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CORR IGENDUM
Biodiversity effects on ecosystem functioning change along
environmental stress gradients
Bastian Steudel,1,2* Andy Hector,3 Thomas Friedl,4 Christian L€ofke,5 Maike Lorenz,4 Moritz Wesche4 and Michael Kessler1
1Systematic Botany, University of Zurich, Zollikerstrasse 107, CH-8008, Zurich, Switzerland, 2Biodiversity, Macroecology & Conservation Biogeography Group, Faculty
of Forest Sciences and Forest Ecology, Georg-August-University G€ottingen, B€usgenweg 2, D-37077, G€ottingen, Germany, 3Institute of Evolutionary Biology and
Environmental Studies, University of Zurich, Winterthurerstrasse 190, CH-8057, Zurich, Switzerland, 4Department of Experimental Phycology and Culture Collection
of Algae (SAG), Albrecht-von-Haller-Institute for Plant Sciences, Georg-August-University G€ottingen, Nikolausberger Weg 18, D-37073, G€ottingen, Germany and5Institute of Applied Genetics and Cell Biology (IAGZ), University of Natural Resources and Life Sciences (BOKU), Muthgasse 18, A-1190, Vienna, Austria
*Correspondence: E-mail: [email protected]
Ecology Letters (2013) 16: 568–569
We regret that two errors were inadvertently introduced in the
paper by Steudel et al. (2012); their correction required changes to
Figs 2, S5 and S8 as well as to Tables 2 and 3:
1) Our erroneous inclusion of stress response intensity (SRI) in the
formula for calculating the relative stress-response buffering effect
(rSRBE) positively biased the slope of the relationship between the
Table 2 Empirical studies used for analyzing relationships between the relative stress-response buffering effect (rSRBE) and stress response intensity (SRI).
Reference Treatment log (aSRBE)
log (aSRBE) without
monocultures rSRBE
rSRBE without
monocultures
Stress response
intensity (SRI)
Allison 2004 Low 1 �0.416 NA 0.920 NA 0.73
Allison 2004 Low 2 �1.050 NA �0.481 NA 0.48
Caldeira et al. 2005 �1.653 NA 1.375 NA 0.84
De Boeck et al. 2008 A �0.916 NA �0.222 NA 0.33
De Boeck et al. 2008 B �1.050 NA �0.291 NA 0.29
De Boeck et al. 2008 C �0.223 NA 0.167 NA 0.40
De Boeck et al. 2008 D �0.844 NA �0.375 NA 0.25
De Boeck et al. 2008 E �0.619 NA �0.213 NA 0.20
De Boeck et al. 2008 F 0.890 NA �0.663 NA 0.17
Downing & Leibold 2010 Macrophyte �0.811 NA �0.089 NA 0.37
Downing & Leibold 2010 Herbivore �0.172 NA 0.470 NA 0.45
Dukes 2002 New 0.513 1.386 0.818 0.065 0.35
Dukes 2002 Established 0.030 0.715 0.109 �0.069 0.33
Goodsell & Underwood 2008 Bungan Head 0.932 NA 0.223 NA 0.21
Goodsell & Underwood 2008 Narrabeen Head 0.560 NA 0.129 NA 0.24
Hughes & Stachowicz 2004 1.887 �0.260 0.196 0.163 0.48
Ji et al. 2009 Grasses 2004 0.194 NA 0.249 NA 0.34
Ji et al. 2009 N-fixers 2004 �1.444 �1.641 �1.327 �0.243 0.50
Ji et al. 2009 N-fixers 2005 �0.007 0.755 1.589 1.316 0.60
Ji et al. 2009 Forbs 2005 0.087 NA 0.371 NA 0.22
Joshi et al. 2000 0.513 �0.065 2.900 0.1 0.71
Langenheder et al. 2012 �0.074 NA 0.042 �0.156 0.14
Lanta et al. 2012 2003 �0.239 NA �0.037 0.053 0.12
Lanta et al. 2012 2004 0.125 NA 0.371 0.432 0.32
Lanta et al. 2012 2005 �1 NA �0.338 �0.256 0.13
Liiri et al. 2002 �0.083 NA 0.933 NA 0.47
Mulder et al. 2001 2.140 NA 0.553 NA 0.34
Nagase & Dunnett 2010 Root �0.827 1.078 0.487 2.079 0.56
Nagase & Dunnett 2010 Shoot 0.000 0.047 0.005 0.212 0.29
Roger et al. 2012 High temperature NA NA �0.725 NA 0.47
Roger et al. 2012 Low salinity NA NA �0.386 NA 0.53
Steudel et al. 2011 Above-ground drought 0.573 0.570 0.270 0.262 0.21
Steudel et al. 2011 Above-ground salt 0.610 0.525 0.284 0.225 0.20
Steudel et al. 2011 Above-ground shade 0.772 0.733 0.543 0.488 0.38
Steudel et al. 2011 Below-ground drought 0.578 0.788 0.785 1.094 0.49
Steudel et al. 2011 Below-ground salt 0.501 0.564 0.495 0.493 0.36
Steudel et al. 2011 Below-ground shade �0.675 0.960 3.018 8.096 0.82
© 2013 Blackwell Publishing Ltd/CNRS
Ecology Letters, (2013) 16: 568–569 doi: 10.1111/ele.12079
relative biodiversity effect of the control treatment (rBEc) and the
predicted slope at high stress intensities. The correct rSRBE is the
difference between the relative biodiversity effect of the stress treat-
ment (rBEs) and the rBEc (rBEs-rBEc). Reanalysis of the corrected
data resulted in a positive relationship between rSRBE and SRI
when the monoculture data are excluded in our mixed models anal-
ysis with literature and our own experimental data combined (Fig. 2,
Table 2, Table 3) and with literature data only (Fig. 2, Table 2).
However, reanalysis of only our experimental data revealed no sig-
nificant relationship (Fig. S5A). With the monoculture data included,
the relationship between rSRBE and SRI was positive for the litera-
ture data alone and in combination with our experimental data (Fig.
S8). Again, reanalysis of our experimental data only revealed no sig-
nificant relationship (Fig. S5B). Addition of three new case studies
to the literature analysis with our experimental data included
(Langenheder et al. 2012, Lanta et al. 2012, Roger et al. 2012) con-
firmed the positive relationship when monoculture data are
excluded from the analysis (Fig. 2) or included in the analysis (Fig.
S8). Thus, despite the miscalculation of the rSRBE in our original
paper, the main conclusion of a positive relationship between
rSRBE and SRI is essentially confirmed by the correct analysis. We
thank Dr. T. Banitz for pointing out the mistake.
2) In the figure of Box 1, the absolute stress-response buffering
effect (aSRBE) was incorrectly defined as aBEc/aBEs instead of
aBEs/aBEc, as was correctly stated in the main text. This typo-
graphical error had no consequences for the reported results or
conclusions.
REFERENCES
Langenheder, S., Bulling, M.T., Prosser, J.I. & Solan, M. (2012). Role of
functionally dominant species in varying environmental regimes: evidence for
the performance-enhancing effect of biodiversity. BMC Ecology, 12, 14.
Lanta, V., Dolezal, J., Zemkova, L. & Leps, J. (2012). Communities of different
plant diversity respond similarly to drought stress: experimental evidence from
field non-weeded and greenhouse conditions. Naturwissenschaften, 99, 473–482.Roger, F., Godhe, A. & Gamfeldt, L. (2012). Genetic diversity and ecosystem
functioning in the face of multiple stressors. PloS One, 7, e45007.
Steudel, B., Hector, A., Friedl, T., L€ofke, C., Lorenz, M., Wesche, M. & Kessler,
M. (2012). Biodiversity effects on ecosystem functioning change along
environmental stress gradients. Ecol. Lett., 15, 1397–1405.
Table 3 Measurements of stress-response buffering effects (SRBE) and stress response intensity (SRI) of our algal experiment.
Salinity or temperature log (aSRBE)
log (aSRBE)
without monocultures rSRBE
rSRBE
without monocultures
Stress response
intensity (SRI)
0.13% 0.488 0.472 0.288 0.356 0.24
0.25% 0.155 0.258 0.148 0.242 0.25
0.50% �0.180 �0.321 0.052 0.002 0.25
1.00% �0.248 �0.183 0.125 0.157 0.39
1.50% �0.847 �1.264 �0.047 �0.174 0.40
2.50% �1.724 �0.816 �0.193 �0.057 0.46
27.5 °C 0.151 0.211 0.178 0.125 0.06
30.0 °C 0.538 0.538 0.536 0.613 0.32
32.5 °C 0.311 0.705 0.631 1.007 0.40
35.0 °C 0.032 �0.280 0.279 0.086 0.45
37.5 °C �1.553 �1.333 �0.022 �0.069 0.65
40.0 °C �1.305 �0.889 0.036 0.307 0.72
Figure 2 Relationships between relative stress-response buffering effect (rSRBE)
calculated without monoculture data and stress response intensity (SRI) derived
from monoculture data. Black dots represent literature data, grey dots data from
our algal experiment. Black triangles represent studies not included in the
published paper. The black line is the regression line of a linear mixed model
including published data only, with ‘study’ treated as random factor
(intercept = �4.24, SE = 1.17, t = �3.63; slope = 10.36, SE = 1.98, t = 5.22;
P = 0.001, n = 6). The grey line is the regression line of a linear mixed model
including published data and those of the present experiment, with ‘study’
treated as random factor (intercept = �1.26, SE = 0.76, t = �1.66,
slope = 4.45, SE = 1.52; t = 2.92, P = 0.009, n = 7). The dashed line is the
regression line of a linear mixed model including all data (published, algae, and
new studies), with ‘study’ treated as random factor (intercept = �1.02,
SE = 0.58, t = �1.94, slope = 2.23, SE = 0.55, t = 4.07, P = 0.0046, n = 9).
© 2013 Blackwell Publishing Ltd/CNRS
Corrigendum Corrigendum 569