António M. de Frias Martins’s research while affiliated with CIBIO Research Center in Biodiversity and Genetic Resources and other places

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Publications (47)


Supplementary Material_European Terrestrial Molluscs.pdf
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August 2019

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420 Reads

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2 Citations

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Figure 3. Population trends of European terrestrial molluscs; all species: outer ring; threatened species only: inner ring.
Figure 4. The proportion of European terrestrial molluscs known to occur within a protected area; all species: outer ring; threatened species only: inner ring.
Figure 5. Overall species richness of European terrestrial molluscs.
Figure 6. Distribution of endemic European terrestrial molluscs.
Figure 7. Distribution of threatened terrestrial molluscs in Europe.

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EUROPEAN RED LIST OF TERRESTRIAL MOLLUSCS: SNAILS, SLUGS, AND SEMI-SLUGS

July 2019

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3,820 Reads

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29 Citations


The Echinoderm Fauna of the Azores (NE Atlantic Ocean)

July 2019

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74 Reads

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9 Citations

Zootaxa

In more than 150 years of research in the waters surrounding the Azores, several publications on the fauna of echinoderms of the archipelago have been produced, in the form of papers, notes, reports, reviews, and monographs. This work attempts to summarize the present knowledge on this marine group in the Azorean exclusive economic zone (i.e., waters within 200 nautical miles of the archipelago’s shores). A short review of the history of the species’ taxonomy is given, with key references, geographical distribution, ecology, additional notes and, when possible, figures. We herein report 172 species of echinoderms (6 crinoids, 55 ophiuroids, 45 asteroids, 36 holothurians, and 30 echinoids) from the Azores Archipelago, most of them inhabiting deep waters (>200 m). Only 29 shallow-water species were recorded locally (≤50 m depth). In general, the echinoderm species present in the Azores are characterized by a wide geographical distribution in the Atlantic Ocean. Only nine taxa (all deep-water species, >840 m) appear to be restricted to the Azorean waters. Overall, the knowledge of the echinoderm fauna of the Azores is out-dated, with many species last collected in the archipelago over 100 years ago. A recent interest in the Azorean Mid-Atlantic waters has brought oceanographic cruises back to the archipelago, thus providing new opportunities for the renewal of 150 years of echinoderm studies in the area.


Figure 1. Gene map of the Melarhaphe neritoides mitogenome. Genes encoded on the plus strand are mapped outside the outer circle and are transcribed counterclockwise. Genes encoded on the minus strand are mapped inside the outer circle and are transcribed clockwise. The inner circle plot represents G + C% content; the darker the lines are, the higher their G + C% is. Photo credit: Yves Barette (RBINS).
Figure 2. Evolutionary rates (ω) of amino acid substitutions for each protein-coding gene among four littorinid mitogenomes.
Figure 3. Relative synonymous codon usage (RSCU) of the mitochondrial genome of Melarhaphe neritoides. The 22 codon families consisting of a total of 62 two-and four-fold degenerate synonymous codons are plotted on the x-axis. The label for the 2 or 4 codons that compose each family is shown in the boxes below the x-axis, and the colours correspond to the colours in the stacked columns. The most used synonymous codon in each family is in green. The RSCU values are shown on the y-axis.
Figure 4. Gene order of the 13 protein-coding genes of Melarhaphe neritoides mitogenome drawn into a phylogenetic context including a total of 68 Caenogastropoda. Underlined genes are encoded on the minus strand. Symbol letters for tRNAs indicate the encoded amino acid and follows the IUPAC-IUB nomenclature for amino acids. Branches are colour-coded to represent the putative clades Architaenioglossa (red), Cerithiimorpha (orange), Latrogastropoda (green), non-Latrogastropoda Hypsogastropoda (pink), and outgroup taxa are left in black. Numbers at the nodes are Bayesian posterior probabilities (left) and ML bootstrap values (right). Branches with posterior probability >0.95 and bootstrap support value >70% are considered to be strongly supported. Scale bar is substitutions/site. Plus sign indicates long branch.
Relation between mitochondrial DNA hyperdiversity, mutation rate and mitochondrial genome evolution in Melarhaphe neritoides (Gastropoda: Littorinidae) and other Caenogastropoda

December 2018

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845 Reads

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37 Citations

Mitochondrial DNA hyperdiversity is primarily caused by high mutation rates (μ) and has potential implications for mitogenome architecture and evolution. In the hyperdiverse mtDNA of Melarhaphe neritoides (Gastropoda: Littorinidae), high mutational pressure generates unusually large amounts of synonymous variation, which is expected to (1) promote changes in synonymous codon usage, (2) reflect selection at synonymous sites, (3) increase mtDNA recombination and gene rearrangement, and (4) be correlated with high mtDNA substitution rates. The mitogenome of M. neritoides was sequenced, compared to closely related littorinids and put in the phylogenetic context of Caenogastropoda, to assess the influence of mtDNA hyperdiversity and high μ on gene content and gene order. Most mitogenome features are in line with the trend in Mollusca, except for the atypical secondary structure of the methionine transfer RNA lacking the TΨC-loop. Therefore, mtDNA hyperdiversity and high μ in M. neritoides do not seem to affect its mitogenome architecture. Synonymous sites are under positive selection, which adds to the growing evidence of non-neutral evolution at synonymous sites. Under such non-neutrality, substitution rate involves neutral and non-neutral substitutions, and high μ is not necessarily associated with high substitution rate, thus explaining that, unlike high μ, a high substitution rate is associated with gene order rearrangement.





Beyond the Last Glacial Maximum: Island endemism is best explained by long-lasting archipelago configurations

November 2018

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647 Reads

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46 Citations

Global Ecology and Biogeography

Aim To quantify the influence of past archipelago configuration on present‐day insular biodiversity patterns, and to compare the role of long‐lasting archipelago configurations over the Pleistocene to configurations of short duration such as at the Last Glacial Maximum (LGM) and the present‐day. Location 53 volcanic oceanic islands from 12 archipelagos worldwide—Azores, Canary Islands, Cook Islands, Galápagos, Gulf of Guinea, Hawaii, Madeira, Mascarenes, Pitcairn, Revillagigedo, Samoan Islands and Tristan da Cunha. Time period The last 800 kyr, representing the nine most recent glacial–interglacial cycles. Major taxa studied Land snails and angiosperms. Methods Species richness data for land snails and angiosperms were compiled from existing literature and species checklists. We reconstructed archipelago configurations at the following sea levels: the present‐day high interglacial sea level, the intermediate sea levels that are representative of the Pleistocene and the low sea levels of the LGM. We fitted two alternative linear mixed models for each archipelago configuration using the number of single‐island endemic, multiple‐island endemic and (non‐endemic) native species as a response. Model performance was assessed based on the goodness‐of‐fit of the full model, the variance explained by archipelago configuration and model parsimony. Results Single‐island endemic richness in both taxonomic groups was best explained by intermediate palaeo‐configuration (positively by area change, and negatively by palaeo‐connectedness), whereas non‐endemic native species richness was poorly explained by palaeo‐configuration. Single‐island endemic richness was better explained by intermediate archipelago configurations than by the archipelago configurations of the LGM or present‐day. Main conclusions Archipelago configurations at intermediate sea levels—which are representative of the Pleistocene—have left a stronger imprint on single‐island endemic richness patterns on volcanic oceanic islands than extreme archipelago configurations that persisted for only a few thousand years (such as the LGM). In understanding ecological and evolutionary dynamics of insular biota it is essential to consider longer‐lasting environmental conditions, rather than extreme situations alone.


Fig. 1. Geographical distribution of Sclerasterias richardi in the Mediterranean Sea and NE Atlantic. The square indicates the type locality (Perrier 1882, in Milne-Edwards 1882), circles the historical records (Marenzeller 1893, 1895; Perrier 1894; Ludwig 1897; Pruvot 1897; Baldelli 1914; Fisher 1928; Gallo 1933; Gautier-Michaz 1958; Santarelli 1964; Tortonese 1965; Falconetti et al. 1976, 1977; Febvre et al. 1981; Munar 1984; Borri et al. 1990; Mastrototaro & Mifsud 2008; Mifsud et al. 2009) and the star the new record from the Azores (DBUA-ECH 357).
Table 1 . Size (Rmax, r) of the specimens from the Azores and corresponding arm length, number of arms and madreporites.
Fig. 2. Sclerasterias richardi (Perrier, in Milne-Edwards, 1882) (DBUA-ECH 357). a) aboral view; b) oral view; c) lateral view; d) detail of the oral region; e) oral view of the arm; f) S-shaped madreporite. All white scale bars are 1 mm Description of the specimens: Two animals with six arms of unequal size, three larger and three smaller; one specimen with three arms of similar dimensions to the larger arms of the six-rayed specimens (Table 1). Arms broad, pentagonal in cross-section, narrowing gradually into a round arm tip wholly covered by the terminal plate. Arms weakly attached to the disc. Reticular plating on the arms arranged in fairly regular longitudinal plate series (carinal, dorsolateral, superomarginal, inferomarginal, adambulacral); arm plates have a round fourlobbed shape with the lateral arms extending towards the corresponding lobe of the adjacent plates series with exception of the small bridgelike dorsolateral plates that serve as an intermediary link between superomarginal and carinal plates. Papulae occupying the interstices between plates, forming two longitudinal rows on 
First record of the Mediterranean asteroid Sclerasterias richardi (Perrier in Milne-Edwards 1882) in the Azores Archipelago (NE Atlantic Ocean)

November 2017

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463 Reads

The first occurrence of the Mediterranean fissiparous asteroid Sclerasterias richardi (Perrier in Milne-Edwards, 1882) is reported from the Azores based upon dredged material off the south coast of São Miguel Island, at 135 m depth. This record represents a considerable expansion of the species’ geographic range, otherwise reported with certainty only from the Mediterranean Sea. S. richardi is capable of producing long-lived planktotrophic larvae with high dispersal potential to reach remote areas such as the Azores. Alternatively, this species is also capable of reproducing asexually through fission, which could insure the maintenance of viable numbers in a stranded population. The presence of S. richardi in Azorean waters and its rarity in an otherwise thoroughly investigated area does not necessarily imply a recent arrival nor a human-mediated introduction, as the depths in consideration (80-700 m) are also the least studied in the archipelago.



Citations (28)


... Species with more or less wide ecological tolerance were also found in the poplar woodlands along the Bregalnitsa River valley (N=3) Among the investigated gastropod fauna from the poplar woodlands along the Bregalnitsa River valley, there are no species included in the threatened categories of IUCN Red List (Neubert et al. 2019). The newly described species, Vitrea melovskii sp. ...

Reference:

Inventory of the Terrestrial Gastropods in a Poplar Forest in the Valley of the Bregalnitsa River, Republic of North Macedonia, with the description of a new species of the genus Vitrea Fitzinger, 1833
Supplementary Material_European Terrestrial Molluscs.pdf

... snails, rats, flatworms) (Holland 2009;Chiba and Cowie 2016). Particularly for European land snail species, the most significant threats are natural ecosystem modifications, residential and commercial development and agriculture (Neubert et al. 2019). ...

EUROPEAN RED LIST OF TERRESTRIAL MOLLUSCS: SNAILS, SLUGS, AND SEMI-SLUGS

... The genus Marthasterias, first described by Jules Jullien in 1878 as a group from the family Asteriidae Gray, 1840, is characterized by having ambulacral tubes 2 in series of four, dorsal skeleton reticulated, five arms, marginal 3 plates 4 bordered by a membrane in which the marginal spines are lodged, pedicellariae 5 straight, and sessile ( Table 2) [13,21]. Marthasterias was considered an outgroup of the genus Asterias [22]; nevertheless, in a more recent study, Marthasterias is now accepted as an outgroup to the entire clade Asteriidae [23]. ...

The Echinoderm Fauna of the Azores (NE Atlantic Ocean)
  • Citing Article
  • July 2019

Zootaxa

... Differences between the resulting assemblies were reconciled using raw paired-end sequence data. Automated mitogenome annotation (MITOS; Bernt et al. 2013;Donath et al. 2019) was checked using criteria established by Fourdrilis et al. (2018) through Snapgene (Dotmatics). The nuclear rDNA cassette of each of the 24 snails was reconstructed manually from RNA-seq data by iterative blasting, initiated with P. acuta ITS sequences (GenBank KF316326-9). ...

Relation between mitochondrial DNA hyperdiversity, mutation rate and mitochondrial genome evolution in Melarhaphe neritoides (Gastropoda: Littorinidae) and other Caenogastropoda

... This confounding effect of the archipelago's geography could substantially impact the interpretation of phylogenies in dynamic contexts, especially in the context of islands. As islands are surrounded by water, sea-level variation is another geographical factor altering island area and connectivity between islands over time (Rijsdijk et al. 2014;Fernández-Palacios et al. 2016;Borregaard et al. 2017;Norder et al. 2018Norder et al. , 2019. Because sea-level fluctuations occur on a faster timescale than ontogenetic changes and and because we found that rapid past geo-environmental changes may have a substantial imprint on phylogeny structure, sea level fluctuations are expected to introduce additional complexity when attempting to reconstruct the biogeographic history of a community based on its phylogenetic patterns. ...

Beyond the Last Glacial Maximum: Island endemism is best explained by long-lasting archipelago configurations
  • Citing Article
  • November 2018

Global Ecology and Biogeography

... The remaining COI sequence composition of D. cornus across the west coast of Australia was relatively homogeneous and likely correspond to those of a single species. The relatively high Φ ST value between the D. cornus from Ningaloo Reef compared to the Abrolhos Islands could reflect differing sample sizes and/or higher levels of haplotype diversity (Fourdrilis et al. 2016), however, we cannot rule out the possibility that there is a real difference between the D. cornus assemblages at these two sites, especially as the results of the power analysis suggest that our COI data set did not have sufficient power to detect subtle levels of genetic differentiation, and as Rottnest Island group did not significantly differ from either of the northern groups. Future research should use more intricate genomic data, e.g., Single Nucleotide Polymorphisms (SNPs), to provide a higher-resolution test of differentiation. ...

Mitochondrial DNA hyperdiversity and its potential causes in the marine periwinkle Melarhaphe neritoides (Mollusca: Gastropoda)

... Even though conservation efforts focused on island biodiversity may greatly benefit from the ecological information generated by SDMs, research to-date on SDMs has tended to focus on species with broad ranges and for which there is a large amount of occurrence information, corresponding typically to continental species (Hickisch et al., 2019, Leroy, 2022. Historically, there have been fewer applications of SDMs in island environments and for island species, although recently this situation has started to change (e.g., Price et al., 2012;Vergilio et al., 2016;Spiers et al., 2018;Goedecke et al., 2020;Barlow et al., 2021). The increasing implementation of SDMs in island studies provides an opportunity for evaluating how two key considerations for developing robust models for islands species have been handled: data limitations (Pearson et al., 2007;Lannuzel et al., 2021) and the restricted spatial context of island environments (Kier et al., 2009;Whittaker et al., 2023). ...

Assessing the efficiency of protected areas to represent biodiversity: a small island case study

Environmental Conservation

... More recently, Ahuir Galindo [2016] described I. alonensis labiatus from Nerja (Sierras de Tejeda, Almijara y Alhama, Málaga, Spain) easily distinguishable by a large shell size and a lip more developed than average. Nevertheless, a large body of scientific evidence has proved shell morphology to be often unsuitable as an isolated tool for delimiting and recognising species of pulmonate gastropods [Giusti, Manganelli, 1992;Schilthuizen, Gittenberger, 1996;Young et al., 2001;Korte, Armbruster, 2003;Uit de Weerd et al., 2004;Geenen et al., 2006;Pfenninger et al., 2006;Triantis et al., 2016;Collado et al., 2019;Vinarski et al., 2020;Liétor et al., 2024a]. ...

Discordance between morphological and taxonomic diversity: Land snails of oceanic archipelagos
  • Citing Article
  • April 2016

Journal of Biogeography

... This species is also reported from the Lower Pliocene of Azores [105] and the Canary Islands (Lanzarote, Fuerteventura and Gran Canaria [106]), ; the Pleistocene of the Canary Islands and Porto Santo (Madeira Archipelago; [25]); and from the Last Interglacial (LIG) fossil record of Azores [107,108], Selvagens [109], Canary Islands [106] and Cabo Verde [25]. Today, it is reported for all Macaronesian archipelagos [110,111]. In the oldest Azorean Island, Santa Maria, the two Pliocene outcrops from where this bivalve species is reported (Ávila, unpublished data) are Pedra-que-pica (4.78 ± 0.13 Ma to 4.13 ± 0.19 Ma) and Ponta do Castelo (4.13 ± 0.19 Ma to 3.98 ± 0.05 Ma) [112]. ...

Checklist of the littoral gastropods (Mollusca: Gastropoda) from the Archipelago of the Azores (NE Atlantic)

Biodiversity

... Ввиду отсутствия единой системы олигохет, поддержанной как морфологическими, так и молекулярными данными (Kaygorodova, 2010), мы следуем системе Тимма (Timm, 2009). Данные по распространению получены из видовых сводок (Попченко, 1988;Timm, 2009) и с использованием ресурса «PESI» (de Jong et al., 2015). ...

PESI - A taxonomic backbone for Europe