To identify the Rattus species dominating islands in the reservoir, we collected tissue samples from multiple sites in the reservoir; all individuals were identified as Rattus tiomanicus
Trang 1www.sciencemag.org/content/341/6153/1508/suppl/DC1
Supplementary Materials for
Near-Complete Extinction of Native Small Mammal Fauna 25 Years
After Forest Fragmentation
*Corresponding author E-mail: lggibson@nus.edu.sg (L.G.); fhe@mail.sysu.edu.cn (F.H.);
dbsbdp@nus.edu.sg (D.P.B.)
Published 27 September 2013, Science 341, 1508 (2013)
DOI: 10.1126/science.1240495
This PDF file includes:
Materials and Methods
Figs S1 to S3
Tables S1 to S3
References (31–38)
Trang 2Supplementary Materials
Materials and Methods: We surveyed islands in Chiew Larn Reservoir in Surat Thani province,
Thailand 5-7 years following isolation (1992-1994) and 25-26 years following isolation (2012-2013) We selected islands of various sizes (< 1 to > 50 ha) in remote parts of the reservoir, mostly in the upper reservoir where there are more islands and where there is little human
disturbance We did not survey islands where there was any human presence The same 12 islands were sampled during both time periods, but most were small islands (Table 1) To ensure findings from the large islands were representative, we also sampled four additional large islands
in the most recent surveys
We used trapping transects to survey small mammal communities Sampling effort was
small islands (~ 1 ha), 4-5 transects on medium islands (~ 10-25 ha), and approximately 8-10
transects on large islands (~ 50 ha) (31) Consequently, larger islands were sampled more
intensively than smaller islands on an absolute basis, but less intensively per unit area Trapping transects spanned 135 m In each transect, 10 Tomahawk live traps were placed on the ground at every 15 m, and 4 Sherman live traps were mounted on lianas or fallen trees 0.5-2 m above the ground every 45 m Traps were baited with a mixture of bananas and coconut pieces covered in peanut butter Each island was sampled for seven consecutive days and traps were checked before 11:00 am to ensure the safety of trapped animals
Captured animals were handled briefly for identification, marked using ear tags, and released unharmed within a few minutes Species were identified using a regional guidebook
Trang 3(24) To identify the Rattus species dominating islands in the reservoir, we collected tissue samples from multiple sites in the reservoir; all individuals were identified as Rattus tiomanicus
by J-F Cosson using genetic markers
To compare the number of species on islands between different sampling periods, we applied a generalized linear model with a gamma error distribution and log-link function to account for the non-normal nature of our response variable and for predictor heteroscedasticity
We compared and ranked models using Akaike’s information criterion corrected for small
via its percent deviance explained (%DE)
We developed an island biogeographic model to predict the number of species on forest fragments after time since isolation Before isolation, the equilibrium number of species on an
island is assumed to follow a power-law model (34)
island, and c and z are constants Simple power-law species-area relationships generally perform best across datasets (35)
The theory of island biogeography postulates that the change in the number of species on
an island would be
new species immigrating to an island during the elapsed time interval (t, t+1), and E is the
Trang 4number of extinctions (including permanent emigration) on an island during the elapsed time
interval There are several ways to define I and E For example, they can be functions of island
size and the number of resident species on the island The number of parameters can quickly increase if we consider both area and number of species for each parameter Here, we consider a simple model
𝑑𝑆
rates This leads to
𝑆𝑡= 𝐼0 𝑆𝑚
𝐼0+𝐸0− �𝐼0 𝑆𝑚
number of species of the original system Substituting model (S1) into the above equation and
simplifying notation, we obtain
the main text fits our data well (R 2 = 0.783; Fig S1)
that have been used to model SAR for relatively small areas (as in our study) are the Gleason
Trang 5S1), but model (S5) with the S0 Gleason SAR substitution provided a poorer fit (R2 = 0.704) We therefore only present results based on the more common power-law model in the main text
We completed all statistical analyses and figures using the R statistical package, version
2.12.2 (38)
Trang 6Fig S1 Rarefied small mammal species richness in large (10.1-56.3 ha, n = 7) and small
(0.3-4.7 ha, n = 9) islands 5-7 years (dark tones) and 25-26 years (light tones) following isolation
Rarefaction was based on 10 samples for each island; islands with fewer than 10 individuals were excluded We also used rarefied levels of 5 and 8 individuals, but the results remained the same and are not reported Plotted are median values, interquartile ranges, and full ranges The upper horizontal dashed line represents the number of small mammal species found on the mainland (Table S3)
Trang 7Fig S2 Mean small mammal species richness per transect in large (10.1-56.3 ha, n = 7) and
small (0.3-4.7 ha, n = 9) islands 5-7 years (dark tones) and 25-26 years (light tones) following
isolation Plotted are median values, interquartile ranges, and full ranges The upper horizontal dashed line represents the number of small mammal species found on the mainland (Table S3)
Trang 8Fig S3 Predicted vs observed number of species on forest fragments Predicted number of
species is based on model (1)
Trang 9y
Trang 105 1 3 1 2 1 1 6
Trang 1112 1 11 1 3
Trang 12X3 1 8 1
Trang 13X3 1 1 10 2
Table S1 Small mammal abundance and richness per transect on islands in Chiew Larn
Reservoir Three sampling periods were made 5-7 years following isolation (1992-1994), and two were made 25-26 years following isolation (2012-2013) Total species richness per transect
is listed in the final column
Trang 14Model LL k ΔAICc wAIC c %DE
Table S2 Predictors of species richness for forest fragments (years since fragment isolation and
island area) Shown are the top-ranked generalized linear models testing five potential
predictors Included for each model is maximum log-likelihood (LL), number of parameters (k),
change in Akaike’s information criterion corrected for small samples relative to the top-ranked
Trang 15Table S3 Small mammal abundance and richness on mainland control sites surrounding Chiew Larn Reservoir Order, family, and
species names are listed The three same sites were surveyed 5, 6, 7, and 25 years following isolation (1992-1994, 2012); a different site was surveyed 26 years following isolation (2013) due to changes in the direction of research All sites were located adjacent to the
reservoir and within a few kilometers from other island sites Sampling methods were identical to those used on islands (18) Total
Trang 16species richness per site is listed in the final column Rattus tiomanicus does not occur naturally in undisturbed forest surrounding
Chiew Larn Reservoir; all other species are native
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