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1,338 results for “Iberian Peninsula.”
Fig. 5 in A new early Pliocene murine rodent from the Iberian Peninsula and its biostratigraphic implications
Fig. 5. Biostratigraphic distribution and evolution of the European Paraethomys species, showing their chronological ranges. The localities marked with an asterisk are calibrated with paleomagnetic data (Opdyke et al. 1997; Martín-Suárez et al. 1998, 2000; Oms et al. 1999; Gibert et al. 2013; Garcés et al. 1998, 2001; Hüsing et al. 2010; Mansino et al. 2015b; Piñero et al. 2017b, 2018). The sites with two species of Paraethomys in coexistence are in bold. Abbreviations: AC, Alcoi Cristian; ATNTS, Astronomically Tuned Neogene Time Scale; CEL, Celadas; CLC, Calicasas ELMA, European Land Mammal Ages; LG, La Gloria (Adrover et al. 1993); M., Mimomys; MN, Mammal Neogene; P., Paraethomys; PUR, Purcal; VAR, Villalba Alta Río.
Fig. 4 in A new early Pliocene murine rodent from the Iberian Peninsula and its biostratigraphic implications
Fig. 4. Ranges of size variation (in mm) in the upper (M1–M3) and lower (m1–m3) teeth of Paraethomys baeticus sp. nov. from Baza-1 (type locality; this paper), Paraethomys jaegeri from Gorafe-2 (type locality; Montenat and De Bruijn 1976), Paraethomys abaigari from Villalba Alta Río (type locality) and La Judería (Adrover et al. 1988), Paraethomys meini from Sète (type locality; Michaux 1969; Adrover 1986) and Sifón-61 (Piñero and Agustí 2019), Paraethomys belmezensis from Bélmez-1 (type locality; Castillo Ruiz 1992), and Paraethomys balearicus from Na Burguesa-1 (type locality; TorresRoig et al. 2019). Mean sizes are marked by symbols inside the boxes.
Figs. 2–8 in A new cave species of Pseudosinella (Collembola, Entomobryomorpha, Entomobryidae) from Sima del Campamento (Jaén, Southern Iberian Peninsula).
Figs. 2–8.- Pseudosinella perezi sp. nov. 2.- Habitus. 3.- Labial chaetotaxy. 4.- Chaetotaxy of second abdominal tergite. 5.- Cephalic chaetotaxy and eyes. 6.- Macrochaetae and chaetae complex from anterior bothriotrichum of abdominal tergite IV. 7.- Unguis and unguiculus of leg III. 8.- mucro (scale¡ 25 micrometers).
Figures 10-16. Theodoxus meridionalis. 10-15 in On the identity of Neritina baetica Lamarck, 1822 and Nerita meridionalis Philippi, 1836 (Gastropoda: Neritidae) from the Iberian Peninsula
Figures 10-16. Theodoxus meridionalis. 10-15: Syntypes of Theodoxus meridionlis (Philippi, 1836), 16: original lable.
Figures 2-6 in On the identity of Neritina baetica Lamarck, 1822 and Nerita meridionalis Philippi, 1836 (Gastropoda: Neritidae) from the Iberian Peninsula
Figures 2-6. The operculum of Theodoxus fluviatilis (2-4), Th. baeticus (5), and Th. meridionalis (6). Abbreviations: ca = callus, eo = embryonic operculum, la = left adductor, ap = apophysis, pa = pseudo-apophysis, ra = right adductor, rp = rib pouch, rs = rib shield.
Figures 7-9 in On the identity of Neritina baetica Lamarck, 1822 and Nerita meridionalis Philippi, 1836 (Gastropoda: Neritidae) from the Iberian Peninsula
Figures 7-9. Opercula of Theodoxus baeticus. 7: Photo of Mermod's depicted operculum (reproduction, rotated for better comparison), 8-9: actual photos the opercula of the two syntypes (MHNG-MOLL-51319).
Figure 1 in On the identity of Neritina baetica Lamarck, 1822 and Nerita meridionalis Philippi, 1836 (Gastropoda: Neritidae) from the Iberian Peninsula
Figure 1. Reproduction of Mermod's figure of Lamarck's syntypes of Theodoxus baeticus (from Mermod 1953:155, fig. 169).
Fig. 1 in First records of Cixidia maroccana Anufriev, 1969 from the Iberian Peninsula and some additional new records of Achilidae Stṏl, 1839 (Auchenorrhyncha: Fulgoromorpha)
Fig. 1.- Adult female of Cixidia cf. lapponica, 1.5 km northeAst of L'Ampolla (Tarragona, Spain), 28.IV.2023. Photo: M.C. de Haas.
Fig. 4 in First records of Cixidia maroccana Anufriev, 1969 from the Iberian Peninsula and some additional new records of Achilidae Stṏl, 1839 (Auchenorrhyncha: Fulgoromorpha)
Fig. 4.- Habitat of place where nymphs and adults of Cixidia maroccana were found, Quinta de Marim (Olhão, Portugal). Photo: T. Valkenburg.
Fig. 2 in Micropeplus marietti Jacquelin du Val, 1857, new species for the Iberian Peninsula (Coleoptera: Staphylinidae: Micropeplinae)
Fig. 2.- Aedeagus of Micropeplus marietti Jacquelin du Val, 1857. Left, ventral view. Right, lateral view.
Fig. 1 in Fulvius oxycarenoides (Reuter, 1878), first records of the subfamily Cylapinae (Heteroptera: Miridae) in Catalonia and Aragon (NE Iberian Peninsula)
Fig. 1.- Male specimen of Fulvius oxycarenoides (Reuter, 1878) from ̏rrius, Barcelona, 1/11/2021, in alcohol.
Fig. 2 in Corythucha arcuata (Say, 1832) (Hemiptera: Tingidae), new species for the Iberian Peninsula
Fig. 2.- Corythucha arcuata captured on Quercus robur in Quinta de Chão de Carvalhos (Vila Nova de Gaia, Porto).
Fig. 1 in Aportaciones al inventario de los Heteroptera (Hemiptera) de Galicia (N.O. Península Ibérica). VII. Familia Aradidae Brullé, 1836 Contributions to the inventory of the Heteroptera (Hemiptera) of Galicia (N.W. Iberian Peninsula). VII. Family Aradidae Brullé, 1836
Fig. 1.- Aneurus (Aneurodes) avenius (Dufour, 1833), ♀, A Cortevella (Lugo), 27/04/2004. (Foto: J.P. Valcárcel). Fig. 2.- Aradus (Aradus) cinnamomeus Panzer, 1806, ♂, Praia de Area Grande (O Grove, Pontevedra), 14/11/1998. (Foto: J.P. Valcárcel).
FIGURE 5 in A subspecies of marbled newt (Triturus marmoratus) in the Iberian Peninsula newly resolved from congruent nuclear and mitochondrial DNA data
FIGURE 5 The Iberian Peninsula with the ranges of Triturus pygmaeus in light red and T. rudolfi in brown (Arntzen, 2023, 2024). Populations of the counterpart species T. marmoratus are coloured according to the dominant mitochondrial haplogroups with colours as in the legend and fig. 4. The solid or interrupted black line shows the northern range of T. m. harmannis ssp. nov., as determined by the green, yellow and blue sections in fig. 1. Note that haplogroups 1 and 2 are associated with T. m. marmoratus and that haplogroups 3, 4 and 5 are associated with T. m. harmannis ssp. nov. Haplogroup 6 is associated with T. pygmaeus and T. rudolfi (for details see table 2). Areas shown in white fall outside the documented range of the T. marmoratus species group and areas shown in grey are distant from a sampled locality.
FIGURE A1 in A subspecies of marbled newt (Triturus marmoratus) in the Iberian Peninsula newly resolved from congruent nuclear and mitochondrial DNA data
FIGURE A1 Holotype of Triturus marmoratus harmannis ssp. nov. at right and ventral view. Size bar is 1 cm. Stored at the Museo Nacional de Ciencias Naturales, Madrid, Spain under catalogue number 51792.
FIGURE 3 in A subspecies of marbled newt (Triturus marmoratus) in the Iberian Peninsula newly resolved from congruent nuclear and mitochondrial DNA data
FIGURE 3 Histogram of scores along the first axis for the discriminant analysis of size corrected morphometric data for Triturus marmoratus marmoratus (shaded bars) and T. m. harmannis ssp. nov. (open bars). This first discriminant axis is most strongly correlated with extremity lengths and not the other characters. Highest loadings on the second axis are for head length and head width (results not shown).
FIGURE 1 in A subspecies of marbled newt (Triturus marmoratus) in the Iberian Peninsula newly resolved from congruent nuclear and mitochondrial DNA data
FIGURE 1 Classification and geographical distribution of European marbled and pygmy newts from a panel of 32–33 nuclear genetic markers (data from Kazilas et al., 2024). (A) HIests plot with ancestry and heterozygosity for within marbled newts (top panel, with Triturus m. marmoratus left and T. m. harmannis ssp. nov. to the right) and for pygmy newts (bottom panel, with T. rudolfi to the left and T. pygmaeus to the right). (B) Investigated Iberian populations shown by black dots with surrounding areas coloured as in A. Areas shown in white fall outside the documented range of the T. marmoratus species group and areas in shown grey are distant from a sampled locality. The open square symbol in the Lisbon Peninsula corresponds to the open round symbol in A.
FIGURE 2 in Morphological and genetic diversification of Old-World marbled newts, with the description of a new and 'not-at-all-cryptic' subspecies from the Iberian Peninsula (Triturus, Salamandridae)
FIGURE 2 The distribution of two species of marbled newts over the western part of the Iberian Peninsula, as inferred from the morphological character Nlinks. Triturus marmoratus is shown in two shades of blue, T. pygmaeus in two shades of red and four localities with both species are shown in grey (see colour legend). The spatial extrapolation does not exceed ca. 50 km. Note that southern Iberian populations are all T. pygmaeus, irrespective of high (cluster C1), low (C2), or bimodal Nlink counts (Doñana National Park). Populations that were studied morphometrically are highlighted by a box. The type locality for T. pygmaeus lusitanicus ssp. nov. is Granja, Portugal and is marked by an asterisk.
FIGURE 4 in Morphological and genetic diversification of Old-World marbled newts, with the description of a new and 'not-at-all-cryptic' subspecies from the Iberian Peninsula (Triturus, Salamandridae)
FIGURE 4 Morphological and genetic variation in Triturus pygmaeus from in and around Doñana National Park (DNP). A – histograms of Nlink counts for four population groups with, from top to bottom: southwestern cluster of T. pygmaeus (localities 65, 436, 438 and 1004 in the south of Portugal, together marked C1 in fig. 2), populations in the northern section of DNP (ER, locality 1005 and BS, locality 1006), population in the southern section of DNP (locality 271) and the Betic cluster of T. pygmaeus (localities 270, 463, 465 and 1003 in the very south of Spain, together marked C2 in fig. 1). Exceptionally, the northern Doñana museum material contains 15 juvenile specimens (open bars) along with three adults (shaded bars). B – geographical cline in microsatellite genetic variation. The horizontal axis shows 'Distance from the Guadalquivir River' in km and the vertical axis presents Structure Q-scores. The solid round symbols represent populations and the grey area shows the 95% credibility interval. The Structure Q-scores were extracted from a published figure (Albert & García-Navas, 2022: Figure 4) and are unavoidably imprecise. The position of the 'Torre Carbonero', a cultural landmark at the Doñana beach, is shown by an arrow (TC). Three populations with morphological data available, that can be associated to the transect are El Rocío (arrow marked ER) and the biological station (BS) in northern Doñana and Zacallón C. de los Junqueros in southern Doñana (arrow marked 271). For details, see table 1 and supplementary table S1.
FIGURE 3 in Morphological and genetic diversification of Old-World marbled newts, with the description of a new and 'not-at-all-cryptic' subspecies from the Iberian Peninsula (Triturus, Salamandridae)
FIGURE 3 Nine marbled newts from three (sub)species each in dorsal and ventral view. Link counts for the left and right side of the body are given in parentheses. Top row – Triturus marmoratus from Jublains, France; left male (3, 2) and right female (1, 1). Middle row – T. pygmaeus lusitanicus ssp. nov. from Cardeña, Spain; from left to right female (2, 4), male (4, 3) and male (4, 5). Bottom row – T. p. pygmaeus from Salinas, Spain; from left to right male (2, 1), male (1, 2) male (2,0) and female (3, 1). Note that the colour pattern in T. marmoratus and T. p. pygmaeus is horizontally banded whereas in T. p. lusitanicus ssp. nov. it is reticulated. PHOTOGRAPHY L. A. VAN DER LAAN
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Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
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DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.