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South African Journal of Animal Science

versión On-line ISSN 2221-4062
versión impresa ISSN 0375-1589

S. Afr. j. anim. sci. vol.42 no.5 Pretoria ene. 2012

 

The use of near infrared spectroscopy (NIRS) to predict the chemical composition of feed samples used in ostrich total mixed rations

 

 

E. SwartI, III; T.S. BrandI, II, #; J. EngelbrechtIV

IElsenburg Institute for Animal Production, Dept of Agriculture: Western Cape, Private Bag XI, Elsenburg, 7607, South Africa
IIDept of Animal Sciences, Stellenbosch University, Private Bag X1, Matieland, 7602
IIINelson Mandela Metropolitan University, George Campus: Saasveld, Private Bag X6531, George, 6530
IVDepartment of Physics, Nelson Mandela Metropolitan University, Port Elizabeth, 6031, South Africa

 

 


ABSTRACT

The wet chemical analysis of feed samples is time consuming and expensive. Near infrared spectroscopy (NIRS) was developed as a rapid technique to predict the chemical composition of feeds. The prediction of accuracy of NIRS relies heavily on obtaining a calibration set which represents the variation in the main population, accurate laboratory analyses and the application of the best mathematical procedures. In this study NIRS was used to determine the chemical composition of total mixed rations (TMRs) used in ostrich diets. A sample population of 479 ostrich feed samples was used in the calibration and 94 samples were used in the independent validation of dry matter (DM), ash, crude protein (CP), ether extract (EE), crude fibre (CF), acid detergent fibre (ADF), neutral detergent fibre (NDF), gross energy (GE), calcium (Ca) and phosphorus (P). Coefficient of determination in validation (r2v) and standard error of prediction (SEP) was satisfactory (r2v values higher than 0.80). Coefficient of determination and SEP values for CP, EE, CF, ADF, NDF and GE were 0.97% and 0.74%, 0.89% and 0.50%, 0.94% and 1.41%, 0.89% and 2.67%, 0.95% and 2.81% and 0.80% and 0.28 MJ/kg, respectively. Less accurate values (r2v below 0.80) were obtained for DM, ash, Ca and P being 0.57% and 0.28%, 0.67% and 1.29%, 0.43% and 0.59% and 0.49% and 0.11%, respectively. The study indicated that NIRS is a suitable tool for a rapid, non-destructive and reliable prediction of the chemical composition of ostrich TMRs.

Keywords: NIRS, ostrich TMR, chemical composition, nutritive value


 

 

Introduction

For adequate feeding of livestock, farmers need information about the nutritive value of available feedstuffs (Goedhart, 1990). Livestock selected for high production require an adequate supply of nutrients. This is essential not only for the health of the animals, but also from an economic viewpoint (Givens et al., 1997). The wet chemical analyses of feed samples to determine their chemical composition are time consuming and expensive. Plant breeders, farmers and animal nutritionists require an accurate, precise, rapid and cost-effective method of assessing the nutritive value of pastures and feeds (Smith & Flinn, 1991). Near infrared spectroscopy (NIRS) provides an opportunity to determine the chemical composition of feedstuffs. Apart from its rapidity, NIRS is a physical non-destructive method, requiring minimal sample preparation, with high accuracy. In contrast to traditional chemical analyses, NIRS requires no reagents, producing no waste. It is furthermore a multi-analytical technique as several determinations can be made simultaneously and once the NIRS is calibrated, it is simple to use and operate (Givens et al, 1997). For example, conventional chemical analysis of feeds will take two to three days, while a similar analysis can be completed in 2 - 3 minutes by NIRS (Corson et al, 1999). However, calibration sets with insufficient distribution of the samples could lead to inaccurate calibrations (Viljoen et al., 2005).

The chemical composition of ostrich total mixed rations (TMRs) varies considerably due to the wide range of raw materials and by-products used. The prediction of the composition of compound feeds is generally less accurate compared to the calibrations to predict the chemical composition of raw materials. This is mainly because of the variation in range and quantity of raw materials which may exhibit different spectral characteristics for a compound feed with apparently the same chemical composition (Givens & Deaville, 1999). Aufrère et al. (1996) stated that NIRS is not widely used for concentrates and compound feeds as a large number of samples are required for the calibration. Compound feeds are further spectrally complicated because of the wide choice of raw materials used in such feeds as an infinite number of combinations is possible (de Boever et al., 1995). In this study the possibility of using NIRS to predict the chemical composition of ostrich TMRs was examined.

 

Materials and Methods

A total of 479 ostrich TMRs were subjected for chemical analysis for dry matter (DM), ash, crude protein (CP), ether extract (EE), crude fibre (CF), acid detergent fibre (ADF), neutral detergent fibre (NDF), gross energy (GE), calcium (Ca) and phosphorus (P). The DM percentage of feeds was determined by loss of weight after drying a 2 g aliquot of each sample for 24 hours at 100 °C (AOAC, 2005). The ash content was determined by ashing an aliquot of the sample at 500 °C for 5 hours in a Labcon Muffle furnace RM7 (AOAC, 2003). Nitrogen (N) was analysed by using a Leco FP428 Nitrogen analyser according to the Dumas Combustion Method. A factor of 6.25 was used to estimate the CP content (AOAC, 2003). Analyses for NDF and ADF were carried out according to Goering & Van Soest (1970). Neutral detergent fibre and CF were determined by using a Velp Scientifica FIWE Raw Fiber Extractor while ADF was determined by using a JP Selecta Dosi-Fiber Cellulose and Fibre Determination Extractor. Ether Extract was determined by a Soxtec system HT 1043, using diethyl-ether as an extraction fluid (AOAC, 2005). The Ca and P content of feeds were determined by Agri Laboratory Association of South Africa method number 6.1.1 using the dry ashing method and reading the samples on a Thermo Electron iCap 6000 series Inductively Coupled Spectrophotometer (ICP).

The sample population used in the calibration consisted of 479 ostrich TMR samples while 94 samples were used in the cross validation. The ostrich TMR samples selected for this study varied widely in their chemical composition, as feed samples of feeds used in different growth stages such as pre-starter; starter, grower and maintenance feeds were collected. Samples were ground through a 1mm sieve and scanned in small ring cups. The samples were scanned in the reflectance mode between 1100 - 2500-nm of the near-infrared region on an InfrAlyzer 500 near infrared reflectance spectrometer (IA-500) using Bran+Leubbe SESAME Version 2.00 software (Bran + Luebbe GmbH, Norderstedt, Germany). Calibrations were developed for the following chemical components: DM, ash, CP, EE, CF, ADF, NDF, GE, Ca and P. The calibration equations were independently validated on 94 TMR samples and outliers were removed, as suggested by the instrument.

The method relies on the measurement of light absorption by a feed sample when scanned using wavelengths in the near-infrared region (1100 - 2500 nm) with reflectances measured (as log 1/reflectance) at 2-nm intervals to obtain the NIRS spectra. The resulting absorption spectrum depends on the chemical bonds within the components of the scanned sample and it is therefore possible to identify specific regions of the spectrum correlated with constituents such as starch, fibre or crude protein (Mould, 2003). Calibrations were developed by means of partial least-squares regression (PLSR). PLSR is the appropriate multivariate calibration technique to avoid the problem of the very high intercorrelation between absorbances (Goedhard, 1990).

 

Results and Discussion

The statistics of NIRS calibrations for chemical components are presented in Table 1. Coefficient of determination in validation (r2v) and standard error of prediction (SEP) was satisfactory, i.e. r2v higher than 0.80 for CP, EE, CF, ADF, NDF and GE with values being 0.97% and 0.74%, 0.89% and 0.50%, 0.94% and 1.41%, 0.89% and 2.67%, 0.95% and 2.81% and 0.80% and 0.28 MJ/kg, respectively. It was less accurate (r2v below 0.80) for DM, ash, Ca and P. Guidelines for interpretation of r, according to Williams (2001), state that a value of 0.83 to 0.90 for r2 is usable in most applications, including quality assurance. A value of more than 0.98 is usable in any application while r2 values of 0.66 to 0.81 can only be used for screening and possibly some other approximate applications. The calibrations for ash, Ca en P were poor because minerals do not absorb in the near infrared region, which corresponds with results reported by de Boever et al. (1995) for compound feeds for cattle.

The coefficient of correlation, r, indicates the closeness of fit between the NIRS reflectance and reference data over the range of composition. A high r value with a low SEP and bias, together with a slope close to 1.0, means that the NIRS reflectance results are accurate over the anticipated range and likely to remain so, provided that these statistics were based on a sufficient number of observations (Williams, 2001).

The SD/SECV ratio represents the standard deviation of the chemical analyses divided by the standard error of cross validation of the calibration providing a comparison of the performance of all NIRS calibrations irrespective of the different units of the chemical parameters (Park et al., 1998). High values for the SD/SECV (ideally 5 or more, but at least 3) indicate efficient NIR reflectance predictions. The ratio between standard deviation/standard error of cross validation (SD/SECV), presented in Table 1, were the highest for DM and CP at 5.59 and 5.76 respectively. The lowest SD/SECV ratio was for Ca at 1.26. Calibrations for CF and NDF presented a SD/SECV ratio value of less than three, which is regarded as fair, while the SD/SECV ratio values for ash, EE, ADF, GE, Ca and P were poor. Xiccato et al. (2003), Pérez-Marin et al. (2004) and González-Martín (2006) obtained acceptable accurate calibrations for CP, EE and CF in compound feeds.

The relationship between laboratory determined and NIRS predicted values for CP, EE and CF is presented in Figure 1. Results of NIRS calibration indicate good correlations for CP, EE and CF with r2 values higher than 0.81. The high r2 values for CP, EE and CF indicate very good predictive capability compared to DM, ash, Ca and P. The CP and EE predictions were satisfactory for calibration with SEP values of 0.74% and 0.50% and r2v value of 0.97 and 0.89, respectively. For CF values were 0.94% and 1.41% respectively. Bruno-Soares et al. (1998) also reported accurate predictions of CP and CF by NIRS, confirming the findings of the present study. NIRS is most successful when equations are used on sample sets other than those used in calibration development. Therefore, it is necessary to determine whether it is appropriate to analyse a new population with existing NIRS equations (Smith & Flinn, 1991).

 

Conclusions

It seems that good predictions can be obtained from the prediction for CP, EE, CF, ADF, NDF and GE of ostrich TMRs. Less accurate predictions for DM, ash, Ca and P were achieved for ostrich TMRs. Better calibrations will probably be obtained for the latter components if separate calibrations are developed for diets formulated for the different growth stages of ostriches. The study, however, indicates that NIRS is an accurate technique for the prediction of the most important chemical components in ostrich TMRs.

 

Acknowledgements

The authors would like to thank A. Botha, S. September and F. Fransies at the Feeds Laboratory of the Department of Agriculture: Western Cape for the chemical analysis of the feed samples.

 

References

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# Corresponding author: tersb@elsenburg.com

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