Preface to the Princeton Landmarks in Biology Edition vii Preface xi Symbols Used xiii 1. The Importance of Islands 3 2. Area and Number of Speicies 8 3. Further Explanations of the Area-Diversity Pattern 19 4. The Strategy of Colonization 68 5. Invasibility and the Variable Niche 94 6. Stepping Stones and Biotic Exchange 123 7. Evolutionary Changes Following Colonization 145 8. Prospect 181 Glossary 185 References 193 Index 201

The Theory of Island Biogeography

Statistical method for testing the neutral mutation hypothesis by DNA polymorphism.

So far in this course we have dealt entirely with the evolution of characters that are controlled by simple Mendelian inheritance at a single locus. There are notes on the course website about gametic disequilibrium and how allele frequencies change at two loci simultaneously, but we didn’t discuss them. In every example we’ve considered we’ve imagined that we could understand something about evolution by examining the evolution of a single gene. That’s the domain of classical population genetics. For the next few weeks we’re going to be exploring a field that’s actually older than classical population genetics, although the approach we’ll be taking to it involves the use of population genetic machinery. If you know a little about the history of evolutionary biology, you may know that after the rediscovery of Mendel’s work in 1900 there was a heated debate between the “biometricians” (e.g., Galton and Pearson) and the “Mendelians” (e.g., de Vries, Correns, Bateson, and Morgan). Biometricians asserted that the really important variation in evolution didn’t follow Mendelian rules. Height, weight, skin color, and similar traits seemed to

Human biochemical genetics

计量经济分析 = Econometric analysis

The genetic effects of pleistocene ice ages are approached by deduction from paleoenvironmental information, by induction from the genetic structure of populations and species, and by their combination to infer likely consequences. (1) Recent palaeoclimatic information indicate rapid global reversals and changes in ranges of species which would involve elimination with spreading from the edge. Leading edge colonization during a rapid expansion would be leptokurtic and lead to homozygosity and spatial assortment of genomes. In Europe and North America, ice age contractions were into southern refugia, which would promote genome reorganization. (2) The present day genetic structure of species shows frequent geographic subdivision, with parapatric genomes, hybrid zones and suture zones. A survey of recent DNA phylogeographic information supports and extends earlier work. (3) The grasshopperChorthippus parallelusis used to illustrate such data and processes. Its range in Europe is divided on DNA sequences into five parapatric races, with southern genomes showing greater haplotype diversity — probably due to southern mountain blocks acting as refugia and northern expansion reducing diversity. (4) Comparison with other recent studies shows a concordance of such phylogeographic data over pleistocene time scales. (5) The role that ice age range changes may have played in changing adaptations is explored, including the limits of range, rapid change in new invasions and refugial differentiation in a variety of organisms. (6) The effects of these events in causing divergence and speciation are explored usingChorthippusas a paradigm. Repeated contraction and expansion would accumulate genome differences and adaptations, protected from mixing by hybrid zones, and such a composite mode of speciation could apply to many organisms.

https://www.fc.up.pt/mestr_biodiv/aulas/hewitt_1996.pdf

Some genetic consequences of ice ages, and their role in divergence and speciation

Host-associated races of phytophagous insects provide a model for understanding how adaptation to a new environment can lead to reproductive isolation and speciation, ultimately enabling us to connect barriers to gene flow to adaptive causes of divergence. The pea aphid (Acyrthosiphon pisum) comprises host races specializing on legume species and provides a unique system for examining the early stages of diversification along a gradient of genetic and associated adaptive divergence. As host choice produces assortative mating, understanding the underlying mechanisms of choice will contribute directly to understanding of speciation. As host choice in the pea aphid is likely mediated by smell and taste, we use capture sequencing and SNP genotyping to test for the role of chemosensory genes in the divergence between eight host plant species across the continuum of differentiation and sampled at multiple locations across western Europe. We show high differentiation of chemosensory loci relative to control loci in a broad set of pea aphid races and localities, using a model-free approach based on principal component analysis. Olfactory and gustatory receptors form the majority of highly differentiated genes and include loci that were already identified as outliers in a previous study focusing on the three most closely related host races. Consistent indications that chemosensory genes may be good candidates for local adaptation and barriers to gene flow in the pea aphid open the way to further investigations aiming to understand their impact on gene flow and to determine their precise functions in response to host plant metabolites.

https://onlinelibrary.wiley.com/doi/pdf/10.1111/mec.13818

Targeted re-sequencing confirms the importance of chemosensory genes in aphid host race differentiation

Two subspecies of the grasshopper Chorthippus parallelus form a hybrid zone in the Pyrenees. Transitions across the zone, including changes in mating signals and reproductive isolation have been intensively studied. Cuticular pheromones have been identified as likely mate recognition signals. Since the major role of the cuticle is in waterproofing, environmental adaptation of cuticular composition has the interesting potential to generate assortative mating as an incidental by-product. We describe the pattern of variation in cuticular hydrocarbon blend in four transects through the hybrid zone. We find no evidence for a previously observed displaced cline in one blend component. There were differences between subspecies but these varied among transects and were small compared with variation between transects. We examined environmental variation within one transect and found a correlation between vegetation and cuticular composition, suggesting that environment influences the constitution of the cuticle, and hence natural selection may interact with mating signals in this species. © 2003 The Linnean Society of London, Biological Journal of the Linnean Society, 2003, 78, 193−201.

http://www.selfishgene.org/Tom/Papers/SHBetal_BiolJLinnSoc03.pdf

Transitions in cuticular composition across a hybrid zone: historical accident or environmental adaptation?

Genetics and the boundaries of species' distributions

Aim: Community assembly is traditionally assumed to result from speciation and colonization mediated by available niche space. This paradigm is expanded by the theory that niche space can also be saturated by intersexual adaptive divergence (ecological sexual dimorphism) when interspecific competition is relaxed. This theory (here termed ‘niche-packing equivalence’) predicts that the evolution of ecological sexual dimorphism constrains the ecological opportunity that would otherwise lead to ecological speciation or colonization, and that saturation of niches by different species constrains divergent selection for divergence between the sexes. Therefore, sexes and species are equivalent, yet antagonistic units of niche occupation. We present the most comprehensive test of the niche-packing equivalence theory at ecological time-scales (assemblage level) to date.
Location: South America
Major taxa studied: Liolaemus lizards.
Methods: We identified 23 Liolaemus assemblages varying in species richness and sexual size dimorphism (SSD), distributed across a wide environmental range. We used mixed effects models, permutation tests and Markov Chain Monte Carlo (MCMC) regressions to quantify the relationship between SSD and species richness. We then partitioned the body size niche dimension between the sexes and amongst species, and tested for non-overlapping body size distributions. We regressed SSD and species richness of each assemblage against environmental predictors, using multi-model inference and structural equation modelling.
Results: Sexual dimorphism declines with increasing species richness, and a strong signal of tension between the two remains following phylogenetic control. This pattern is accompanied by evidence of constraints on body-size partitioning amongst species and between the sexes: the two units of niche saturation tend not to overlap. However, across assemblages, species richness and SSD correlate with different environmental variables, suggesting that their tension is context-specific.
Main conclusions: Our evidence supports the prediction that sexual dimorphism and species richness are alternative outcomes of adaptive radiation. However, this antagonism is mediated by a suite of environmental predictors that influence dimorphism and species richness differentially.

/pdf/sexes-and-species-as-rival-units-of-niche-saturation-during-3mnan50ody.pdf

Sexes and species as rival units of niche saturation during community assembly

Chromosomal rearrangements can alter the rate and patterns of gene flow within or between species through a reduction in the fitness of chromosomal hybrids or by reducing recombination rates in rearranged areas of the genome. This concept, together with the observation that many species have structural variation in chromosomes, has led to the theory that the rearrangements may play a direct role in promoting speciation. Australian morabine grasshoppers (genus Vandiemenella, viatica species group) are an excellent model for studying the role of chromosomal rearrangement in speciation because they show extensive chromosomal variation, parapatric distribution patterns, and narrow hybrid zones at their boundaries. This species group stimulated development of one of the classic chromosomal speciation models, the stasipatric speciation model proposed by White in 1968. Our population genetic and phylogeographic analyses revealed extensive non-monophyly of chromosomal races along with historical and on-going gene introgression between them. These findings suggest that geographical isolation leading to the fixation of chromosomal variants in different geographic regions, followed by secondary contact, resulted in the present day parapatric distributions of chromosomal races. The significance of chromosomal rearrangements in the diversification of the viatica species group can be explored by comparing patterns of genetic differentiation between rearranged and co-linear parts of the genome.

https://www.mdpi.com/2075-4450/2/1/49/pdf

Roger K. Butlin

Papers

Targeted re-sequencing confirms the importance of chemosensory genes in aphid host race differentiation

Transitions in cuticular composition across a hybrid zone: historical accident or environmental adaptation?

Genetics and the boundaries of species' distributions

Sexes and species as rival units of niche saturation during community assembly

Chromosomal Speciation Revisited: Modes of Diversification in Australian Morabine Grasshoppers (Vandiemenella, viatica Species Group).