Abstract

The notion of islands as natural testbeds for evolutionary study is nearly as old as the theory of evolution itself. The restricted scale, isolation, and sharp boundaries of islands create unique selective pressures, often to dramatic effect. Following what’s known as the “island rule,” small animals evolve into outsize versions of their continental counterparts while large animals shrink. Once restricted to islands, small animals often lacked predators and the competition between species that constrained the growth of their relatives on the mainland. Large mammals, on the other hand, no longer had access to vast grasslands and other abundant food sources and grew smaller to survive. Giant tortoises and iguanas still inhabit the Galapagos and a few other remote islands today, but only fossils remain of the dwarf hippopotami, elephants, and deer that once lived on islands in Indonesia, the Mediterranean, and the Pacific Ocean. The fossil record suggests that these size changes (as well as other morphological changes) occur rapidly after species become isolated on islands, but this assumption has never been empirically examined in a systematic manner. In a new study, Virginie Millien puts this longstanding hypothesis to the test by analyzing the fossil record and data from living species. Comparing the rates of evolutionary change between island and mainland populations for 88 species at intervals ranging from 21 years to 12 million years, Millien confirmed that island species undergo accelerated evolutionary changes over relatively short time frames, between decades and several thousand years. (One can imagine rats of horror movie proportions if such rates persisted for millions of years.) Measuring rates of evolutionary change has proven difficult because the fossil record rarely captures every morphological shift in a lineage, precise dating isn’t always possible, and it’s often not clear when the ancestral form first appeared on the island. To get a robust sample of island and mainland mammalian species, Millien collected data from text, figures, and tables in an extensive survey of the published literature. From these datasets, she calculated a total of 826 evolutionary rates for 170 populations representing the 88 species. (Rates of evolutionary change are measured in units called, appropriately enough, “darwins.”) Evolution rates, she found, decreased over time intervals for both island and mainland species, with a slower rate of decrease for island species. The differences in evolutionary rates between island and mainland pairs also decreased over time, becoming statistically insignificant for intervals over 45,000 years. Overall, island species evolved faster than mainland species—a phenomenon that was most pronounced for intervals between 21 years through 20,000 years. Island evolution theory predicts that the most extreme effects of isolation will be seen on the smallest, most far-flung islands. In keeping with theory, Millien found that evolutionary rates for different populations of the same species varied with island locale. Thus, the rate of evolution does not appear to be an evolutionarily conserved trait, like metabolic rate or whiskers. Because rodents make up nearly half of the world’s mammalian species—and over 70% of taxa on some islands in this study—Millien repeated her analysis on a subset of the data with equal numbers of rodent and non-rodent taxa. The overrepresentation of rodents had no effect on the results, which still revealed significant differences between island and mainland evolution rates for the same species or populations. The finding that mammals evolve faster on islands, Millien argues, comports with the island evolution theory prediction that mammals respond to their new island homes with rapid morphological and size adaptations. The brisk pace of these changes may explain why the fossil record harbors few examples of intermediate forms between the mainland ancestor and island descendant. Millien’s results also conform with the hypothesis that evolution rates for island species slow down after the initial period of accelerated change, approaching rates on the mainland. If island species can evolve quickly, Millien argues, it stands to reason that mainland species retain a similar capacity. As habitat destruction continues to pose the number one threat to biodiversity, many mainland habitats are beginning to resemble islands, with isolated pockets of wildlife separated by degraded or developed lands. Thus, island species may serve as a model for understanding how mainland species will adapt to the rapidly changing environmental conditions brought on by habitat destruction and global warming. It appears that some mainland species are already responding like island species: a 1989 study followed the island rule in linking fragmented habitat to body size changes in 25 European mammals over the past 200 years. How long animals can continue to evolve in the face of these changes, however, remains to be seen.

Highlights

  • Fusion of two plasma membranes is central to exocytosis, the process by which a cell secretes neurotransmitters, digestive enzymes, and other products

  • When the others bind to their respective SNAREs, they leave the SNAREs in an open conformation, available for interacting with others and forming the complexes that drive membrane fusion

  • Synaptobrevin is a known partner for syntaxin, and it has been shown that the addition of synaptobrevin drives syntaxin in conjunction with SNAP-25 into SNARE complexes

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Summary

Synopses of Research Articles

Fusion of two plasma membranes is central to exocytosis, the process by which a cell secretes neurotransmitters, digestive enzymes, and other products. By deleting SNAP-25, the authors verified its essential role in displacing Munc181 from syntaxin, suggesting there is an intermediate complex formed by Munc, syntaxin, synaptobrevin, and SNAP-25 These results shed light on the actual function of Munc, but allow the development of a more coherent picture of SM proteins, in which Munc is no longer the oddball. HIV-1 exploits retrograde transport of tRNAs in human cells to promote nuclear import of its reverse transcription complex. Using a high-speed centrifuge, they separated cytoplasm from cultured cells into fractions and tested each fraction for its ability to promote nuclear import of the RTCs in the gutted cells As expected, when they added in the fraction containing several known nuclear transport factors, the RTCs could enter the nucleus.

Chance Fluctuations in mRNA Output in Mammalian Cells
Transposon Silencing Keeps Jumping Genes in Their Place
Offspring of plants that had both
Protein Kinases and Plant Pores
Infection Status Drives Interspecies Mating Choices in Fruit Fly Females
Gut Bacteria Cospeciating with Insects
Predicting Species Abundance in the Face of Habitat Loss
Disrupted Intercellular Communication Causes a Disfiguring Birth Defect
Learning New Movements Depends on the Statistics of Your Prior Actions
Findings
Islands Spark Accelerated Evolution
Full Text
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