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First continuous pre-Jaramillo to Jaramillo terrestrial vertebrate succession from Europe


In this paper, the early Pleistocene small vertebrate sequence of Quibas-Sima (Quibas karstic complex, Murcia, SE Spain) is presented. The available magnetostratigraphic information together with the small vertebrate association, allow to reliably constrain the age of the different units. The basal unit of the section has recorded a reversed polarity assigned to the pre-Jaramillo Matuyama (C1r.2r, i.e., between 1.2 and 1.07 Ma). The intermediate units have recorded a normal polarity correlated directly with the Jaramillo subchron (C1r.1n, between 1.07 and 0.99 Ma), while the upper units record the post-Jaramillo reverse polarity (C1r.1r, i.e., between 0.99 and 0.78). Jaramillo subchron is especially significant regarding the earliest hominin dispersal in Western Europe. However, vertebrate faunas unambiguously correlatable with Jaramillo subchron are extremely rare in Europe. Thereby, the study of the Quibas-Sima sequence allows to characterize the vertebrate association synchronous to this paleomagnetic episode in southern Iberian Peninsula, and contributes to increase knowledge of the biotic and climatic events that took place in southern Europe at the beginning of the Early-Middle Pleistocene transition, prior to the Matuyama-Brunhes boundary. A continuous small vertebrate succession has been reported, including representatives of the families Bufonidae, Pelodytidae, Testudinidae, Gekkonidae, Blanidae, Lacertidae, Colubridae, Viperidae, Soricidae, Erinaceidae, Rhinolophidae, Vespertilionidae, Muridae, Gliridae, Sciuridae, Leporidae and Ochotonidae The ecological affinities of the faunal association suggest a progressive reduction in forest cover in the onset of the Jaramillo subchron.


The Jaramillo subchron (1.07–0.99 Ma) is a normal polarity episode reported within the upper part of Matuyama Chron. This paleomagnetic interval characterizes the early phase of the Early-Middle Pleistocene transition (1.2–0.5 Ma), a time span that represents an important change in the Earth’s climate. Moreover, this episode is particularly relevant concerning the earliest hominin occurrence in Western Europe. Unfortunately, European terrestrial vertebrate sequences recording the Jaramillo subchron are very rare. The combination of biochronology and magnetochronology has vantage to precisely constrain the geochronology of the studied site. On the basis of a sound taxonomy of the small vertebrate fauna and solid magnetostratigraphy, the Quibas-Sima section (Spain) is here dated between 1.2 and 0.78 Ma. This implies that, for the first time in Europe, a continuous continental succession recording pre-and syn-Jaramillo vertebrate faunas is reported. For this reason, Quibas-Sima offers an excellent opportunity to increase our knowledge about the faunal and paleoenvironmental context of the time span comprised between roughly 1.2 and 0.99 Ma (Epivillafranchian). This paper provides new data that will help to understand better faunal composition of ecosystems in southwestern Europe during a relevant time interval such as the late early Pleistocene and its paleoclimatic implications.


The subchron C1r-1n (1.07–0.99 Ma)1, better known as Jaramillo, is a very significant stratigraphic marker within the early Pleistocene. The Jaramillo subchron covers MIS 28–31. This interval is of great interest and relevance in relation to the first occurrence of hominin presence in Western Europe (Barranco León 5, Fuente Nueva 3, Sima del Elefante 9c, Le Vallonet)2,3,4,5. Unfortunately, early Pleistocene small vertebrate successions with a well dated framework immediately prior or younger than this paleomagnetic reversal are scarce in Europe6,7,8,9, whereas small vertebrate faunas unambiguously correlatable with Jaramillo subchron are extremely rare10,11. In Eastern Europe, small mammals from the Ostrogozh layer of the Korotoyak section (Russia), according to paleomagnetic evidence, were correlated with the Jaramillo subchron12. In Western Europe, the Colle Curti sequence (central Italy) covers a part of the Matuyama epoch which includes the Jaramillo subchron13. The Castagnone section (northern Italy) recorded normal polarity deposits with microfauna correlated with the Jaramillo subchron14. Kahlke15 correlated the site of Untermassfeld (Germany) with the Jaramillo subchron. The normal polarity sequence detected in the archaeological deposits from Le Vallonnet (France) was first correlated with the Jaramillo subchron16. However, later U-Pb data, in combination with paleomagnetic constraints, associated it with the somewhat older Cobb Mountain subchron5.

In Spain, the Jaramillo subchron has been directly identified at the section of Torrent de Vallparadís (Terrassa, northeastern Spain) with the fossiliferous levels EVT10 and EVT128. So far, it was the only section in the Iberian Peninsula where this normal event has been reliably identified. Despite the excellent continuous biostratigraphic succession of the interval around the Jaramillo subchron recorded in both Atapuerca sites of Sima del Elefante (TE) and Gran Dolina (Burgos, Spain), coeval fossiliferous levels with this geomagnetic subchron have not been directly identified9,17,18. Similarly, although the Guadix-Baza Basin (Granada, southern Spain) presents one of the best continental records from the late Miocene to the middle Pleistocene in western Europe, a biostratigraphic gap is present covering the coeval Jaramillo deposits19,20.

The site of Quibas (Murcia, Spain) (Fig. 1a) is a karstic complex of cavities filled by sediments of early Pleistocene age (see “The site of Quibas” in Supplementary Information for details). The main structures of this complex with paleontological record consist of a gallery called Quibas-Cueva (QC; up to 5 m wide, 9 m high and more than 30 m in length) and a vertical shaft known as Quibas-Sima (QS; 12 m deep and up to 2 m wide) (Fig. 1b). The Quibas-Sima sequence contains seven distinct detritic units: QS-1 to QS-7 (see “Lithostratigraphic units” in Supplementary Information, and Supplementary Figs. S1 and S2). The lowest unit has been subdivided from the base to the top into QS-1.1, QS-1.2 and QS-1.3. The upper units, QS-5 and QS-6 yielded no fossils other than gastropods, while all the underlying units and the uppermost one contained as well vertebrate remains.

Figure 1

Geographic and structural context of the Quibas site. (a) Geographic location of the Quibas karstic complex. (b) View of the two main structures of the Quibas site in 2015.

Paleomagnetism and in particular magnetic reversal stratigraphy, coupled with biochronology, provides very often a solid time framework in sedimentary rocks. The aim of the present article is to provide an overview of the microvertebrate succession recovered from the Quibas-Sima sequence, as well as to date accurately this section based on its magnetostratigraphic and paleontological data, the later also including the Quibas-Cueva fragmentary record.


The general paleomagnetic results from the Quibas-Sima permit a magnetostratigraphic correlation. Samples always display enough intensity to be measured, although in the QS-1 subunits it is generally lower (between 5 and 10 mA/m) compared to the higher values measured in the rest of the succession (reaching values generally between 10 and less than 100 mA/m). During demagnetization, no major shifts in susceptibility were detected and the resulting orthogonal plots display a stable behavior with up to three components. In some samples, an initial viscous and secondary component is observed from room temperature to around 150 °C which is likely to be an overprint of the present-day/recent geomagnetic field. At temperatures between 150 °C and 250–300 °C, a low temperature component is detected (Fig. 2), while a high temperature one can be detected between 250–300 °C and 600 °C. This high temperature component is always directed towards the origin (demagnetization state) and is considered the characteristic one to derive the inclination and declination values of the paleofield at the moment of rock formation. The substantial amount of magnetization above 600 °C observed in the demagnetization plots, and Isothermal Remanent Magnetization (IRM) acquisition curves, reveal the presence of hematite as carrier of magnetization in the high temperature component. The demagnetization plots from the Quibas-Sima section display both reverse polarities (such as Fig. 2a–c), and normal ones (such as Fig. 2d,e). The few samples from Quibas-Cueva (see “Paleomagnetism” in Supplementary Information, and Fig. S3) show only reverse polarities (Fig. 2h–k). In some specimens, unconsistent values are observed, such as having positive inclination and southwards declination (Fig. 2f,g), which may be the result of postdepositional processes such as tilting or reworking. The values of the characteristic component (declination and inclination) were used to caculate the VGP (Virtual Geomagnetic Poles) latitude. The values of these latitudes are used to build a local magnetostratigraphy. Since each stratigraphic sampling level is typically represented by one or two samples (34 and 16 cases, respectively), no mean per site can be calculated for all the section. Thus, quality assessment of samples is carried out by integrating all data belonging to each stratigraphic/paleontologic unit (see Figs. 3 and S4).

Figure 2

Orthogonal demagnetization plots from the Quibas-Sima section (ag, see location in Fig. 3) and Quibas-Cueva (hk, see location in Fig. S3). (ac) Indicate reverse polarities, and (d,e) indicate normal ones. (f,g) Samples are of undefined polarity. (h–k) samples (Quibas-Cueva) are of reverse polarity. Abbreviations: NRM, Natural Remanent Magnetization (room temperature); RM, Remanent Magnetization at a specific temperature.

Figure 3

Stratigraphic units (coincident with micromammals sampling units) and magnetostratigraphic results from the Quibas-Sima section.

In units QS-1.1, QS-1.2 and QS-1.3, the observed polarity is mainly reverse, with most of the samples grouped around consistent values (i.e., south-directed and negative inclinations). On the other hand, in units QS-2 and QS-3 clear normal polarities are detected, with consistent mean values poiting northwards and having positive inclinations. QS-4 is less consistent, but VGP latitudes are dominantly normal (Fig. 3). QS-5 has consistent normal polarities and VGP latitudes. In units QS-6 and QS-7 few samples could be obtained and, although results may be rather dispersed, VGP latitudes are reverse. Regarding the few samples taken at the base of the Quibas-Cueva structure, they showed clear reverse polarities.

Small Vertebrate Succession

The small vertebrate assemblage from the Quibas-Sima section comprises amphibians (Bufonidae, Pelodytidae), reptiles (Testudinidae, Gekkonidae, Blanidae, Lacertidae, Colubridae, Viperidae) and, among mammals, insectivores (Soricidae, Erinaceidae), bats (Rhinolophidae, Vespertilionidae), rodents (Arvicolinae, Muridae, Gliridae, Sciuridae) and lagomorphs (Leporidae, Ochotonidae) (Figs. 4 and 5).

Figure 4

Distribution chart of the taxa found in the Quibas-Sima section.

Figure 5

ESEM photographs of representative small-mammal teeth from Quibas-Sima. (a) Left maxilla of Apodemus sylvaticus with M1 and M2 from QS-3, IPHES-QS-3-R/P25. (b) Right M1 and M2 of Castillomys rivas from QS-1.3, IPHES-QS-1Z-R/J1. (c) Left M1-2 of Eliomys quercinus from QS-1.2, IPHES-QS-1A-R/G6. (d) Left M3 of Allophaiomys sp. from QS-1.1, IPHES-QS-1Z-R-K32. (e) Left P4 of Sciurus aff. magistri from QS-1.2, IPHES-QS-1A-R/AB1. (f) Left upper molariform of Oryctolagus cf. giberti from QS-3, IPHES-QS-3-L/V8. (g) Right p3 and p4 of Prolagus calpensis from QS-3, IPHES-QS-3-L/V12. (h) Right M1 of Crocidura kornfeldi from QS-1.3, IPHES-QS-1Z-I/AC2. (i) Right M1 of Neomys sp. from QS-1.3, IPHES-QS-1Z-I/AC1. (j) Right m2 of Erinaceus sp. from QS-3, IPHES-QS-3-I/AC1. (k) Right m1 of Rhinolophus ferrumequinum from QS-3, IPHES-QS-3-Q/V15. (l) Left M1 of Miniopterus cf. horaceki from QS-1.2, IPHES-QS-1A-Q/W2. (m) Left M2 of Myotis myotis from QS-4, IPHES-QS-4-Q/Z1. (n) Right M3 of Rhinolophus euryale from QS-1.2, IPHES-QS-1A-Q/W18. (o) Left M3 of Rhinolophus hipposideros from QS-1.2, IPHES-QS-1A-Q/W19. The 2 mm scale bar goes with figure (j) and the 1 mm scale bar goes with the remaining figures.

The lower unit from the Quibas-Sima sequence (QS-1.1, QS-1.2, QS-1.3), is in general characterized by an association which presents a diversified small vertebrate assemblage, including anurans (Pelodytes sp.), lizards (Blanus gr. B. cinereus, Tarentola gr. T. mauritanica, a small sized Lacertidae), snakes (Coronella girondica), insectivores (Neomys sp., Crocidura kornfeldi), bats (Rhinolophus ferrumequinum, Rhinolophus euryale, Rhinolophus hipposideros, Myotis nattereri, Miniopterus cf. horaceki), rodents (Allophaiomys sp., Apodemus sylvaticus, Castillomys rivas, Eliomys quercinus, Sciurus aff. magistri) and lagomorphs (Prolagus calpensis, Oryctolagus cf. giberti). Many of these elements are related to living forms which indicate a Mediterranean climate, such as Blanus cinereus, Tarentola mauritanica, Rhinolophus ferrumequinum or Rhinolophus hipposideros.

Among the insectivores, the presence of the shrew Neomys in the Iberian small mammal assemblages becomes rather frequent close to the transition from the early to middle Pleistocene, as it is the case of the latest early Pleistocene sites of Almenara-Casablanca 3 and Gran Dolina TD3-TD821,22, replacing the neomyini species Asoriculus gibberodon, present in many early Pleistocene sites such as Fuente Nueva 3 and Barranco León 5 (Guadix-Baza Basin) and Sima del Elefante (TE7-TE14), which record the earliest hominin presence in Western Europe9,20,23,24,25. All the extant Neomys species have aquatic habits. This is why the occurrence of the genus is usually considered as indicative of the presence of water bodies in the surrounding area. Up to date, the occurrence of Neomys in Quibas-Sima is probably the oldest record of this genus in Spain. Other than the presence of a Neomys species in the subunits QS-1.1, QS-1.2 and QS-1.3, the insectivore assemblage is clearly dominated by the species Crocidura kornfeldi. It is widely known that crocidurine shrews are better adapted to milder and more arid climates than their soricine counterparts. Since its entry in the Iberian Peninsula at about 1.5 Ma, Crocidura kornfeldi persisted until the early-middle Pleistocene transition in sites such as Cueva Victoria26, Almenara-Casablanca 321 and Gran Dolina TD3-TD89.

In the case of extinct rodent species, development of ever-growing molars in the microtine Allophaiomys sp. lineages or the development of longitudinal ridges between cusps (stephanodonty) in the murine Castillomys rivas, have been interpreted as dental adaptations to foraging in open grasslands27,28,29. However, the presence of a forested habitat is attested by the occurrence of Rhinolophus hipposideros, Apodemus sylvaticus and, most specially, the squirrels of the species Sciurus aff. magistri. Moreover, the dormouse Eliomys quercinus is particularly frequent in these lower levels of Quibas-Sima, reaching a 14% at the subunit QS-1.3. This species currently occupies habitats of low-density deciduous and conifer forests, rocky areas with some vegetation and woodland edges from the Iberian Peninsula to the Ural Mountains. Areas with abundant herbaceous vegetation seem to be a limiting factor on its presence30. The presence of favourable environmental conditions are supported by the number of bat species identified in this level (up to five species). The occurrence of Blanus gr. B. cinereus in QS-1.1, QS-1.2 and QS-1.3, a species linked to humid and covered areas, together with Pelodytes sp. in QS-1.3 would probably suggest locally wetter and more forested environmental conditions than in the overlying units in the sequence. This is consistent with the record of the anguid Ophisaurus manchenioi in the base of Quibas-Cueva, correlated with QS-1, a taxon linked to subtropical humid conditions31.

The unit QS-2 retains most of the species found in QS-1. However, the parsley frog Pelodytes sp., the shrew Neomys sp. (the insectivores becoming represented only by Crocidura kornfeldi) and the bats Rhinolophus hipposideros and Miniopterus cf. horaceki do not reappear at any of the remaining units of Quibas-Sima. Other taxa absent in QS-2 such as the bat Rhinolophus euryale or the lagomorph Prolagus calpensis reappear in more recent units of the Quibas-Sima sequence. Among the reptiles, the punctual presence of the snake Zamenis scalaris, and the first occurrence of chelonids (Testudo sp.), a large-sized lizard and the snake Malpolon monspessulanus must be pointed out, besides Tarentola gr. T. mauritanica, Coronella girondica and a small-sized lizard. The representatives of the genus Testudo are terrestrial chelonians that prefer semi-arid habitats, with Mediterranean vegetation and open areas with a strong insolation such as the Mediterranean forest and shrub. Malpolon monspessulanus is a thermophilous snake very well adapted to all types of Mediterranean ecosystems, showing a certain preference for shrubland of warm and dry climate32,33.

Although the presence of Apodemus sylvaticus, Sciurus aff. magistri or Zamenis scalaris points to the persistence of forest or open-forest formations at this unit, an environmental change between QS-1 and QS-2 is attested by the extirpation of Neomys sp. and the occurrence of species with preferential affinity for more open habitats such as Malpolon monspessulanus and Testudo sp.

A number of changes in the small vertebrate association is observed in QS-3 and QS-4 when compared to the association at QS-2. The snake Vipera latastei and the anuran Bufotes viridis appear for the first time. Vipera latastei is a discontinuously distributed Iberian and North African species that preferentially lives in deteriorated scrubs and mountainous dry areas, showing special affinity for open areas with little or no vegetation such as scree environments34. Green toads (Bufotes viridis sensu lato) belong today to a widespread group of closely related species with a range that extends from eastern France and Italy to central Asia, including northern Africa and numerous Mediterranean islands. They inhabit mesic to arid environments, from subtropical to cold temperate, ranging in altitudes from below sea level in Israel to more than 4000 m.a.s.l. in the Himalayas35. Fossils belonging to this group have been reported in late early Pleistocene sites in Spain, such as Barranco León36,37, Almenara-Casablanca 338 and Cueva Victoria39. It is also known in northern Africa at the early Pleistocene site of Ahl al Oughlam (Casablanca, Morocco40). The last record of Bufotes viridis so far comes from the late early Pleistocene of Cueva Victoria, being absent since then from the continental record of the Iberian Peninsula.

Among the insectivores, unit QS-3 records the presence of Erinaceus sp. and Crocidura kornfeldi. Erinaceus is usually considered as a generalistic taxon, able to occupy habitats with different environmental conditions, although it usually avoids extreme conditions such as in deserts or ever-frozen regions. Concerning bats, QS-3 and QS-4 record the entry of Myotis myotis and the reappearance of Rhinolophus euryale. Perhaps the most significant change compared to the lower units of Quibas-Sima is the absence of the squirrels of the species Sciurus aff. magistri, which is probably indicative of a decrease in arboreal cover. This observation is consistent with the presence of species preferentially linked to open-land environments, such as Testudo sp., Vipera latastei, Malpolon monspessulanus or Erinaceus sp.

Vertebrates are apparently absent from the upper units of Quibas-Sima (QS-5, QS-6) with the exception of the uppermost part of the sequence (QS-7), which delivered some scarce remains of Blanus gr. B. cinereus, Tarentola gr. T. mauritanica, a small-sized lacertid, Apodemus sylvaticus and Eliomys quercinus.

Therefore, the faunal succession of Quibas-Sima points to a progressive reduction of tree cover from QS-1 to QS-4. This section is clearly divided into two paleoenvironmental episodes: a first one (unit QS-1) is characterized by the presence of a forested mosaic habitat with moderately moist conditions, and a second one (QS-2, QS-3 and QS-4) is indicative of a more open landscape with relatively drier environmental conditions.

Magnetobiostratigrafic Correlation

The joint presence of Castillomys rivas and an archaic representative of Allophaiomys in Quibas-Sima and the lower part of Quibas-Cueva places them in the late early Pleistocene (Biharian mammal age)41,42,43. The age of these two sections can be finely constrained on the basis of the correlation of the obtained polarities with the Geomagnetic Polarity Time Scale and the available biostratigraphic data from other Spanish late early Pleistocene sites such as Fuente Nueva-3 (FN-3, Guadix-Baza Basin), Vallparadís (Terrasa, NE Spain), Cueva Victoria (SE Spain) and Gran Dolina (TD, Atapuerca karstic complex). The entire lower part of Quibas-Cueva records a reversed polarity interval, whereas the Quibas-Sima section records a reversed-normal polarity sequence. So while the unit QS-1 is included in a reversed interval, the units QS-2 to QS-5 have provided a normal polarity. To this is added the record of a second reverse polarity in QS-6 and QS-7.

According to the micromammal content, the reversed Quibas-Cueva section can be correlated with the reversed base of Quibas-Sima, both of which share the presence of Neomys sp. and Castillomys rivas44,45, as well as Apodemus sylvaticus, Sciurus aff. magistri, Allophaiomys sp. and Eliomys quercinus, among others. Paleomagnetic data from FN-3 show that this site is placed in a reversed chron identified as upper Matuyama46. The radiometric data indicated that FN-3 is placed below the Jaramillo subchron7. Duval et al.7 and Lozano-Fernández et al.47 dated FN-3 to 1.2 Ma. Quibas-Sima shares with this site the presence of an endemic species of Allophaiomys (Allophaiomys sp.), which suggests a roughly similar age. However, as we have mentioned previously, the occurrence of Neomys in Quibas-Sima probably represents the oldest record of this genus in Spain. This genus is still absent in FN-3 where Asoriculus has not yet been replaced by Neomys, which indicates that QS-1 is somewhat younger. In this way, the correlation of the reversed polarity observed in the lower part of Quibas-Sima and Quibas-Cueva to the pre-Olduvai Matuyama interval is discarded. Otherwise, the last occurrence of Castillomys rivas is recorded in the level Cúllar-Baza B19. It is located in the lower part of the section of Cúllar-Baza, Guadix-Baza Basin. Magnetobiostratigraphic correlations from Cúllar-Baza placed the reversed interval of this part of the section in the uppermost Matuyama chron, immediately before the Matuyama-Bruhnes boundary (between 0.99 and 0.78 Ma)19. Castillomys is already absent in the lowermost levels of Gran Dolina (TD4 to TD7, shortly after the Jaramillo subchron but before the Matuyama-Bruhnes boundary at 0.9 Ma9,18,48). Thus, this genus became extinct before the early-middle Pleistocene boundary. The presence of Castillomys rivas in Quibas-Sima allows us to discard the assignament of the upper normal polarity from QS-2 to QS-5 to the Bruhnes chron. This is confirmed by the record of a reverse polarity in the overlying QS-6 and QS-7. In addition, the arvicolid species found in the studied section is already absent from the nearby site of Cueva Victoria where it has been replaced by the more advanced arvicolid Allophaiomys chalinei. Moreover, the cricetid Allocricetus bursae is still absent in Quibas-Sima and present in Cueva Victoria. The latter site has been placed in the upper Matuyama chron between Jaramillo and Brunhes and correlated with MIS-22, at about 0.9 Ma49.

The paleontological sites of Quibas are also older than EVT12 and EVT10, from the section of Vallparadís. These two levels are placed in a normal polarity interval which has been correlated with the Jaramillo subchron8. In these levels Iberomys huescarensis is already present, a microtine species which is common in latest early Pleistocene localities such as those of Gran Dolina (TD3/4, TD5, TD6 and TD8), in Atapuerca, or Huéscar and Loma Quemada, in the Guadix-Baza Basin. However, this species has not been recorded at any level of the entire sequence of Quibas-Sima, pointing to an older age. Therefore, contrary to the Vallparadís section, the Quibas-Sima sequence covers the lower boundary between the upper Matuyama and Jaramillo chrons. The entry of Iberomys huescarensis must have taken place within the Jaramillo subchron, some time between the deposition of QS-4 from the Quibas-Sima sequence and EVT12 from the Vallparadís sequence.

Therefore, the age of the base of Quibas-Cueva and Quibas-Sima (QS-1) can be roughly constrained between 1.2 (age of FN-3) and 1.07 Ma, whereas the normal polarity detected at QS-2, QS-3, QS-4 and QS-5 can be correlated with the subchron Jaramillo, between 1.07 and 0.99 Ma (Fig. 6). This correlation is consistent with the macromammal association from Quibas-Cueva described by Montoya et al.44,45, Piñero and Alberdi50 and Alba et al.51, which includes two species of horses (Equus altidens and Equus suessenbornensis) and the macaque Macaca sylvanus florentina.

Figure 6

Magnetobiostratigraphic correlation of several European localities2,7,8,17,18,19,46,49 and location of the Quibas-Sima units (QS-1 to QS-7) and the base of Quibas-Cueva. GPTS (Geomagnetic Polarity Time Scale) shows Bruhnes, and two normal polarity intervals within Matuyama: subchrons Jaramillo (1.07–0.99 Ma) and Cobb Mountain (1.22–1.19 Ma)53.


The Quibas-Sima section records a polarity change from a reverse interval (QS-1) to a normal one (QS-2, QS-3, QS-4, QS-5) plus a second reverse one (QS-6 and QS-7). This normal polarity interval bounded by reverse polarities, is identified as the Jaramillo subchron. In Europe, vertebrate assemblages unambiguously assigned to Jaramillo subchron are very scarce. Up to now, the Quibas-Sima sequence represents the longest and most complete pre-Jaramillo and Jaramillo continental vertebrate succession from this continent. This section thus provides a unique chance to increase our knowledge on the paleoenvironmental and faunal context of the time interval comprised between 1.2 and 0.99 Ma. This time span is the prelude to the transition from the early to the middle Pleistocene, marked by major changes in the climatic cyclicity of the Earth. Under these circumstances, the information provided from the study of the Quibas-Sima sequence is an important contribution to our understanding of the climatic and faunal events that occurred at the beginning of the early-middle Pleistocene transition. A significant change in the small vertebrate composition has been observed from QS-1 to QS-4. Among the small mammals, this change involved the extirpation of species associated to woodland habitats and water bodies such as Sciurus aff. magistri and Neomys sp., respectively, as well as a drop in the bat diversity. Among reptiles, it involved a shift towards species with a preference for dry and open areas, such as Testudo sp., Vipera latastei and Malpolon monspessulanus. Therefore, it seems that close to the onset of the Jaramillo subchron, a progressive environmental change involving a reduction of tree cover and spreading of shrublands or grasslands took place. At the Quibas-Sima section, this change is coincident with the transition from MIS 31 to MIS 30. While in northern latitudes the transition from interglacial to glacial conditions involved a decrease in global temperatures. It seems that this was not the case for lower latitudes such as the southern part of the Iberian Peninsula. While interglacial conditions such as MIS 31 favoured at these latitudes the extension of woodlands or open woodlands, during glacial times as was the case of MIS 30, all evidence points to increased aridity leading to a reduction of forested formations and the extension of open-land habitats.

Materials and Methods

Most of the small-vertebrate sample was collected from the Quibas-Sima section during the sampling campaing of 2014, but it is also included material recovered during the systematic excavation campaigns of 2015, 2016, 2017 and 2018. All the sediment was water-screening using superimposed 4, 1 and 0.5 mm mesh screens. The Quibas-Sima sample includes 2584 identified small-vertebrate remains corresponding to 29 taxa. QS-1.1 has yielded 26 remains representing 11 species, the material from QS-1.2 comprises 423 small-vertebrate fossils of at least 18 species, the sample of QS-1.3 consists of 831 specimens ascribed to 15 taxa, QS-2 has yielded 141 specimens comprising 18 taxa, the material from QS-3 consists of 796 identified remains representing 21 small-vertebrate species, the sample from QS-4 contains 243 remains assigned to 19 taxa, and QS-7 is the poorest unit with only nine specimens belonging to five taxa. The recovered fossils are currently kept at the Institut de Paleoecologia Humana i Evolució Social (IPHES; Tarragona, Spain). Small-mammal teeth are illustrated by means of micrographs taken with Environmental Scanning Electron Microscopy (ESEM) at the Servei de Recursos Científics i Tècnics de la Universitat Rovira i Virgili (Tarragona).

For this paleomagnetic study at the Quibas karstic complex, the Quibas-Sima section was sampled in some 50 levels with an electrical drill. Each sample was a single core that, if long enough, was cut into several samples. These specimens underwent a paleomagnetic study, accounting for a whole of some 70 studied samples. These samples underwent a stepwise thermal demagnetization and measuring of remanence in a triaxial cryogenic magnetometer at in Laboratory of Paleomagnetism at Universitat de Barcelona (SCT-CSIC). Thermal demagnetiser TSD-1 (Schonstedt) was used for this study, while bulk susceptibility was measured with the KLY-2 susceptibilimeter (Geofyzika Brno). Paleomagnetic components were derived with the Koymans et al.52 software. A thermal demagnetization protocol including from 8 to 13 steps was applied to the studied samples. This protocol ranged from NRM (Natural Remanent Magnetization) to 600 °C. The basal part of the lateral (cave) section was also sampled with few additional cores.


  1. 1.

    Gradstein, F. M., Ogg, J. G., Schmitz, M. D. & Ogg, G. The Geologic Time Scale 2012, p. 1144 (Elsevier, Amsterdam, 2012).

  2. 2.

    Oms, O. et al. Early human occupation of Western Europe: paleomagnetic dates for two paleolithic sites in Spain. Proc. Natl. Acad. Sci. USA 97, 10666–10670 (2000).

    Article  ADS  CAS  Google Scholar 

  3. 3.

    Carbonell, E. et al. The first hominin of Europe. Nature 452, 465–469 (2008).

    Article  ADS  CAS  Google Scholar 

  4. 4.

    Toro-Moyano, I. et al. The oldest human fossil in Europe, from Orce (Spain). J. Hum. Evol. 65, 1–9 (2013).

    Article  Google Scholar 

  5. 5.

    Michel, V. et al. New dating evidence of the early presence of hominins in Southern Europe. Sci. Rep. 7, 10074 (2017).

    Article  ADS  CAS  PubMed  PubMed Central  Google Scholar 

  6. 6.

    Duval, M. et al. ESR dating of the Early Pleistocene archaeological site at Vallparadís (Terrassa, Cataluña, Spain). Trab. Prehist. 68, 7–24 (2011).

    Article  Google Scholar 

  7. 7.

    Duval, M. et al. On the limits of using combined U-series/ESR method to date fossil teeth from two Early Pleistocene archaeological sites of the Orce area (Guadix-Baza basin, Spain). Quat. Res. 77, 482–491 (2012).

    Article  CAS  Google Scholar 

  8. 8.

    Minwer-Barakat, R. et al. Pleistocene rodents from the Torrent de Vallparadís section (Terrassa, northeastern Spain) and biochronological implications. J. Vert. Paleontol. 31, 849–865 (2011).

    Article  Google Scholar 

  9. 9.

    Cuenca-Bescós, G. et al. Comparing two different Early Pleistocene microfaunal sequences from the caves of Atapuerca, Sima del Elefante and Gran Dolina (Spain): biochronological implications and significance of the Jaramillo subchron. Quat. Int. 389, 148–158 (2015).

    Article  Google Scholar 

  10. 10.

    Markova, A. K. Pleistocene mammal faunas of Eastern Europe. Quat. Int. 160, 100–111 (2007).

    Article  Google Scholar 

  11. 11.

    Markova, A. K. “The European small mammal faunas synchronous to the Jaramillo paleomagnetic episode” in Geological Neogene and Quaternary Events in Russia: Modern Condition of the Stratigraphic Schemes and Palaeogeographic Reconstructions, pp. 60–65 (GEOS press, Moscow, 2007).

  12. 12.

    Semenov, V. V. “Palaeomagnetism” in The Lower-Middle Pleistocene of the Upper Don Basin. Guidebook for excursion, Iosifova, Yu. & Krasnenkov, R. V., Eds., pp. 146–149 (Geosynthes, Moscow, 1994).

  13. 13.

    Coltorti, M. et al. The Colle Curti mammal site in the Colfiorito area (Umbria-Marchean Apennine, Italy): geomorphology, stratigraphy, paleomagnetism and palynology. Quat. Int. 47, 107–116 (1998).

    Article  Google Scholar 

  14. 14.

    Giraudi, C., Mottura, A., Sala, B., Siori, M. S. & Bormioli, D. The Castagnone site (Cerrina valley, Monferrato hills, NW Italy): early Pleistocene sedimentary record and biochronology. Riv. Ital. Paleontol. S. 109, 517–526 (2003).

    Google Scholar 

  15. 15.

    Kahlke, R. D. The Early Pleistocene (Epivillafranchian) Faunal Site of Untermassfeld (Thuringia, Central Germany). Synthesis of New Results. Eraul 92, 123–138 (2000).

    Google Scholar 

  16. 16.

    De. Lumley, H., Fournier, A. & Krzepkowska, A. Echasoux, L’industrie du Pleistocene inférieur de la grotte du Vallonet, Roquebrune-Cap-Martin, Alpes Maritimes. L’Anthropologie 92, 501–614 (1988).

    Google Scholar 

  17. 17.

    Cuenca-Bescós, G. et al. The small mammals of Sima del Elefante (Atapuerca, Spain) and the first entrance of Homo in Western Europe. Quat. Int. 295, 28–35 (2013).

    Article  Google Scholar 

  18. 18.

    Parés, J. M. et al. Chronology of the cave interior sediments at Gran Dolina archaeological site, Atapuerca (Spain). Quat. Sci. Rev. 186, 1–16 (2018).

    Article  ADS  Google Scholar 

  19. 19.

    Agustí, J., Oms, O. & Pares, J. M. Calibration of the Early-Middle Pleistocene transition in the continental beds of the Guadix–Baza Basin (SE Spain). Quat. Sci. Rev. 18, 1409–1417 (1999).

    Article  ADS  Google Scholar 

  20. 20.

    Agustí, J. et al. Chronological and environmental context of the first hominin dispersal into Western Europe: The case of Barranco León (Guadix-Baza Basin, SE Spain). J. Hum. Evol. 87, 87–94 (2015).

    Article  Google Scholar 

  21. 21.

    Agustí, J. et al. The late Neogene-early Quaternary small vertebrate succession from the Almenara-Casablanca karst complex (Castellón, Eastern Spain): Chronologic and paleoclimatic context. Quat. Int. 243, 183–191 (2011).

    Article  Google Scholar 

  22. 22.

    Furió, M., van den Hoek Ostende, L. W., Agustí, J. & Minwer-Barakat, R. Evolución de las asociaciones de insectívoros (Eulipotyphla, Mammalia) en España y su relación con los cambios climáticos del Neógeno y el Cuaternario. Ecosistemas 27, 38–51 (2018).

    Article  Google Scholar 

  23. 23.

    Rofes, J. & Cuenca-Bescós, G. First evidence of the Soricidae (Mammalia) Asoriculus gibberodon (Petényi, 1864) in the Pleistocene of North Iberia. Riv. Ital. Paleontol. S. 112, 301–315 (2006).

    Google Scholar 

  24. 24.

    Furió, M. Los Insectívoros (Soricomorpha, Erinaceomorpha, Mammalia) del Neógeno superior del Levante Ibérico. PhD dissertation, p. 299 (Universitat Autònoma de Barcelona, Barcelona, 2007).

  25. 25.

    Agustí, J., Blain, H.-A., Furió, M., De Marfà, R. & Santos-Cubedo, A. The early Pleistocene small vertebrate succession from the Orce region (Guadix-Baza Basin, SE Spain) and its bearing on the first human occupation of Europe. Quat. Int. 223–224, 162–169 (2010).

    Article  Google Scholar 

  26. 26.

    Furió, M., Gibert, L., Ferràndez, C. & Sevilla, P. The insectivores (Soricidae, Erinaceidae; Eulipotyphla; Mammalia) from Cueva Victoria (Early Pleistocene, Murcia, Spain). Neues Jahrb. Geol. Paläontol. 275, 151–161 (2015).

    Article  Google Scholar 

  27. 27.

    van Dam, J. A. & Weltje, G. J. Reconstruction of the Late Miocene climate of Spain using rodent palaeocommunity successions: an application of end-member modelling. Palaeogeogr. Palaeoclimatol. Palaeoecol. 151, 267–305 (1999).

    Article  Google Scholar 

  28. 28.

    Gómez Cano, A. R., Hernández Fernández, M. & Álvarez-Sierra, M. A. Dietary ecology of Murinae (Muridae, Rodentia): a geometric morphometric approach. PloS One 8, e79080 (2013).

    Article  ADS  PubMed  PubMed Central  Google Scholar 

  29. 29.

    Renaud, S. et al. Morphological evolution, ecological diversification and climate change in rodents. Proc. R. Soc. B. 272, 609–617 (2005).

    Article  Google Scholar 

  30. 30.

    López-García, J. M. et al. Small mammals from the middle Pleistocene layers of the Sima del Elefante (Sierra de Atapuerca, Burgos, northwestern Spain). Geol. Acta 9, 29–43 (2011).

    Google Scholar 

  31. 31.

    Blain, H.-A. & Bailon, S. Extirpation of Ophisaurus (Anguimorpha, Anguidae) in Western Europe in the context of the disappearance of subtropical ecosystems at the Early-Middle Pleistocene transition. Palaeogeogr. Palaeoclimatol. Palaeoecol. 520, 96–113 (2019).

    Article  Google Scholar 

  32. 32.

    Pleguezuelos, J. M. “Malpolon monspessulanus (Hermann, 1804)” in Fauna Ibérica, Vol. 10, Salvador, A., Ed., pp. 408–427 (Museo Nacional de Ciencias Naturales, CSIC, Madrid, 1997).

  33. 33.

    Carmen Blazquez, M. & Pleguezuelos, J. M. “Malpolon monspessulanus” in Atlas y libro rojo de los Anfibios y Reptiles de España, Pleguezuelos, J. M., Marquez, M. & Lizanam, M. Eds., pp. 284–286 (Dirección General de Conservación de la Naturaleza, Asociación Herpetológica Española, Madrid, 2004).

  34. 34.

    Pleguezuelos, J. M. & Santos, X. “Vipera latasti” in Atlas y libro rojo de los Anfibios y Reptiles de España, Pleguezuelos, J. M., Marquez, M. & Lizanam, M. Eds., pp. 298–300 (Dirección General de Conservación de la Naturaleza, Asociación Herpetológica Española, Madrid, 2004).

  35. 35.

    Dessauer, H. D., Nevo, E. & Chuang, K. High genetic variability in an ecologically variable vertebrate. Bufo viridis. Biochem. Genet. 13, 651–661 (1975).

    Article  CAS  Google Scholar 

  36. 36.

    Blain, H.-A. & Bailon, S. “Anfibios y escamosos del Pleistoceno inferior de Barranco León y de Fuente Nueva 3 (Orce, Andalucía, España)” in Ocupaciones humanas durante el Pleistoceno inferior y medio de la Cuenca de Guadix-Baza, Toro, I., Martínez-Navarro, B. & Agustí, J. Eds., pp. 165–183 (Arqueología Monografías. Junta de Andalucía, Sevilla, 2010).

  37. 37.

    Blain, H.-A., Bailon, S., Agustí, J., Martínez-Navarro, B. & Toro, I. Paleoenvironmental and paleoclimatic proxies to the Early Pleistocene hominids of Barranco León D and Fuente Nueva 3 (Granada, Spain) by means of their amphibian and reptile assemblages. Quat. Int. 243, 44–53 (2011).

    Article  Google Scholar 

  38. 38.

    Blain, H.-A., Bailon, S. & Agustí, J. Anurans and squamate reptiles from the latest Early Pleistocene of Almenara-Casablanca-3 (Castellón East of Spain). Systematic, climatic and environmental considerations. Geodiversitas 29, 269–295 (2007).

    Google Scholar 

  39. 39.

    Blain, H.-A., Gibert, L. & Ferrandez-Cañadell, C. First report of a green toad (Bufo viridis sensu lato) in the Early Pleistocene of Spain: Palaeobiogeographical and palaeoecological implications. C. R. Palevol. 9, 487–497 (2010).

    Article  Google Scholar 

  40. 40.

    Bailon, S. Amphibiens et reptiles du Pliocène terminal d’Ahl al Oughlam (Casablanca Maroc). Geodiversitas 22, 539–558 (2000).

    Google Scholar 

  41. 41.

    Piñero, P., Agustí, J., Blain, H.-A., Furió, M. & Laplana, C. Biochronological data for the Early Pleistocene site of Quibas (SE Spain) inferred from rodent assemblage. Geol. Acta 13, 229–241 (2015).

    Google Scholar 

  42. 42.

    Agustí, J. et al. Early to Middle Pleistocene rodent biostratigraphy of the Guadix-Baza basin (SE Spain). Quat. Int. 389, 139–147 (2015).

    Article  Google Scholar 

  43. 43.

    Cuenca-Bescós, G. et al. Biochronology of Spanish Quaternary small vertebrate faunas. Quat. Int. 212, 109–119 (2010).

    Article  Google Scholar 

  44. 44.

    Montoya, P. et al. La fauna del Pleistoceno Inferior de la Sierra de Quibas (Abanilla, Murcia). Estud. Geol. 55, 127–161 (1999).

    Article  Google Scholar 

  45. 45.

    Montoya, P. et al. Une faune très diversifiée du Pléistocène inférieur de la Sierra de Quibas (provincia de Murcia, Espagne). C. R. Acad. Sci. 332, 387–393 (2001).

    Article  Google Scholar 

  46. 46.

    Álvarez, C. et al. New magnetostratigraphic and numerical age of the Fuente Nueva-3 site (Guadix-Baza basin, Spain). Quat. Int. 389, 224–234 (2015).

    Article  Google Scholar 

  47. 47.

    Lozano-Fernández, I., Blain, H.-A., López-García, J. M. & Agustí, J. Biochronology of the first hominid remains in Europe using the vole Mimomys savini: Fuente Nueva 3 and Barranco León D, Guadix-Baza Basin, south-eastern Spain. Hist. Biol. 27, 1021–1028 (2015).

    Article  Google Scholar 

  48. 48.

    Parés, J. M. & Pérez-González, A. Magnetochronology and stratigraphy at Gran Dolina section, Atapuerca (Burgos, Spain). J. Hum. Evol. 37, 325–342 (1999).

    Article  Google Scholar 

  49. 49.

    Gibert, L. et al. Chronology for the Cueva Victoria fossil site (SE Spain): Evidence for Early Pleistocene Afro-Iberian dispersals. J. Hum. Evol. 90, 183–197 (2016).

    Article  Google Scholar 

  50. 50.

    Piñero, P. & Alberdi, M. T. Estudio de los caballos del yacimiento de Quibas, Pleistoceno Inferior final (Abanilla, Murcia, España). Estud. Geol. 71, e034 (2015).

    Article  Google Scholar 

  51. 51.

    Alba, D. M. et al. Fossil remains of Macaca sylvanus florentia (Cocchi, 1972) (Primates, Cercopithecidae) from the Early Pleistocene of Quibas (Murcia, Spain). J. Hum. Evol. 61, 703–718 (2011).

    Article  Google Scholar 

  52. 52.

    Koymans, M. R., Langereis, C. G., Pastor-Galan, D. & van Hinsbergen, D. J. J. An online multi-platform open source environment for paleomagnetic data analysis. Comput. Geosci. 93, 127–137 (2016).

    Article  ADS  Google Scholar 

  53. 53.

    Singer, B. S. A Quaternary geomagnetic instability time scale. Quat. Geochronol. 21, 29–52 (2014).

    Article  Google Scholar 

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This work was supported by the Comunidad Autónoma de la Región de Murcia (ARQ115/2018, Subvención para la Investigación e Intervención en el Patrimonio Arqueológico y Paleontológico de la Región de Murcia), the Spanish Agencia Estatal de Investigación and the European Regional Development Fund of the European Union (CGL2016-80000-P, CGL2016-75109-P, CGL2016-76431-P and CGL2017-82654-P, AEI/FEDER EU), and the Generalitat de Catalunya (2017/SGR/859, CERCA Programme). One author (P.P.) is beneficiary of a postdoctoral fellowship from the Argentinian Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET). We would like to dedicate this paper to Miguel A. Mancheño, professor of the University of Murcia, who directed the site of Quibas from 2002 to 2009. We are especially grateful to Gregorio Romero and the Servicio de Patrimonio Histórico de la Dirección General de Bienes Culturales de la Región de Murcia for their facilities to carry out the research at the Quibas site. We would like to express our gratitude to the Quibas excavation team, who helped with the extraction, sieving, and washing of sediments. The authors wish to thank the Town Hall of Abanilla for their support. Last but not least, we gratefully acknowledge the valuable comments provided by two anonymous reviewers and by editor Chenglong Deng.

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P.P. and J.A. designed research; P.P., J.A. and O.O. performed research; P.P., J.A., O.O., H.-A.B, M.F., C.L., P.S., A.R. and J.V. analyzed data; and P.P., J.A. and O.O. wrote the paper.

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Correspondence to Pedro Piñero.

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Piñero, P., Agustí, J., Oms, O. et al. First continuous pre-Jaramillo to Jaramillo terrestrial vertebrate succession from Europe. Sci Rep 10, 1901 (2020).

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