling and measurements
The worm seed stock and the fresh manure are mixed and
placed in plastic baskets.
The DM of the substrate will be analysis at weekly intervals
to adjust to the optimal humidity for earth worms. At the end of experiment the
adult worms, immature worms, worm eggs and residual substrate will be separated
and weighed.
Statistical analysis
The data will be analysed by analysis of variance using the
General Linear Model procedure of the
Minitab Software (Version 12). The model is:
Yij = µ + ai + bj + (ab)ij + eij
Y = Response
parameter
µ = Overall mean.
a =
Effect of seeding rate i
b = Effect of kind
of substrate j
e = Error
ab =
Interaction between seeding rate and substrate
Mini-project 16
Farmer observations in the Mekong delta (Nguyen Thi
Samples will be taken of leaves at the top and from the
bottom of mature trees. They will be dried and analysed for DM, N and
water-extractable DM and N using the
washing machine technique
Young leaves will have higher nutritive value than old leaves when assessed by the water extractable dry matter and nitrogen technique.
Objectives:
Samples will be taken of leaves at the top and from the
bottom of mature trees. The trees to be tested are: Cassava, Hibiscus
rosa-sinuensis, Gliricidia sepium, Acacia auriculiformis, Erythrina variata and Muntingia calabura.
The two treatments are the ages of the leaves, and the species of the tree/shrub, from which they were collected, it being assumed that the leaves at the top of the tree or shrub are the young leaves and that the leaves at the bottom are the old leaves.
The fresh leaves are analysed for DM by the micro-wave
radiation method (Undersander et al 19??), N (AOAC 1990) and water extractable
DM and N (Ly et al 20??).