Rodents typically avoid illuminated and open areas, favoring dark or sheltered environments for activity. Indeed, higher activity was described in numerous field and laboratory studies of nocturnal species tested in the dark, compared with their activity when tested under light. For example, common spiny mice (Acomys cahirinus) decreased activity and foraging in open spaces under moonlit compared with dark nights [1]. When tested in the dark, laboratory rats increase their activity and display behaviors that indicate reduced habituation, fear and anxiety [2]. Deermice (Peromyscus maniculatus) were shown to reduce activity in the open during moonlit nights and were active only near objects such as rocks, grasses, and walls, where they could successfully evade a predator attack [3]. Thus, it appears that rodents perceive increased risk of predation in open spaces and/or during moonlit nights and in consequence shift their activity to more protected microhabitats [4-7]. While many of these studies used indirect measures of locomotor activity, such as footprints [8], the present laboratory study was aimed at direct observation of locomotor behavior under various light levels and arena complexities.
The 'open field' is a widely used apparatus in laboratory studies of rodents' locomotor activity [9]. This apparatus has been criticized for being "a poor and explicitly aversive environment with excess light and open spaces..."[10]. Nevertheless, it is a relatively simple testing environment for a variety of species, in which they display a typical behavioral structure [11] that withstands drastic environmental changes [12]. Studies in wild and laboratory rodents in an illuminated open field (e.g., [9,11-14]) have shown that their locomotor behavior is organized in reference to a key location – the home-base. At the home base, the rodent demonstrates typical behaviors (e.g. grooming and crouching), and sets out on round trips in the area. The building block of the round trip is a stop, with an upper limit of 8–10 stops per trip [15]. The limited number of stops/trip is preserved by scaling the distance between successive stops and adjusting the number of trips, even under large changes in arena size [12,16]. Accordingly, rodents in a larger area made fewer yet longer trips, whereas in a small area they made shorter but more frequent trips. Following these earlier studies, the present study tested open field behavior under varying light level and arena complexity.
The common spiny mouse (Acomys cahirinus) was selected for this study since it is a strictly nocturnal species that displaces other species to crepescular or diurnal activity [17,18]. Common spiny mice were thus expected to be sensitive to tests in illuminated compared with dark environments. Also, they live in rocky environments, nimbly foraging in crevices between and under rocks and boulders [18,19], where the complex habitat structure provides shelter and escape from predators. They were thus expected to be also sensitive to changes in environmental complexity. Three questions were posed in this study of common spiny mice: i) is their behavior in an illuminated arena similar to that seen in mice, rats, and voles? ii) does behavior change in dark arena and/or with increased environmental complexity? iii) what is the functional mechanism that may underlie behavioral changes in dark or complex environments? As shown below, activity increased in dark or in complex environment, and took a different form of short straight trajectories. In contrast, spiny mice traveled through the center in a convoluted path in either lit or dark empty arenas. This later form of progression may have a defensive advantage.