A new Eurasian phylogeographical paradigm? Limited contribution of southern populations to the recolonization of high latitude populations in Juniperus communis L. (Cupressaceae)
Abstract:Aim The aims of this population genetics study of the common juniper across Eurasia were to (1) assess the contribution of southern mountain ranges to the post-glacial recolonization of high latitudes and (2) test whether recent expansion or high gene flow could explain the low genetic differentiation in Northern Eurasia.Location Northern Eurasia and mountain regions of Central Europe and Asia.Methods Six hundred and twenty-two individuals were sampled in 42 populations. Two chloroplast DNA (cpDNA) fragments w… Show more
“…However, the events related to this range expansion took place apparently long before the migrations resulted in the modern structure of Scots pine populations. The presence of the secondary center of the re-colonization under the initially European origin is not a feature unique to Scots pine and was noted for some other species of forest biota of Northern Eurasia, for example -Calluna vulgaris (Sannikov et al 2014) and Juniperus communis (Hantemirova et al 2017). Clearly, migration of P. sylvestris (as well as C. vulgaris and J. communis) to the Urals from Central Europe could be related to the restoration of forest zone after one of the most severe glacial intervals, when forest vegetation disappeared completely on the plains of Eastern Europe and Western Siberia and in the mountainous regions of the Urals, for example -during MIS8 (270-250 kya) or , when the boundary of glaciation in Western Siberia reached 60°-62° N, respectively (Volkova 2002).…”
During Quaternary glaciations the ranges of Northern Eurasia forest biota species periodically experienced contraction followed by subsequent recolonizations in the interglacial intervals. However, unlike the broadleaf trees of temperate forests, taiga species seem not fully retreated to southern regions in unfavorable periods and possibly survived at mid-latitudes in multiple refugia. It is supported by this study of genetic variation of three mitochondrial DNA markers in 90 populations of Scots pine (Pinus sylvestris) located from Eastern Europe to Eastern Siberia. Geographic distribution of nine mitochondrial haplotypes (mitotypes) demonstrated the split between western and eastern populations approximately along the 38 th meridian. Genetic diversity in the western part was significantly higher than in the eastern one. 2 Six haplotypes were western-and two eastern-specific. One haplotype was common in both regions, but in the eastern part it occurred only in the South Urals and adjacent areas. The structure of the mitotype geographical distribution supports the hypothesis of the post-glacial recolonization of the studied territory from the European and Ural refugia.
“…However, the events related to this range expansion took place apparently long before the migrations resulted in the modern structure of Scots pine populations. The presence of the secondary center of the re-colonization under the initially European origin is not a feature unique to Scots pine and was noted for some other species of forest biota of Northern Eurasia, for example -Calluna vulgaris (Sannikov et al 2014) and Juniperus communis (Hantemirova et al 2017). Clearly, migration of P. sylvestris (as well as C. vulgaris and J. communis) to the Urals from Central Europe could be related to the restoration of forest zone after one of the most severe glacial intervals, when forest vegetation disappeared completely on the plains of Eastern Europe and Western Siberia and in the mountainous regions of the Urals, for example -during MIS8 (270-250 kya) or , when the boundary of glaciation in Western Siberia reached 60°-62° N, respectively (Volkova 2002).…”
During Quaternary glaciations the ranges of Northern Eurasia forest biota species periodically experienced contraction followed by subsequent recolonizations in the interglacial intervals. However, unlike the broadleaf trees of temperate forests, taiga species seem not fully retreated to southern regions in unfavorable periods and possibly survived at mid-latitudes in multiple refugia. It is supported by this study of genetic variation of three mitochondrial DNA markers in 90 populations of Scots pine (Pinus sylvestris) located from Eastern Europe to Eastern Siberia. Geographic distribution of nine mitochondrial haplotypes (mitotypes) demonstrated the split between western and eastern populations approximately along the 38 th meridian. Genetic diversity in the western part was significantly higher than in the eastern one. 2 Six haplotypes were western-and two eastern-specific. One haplotype was common in both regions, but in the eastern part it occurred only in the South Urals and adjacent areas. The structure of the mitotype geographical distribution supports the hypothesis of the post-glacial recolonization of the studied territory from the European and Ural refugia.
“…Although the western migration reached the Ural Mountains, this lineage has not been found farther west than the Perm region on the western slopes of the Urals. As with the 3a1 clade in brown bears, the common juniper ( Juniperus communis ) also has a dominant and widespread clade in Eurasia (Hantemirova et al., ), although it does not reach as far east.…”
Aim
Climatic changes during the Late Pleistocene had major impacts on populations of plant and animal species. Brown bears and other large mammals are likely to have experienced analogous ecological pressures and phylogeographical processes. Here, we address several unresolved issues regarding the Late Pleistocene demography of brown bears: (1) the putative locations of refugia; (2) the direction of migrations across Eurasia and into North America; and (3) parallels with the demographic histories of other wild mammals and modern humans.
Location
Eurasia and North America.
Methods
We sequenced 110 complete mitochondrial genomes from Eurasian brown bears and combined these with published sequences from 138 brown bears and 33 polar bears. We used a Bayesian approach to obtain a joint estimate of the phylogeny and evolutionary divergence times. The inferred mutation rate was compared with estimates obtained using two additional methods.
Results
Bayesian phylogenetic analysis identified seven clades of brown bears, with most individuals belonging to a very large Holarctic clade. Bears from the widespread clade 3a1, which has a distribution from Europe across Asia to Alaska, shared a common ancestor about 45,000 years ago.
Main conclusions
We suggest that the Altai‐Sayan region and Beringia were important Late Pleistocene refuge areas for brown bears and propose large‐scale migration scenarios for bears in Eurasia and to North America. We also argue that brown bears and modern humans experienced a demographic standstill in Beringia before colonizing North America.
“…The single Caucasus population included in this study (Figure a; Georgia – from Buchovska et al., ) was composed of mitotypes a and b – the former widely distributed in the whole of Europe including Turkey, and the latter present at a particularly high frequency in Finland, Central Europe and NW Russia (Figure a); the mitotype d specific to Turkey was not present in the Caucasus population. Thus, based on these limited data there remains uncertainty regarding whether glacial refugia for Scots pine existed in the Caucasus but were not active during repopulating, similar to some other species (Petit, Brewer, & Bordács, ; Skrede, Eidesen, Piñeiro Portela, & Brochman, ) or whether this region was colonized from northern direction, as for example in case of common juniper ( Juniperus communis L.) (Hantemirova et al., ).…”
Aim: Scots pine is one of the dominant tree species in forest ecosystems of the temperate and boreal zones in Eurasia. Since the Tertiary, it has persisted also in the Mediterranean region, forming relict populations. In this study, we investigate rangewide genetic diversity of Scots pine, aiming to provide comprehensive information on the phylogeography and genetic resources of the species.Location: Europe and Asia. Methods: Thirteen paternally inherited chloroplast microsatellite (cpSSR) loci were used to investigate the genetic structure of 62 populations from Fennoscandia and 30 populations from the Mediterranean. We also surveyed variability of two maternally inherited mitochondrial DNA (mtDNA) regions and additionally included literature data from 156 populations (248 populations in total).Results: Scots pine retains an overall high genetic diversity in the chloroplast genome but, unexpectedly, the historically younger populations from Fennoscandia showed statistically higher mean intrapopulation diversity than the Mediterranean stands (0.807 and 0.750, respectively). The latter also contained a lower number of private cpSSR haplotypes.Population differentiation with respect to mtDNA was higher (G ST = 0.628) than at cpSSR (G ST = 0.015) indicating an efficient pollen-mediated gene flow among refugial populations of the species. One novel haplotype mtDNA was found, increasing the number of known mitotypes for the species from 4 to 5. The geographic distribution of mitotypes was structured into four groups corresponding to the main refugial areas of the species. Main conclusions: Genetic impoverishment of the Mediterranean populations may enhance their vulnerability to future environmental changes. The spatial distribution of two mitotypes in Fennoscandia, featuring predominance of mitotype a in Norway and Sweden and mitotype b in Finland, gives strong support for dual colonization of that region from south-eastern (Finland) and south-western (Sweden) directions. These results thus provide new insights into both Holocene expansion of Scots pine and the present distribution of species' genetic resources. | 541 DERING Et al.
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