META-ANALYSIS
DATA FOR MULTI-TROPHIC LEVEL INTERACTIONS IN TROPICAL VERSUS TEMPERATE SYSTEMS.
These data are presented to complement publications that
include these studies in meta-analyses. If you plan to use these data for other
analyses, please contact Lee Dyer for more details: ldyer@mesastate.edu.
Descriptions of the data and literature cited are below the table.
Click here if you cannot see the table below
lat |
conx |
conn |
constd |
expx |
expn |
expstd |
IV |
DV |
DVm |
effect |
paper |
tmp |
5.20 |
195.00 |
1.80 |
7.20 |
195.00 |
1.80 |
res |
plt |
bio |
dirpos |
Abrahamson et al. 1988 |
tmp |
5.90 |
5.00 |
1.57 |
15.00 |
5.00 |
2.68 |
res |
plt |
bio |
dirpos |
Aerts 1989 |
trop |
0.06 |
40.00 |
0.00 |
0.18 |
9.00 |
0.08 |
hrb |
plt |
bio |
dirneg |
Aide 1992 |
trop |
86.16 |
21.00 |
8.60 |
3.41 |
22.00 |
2.42 |
hrb |
plt |
bio |
dirneg |
Anderson and Lee 1995 |
tmp |
5.50 |
5.00 |
1.50 |
2.30 |
5.00 |
1.12 |
prd |
hrb |
bio |
dirneg |
Atlegrim 1989 |
trop |
31.30 |
6.00 |
10.29 |
47.50 |
6.00 |
17.64 |
prd |
plt |
bio |
inpos |
Bach 1991 |
trop |
120.00 |
6.00 |
36.74 |
52.00 |
6.00 |
39.19 |
prd |
hrb |
bio |
dirneg |
Bach 1991 |
trop |
120.00 |
6.00 |
36.74 |
52.00 |
6.00 |
39.19 |
prd |
hrb |
bio |
inpos |
Bach 1991 |
tmp |
54.60 |
30.00 |
0.00 |
47.30 |
30.00 |
0.00 |
chm |
hrb |
bio |
dirneg |
Bauer and Nordin 1988 |
tmp |
1.23 |
16.00 |
0.32 |
1.69 |
16.00 |
0.52 |
res |
plt |
bio |
dirpos |
Bjorkman et al. 1991 |
tmp |
2.10 |
16.00 |
0.40 |
2.45 |
16.00 |
0.40 |
res |
plt |
chm |
dirpos |
Bjorkman et al. 1991 |
tmp |
57.00 |
10.00 |
28.00 |
69.90 |
10.00 |
24.30 |
res |
hrb |
bio |
inneg |
Bjorkman et al. 1991 |
tmp |
7.80 |
10.00 |
4.20 |
0.20 |
10.00 |
0.40 |
chm |
prd |
bio |
inneg |
Boeve 1991 |
trop |
25.59 |
27.00 |
50.19 |
180.68 |
27.00 |
143.67 |
chm |
hrb |
bio |
dirneg |
Braker and Chazdon |
tmp |
3.00 |
4.00 |
0.20 |
3.10 |
4.00 |
0.20 |
res |
plt |
chm |
dirneg |
Bryant et al. 1987 |
tmp |
3.10 |
4.00 |
0.20 |
4.60 |
4.00 |
1.00 |
res |
plt |
chm |
dirpos |
Bryant et al. 1987 |
tmp |
3.30 |
10.00 |
1.58 |
6.80 |
10.00 |
1.58 |
res |
plt |
bio |
dirpos |
Bryant et al. 1987 |
tmp |
94.00 |
10.00 |
3.16 |
1.00 |
10.00 |
0.50 |
res |
hrb |
bio |
inneg |
Bryant et al. 1987 |
trop |
0.56 |
9.00 |
0.20 |
1.41 |
9.00 |
0.41 |
prd |
hrb |
bio |
inpos |
Buckley 1990 |
trop |
0.85 |
5.00 |
0.32 |
0.22 |
5.00 |
0.22 |
prd |
prd |
bio |
dirneg |
Buckley and Gullan 1991 |
trop |
8.00 |
9.00 |
3.00 |
10.80 |
9.00 |
3.00 |
res |
plt |
bio |
dirpos |
Burslem et al. 1996 |
tmp |
96.00 |
20.00 |
27.95 |
71.00 |
20.00 |
27.95 |
hrb |
plt |
bio |
dirneg |
Cain et al. 1991 |
trop |
144.20 |
8.00 |
17.50 |
398.50 |
8.00 |
89.10 |
res |
plt |
bio |
dirpos |
Chazdon and Pearcy 1986 |
tmp |
1.50 |
34.00 |
8.75 |
3.40 |
29.00 |
2.64 |
res |
plt |
sur |
dirpos |
Collinge and Louda 1989 |
tmp |
2.90 |
31.00 |
2.23 |
3.40 |
29.00 |
2.64 |
hrb |
plt |
sur |
dirpos |
Collinge and Louda 1989 |
trop |
56.67 |
10.00 |
12.65 |
91.11 |
10.00 |
21.08 |
hrb |
plt |
bio |
dirpos |
Dangerfield and Modukanele
1996 |
tmp |
28.00 |
6.00 |
17.15 |
12.00 |
6.00 |
9.80 |
hrb |
plt |
bio |
dirneg |
D'Antonio et al. 1993 |
trop |
9.40 |
5.00 |
2.60 |
13.40 |
5.00 |
4.10 |
hrb |
plt |
div |
dirpos |
Debrot and de Freitas 1993 |
trop |
46.30 |
5.00 |
21.20 |
17.40 |
5.00 |
14.90 |
hrb |
plt |
bio |
dirneg |
Debrot and de Freitas 1993 |
trop |
0.27 |
16.00 |
0.14 |
0.48 |
16.00 |
0.17 |
prd |
plt |
sur |
inpos |
del Claro et al. 1996 |
trop |
17.70 |
15.00 |
4.46 |
10.80 |
15.00 |
1.93 |
prd |
hrb |
bio |
dirneg |
del Claro et al. 1996 |
tmp |
64.30 |
8.00 |
14.10 |
144.20 |
8.00 |
26.20 |
res |
plt |
bio |
dirpos |
DeLucia et al. 1989 |
trop |
15.00 |
14.00 |
8.98 |
38.00 |
40.00 |
8.85 |
res |
plt |
div |
inpos |
Duivenvoorden 1996 |
trop |
202.80 |
12.00 |
219.97 |
0.30 |
3.00 |
1.04 |
prd |
hrb |
bio |
dirneg |
Escalante and Benado 1990 |
tmp |
13.80 |
9.00 |
9.00 |
83.30 |
6.00 |
14.30 |
chm |
hrb |
bio |
inpos |
Faeth 1985 |
trop |
0.08 |
10.00 |
0.01 |
0.10 |
10.00 |
0.01 |
hrb |
res |
bio |
dirpos |
Farji Brener and Silva 1995 |
trop |
0.17 |
4.00 |
0.13 |
0.14 |
12.00 |
0.04 |
chm |
hrb |
bio |
dirneg |
Farnsworth and Ellison 1991 |
trop |
1075.00 |
12.00 |
259.81 |
640.00 |
16.00 |
86.60 |
res |
plt |
chm |
dirneg |
Feller 1996 |
trop |
0.03 |
10.00 |
0.02 |
0.08 |
10.00 |
0.05 |
res |
hrb |
bio |
dirpos |
Feller and Mathis 1997 |
trop |
3.90 |
20.00 |
2.41 |
17.27 |
20.00 |
6.73 |
chm |
hrb |
bio |
dirneg |
Filip et al. 1995 |
tmp |
44.80 |
16.00 |
10.00 |
12.10 |
16.00 |
3.20 |
hrb |
plt |
bio |
dirneg |
Fox and Morrow 1992 |
tmp |
7.09 |
22.00 |
0.94 |
7.47 |
22.00 |
0.75 |
res |
hrb |
bio |
inpos |
Fox et al. 1990 |
trop |
680.00 |
3.00 |
94.00 |
337.00 |
3.00 |
43.00 |
chm |
hrb |
bio |
dirneg |
Ganzhorn 1992 |
tmp |
16.00 |
4.00 |
5.00 |
22.00 |
4.00 |
3.00 |
res |
plt |
bio |
dirpos |
Gebauer et al. 1987 |
trop |
16.70 |
3.00 |
16.00 |
63.70 |
5.00 |
7.20 |
res |
plt |
div |
dirpos |
Gentry and Emmons 1986 |
trop |
0.49 |
17.00 |
0.27 |
0.09 |
6.00 |
0.02 |
hrb |
plt |
bio |
dirneg |
Georgiadis 1989 |
trop |
15.20 |
5.00 |
2.10 |
21.70 |
5.00 |
2.10 |
res |
plt |
bio |
dirpos |
Georgiadis 1989 |
trop |
70.10 |
3.00 |
33.60 |
318.00 |
3.00 |
43.82 |
res |
plt |
bio |
dirpos |
Gerwing 1995 |
tmp |
20.60 |
129.00 |
10.50 |
24.60 |
108.00 |
9.60 |
res |
hrb |
bio |
dirpos |
Glyphis and Puttick 1989 |
tmp |
21.40 |
127.00 |
11.40 |
17.70 |
212.00 |
8.10 |
res |
hrb |
bio |
inneg |
Glyphis and Puttick 1989 |
tmp |
60.00 |
3.00 |
4.00 |
83.00 |
3.00 |
9.00 |
res |
plt |
chm |
dirpos |
Glyphis and Puttick 1989 |
tmp |
334.70 |
136.00 |
106.80 |
262.00 |
133.00 |
112.50 |
res |
plt |
bio |
dirpos |
Glyphis and Puttick 1989 |
tmp |
2.80 |
6.00 |
6.80 |
58.30 |
14.00 |
7.00 |
prd |
prd |
bio |
dirneg |
Gunnarsson 1985 |
trop |
2380.00 |
11.00 |
2197.00 |
774.00 |
11.00 |
881.00 |
hrb |
plt |
bio |
dirneg |
Guy 1989 |
tmp |
9.70 |
10.00 |
0.63 |
3.80 |
10.00 |
3.48 |
chm |
prd |
bio |
inneg |
Hare and Eisner 1993 |
tmp |
221.63 |
19.00 |
56.84 |
115.53 |
13.00 |
42.91 |
chm |
hrb |
bio |
dirneg |
Harrison and Karban 1986 |
tmp |
32.30 |
5.00 |
6.83 |
51.40 |
5.00 |
9.16 |
res |
plt |
bio |
dirpos |
Haukioja et al. 1985 |
tmp |
862.50 |
2.00 |
335.90 |
375.50 |
2.00 |
33.20 |
prd |
hrb |
bio |
dirneg |
Haukioja et al. 1985 |
tmp |
6.50 |
12.00 |
1.39 |
6.20 |
12.00 |
0.69 |
hrb |
plt |
div |
dirneg |
Heske et al. 1993 |
tmp |
390.00 |
12.00 |
103.92 |
250.00 |
12.00 |
173.21 |
hrb |
plt |
bio |
dirneg |
Heske et al. 1993 |
trop |
1025.00 |
10.00 |
155.00 |
415.00 |
10.00 |
90.00 |
prd |
hrb |
bio |
dirneg |
Houston 1987 |
trop |
47.30 |
24.00 |
6.40 |
42.00 |
24.00 |
8.60 |
chm |
hrb |
bio |
dirneg |
Howard 1990 |
trop |
2.90 |
158.00 |
2.80 |
4.10 |
158.00 |
0.60 |
res |
plt |
sur |
dirpos |
Howe 1990 |
trop |
15.30 |
3.00 |
3.50 |
5.70 |
3.00 |
4.00 |
hrb |
plt |
sur |
dirneg |
Howe 1990 |
trop |
0.13 |
20.00 |
0.36 |
0.36 |
10.00 |
0.41 |
res |
prd |
bio |
inpos |
Hustler and Howells 1990 |
tmp |
71.40 |
5.00 |
2.68 |
64.40 |
5.00 |
2.24 |
chm |
hrb |
bio |
dirneg |
Jensen 1988 |
tmp |
1.50 |
12.00 |
1.73 |
1.70 |
12.00 |
2.77 |
chm |
hrb |
bio |
none |
Johnson et al. 1985 |
tmp |
0.19 |
25.00 |
0.15 |
2.70 |
25.00 |
0.50 |
res |
plt |
bio |
dirpos |
Julkunen-Tiitto et al. 1993 |
tmp |
2.60 |
25.00 |
2.00 |
12.50 |
25.00 |
1.50 |
res |
plt |
chm |
dirpos |
Julkunen-Tiitto et al. 1993 |
tmp |
10.00 |
25.00 |
4.00 |
5.00 |
25.00 |
1.00 |
res |
plt |
chm |
dirneg |
Julkunen-Tiitto et al. 1993 |
tmp |
48.00 |
6.00 |
17.00 |
7.00 |
6.00 |
4.00 |
chm |
prd |
bio |
inneg |
Kearsley and Whitham 1992 |
tmp |
1.10 |
32.00 |
1.13 |
0.53 |
32.00 |
0.57 |
prd |
hrb |
bio |
dirneg |
Kelly 1986 |
tmp |
17.30 |
12.00 |
41.20 |
57.20 |
18.00 |
50.80 |
prd |
plt |
bio |
inpos |
Kelly 1986 |
tmp |
4.40 |
5.00 |
1.34 |
5.60 |
8.00 |
0.51 |
plt |
hrb |
div |
dirpos |
Kemp et al. 1990 |
tmp |
9.00 |
7.00 |
5.29 |
73.00 |
9.00 |
105.00 |
plt |
hrb |
bio |
dirpos |
Kimberling et al. 1990 |
tmp |
810.00 |
9.00 |
69.00 |
660.00 |
16.00 |
68.00 |
hrb |
plt |
bio |
dirneg |
Kinsman and Platt 1984 |
tmp |
27.00 |
4.00 |
12.00 |
45.00 |
4.00 |
6.00 |
res |
plt |
bio |
dirpos |
Koch et al. 1989 |
tmp |
35.40 |
6.00 |
2.94 |
38.20 |
6.00 |
4.41 |
hrb |
plt |
div |
dirpos |
Korn and Korn 1989 |
tmp |
234.00 |
60.00 |
89.00 |
122.60 |
60.00 |
17.00 |
hrb |
plt |
bio |
dirneg |
Korn and Korn 1989 |
tmp |
0.26 |
30.00 |
0.02 |
0.23 |
30.00 |
0.03 |
chm |
hrb |
bio |
dirneg |
Krischik et al. 1991 |
trop |
1.00 |
5.00 |
1.19 |
0.40 |
5.00 |
0.69 |
chm |
hrb |
bio |
dirneg |
Kursar and Coley 1992 |
trop |
0.01 |
525.00 |
0.00 |
0.02 |
750.00 |
0.01 |
chm |
hrb |
bio |
inpos |
Lacerda et al. 1986 |
trop |
294.00 |
36.00 |
132.00 |
77.50 |
20.00 |
101.00 |
hrb |
plt |
sur |
dirneg |
Lam and Dudgeon 1985a |
trop |
200.00 |
75.00 |
19.60 |
114.70 |
75.00 |
19.60 |
hrb |
plt |
bio |
dirneg |
Lee 1991 |
trop |
0.27 |
3.00 |
0.10 |
0.05 |
3.00 |
0.01 |
prd |
hrb |
bio |
dirneg |
Letourneau and Dyer 1998 |
trop |
5.70 |
3.00 |
6.06 |
560.30 |
3.00 |
328.05 |
hrb |
plt |
bio |
dirneg |
Letourneau and Dyer 1998 |
trop |
560.30 |
3.00 |
328.05 |
5.70 |
3.00 |
6.06 |
prd |
plt |
bio |
inpos |
Letourneau and Dyer 1998 |
trop |
0.24 |
30.00 |
0.27 |
0.06 |
45.00 |
0.13 |
prd |
hrb |
bio |
dirneg |
Letourneau et al. 1993 |
tmp |
0.03 |
15.00 |
0.03 |
0.15 |
15.00 |
0.08 |
res |
hrb |
bio |
inpos |
Lightfoot and Whitford 1990 |
tmp |
6.86 |
20.00 |
1.78 |
5.78 |
20.00 |
2.42 |
chm |
hrb |
bio |
dirneg |
Lincoln and Couvet 1989 |
trop |
5.80 |
12.00 |
1.70 |
3.90 |
12.00 |
1.10 |
prd |
hrb |
div |
dirneg |
Lounibos et al. 1987 |
trop |
13.00 |
12.00 |
3.80 |
0.00 |
12.00 |
0.03 |
prd |
hrb |
bio |
dirneg |
Lounibos et al. 1987 |
trop |
34.70 |
121.00 |
4.60 |
18.90 |
37.00 |
4.60 |
prd |
prd |
bio |
dirneg |
Lounibos et al. 1987 |
trop |
2.90 |
10.00 |
1.90 |
10.80 |
10.00 |
4.90 |
res |
plt |
chm |
dirpos |
Lowman 1992 |
tmp |
22.40 |
11.00 |
2.32 |
16.00 |
12.00 |
1.73 |
chm |
hrb |
bio |
dirneg |
Manuwoto and Scriber 1986 |
tmp |
0.40 |
9.00 |
0.15 |
0.80 |
9.00 |
0.24 |
res |
plt |
bio |
dirpos |
Marks and Clay 1990 |
tmp |
6.30 |
4.00 |
2.20 |
2.90 |
4.00 |
1.00 |
prd |
hrb |
bio |
dirneg |
Meserve et al. 1993 |
tmp |
16.20 |
3.00 |
1.04 |
6.50 |
3.00 |
0.35 |
res |
plt |
bio |
dirpos |
Methy et al. 1990 |
tmp |
0.25 |
10.00 |
0.16 |
0.13 |
10.00 |
0.06 |
chm |
hrb |
bio |
dirneg |
Meyer and Montgomery 1987 |
tmp |
39.50 |
10.00 |
7.43 |
28.90 |
10.00 |
10.34 |
hrb |
plt |
bio |
dirneg |
Meyer and Whitlow 1992 |
tmp |
5.10 |
12.00 |
1.73 |
3.10 |
12.00 |
1.70 |
res |
plt |
chm |
dirneg |
Mihaliak and Lincoln 1985 |
tmp |
0.22 |
7.00 |
0.08 |
0.39 |
15.00 |
0.15 |
hrb |
plt |
bio |
dirpos |
Mihaliak and Lincoln 1989 |
tmp |
6.38 |
6.00 |
3.40 |
4.89 |
9.00 |
1.35 |
res |
plt |
chm |
dirneg |
Mihaliak and Lincoln 1989 |
tmp |
16.00 |
17.00 |
12.37 |
50.00 |
25.00 |
40.00 |
res |
hrb |
bio |
inpos |
Minkenberg and Ottenheim
1990 |
tmp |
50.00 |
25.00 |
40.00 |
16.00 |
17.00 |
12.37 |
chm |
hrb |
bio |
dirneg |
Minkenberg and Ottenheim
1990 |
tmp |
583.00 |
25.00 |
155.00 |
1763.00 |
17.00 |
387.57 |
res |
plt |
bio |
dirpos |
Minkenberg and Ottenheim
1990 |
tmp |
549.50 |
24.00 |
584.94 |
560.10 |
24.00 |
750.03 |
plt |
hrb |
bio |
none |
Munger 1992 |
tmp |
1086.60 |
16.00 |
713.20 |
1692.60 |
16.00 |
458.40 |
prd |
hrb |
bio |
none |
Munger 1992 |
trop |
6.00 |
117.00 |
9.08 |
0.80 |
51.00 |
1.14 |
chm |
hrb |
bio |
dirneg |
Murali and Sukumar 1993 |
trop |
22.00 |
15.00 |
38.73 |
0.00 |
15.00 |
0.00 |
prd |
hrb |
bio |
dirneg |
Naeem 1988 |
trop |
5.45 |
28.00 |
2.59 |
1.72 |
28.00 |
2.12 |
chm |
hrb |
bio |
dirneg |
Newbery and de Foresta 1984 |
trop |
7.79 |
12.00 |
1.97 |
3.79 |
6.00 |
1.49 |
res |
hrb |
bio |
inneg |
Newbery and de Foresta 1984 |
trop |
-0.20 |
9.00 |
0.90 |
3.50 |
10.00 |
2.53 |
res |
plt |
bio |
dirpos |
Nichols-Orians 1991 |
trop |
6.60 |
9.00 |
1.50 |
12.00 |
10.00 |
3.16 |
res |
plt |
chm |
dirpos |
Nichols-Orians 1991 |
trop |
-0.16 |
3.00 |
0.30 |
1.33 |
3.00 |
0.36 |
res |
plt |
bio |
dirpos |
Oberbauer and Strain 1985 |
tmp |
17.90 |
29.00 |
4.10 |
25.20 |
43.00 |
6.10 |
res |
hrb |
bio |
inpos |
Ohmart et al. 1985 |
tmp |
17.90 |
29.00 |
4.10 |
25.20 |
43.00 |
6.10 |
chm |
hrb |
bio |
inpos |
Ohmart et al. 1985 |
tmp |
27.60 |
10.00 |
3.80 |
19.80 |
38.00 |
2.00 |
res |
plt |
chm |
dirneg |
Ohmart et al. 1985 |
trop |
14.30 |
6.00 |
4.30 |
9.70 |
6.00 |
6.30 |
prd |
hrb |
div |
dirneg |
Otis et al. 1986 |
trop |
58.20 |
6.00 |
24.40 |
32.70 |
6.00 |
24.10 |
prd |
hrb |
bio |
dirneg |
Otis et al. 1986 |
trop |
0.39 |
20.00 |
0.45 |
1.30 |
20.00 |
0.49 |
hrb |
plt |
bio |
dirpos |
Oyama and Mendoza 1990 |
trop |
0.04 |
20.00 |
0.03 |
0.19 |
20.00 |
0.03 |
hrb |
plt |
bio |
dirneg |
Parra-Tabla and Bullock 1998 |
trop |
80.00 |
20.00 |
17.89 |
61.00 |
20.00 |
8.94 |
res |
plt |
bio |
dirpos |
Parra-Tabla and Bullock 1998 |
tmp |
52.60 |
1.00 |
8.20 |
15.30 |
2.00 |
4.10 |
prd |
hrb |
bio |
dirneg |
Pech et al. 1992 |
tmp |
33.80 |
6.00 |
9.80 |
26.10 |
6.00 |
6.12 |
hrb |
plt |
bio |
dirneg |
Polley and Detling 1988 |
tmp |
32.90 |
5.00 |
14.53 |
28.30 |
5.00 |
13.86 |
res |
hrb |
bio |
inneg |
Potter 1992 |
tmp |
329.70 |
5.00 |
86.76 |
426.50 |
5.00 |
122.54 |
res |
plt |
bio |
dirpos |
Potter 1992 |
tmp |
8.40 |
8.00 |
0.50 |
1.40 |
8.00 |
0.30 |
chm |
hrb |
sur |
dirneg |
Potter and Kimmerer 1989 |
tmp |
117.90 |
8.00 |
12.20 |
2.40 |
8.00 |
0.70 |
chm |
hrb |
bio |
dirneg |
Potter and Kimmerer 1989 |
tmp |
2.40 |
8.00 |
1.41 |
0.40 |
8.00 |
0.85 |
hrb |
plt |
div |
dirneg |
Prins and Nell 1990 |
tmp |
3.88 |
10.00 |
1.01 |
2.83 |
10.00 |
1.36 |
hrb |
plt |
sur |
dirneg |
Prins and Nell 1990 |
tmp |
168.30 |
79.00 |
44.30 |
123.50 |
79.00 |
23.90 |
chm |
hrb |
bio |
dirneg |
Puttick 1986 |
tmp |
3.80 |
11.00 |
3.20 |
19.70 |
11.00 |
12.10 |
chm |
hrb |
bio |
dirpos |
Rank 1992 |
tmp |
1.90 |
10.00 |
3.79 |
13.00 |
10.00 |
9.17 |
res |
plt |
bio |
dirpos |
Reichardt et al. 1991 |
tmp |
5.00 |
4.00 |
2.00 |
9.00 |
4.00 |
2.40 |
res |
plt |
chm |
dirpos |
Reichardt et al. 1991 |
tmp |
26.00 |
10.00 |
1.90 |
45.50 |
10.00 |
4.43 |
res |
hrb |
bio |
inpos |
Reichardt et al. 1991 |
trop |
16.30 |
6.00 |
5.90 |
0.00 |
2.00 |
0.00 |
prd |
plt |
bio |
dirneg |
Renner and Ricklefs 1998 |
tmp |
22.00 |
8.00 |
8.49 |
40.00 |
8.00 |
33.94 |
res |
plt |
bio |
dirpos |
Ritchie and Tilman 1993 |
tmp |
22.00 |
8.00 |
8.50 |
10.00 |
8.00 |
8.49 |
hrb |
plt |
bio |
dirneg |
Ritchie and Tilman 1993 |
tmp |
0.39 |
15.00 |
0.23 |
0.05 |
15.00 |
0.06 |
prd |
prd |
bio |
dirneg |
Rosenheim et al. 1993 |
tmp |
0.40 |
15.00 |
1.20 |
0.80 |
15.00 |
1.20 |
prd |
hrb |
bio |
inpos |
Rosenheim et al. 1993 |
tmp |
1.90 |
15.00 |
1.16 |
0.40 |
15.00 |
1.16 |
prd |
hrb |
bio |
dirneg |
Rosenheim et al. 1993 |
tmp |
30.00 |
5.00 |
15.65 |
6.00 |
5.00 |
0.00 |
hrb |
plt |
bio |
dirneg |
Schaffer and Mason 1990 |
tmp |
18.00 |
20.00 |
4.47 |
50.00 |
20.00 |
8.94 |
res |
plt |
bio |
dirpos |
Schmid et al. 1990 |
tmp |
4.50 |
4.00 |
1.20 |
8.20 |
4.00 |
1.60 |
res |
plt |
bio |
dirpos |
Schmitz 1993 |
tmp |
8.20 |
4.00 |
1.60 |
4.00 |
4.00 |
1.60 |
hrb |
plt |
bio |
dirneg |
Schmitz 1993 |
tmp |
8.20 |
4.00 |
1.60 |
5.00 |
4.00 |
2.00 |
prd |
plt |
bio |
inpos |
Schmitz 1993 |
tmp |
1.50 |
4.00 |
1.00 |
1.00 |
4.00 |
0.50 |
res |
plt |
bio |
none |
Simms 1987 |
tmp |
3.00 |
4.00 |
2.00 |
8.00 |
|
4.00 |
res |
plt |
bio |
dirpos |
Simms 1987 |
tmp |
1.01 |
14.00 |
0.69 |
0.01 |
27.00 |
0.64 |
chm |
hrb |
bio |
dirneg |
Speiser et al. 1992 |
trop |
268.70 |
3.00 |
77.70 |
78.70 |
3.00 |
31.70 |
prd |
prd |
bio |
dirneg |
Spiller and Schoener 1990 |
tmp |
15.80 |
8.00 |
1.70 |
6.40 |
8.00 |
4.24 |
prd |
hrb |
bio |
dirneg |
Stamp and Bowers 1988 |
tmp |
0.44 |
5.00 |
0.03 |
0.29 |
5.00 |
0.08 |
prd |
hrb |
bio |
dirneg |
Stamp and Bowers 1991 |
tmp |
9.10 |
22.00 |
0.70 |
7.20 |
22.00 |
0.47 |
chm |
prd |
bio |
inneg |
Stamp et al. 1991 |
trop |
1.95 |
10.00 |
0.38 |
1.69 |
10.00 |
0.27 |
prd |
hrb |
bio |
dirneg |
Suarez et al. 1998 |
tmp |
1.00 |
3.00 |
0.15 |
8.20 |
3.00 |
2.00 |
res |
plt |
bio |
dirpos |
sun Lee et al. 1986 |
tmp |
97.00 |
3.00 |
1.00 |
5.00 |
3.00 |
3.00 |
chm |
hrb |
bio |
dirneg |
Tahvanainen et al. 1985 |
tmp |
73.90 |
8.00 |
1.70 |
95.60 |
8.00 |
4.40 |
res |
plt |
bio |
dirpos |
Taylor and Davies 1986 |
tmp |
2.29 |
95.00 |
0.77 |
1.57 |
95.00 |
0.59 |
chm |
hrb |
bio |
dirneg |
Tscharntke 1988 |
trop |
1.60 |
3.00 |
1.70 |
5.20 |
3.00 |
5.00 |
res |
plt |
bio |
dirpos |
van der Meer et al. 1998 |
trop |
0.50 |
15.00 |
6.97 |
22.60 |
15.00 |
18.98 |
prd |
plt |
bio |
inpos |
Vasconcelos 1991 |
trop |
24.50 |
15.00 |
22.85 |
0.70 |
15.00 |
0.39 |
prd |
hrb |
bio |
dirneg |
Vasconcelos 1991 |
trop |
0.89 |
97.00 |
0.49 |
0.58 |
30.00 |
0.38 |
hrb |
plt |
bio |
dirneg |
Vasconcelos and Casimiro
1997 |
trop |
2.25 |
8.00 |
1.58 |
0.21 |
47.00 |
0.55 |
prd |
hrb |
bio |
dirneg |
Vasconcelos and Casimiro
1997 |
trop |
17.80 |
3.00 |
3.00 |
1.70 |
3.00 |
0.50 |
hrb |
plt |
sur |
dirneg |
Vasconcelos and Cherrett
1997 |
trop |
29.70 |
16.00 |
12.00 |
7.60 |
22.00 |
11.26 |
hrb |
plt |
bio |
dirneg |
Vasconcelos and Cherrett
1997 |
tmp |
0.69 |
4.00 |
0.20 |
0.25 |
4.00 |
0.10 |
hrb |
plt |
bio |
dirneg |
Vinton and Hartnett 1992 |
tmp |
26.10 |
35.00 |
25.44 |
14.90 |
35.00 |
12.42 |
prd |
plt |
chm |
inneg |
Vrieling et al. 1991 |
tmp |
1.10 |
60.00 |
1.16 |
0.60 |
60.00 |
0.77 |
hrb |
plt |
bio |
dirneg |
Vuorisalo et al. 1990 |
tmp |
4.00 |
20.00 |
1.34 |
7.80 |
20.00 |
1.30 |
hrb |
plt |
chm |
dirpos |
Wagner and Evans 1985 |
trop |
3.60 |
16.00 |
0.80 |
4.70 |
16.00 |
0.80 |
res |
plt |
bio |
dirpos |
Walker and Aplet 1994 |
tmp |
2.40 |
11.00 |
1.99 |
4.00 |
10.00 |
3.16 |
res |
hrb |
bio |
inpos |
Wallace and O'Dowd 1989 |
tmp |
13.00 |
29.00 |
7.00 |
7.80 |
31.00 |
3.90 |
res |
plt |
bio |
inneg |
Wallace and O'Dowd 1989 |
tmp |
30.40 |
19.00 |
20.05 |
0.60 |
18.00 |
0.42 |
hrb |
plt |
bio |
dirneg |
Wallace and O'Dowd 1989 |
tmp |
50.80 |
4.00 |
56.00 |
32.50 |
4.00 |
31.90 |
prd |
hrb |
sur |
dirneg |
Warrington 1985 |
tmp |
5.37 |
7.00 |
0.50 |
4.18 |
5.00 |
0.47 |
hrb |
plt |
bio |
dirneg |
Warrington et al. 1989 |
tmp |
5.70 |
4.00 |
1.80 |
4.75 |
4.00 |
1.40 |
res |
plt |
bio |
dirpos |
Watt 1989 |
tmp |
142.60 |
3.00 |
16.20 |
212.20 |
3.00 |
45.70 |
res |
plt |
chm |
dirpos |
Watt 1989 |
trop |
5.29 |
7.00 |
3.41 |
2.14 |
7.00 |
1.38 |
prd |
hrb |
bio |
dirneg |
Whalen and Mackay 1988 |
tmp |
1.80 |
10.00 |
0.63 |
10.10 |
10.00 |
3.48 |
res |
plt |
bio |
dirpos |
Widmann et al. 1990 |
tmp |
6.30 |
5.00 |
0.67 |
5.50 |
5.00 |
0.67 |
hrb |
plt |
bio |
dirneg |
Willis et al. 1993 |
lat = latitude; tmp = temperate; trop = tropical
conx/expx = control/experimental mean
conn/expn = control/experimental sample size
constd/expstd = control/experimental standard deviation
IV = independent variable
DV = dependent variable
DVm = response measured for the dependent variable
dirpos =
direct positive effect
inpos =
indirect positive effect
dirneg =
direct negative effect
inneg =
indirect negative effect
res = plant
resources (minerals or light)
hrb =
herbivores
prd =
predators
chm = plant
defense
plt = plants
bio = biomass
sur = survivorship/fitness
div =
diversity
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