Godfrey M. Hewitt’s research while affiliated with University of East Anglia and other places

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Publications (218)


Figure 2. Neighboring graph. 
Figure 4. Color plot corresponding to the first three components. 
Figure 3 of 3
spatialtrends sup
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September 2015

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253 Reads

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Dalimitra S
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Climate changes and vegetation responses during the past 140000 years (kyr). (A) 21 June insolation 65°N [65]; (B) Sea-level reconstructions (light-blue line: [58]); dark-blue line: [59]; black squares: [62]; (C) atmospheric CO2 concentration in Antarctic ice cores [63]; (D) reconstructed δ18O composition of ice in Greenland synthetic (GLT-syn) record [66]; changes in arboreal pollen (AP) percentages in the Grande Pile record, Vosges Mountains, France [67]; changes in temperate (orange) and pioneer (Pinus, Betula, and Juniperus) pollen percentages in the Ioannina 284 record, northwest Greece [68]. Marine Isotopic Stages and Substages (MIS) are indicated. Also indicated are climato- and chronostratigraphic units: Penultimate Glacial (PG), Last Interglacial (LIG), Early Glacial (EG), Early Pleniglacial (EPG), Middle Pleniglacial (MPG), Late Pleniglacial (LPG), Lateglacial (LG), and Holocene (HOL). Heinrich Stadials 1 and 2 (HS1 and HS2) are shown by vertical bars and the Greenland Interstadial 3 (GIS3) is also shown.
European paleoenvironments during the Late Pleniglacial. Maximum extent of ice (white) [69,70] and continuous and discontinuous permafrost (large and small crosses, respectively) [46] is shown. Also shown is the distribution of macrofossil and pollen sites and inferred tree presence (Tables S1 and S2 and Figure S1 in the supplementary material online): boreal dwarf shrubs: Betula nana (dwarf birch) and Salix (willow); boreal and/or mountain conifers: Picea (spruce) and Larix (larch); boreal and/or mountain summergreen trees: Betula (birch), Populus (poplar), Salix, and Alnus (alder); Pinus (pine); Juniperus (juniper); temperate trees: deciduous and evergreen Quercus (oaks), Ulmus (elm), Corylus (hazel), Tilia (lime), Fraxinus (ash), Vitis (vine), Carpinus betulus (hornbeam), Ostrya (hop hornbeam), Castanea (sweet chestnut), Fagus (beech), Abies (fir), Cedrus (cedar), and Alnus; Mediterranean sclerophylls: Olea (olive), Phillyrea, and Pistacia (lentisc and terebinth). Question marks over vegetation symbols denote uncertainty (see footnotes in Table S2 in the supplementary material online).
Cryptic or mystic? Glacial tree refugia in northern Europe

September 2013

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612 Reads

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373 Citations

Trends in Ecology & Evolution

Here, we examine the evidence for tree refugia in northern Europe during the Late Pleniglacial (LPG) interval of maximum tree-range contraction. Our review highlights the often equivocal nature of genetic data and a tendency to overestimate potential tree distributions due to warm climate-model bias, and also reveals a convergence of macrofossil and pollen evidence. What emerges is the absence of temperate trees north of 45°N and a west-east (W-E) asymmetry in boreal tree distribution, with a treeless Western Europe north of 46°N, while restricted boreal populations persisted in Eastern Europe up to 49°N, and higher latitudes east of the Fennoscandian ice-sheet. These results have implications for current thinking on European genetic diversity patterns, species migration capacity, and conservation strategies.



Founder takes all: Density-dependent processes structure biodiversity

February 2013

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508 Reads

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437 Citations

Trends in Ecology & Evolution

Density-dependent processes play a key role in the spatial structuring of biodiversity. Specifically, interrelated demographic processes, such as gene surfing, high-density blocking, and competitive exclusion, can generate striking geographic contrasts in the distributions of genes and species. Here, we propose that well-studied evolutionary and ecological biogeographic patterns of postglacial recolonization, progressive island colonization, microbial sectoring, and even the 'Out of Africa'pattern of human expansion, ...


Fig. 3 Adaptive introgression and hybrid speciation. Divergently selected loci (depicted as black and grey solid lines) in two populations can be combined by recombinant hybridization. The resulting hybrid combination can potentially be adaptive and favoured in a new habitat and can give rise to an independent hybrid taxon (hybrid speciation), or it can allow one population to evolve further, replacing the original genome (adaptive introgression). Globally adaptive variation as well as neutral variation (both depicted as broken lines) can be exchanged between all populations via gene flow through hybridization.
Hybridization and speciation

February 2013

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6,340 Reads

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2,020 Citations

Journal of Evolutionary Biology

Hybridization has many and varied impacts on the process of speciation. Hybridization may slow or reverse differentiation by allowing gene flow and recombination. It may accelerate speciation via adaptive introgression or cause near-instantaneous speciation by allopolyploidization. It may have multiple effects at different stages and in different spatial contexts within a single speciation event. We offer a perspective on the context and evolutionary significance of hybridization during speciation, highlighting issues of current interest and debate. In secondary contact zones, it is uncertain if barriers to gene flow will be strengthened or broken down due to recombination and gene flow. Theory and empirical evidence suggest the latter is more likely, except within and around strongly selected genomic regions. Hybridization may contribute to speciation through the formation of new hybrid taxa, whereas introgression of a few loci may promote adaptive divergence and so facilitate speciation. Gene regulatory networks, epigenetic effects and the evolution of selfish genetic material in the genome suggest that the Dobzhansky–Muller model of hybrid incompatibilities requires a broader interpretation. Finally, although the incidence of reinforcement remains uncertain, this and other interactions in areas of sympatry may have knock-on effects on speciation both within and outside regions of hybridization.


Comment on "Glacial Survival of Boreal Trees in Northern Scandinavia"

November 2012

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229 Reads

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69 Citations

Science

Parducci et al. (Reports, 2 March 2012, p. 1083) fail to present convincing evidence for glacial survival of Pinus and Picea in northern Scandinavia. Their methodology does not exclude contamination. Additionally, they should consider the lack of suitable habitats, the apparent extinction of both taxa after deglacial warming, and alternative hypotheses for the distribution of the Picea genetic marker haplotype A.


Genetic analysis of a contact zone between two lineages of the ocellated lizard (Lacerta lepida Daudin 1802) in south-eastern Iberia reveal a steep and narrow hybrid zone

October 2012

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252 Reads

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30 Citations

Measuring the diffusion of genes between diverging taxa through zones of secondary contact is an essential step to understand the extent and nature of the reproductive isolation that has been achieved. Previous studies have shown that the ocellated lizard (Lacerta lepida Daudin, 1802) has endured repeated range fragmentation associated with the climatic oscillations of the Plio-Pleistocene that promoted diversification of many different evolutionary units within the species. However, the oldest divergence within the group is estimated to have occurred much earlier, during the Miocene, around 9 Ma and corresponds to the split between the subspecies Lacerta lepida nevadensis Buchholz (1963) and Lacerta lepida lepida Daudin (1802). Although these two evolutionary units have documented genetic and morphological differentiation, most probably accumulated during periods of allopatry, little is known about patterns of gene flow between them. In this study, we performed a population genetic analysis of a putative area of secondary contact between these two taxa, using mtDNA and microsatellite data. We assessed levels of gene flow across the contact zone to clarify to what extent gene flow may be occurring. Hybridization between the subspecies was observed by the presence of genetically introgressed individuals. However, the overall coincidence of mitochondrial and multilocus nuclear clines and generally steep clines support the idea that this contact zone is acting as a barrier to gene flow. Taken together, these results suggest that L. l. lepida and L. l. nevadensis are in independent evolutionary trajectories and should be considered as two different species.


Numts help to reconstruct the demographic history of the ocellated lizard ( Lacerta lepida ) in a secondary contact zone

February 2012

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221 Reads

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31 Citations

Molecular Ecology

In northwestern Iberia, two largely allopatric Lacerta lepida mitochondrial lineages occur, L5 occurring to the south of Douro River and L3 to the north, with a zone of putative secondary contact in the region of the Douro River valley. Cytochrome b sequence chromatograms with polymorphisms at nucleotide sites diagnostic for the two lineages were detected in individuals in the region of the Douro River and further north within the range of L3. We show that these polymorphisms are caused by the presence of four different numts (I-IV) co-occurring with the L3 genome, together with low levels of heteroplasmy. Two of the numts (I and II) are similar to the mitochondrial genome of L5 but are quite divergent from the mitochondrial genome of L3 where they occur. We show that these numts are derived from the mitochondrial genome of L5 and were incorporated in L3 through hybridization at the time of secondary contact between the lineages. The additional incidence of these numts to the north of the putative contact zone is consistent with an earlier postglacial northward range expansion of L5, preceding that of L3. We show that genetic exchange between the lineages responsible for the origin of these numts in L3 after secondary contact occurred prior to, or coincident with, the northward expansion of L3. This study shows that, in the context of phylogeographic analysis, numts can provide evidence for past demographic events and can be useful tools for the reconstruction of complex evolutionary histories.


Mediterranean Peninsulas: The Evolution of Hotspots

August 2011

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644 Reads

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269 Citations

The Mediterranean peninsulas contain much genetic and species diversity, which decreases toward higher latitudes in Europe. In considering how such diversity evolved, three areas of activity seem important – Paleogeology, Paleoclimatology, and Phylogeography. The complex collision of the African and European tectonic plates produced the very different peninsulas of Iberia, Italy, and the Balkans. The climate cooled from 50 Mya with increasingly severe ice ages over the last 2 My that repeatedly modified species distributions and hence species evolution. As well as many endemic species, genetic methods show the peninsulas to have distinct genotypes in many species, with various postglacial histories. Their mountainous topography appears important for the survival of species through the ice ages and previously. In Iberia, mountains are the focus for multiple refugia, producing several diverged genetic lineages. Italy shows more recent subdivision through multiple refugia, particularly in the south. The Balkans has many more endemics, but fewer phylogeographic studies than other peninsulas. Multiple refugia and a range of lineage ages indicate continuous divergence and speciation over many millions of years to the present. The peninsulas are important as refugia for the survival of species and engines of speciation.


Phylogeography and demographic history of Lacerta lepida in the Iberian Peninsula: Multiple refugia, range expansions and secondary contact zones

June 2011

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377 Reads

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75 Citations

BMC Evolutionary Biology

The Iberian Peninsula is recognized as an important refugial area for species survival and diversification during the climatic cycles of the Quaternary. Recent phylogeographic studies have revealed Iberia as a complex of multiple refugia. However, most of these studies have focused either on species with narrow distributions within the region or species groups that, although widely distributed, generally have a genetic structure that relates to pre-Quaternary cladogenetic events. In this study we undertake a detailed phylogeographic analysis of the lizard species, Lacerta lepida, whose distribution encompasses the entire Iberian Peninsula. We attempt to identify refugial areas, recolonization routes, zones of secondary contact and date demographic events within this species. Results support the existence of 6 evolutionary lineages (phylogroups) with a strong association between genetic variation and geography, suggesting a history of allopatric divergence in different refugia. Diversification within phylogroups is concordant with the onset of the Pleistocene climatic oscillations. The southern regions of several phylogroups show a high incidence of ancestral alleles in contrast with high incidence of recently derived alleles in northern regions. All phylogroups show signs of recent demographic and spatial expansions. We have further identified several zones of secondary contact, with divergent mitochondrial haplotypes occurring in narrow zones of sympatry. The concordant patterns of spatial and demographic expansions detected within phylogroups, together with the high incidence of ancestral haplotypes in southern regions of several phylogroups, suggests a pattern of contraction of populations into southern refugia during adverse climatic conditions from which subsequent northern expansions occurred. This study supports the emergent pattern of multiple refugia within Iberia but adds to it by identifying a pattern of refugia coincident with the southern distribution limits of individual evolutionary lineages. These areas are important in terms of long-term species persistence and therefore important areas for conservation.


Citations (69)


... Subspecies are traditionally held as geographically separate and genetically distinct populations within the species' range, permitting gene flow in the area of contact (Wilson and Brown 1953;O'Brien and Mayr 1991;Patten and Unitt 2002). Despite possible interbreeding between subspecies, subspecies may retain differences in respective life cycles or other traits (Hewitt 2002;Kothera et al. 2009). Among birds, high subspecies richness was associated with large breeding ranges, island dwelling, inhabiting montane regions, habitat heterogeneity and low latitude; on the other hand, species phylogenetic age was a poor predictor of subspecies richness (Phillimore et al. 2007). ...

Reference:

Revision of Tipula (Yamatotipula) stackelbergi Alexander (Diptera, Tipulidae), and a short discussion on subspecies among crane flies
Hybrid Zones
  • Citing Chapter
  • May 2003

... P < 0.02) only for an easterly located population, Erzincan, which was also supported by small SSD and HRag values, implying that this population underwent population growth in the past. In this study cyt b and ITS2 data weakly supported each other; however, the former is used to explain the relatively recent past, while the latter points to the more ancient past (Zhang & Hewitt, 2003). In general, it seems that historical factors in the past have imposed their effects on C. quercusfolii populations in Turkey, resulting in the more ancient population expansion from eastern to western Turkey as suggested by the ITS2 data and continuing more recent historical expansion as indicated by the cyt b gene data. ...

Nuclear DNA analyses in genetic studies of populations: practice, problems and prospects (vol 12, pg 563, 2003)
  • Citing Article
  • June 2003

Molecular Ecology

... Different connection networks were tested and a comparison of the results led us to choose as connection network the optimal number (K) of nearest neighbors (K = 10), which maximizes the clear separation of breeds. Spatial structures detected by sPCA were tested using the global and local permutation tests and Moran's eigenvector maps [35]. The elevation map that is necessary for the next steps was produced using the Raster package [36]. ...

Spatial Trends of Genetic Variation of Domestic Ruminants in Europe

... In China, especially in the Qinghai-Tibet Plateau (QTP) and adjacent regions, significant progress has been made in inferring the Quaternary phylogeographic histories of plant species using population genetics approaches [9][10][11][12][13]. Studies have shown that the QTP acted as a barrier against glaciation within the warm temperate zones of China, resulting in arid climates that persisted for thousands of years [14][15][16][17][18][19]. Thus, the present warm temperate region likely served as glacial refugia for plant species during the Last Glacial Maximum (LGM), approximately 23,000 to 18,000 years ago. ...

Cryptic or mystic? Glacial tree refugia in northern Europe

Trends in Ecology & Evolution

... Holderegger and Thiel-Egenter (2009) define three different types of refugia for mountain species during glacial periods: isolated microrefugia on mountain peaks above the glaciers in the center of mountain systems (nunataks); peripheral refugia that maintained some snow-free periods towards the borders of mountain systems; and lowland refugia outside mountain systems and beyond the limits of ice shields. In Europe, Alpine Lepidoptera undertook elevation range shifts to persist during glacial periods in lowland refugia (Haubrich and Schmitt 2007;Schmitt and Hewitt 2004), but some less dispersive alpine plant species (potentially with associated insects) are inferred to have survived in high-altitude nunataks (Holderegger and Thiel-Egenter 2009). ...

Molecular Biogeography of the arctic-alpine disjunct burnet moth species Zygaena exulans (Zygaenidae, Lepidoptera) in the Pyrenees and Alps
  • Citing Article
  • June 2004

Journal of Biogeography

... The complete mitochondrial genome of D. angustivirgatus Kishida, 1933 has been sequenced with gene arrangement typical of mitochondrial genomes of Entelegynae spiders (Wang et al., 2020). Ten polymorphic microsatellite DNA loci were developed for D. plantarius for use in paternity studies and for analysis of population genetics (Ji et al., 2004). The newly available subgenomic data with ultraconserved elements of Dolomedes worldwide will be useful, beyond phylogenomics, in efforts to generate new sets of microsatellites (Raposo do Amaral et al., 2015). ...

Ten polymorphic microsatellite DNA loci for paternity and population genetics analysis in the fen raft spider (Dolomedes plantarius)
  • Citing Article
  • June 2004

Molecular Ecology Notes

... The X chromosome shows a distal heterochromatic band in CPP that is absent in CPE. However, in CPE, the X-chromosome displays an exclusive interstitial band that cannot be explained by an inversion, but rather by the recent amplification and heterochromatinization of specific sequences [7,12]. ...

A hybrid zone between Chorthippus parallelus parallelus and Chorthippus parallelus erythropus (Orthoptera: Acrididae): Chromosomal differentiation

... Survival in such areas was likely enabled by the groups' close association to the temperature-buffering soil environment and their diverse diets (von Saltzwedel et al. 2016). During these cold periods, populations were isolated and reduced in size, resulting in the erosion of genetic diversity, potentially amplifying the creation of genetically distinct and geographically separated lineages (Avise 2009;Waters et al. 2013). In this respect, it is intriguing that the two A. bisetosa sp. ...

Founder takes all: Density-dependent processes structure biodiversity
  • Citing Article
  • February 2013

Trends in Ecology & Evolution

... The results of the ECONOGENE project demonstrated the power of microsatellite markers to investigate within-breed genetic diversity and between-breed genetic relationships. Sheep breeds located near the domestication centre and southeast regions harbour higher levels of genetic diversity [21]. On the other hand, a geographical differentiation among breeds was suggested by PCA and STRUCTURE results, indicating a genetic cline from the Middle Eastern and southeastern European breeds towards north-western and western European breeds. ...

Spatial Trends of Genetic Variation of Domestic Ruminants in Europe European Cattle Genetic Diversity Consortium and Econogene Consortium

... Suture zones that assort non-randomly in space provide historical evidence for this phenomenon where organisms expand out of their refugia and come into secondary contact in these regions (Hewitt 1988(Hewitt , 2001Remington 1968). In Europe, several suture zones have been identified, as illustrated by the contemporary distributions of three well-studied species: the meadow grasshopper, Pseudochorthippus parallelus (Butlin and Hewitt 1985;Cooper et al. 1995;Hagberg et al. 2022), the European hedgehog, Erinaceus europeus (Bolfíková and Hulva 2012;Santucci et al. 1998;Seddon et al. 2002), and the brown bear, Ursus arctos (Taberlet and Bouvet 1997;Waits et al. 2000). For each of these suture zones, mountain ranges such as the Pyrenées and Alps act as physical barriers to the expansion of refugial populations from Iberia, Italy, the Balkans, and/ or Caucasus (Hewitt 2000(Hewitt , 2001. ...

Caucasus Mountains divide postulated postglacial colonization routes in the white-breasted hedgehog, Erinaceus concolor
  • Citing Article
  • May 2002

Journal of Evolutionary Biology