Dr. Wulfila Gronenberg Print E-mail
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Associate Professor of Neuroscience and Ecology and Evolutionary Biology

Ph.D. 1984, Free University of Berlin


Office: Gould-Simpson Bldg. Rm. 422
E-mail: This e-mail address is being protected from spambots. You need JavaScript enabled to view it
Phone: (520) 626-5422
Fax: (520) 621-8282
Gronenberg Lab Group

Neuronal control of complex behavior; multimodal information processing and brain plasticity

I am interested in the neuronal control of behavior at different levels of behavioral complexity. In my lab, we favor the comparative approach towards neuroethology, focusing on the brain and behavior of Hymenoptera (bees, ants, and wasps). In addition to simple behavior, social insect colonies depend on communication, kin recognition, navigation, exploration and recollection of territories, food sources, and nest positions, and adaptive foraging strategies to cope with changing colony needs and food availability.

 

 

Sensory-motor reflexes. The mandibles are the most important tools of most insects and they are used for many different tasks requiring a wide range of force output and movement velocities (biting, cutting, defense, seed cracking, digging, grooming, brood care, etc.). In biting insects (e.g. ants and wasps), jaws are powered by particularly large muscles. Using electrophysiology, force- and movement measurements and anatomical methods, we investigate how the relatively small number of motor neurons that control the jaw muscles can generate the wide range of movements, among which are some of the fastest reflexes known (in trap-jaw ants).

Brain and behavior. Most insects and all ants rely on olfaction and tactile cues for communication and orientation. Wasps and bees, and some ants are expressively visual animals that use their keen sight to navigate by visual landmarks, the position of the sun or moon, or the polarization pattern of the skylight. They rely on vision to find flowers, nests, or lekking points, to catch prey (wasps and ants) and even for individual 'face' recognition (some paper wasps).By comparing the brains of insects that rely on different sensory cues and show very different behavior we try to get insights into the function of particular brain structures. The brains of Hymenoptera comprise prominent antennal lobes that process odor information, and the visual brain centers are large in bees and wasps, but small small in most ants. The antennal and optic lobes assess significant stimulus features (such as odor quality and strength, light color, pattern, movement). Other brain compartments concatenate these features and determine their significance with regard to temporal and spatial conditions and previous experience to give rise to complex behavior. The so-called mushroom bodies are involved in the generation of such complex decision-making. These central brain structures process multimodal information and supposedly control orientation, complex movement and learning and memory. The mushroom bodies are particularly large in ants and bees, suggesting a correlation with their rich behavioral repertoire. We analyze the brains and nerve cells of different species and castes to quantify differences in their brain design. These data are compared to the behavioral performance of the respective species in quantitative laboratory tests (walking, orientation, learning paradigms). We are particularly interested in the structure and function of neurons associated with the mushroom bodies and try to find out how visual and olfactory information is represented in and processed by mushroom body neurons. Behavioral deficits resulting from focused brain ablations help to determine the functional significance of certain brain sub-compartments and groups of neurons.


Neuronal and behavioral plasticity. In addition to their overall complex behavior, social insect colonies are based on caste systems. Besides reproductive males and females, the majority of individuals in the colonies are workers (e.g. nurses, foragers, soldiers). In many ant species, worker castes may differ morphologically (e.g. body size). Although genetically almost identical, these workers show cast-specific responses when confronted with particular stimuli. Moreover, their individual behavior may change over time as virgins become queens or as nurses become foragers. We assess their changing behavior and learning abilities and analyze concomitant changes in the neuronal substrate, particularly in the mushroom bodies. Neuronal changes associated with such behavioral transitions are also examined in deprivation experiments in which the importance of sensory experience for the development of the brain and of normal behavior is assessed. Similar neuronal changes occur in vertebrates as they become more experienced, but it is easier to examine such effects in social insects.

 

Selected Recent Publications

Gilbert C, Gronenberg W, Strausfeld NJ. Oct 1995. Oculomotor control in calliphorid flies: head movements during activation and inhibition of neck motor neurons corroborate neuroanatomical predictions. J Comp Neurol, 361:285-97

Gronenberg W, Milde JJ, Strausfeld NJ. Oct 1995. Oculomotor control in calliphorid flies: organization of descending neurons to neck motor neurons responding to visual stimuli. J Comp Neurol, 361:267-84

Gronenberg W, Strausfeld NJ. Feb 1992. Premotor descending neurons responding selectively to local visual stimuli in flies. J Comp Neurol, 316:87-103

Gronenberg W, Strausfeld NJ. Oct 1991. Descending pathways connecting the male-specific visual system of flies to the neck and flight motor. J Comp Physiol [A], 169:413-26

Gronenberg W, Strausfeld NJ. Dec 1990. Descending neurons supplying the neck and flight motor of Diptera: physiological and anatomical characteristics. J Comp Neurol, 302:973-91

Strausfeld NJ, Gronenberg W. Dec 1990. Descending neurons supplying the neck and flight motor of Diptera: organization and neuroanatomical relationships with visual pathways. J Comp Neurol, 302:954-72

Gronenberg W. Apr 1990. The organization of plurisegmental mechanosensitive interneurons in the central nervous system of the wandering spider Cupiennius salei. Cell Tissue Res, 260:49-61

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