2.9 Aroids for Rural Agro-Industrialisation
The condition of the leaves is a good maturity
index for assessing the readiness of corms for harvest. The length of the growing
season and yield varies among the cocoyam varieties. Taro matures in 240-300
days from planting but the eddo type matures in 180-210 days. Taro yields may
range from 4-6 t.ha-1 and up to 15 t.ha-1. Tannia matures
in 240-420 days after planting and produces small edible cormels 15-22 cm in
length attached to large corms. These cormels should be harvested before they
produce new shoots. Tannia yields about 6-12 t.ha-1 of corms, but
yields of 12-20 t.ha-1 can be achieved. Data on length of growing
season and crop yield are useful in planning harvesting and post-harvest requirements
for labour, packaging, transportation, storage, quality control and marketing.
Edible
aroids are mature for harvesting when the leaves begin to turn yellow and start
to wither. Harvesting is carried out by lifting the corms by hand. Simple tools
such as hoe and knife are used to remove the soil around the corm. Shovels are
also used. Although experimental mechanical lifters have been studied, there
are no commercial equipment dedicated to harvesting aroids. Mature taro produces
a large edible main corm and a few lateral cormels, about 4-10 in number. The
main tuber is often harvested with the smaller corms left to develop later.
For tannia, on the other hand, mature cormels may be harvested continuously
for 500 days or more, leaving the main corm in the ground to develop new cormels.
The
main objective of harvesting is to remove the mature crop without physical damage.
Most subsistent small-scale farmers harvest their crop for immediate consumption
and/or sale while the rest are left underground as a storage strategy until
required. Corms are susceptible to damage during harvesting. Damage can occur
as a result of the harvesting tool injuring the corm, or as a consequence of
rough handling (e.g. corm-to-corm impact by throwing harvested corms into a
pile). Physical damage such as punctures, cuts or abrasion lead to high rates
of moisture loss and provide avenues for microbial infection. These conditions
lead to high incidence of shrinkage and postharvest losses down the handling
chain. In many regions, corm harvesting is generally carried out by women who
also have to trek considerable distance back to the family house or market.
Developing simple and appropriate tools to remove the drudgery of manual harvesting,
particularly when the soil is dry and ‘hard’ would be beneficial
engineering inputs under these conditions.
Harvested corms are stored on-farm or transported
immediately to the home, nearby market or handling facility. In many rural subsistence
farming systems, the corms are put in a woven basket and carried on the head
as in parts of West Africa or on the shoulder where a basket is tied to each
end of a stick as in the South Pacific. Bicycles and motorised transport are
increasingly being used for transportation, especially where a large quantity
of crop is harvested. The quantity of crop and expected market value are important
considerations is selecting an appropriate transport system. Mechanised transport
has the potential to induce physical damage during haulage on “bumpy”
roads. Good shock and vibration absorbers and careful driving will assist in
reducing the incidence of damage.
Although not desirable for good quality produce, wounding of corms occurs during harvesting and trimming, and it is therefore important that harvested crop is cured before long-term storage so as to promote a rapid wound repair process. Curing slows down the rates of physiological and pathological deterioration which lead to losses in quality and quantity. Several wounds are made on tannia corm when the cormels (usually 4-10 in number) are removed, and one wound is ultimately made on taro cormels when they are cut off from the parent corm. Additional wound is also made during trimming to remove the residual planting material from the base of the corms and the petiole of leaf base. These regions have poor healing properties and require curing to prevent subsequent infection and spoilage.
Under traditional post-harvest systems, curing
is accomplished by placing corms in the sun until the wounded surface dries
out. Corms can also be cured in naturally ventilated barns or other storage
structures. Curing is less effective if damage on corms is extensive. Fungicide
treatment may be necessary if base trimming is practised. Curing can also be
achieved at elevated temperatures in high humidity environment, but chemical
application to suppress sprouting has been suggested to cause an inhibitory
effect on wound healing and periderm formation (Passam, 1982). Curing corms
at 35°C and 95% rh for 5 days reduced the rate of sprouting and weight loss
in tannia (Passam, 1982; Been et al., 1975), and temperatures below 20°C
have been reported to cause very slow wound healing of dasheen cormels. It was
recommended that brief storage of corms under tropical ambient conditions (24
or 30°C with 85% rh) promoted curing in taro and tannia corms (Agbo-Egbe
and Rickard, 1991). Other studies reported that the best conditions for wound
healing were 34-36°C with 95-100% rh (Rickard, 1981). Under these conditions,
wound healing occurred more readily at the top of corms than at the base and
sometimes did not occur at the base.
Cleaning the edible aroids to meet strict
export quarantine requirements is an essential part of the postharvest handling
system. Currently, New Zealand regulation stipulates that no more than 25 grams
of soil per 600 units (or corms) samples. Scraping and/or washing in water at
the packhouse clean taro destined for export by hand. Hand cleaning is labour-intensive
and takes considerable time and work quality is difficult to control. Although
experimental washing of taro corms grown in paddy conditions has been reported,
no mechanised cleaning equipment is yet available (IRETA, 1997). Based on an
assessment of several crop cleaning machines in Samoa in terms of time taken
to clean to export crop standard, uniformity of cleaning, damage to corms, complexity
of the machine, and cost, it was recommended that the carrot barrel washer with
some manual finishing could be used for cleaning taro corms to meet export standards.
The cost of this machine was about US$5000 in 1995.
The two main packaging systems used are woven
baskets and crates. The baskets are made of palm tree leaves or coconut leaves.
They are suitable for manual transport due the lack impacts and/or vibration
that can lead to physical damage of corms. When used in mechanical transport
systems, these baskets collapse easily under compression loading. During mechanical
transportation, wooden or plastic crates are preferred because they are firm
and reduce the incidence of mechanical damage to corms. Crates can be cleaned,
thereby contributing to better hygiene and reduced microbial infection of corms.
They are also most suited for long distance marketing and exportation.
Storage of fresh corms is important for distant
marketing, to free farmland for new cropping, and to ensure the availability
of seed cormels in the next planting season. But edible aroids have a short
period of shelf life, and this creates specific problems with the supply of
new planting materials. In particular, storage at ambient temperatures is considered
impossible due to very high incidence of fungal decay.
There is considerable variation in the storage
behaviour of the different edible aroids. For the two most important edible
aroids, taros are more difficult to store than tannia. Under high storage temperature
(25°C and above) and humidity (85% and above), it has been found that more
sprouting and decay occurred with taro than with tannia cormels (Agbo-Egbe and
Rickard, 1991). However, less sprouting and decay occurred with taro at high
temperature and low humidity than at high temperature and high humidity but
weight loss was higher. Under tropical ambient conditions, tannia cultivars
were stored successfully for about 5-6 weeks but up to 60% decay occurred in
taro corms.
Traditional Storage
Aroids are stored in a variety of traditional
low-cost structures such as shade, hut and underground pits. Sometimes, the
corms are placed in boxes before loading into the building while others are
placed directly on the storage floor. Corms may also be stored in heaps in a
shade and/or covered with straw or plantain leaves. In parts of southern China,
it is common practice to pile the corms in heaps and cover them with soil or
seal them in leaf-lined pits in the ground (Plucknett and White, 1979). In parts
of the Philippines, corms are stored in wooden platforms with the corms arranged
in irregular rows and covered with dry grass and finally with soil. As practised
in some parts of the South Pacific, corms may be harvested with about 30 cm
of their basal petioles attached, tied into bundles and stored suspended in
the shade. In pit storage, corms are placed inside pits and covered with leaves
and soil. Storage in leaf-lined soil pits is also practised. The pits or trenches
are usually dug in well-drained soil in shaded areas. The trenches may also
covered with dry grass and finally soil. These traditional storage conditions
reduce moisture loss and promote the curing of wounds. Under these conditions,
the storage life of taro corms has been extended for up to 4 weeks with no beneficial
effect on the storage of tannia. Fungal infection is also reduced.
Storage losses can be reduced by minimising
the occurrence mechanical damage and leaving the corms untrimmed during storage
(Cooke et al., 1988). Taro can be stored in shaded pits for about 4 months without
significant losses in quality and quantity, and satisfactory storage has been
achieved for up 3 months under a variety of tropical conditions. In general,
tannia keeps better in traditional pit storage better than ventilated room or
barn storage. Mature tannia corms do not deteriorate if left in the ground and
it is also common practice to harvest corms for immediate utilisation as required.
Traditional storage systems are mainly suited
for short-term storage and have limited success with long-term storage, which
is necessary for marketing beyond the harvest period. Existing results are largely
variable and in many instances the corms decay and become unfit for human consumption
after a short period. Different levels of corm wastage and losses have been
reported for different lengths of storage and for the different types of edible
aroids (Section 3). It has been shown that edible aroids can be stored at tropical
ambient conditions (24-29°C with 86-98% rh) for at least 2 weeks without
significant changes in nutritional values (Agbo-Egbe and Rickard, 1991) such
as crude protein content and total amino acids. However, resulted in a significant
reduction in starch content and increase in total sugar content. The limitations
of traditional storage structures have resulted in the search for improved storage
systems such as ventilated and refrigerated storage. Appropriate storage technique
must be selected based on crop economic value of crop, the intended use, and
the skills necessary to operate and maintain the technology under local conditions.
Ventilated Storage
During storage in well ventilated stores (~26°C and 76% rh), tannia corms had 1% weight loss per week but sprouting occurred after 6 weeks. The corms were still edible after 9 weeks storage (Thompson, 1996). Other studies showed that tannia corms may be stored in well-ventilated conditions for up to 6 months (Kay, 1987), although loss of eating quality was observed after 8 weeks. Ventilated storage of corms in the dark at 24°C resulted in 30% decay after 1-3 weeks (Kay, 1987). Factors such as corm maturity, environmental condition, agro-climatology, degree of physical damage, and a host of pre-harvest factors contribute to the variability of results reported. Results in the literature must be tested and adapted under local conditions.
Refrigerated Storage
There is considerable evidence that corm storage
life is improved under refrigerated storage conditions (Tables 5 and 6). It
must be noted though, that refrigeration
technology cost more than traditional and ventilated storage methods, and investments
in capital equipment, packaging, technical skill, and power supply are necessary.
Table 5: Recommended storage conditions for tannia (Xanthosoma spp. X. sagittifolium, Araceae).
|
Temperature (°C) |
Relative humidity (%) |
Length of storage |
|
7 |
80 |
17.1-18.6 weeks |
|
7.2 |
80 |
18 weeks |
|
7-10 |
80 |
16-20 weeks |
|
15 |
85 |
5-6 weeks |
Sources: (Tindall, 1983; Agbo-Egbe
and Rickard, 1991; Snowdown, 1991)
Table 6: Recommended storage conditions for taro (Colocasia esculenta, Araceae).
|
Temperature (°C) |
Relative humidity (%) |
Length of storage |
|
4.4 |
- |
3½ months |
|
6.1-7.2 |
80 |
- |
|
7.2 |
70-80 |
90 days‡ |
|
7.2 |
85-90 |
120-150 days# |
|
7-10 |
85-90 |
4-5 months |
|
10 |
- |
up to 180 days† |
|
10 |
- |
6 months |
|
11.1-12.8 |
85-90 |
21 weeks |
|
11-13 |
85-90 |
5 months |
|
12 |
90 |
5 months |
|
13.3 |
85-90 |
42-120 days |
|
20 |
60 |
2-4 weeks |
†= Dasheen type; ‡= Malanga type; #= taro root.
Sources: (Tindall, 1983; Thompson,
1996; Snowdown, 1991; Wardlaw, 1937; SeaLand, 1991; Mercantilia, 1989)
Storage life is generally improved at conditions
of lower temperature and high humidity. If storage environment can be maintained
at 11-13°C and 85-90% rh, the length of storage of taro can be extended
to about 150 days. At low temperature (15°C) and high humidity (85%), both
taro and tannia were successfully stored for 5-6 weeks (Agbo-Egbe and Rickard,
1991). For tannia, storage at 7°C and 80% rh was found to maintain corms
in good condition and good eating quality for about 120-130 days (Tindall, 1983).
Storage of taro packed in soil in brick-built containers or in pits stored for
up to 5 months in China at ambient temperature of 8-15°C or lower (Cooke
et al., 1988). Storage periods of 6-7 months have also been recorded under similar
conditions (Plucknett and White, 1979).
International sea- and air-freighting of taro
in refrigerated containers and chambers and subsequent storage at 3-5°C
in market stores is a common practise for taro grown in the South Pacific and
destined. The corms remain in good condition for up to 6 weeks, but once they
are exposed to ambient conditions they deteriorate rapidly after 24 hours (Wilson,
1983). Tannia export shipments at 13-14°C from Puerto Rico to the USA were
generally in poor condition on arrival after the 9-day journey. The corms decayed
after subsequent storage at 15°C and 65% rh for 30 days.
Other Storage Techniques
Successful storage of aroids in plastic bags
alone or in combination of traditional storage structures has been reported.
The conditions created inside the bag reduce moisture loss and facilitate the
curing of wounds. Packing taro corms in plastic bags and closely tying the open
end with rubber bands reduced the decay severity and percentage weight loss
(Quevedo et al., 1991). For commercial handling purposes, packing in polyethylene
bags often follows the selection of good quality corms, fungicide application
and draining, and air-drying. It was reported that the storage life of corms
in such bags was 26-40 days over those packed in cartons (Kay, 1987). Taros
stored in polyethylene bags showed a 6% loss in fresh weight and 50% decay while
tannia suffered a 9% weight loss and 30% decay (Passam, 1982). In comparison
with traditional storage in trenches or pits, corms kept in polyethylene bags
survived well for up to 30 days without appreciable changes in taste and texture.
Dipping corms in NaCl (1%) before storage in polythene bags provided additional
protection against fungal infection (Rickard, 1983), and the best storage results
were obtained when the petioles and corm apex were left intact.
Other storage environments such as coir dust
and hull ash have been reported to increase storage life and reduce the severity
of decay of corms. In trials with Colocasia (dasheen type), placing corms in a medium of rice hull ash extended
its usual storage life of corms by 14 days and reduced the incidence of decay
(Quevedo et al., 1991). Tannia corms can be stored satisfactorily in damp coir
media with significant reductions in weight loss and decay incidence. During
a 6-week storage trial in which edible aroids were put in boxes containing coir
dust and stored under ambient conditions (27-32°C), taro corms showed a
28% weight loss and 50% decay, while weight loss and decay were 30% and 25%,
respectively (Passam, 1982). When corms were stored in boxes containing moist
coir, taro showed a 21% weight loss and 50% decay, while weight loss and decay
were only 7% and 5%, respectively. For best results, it is important to ensure
that the moisture content of the coir is damp and not wet as the latter would
facilitate the decay of corms.
Taro small starch grains (1-4 µm) compared
to the large grains of tannia (17-20 µm), and this makes taro suitable
for several food products, especially as food for potentially allergic infants,
and persons with gastro-intestinal disorders. Among the root crops, taro is
perhaps most widely prepared or processed into more consumable forms. These
include poi (fresh or fermented paste, canned, and canned-acidified), flour,
cereal base, beverage powders, chips, sun-dried slices, grits, and drum-dried
flakes.
Flour can be produce in several ways, but
the key unit operations include: peeling fresh or pre-cooked corms and cormels,
drying, and grinding into flour. In commercial practice, the flour is made by
peeling the corms and cormels, slicing them, and washing them thoroughly with
water to remove adhering mucilage. After soaking in water overnight, the slices
are washed and immersed in 0.25% sulphurous acid for 3 hr. Finally, the slices
are blanched in boiling water for 4-5 min, dried thoroughly at 57-60°C,
and then milled into flour. Readers interested in a much detailed and comparative
analysis of alternative processes for manufacturing cocoyam flour in different
regions should consult Wang (1983).
Taro can also be processed into “poi” which is very a purplish-gray paste, which is considered an excellent
food and is popular in Hawaii and the South Pacific. It is sold commercially
in plastic bags, jars, or can in Hawaii. Poi is prepared in the following way:
(1) the corms and cormels are pressure-cooked, washed, peeled, and mashed into
a semi-fluid consistency; (2) the product is then passed through a series of
strainers, the final strainer having 0.5 mm diameter grade; and (3) the product
is bagged and sold as fresh drink or stored in room temperature to ferment owing
to the action of Lactobacills spp bacteria. Following the fermentation, the product becomes more
acidic (pH declines from about 5.7 to 3.9). In some areas, coconut products
may be added to the fermented “poi” before consumption.
Canned fresh poi (“ready-to-eat”
poi) is the unfermented product less than 4 hr old containing 18% total solids
or more. For a standard 566-gm can, the thermal process requires about 100 min.
cooking time at 116°C (54). On the other hand, canned-acidified poi is the
unfermented product less than 4 hr old to which 1% w/w commercial grade lactic
acid (50% lactic acid) has been added. It usually contains 18% or more total
solids, with a shelf life comparable to other canned foods (Sherman et al.,
1952). In trials with gamma-radiation, a minimum of 7 kGy was required to increase
the shelf life of poi to 7-10 days (Moy et al., 1967). High quality dehydrated
poi made by freeze drying which had acceptable quality has been reported; however,
the process was considered expensive.
The edible aroids and in particular taro,
can be made into about a dozen of different food products. An extensive review
of the experimental and commercial processes for these products can be found
in Wang (1983), and readers interested in these details are advised to consult
this reference. In summary, these reports contained this publication demonstrate
that stable, intermediate products such as flour and dried slices could be prepared
and further extruded into convenient, ready-to-use, stable forms such as taro
rice, noodles, and macaroni.
Manufacture of Animal Feedstuff
Edible aroids have considerable potential
in the livestock industry in rural areas that is dominated by small-scale farmers.
In many parts of the tropics and sub-tropics where cocoyam and other root crops
are grown as staple food, development of the livestock industries is still hampered
by the lack of or inadequate production of feeds. Often, imported feeds are
too expensive for farmers in these subsistence environments. The use of cocoyam
by-products including leaves has the potential to maximise animal production
at minimum expense to assist in meeting the food requirements in these areas.
Producing animal feed from cocoyams could become a new source of income for
some families, and also increase the ability to feed more domestic livestock.
Additionally, removal of the leaves would improve field sanitation, and reduce
the subsequent land preparation required.
Root crops in general and taro in particular
can make an excellent source of animal feed (Coursey and Halliday, 1975). Silage
made from the entire crop has been specifically suggested. Indeed, taro corms,
cormels, and leaves are used to a limited extent as animal feed. This limited
use is attributed to the acridity problem, which renders the leaves, petioles,
and corms unacceptable for use without costly, high-energy preparation (Tang
and Sakai, 1983). All parts of the plant contain acrid principles, which are
irritating to the mouth and oesophagus, and these can be removed by cooking
or fermentation.
The potential of cocoyams as an animal feed
is considerable and should not be ignored because of the high yield of petioles,
top, and leaves. Based on an average of 2 kg of taro tops per plant per 31 weeks
and a spacing of 80 x 80 cm, a yield of 52.5 metric tonnes per ha per year was
estimated (Carpenter et al., 1983). Some aroids such as giant taro can yield
up to 167.8 metric tonnes of leaves and stems per ha per year. Optimum fertiliser
application raised the yield from 226.8 metric tonnes per ha per year, the equivalent
of 27.2 metric tonnes dry matter with 34% crude protein and 17% carbohydrates.
Experimental trials indicate that up to 7 metric tonnes of taro leaves and petioles
per ha can be achieved in a 3-month period. Yields of 9-14 and 16-25 tonnes
per ha per year fresh weight of tops have been reported for some varieties (Carpenter
and Steinke, 1983).
Experimental trench silos have been constructed
and used successfully to ensile the leaf, petiole, and whole parts of taro (Wang
et al., 1981). Based on test results, it was found that the acrid factor or
factors in taro was either neutralised or destroyed whereas the raw, unensiled
material was quite acrid and caused irritation to workers handling the material.
In addition to these results, other studies on the feeding value of taro silage
showed that the fermentation characteristics were comparable with other silage,
and that taro silage could meet much of the feed needs for brood sows with no
reproductive problems and good litter performance (Carpenter and Steinke, 1983).
The problem posed by the high moisture content of taro silage (90-92% water)
as an animal feed can be minimised by ensiling taro tops along with other feedstuffs
(Table 7). This ensiling process also allows the preservation of taro forage
without the use of energy for drying.
Table 7: Types of feeds satisfactorily ensiled with taro tops
|
Energy Feeds |
Dry roughness + grasses |
Agricultural by-products |
|
Rolled barley |
Rice straw |
Rice bran |
|
Rolled corn |
Guinea grass hay |
Chopped banana plant |
|
Pineapple bran |
Pangola grass |
Whole pant sugarcane |
|
Molasses |
Paragrass |
Seedcane tops; Cane trash |
Source: (Carpenter and Steinke,
1983)
In many tropical developing countries, edible
aroids and other indigenous non-conventional feedstuffs can help to lower feed
energy costs and save some quantity of cereals for human food. Results of chicken
feeding trials have demonstrated that root crops like taro can serve as base
feeds in replacement of cereal (corn) at better cost and performance (Anigbogu,
1995 & 1996; Galvaz, 1980). Analysis of the economic costs of using taro
in broiler rations in the Philippines showed that the use of taro meals at 12.5%
yielded a profit better and had better rate of return on investment than the
control with corn as the base feed, and it was concluded that taro meal can
replace corn in terms of profit for broilers at 49 days (Anigbogu, 1996). A
minimum of 20 chicks were used for each treatment. Typical composition of different
rations and the performance evaluation on broiler chicks are shown in Tables
8 and 9.
Table 8: Composition of different taro-based rations and a control used in feedstuff evaluation.
|
Feedstuff |
Rations |
||||
|
|
A% |
B% |
C% |
D% |
E% |
|
Taro |
0 |
12.5 |
25.0 |
37.5 |
50.0 |
|
Corn (yellow) |
50.0 |
37.5 |
25.5 |
12.5 |
0 |
|
Rice bran |
5.0 |
5.0 |
5.0 |
5.0 |
5.0 |
|
Copra meal |
12.0 |
9.8 |
7.7 |
5.6 |
3.5 |
|
soybean oil meal |
18.0 |
20.0 |
22.0 |
21.0 |
26.0 |
|
Fish meal |
10.0 |
10.0 |
10.5 |
10.0 |
10.0 |
|
Ipil-Ipil leaf meal |
3.0 |
3.0 |
3.0 |
3.0 |
3.0 |
|
Bone meal |
1.0 |
1.0 |
1.0 |
1.0 |
1.0 |
|
Vegetable oil |
0 |
0.2 |
0.3 |
0.4 |
0.5 |
|
Salt |
0.5 |
0.5 |
0.5 |
0.5 |
0.5 |
|
Vitamin-mineral premix |
0.5 |
0.5 |
0.5 |
0.5 |
0.5 |
|
Total |
100.0 |
100.0 |
100.0 |
100.0 |
100.0 |
|
Calculated analysis |
|
|
|
|
|
|
Protein (%) |
21.79 |
21.79 |
21.84 |
21.84 |
21.86 |
|
Fat (%) |
4.33 |
4.17 |
3.92 |
3.66 |
3.37 |
|
Fibre (%) |
4.96 |
4.91 |
4.86 |
4.82 |
4.78 |
|
Energy (Kcal.kg-1) |
2993.27 |
3025.23 |
3052.04 |
3078.85 |
3105.66 |
|
Protein-energy ratio |
1:137.37 |
1:138.34 |
1:139.75 |
1:140.97 |
1:142.07 |
Source: (Anigbogu, 1996)
Table 9: Cost and feed performance analysis on broiler chicks fed on taro meal.
|
|
Treatment |
|||||
|
Taro meal |
0% |
12.5% |
25% |
37.5% |
50% |
CV (%) |
|
Cost of production (P)† |
25.85 a‡ |
24.24 abc |
25.44 ab |
25.04 abc |
22.04 d |
4.73 |
|
Profit (P) |
4.36 b |
6.16 a |
0.84 c |
-3.72 d |
-3.77 e |
48.59 |
|
Return on investment (P) |
16.89 b |
25.41 a |
3.21 c |
-14.87 d |
-17.11 e |
23.54 |
|
Feed cost per kg live weight (P) |
15.26 d |
14.99 d |
17.77 c |
24.95 b |
30.97 a |
3.97 |
|
Initial weight (kg) |
46.9 |
46.9 |
46.9 |
46.9 |
46.9 |
- |
|
Weight gain (kg) |
1324.8 ab |
1335.1 a |
1148.6 c |
922.1 d |
798.47 d |
6.28 |
|
Feed consumption (kg) |
3634 cd |
3638.2 cd |
3770.9 c |
4342.2 b |
4678.3 a |
4.25 |
|
Feed conversion efficiency |
2.05 cd |
2.02 cd |
2.35 c |
3.24 b |
4.12 a |
8.34 |
† P=Philipine pesos; ‡ Any two means having a common letter in a row are not significantly different at 5% using DMRT. Source: (Anigbogu, 1996).
Industrial Raw Materials
Industrial use of edible aroids is very limited
although the starch content of taro, for instance, accounts for nearly 78% of
the carbohydrate fraction (Table 10). The small size of the taro starch grains
(1-4 µm) makes them readily digestible as a food material, but unsuitable
as a source of industrial starch. The protein content of taro corms (1.4-3.0%
fresh weight basis and about 7% on dry weight basis) is slightly higher than
that of other major root and crops. It is also rich in essential amino acids,
it is rather low in histidine, lysine, isoleucine, tryptophan, and methionine.
Table 10: Fractional analysis of carbohydrate content of taro corm.
|
Component |
% |
|
Starch |
77.9 |
|
Pentosans |
2.6 |
|
Crude protein |
1.4 |
|
Dextrin |
0.5 |
|
Reducing sugars |
0.5 |
|
Sucrose |
0.1 |
|
Amylose |
17-28 |
Source: (Coursey, 1968; Oyenuga,
1968)
The special quality attributes of aroid starch,
which are important for industrial application includes particle size, pasting
temperature, and amylose content. The particle size of starch of aroids sets
them apart distinctly from more familiar commercial starches. Comparison of
the results of microscopy and laser light scattering studies showed that several
taro varieties have particle size 1-6.5 µm mean diameter, compared with
rice starch at about 5 µm which is the finest of the commonly available
starches (Griffin and Wang, 1983). Thus, taro starch literally takes over where
the commercial starches finish. On the other hand, the starch of tannia has
relatively large grains with average diameter of 17-20 µm. Edible aroids,
therefore, cover a unique wide range of particle sizes.
In addition to particle size, pasting or gelation temperature of starch
is also important during processing and industrial applications. Data available
indicates that aroids have high gelation temperatures compared with traditional
starch sources (Table 11). These data indicate that edible aroids and taro in
particular, could provide a unique combination of small particles with high
gelation temperatures.
Table 11: Particle size and gelation temperatures of taro starch, cereal starches, and potato starch.
|
Type of crop |
Particle size (µm) |
Pasting or gelation temperature (°C) |
|
Taro -Akalomama |
6 |
64 |
|
-Bun-Long |
5 |
71 |
|
-Antiquorum (cv Martin) |
3.5 |
68 |
|
Wheat |
15 (circa) |
54 |
|
Rice |
5 |
64 |
|
Potato |
50 |
60 |
Source: (Griffin and Wang,
1983).
The literature on starch application technology
highlights specific areas in which the properties of aroids starch can be applied
in commercial industries. These areas include cosmetics, syrups, gums, modified
atmosphere packaging film, fillers/modifiers for plastics, and renewable energy.
These industrial applications have been extensively reviewed elsewhere (Wang,
1983) and only a summary of the major potential uses is warranted here.
Syrup Production
World production and demand for industrial
syrup has increased considerably in the last few decades and is predicted to
continue in the future. Like other vegetable starches, aroid starches could
be processed into high fructose enriched syrups (HFES) which is a liquid sugar
(sweetener) made from starch. The nutritional value of HFES is similar to that
of sucrose, and it is also desirable, inexpensive, and easy to use sweetener.
Facilities can be built in areas where starch is available and inexpensive.
Local uses include canning, jams, jellies, and soft drinks.
Gum Production
Aroids contain a gum-like substance, which
swells in water and becomes hydrated. This gum has potential usefulness as an
emulsifying, thickening, and smoothing agent for creams, suspensions, and other
colloidal food preparations. Extraction of the gum would also alter the properties
of aroid products and reduce their stickiness and viscosity.
Renewable Energy Source
There is considerable global concern on the
depletion of non-renewable energy sources and the deleterious effects of fossil
fuel on environmental degradation. In most developing countries, low-energy
input is often a major limitation to increasing agricultural productivity and
overall rural development. Many countries could reduce their dependence on imported
oil appreciably by replacing part of their petroleum consumption with alcohol
produced from sugar or starch-containing crops Given a favourable domestic economy,
the edible aroids would serve well as a feed material for energy generation.
The alcohol yield of taro is lower than that of cassava and cereal crops but
higher than that of sugarcane and sweet corn (Table 12). The accepted starch-to-alcohol
conversion ratio is about 1.67 kg of starch to 1 litre of alcohol, and in the
USA alcohol production cost from taro was considered similar to cassava or sugarcane
and estimated to be $0.15 per litre in 1978 in comparison to ethanol production
from corn at $0.11 per litre.
Table 12: Estimated alcohol yield per tonne (wet weight) and cropping cycle for selected crops.
|
Crop |
Alcohol yield (litre.t-1) |
Cropping cycle (months) |
|
Taro |
142 |
9-15 |
|
Sweet potato |
142 |
5 |
|
Sugarcane |
67 |
10-22 |
|
Sweet sorghum |
76.7 |
4 |
|
Cassava |
180 |
12 |
|
Corn |
385 |
3.5 |
|
Spring wheat |
368 |
4 |
|
Grain sorghum |
389 |
3.5 |
Modified from (Wang, 1983).
Modification of Plastics
Starch can make up to 40% of plastic compounds
based on such polymers as polystyrene, polyethylene, polyvinyl chloride (PVC),
and the addition of modest amounts of starch does not materially affect the
original physical properties of the plastics. Taro starch is biodegradable and
when it is used in appropriate formulation in the production of plastics, it
accelerates the biodegradability of the parent polymer. In addition, the starch
does not exclude the possibility of recycling the majority of plastics composition.
With the increasing global demand and utilisation of processed food and raw
materials in general, biodegradability has become increasingly an important
requirement in agro-industrial waste management. The small size of taro starch
granules (about one-tenth of the size of maize starch granules) makes them superior
to other starches for the production of biodegradable plastics. The advantages
of using taro starch in plastic production are summarised in Table 14.
Aroid-based Edible Films for Modified Atmosphere
Packaging (MAP)
MAP technology utilises the permeability characteristics
of films and other packaging materials to influence the exchange of O2
and CO2 mainly to control the rate of ripening and other physiological
activities of fresh food products inside a package. Starch-filled polyethylene
films showed a significant decrease in gas permeability with increasing starch
content, and this effect was attributed to the high degree of crystallinity
of the starch filler material, a property that is also shared by mineral fillers
(Griffin and Wang, 1983). The low fixed gas permeability of taro starch makes
it a potential candidate in developing appropriate MAP technologies, especially
in the tropical root crops regions where production of root crops is a major
part of agricultural production. A taro-based packaging film has been successfully
developed but was found expensive compared with low-cost synthetics (Simmonds
et al., 1943).
Table 13: Advantages of using taro starch in plastic production compared with other minerals
|
|
Taro starch |
Minerals |
|
1. |
Density comparable with plastics 1.49 t.m-3 |
High density, ranging from 2.6 t.m-3 for silica to 4.6 t.m-3 for barytes. |
|
2. |
Narrow particle size range. Low porosity. Very small particle size; can therefore be used in surface coatings or very thin films. |
Broad particles size range with often a high fines content. Very low porosity, except certain chalks, dolomites and clays. |
|
3. |
Simple particle geometry approaching spherical and regular, minimum disturbance to melt rheology. |
Irregular particles, mostly fracture fragments from grinding operations. High surface area. |
|
4. |
Very low abrasive properties. |
Often extremely abrasive. |
|
5. |
Colourless and most transparent, can yield translucent or near-transparent products. |
Usually colourless but of high refractive index, e.g., calcite-1.66; wollanstonite-1.63; talc-1.59; blends with polymers are white and opaque. |
|
6. |
No significant metallic content, starch itself is an accepted food product. |
Transition metals may be released, possible interference with antioxidant function, possible toxicity questions. |
|
7. |
Thermally stable to 250°C. |
Thermally stable to very high temperatures. |
|
8. |
Not water soluble, but hygroscopic. Also hygroscopic in situ. |
Some minerals retain traces of water tenaciously, but not normally hygroscopic in situ. |
|
9. |
Low fixed gas permeability. |
Very low fixed gas permeability. |
|
10. |
Biodegradable formulations possible. |
Permanent in a biologically active environment. |
Source: (Plucknett, 1979).