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Bootstrap coalescent species trees of the family Talpidae estimated using (A) ASTRAL-II, and (B) SVDquartets. Support values are provided for all non-highly supported nodes (posterior probabilities [PP] <0.95 or bootstrap values [BS] <90). 

Bootstrap coalescent species trees of the family Talpidae estimated using (A) ASTRAL-II, and (B) SVDquartets. Support values are provided for all non-highly supported nodes (posterior probabilities [PP] <0.95 or bootstrap values [BS] <90). 

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The mammalian family Talpidae (moles, shrew moles, desmans) is characterized by diverse ecomorphologies associated with terrestrial, semi-aquatic, semi-fossorial, fossorial, and aquatic-fossorial lifestyles. Prominent specializations involved with these different lifestyles, and the transitions between them pose outstanding questions regarding the...

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... coalescent species tree estimations were highly con- gruent with the concatenated trees at the tribal level ( fig. 2 and supplementary fig. S1B and C, Supplementary Material online), though most tribal interrelationships, including the positions of the star-nosed mole and the desmans, were not resolved. In addition, while Scapanulus was unambiguously placed within Scalopini, its sister-relationship with Parascalops only received modest support (BS ¼ ...
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... the interre- lationships among Southeast Asian Euroscaptor, and be- tween long-tailed moles and the two shrew-mole tribes, though support scores for these alternative nodes were low (BS ¼ 49-74). SVDquartets further placed Euroscaptor parvidens sister to a clade containing other Southeast Asian Euroscaptor plus Parascaptor þ Scaptochirus ( fig. 2B), result- ing in a polyphyletic Euroscaptor (BS ¼ ...
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... between Chinese and North American scalopins, between European and Asian talpins, and between the two long-tailed mole lineages all occurred in the mid-Miocene (ca. 16 Ma; 95% CI = 22-10 Ma). Finally, divergences between sister genera generally occurred between 18 and 7 My (95% CI ¼ 26-4 Ma). The lineage-through-time (LTT) plot (supple mentary fig. S2A, Supplementary Material online) showed an increasing diversification rate beginning ca. 10 Ma. However, the Pybus and Harvey's c-value was insignificantly negative (À0.70; P ¼ 0.24), while the likelihood-based test found pure- birth as the best constant rate model (AIC ¼ 68.67) and the yule-3-rate as the best rate variable model (AIC ¼ ...
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... and Harvey's c-value was insignificantly negative (À0.70; P ¼ 0.24), while the likelihood-based test found pure- birth as the best constant rate model (AIC ¼ 68.67) and the yule-3-rate as the best rate variable model (AIC ¼ 67.94), sug- gesting that speciation rate did not shift significantly through time. The fossil-diversity plot (supplementary fig. S2B, Supplementary Material online) demonstrated that the num- ber of semi-fossorial and nonfossorial species have substantially declined in the last four million ...
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... For example, the fossil history of Uropsilinae (includ- ing Asthenoscapter and Desmanella) extends much further back in Europe than it does in Asia ( Qiu and Storch 2005). Similarly, members of the North American tribes Neurotrichini, Condylurini, and Scalopini were also distrib- uted in Europe during the Oligocene to Pleistocene (supple mentary fig. S2C, Supplementary Material online), but have since been extirpated (van den Hoek Ostende et al. 2005). This decline of non-fossorial talpids was clearly evident on the fossil-diversity plot (supplementary fig. S2B, Supplementary Material online), but not accounted for on the LTT plot using living species only (supplementary fig. S2A, ...
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... tribes Neurotrichini, Condylurini, and Scalopini were also distrib- uted in Europe during the Oligocene to Pleistocene (supple mentary fig. S2C, Supplementary Material online), but have since been extirpated (van den Hoek Ostende et al. 2005). This decline of non-fossorial talpids was clearly evident on the fossil-diversity plot (supplementary fig. S2B, Supplementary Material online), but not accounted for on the LTT plot using living species only (supplementary fig. S2A, Supplementary Material ...
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... (supple mentary fig. S2C, Supplementary Material online), but have since been extirpated (van den Hoek Ostende et al. 2005). This decline of non-fossorial talpids was clearly evident on the fossil-diversity plot (supplementary fig. S2B, Supplementary Material online), but not accounted for on the LTT plot using living species only (supplementary fig. S2A, Supplementary Material ...

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... Furthermore, the mean resting metabolic rate decreases during increasing up to 30°C and it is suggested that over 30°C leads to a risk of overheating (Frears, 1993). Both Talpa and Mogera are closely related Palaearctic taxa (He et al., 2017) and inhabit temperate regions in Europe and Japan, respectively (Loy & Corti, 1996;Ohdachi et al., 2015). Therefore, it is estimated that the thermoneutral zone of Mogera likely ranges from 23°C to around 30°C (Frears, 1993;Kashimura et al., 2010). ...
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... Remarks.-In the paleontological literature, desmans are traditionally considered as a subfamily. However, genetic data (e.g., He et al., 2016) suggest its inclusion within the Talpinae, which is followed here. Additionally, we refer here to the genus Archaeodesmana Topachevsky and Pashkov, 1983, rather than Ruemkelia Rzebik-Kowalska and Pawłowski, 1994, an alternative name meant to replace Dibolia (see Rzebik-Kowalska and Rekovets, 2016). ...
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... The existing phylogenetic trees of moles differ in the position of the Japanese mountain mole Oreoscaptor mizura relative to representatives of the genera Mogera and Euroscaptor. Some researchers place it basal to these genera [3,4,10,11] and others place it in a separate clade together with Mogera, different from the branch leading to Euroscaptor, Parascaptor, and Scaptochirus [2,7]. ...
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... ground lifestyle of the Talpini results in similar physical traits of moles and makes it difficult to differentiate them, leading to the underestimation of the species diversity [2]. In Talpini, the genus Talpa is widely distributed from Western Europe to Asia. ...
... The phylogeny of the Talpini tribe is now well established. Genetic research provided good support for phylogenies based on morphological data [2,3,6]. High genetic differentiation within the most successful genus Talpa allowed to identify 4 clades with a strict geographical reference for the European and Caucasian group of species, as well as the "davidiana" group, the re-colonization of Europe from Asia was shown [7]. ...
... We have shown that each stage of species divergence within the genus is marked by certain rearrangements in half of the autosomes, which have undergone changes in contrast to the rest of the autosomes (homologs EPAR 5, 8, 10-15), which were conserved (Table 1, Figure 3). The Japanese mountain mole, Oreoscaptor mizura, formerly treated as E. mizura, was suggested to be elevated to genus level [2,4,10,11,36]. Its karyotype differs from the Euroscaptor by the absence of evolutionary rearrangements, which gives reason to assume its chromosome set is the most conservative and close to the ancestral karyotype of the genus. Moreover, its similarity to the karyotype of M.wogura, a species from another genus [16], suggests that these species retained a chromosomal set of an ancestor common to both genera. ...
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In recent years, the number of mole species for which the species status has been confirmed using genetic methods has been continuously increasing. Unfortunately, cytogenetic analysis is not available for all species. Here, for the first time, a GTG-banded karyotype of the small-toothed mole from Vietnam, Euroscaptor parvidens, a representative of the eastern clade of the genus Euroscaptor, was described. Through comparative analysis of available Euroscaptor (E. parvidens, E. klossi, and E. malayana) and Oreoscaptor (O.mizura) karyotypes we find cytogenetic signatures. Zoo-FISH with sorted chromosomes of the Siberian mole Talpa altaica on chromosome sets of the small-toothed mole E. parvidens, the small Japanese mole M. imaizumii from the close genus Mogera and the Japanese shrew mole Urotrichus talpoides from the tribe Urotrichini made it possible to identify syntenic regions between species that diverged about 35 million years ago. The low rate of chromosomal changes within the species of the genus Talpa - T.altaica and T.europaea - and the high rate of karyotypic reshuffling within the Asian genera of the tribe were confirmed. The pericentric inversions on four pairs of autosomes are shared between the closely related genera Euroscaptor, Oreoscaptor, and Mogera, while many more apomorphic rearrangements have occurred in each lineage additionally. The highest rate of chromosomal changes was recorded in the lineage of the small-toothed mole.
... The species typically occurs in evergreen broad-leaved forests, shrubs, and near farm fields at elevations of 1300-3600 m (Wilson and Mittermeier 2018). It is considered a relict species because its closest relatives are distributed in Japan (Dymecodon and Urotrichus) and North America (Neurotrichus), which diverged from long-tailed moles approximately 30 million years ago (He et al. 2017). ...
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... Shinohara et al. found that the North American moles and Eurasian moles are not monophyletic groups, and thus proposed that there have been at least two separate evolution processes of Talpidae [12]. He et al. confirmed that Gansu mole (Scapanulus oweni) is the only living Asian population in North America based on mitochondrial and nuclear gene sequences [2]. However, with the reported new species belonging to the family Talpidae, such as Talpa aquitania, Uropsilus dabieshanensis sp. ...
... The phylogenetic relationship of Talpidae is a controversial topic in ecological research. He et al. used 19 nuclear genes and two mitochondrial genes to construct the phylogenetic trees of about 60% of Talpidae animals in 17 genera, preliminarily elucidating the evolutionary relationships of the Talpidae animals [2]. However, with the emergence of new species of Talpidae in recent years (e.g., Talpa aquitania, Uropsilus dabieshanensis sp. ...
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... Convergent evolution among specialized clades has created major discrepancies between talpid molecular and morphological phylogenies (Douady et al., 2002;Symonds, 2005;Sánchez-Villagra et al., 2006;He et al., 2016). Similar morphology among clades makes it difficult to choose morphological characters independent of ecology, and most molecular studies also lack confidence on cluster positions. ...
... Talpidae is an ecologically diverse family consisting of: terrestrial shrew moles, semi-fossorial shrew moles, semi-aquatic desmans, as well as semi-fossorial and fossorial moles (Koyabu et al., 2011). Currently, the most parsimonious phylogenetic hypothesis comes from He et al. (2016). There are three subfamilies within Talpidae: Uropsilinae (Asian shrew-like moles), Talpinae (Old World moles, desmans, and shrew moles), and Scalopinae (New World moles), and there are seven tribes: Scalopini (North American/Asian fossorial moles), Scaptonychini (Chinese fossorial long-tailed moles), Urotrichini (Japanese semi-fossorial shrew moles), Neurotrichini (North American semi-fossorial shrew moles), Condylurini (North American semi-fossorial star-nosed mole), Desmanini (Eurasian semi-aquatic desmans), and Talpini (Eurasian fossorial moles). ...
... Two of the six clusters are exclusively fossorial: the Eurasian Talpini and North American/Asian Scalopini. It is hypothesized that these two clusters convergently evolved similar derived morphological specializations for fossorial life (Gorman and Stone, 1990;Piras et al., 2012;Meier et al., 2013;He et al., 2016). ...
... The phylogenetic relationships of Talpidae have been the subject of ongoing debate for decades (Whidden 2000;Shinohara et al. 2003;Bannikova et al. 2015;He et al. 2016; This article is protected by copyright. All rights reserved. ...
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The evolution of complex morphological structures can be characterized by the interplay between different anatomical regions evolving under functional integration in response to shared selective pressures. Using the highly derived humeral morphology of talpid moles as a model, here we test whether functional performance is linked to increased levels of evolutionary integration between humerus sub‐units and, if so, what the strength is of the relationship. Combining 2D geometric morphometrics, phylogenetic comparative methods and functional landscape modelling, we demonstrate that the high biomechanical performance of subterranean moles’ humeri is coupled with elevated levels of integration, whereas taxa with low performance values show intermediate or low integration. Theoretical morphs occurring in high‐performance areas of the functional landscape are not occupied by any species, and show a marked drop in covariation levels, suggesting the existence of a strong relationship between integration and performance in the evolution of talpid moles’ humeri. We argue that the relative temporal invariance of the subterranean environment may have contributed to stabilize humeral morphology, trapping subterranean moles in a narrow region of the landscape and impeding any attempt to reposition on a new ascending slope. This article is protected by copyright. All rights reserved
... In particular, the mountain ranges of Southwest China are viewed as among the most important montane biodiversity hotspots (Mittermeier et al. 2011), where past environmental changes have significantly contributed to the speciation and regional biodiversity (Wan et al. 2021). Indeed, in the last decade, several new cryptic mammal species have been uncovered in this area (Abramov et al. 2009;He et al. 2017;Liu et al. 2018;Wan et al. 2018;Bannikova et al., 2019;Chen et al. 2020). ...
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During a small mammal survey in Wanglang National Natural Reserve, Sichuan, China in August–October 2018, we collected four specimens of an Asiatic striped squirrel (genus Tamiops) that could not be assigned morphologically to any described species. Phylogenetic analyses of CYTB and nuDNA sequences strongly supported them in the genus Tamiops. The p-distances of CYTB between these individuals and other species of Tamiops ranged from 17.4 to 19.1%. Morphologically, they differed from their congeners, including T. maritimus, T. mcclellandii, T. rodolphii, and T. swinhoei by pelage, skull, and baculum characteristics. Based on the results of morphological comparisons and molecular analyses, we describe the four specimens as the new species Tamiops minshanica sp. nov.