Supporting Online Material for

Similar documents
The Origin of Species: Lizards in an Evolutionary Tree

LOOK WHO S COMING FOR DINNER: SELECTION BY PREDATION

Experimental evidence that competition and habitat use shape the individual fitness surface

Is it better to be bigger? Featured scientists: Aaron Reedy and Robert Cox from the University of Virginia Co-written by Matt Kustra

Hind-Limb Length Plasticity in Anolis carolinensis

LIZARD EVOLUTION VIRTUAL LAB

Pulses of marine subsidies amplify reproductive potential of lizards by increasing individual growth rate

Effects of Hind-Limb Length and Perch Diameter on Clinging Performance in Anolis Lizards from the British Virgin Islands

The Origin of Species: Lizards in an Evolutionary Tree

Effects of prey availability and climate across a decade for a desert-dwelling, ectothermic mesopredator. R. Anderson Western Washington University

Chapter 16: Evolution Lizard Evolution Virtual Lab Honors Biology. Name: Block: Introduction

City slickers: poor performance does not deter Anolis lizards from using artificial substrates in human-modified habitats

Egg environments have large effects on embryonic development, but have minimal consequences for hatchling phenotypes in an invasive lizard

Larval thermal windows in native and hybrid Pseudoboletia progeny (Echinoidea) as potential drivers of the hybridization zone

Seasonal Shifts in Reproductive Investment of Female Northern Grass Lizards ( Takydromus septentrionalis

1.5 C: Role of the Environment in Evolution Quiz

Adjustment Factors in NSIP 1

Gulf and Caribbean Research

A Population Analysis of the Common Wall Lizard Podarcis muralis in Southwestern France

Morphological Variation in Anolis oculatus Between Dominican. Habitats

Habitats and Field Methods. Friday May 12th 2017

Incubation temperature and phenotypic traits of Sceloporus undulatus: implications for the northern limits of distribution

THERE S A NEW KID IN TOWN HOW NATIVE ANOLES AVOID COMPETITION FROM INVASIVE ANOLES

STAT170 Exam Preparation Workshop Semester

SEXUAL DIMORPHISM IN BODY SHAPE WITHOUT SEXUAL DIMORPHISM IN BODY SIZE IN WATER SKINKS (EULAMPRUS QUOYII)

DECREASED SPRINT SPEED AS A COST OF REPRODUCTION IN THE LIZARD SCELOPORUS OCCIDENTALS: VARIATION AMONG POPULATIONS

Consequences of Extended Egg Retention in the Eastern Fence Lizard (Sceloporus undulatus)

Name Class Date. How does a founding population adapt to new environmental conditions?

Relationship between hatchling length and weight on later productive performance in broilers

Biochemical HA T FT AD Iceland (1,2) Cohort IM Clinical HA. 10 follicles 2 10 mm or > 10 cc volume. > 63 ng/dl NA >3.8 ng/ml. menses/yr.

Supplementary Fig. 1: Comparison of chase parameters for focal pack (a-f, n=1119) and for 4 dogs from 3 other packs (g-m, n=107).

Effects of nest temperature and moisture on phenotypic traits of hatchling snakes (Tropidonophis mairii, Colubridae) from tropical Australia

EXPERIMENTAL ANALYSIS OF AN EARLY LIFE-HISTORY STAGE: SELECTION ON SIZE OF HATCHLING TURTLES

The influence of invasive fire ants on survival, space use, and patterns of natural selection in juvenile lizards

PROCEEDINGS OF THE FORTEENTH SYMPOSIUM ON THE NATURAL HISTORY OF THE BAHAMAS

SUPPLEMENTARY INFORMATION

Pierre-Louis Toutain, Ecole Nationale Vétérinaire National veterinary School of Toulouse, France Wuhan 12/10/2015

Variation in Piglet Weights: Development of Within-Litter Variation Over a 5-Week Lactation and Effect of Farrowing Crate Design

The effect of weaning weight on subsequent lamb growth rates

STATISTICAL REPORT. Preliminary Analysis of the Second Collaborative Study of the Hard Surface Carrier Test

Econometric Analysis Dr. Sobel

A COMPARATIVE TEST OF ADAPTIVE HYPOTHESES FOR SEXUAL SIZE DIMORPHISM IN LIZARDS

17 th Club Phase 1 Annual Meeting April 5, Pierre Maison-Blanche Hopital Bichat, Paris, France

CAMBRIDGE, MASS. 26 MARCH 2010 NUMBER 519 CRUISE FORAGING OF INVASIVE CHAMELEON (CHAMAELEO JACKSONII XANTHOLOPHUS) IN HAWAI I

Appendix from T. J. Ord and J. A. Stamps, Species Identity Cues in Animal Communication

THE EFFECTS OF MORPHOLOGY AND PERCH DIAMETER ON SPRINT PERFORMANCE OF ANOLIS LIZARDS

Bio4009 : Projet de recherche/research project

Grade: 8. Author: Hope Phillips

Supplement of Changes in soil carbon and nutrients following 6 years of litter removal and addition in a tropical semi-evergreen rain forest

A Comparison of morphological differences between Gymnophthalmus spp. in Dominica, West Indies

Impact of colour polymorphism in free ranging asp vipers

Genetics of temperament: What do we know about the back test?

Dominance/Suppression Competitive Relationships in Loblolly Pine (Pinus taeda L.) Plantations

A Genetic Comparison of Standard and Miniature Poodles based on autosomal markers and DLA class II haplotypes.

Biodiversity and Extinction. Lecture 9

Population Size, Trend, and Immigration in a Tennessee Population of Mediterranean Geckos (Hemidactylus turcicus)

Larkey Genetics Code

Dr. Jerry Shurson 1 and Dr. Brian Kerr 2 University of Minnesota, St. Paul 1 and USDA-ARS, Ames, IA 2

Chapter 18: Categorical data

Climatic control of trophic interaction strength: the evect of lizards on spiders

Detective Work in the West Indies: Integrating Historical and Experimental Approaches to Study Island Lizard Evolution

Phenotypic correlates of hybridisation between red and sika deer (genus Cervus)

Comparative Morphology of Western Australian Varanid Lizards (Squamata: Varanidae)

SCIENTIFIC REPORT. Analysis of the baseline survey on the prevalence of Salmonella in turkey flocks, in the EU,

Texas Quail Index. Result Demonstration Report 2016

from an experimental bag net SHIODE, DAISUKE; TAKAHASHI, MUTSUKI Proceedings of the 6th Internationa SEASTAR2000 workshop) (2011): 31-34

SEVERAL fundamental studies in community ecology

This is the book of David, the son of Abraham and the father of Jesus Christ Matthew 1.1. Declaration

COOPERATIVE EXTENSION Bringing the University to You

COMPARING BODY CONDITION ESTIMATES OF ZOO BROTHER S ISLAND TUATARA (SPHENODON GUNTHERI) TO THAT OF THE WILD, A CLINICAL CASE

Motuora island reptile monitoring report for common & Pacific gecko 2016

SEDAR31-DW30: Shrimp Fishery Bycatch Estimates for Gulf of Mexico Red Snapper, Brian Linton SEDAR-PW6-RD17. 1 May 2014

Rubber Boas in Radium Hot Springs: Habitat, Inventory, and Management Strategies

Post-Release Success of Captive Bred Louisiana Pine Snakes

The Power of NSIP to Increase Your Profits. August 17, 2015 Rusty Burgett, Program Director

Selection for Egg Mass in the Domestic Fowl. 1. Response to Selection

Effects of Natural Selection

Analysis of Sampling Technique Used to Investigate Matching of Dorsal Coloration of Pacific Tree Frogs Hyla regilla with Substrate Color

RELATIONSHIP BETWEEN GROWTH OF SUFFOLK RAMS ON CENTRAL PERFORMANCE TEST AND GROWTH OF THEIR PROGENY

Maturity and Other Reproductive Traits of the Kanahebi Lizard Takydromus tachydromoides (Sauria, Lacertidae) in Mito

Comparison of different methods to validate a dataset with producer-recorded health events

Habitats and Field Techniques

COULD YOU HAVE RIDDEN A HORSE MILLIONS OF YEARS AGO? Horse evolution goes back more than 55 million years

PATTERNS OF EVOLUTION STATIONS

Tuesday, December 6, 11. Mesozoic Life

The Effect of Phase Shifts in the Day-Night Cycle on Pigeon Homing at Distances of Less than One Mile

The island syndrome in lizards

Adjustments In Parental Care By The European Starling (Sturnus Vulgaris): The Effect Of Female Condition

An Estimate of the Number of Dogs in US Shelters. Kimberly A. Woodruff, DVM, MS, DACVPM David R. Smith, DVM, PhD, DACVPM (Epi)

Anole Density and Biomass in Dominica. TAMU Study Abroad Dr. Woolley, Dr. Lacher Will Morrison Lori Valentine Michael Kerehgyarto Adam Burklund

SEASONAL PATTERNS OF NESTING IN THE RED-WINGED BLACKBIRD MORTALITY

206 Adopted: 4 April 1984

Lab Report These are the questions you are asked to answer as you go through the lab. Your lab notebook begins after the questions (page 3).

POPULATION TRENDS OF THE COMMON QUAIL (Coturnix coturnix) IN FRANCE AND SPAIN: CONFLICTING DATA OR CONTROVERSIAL CENSUS METHODOLOGIES?

PROBABLE NON-BREEDERS AMONG FEMALE BLUE GROUSE

Multiclass and Multi-label Classification

Active Bacterial Core Surveillance Site and Epidemiologic Classification, United States, 2005a. Copyright restrictions may apply.

NSIP EBV Notebook June 20, 2011 Number 2 David Notter Department of Animal and Poultry Sciences Virginia Tech

LIZARD HOME RANGES REVISITED: EFFECTS OF SEX, BODY SIZE, DIET, HABITAT, AND PHYLOGENY

Section A. Answer all questions. Answer each question in the space provided for that question. Use 90 and Over on page 2 of the Data Sheet.

Transcription:

www.sciencemag.org/cgi/content/full/314/5802/1111/dc1 Supporting Online Material for Rapid Temporal Reversal in Predator-Driven Natural Selection Jonathan B. Losos,* Thomas W. Schoener, R. Brian Langerhans, David A. Spiller *To whom correspondence should be addressed. E-mail: jlosos@oeb.harvard.edu This PDF file includes: Materials and Methods Fig. S1 Table S1 Reference Published 17 November 2006, Science 314, 1111 (2006) DOI: 10.1126/science.1133584

1 Supplementary Information Methods L. carinatus were introduced to islands near Great Abaco, Bahamas, in early June, 2003 (details in (S1)). Prior to this introduction, we captured A. sagrei (> 33 mm snoutvent length) on all 12 islands. For individual identification, each lizard received an island-unique pattern of colored marks by injecting elastomer (Northwest Marine Technologies) subdermally into two limb segments. In November 2003 and May 2004, we censused nearly exhaustively on each island to determine surviving individuals. Standardized selection gradients were calculated on relative hindlimb length for each island for 0-6 and 6-12 months. Relative hindlimb length was calculated (using only males) as the residual of ln-transformed hindlimb length versus ln snout-vent length (SVL) using the regression for all individuals from all islands (between-island heterogeneity in slope is not significant in ANCOVA). SVL was also included in the regression equation used to calculate selection gradients. Selection gradients could only be calculated on islands for which some, but not all, lizards died. Because survival of marked lizards was either 0 or 100% on some islands in some of the time periods, our sample size was reduced to nine islands in the first time period and five in the second time period; those five islands were used in the repeated measures analysis. On these islands, an average of 20.6 males was measured at the start of the experiment; survival rates were 33% and 58% in the 0-6 and 6-12 month periods. Habitat-use data were recorded immediately prior to and after the introduction as in (S1). Data on marked individuals were collected on all 12 islands in November 2003 and May 2004, whereas in May 2003 habitat data on marked individuals were only

2 collected on two introduction and two control islands. Habitat data were logtransformed. The time*treatment interaction from a repeated-measures ANCOVA was used to test differences in selection gradients after the first versus second six-month periods; the model included log-transformed island vegetated area as a covariate, and the repeated factors time and time*area were also significant (P = 0.0l3, 0.014). We report the unweighted (by sample size), rather than, as in reference (S1), the weighted analysis because sample size changed from the first to the second time period; using the mean sample size as weights gave only a slightly higher P value for the interaction of interest (P = 0.021 vs. 0.017). An alternative explanation for these results is that selection favored the same limb length in both treatments in the second time period, but that because of differences in trait distribution between the treatments, selection gradients differed between them. However, analysis of selection gradients calculated from quadratic regression reveals no consistent evidence across islands for stabilizing selection in either treatment; moreover, examination of survival vs. non-survival over the range of limb lengths found in both treatments reveals a clear difference in patterns of selection (Figure S1). A second repeated-measures analysis tested the significance of the time*treatment interaction for perch diameter using data from the beginning and end of the second sixmonth period (Nov. 2003 and May 2004); no covariate was used here. On September 3, 2004, the experiment was terminated by the storm surge associated with Hurricane Frances.

3 References: S1. J. B. Losos, T. W. Schoener, D. A. Spiller. Nature 432, 505 (2004). Figure S1 caption Selection gradients calculated with data pooled across islands within treatments were highly similar to estimated treatment means using island-specific gradients (n = 4, r = 0.98, P = 0.017). Therefore, we used the pooled dataset with its higher sample size to visualize the fitness functions. Fitness functions were generated using the nonparametric cubic-spline regression technique. The solid line represents mean survival probability and the dashed lines indicate ± 1 SE of predicted values from 1000 bootstrap replicates of the fitness function. To control for possible effects of differences in the phenotypic range among treatments, fitness functions were generated excluding individuals with limb lengths not present in the alternative treatment (i.e., three lizards in the experimental treatment had relatively longer limbs than any lizard in the control treatment and two lizards in the control treatment had shorter limbs than any lizard in the experimental treatment).

4 Supplementary Figure 1 Control Islands Introduction Islands 1.0 1.0 0.9 0.9 0.8 0.8 0.7 0.7 Survival 0.6 0.5 0.4 Survival 0.6 0.5 0.4 0.3 0.3 0.2 0.2 0.1 0.1 0.0 0.0-0.03-0.02-0.01 0.00 0.01 0.02 0.03 0.04-0.03-0.02-0.01 0.00 0.01 0.02 0.03 0.04 Relative Limb Length Relative Limb Length

5 Table S1. Selection gradients ± 1 SE for relative hindlimb length (adjusted for vegetated island area using ANCOVA; see Methods), and mean limb lengths (residual values 100 ± 1 s.e.) for lizards that either died or survived. Subscripts indicate the time period examined (1: first six months, 2: second six months, 1+2: all 12 months). Note that the survivors for the second period are the same as the survivors for the 12 month period. NA indicates that the standard error is not available because it could not be calculated due to a lack of degrees of freedom. Selection Gradient Mean Relative Hindlimb Length Island β 1 β 2 β 1+2 Died 1 Lived 1 Died 2 Lived 2, 1+2 Died 1+2 Control Islands -0.07 ± 0.25-0.17 ± 0.29-0.11 ± 0.59 0.01 ± 0.28 0.12 ± 0.27 0.52 ± 0.32-0.01 ± 0.45 0.09 ± 0.32 1-0.15 ± 0.12 (25) 0.07 ± 0.14 (19) -0.18 ± 0.15 (25) 1.48 ± 0.57 0.17 ± 0.34-0.05 ± 0.23 0.23 ± 0.42 0.87 ± 0.74 6-0.28 ± 0.48 (25) -0.59 ± 0.39 (4) -0.67 ± 0.54 (25) -0.58 ± 0.42-2.08 ± 0.53-0.10 ± 0.00-2.73 ± 1.40-0.56 ± 0.44 Buddy 0.21 ± 0.46 (12) 0.01 ± NA (3) 0.52 ± 0.70 (12) 0.42 ± 0.41 2.70 ± 0.28 3.40 ± 0.00 2.35 ± 0.61 0.72 ± 0.52 Introduction Islands 0.70 ± 0.32-1.68 ± 0.36-0.59 ± 0.74 0.82 ± 0.42 1.48 ± 0.34 2.44 ± 0.33-0.06 ± 0.66 1.23 ± 0.42 5 1.03 ± 0.32 (23) -1.39 ± 0.42 (8) 0.17 ± 0.51 (23) 1.26 ± 0.52 1.93 ± 0.44 2.50 ± 0.61 0.58 ± 0.78 1.52 ± 0.55 x3 0.37 ± 0.41 (14) -1.97 ± 0.28 (5) -1.35 ± 1.12 (14) 0.09 ± 0.69 1.38 ± 0.17 2.38 ± 0.28-2.60 ± 0.00 0.79 ± 0.67