Can rats and ants exchange information between the horizontal and vertical domains?

Since traveling in nature involves encountering various vertical structures, integration of horizontal and vertical spatial information is required. One form of such integration is to use information acquired in one plane for spatial navigation in another plane. Here we tested whether rats and ants that learned a reward location in a horizontal maze could utilize this information when the maze was rotated to a vertical orientation and vice versa. Rats that were trained in a horizontal Y-maze required more time to reach the reward when the maze was vertically rotated, but they were more accurate in choosing the correct arm. In contrast, rats tested in a horizontal maze after being trained in a vertical maze were less accurate but reached the reward faster. Changes after maze rotation were moderate and non-significant in ants, perhaps since the number of ants arriving at the reward increased over trials, diminishing the effect of maze rotation in ants compared to rats. According to the notion that horizontal spatial information is encoded in more detail than vertical information, the slow performance of rats in the vertical domain could be due to a more physically demanding task whereas their accuracy was due to a preceding detailed horizontal encoding. In contrast, rats in the vertical maze could gather less detailed information and therefore were less accurate in subsequent horizontal trials, where the lower energy cost enabled them to swiftly correct wrong choices. Altogether, the present results provide an indication for transferring spatial information between horizontal and vertical dimensions.

Rodents Prefer Going Downhill All the Way (Gravitaxis) Instead of Taking an Uphill Task.

We directly tested whether, when given the choice to ascend or descend, rodents would favor traveling downwards or upwards. The test incorporated different rodent species that dwell in different habitats and display different life and motor styles. Testing was performed in a three-dimensional Y-maze in which the basis was horizontal and, by rotating it, one arm of the maze could be pointing upwards at a certain angle and the other arm pointed downwards at the same angle. All the tested species displayed a general preference for descent, with rodents from complex habitats being less affected by inclination compared with rodents from flatlands. Unlike laboratory rats, wild species traveled greater distances along the lower compared to the upper maze arm. All the rodents initially tended to travel the entire length of the inclined maze arms, but such complete trips decreased with the increase in inclination. When introduced into the maze from top or bottom, flatland dwellers traveled mainly in the entry arm. Overall, when given the choice to ascend or descend, all the tested species displayed a preference to descend, perhaps as attraction to the ground, where they usually have their burrows.

The sounds of silence: Barn owl noise in landing and taking off.

A barn owl swooping down generated a quieter, almost silent, noise (acoustic impulses) compared to a louder noise generated by the owl when taking off. These acoustic impulses are at low frequencies which are below the auditory threshold to most rodents. Therefore, rodents are less likely to hear these noises of owl flight. A previous study revealed that rodents exhibit frantic response to an owl taking off (as opposed to their typical freezing response during owl attack). The frantic response could be the result of tactile reception of the air-puffs generated by the owl's wingbeats and may reduce the success in subsequent attacks.

Rats do not eat alone in public: Food-deprived rats socialize rather than competing for baits.

Limited resources result in competition among social animals. Nevertheless, social animals also have innate preferences for cooperative behavior. In the present study, 12 dyads of food-deprived rats were tested in four successive trials, and then re-tested as eight triads of food-deprived rats that were unfamiliar to each other. We found that the food-deprived dyads or triads of rats did not compete for the food available to them at regular spatially-marked locations that they had previously learnt. Rather, these rats traveled together to collect the baits. One rat, or two rats in some triads, lead (ran ahead) to collect most of the baits, but "leaders" differed across trials so that, on average, each rat ultimately collected similar amounts of baits. Regardless of which rat collected the baits, the rats traveled together with no substantial difference among them in terms of their total activity. We suggest that rats, which are a social species that has been found to display reciprocity, have evolved to travel and forage together and to share limited resources. Consequently, they displayed a sort of 'peace economy' that on average resulted in equal access to the baits across trials. For social animals, this type of dynamics is more relaxed, tolerant, and effective in the management of conflicts. Rather than competing for the limited available food, the food-deprived rats socialized and coexisted peacefully.

Modulation of quinpirole-induced compulsive-like behavior in rats by environmental changes: implications for OCD rituals and for exploration and navigation.

BACKGROUND: Rats treated chronically with the D2-3 dopamine agonist quinpirole were previously proposed as an animal model of obsessive-compulsive disorder (OCD) since their behavior is based on repeated, compulsive-like persistent traveling between a few places in the open field. The aim of the present study was to determine properties of the physical environment that shape such behavior. For this, quinpirole-treated rats were first exposed to an arena with an array of objects (landmarks) and after the development of compulsive-like behavior, the arena was manipulated by multiplying the number of objects, changing their spacing, relocating object array, or removing the objects. RESULTS: When the number of objects was retained but they were spaced further apart, rat routes converged at 1-2 of the objects and at the corner at which the rats had been introduced into the arena (start corner). When object spacing was retained but their number was increased, the rats traveled between the objects with the routes converging only at the start corner. Finally, when object array was relocated to different places within the arena, the rats extended their routes from the start corner to the object array, regardless of array location. CONCLUSION: Quinpirole-treated rats organized and updated their progression primarily according to the proximal layout of landmarks, but did so with excessive repetitions compared with saline-treated rats. The behavior of quinpirole-treated rats paralleled human OCD rituals that are linked to the immediate physical environment, featuring an excessive rate of performance. Finally, when only a few objects were present, they were perceived by the rats as positional cues (beacons) that routes converged at them. In contrast, in the presence of many objects, the routes passed between the objects as if using them as directional cues.

Exploration in a dark open field: a shift from directional to positional progression and a proposed model of acquiring spatial information.

Exploration in a dark open field undergoes three progressive changes: (i) an initial phase of spending equal amounts of time in various zones of the arena changes to staying in the corners, and ultimately spending most of the time in one corner; (ii) travel paths are first circular and scattered all over the arena, but gradually become anchored to one corner at which they start and end; (iii) traveled distance gradually decreases to that of the initial level seen in a lit open field. Altogether, rodents shift from a 'looping' exploration mechanism with feeble coupling with the environment, to 'home base' exploration which is firmly anchored to the environment. This shift also involves switching from momentary and sporadic to repeated returns to a specific, presumably familiar place, to which the animal navigates back from various other places. We suggest that this switching illustrates navigation first by directional and then by positional environmental cues, as hypothesized in the 'parallel map theory'. We also suggest that the transition from looping to home base behavior is part of a hierarchal construction of space representation via three modes of spatial information processing: (i) piloting--sequential processing, based on moving from one landmark to the next; (ii) orienting--parallel processing, based on moving from one point to the next, with the same starting and ending point; (iii) navigating--continuous processing, based on continuously updating the position in relation to several locations in the environment (map navigation).

'Looping'-an exploration mechanism in a dark open field.

The behavior of Tristram's jird (a species of gerbil) in an illuminated open field resembled that of other rodents, comprising round trips to a home base and alternating between periods of progression (locomoting) and of stopping. In this study, we compared the characteristics of exploration in a dark arena with exploration by the same individuals in a lit arena. In the dark arena, stopping episodes were brief and fewer, suggesting almost continuous locomotion by the rodents. The clear distinction between progression and stopping that had characterized locomotion in an illuminated arena, thus diminished in the dark. There was also no apparent home base in the dark and traveling consisted in moving in a circular path, closing a loop to a recently traveled place that varied from one loop to the next. Locomotion in the dark may thus be regarded as a set of loops (round trips) to a continuously shifting home base, whereas with lights on the round trips converge to a home base using visible environmental landmarks. We suggest that a similar looping mechanism may be applicable to the behavior of hippocampal rats displaying hyperactivity and diversified locomotion, reminiscent of that seen in jirds in a dark arena.