Neuronal control of complex behavior; multimodal information processing and brain plasticity
We are interested in the neuronal control of behavior at different levels of behavioral complexity. In our lab, we favor the comparative approach towards neuroethology, focusing on the brain and behavior of Hymenoptera (bees, ants, and wasps) and some arachnids (spiders and their kin).
Some Hymenoptera have evolved social lifestyles (e.g. honey bees, paper wasps, ants). Individual social insects often show sophisticated behaviors (e.g. communication, navigation, etc.) and pronounced learning and memory capabilities and we are interested in the neural basis of such behavioral feats (e.g. color and odor learning).
Brain and behavior. Most insects rely on olfaction and tactile cues for communication and orientation. Wasps and bees, and some ants use their keen sight to navigate by visual landmarks, to find flowers, nests, or mating points, to catch prey 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 odor-processing centers (antennal lobes) and large visual centers (bees and wasps, some ants). Central brain structures such as the so-called mushroom bodies process multimodal information and are involved in orientation, decision-making, learning and memory.
Brain and brain component size and activity. For a long time people have been intrigued by correlations between animals’ brain or brain component size or brain organization and behavioral capacities. We compare brain and brain component size and metabolic brain activity across species and castes and we ask what the behavioral advantages of larger or more active brains or brain components are, keeping in mind that even tiny insects with minuscule brains are doing just fine in their respective environments.
The mushroom bodies are particularly large in behaviorally advanced hymenopteran species, suggesting a correlation with their rich behavioral repertoires. 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 and learning paradigms in particular.
Neuronal and behavioral plasticity. Most individuals in social insect colonies are workers (e.g. nurses, foragers, soldiers). Although genetically almost identical, these workers show cast-specific behaviors and their individual behavior may change over time. We assess their changing behavior and learning abilities and analyze concomitant changes in the neuronal substrate.
Compared to insects, very little is known about the nervous systems of spiders and their kin. Arachnids are very sensitive to mechanical stimuli (touch, vibration, wind, etc.) and some have very acute vision (e.g. jumping spiders) whereas other do not. While our knowledge about chemical senses in spiders is severely lacking, it is known that spiders, scorpions and other arachnid orders have chemoreceptors on their legs, feelers or specialized organs. Next to nothing is known about where in their brains this chemical information is processed, and we are trying to find out. We found structures indicative of olfactory information processing (glomeruli) in the central nervous systems of spiders and harvestmen and in the exceedingly large mushroom bodies of whip spiders. The latter is of particular interest as whip spiders reportedly navigate using their sense of smell and their brain may comprise chemical ‘maps’ which, we think, may reside in their large mushroom bodies.
Selected Recent Publications
Kamhi JF, Gronenberg W, Robson SKA, James F. A. Traniello JFA (2016) Social complexity influences brain investment and neural operation costs in ants. Proc R Soc B (in press)
Amador-Vargas S, Gronenberg W, Wcislo W, Mueller U (2015) Specialization and group size: brain and behavioral correlates of colony size in ants lacking morphological castes. Proc R Soc B DOI: 10.1098/rspb.2014.2502
Muscedere ML, Gronenberg W, Moreau CS, Traniello JFA (2014) Investment in higher-order central processing regions is not constrained by brain size in social insects. Proc. R. Soc. B 281: 20140217. http://dx.doi.org/10.1098/rspb.2014.0217
Gronenberg W, Raikhelkar A, Abshire E, Stevens J, Epstein E, Loyola K, Rauscher M, Buchmann S (2014) Honey bees (Apis mellifera) learn to discriminate the smell of organic compounds from their respective deuterated isotopomers. Proc. R. Soc. B 20133089. http://dx.doi.org/10.1098/rspb.2013.3089
Jones MB, Leonard AS, Papaj DR, Gronenberg W (2013) Plasticity of the worker bumblebee brain in relation to age and rearing environment. Brain Behav. Evol. 82:250-261 (DOI: 10.1159/000355845)
Milton Giraldo Y, Patel E, Gronenberg W, Traniello JFA(2013) Division of labor and structural plasticity in a serotonergic extrinsic mushroom body neuron in the ant Pheidole dentate. Neurosci Letters 534: 107– 111
Mota T, Gronenberg W, Giurfa M, Sandoz JC (2013) Chromatic Processing in the Anterior Optic Tubercle of the Honey Bee Brain. J Neurosci. 33:4-16
Riveros AJ, Gronenberg W (2012) Decision-making and associative color learning in harnessed bumblebees (Bombus impatiens). Anim. Cogn. 15: DOI: 10.1007/s10071-012-0542-6
Mota T, Yamagata N, Giurfa M, Gronenberg W, Jean-Christophe Sandoz J-C (2011) Neural organization and visual processing in the anterior optic tubercle of the honeybee brain. J. Neurosci. 31: 11443-11456.
Riveros AJ, Gronenberg W (2010) Brain allometry and neural plasticity in the bumblebee Bombus occidentalis, Brain Behav Evol. 75(2):138-148.
Gronenberg W, Couvillon M, (2010) Brain composition and olfactory learning in honey bees, Neurobiol Learn Mem, 93(3):435-443.
Riveros AJ, Gronenberg W (2009) Learning from learning and memory in bumblebees, Commun Integr Biol. 2(5):437-440.
Couvillon MJ, DeGrandi-Hoffman G, Gronenberg W ( 2009) Africanized honeybees are slower learners than their European counterparts, Naturwissenschaften,97(2):153-160.
Paulk AC, Dacks AM, Phillips-Portillo J, Fellous JM, Gronenberg W (2009) Visual processing in the central bee brain, J Neurosci. 29(32):9987-9999.
Snell-Rood EC, Papaj DR, Gronenberg W (2009) Brain size: a global or induced cost of learning? Brain Behav Evol.73(2):111-128.
Riveros AJ, Gronenberg W (2009) Olfactory learning and memory in the bumblebee Bombus occidentalis, Naturwissenschaften,96(7):851-856