Title: Effects of predatory fish and agricultural practices on the

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Table S1. Correlation matrix of variables used in the structural equation modeling to explain the spatial
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distribution of tadpoles in rice fields. The Pearson correlation coefficient is calculated by treating the
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survey year and modernization of ditch as dummy variables (year: 2009 = 0 and 2010 = 1, modernization:
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unlined drainage ditch = 0 and lined with concrete = 1). Relative densities of six predator/competitor
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species groups are log (x + 0.5)-transformed to normalize their distributions.
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Variable
1
2
3
4
5
6
7
8
9
-
1. Year
-
2. Modernization
0.00
-
3. Flood period
0.35**
-0.46***
-
4. Egret
0.06
-0.53***
0.22*
-
5. Adult loach
0.17
-0.38***
0.33**
0.27*
-
6. Young loach
0.28*
-0.54***
0.40***
0.55***
0.38***
-
7. Crayfish
0.13
-0.52***
0.30*
0.20
0.31**
0.30*
-
8. Insect predators
-0.15
0.44***
-0.35***
-0.43***
-0.22*
-0.28*
-0.14
-
9. Insect consumers
0.26*
0.07
0.02
-0.09
-0.11
-0.06
0.13
0.01
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*P < 0.05; **P < 0.005; ***P < 0.0005, indicating a significant correlation between variables.
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1
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Table S2. Results of the final model of structural equation modeling examining the direct, indirect and
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total effects of three abiotic (survey year, modernization of ditch and flood-irrigation period) and six biotic
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(relative densities of egret, adult and young loach, crayfish, insect predators and consumers) variables on
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the density of Japanese tree frog tadpoles in rice fields. P value of direct paths is also shown. Details for
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the calculation of direct, indirect and total effects are shown in the main text.
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Path from
Year
Modernization
To
Effects
Direct
Total
P
Young loach
0.27
0.27
<0.001
Insect consumers
0.26
0.26
<0.01
Egret
-0.53
-0.53
<0.001
Adult loach
-0.28
-0.28
<0.01
Young loach
-0.54
-0.54
<0.001
Crayfish
-0.52
-0.52
<0.001
0.35
0.35
<0.001
Insect predators
Tadpoles
Flood period
Indirect
Adult loach
Insect predators
0.12
0.12
0.20
0.20
0.05
-0.21
-0.21
<0.05
0.33
<0.001
Tadpoles
0.41
-0.08
Adult loach
Tadpoles
-0.18
-0.18
0.07
Insect predators
Tadpoles
0.20
0.20
<0.05
15
16
2
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Table S3. Results of the general linear model examining the relationship between mean body size of the
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tree frog tadpoles and the flood-irrigation period in the rice fields in 2009 and 2010. 16 and 10 out of 48
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fields in each year were removed for the analysis because no tadpole was captured by the traps and thus
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body size could not be calculated. The response variable was the mean body size (cm) of tadpoles in each
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field and the explanatory variables were the flood-irrigation period and the survey year (2009 = 0 and
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2010 = 1). Scatter plot is shown in Fig. S3.
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Variable
Coeff.
SE
P
Intercept
1.21
0.48
Year
0.41
0.13
<0.005
Flood period
0.04
0.01
<0.005
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25
3
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Figure S1. The study site lies along the southern shore of Lake Kasumigaura in Ibaraki Prefecture, Kanto
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region, central Japan (36°02′N, 140°17′E). The location of four areas for tadpole surveys was shown with
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black-line boxes. As an example, rice fields for the surveys (diagonally lined areas) in four blocks
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(black-line boxes) in Area 2 are also shown in the inset.
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“Area”
0
N
1km
0
10km N
Pacific
Ocean
Study site
Lake Kasumigaura
1
Kanto region
2
3
“Block”
Lake
Kasumigaura
0
4
200m N
Towns and mountains
Key
Rice paddy region
Rice fields for sampling
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32
Breeding colony of egrets
4
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Figure S2. The periods of flood-irrigation (i.e., the number of days from the flood-irrigation date to the
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survey date of tadpoles) in 48 rice fields in 2009 (white bars) and 2010 (black bars). Tadpole surveys in
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the fields were conducted on 25–26 May 2009 and 27–28 May 2010. On the Y axis the fields were sorted
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by the type of cultivation (M: modern field; T: traditional field) and chronologically from the beginning of
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the flood-irrigation in 2010.
38
39
40
41
42
43
44
45
46
47
48
49
5
50
Figure S3. Frequency histograms of body size distributions for dojo loach, crayfish and Japanese tree frog
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tadpoles in rice fields in late May 2009 (white bars) and 2010 (black bars). Dojo loach was counted by the
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night-time census, and the other two species were captured by the minnow traps (for more details please
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see the main text).
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250
Dojo loach
2009
2010
200
Number of individuals
150
55
56
100
50
0
1.1 - 2.1 - 3.1 - 4.1 - 5.1 - 6.1 - 7.1 - 8.1 - 9.1 - 10.1 2.0 3.0 4.0 5.0 6.0 7.0 8.0 9.0 10.0 14.0
Total length (cm)
25
Crayfish
1000
20
800
15
600
10
400
5
200
0
0
01.0 - 2.0 - 3.0 0.9
1.9
2.9
3.9
Carapace length (cm)
Tadpole
1.0 - 2.0 - 3.0 - 4.0 1.9
2.9
3.9
5.0
Total length (cm)
6
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Figure S4. Moran's correlograms for residuals of the six biotic variables in the best model in 2009 (circle
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and solid line) and 2010 (square and dotted line). The abscissa is distance classes, which were defined at
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100 m intervals to confirm the presence of patch structure at a small spatial scale. The ordinate is Moran’s
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coefficients estimated for different distance classes. Moran’s coefficients usually range from -1 (indicating
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regular distribution of loach at the spatial scale) to 1 (clumped distribution). Zero value indicates a random
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spatial distribution. Filled circles/squares indicate significant coefficients for each distance class, which
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was tested by performing 1000 permutations of the original data with Bonferroni correction.
1
64
65
Adult loach
0.5
0.5
0
0
-0.5
-0.5
100
69
70
71
Moran’s coefficients
68
300
500
700
1
67
100
900
Egret
300
500
1
0.5
0.5
0
0
-0.5
-0.5
700
900
Crayfish
-1
-1
100
300
1
500
700
100
900
Predatory insects
0.5
0
0
-0.5
-0.5
-1
300
500
700
900
Consumer
insects
1
0.5
-1
100
300
500
700
1
72
Young loach
-1
-1
66
1
900
100
Tadpole
0.5
300
500
700
900
2009
2010
0
73
74
-0.5
-1
100
300
500
700
900
Spatial scale (m)
7
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Figure S5. Scatter plot on the relationship between the mean body size (cm) of tree frog tadpoles and the
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flood-irrigation period in the 32 and 40 rice fields in 2009 and 2010, respectively. General linear model
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showed that their mean body size in each field is positively correlated with the flood-irrigation period (see
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Table S3).
Mean body size (cm)
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4
3
2
2009
1
2010
0
20
30
40
50
Flood period (number of date)
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