Tomás Gallardo’s research while affiliated with Complutense University of Madrid and other places

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Publications (59)


Table 1 Survival temperature interval (STI) and threats over seaweeds
Fig. 3 Extent of Occurrence (EOO) for the warm-temperate red algae Gelidium corneum. Ecological regions correspond to those described by Ramos et al. (2016), Tuya et al. (2012) and Bermejo et al. (2012) (see "Materials and methods"). Numbered lines correspond to the limits of the ecological units. RVi Ría Villaviciosa, RV Ria de Viveiro, FC Finisterre Cape, SP-PT Spain-Portugal border, NC Nazaré Canyon. The outer coastline represents the algal distribution during Period 1 (1980's-1990's), dark polygons correspond to estimated EOO. The inner coastline corresponds to Period 2 (2013-2016), dark polygons correspond to estimated EOO; light polygons correspond to areas where a sharp decline in G. corneum meadows was observed
Extent of Occurrence (EOO) of warm-temperate kelps with an intertidal and subtidal distribution (Laminaria ochroleuca and Saccorhiza polyschides). Ecological regions correspond to those described by Ramos et al. (2016), Tuya et al. (2012) and Bermejo et al. (2012) (see “Materials and methods”). Numbered lines correspond to the limits of ecological units. FR–SP France–Spain border, RVi Ría Villaviciosa, RV Ria de Viveiro, FC Finisterre Cape, SP–PT Spain–Portugal border, NC Nazaré Canyon, PT–SP Portugal–Spain border, PC Punta Camarinal, Gib Gibraltar. The outer coastline represents kelp distribution during Period 1 (1980’s–1990’s), dark polygons correspond to estimated EOO. The inner coastline corresponds to Period 2 (2013–2016), dark polygons correspond to estimated EOO; dashed lines indicate areas where the kelps have not been found; light polygons correspond to areas where sparse isolated individuals have been found in the deep subtidal zone
Extent of Occurrence (EOO) for cold-temperate kelps with an intertidal and subtidal distribution (Laminaria hyperborea and Saccharina latissima). Ecological regions correspond to those described by Ramos et al. (2016) and Tuya et al. (2012) (see “Materials and methods”). Numbered lines correspond to the limits of the ecological units. RVi Ría Villaviciosa, RV Ria de Viveiro, FC Finisterre Cape, SP–PT Spain–Portugal border, NC Nazaré Canyon. The outer coastline represents the kelp distribution during Period 1 (1980’s–1990’s), dark polygons correspond to estimated EOO. The inner coastline corresponds to Period 2 (2013–2016), dark polygons correspond to estimated EOO; dashed lines indicate areas where the kelps have not been found; light polygons correspond to areas where sparse isolated individuals have been found in the deep subtidal zone
Extent of Occurrence (EOO) for fucoids with intertidal distribution (Himanthalia elongata and Fucus serratus). Ecological regions correspond to those described by Tuya et al., (2012) and Ramos et al. (2016) (see “Materials and methods”). Numbered lines correspond to the limits of the ecological units. RVi Ría Villaviciosa, RV Ria de Viveiro, FC Finisterre Cape, SP–PT Spain–Portugal border, NC Nazaré Canyon. The outer coastline represents the fucoids’ distribution during Period 1 (1980’s–1990’s), dark lines correspond to estimated EOO. The inner coastline corresponds to Period 2 (2013–2016), dark lines correspond to estimated EOO; dashed lines indicate areas where the fucoids have not been found; light lines correspond to areas where sparse isolated individuals have been found
Distributional shifts of canopy-forming seaweeds from the Atlantic coast of Southern Europe
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April 2019

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194 Reads

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91 Citations

Biodiversity and Conservation

P Casado-Amezúa

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Canopy-forming seaweeds sustain critical ecosystem services in coastal habitats. Around the world, many of these seaweeds are suffering strong declines, mainly attributed to the progressive increase in sea surface temperature, in combination with other stressors due to current global changes. The southernmost part of the NE Atlantic is among those areas most affected by climate change. In this study, we estimated the distributional contractions of seven of the most conspicuous seaweeds from the Atlantic coasts of the Iberian Peninsula using an "Extent of Occurrence" methodology. Overall, during the last three decades , range shifts have been more pronounced east of the Cantabrian Sea than along the western coast of the Iberian Peninsula. In particular, regions with a semi-permanent summer upwelling seem to be critical to the persistence of brown seaweeds, fucoids and kelps. Range contractions of the cold-temperate fucoids were estimated to be ca. 21% and 45% for Himanthalia elongata and Fucus serratus, respectively; and for the kelps Saccharina latis-sima and Laminaria hyperborea, 6% and 14%, respectively. Range contractions for warm-temperate kelps were estimated to be ca. 13% and 10% for Saccorhiza polyschides and L. ochroleuca, respectively. Finally, a decline in the warm-temperate red algae Gelidium corneum occurred only in the easternmost area of the Cantabrian Sea (Basque Country), leading to a distributional contraction of 7%. We recommend conservation actions to better manage the remnant populations of these canopy-forming seaweeds, and their inclusion in national and regional catalogues of endangered species and on international Red Lists.

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NUEVA LISTA CRÍTICA DE LAS ALGAS BENTÓNICAS MARINAS DE ESPAÑA. A new checklist of benthic marine algae of Spain. Algas. Bol. Inf. Soc. Esp. Ficol. 51,7-52

June 2016

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152 Reads

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9 Citations

En 2012 responsables del Ministerio de Agricultura, Alimentación y Medioambiente de España (MAGRAMA) a través de su División para la Protección del Mar, se pusieron en contacto con la Sociedad Española de Ficología (SEF), solicitando su colaboración en la elaboración de la denominada Lista Patrón de las Especies Marinas Presentes en España, elemento básico de la Ley 41/2010 de Protección del Medio Marino. El compromiso de la SEF y de algunos de su miembros, fue el de participar de manera desinteresada en la elaboración de la parte de la Lista correspondiente a las algas bentónicas y fanerógamas marinas españolas. La Lista se ha estructurado siguiendo los criterios sistemáticos y taxonómicos de la base de datos AlgaeBase (Guiry & Guiry 2016), ampliamente aceptados en la actualidad. Se han catalogado las especies y taxones subespecíficos (subespecies, variedades y formas) citados para el litoral ibérico, baleárico, norteafricano y canario, indicando su presencia en cada una de las Demarcaciones Marinas.




Fig. 2. Distribution of Himanthalia elongata. Locations visited are indicated by black (presence), white (absence) and grey (sporadic populations) circles and also pointed by grey arrows. (A) Surveys of 1889e1911, (B) 1955e1962, (C) 1975e77 and 1990. Names of the range boundary locations are shown. See text for bibliographic references.  
Recent and historical range shifts of two canopy-forming seaweeds in North Spain and the link with trends in sea surface temperature

August 2013

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614 Reads

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88 Citations

Acta Oecologica

Geographical range shifts of two canopy-forming seaweeds, Himanthalia elongata (L.) S.F. Gray and Fucus serratus L. were investigated at their southern range boundary in Northern Spain from the end of nineteenth century to 2009. Given the good dispersal abilities of H. elongata and its short life-span, we hypothesize that this species will track environmental changes at a faster rate than the perennial and short-distance disperser F. serratus. Our results show a continuous and drastic westward retraction of H. elongata, which has nowadays virtually vanished in Northern Spain, whereas F. serratus is still found in the westernmost area. Despite this, the first species is still relatively abundant in the Iberian Peninsula, whereas the presence of the latter is scattered and reduced. Overall, range shifts fit with the warming trend in sea surface temperature (SST), whereas it is unlikely that increases in grazing pressure or coastal pollution have driven the observed changes, particularly the rapid trend in recent years. Differences in species traits are linked to range dynamics. The higher persistence of F. serratus at eastern shores may thus be related to its longer life span and its greater thermal tolerance. The presence of sporadic populations of H. elongata outside the zone of continuous distribution can be attributed to long-distance dispersal events during cold pulses. Relict populations in isolated and estuarine locations were left behind in the contracting range margins, particularly for F. serratus. In Northern Spain, the westward retreat of large canopy-forming algae seems to be a general phenomenon, involving other species such as kelps. Therefore, an evident reorganization of coastal assemblages is expected, though the temporal extent of changes and the consequences for ecosystem services need to be evaluated.


Fig. 34. Maximum likelihood tree derived from the combined LSU (full) and rbc L alignment for representatives of the Gigartinales and two outgroups (Bonnemaisoniales and Peyssonneliales). Bootstrap values are displayed along branches with . 50 % support, followed by posterior probabilities from the Bayesian analyses when support was . 0.95. Branches resolved with full support in both analyses are denoted with an asterisk. 
Figs 1-5. Pseudopolyides furcellarioides gen. et sp. nov. Habitat and habit. Fig. 1. Lugo, Peinza´sPeinza´s (type locality), April 1998, lower intertidal with Lithophyllum incrustans and Corallina elongata. Scale bar ¼ 10 lm. Fig. 2. Lugo, Punta del Castro, May 2003, lower intertidal. Scale bar ¼ 10 lm. Fig. 3. A Coruña, Cambre, June 2008, lower intertidal with Bifurcaria bifurcata, Jania rubens, Halopteris scoparia, Dictyota dichotoma and Sargassum muticum. Scale bar ¼ 20 lm. Fig. 4. Polyides rotundus, A Coruña, Lourido, April 2009, SANT-Algae 21694. Scale bar ¼ 5 cm. Fig. 5. Furcellaria lumbricalis (arrow) intermingled with Pseudopoplyides furcellarioides (arrowhead), Asturias, Canda´sCanda´s, November 2007, SANT-Algae 19547. Scale bar ¼ 5 cm.
Figs 6-13. Pseudopolyides furcellarioides gen. et sp. nov. External vegetative morphology. Fig. 6. Pseudopolyides furcellarioides as Polyides rotundus, Jove, Gijón, August 1934, lower intertidal, F. Miranda's personal herbarium No. 290. Scale bar ¼ 5 cm. Fig. 7. Furcellaria lumbricalis, Jove (Gijón), August 1936, lower intertidal, F. Miranda's personal herbarium No. 326. Scale bar ¼ 5 cm. Fig. 8. Images of type material, Peinza´sPeinza´s, December 2007, subtidal (1 m) over rock, SANT-Algae 19559, image of holotype (arrow). Scale bar ¼ 5 cm. Fig. 9. Image of holotype in detail, Peinza´sPeinza´s, December 2007, SANT-Algae 19559. Scale bar ¼ 5 lm. Fig. 10. Mammillated, crustose holdfast producing erect axes, Asturias, Canda´sCanda´s, November 2007, SANT-Algae 19548. Scale bar ¼ 1 cm. Fig. 11. Crustose holdfast with abundant erect axes, Lugo, Punta del Castro, May 2003, SANT-Algae 18954. Scale bar ¼ 1 cm. Fig. 12. Stout, lower-intertidal morphotype resembling the habit of Polyides rotundus, Lugo, Punta del Castro, May 2003, SANT-Algae 18954. Scale bar ¼ 5 cm. Fig. 13. Slender, upper-subtidal morphotype resembling the habit of Furcellaria lumbricalis, Lugo, Punta del Castro, May 2003, SANTAlgae 18955. Scale bar ¼ 5 cm.
Figs 14-21. Pseudopolyides furcellarioides gen. et sp. nov. Internal vegetative morphology. Fig. 14. Transverse section showing compact medulla and large, radially arranged cells in the inner cortex and outer cortex (F. Miranda's personal herbarium No. 290, Asturias, Jove, 1934, as Polyides rotundus). Scale bar ¼ 200 lm. Fig. 15. Transverse section, Asturias, SANT-Algae 19547. Scale bar ¼ 200 lm. Fig. 16. Longitudinal section with medullar filaments and inner cortex diverging at c. 458 from the medullary filaments (SANT-Algae 13050 and Exsiccata Algae Ibericae No. 167, as Polyides rotundus). Scale bar ¼ 500 lm. Fig. 17. Transverse section. Detail of the medulla with longitudinal filaments interwoven with oblique rhizoids and the abrupt transition to inner cortex (F. Miranda's personal herbarium No. 290, Asturias, Jove, 1934, as Polyides rotundus). Scale bar ¼ 200 lm. Fig. 18. Elongated cells in outer cortex, SANT-Algae 21689. Scale bar ¼ 50 lm. Fig. 19. Domed pit connections between medullar filaments, SANT-Algae 21690. Scale bar ¼ 20 lm. Fig. 20. Domed pit connections in the distal end of a medullar filament, SANT-Algae 21690. Scale bar ¼ 20 lm. Fig. 21. Medullar filaments with ball-and-socket joint pit connections, SANT-Algae 19584. Scale bar ¼ 20 lm.
Figs 35-37. Polyides rotundus and Furcellaria lumbricalis. Internal vegetative morphology. Fig. 35. Polyides rotundus: domed pit connections and refractive inclusions (arrow), A Coruña, Lourido, SANT-Algae 22519. Scale bar ¼ 50 lm. Fig. 36. Polyides rotundus: longitudinal filaments and refractive inclusions (arrow) in the medulla, France, Brittany, SANT-Algae 19570. Scale bar ¼ 200 lm. Fig. 37. Furcellaria lumbricalis: ball-and-socket joint pit connections (France, Brittany, SANT-Algae 19569). Scale bar ¼ 30 lm.
Pseudopolyides furcellarioides gen. et sp. nov. (Gigartinales, Rhodophyta) an erect member of the Cruoriaceae based on morphological and molecular evidence

March 2013

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591 Reads

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15 Citations

Phycologia

Pseudopolyides furcellarioides gen. et sp. nov. (Gigartinales, Rhodophyta) was described from the Atlantic coasts of the northern Iberian Peninsula based on morphological and molecular evidence. This plant was found growing in the lower intertidal to the upper subtidal of moderately exposed rocky coasts, the bases anchored to rocks and often covered by sand. Thalli were perennial, terete, dichotomously branched and erect from a mammillate crustose holdfast. Fronds were multiaxial with a compact filamentous medulla, a densely pseudoparenchymatous inner cortex and an anticlinal outer cortex. Gametophytes were dioecious and isomorphic to tetrasporophytes. Spermatangia were superficial on swollen branch tips. Gonimocarps were spindle-shaped and directed to the thallus interior, while tetrasporangia were zonate. The habit and internal structure resembled those of both Polyides rotundus (characterized by crustose holdfasts, dichotomous or trichotomous branching and similar longitudinal section) and Furcellaria lumbricalis (distinguished by internal gonimocarps and zonate tetrasporangia). All three species occasionally occurred sympatrically in the Iberian Peninsula and were easily misclassified. Molecular phylogenetic analyses placed Pseudopolyides furcellarioides within the previously monogeneric Cruoriaceae, making it the first non-crustose representative of this family.


Citations (32)


... The apical cell initiates a dichotomous primary ramification, which leads to bilateral secondary ramification from the initial cell in the marginal slits. Geographical distribution: Ascophyllum nodosum is found in the Atlantic Ocean (Neto et al., 2020), the White Sea (Smirnova & Mikhailova, 2013), and the Mediterranean (Gallardo et al., 2016;Petrocelli & Cecere, 2019). Previous research on Algerian coasts has found no record of this species. ...

Reference:

Checklist updating of the Mediterranean Western Algeria algae, fifteen first records case of Phaeophyceae, Chlorophyceae and Rhodophyceae
NUEVA LISTA CRÍTICA DE LAS ALGAS BENTÓNICAS MARINAS DE ESPAÑA. A new checklist of benthic marine algae of Spain. Algas. Bol. Inf. Soc. Esp. Ficol. 51,7-52

... nodosum has remained stable in northern Portugal, where sea temperatures rarely exceed 22°C (Seabra et al., 2011), while other cold water species have experienced significant range contraction northwards (Casado-Amezúa et al., 2019;Lima et al., 2006). This realisation raises the question of what actually sets its distribution limit. ...

Distributional shifts of canopy-forming seaweeds from the Atlantic coast of Southern Europe

Biodiversity and Conservation

... Spain Gallardo et al. (1990), Fernández (1991), Juanes & Borja (1991) and Santos (1993: Appendix 1) reviewed the exploitation of the G. sesquipedale resource in Spain. The harvest areas were located in the north coast, mainly in Cantabria, Asturias and Basque Country, in order of decreasing importance. ...

Current state of seaweed resources in Spain
  • Citing Chapter
  • January 1990

... Multiple subsamples were collected from different points at each station and Fig. 1). The material belonging to Chlorophyta according to Gallardo et al. (1993), Phaeophyceae according to Ribera et al. (1992), and Rhodophyta (while Corallinales was based on Bressan & Babbini-Benussi, 1995 according Silva et al. (1996) were determined and nomenclature checked against Guiry and Guiry, 2021). The collected samples were transported to the laboratory in a dark cooler as quickly as possible. ...

Check-list of Mediterranean Seaweeds, 2 Chlorophyceae

Botanica Marina

... El vigente catálogo de la flora marina gallega ) contiene 296 especies de Rhodophyta. Gracias entre otras cosas al aumento de la masa crítica de investigadores y al empleo de herramientas moleculares, en la última década se ha incrementado aún más el conocimiento de Rhodophyta, aportándose nuevas citas y registros corológicos para Galicia (Bárbara et al. , 2006(Bárbara et al. , 2008a(Bárbara et al. ,b, 2011(Bárbara et al. , 2012(Bárbara et al. , 2016Cremades et al. 2007;Peña & Bárbara 2006a,b, 2008, 2010Escudero et al. 2009;Díaz Tapia et al. 2013a,c;Díaz Tapia & Bárbara 2013Carro et al. 2014;Pardo et al. 2014Pardo et al. , 2015Hernández-Kantún et al. 2015;Peña et al. 2015a) e, incluso, se han descrito nuevos géneros y especies, algunas de ellas endémicas (Peña et al. , 2015bBárbara et al. 2013a, b;Díaz-Tapia et al. 2013b;Díaz-Tapia & Bárbara 2013;Robuchon et al. 2014). En este nuevo catálogo de las Rhodophyta de Galicia se añaden 37 especies encontradas en la última década en aguas gallegas, alguna de ellas de gran interés taxonómico y biogeográfico, por lo que actualmente la lista Rhodophyta de Galicia asciende a 333 especies. ...

Reference:

RHODOPHYTA
Mapas de distribución de algas marinas de la Península Ibérica e Islas Baleares. XXIII. Acrosorium, Cryptopleura, Gonimophyllum (Delesseriaceae, Ceramiales, Rhodophyceae)

Botanica Complutensis

... For the Italian coast of Adriatic Sea there are several check lists of algae by [3] and [4,5]. Very useful are also papers of green algae by Gallardo et al. [6], Fucophyceae by Ribera et al. [7] and Ceramiales by Gomez Garreta et al. [8] but these checklists are referring to the all Mediterranean Sea and Adriatic Sea is considered as one single region. For the Eastern Adriatic coast the most comprehensive checklists so fare are for Chlorophyta, Phaeophyceae and Ceramiales by Antolić et al. [9][10][11]. ...

Nomenclatural Notes on Some Mediterranean Algae, I: Phaeophyceae
  • Citing Article
  • May 1992

Taxon

... Gonimophyllum buffhamii se encuentra epífito tanto sobre Cryptopleura ramosa como sobre Acrosorium ciliolatum, siendo más frecuente sobre C. ramosa; vive tanto en el litoral inferior como en el infralitoral en localidades expuestas al oleaje. Se encuentra distribuido en las costas europeas (Maggs & Hommersand 1993); su distribución geográfica en la Península Ibérica y las Islas Baleares se limita a las costas atlánticas, en Galicia, provincias de La Coruña y de Pontevedra, y en la ría de Eo en Asturias (Bárbara et al. 2005, Gallardo & Escudero 2011. ...

Gonimophyllum buffhamii Batters (Delesseriaceae, Rhodophyceae) from the Iberian Peninsula: Description of Morphological and Reproductive Structures
  • Citing Article
  • February 2011

Cryptogamie Algologie

... Based on the sampling design and the cluster analysis (Fig. 2), we identified three distinct ecoregions according to the taxonomic distribution of seaweeds and peracarids: Northern Europe, the Iberian Peninsula, and Macaronesia. These findings are consistent with earlier studies conducted by Spalding et al. (2007) and Alvarez et al. (1988), with some discrepancies observed for Norway, Scotland, and Iceland. Notably, Almada et al. (2013) and Vieira et al. (2022) proposed a differentiation between the Iberian Peninsula and Macaronesia based on fish and peracarids, respectively, a classification that aligns with our results on seaweeds. ...

A reassessment of North Atlantic seaweed biogeography
  • Citing Article
  • June 1988

Phycologia

... This region has witnessed large-scale green tides annually for a decade, which makes the appearance of this particular bloom even more significant . Rojo et al. (2014) carried out a study in Spain to understand the temporal patterns of coexistence and reproductive characteristics in Codium species, encompassing both native and invasive populations. They documented a marked rise in individuals with gametangia in February compared to July. ...

Coexistence of congeneric native and invasive species: The case of the green algae Codium spp. in northwestern Spain
  • Citing Article
  • October 2014

Marine Environmental Research

... The checklist of marine macroalgae in western Algeria is based on data from this study and literature references (Perret-Boudouresque & Seridi, 1989;Ribera et al., 1992;Gallardo et al., 1993;Gomez et al., 2001;Seridi, 2007; Bachir Bouiadjra, Table 1. List of species inventoried in the study area (see Figure 1). ...

Checklist of Mediterranean Seaweeds. II. Chlorophyceae Wille s.l
  • Citing Article
  • September 1993

Botanica Marina