Module 7- Nutrient digestibility Flashcards
digestibility
proportion of a feed that is not excreted in feces and therefore assumed to be absorbed
what is the major determinant of nutritional value of feeds
digestibility
high digestibility = ( ) nutrient retention = ( ) performance
high, high
3 ways to measure feed digestibility + example for each
1) in vivo
- total fecal collections
- indicator method
2) in situ
- nylon bag
3) in vitro
- tilley & terry method
nylon bag technique
feed is contained in nylon bag & placed in rumen
in situ means
between in vivo + in vitro
why is an adaptation period required for in vivo digestibility measurement? (3)
1) need time for residual feed from previous diet to be totally excreted
- takes several days for ruminants
2) GI tract needs to adapt
3) adapt to new environment
why is a balloon inflated with distilled water in bladder catheter for total urine collection?
so catheter stays in place
metabolism crates only use what sex of animal? why?
male, urine is diverted into funnel below crate
adaptation period for metabolism stalls vs crates
stalls: 4-14
crates: 2-3 days
issues with digestibility harness
bags fill up fast & become heavy
- more labour to empty bags frequently
true digestibility is always going to be ( ) than apparent digestibility. why?
higher, bc of sloughed off epithelial cells/enzymes
- overestimating proteins in feces
what is the protein in feces? (2)
undigested protein from feed & endogenous protein
NDF will always use ( ) digestibility bc no NDF secreted in GI tract
true
indirect measurement of digestibility
use basal diet digestibility & compare with test ingredient digestibility
associative effects of indirect measurement of digestibility (problem)
assumes digestibility of test ingredient stays at that % when mixed with other ingredients
2 problems with total collections
1) accurate estimate of feed intake
2) must collect ALL fecal output
measuring digestibility with the indicator method
add indicator to feed at low level & measure the concentration in the feces
indicator is often added at (%)
0.5
steady state
consistent feed intake & fecal output
DM digestibility using indicator/marker =
100 - (% indicator in feed) x 100) / (% indicator in feces)
specific nutrient digestibility =
100 - (% indicator in feed) x (% nutrient in feces ) x 100 / (% indicator in feces) x (% nutrient in feed)
concentration of indicator in the feces is always going to be ( ) than it is in the feed. why?
greater, as feed gets digested = concentrates indicator
7 properties of an ideal indicator or marker
1) cannot be digested/absorbed
2) no negative impacts
3) associated with material that it is to mark
4) uniformly excreted in feces each time
5) inexpensive
6) readily available
7) easily detected / easy to measure
2 types of digestibility markers + examples
1) internal markers -> already contained in test feed
- lignin
2) external markers -> chemical added to test feed
- chromic oxide
most common external marker used
chromic oxide