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Herrnberger, L.

Publications and source records attributed to Herrnberger, L..

2 recordsLinked to original sources

No decoy effect in bees: rewardless flowers do not increase bumblebees' preference for neighbouring flowers

Nectarless flowers are common among flowering plants, which often retain colour-changed, rewardless flowers instead of shedding them. Yet, how these flowers influence pollinators foraging choices within an inflorescence remains unclear. We hypothesised that rewardless flowers in an inflorescence may act as "decoys", causing the rewarding flowers in the inflorescence to be perceived as more valuable by contrast. Using artificial inflorescences, we presented individual bumblebees (Bombus terrestris) with a binary choice between two equally rewarding inflorescences, one of which included additional unrewarded, differently coloured flowers. We found that the presence of rewardless flowers did not increase bees preference for neighbouring flowers, nor did it affect their overall choice between inflorescences. However, bees quickly learned to avoid the unrewarded flowers, drastically reducing visits and probing within a few foraging bouts. We review research on decoy effects in bees, and find very little support for their presence. Our findings contribute to the growing body of evidence that rewardless flowers do not induce decoy effects in bees, and highlight the need for further research into the ecological role of nectarless flowers within floral patches. It may be time to abandon the search for classical decoy effects in pollinators.

animal behavior and cognition↗

The extracellular matrix protein fibronectin modulates metanephric kidney development

Complex interactions of the branching ureteric bud and surrounding mesenchymal cells during metanephric kidney development determine the final number of nephrons. Alterations that result in impaired nephron endowment predispose to arterial hypertension and chronic kidney disease. In the kidney, extracellular matrix (ECM) proteins are usually regarded as acellular scaffolds or as the common histological end-point of chronic kidney diseases. Only little is known about their physiological role in kidney development. The ECM protein fibronectin is expressed at early time points of kidney growth. Therefore, we were interested in the characterization of its expression and role in kidney development. In mouse, fibronectin was expressed during all stages of kidney development with significant changes over time. At embryonic day (E) 12.0 and E13.5 fibronectin lined the ureteric bud epithelium, which was less pronounced at E16.5 and then switched to a glomerular expression in the postnatal and adult kidneys. Similar results were obtained in human kidneys. Deletion of fibronectin at E13.5 in cultured metanephric mouse kidneys resulted in reduced kidney sizes, impaired branching morphogenesis and decreased glomerulogenesis. In line with these findings, fibronectin deletion led to reduced cell proliferation of the branching epithelial cells. Fibronectin colocalized with alpha8 integrin and fibronectin loss caused a reduction in alpha8 integrin-dependent formation of glial cell line-derived factor and expression of Wnt11, both of which are essentially involved in promoting ureteric bud branching. In conclusion, the ECM protein fibronectin acts as a regulator of metanephric kidney development and is a determinant of nephron number.

developmental biology↗