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Cassava (Manihot esculenta, Crantz) leaf meal as a protein source for young cattle fed rice straw
 

Ho Thanh Tham

Literature review

Planting cassava in Vietnam

Cassava or tapioca (Manihot esculenta, Crantz), of the family Euphorbiaceae, is an annual root crop that grows widely in tropical and sub-tropical areas. It can easily thrive in sandy-loam soil with low organic matter, receiving low rainfall and high temperatures (Wanapat 1999). In Vietnam, cassava production has steadily increased during recent years and has rapidly changed its role from a food crop to an industrial crop, mainly because of increases in both area planted and yield per hectare. Cassava is the third crop after rice and maize, with about 423.800 ha planted in 2005 (General Statistics Office of Vietnam 2006). Cassava is mostly cultivated in the South-East region of Vietnam (Table 1), which includes Ninh Thuan, Binh Thuan, Binh Phuoc, Tay Ninh, Binh Duong, Dong Nai, Ba Ria-Vung Tau provinces and Ho Chi Minh city. The varieties most popular with farmers are considered to be: Gon, "Japan", "India", KM60, KM94 and KM95 (Phuc et al 1996). The common cassava production system in Vietnam aims at optimising the root yield harvested after a growing period of almost one year, with the foliage being left in the field.

Table 1. Planted area of cassava in Vietnam (thousand ha)

Locations

2003

2004

2005

Red River Delta

7.6

7.4

7.3

North East

47.5

49.4

49.4

North West

37.5

40.6

42.5

North Central Coast

44.5

48.4

52.8

South Central Coast

42.9

51.7

58.3

Central Highlands

65.4

70.6

88.3

South East

109.8

114.1

118.8

Mekong River Delta

10.4

6.4

6.4

Whole country

371.9

388.6

423.8

Source: General Statistics Office of Vietnam (2006)

With increasing demand for high quality feeds for cattle there is a growing interest to also utilize the cassava foliage as a protein supplement, which may lead to the cassava production system developing into a dual-purpose crop (Khang 2004). One hectare of cassava can produce a foliage yield of 0.64 tonnes DM/ha at root harvesting (Khang 2004), which on a national basis would be the equivalent of about 270,000 tonnes cassava foliage DM per year.

Intercropping cassava with a leguminous shrub such as Flemingia (Flemingia macrophylla) improves soil fertility and increases the protein content of the cassava foliage (Dung and Preston 2007). Previously, cassava has been characterized as an "exploitive" crop, destructive of soil fertility. However, when cassava is grown as a component of a farming system, in which livestock and crops are closely integrated, its capacity to "exploit" the nutrients in live stock manure becomes a valuable asset (Preston 2001).

Nutrient composition of cassava leaves

The mineral profile of cassava leaf meal (CLM) prepared from leaves remaining after the harvest of cassava roots showed it to be good sources of most minerals, particularly of calcium and trace minerals. The P and Na contents, however, were low (Ravindran and Ravindran 1988). The chemical composition of fresh cassava leaves, and after ensiling or sun-drying, are presented in Table 2. The CP in the leaves ranged from 23.9 to 34.7% and the fibre from 9 to 14% (both as % of DM) (Phuc et al 1996). While cassava leaf protein is low in sulphur amino acids (Gomez and Valdivieso 1984), the content of most other essential amino acids is higher than in soya bean meal (Eggum 1970). The high protein content and a relatively good profile of essential amino acids are reasons for believing that cassava leaves could be a potential protein source for monogastric animals (Phuc et al 2001), while stems plus petioles or whole plant are more suitable for ruminants (Borin 2005).

Table 2. Chemical composition of cassava leaves

 

% of DM

References

 

DM

CP

ADF

NDF

Ash

CLM

89.94

20.36

20.91

27.65

7.84

Tham et al (2007)

91.72

22.54

18.85

25.6

8.53

Khang (1999)

FCF

20.12

21.51

28.8

38.17

5.78

Khang (2004)

29.2

18.8

34.2

51.8

6.3

Man (2001)

20.3

16.9

37.1

48.7

6.4

Dung (2003)

ECF

39.27

20.3

37.16

50.1

6.89

Khang (2004)

31

21.5

34.6

51.2

5.8

Man (2001)

CH

92.4

18.9

29.7

39.5

10.7

Dung (2003)

93.4

24.9

27.0

34.4

6.6

Wanapat et al. (1997)

PCF

90.18

20.62

36.71

49.09

6.89

Khang (2004)

CLMCLM=Cassava leaf mea; FCF=Fresh cassava foliage; ECF=Ensiled cassava foliage ; CH=Cassava hay; PCF=Pelleted cassava foliage

Influence of processing methods and storage time on hydrocyanide acid (HCN), and condensed tannins (CT) of cassava leaves

Understanding of the influences on tannin content is essential for the manipulation of tannins to maximise nutritive value for animals (Norton 2000). Cassava leaves have good potential as an animal feed in the tropics on the basis of their protein, amino acid and mineral contents (Ravindran et al 1982). However, CT and cyanide are two anti-nutritional factors in cassava leaves that may reduce the nutritional quality of the leaf meal (Padmaja 1989). Fresh cassava leaves contain high levels of cyanogenic glucosides (Lancaster and Brooks 1983), which after enzymic hydrolysis give rise to toxic hydrocyanic acid. Cyanide content in cassava foliage can be reduced to levels that are safer for animals by drying (Ravindran et al 1987; Phuc et al 2001) or ensiling (Man 2001). Phuc et al (1995) reported that the HCN content (DM basis) was reduced by sun-drying from 190 mg/kg DM in the fresh leaf to 20 mg/kg DM in the leaf meal. Similarly, the HCN content was reduced by drying from 86 mg/kg in the leaf meal dried at 60oC, to 28 mg/kg in the leaf meal dried at 105oC (Phuc et al 2001). At 105oC the drying temperature had a marked effect on the cyanide content of cassava leaves and their consequent toxicity (Ravindran 1993). As has been reported by Wanapat and Rowlinson (2005) that sun-drying eliminated more than 90% of the HCN and enhanced the palatability and long-term storage. Khang (2004) found that cyanide content was reduced by 92% in pelleted cassava foliage and 78% in cassava foliage silage after drying and ensiling, respectively. The effect of three processing methods (drying, chopping and wilting), their combinations and the storage time on HCN and the crude protein (CP) content of CLM were evaluated by Ravindran et al (1987). Fresh cassava leaves contained an average of 1436 mg HCN/kg DM and simple drying (sun- or oven-) eliminated almost 90% of the HCN. A combination of chopping and 3-day wilting before drying proved most effective, lowering the cyanide potential of the final product to about 55 mg/kg DM. The HCN content of CLM declined by 58.2% during an 8-month post-processing storage.

CT was generally found to have a higher value in mature cassava leaves, but levels were lower in cassava hay harvested at a younger stage (Wanapat 2001). Sun-drying of leaves is the method of processing commonly used by farmers.

Tannins in plant leaves are considered to be detrimental when they exceed 4 to 5% in the DM by reducing palatability and digestibility (Kumar and D'Mello 1995). However, at lower levels they can be beneficial by protecting the protein from rumen microbial attack through the formation of insoluble complexes with the protein (Barry 1989). The tannin content of plants is affected by plant species, genotype and stage of growth, and may vary with plant part (leaf, stem, inflorescence, seed), season of growth and other specific environmental factors such as temperature, rainfall, cutting and defoliation by grazing herbivores including insects (Norton 2000). Free tannin contents of cassava leaves were markedly lowered by drying (Padmaja 1989). Similar effects were also found by Khang (2004) and Borin (2005), who reported that sun drying and ensiling reduced tannin contents in cassava foliage, although ensiling after sun wilting was more effective. Tannin content was reduced from 3.51% in fresh cassava foliage to 2.42% and 2.74% after drying and ensiling, respectively. Therefore, wilted and ensiled, or dried and pelleted cassava foliage can be used as a safe protein source in cattle diets to improve the productivity, without negative effects on thyroid gland and liver functions. In their study, Man (2001) demonstrated that a reduction of 25% in the tannin content of fresh cassava tops was found after ensiling; and storage time had little effect on the tannin content.

HCN and tannin contents of cassava leaves processed in different ways are summarized in Table 3.

Table 3. HCN and tannins contents of cassava leaves processed in different ways

 

HCN
(mg/kg DM)

Reference

CT
(g/kg DM)

Reference

FCF

840

Man (2001)

40

Chantaprasarn (2005)

983

Khang (2004)

35.1

Khang (2004)

CH

120

Ho Bunyeth (2005)

31

Wanapat et al. (2000)

128

Dung (2003)

23

Dung (2003)

PCF

341

Khang (2004)

24.2

Khang (2004)

ECF

408

Khang (2004)

27.4

Khang (2004)

292

Man (2001)

45

Man (2001)

CLM

-

 

31

Khang (2004)

CT=Condensed tannins; FCF=Fresh cassava foliage; CH=Cassava hay; PCF=Pelleted cassava foliage; ECF=Ensiled cassava foliage ; CLM=Cassava leaf meal

In the rainy season, it is difficult to sun-dry. Thus, ensiling is an appropriate method during this period, but is less advantageous because it increases labour costs and the risks of unfavourable microbial processes during the time of ensiling and storing, which affect the palatability and nutrient content and may lead to the development of toxic substances (Man 2001). From a practical and economic point of view, sun-drying would be the method of choice in the developing countries of the tropics (Phuc et al 2000).

Use of cassava leaves as a protein supplementation for ruminants

A considerable amount of new research information about the use of cassava as animal feed is becoming available from ongoing research in Vietnam, Thailand and Cambodia. Recent experimental findings on the use of cassava foliage as a protein supplement for pigs (the ensiled leaves), goats and cattle (the fresh or hay foliage), and buffaloes are encouraging and lay the basis for future research and development activities that promise to have a major impact in tropical farming systems. The most immediate prospects for the use of cassava leaf products are in the following areas: (i) low level inclusion of leaf meal in feed formulations for monogastric animals, and (ii) fresh foliage or cassava hay as a protein supplement to low-quality roughages in ruminant feeding.

In Thailand, cassava leaves have been used as a protein source for ruminants, especially for dairy cattle when collected at tuber harvesting time (Wanapat et al 2000). These authors considered that cassava hay was an excellent source of supplemental by-pass protein for dairy cattle especially during the long dry season and had the potential to increase productivity and profitability. The ruminal protein degradation of cassava hay was relatively low (48.8%) which Wanapat et al (2000) ascribed to the presence of tannins forming protein complexes, with the net result that it would act as a source of by-pass protein for digestion in the small intestine. According to Hong et al (2003), supplementation with cassava hay at 2-3 kg/hd/d or its provision as a sole source of roughage in dairy cattle could remarkably reduce concentrate supplementation and increase the fat and protein content of milk thus resulting in increased economic returns. These authors also suggested that cassava hay supplementation in dairy cattle could significantly increase milk thiocyanate which would possibly enhance milk quality and milk storage especially in small holder-dairy farming.

In contrast with the cassava research programme in Thailand, which is mainly based on production and utilization of cassava hay for dry season feeding (Wanapat 2001), in Cambodia the emphasis is on use of the fresh foliage on a year-round basis. For cattle, the emphasis has been on the use of the cassava foliage to supplement untreated rice straw as a fattening system for local yellow cattle. The results were encouraging, especially when the cassava foliage was combined with a single drench of vegetable oil at the beginning of the fattening period (Seng Mom et al 2001).

For cattle, fresh cassava foliage has been successfully fed as the only protein supplement in diets based on molasses-urea (Ffoulkes and Preston 1978). In an experiment with urea-treated rice straw fed to Sindhi x yellow cattle plus 0.72 kg DM/day of Napier grass and 0.26 kg DM/day of cassava root meal per 100 kg LW, provision of 100 g CP/day of fresh cassava foliage per 100 kg LW increased LW gain with an indication of reduced levels of nematode eggs in the faeces (Khuong and Khang 2005).

In an experiment with different levels of wilted cassava foliage fed to growing goats (Vanthong and Ledin 2006), the highest weight gain was recorded with 40% of wilted cassava foliage in the basal diet of Gamba grass (Andropogon gayanus).

In Paper I, it was shown that using CLM as a protein supplement to rice straw sprayed with a mixture of urea and molasses in cattle, led to an increase of total DM intake per kg LW and growth rates that were 73% higher (214 g/day) for cattle given CLM at 0.5% of body weight compared with the control treatment with no CLM (58 g/day). There was a linear increase in LW gain (R2=0.88) as proportion of CLM CP in total CP of the diet increased. The linear nature of the response curve indicates that higher levels of CLM protein might be needed to maximize LW gain.

Various methods for protecting feed protein from degradation by rumen bacteria

The protein value of feeds for ruminants is based on an estimate of the quantity of dietary protein that reaches the sites of enzymic digestion in the intestine (Preston and Leng 1987). Dietary proteins that escape degradation in the rumen are thus a significant factor in determining the protein value of feeds (Aufrère et al 2001). Manget (1997) reported that protein meals with high level of naturally available rumen-undegradable protein (RUP) or bypass protein should be preferred for incorporation in the diet of lactating and growing animals. However, if such resources are non-available or are expensive, protein meals having high rumen degradability can be carefully subjected to heat or formaldehyde treatment to achieve desired level of rumen bypass capacity (Manget 1997). The processing of protein sources to increase the RUP fraction with heat by roasting, extruding, and expelling, and by treating with formaldehyde and lignosulfonate has therefore received much attention recently (Eastridge 2006).

Heating

Heating is one of the factors which may affect the rumen degradability of protein (Dakowski et al 1996). For highly producing ruminants, heat treatment of protein supplements has been used for increasing the amount of dietary protein escaping rumen degradation, and to increase the amino acid pool entering the small intestine (McKinnon et al 1995). However, heating above the optimal temperature may overprotect the protein to a degree where it is neither fermented in the rumen nor digested in the intestine because of the Maillard reaction (Dakowski et al 1996). Thus, the application of heat must be a balance between beneficial and destructive effects.

In Tham et (2007b), it was shown that heating the various sources of leaves to 140oC for 2 hours remarkably increased fraction B3 that is considered to escape the rumen (Sniffen et al 1992). However, it was also apparent that the proportion of the dietary protein in the B3 fraction was not well correlated with the observed nutritive values of the different leaves based on animal feeding trials. Indeed the water hyacinth leaves, which had the highest proportion of the B3 fraction have been shown to be a poor source of protein for growing goats (Sunday 2002). In contrast, the B2 fraction, which appeared to be best correlated with expected animal performance, was decreased markedly by heat treatment.

Formaldehyde treatment

In vivo studies have demonstrated quite clearly that formaldehyde treatment of protein sources can lead to an increased quantity of dietary amino acids reaching the duodenum undegraded (eg: Nishimuta et al 1974). Formaldehyde reduces protein degradability by forming cross-links between protein chains and has anti-microbial properties that may alter the bacterial population (Nagel and Broderick 1992). However, application of formaldehyde is difficult because of its corrosive nature and cost.

Various methods for estimating forage protein degradation in the rumen

Protein degradation information is important according to NRC (1985). Several methods have been performed to obtain reasonably accurate estimates of rumen-degradable protein (RDP) and rumen-undegradable protein (RUP). These methods include in vivo, in situ, and a variety of in vitro methods (Schwab et al 2003).

In vivo

The in vivo method is considered ideal for protein source evaluation because feeds experience normal digestion processes. With in vivo measures, microbial and endogenous nitrogen needs to be distinguished from dietary nitrogen, which can lead to difficulty in estimation of ruminal protein degradability (Vanzant et al 1996). Most importantly, in vivo measures of ruminal protein degradability are not practical for routine evaluation of feeds due to cost, timeliness, and the need for cannulated animals.

In situ or in sacco

The in situ approach is the most widely used research approach for measuring ruminal protein degradation (NRC 2001) because they utilize the actual ruminal environment (Nocek 1988). The in sacco method of Ørskov and McDonald (1979), with various modifications, is one of the most widely adopted methods for measuring rumen degradable and undegradable protein of feeds. In brief, the in situ procedure involves placing multiple samples of a feed into nylon or Dacron polyester bags with a 40 to 60 μm pore size and then placing the bags into the rumen of ruminally cannulated animals. The bags are removed at varying times of ruminal incubation and washed, and the quantity of undigested crude protein is determined. The NRC (2001) suggests that samples be incubated for 0, 2, 4, 8, 16, 24, and 48 h (72 h for forages). Ruminally undegradable protein is that percentage of the original CP remaining in the bag at the defined endpoint of degradation.

The primary shortcoming of the in situ method is that it is labour intensive and requires the use of cannulated animals, both of which makes it a costly method for obtaining the RDP and RUP values for a feedstuff (Schwab et al 2003). Another shortcoming of this method is the disappearance from the bag of soluble proteins and protein in small particles through the pores (Martin 2001).

In vitro

In vitro methods for estimating protein degradability can be broadly classified under the following headings: solubility in buffers containing proteases, ammonia release from rumen fluid incubated in vitro, solubility in buffer and detergents and degradability predicted using near infrared reflectance spectroscopy (NIRS) (White and Ashes 1999).

Several different in vitro enzymatic methods have been evaluated to identify a method that performs at least as well as in the in situ method (Schwab et al 2003). Most of the cell-free enzymes that have been evaluated have been commercial proteases rather than proteases extracted from mixed ruminal microbes. A goal has been to identify a protease or mixture of proteases that would yield estimates of degradation fractions and rates that are similar to those generated by mixed ruminal microorganisms. The two most studied enzymes have been Streptomyces griseus and ficin. In this case, the rate of protein degradation is calculated from the rate of accumulation of amino acid and ammonia, the products of protein degradation. The usual approach has been to correlate estimates of the "extent" of ruminal protein degradation obtained with the proteases to in situ estimates of the "extent" of degradation.

The use of in vitro enzymatic methods to predict rates of protein degradation in the rumen offers laboratory utility and analytical precision. However, no single method has emerged as being universally acceptable for all feedstuffs. Challenges associated with interfering compounds (e.g., starches and fibre), and identification of the appropriate enzyme/substrate ratio are still to be resolved.

In vitro methods using rumen fluid are useful for evaluating relative protein degradability of high protein feeds (White and Ashes 1999). There are batch and continuous flow systems. The continuous flow systems are expensive and not commonly used for routine laboratory analysis of feeds. Batch methods are relatively cheap, rapid, and can be applied to a large number of samples simultaneously. They are based on the measurement of net ammonia release from a feed sample incubated in isolated rumen culture. The method partly simulates the rumen environment and so overcomes one of the criticisms of using isolated commercial proteases. The main disadvantage is the need to keep fistulated animals to supply rumen fluid. Moreover, the method is not appropriate for feeds that contain low protein fractions and high soluble carbohydrate fractions because more nitrogen can be taken up by the bacteria than released. This defect can be corrected using 15N to measure nitrogen recycling by bacteria, or by using chemical inhibitors of nitrogen uptake (chloramphenicol with hydrazine sulphate) by microbes (Broderick 1987).

Protein solubility in buffer and detergents (In vitro multi-chemical methods)

The multi-chemical approach for quantifying nitrogen fractions in feedstuffs is the protein fractionation scheme used in the CNCPS model (Sniffen et al 1992). The CNCPS partitions crude protein into 5 fractions using 3 solvents and a protein-precipitating agent. Details of the method are described by Licitra et al (1996) (Figure 1).

The 5 fractions are fraction A (NPN; soluble in borate-phosphate buffer but not precipitated with Trichloroacetic acid), fraction B (true protein). This model divides true protein in feed (using Trichloroacetic acid precipitate) into three fractions (B1, B2 and B3) and fraction C (unavailable true protein or bound protein). The rapidly degradable fraction (B1) is soluble in phosphate buffer pH 6.8 and is estimated using the method of Krishnamoorthy et al (1982). Fraction C is determined by acid-detergent insoluble protein (ADIP). Protein soluble in neutral detergent solution is described as degradable (B2) but at an intermediate rate. Protein insoluble in neutral detergent (NDIP) but soluble in acid detergent is termed the slowly degradable fraction (B3). Fraction A is assumed to be 100% degraded in the rumen and fraction C is assumed to be undegradable.

Shannak et al (2000) utilized the fractionation of feed crude protein by the CNCPS model as a basis for estimating undegraded dietary protein (UDP) values of a range of feeds. They claimed that the values of UDP obtained from in situ trials could be reliably and accurately predicted from chemical fractionation of feed crude protein by the CNCPS model. In contrast, the CNCPS model did not provide realistic predictions of milk production when a forage (alfalfa silage) was the sole or major dietary ingredient (Aquino et al 2003).

The use of the CNCPS model to estimate protein fractions of various feeds used for ruminant production in the Mekong Delta of Vietnam (Paper II) was not satisfactory as the B3 fraction, considered to best represent the "bypass" protein, was highest in water hyacinth leaves (which are considered to have a low nutritive value for ruminants), while insignificant amounts of the B3 fraction were observed in cassava leaf meal and in sesbania leaves, which have been shown to significantly increase growth rates of cattle fed low protein basal diets (eg: CLM in Paper I, and Ffoulkes and Preston 1978) or to support high rates of live weight gain in goats fed sesbania leaves as the basal diet (eg: Dahlanuddin 2001; Nhan 1998)

Characterization of protein sources and beneficial effects of rumen-undegradable protein (RUP) supplements to cattle consuming low quality forage

Broderick (1996) indicated that forages contribute protein to the cattle in two ways: by providing protein that is degraded by the ruminal microbes and by providing protein that escapes microbial breakdown in the rumen (so called rumen bypass protein). Throughout this paper, the terms "bypass", "escape", or "slowly degraded" have been used to describe some proteins. These terms have the same meaning and refer to a protein source's ability to escape breakdown in the rumen. Excellent source of by-pass protein for ruminants include blood meal, meat and bone meal, feather meal (Herold et al 1996), cottonseed meal (Zhang Weixian et al 1994) and fishmeal (Speedy 2004). According to Stock et al (1996), protein sources can be divided into four categories: i) high bypass or slowly degradable protein sources (blood meal, meat meal, fish meal, corn gluten meal, brewers grains); ii) intermediate bypass protein sources (cottonseed meal, linseed meal etc.); iii) low bypass protein sources (soybean meal, corn gluten feed, peanut meal, sunflower meal, feather meal, rape seed etc.); and iv) rapidly degradable protein sources (casein, whey, steep liquor etc.). Research conducted by Promkot and Wanapat (2003) showed that increasing dietary crude protein levels from 10.5 to 13.7% using cottonseed meal as the main source to completely replace soybean meal were beneficial to cows consuming diets based on rice straw and cassava chips. However, bypass protein meals are usually scarce and relatively expensive in most countries in the tropics (Leng 2005). Quality protein can be provided sometimes from various crop residues and by-products of food and drink manufacture, such as cassava leaves, brewers' grain and maize gluten meal. Speedy (2004) emphasized that some of these by-products provide a valuable local source of protein which can be inexpensive, accessible and continuously available from the local food industry. Greater utilization of indigenous feed materials is being encouraged for resource-poor smallholder farmers for increasing ruminant production. The value of a wide range of tropical feeds was mentioned, in particular cassava (Manihot esculenta, Crantz) and the potential of other tree legume sources is being recognized (Leng 1995). Recent research has shown that hay made from cassava foliage has a high content of bypass protein presumably because of its tannin content (Wanapat et al 2000). The potentially very high yields per hectare (Hong et al 2003; Khang 2004) of cassava foliage suggest that this may be a practical and valuable source of bypass protein for ruminant production in South East Asia in the future. It was recommended that response curves to feeding cassava foliage to cattle fed local forages and crop residues should be established and a market created for the sale of foliage meals (Leng 2005). It is clear that the feed industry and others must continue to look for alternative, enhanced and cheaper sources of protein for animal feeds. In addition, the identification of sources of supplemental protein that will accomplish the goal with maximal nutritional efficiency while minimizing environmental concerns and economical costs is important.

In all countries of South East Asia, large ruminants are fed for a major part of the feed year on low protein, crop residues (particularly straws), and wasteland grasses. Numerous studies have shown that on these feeds the priorities are to create an optimum growth medium in the rumen and to optimize metabolisable protein (MP) by feeding supplemental by-pass protein (Leng 2005). As presented in Paper I, it is clear that feed intake was remarkably increased with the increasing level of CLM in the diet of cattle consuming rice straw; and that there was a linear positive response in LW gain to the proportion of the dietary crude protein supplied as CLM. Similar responses were reported by Sath (2007) who found that on a basal diet of untreated rice straw plus rumen supplement, LW gain of Zebu cattle increased with increasing level of protein from sun-dried cassava foliage. Efficiency of nitrogen utilization and the cost to benefit ratio for protein supplements may determine the source and amount of bypass protein to feed to cattle in the future (Ipharraguerre and Clark 2005).

Conclusions

The review of the literature indicated that:

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