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Wulfila Gronenberg

Publications and source records attributed to Wulfila Gronenberg.

6 recordsLinked to original sources

Brain allometry in bumblebee and honey bee workers.

Within a particular animal taxon, larger bodied species generally have larger brains. Increased brain size usually correlates with increased behavioral repertoires and often with superior cognitive abilities. Bumblebees are eusocial insects that show pronounced size polymorphism among workers, whereas in honey bees size variation is much less pronounced. Recent studies suggest that within a given colony, large bumblebee workers are more efficient foragers and are better learners than their smaller sisters. Here we examine the allometric relationship between brain and body size of worker bumblebees and honey bees. We find that larger bees have larger brains and that most brain components show a similar size increase as the overall brain. One particular brain structure, the central body, is relatively smaller in large bumblebees compared to small bees. The same is true for the mushroom body lobes, whereas the mushroom body calyces, which receive sensory input, are not reduced in larger bumblebees or honey bees. Honey bees have relatively smaller brains, as well as smaller mushroom bodies, than bumblebee workers. We discuss why brain or mushroom body size does not necessarily correlate with the degree of a species' social organization.

Animals↗

Electrical potentials indicate stimulus expectancy in the brains of ants and bees.

In vertebrates, and in humans in particular, so-called 'omitted stimulus potentials' can be electrically recorded from the brain or scalp upon repeated stimulation with simple stimuli such as light flashes. While standard evoked potentials follow each stimulus in a series, 'omitted stimulus potentials' occur when an additional stimulus is expected after the end of a stimulus series. These potentials represent neuronal plasticity and are assumed to be involved in basic cognitive processes. We recorded electroretinograms from the eyes and visually evoked potentials from central brain areas of honey bees and ants, social insects to which cognitive abilities have been ascribed and whose rich-behavioral repertoires include navigation, learning and memory. We demonstrate that omitted stimulus potentials occur in these insects. Omitted stimulus potentials in bees and ants show similar temporal characteristics to those found in crayfish and vertebrates, suggesting that common mechanisms may underlie this form of short-term neuronal plasticity.

Animals↗

Mushroom body volumes and visual interneurons in ants: comparison between sexes and castes.

The mushroom bodies are brain centers involved in complex behaviors such as learning and orientation. Here we examine the organization of mushroom bodies in ants, focusing on visual input. We describe the structure of visual neurons and compare the volume of brain structures involved in visual processing, especially the optic lobes and parts of the mushroom bodies receiving visual input in males, winged females, and workers of carpenter ants (Camponotus). A relatively small number of neurons connect the medulla with the mushroom bodies, and these neurons have relatively large dendritic fields in the medulla, suggesting low spatial resolution in ants. These neurons terminate in different yet overlapping strata in the mushroom bodies' collar region. While males have larger optic lobes than workers, their collar region is smaller than in females. Male ants have an additional type of medulla-mushroom body neuron with dendrites probing the distal medulla. These neurons are absent in female and worker ants. Most mushroom body Kenyon cells that are postsynaptic to visual input neurons appear to integrate visual as well as antennal input. This is in contrast to honey bees, where visual input to the mushroom bodies is more prominent and where Kenyon cells are not known to combine visual and antennal input.

Animals↗

Segregation of visual input to the mushroom bodies in the honeybee (Apis mellifera).

Insect mushroom bodies are brain regions that receive multisensory input and are thought to play an important role in learning and memory. In most neopteran insects, the mushroom bodies receive direct olfactory input. In addition, the calyces of Hymenoptera receive substantial direct input from the optic lobes. We describe visual inputs to the calyces of the mushroom bodies of the honeybee Apis mellifera, the neurons' dendritic fields in the optic lobes, the medulla and lobula, and the organization of their terminals in the calyces. Medulla neurons terminate in the collar region of the calyx, where they segregate into five layers that receive alternating input from the dorsal or ventral medulla, respectively. A sixth, innermost layer of the collar receives input from lobula neurons. In the basal ring region of the calyx, medulla neuron terminals are restricted to a small, distal part. Lobula neurons are more prominent in the basal ring, where they terminate in its outer half. Although the collar and basal ring layers generally receive segregated input from both optic neuropils, some overlap occurs at the borders of the layers. At least three different types of mushroom body input neurons originate from the medulla: (a) neurons with narrow dendritic fields mainly restricted to the vicinity of the medulla's serpentine layer and found throughout the medulla; (b) neurons restricted to the ventral half of the medulla and featuring long columnar dendritic branches in the outer medulla; and (c) a group of neurons whose dendrites are restricted to the most ventral part of the medulla and whose axons form the anterior inferior optic tract. Most medulla neurons (groups a and b) send their axons via the anterior superior optic tract to the mushroom bodies. Neurons connecting the lobula with the mushroom bodies have their dendrites in a defined dorsal part of the lobula. Their axons form a third tract to the mushroom bodies, here referred to as the lobula tract. Our findings match the anatomy of intrinsic mushroom body neurons (Strausfeld, 2002) and together indicate that the mushroom bodies may be composed of many more functional subsystems than previously suggested.

Animals↗

Motor control of the mandible closer muscle in ants.

Despite their simple design, ant mandible movements cover a wide range of forces, velocities and amplitudes. The mandible is controlled by the mandible closer muscle, which is composed of two functionally distinct subpopulations of muscle fiber types: fast fibers (short sarcomeres) and slow ones (long sarcomeres). The entire muscle is controlled by 10-12 motor neurons, 4-5 of which exclusively supply fast muscle fibers. Slow muscle fibers comprise a posterior and an antero-lateral group, each of which is controlled by 1-2 motor neurons. In addition, 3-4 motor neurons control all muscle fibers together. Simultaneous recordings of muscle activity and mandible movement reveal that fast movements require rapid contractions of fast muscle fibers. Slow and subtle movements result from the activation of slow muscle fibers. Forceful movements are generated by simultaneous co-activation of all muscle fiber types. Retrograde tracing shows that most dendritic arborizations of the different sets of motor neurons share the same neuropil in the subesophageal ganglion. In addition, fast motor neurons and neurons supplying the lateral group of slow closer muscle fibers each invade specific parts of the neuropil that is not shared by the other motor neuron groups. Some bilateral overlap between the dendrites of left and right motor neurons exists, particularly in fast motor neurons. The results explain how a single muscle is able to control the different movement parameters required for the proper function of ant mandibles.

Journal Article↗

Reduction of brain volume correlates with behavioral changes in queen ants.

The behavior of reproductive female ants distinctly changes during the transition from virgin to mature, egg-laying queen. A winged female ant flies only once during her lifetime when she engages in the nuptial flight. Once she is mated she sheds her wings, excavates a nest and starts laying eggs, the basis for her future colony. We show for two species of harvester ants that this transition is accompanied by changes in the performance of behavioral tests: flying virgins are positively phototactic and prefer open areas, whereas young queens prefer the dark, avoid open areas and, given the opportunity, dig into the soil. These behavioral changes coincide with morphological changes in the brain. The brains of mature queens are significantly smaller than those of virgin females at the time of their mating flight. A disproportionately large shrinkage occurs in the medulla and other parts of the visual system during the early adult life of the queen. The brain reduction appears to be adaptive as mature queens show reduced behavioral repertoires and live in the dark. In contrast to virgin females, they do not rely on vision and might increase their fitness by reducing metabolically costly neural tissue.

Animals↗