Two iron repletion experiments using hemoglobin as a response criterio
n were conducted to assess effects of hemicelluloses on iron bioavaila
bility to chicks. In Experiment 1, iron bioavailability from intact fi
ber sources was determined by adding tomato pomace (14.6% hemicellulos
es), soybean hulls (20.6% hemicelluloses), beet pulp (21.5% hemicellul
oses), orchard grass (24.1% hemicelluloses) and corn fiber (55.2% hemi
celluloses) to a casein dextrose basal diet providing 0.4-4.1% hemicel
luloses to the diet. Test foods were analyzed for iron, total dietary
fiber, neutral. detergent residue, neutral detergent fiber, acid deter
gent fiber, acid detergent lignin, pectins and uronic acids. Hemicellu
loses were determined by the difference of neutral detergent residue m
inus acid detergent fiber. Iron bioavailability was determined by the
standard curve method to be (percent relative to ferrous sulfate using
hemoglobin as the response criterion) as follows: tomato pomace, 82.0
; soybean hulls, 94.0; beet pulp, 26.5; orchard grass, 68.9; corn fibe
r, 69.4. Iron bioavailability was not related to hemicellulose content
of test foods or diets. In Experiment 2, the effect of psyllium husk
(a fiber source that contains predominantly hemicelluloses) on iron bi
oavailability from ferrous sulfate was assessed. Bioavailability was d
etermined by the slope ratio method where treatments consisted of grad
ed levels of ferrous sulfate in the presence and absence of 5% dietary
psyllium. Although iron intrinsic to psyllium was unavailable, bioava
ilability of ferrous sulfate iron was not affected (P > 0.05) by the p
resence of psyllium. Thus, there was no clear effect of hemicelluloses
on iron bioavailability. However, some feeds that contained high leve
ls of hemicelluloses had low intrinsic iron bioavailabilities, suggest
ing that other dietary factors are primarily responsible for determini
ng iron bioavailability from these feed components.