Title: GEM and the UW Silage Breeding Project
1GEM and the UW Silage Breeding Project
- J.G. Coors
- D. Majee
- D.T. Eilert
- P.J. Flannery
- Department of Agronomy
- University of Wisconsin
- with acknowledgements to
- J.G. Lauer
- UW Department of Agronomy
- R.D. Shaver
- UW Department of Dairy Science
2- Outline
- Silage quality what is it?
- UW silage breeding system
- GEM contributions silage germplasm
- GEM contributions starch degradability
- Summary
3Dry Matter
Protein
Carbohydrate
Sugars starch
Cell wall
Degradable protein
Bound
Unavailable starch
Sugar and Starch Bugs
Bound with Lignin
Undegradable protein
Fiber Bugs
Digestible energy protein
Absorbed
Metabolizable energy protein
Maintenance
Lactation
Pregnancy
Growth
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5Milk2000
6Processed
Unprocessed
Adapted from Schwab and Shaver, unpublished.
Based on data of Bal et al., 2000 Dhiman et
al., 2000 Rojas-Bourrillon et al., 1987
7GEM Contributions Silage Germplasm
Phase I Silage evaluation of elite GEM topcrosses
(15-25) that were identified in prior years by
other GEM cooperators as having high grain yield
and suitable maturity for Wisconsin (lt120RM).
Phase 2 For those topcrosses with high forage
yield and good nutritional quality in Phase 1
trials, the respective GEM breeding population is
included in the UW inbred development nursery for
further inbreeding and selection Phase 3 Inbred
development testcrosses at S2 to S6 generations
using two to four inbred testers
82004 UW GEM Program
Phase I 17 breeding populations or early
generation GEM inbred families crossed to LH185,
LH198, LH200, LH244, or LH287 were evaluated for
silage potential (GEMNEW). Phase 2 Gem
inbreeding nursery included 400 inbred families
from 10 breeding populations. Most inbred
families (170) were derived from CUBA164
background. Phase 3 160 advanced generation
inbreds from six populations were crossed to two
testers each for evaluation in 2005. Evaluated
50 S3 families topcrosses to two testers
(GEM198, GEM244). 27 promising S4 families
evaluated in topcrossed to two to four testers
each (GEMADV).
9Forage yield for GEMNEW trial in 2004 Entries
marked with will be analyzed for nutritional
quality
102004 UW GEM Program
Phase I 17 breeding populations or early
generation GEM inbred families crossed to LH185,
LH198, LH200, LH244, or LH287 were evaluated for
silage potential (GEMNEW). Phase 2 Gem
inbreeding nursery included 400 inbred families
from 10 breeding populations. Most inbred
families (170) were derived from CUBA164
background. Phase 3 160 advanced generation
inbreds from six populations were crossed to two
testers each for evaluation in 2005. Evaluated
50 S3 families topcrosses to two testers
(GEM198, GEM244). 27 promising S4 families
evaluated in topcrossed to two to four testers
each (GEMADV).
112004 UW GEM Program
Phase I 17 breeding populations or early
generation GEM inbred families crossed to LH185,
LH198, LH200, LH244, or LH287 were evaluated for
silage potential (GEMNEW). Phase 2 Gem
inbreeding nursery included 400 inbred families
from 10 breeding populations. Most inbred
families (170) were derived from CUBA164
background. Phase 3 160 advanced generation
inbreds from six populations were crossed to two
testers each for evaluation in 2005. Evaluated
50 S3 families topcrosses to two testers
(GEM198, GEM244). 27 promising S4 families
evaluated in topcrosses to two or four testers
each (GEMADV).
12Forage yield for GEM198 and GEM244 trials in 2004
13Forage yield for GEMADV trial in 2004
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16Components of GEM Quality Synthetic (GQS) 2003
trial, LH279 topcrosses
17GEM Contributions Starch Degradability
18Rumen Degradability of Starch
19Starch Degradability
Oh43 o2
CHO5015N12-387-1-B
20Correa et al., 2002
21Starch Degradability Studies
Objectives
- Determine whether there is genetic variation for
starch - degradability
- Determine the extent to which kernel vitreousness
is related - to starch degradability
22Starch Study
Entries
32 inbred lines and 1 population (2002) 19
hybrids (2003)
23Procedure Two-Stage Starch Digestion
(Pioneer Hi-Bred International, Inc.)
- STAGE 1 - in-situ ruminal incubation
- Two steers with ruminal cannula 2 wk
adaptation to 70 (DMB) corn silage diet - In-situ procedure
- Corn kernels ground with Wiley Mill (6mm
screen) - 1.5g ground material placed in 5 x 5 cm dacron
bag - Eight replicate bags incubated for each sample
- Placed in rumen for 0 and 14 h,
- Removed, rinsed and dried at 62oC for 24 h
- STAGE 2 - post-ruminal in-vitro incubation
- 14-h ruminal residue subjected to 8 h
incubation - intestinal enzymatic cocktail (pepsin
pancreatic enzymes) - Removed, rinsed and dried at 62oC for 24 h
- Final Action
- Eight replicates for DM disappearance
- Eight replicated bags composited for a single
starch analysis
24½ milk-line stage
25Black layer stage
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27Black layer stage hybrids
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29Summary
GEM has contributed greatly to the UW silage
breeding program by providing 1) Superior and
unique germplasm 2) Better understanding of
nutritional properties of silage
http//silagebreeding.agronomy.wisc.edu