Volume 26, Issue 23, Pages (December 2016)

Slides:



Advertisements
Similar presentations
Toward urgent forecasting of aftershock hazard: Simultaneous estimation of b-value of the Gutenberg-Richter ’ s law of the magnitude frequency and changing.
Advertisements

Ancient Wolf Genome Reveals an Early Divergence of Domestic Dog Ancestors and Admixture into High-Latitude Breeds  Pontus Skoglund, Erik Ersmark, Eleftheria.
Piercing of Consciousness as a Threshold-Crossing Operation
Volume 22, Issue 11, Pages (June 2012)
Volume 23, Issue 19, Pages (October 2013)
Adaptive Evolution of Gene Expression in Drosophila
Araceli Ramirez-Cardenas, Maria Moskaleva, Andreas Nieder 
Volume 21, Issue 8, Pages (April 2011)
Equilibrium Bird Species Diversity in Atlantic Islands
Mark J. Costello, Chhaya Chaudhary  Current Biology 
Biodiversity and Ecosystem Functioning: The Mystery of the Deep Sea
Volume 26, Issue 7, Pages (April 2016)
Volume 25, Issue 24, Pages (December 2015)
With Age Comes Representational Wisdom in Social Signals
Volume 27, Issue 20, Pages e9 (October 2017)
Volume 24, Issue 4, Pages (February 2014)
Aaron C. Hartmann, Andrew H. Baird, Nancy Knowlton, Danwei Huang 
Evolutionary Rewiring of Human Regulatory Networks by Waves of Genome Expansion  Davide Marnetto, Federica Mantica, Ivan Molineris, Elena Grassi, Igor.
Vincent B. McGinty, Antonio Rangel, William T. Newsome  Neuron 
Nathan F. Putman, Katherine L. Mansfield  Current Biology 
Coupling Genetic and Ecological-Niche Models to Examine How Past Population Distributions Contribute to Divergence  L. Lacey Knowles, Bryan C. Carstens,
Human Disruption of Coral Reef Trophic Structure
Archerfish Actively Control the Hydrodynamics of Their Jets
Volume 111, Issue 2, Pages (July 2016)
Double Jeopardy and Global Extinction Risk in Corals and Reef Fishes
Gene-Expression Variation Within and Among Human Populations
Molecular Phylogenetics and the Diversification of Hummingbirds
Volume 23, Issue 10, Pages (October 2016)
Cultural Confusions Show that Facial Expressions Are Not Universal
Morphological Phylogenetics in the Genomic Age
Volume 21, Issue 5, Pages (March 2011)
Volume 25, Issue 1, Pages 1-9 (January 2015)
Nicolas Catz, Peter W. Dicke, Peter Thier  Current Biology 
Volume 27, Issue 14, Pages e8 (July 2017)
Volume 24, Issue 5, Pages (March 2014)
Patterns of Genetic Coding Variation in a Native American Population before and after European Contact  John Lindo, Mary Rogers, Elizabeth K. Mallott,
Volume 26, Issue 21, Pages (November 2016)
Integration Trumps Selection in Object Recognition
BOLD fMRI Correlation Reflects Frequency-Specific Neuronal Correlation
Genomic Flatlining in the Endangered Island Fox
Sriram Sankararaman, Swapan Mallick, Nick Patterson, David Reich 
Volume 19, Issue 15, Pages (August 2009)
A Scalable Population Code for Time in the Striatum
Volume 8, Issue 3, Pages (March 2015)
Volume 28, Issue 4, Pages e6 (February 2018)
Volume 25, Issue 15, Pages (August 2015)
Volume 26, Issue 5, Pages (March 2016)
Adaptation can explain evidence for encoding of probabilistic information in macaque inferior temporal cortex  Kasper Vinken, Rufin Vogels  Current Biology 
Volume 26, Issue 11, Pages (June 2016)
Volume 22, Issue 1, Pages (January 2012)
Benjamin Pettit, Zsuzsa Ákos, Tamás Vicsek, Dora Biro  Current Biology 
Identical Skin Toxins by Convergent Molecular Adaptation in Frogs
Evolution of senescence: Alzheimer's disease and evolution
Selecting a Maximally Informative Set of Single-Nucleotide Polymorphisms for Association Analyses Using Linkage Disequilibrium  Christopher S. Carlson,
Volume 25, Issue 4, Pages (February 2015)
Kevin R. Foster, Thomas Bell  Current Biology 
Humans Can Continuously Optimize Energetic Cost during Walking
Sriram Sankararaman, Swapan Mallick, Nick Patterson, David Reich 
Oligocene CO2 Decline Promoted C4 Photosynthesis in Grasses
Rapid Evolution of the Cerebellum in Humans and Other Great Apes
Ancient Wolf Genome Reveals an Early Divergence of Domestic Dog Ancestors and Admixture into High-Latitude Breeds  Pontus Skoglund, Erik Ersmark, Eleftheria.
Marie P. Suver, Akira Mamiya, Michael H. Dickinson  Current Biology 
Volume 26, Issue 23, Pages (December 2016)
Yafei Mao, Evan P. Economo, Noriyuki Satoh  Current Biology 
Volume 21, Issue 23, Pages (December 2011)
Volume 25, Issue 10, Pages (May 2015)
The Geography of Ecological Niche Evolution in Mammals
Volume 27, Issue 20, Pages e4 (October 2017)
Biodiversity and Ecosystem Functioning: The Mystery of the Deep Sea
Michael S.Y. Lee, Julien Soubrier, Gregory D. Edgecombe 
Presentation transcript:

Volume 26, Issue 23, Pages 3190-3194 (December 2016) Empty Niches after Extinctions Increase Population Sizes of Modern Corals  Carlos Prada, Bishoy Hanna, Ann F. Budd, Cheryl M. Woodley, Jeremy Schmutz, Jane Grimwood, Roberto Iglesias-Prieto, John M. Pandolfi, Don Levitan, Kenneth G. Johnson, Nancy Knowlton, Hiroaki Kitano, Michael DeGiorgio, Mónica Medina  Current Biology  Volume 26, Issue 23, Pages 3190-3194 (December 2016) DOI: 10.1016/j.cub.2016.09.039 Copyright © 2016 Elsevier Ltd Terms and Conditions

Figure 1 Species Richness through Time in the Caribbean (A) Species turnover in Cenozoic Caribbean reef corals based on analyses of the Caribbean Cenozoic Coral Occurrence database [8]. Observed (green) and standardized (light blue) species richness and sampling intensity (dark blue) for 1-million-year intervals from early Miocene to present. Species presence for each time interval was weighted against the range of ages estimated from the locality in which a species occurred (standardization). (B) Occurrences of all recorded Orbicella species between Late Miocene and Early Pleistocene time, together with estimated ranges for the three modern species and the extinct Late Pleistocene O. nancyi. Codes (DR, Dominican Republic; CP, Costa Rica-Panama) indicate unnamed species described by Budd and Klaus [6, 9] and the extinct O. nancyi [5]. Different colors correspond to morphologically defined clades; large dots indicate oldest and youngest age dates estimated for each occurrence. Solid lines indicate age ranges for occurrences, and dotted lines connect occurrences for each species. Estimated ranges of the three modern species and O. nancyi are inferred based on phylogenetic analyses [5, 6]. Occurrence data are provided in Table S1. See also Table S2. Current Biology 2016 26, 3190-3194DOI: (10.1016/j.cub.2016.09.039) Copyright © 2016 Elsevier Ltd Terms and Conditions

Figure 2 Variation in Effective Population Size of Modern Orbicella Species (A and B) Demographic reconstructions from each sequenced diploid genome as a function of time using O. faveolata from Florida (A) and O. franksi (B) as reference. Curves are scaled by a generation time of 35 years [12] and per-generation mutation rate of 4.83 × 10−8 [13, 14]. Thin lines indicate bootstrap replicates, and thick lines indicate actual estimates. Variation among bootstrap replicates increases toward the present. The gray bar indicates period of coral extinction, and dotted lines mark the beginning and end of sea level increase after the coral mass extinction. (C) Global sea level curve relative to the present level (0.1 mya resolution) [15]. Dotted lines indicate onset and end of sea level rise after the coral mass extinction. Genome assembly statistics are shown in Table S1. Figure S1 shows demographic reconstructions using O. annularis as reference. See also reconstructions using diCal v.1.3 in Figure S2. Current Biology 2016 26, 3190-3194DOI: (10.1016/j.cub.2016.09.039) Copyright © 2016 Elsevier Ltd Terms and Conditions

Figure 3 Joint Likelihood Surface for Ancient and Current Effective Population Sizes The point in the surface with the highest likelihood provides estimates of the ancient (anc) and current (cur) effective population sizes under a model with a single size change. Each point in the heatmap shows the likelihood score for the pair of effective size parameters. Warmer colors indicate higher likelihoods, and colder colors indicate lower likelihoods. White spaces reflect the unsampled parameter space. Effective population sizes are scaled by the mutation rate (μ). Estimates for each species were inferred from microsatellite allele frequencies across hundreds of individuals. Fold change and range of the age of the change are shown. Mean values and 95% confidence intervals are given in Table S2. The maximum likelihood values for the ratio of effective population sizes and the time at which the population changed size are given by Nratio = Ncur/Nanc and Tyears, respectively. See full statistics in Table S3. Current Biology 2016 26, 3190-3194DOI: (10.1016/j.cub.2016.09.039) Copyright © 2016 Elsevier Ltd Terms and Conditions

Figure 4 Best-Fit Demographic Model for O. faveolata from Puerto Rico and Mexico Parameters inferred from a derived site frequency spectrum obtained from 75,983 SNPs in 18 individuals. Demographic curves are scaled by a generation time of 35 years [12]. Confidence intervals from 100 non-parametric bootstrap replicates are displayed in parentheses. Likelihood scores and model ranking are shown in Table S4. Best-fitted model is a three-epoch model. See also Figures S3 and S4. Current Biology 2016 26, 3190-3194DOI: (10.1016/j.cub.2016.09.039) Copyright © 2016 Elsevier Ltd Terms and Conditions