Global climate has fluctuated greatly during the past three million years, leading to the recent major ice ages. An inescapable consequence for most living organisms is great changes in their distribution, which are expressed differently in boreal, temperate and tropical zones. Such range changes can be expected to have genetic consequences, and the advent of DNA technology provides most suitable markers to examine these. Several good data sets are now available, which provide tests of expectations, insights into species colonization and unexpected genetic subdivision and mixture of species. The genetic structure of human populations may be viewed in the same context. The present genetic structure of populations, species and communities has been mainly formed by Quaternary ice ages, and genetic, fossil and physical data combined can greatly help our understanding of how organisms were so affected.

http://webpages.icav.up.pt/PTDC/BIA-BEC/105083/2008/hewitt2000.pdf

The genetic legacy of the Quaternary ice ages

Population structure is the result of both present processes and past history. Molecular markers are proving of great value in describing the former, and it is important to similarly determine the latter in order to understand their respective contributions. The study of palaeo-climates has also advanced significantly, and in particular that of the Pleistocene ice ages, which modified species ranges considerably. The last ice age and rapid post-glacial colonization of Europe is summarized. Possible population genetic consequences of expansion northward from southern refugia, and those of remaining in these mountainous regions are discussed. A series of recent case studies are detailed where DNA sequence information has been used to describe species genetic variation and subdivision across Europe. These include a grasshopper, the hedgehog, oak trees, the common beech, the black alder, the brown bear, newts, shrews, water vole, silver fir and house mice. These molecular data confirm southern peninsulas of Europe as major ice age refugia, and in most cases demonstrate that genetically distinct taxa emerged from them. They can thus define genomic differences and so greatly augment previous fossil data. The refugial genomes contributed differently in various species to the re-colonization of Europe, with three broad patterns described as paradigms—«grasshopper», «hedgehog» and «bear». These different expansion patterns produced clusters of hybrid zones where they made contact, and it is argued that many species genomes may be further cryptically subdivided. A reduction in diversity from southern to northern Europe in the extent of allelic variation and species subdivision is seen; this is attributed to rapid expansion northward and the varied topography of southern refugia allowing populations to diverge through several ice ages. The differences in DNA sequence indicate that some species have been diverging in refugial regions for a few ice ages at most, whilst distinct lineages in other species suggest much more ancient separation.

https://www.fc.up.pt/mestr_biodiv/aulas/hewitt_1999.pdf

Post-glacial re-colonization of European biota

http://people.rses.anu.edu.au/lambeck_k/pdf/230.pdf

Sea-level and deep water temperature changes derived from benthic foraminifera isotopic records

The last glacial cycle was characterized by substantial millennial-scale climate fluctuations1,2,3,4,5, but the extent of any associated changes in global sea level (or, equivalently, ice volume) remains elusive. Highstands of sea level can be reconstructed from dated fossil coral reef terraces6,7, and these data are complemented by a compilation of global sea-level estimates based on deep-sea oxygen isotope ratios at millennial-scale resolution8 or higher1. Records based on oxygen isotopes, however, contain uncertainties in the range of ±30 m, or ±1 °C in deep sea temperature9,10. Here we analyse oxygen isotope records from Red Sea sediment cores to reconstruct the history of water residence times in the Red Sea. We then use a hydraulic model of the water exchange between the Red Sea and the world ocean to derive the sill depth—and hence global sea level—over the past 470,000 years (470 kyr). Our reconstruction is accurate to within ±12 m, and gives a centennial-scale resolution from 70 to 25 kyr before present. We find that sea-level changes of up to 35 m, at rates of up to 2 cm yr-1, occurred, coincident with abrupt changes in climate.

Sea-level fluctuations during the last glacial cycle

The oscillations between glacial and interglacial climate conditions over the past three million years have been characterized by a transfer of immense amounts of water between two of its largest reservoirs on Earth -- the ice sheets and the oceans. Since the latest of these oscillations, the Last Glacial Maximum (between about 30,000 and 19,000 years ago), approximately 50 million cubic kilometres of ice has melted from the land-based ice sheets, raising global sea level by approximately 130 metres. Such rapid changes in sea level are part of a complex pattern of interactions between the atmosphere, oceans, ice sheets and solid earth, all of which have different response timescales. The trigger for the sea-level fluctuations most probably lies with changes in insolation, caused by astronomical forcing, but internal feedback cycles complicate the simple model of causes and effects.

Links between climate and sea levels for the past three million years

Existing techniques for estimating natural fluctuations of sea level and global ice-volume from the recent geological past exploit fossil coral-reef terraces or oxygen-isotope records from benthic foraminifera. Fossil reefs reveal the magnitude of sea-level peaks (highstands) of the past million years, but fail to produce significant values for minima (lowstands) before the Last Glacial Maximum (LGM) about 20,000 years ago, a time at which sea level was about 120 m lower than it is today1,2,3,4. The isotope method provides a continuous sea-level record for the past 140,000 years (ref. 5) (calibrated with fossil-reef data6), but the realistic uncertainty in the sea-level estimates is around ±20 m. Here we present improved lowstand estimates—extending the record back to 500,000 years before present—using an independent method based on combining evidence of extreme high-salinity conditions in the glacial Red Sea with a simple hydraulic control model of water flow through the Strait of Bab-el-Mandab, which links the Red Sea to the open ocean. We find that the world can glaciate more intensely than during the LGM by up to an additional 20-m lowering of global sea-level. Such a 20-m difference is equivalent to a change in global ice-volume of the order of today's Greenland and West Antarctic ice-sheets.

M. Fenton

Papers

Magnitudes of sea-level lowstands of the past 500,000 years

Aplanktonic zones in the Red Sea