Coexistence and Intermediate Morphological Forms Between Vipera Aspis and V

Coexistence and Intermediate Morphological Forms Between Vipera Aspis and V

Bol. Asoc. Herpetol. Esp. (2019) 30(1) 35 Coexistence and intermediate morphological forms between Vipera aspis and V. latastei in the intensive agriculture fields of north-western Iberian System Óscar Zuazo1, Inês Freitas2, Ricardo Zaldívar3 & Fernando Martínez-Freiría2 1 Cl. La Puebla, 1. 1º A. 26250 Santo Domingo de la Calzada. La Rioja. Spain. 2 CIBIO/InBIO, Centro de Investigação em Biodiversidade e Recursos Genéticos. Universidade do Porto. Instituto de Ciências Agrárias de Vairão. R. Padre Armando Quintas. 4485-661 Vairão. Portugal. C.e.: [email protected] 3 Avda. de La Paz, 89. 8º O. 26004 Logroño. La Rioja. Spain. Fecha de aceptación: 11 de enero de 2019. Key words: concolor, contact zone, hybridization, landscape transformation, syntopy, Viperinae. RESUMEN: Se presenta la distribución de Vipera aspis y V. latastei en la zona de contacto de Oja-Tirón (noroeste del Sistema Ibérico) caracterizada por un paisaje predominantemente agrícola intensivo. Vipera aspis ha sido detectada en un total de 106 celdas UTM 1x1 km, mientras que V. latastei en 57. Las dos especies se han detectado en simpatría en 15 celdas UTM 1x1 km y en sintopía en cuatro de ellas. De los 549 ejemplares capturados y encontra- dos atropellados se han detectado 46 individuos con características morfológicas intermedias entre las dos especies, incluyendo un ejemplar con coloración gris uniforme (concolor), que constituye el primer registro de una víbora mediterránea occidental con esta coloración en la península ibérica. De manera similar a lo que ocurre en la zona del Alto curso del río Ebro, los ejemplares con características intermedias pueden ser resultado de un proceso de hibridación entre las dos especies de víboras. European vipers (genus Vipera) display pa- the Massif Central in central France (Duguy & rapatric distributions that reflect contrasting Saint-Girons, 1978), in the Bernoises Pre-Alps climatic niches and past evolutionary trajec- of Switzerland (Monney, 1996) and in the Al- tories (Saint-Girons, 1980). In regions of climatic pine region of Lombardy in northern Italy transition, species distributions can meet in (Scali et al., 2011); 2) V. aspis and V. ursinii in the contact, i.e. contact zones, whereas, at local Abruzzo mountains of central Italy (Luiselli et al., scale, species frequently show variable levels of 2007); 3) V. latastei and V. seoanei in the Pene- habitat segregation, in accordance to ecological da-Gerês Mountains of north-western Portugal and evolutionary differentiation (Luiselli, 2006; (Brito & Crespo, 2002); 4) V. aspis, V. berus and Martínez-Freiria et al., 2008; Tarroso et al., 2014; Mebert V. ammodytes in the Julian Alps in north-western et al., 2015; Guiller et al., 2017). Slovenia (Mebert et al., 2015, 2017); and 5) V. aspis, The mechanisms allowing species coexisten- V. latastei and V. seoanei in the High course of the ce among European vipers have been intensively Ebro river in northern Spain (Martínez-Freiría et al., studied in distinct contact zones, including: 2006, 2008, 2009, 2010; Tarroso et al., 2014). 1) Vipera aspis and V. berus in the Atlantic Loi- The Western Mediterranean vipers, V. aspis re region of north-western France (Saint-Gi- and V. latastei, are closely related species that rons, 1975; Naulleau, 1986; Guiller et al., 2017), in exhibit several contact zones across their distri- 36 Bol. Asoc. Herpetol. Esp. (2019) 30(1) Figure 1: Distribution of V. aspis, V. latastei and vipers with interme- diate traits between V. aspis and V. latastei (i.e. intermediate vipers) in the Oja-Tirón contact zone, based on 1x1 km UTM squares (ETRS1989). Location of the study area is showed (top right). Figura 1: Distribución de V. aspis, V. latastei y víboras con caracterís- ticas intermedias entre V. aspis y V. latastei en la zona de contacto de Oja-Tirón, basada en celdas UTM 1x1 km (ETRS1989). Se muestra la localización del área de estudio (arri- ba a la derecha). bution areas (Martínez-Freiría, 2014; Martínez-Frei- High Ebro, sympatry and syntopy were repor- ría et al., 2014). Sympatry between these species ted in a relatively large area of 8 km2, where has been suggested in six areas of the Iberian about 20% of captured specimens showed Peninsula: four in the southern slopes of the intermediate morphology between V. aspis Pyrenees, one in the Iberian System, and one and V. latastei, and were mostly confirmed as in the High course of the Ebro River (Martí- hybrids between these species by genetic stu- nez-Freiría, 2014; Martínez-Freiría et al., 2014). In the dies (Martínez-Freiría et al., 2006; Tarroso et al., 2014). a b Photos Óscar Zuazo Figure 2: Pictures of the landscapes in Oja (a) and Tirón (b) river valleys, where V. aspis and V. latastei occur, res- pectively. Pictures were taken from north to south. Intensive cereal cultures are in the second plane, while Demanda Mountains in the background. Figura 2: Imágenes de los paisajes de los valles del río Oja (a) y Tirón (b), donde se encuentran V. aspis y V. latastei, respectivamente. Las imágenes fueron sacadas desde el norte en dirección sur. Los campos de cultivo se encuentran en segundo plano, mientras que la Sierra de la Demanda en el fondo. Bol. Asoc. Herpetol. Esp. (2019) 30(1) 37 This hybrid zone is coincident with a steep racterised by low levels of precipitation, with an- ecotone between the Atlantic and Mediterra- nual rainfall ranging from 604-1016 mm/year, nean bioclimatic provinces, with hybrids being and low annual temperature, ranging from 4.1 found in areas of suboptimal habitat for paren- to 12.5º C (Hijmans et al., 2005). tal taxa (Tarroso et al., 2014). Aside from this well- The study area was surveyed by foot and studied contact zone, little is known about the car (to find road-killed vipers), along a four- remaining contact zones between V. aspis and years period (March 2015 - November 2018). V. latastei (e.g. Ferrer et al., 2018). In this note, we Alive specimens were captured, measured and report sympatry, syntopy and the existence of photographed, and their geographic position intermediate morphological forms between (UTM coordinates, ETRS1989 datum) re- the two Iberian vipers, V. aspis and V. latastei, corded with a Global Positioning System. in the north-western slopes of the Iberian Sys- Road-killed specimens were collected and tem in north-central Spain. preserved in ethanol for further analyses. Spe- The study area is located north to the De- cimens’ classification as V. aspis, V. latastei, or manda Mountains (Iberian System) and south intermediate forms was done by a set of diag- to La Bureba region (centroid: 30T 495000; nostic morphological traits (see Table 1) fo- 4695000; ETRS1989 datum), between Burgos llowing the criteria used to identify species in and La Rioja provinces (Figure 1). It is shaped the High Ebro contact zone (see Martínez-Freiría by the valleys of two main rivers, the Tirón and et al., 2006, 2009). Specimens were classified as the Oja, tributaries of the Ebro River. Unlike intermediate forms when displaying interme- the High Ebro contact zone, which is embed- diate morphological traits between each spe- ded in a vast natural landscape (Martínez-Freiría cies or a combination of traits which are consi- et al., 2006), the study area is located in a zone dered diagnostic for each species. of substantial anthropogenic disturbance, con- A total of 549 specimens were collected sisting mostly of intensive culture fields of ce- (501 alive, 48 road-killed), 320 classified as reals. Altitude ranges from 480 to 2271 masl. V. aspis (133 females, 154 males) and 186 as The area matches with the transition between V. latastei (82 females, 80 males). Vipera aspis Euro-Siberian and Mediterranean regions, re- was distributed throughout the southern zone sulting in a Mediterranean-Atlantic climatic of the study area, while V. latastei occurred in character (Sillero et al., 2009). The climate is cha- the northern zone (Figure 1). Both species Table 1: Diagnostic morphological traits used to differentiate specimens of V. aspis from specimens of V. latastei (from Martínez-Freiría et al., 2006). Tabla 1: Rasgos morfológicos diagnósticos usados para diferenciar ejemplares de V. aspis y V. latastei (de Mar- tínez-Freiría et al., 2006). Trait V. aspis V. latastei Snout Slightly upwards Snout upwards, forming an appendix Number of apical scales 2 - 3 3 - 9 Shape of the dorsal draw Alternated cross bands with a thin Wide zigzag (type 2) or rounded-rhomboidal vertebral line (type 0) or narrow marks running together to form a wavy or zigzag angular zigzag (type 1) stripe (type 3) Number of dorsal marks 45 - 78 33 - 57 38 Bol. Asoc. Herpetol. Esp. (2019) 30(1) a d g Photos Fernando Martínez-Freiría Fernando Photos b e h c f i Figure 3: Pictures of three individuals classified as intermediate vipers (i.e. vipers with intermediate traits between V. aspis and V. latastei). a), b) and c), correspond to a male with three apical scales, snout slightly upwards, 49 dorsal marks and dorsal draw type 1/2. d), e) and f) correspond to a female with five apical scales, snout upwards, 46 dorsal marks and dorsal draw type 1. g), h) and i) correspond to a male with two apical scales, snout upwards, 42 dorsal marks and dorsal draw type 3. Figura 3: Imágenes de tres individuos clasificados como víboras intermedias (es decir, víboras con rasgos interme- dios entre V. aspis y V. latastei). a), b) y c) corresponden a un macho con tres escamas apicales, hocico levemente hacia arriba, 49 marcas dorsales y diseño dorsal de tipo 1/2. d), e) y f) corresponden a una hembra con cinco escamas apicales, hocico hacia arriba, 46 marcas dorsales y diseño dorsal de tipo 1.

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