2

The richness, diversity, and evenness mean values for various combinations of the domain data sets produced using amplicon length heterogeneity PCR profiling

SampleRichness (S)Diversity (H)Evenness (E)
V1, V3, and V1+V2 domains
NSB 0–5 cm20.33 (± 1.15)a,b2.40 (± 0.05)c,d0.80 (± 0.01)f
NSB 5–15 cm25.67 (± 3.78)a,b2.63 (± 0.18)c0.81 (± 0.04)f
NSB 15–30 cm24.67(± 0.57)a,b2.68 (± 0.12)e0.84 (± 0.03)f
IMP 0–30 cm19.33 (± 1.52)a2.26 (± 0.11)c,d0.76 (± 0.02)f,g
ANOVAF=6.42, P<0.02F= 7.52, P<0.01F= 4.63, P<0.04
V1, V3 domains
NSB 0–5 cm12.89 (± 1.76)h2.03 (± 0.14)i,j0.80 (± 0.04)l
NSB 5–15 cm14.11 (± 2.31)h2.16 (± 0.12)i,j0.82 (± 0.03)l
NSB 15–30 cm14.78 (± 0.83)h2.25 (± 0.10)j0.83 (± 0.03)l
IMP 0–30 cm14.00 (± 0.50)h1.85 (± 0.07)k0.70 (± 0.03)m
ANOVAF=2. 34, P<0.09F=21.52, P<0.01F=28.58, P<0.01
V1, V1+V2 domains
NSB 0–5 cm17.67 (± 1.80)n2.32 (± 0.08)p0.81(± 0.02)s
NSB 5–15 cm21.89 (± 2.14)o2.52 (± 0.15)q0.81(± 0.03)s
NSB 15–30 cm18.33 (± 1.11)n2.33 (± 0.08)p0.80 (± 0.02)s
IMP 0–30 cm18.89 (± 0.92)n2.13 (± 0.09)r0.73 (± 0.03)t
ANOVAF= 12.55, P<0.01F= 19.11, P<0.01F= 22.25, P<0.01
V1+V2, V3 domains
NSB 0–5 cm9.33 (± 0.57)u2.10 (± 0.03)w0.94 (± 0.01)y
NSB 5–15 cm15.67 (± 3.05)v2.51 (± 0.27)w,x0.91 (± 0.05)y
NSB 15–30 cm12.67 (± 0.57)u,v2.44 (± 0.08)w,x0.96 (± 0.02)y
IMP 0–30 cm15.00 (± 0.00)v2.56 (± 0.01)x0.95 (± 0.01)y
ANOVAF=9.82, P<0.01F=6.21, P<0.02F=1.79, P<0.23
SampleRichness (S)Diversity (H)Evenness (E)
V1, V3, and V1+V2 domains
NSB 0–5 cm20.33 (± 1.15)a,b2.40 (± 0.05)c,d0.80 (± 0.01)f
NSB 5–15 cm25.67 (± 3.78)a,b2.63 (± 0.18)c0.81 (± 0.04)f
NSB 15–30 cm24.67(± 0.57)a,b2.68 (± 0.12)e0.84 (± 0.03)f
IMP 0–30 cm19.33 (± 1.52)a2.26 (± 0.11)c,d0.76 (± 0.02)f,g
ANOVAF=6.42, P<0.02F= 7.52, P<0.01F= 4.63, P<0.04
V1, V3 domains
NSB 0–5 cm12.89 (± 1.76)h2.03 (± 0.14)i,j0.80 (± 0.04)l
NSB 5–15 cm14.11 (± 2.31)h2.16 (± 0.12)i,j0.82 (± 0.03)l
NSB 15–30 cm14.78 (± 0.83)h2.25 (± 0.10)j0.83 (± 0.03)l
IMP 0–30 cm14.00 (± 0.50)h1.85 (± 0.07)k0.70 (± 0.03)m
ANOVAF=2. 34, P<0.09F=21.52, P<0.01F=28.58, P<0.01
V1, V1+V2 domains
NSB 0–5 cm17.67 (± 1.80)n2.32 (± 0.08)p0.81(± 0.02)s
NSB 5–15 cm21.89 (± 2.14)o2.52 (± 0.15)q0.81(± 0.03)s
NSB 15–30 cm18.33 (± 1.11)n2.33 (± 0.08)p0.80 (± 0.02)s
IMP 0–30 cm18.89 (± 0.92)n2.13 (± 0.09)r0.73 (± 0.03)t
ANOVAF= 12.55, P<0.01F= 19.11, P<0.01F= 22.25, P<0.01
V1+V2, V3 domains
NSB 0–5 cm9.33 (± 0.57)u2.10 (± 0.03)w0.94 (± 0.01)y
NSB 5–15 cm15.67 (± 3.05)v2.51 (± 0.27)w,x0.91 (± 0.05)y
NSB 15–30 cm12.67 (± 0.57)u,v2.44 (± 0.08)w,x0.96 (± 0.02)y
IMP 0–30 cm15.00 (± 0.00)v2.56 (± 0.01)x0.95 (± 0.01)y
ANOVAF=9.82, P<0.01F=6.21, P<0.02F=1.79, P<0.23

Richness (S)=no. of peaks in each sample; diversity (H)=−Σ(pi)ln(pi), where piis the relative ratio of individual peak heights; evenness (E)=H/Hmax, where Hmax=ln(S); numbers in parentheses are±SD of the calculated means (n=9). Within each domain set, indices followed by the same letter are not significantly different from each other using Bonferroni post-hoc comparisons, P<0.05.

2

The richness, diversity, and evenness mean values for various combinations of the domain data sets produced using amplicon length heterogeneity PCR profiling

SampleRichness (S)Diversity (H)Evenness (E)
V1, V3, and V1+V2 domains
NSB 0–5 cm20.33 (± 1.15)a,b2.40 (± 0.05)c,d0.80 (± 0.01)f
NSB 5–15 cm25.67 (± 3.78)a,b2.63 (± 0.18)c0.81 (± 0.04)f
NSB 15–30 cm24.67(± 0.57)a,b2.68 (± 0.12)e0.84 (± 0.03)f
IMP 0–30 cm19.33 (± 1.52)a2.26 (± 0.11)c,d0.76 (± 0.02)f,g
ANOVAF=6.42, P<0.02F= 7.52, P<0.01F= 4.63, P<0.04
V1, V3 domains
NSB 0–5 cm12.89 (± 1.76)h2.03 (± 0.14)i,j0.80 (± 0.04)l
NSB 5–15 cm14.11 (± 2.31)h2.16 (± 0.12)i,j0.82 (± 0.03)l
NSB 15–30 cm14.78 (± 0.83)h2.25 (± 0.10)j0.83 (± 0.03)l
IMP 0–30 cm14.00 (± 0.50)h1.85 (± 0.07)k0.70 (± 0.03)m
ANOVAF=2. 34, P<0.09F=21.52, P<0.01F=28.58, P<0.01
V1, V1+V2 domains
NSB 0–5 cm17.67 (± 1.80)n2.32 (± 0.08)p0.81(± 0.02)s
NSB 5–15 cm21.89 (± 2.14)o2.52 (± 0.15)q0.81(± 0.03)s
NSB 15–30 cm18.33 (± 1.11)n2.33 (± 0.08)p0.80 (± 0.02)s
IMP 0–30 cm18.89 (± 0.92)n2.13 (± 0.09)r0.73 (± 0.03)t
ANOVAF= 12.55, P<0.01F= 19.11, P<0.01F= 22.25, P<0.01
V1+V2, V3 domains
NSB 0–5 cm9.33 (± 0.57)u2.10 (± 0.03)w0.94 (± 0.01)y
NSB 5–15 cm15.67 (± 3.05)v2.51 (± 0.27)w,x0.91 (± 0.05)y
NSB 15–30 cm12.67 (± 0.57)u,v2.44 (± 0.08)w,x0.96 (± 0.02)y
IMP 0–30 cm15.00 (± 0.00)v2.56 (± 0.01)x0.95 (± 0.01)y
ANOVAF=9.82, P<0.01F=6.21, P<0.02F=1.79, P<0.23
SampleRichness (S)Diversity (H)Evenness (E)
V1, V3, and V1+V2 domains
NSB 0–5 cm20.33 (± 1.15)a,b2.40 (± 0.05)c,d0.80 (± 0.01)f
NSB 5–15 cm25.67 (± 3.78)a,b2.63 (± 0.18)c0.81 (± 0.04)f
NSB 15–30 cm24.67(± 0.57)a,b2.68 (± 0.12)e0.84 (± 0.03)f
IMP 0–30 cm19.33 (± 1.52)a2.26 (± 0.11)c,d0.76 (± 0.02)f,g
ANOVAF=6.42, P<0.02F= 7.52, P<0.01F= 4.63, P<0.04
V1, V3 domains
NSB 0–5 cm12.89 (± 1.76)h2.03 (± 0.14)i,j0.80 (± 0.04)l
NSB 5–15 cm14.11 (± 2.31)h2.16 (± 0.12)i,j0.82 (± 0.03)l
NSB 15–30 cm14.78 (± 0.83)h2.25 (± 0.10)j0.83 (± 0.03)l
IMP 0–30 cm14.00 (± 0.50)h1.85 (± 0.07)k0.70 (± 0.03)m
ANOVAF=2. 34, P<0.09F=21.52, P<0.01F=28.58, P<0.01
V1, V1+V2 domains
NSB 0–5 cm17.67 (± 1.80)n2.32 (± 0.08)p0.81(± 0.02)s
NSB 5–15 cm21.89 (± 2.14)o2.52 (± 0.15)q0.81(± 0.03)s
NSB 15–30 cm18.33 (± 1.11)n2.33 (± 0.08)p0.80 (± 0.02)s
IMP 0–30 cm18.89 (± 0.92)n2.13 (± 0.09)r0.73 (± 0.03)t
ANOVAF= 12.55, P<0.01F= 19.11, P<0.01F= 22.25, P<0.01
V1+V2, V3 domains
NSB 0–5 cm9.33 (± 0.57)u2.10 (± 0.03)w0.94 (± 0.01)y
NSB 5–15 cm15.67 (± 3.05)v2.51 (± 0.27)w,x0.91 (± 0.05)y
NSB 15–30 cm12.67 (± 0.57)u,v2.44 (± 0.08)w,x0.96 (± 0.02)y
IMP 0–30 cm15.00 (± 0.00)v2.56 (± 0.01)x0.95 (± 0.01)y
ANOVAF=9.82, P<0.01F=6.21, P<0.02F=1.79, P<0.23

Richness (S)=no. of peaks in each sample; diversity (H)=−Σ(pi)ln(pi), where piis the relative ratio of individual peak heights; evenness (E)=H/Hmax, where Hmax=ln(S); numbers in parentheses are±SD of the calculated means (n=9). Within each domain set, indices followed by the same letter are not significantly different from each other using Bonferroni post-hoc comparisons, P<0.05.

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