The mechanisms of the evolution and development of the heart in metazoans are highlighted, starting with the evolutionary origin of the contractile cell, supposedly the precursor of cardiomyocytes.... Show moreThe mechanisms of the evolution and development of the heart in metazoans are highlighted, starting with the evolutionary origin of the contractile cell, supposedly the precursor of cardiomyocytes. The last eukaryotic common ancestor is likely a combination of several cellular organisms containing their specific metabolic pathways and genetic signaling networks. During evolution, these tool kits diversified. Shared parts of these conserved tool kits act in the development and functioning of pumping hearts and open or closed circulations in such diverse species as arthropods, mollusks, and chordates. The genetic tool kits became more complex by gene duplications, addition of epigenetic modifications, influence of environmental factors, incorporation of viral genomes, cardiac changes necessitated by air-breathing, and many others. We evaluate mechanisms involved in mollusks in the formation of three separate hearts and in arthropods in the formation of a tubular heart. A tubular heart is also present in embryonic stages of chordates, providing the septated four-chambered heart, in birds and mammals passing through stages with first and second heart fields. The four-chambered heart permits the formation of high-pressure systemic and low-pressure pulmonary circulation in birds and mammals, allowing for high metabolic rates and maintenance of body temperature. Crocodiles also have a (nearly) separated circulation, but their resting temperature conforms with the environment. We argue that endothermic ancestors lost the capacity to elevate their body temperature during evolution, resulting in ectothermic modern crocodilians. Finally, a clinically relevant paragraph reviews the occurrence of congenital cardiac malformations in humans as derailments of signaling pathways during embryonic development. Show less
Wiggers, J.M.R.; Ruijven, J. van; Schaffers, A.P.; Berendse, F.; Snoo, G.R. de 2014
Agricultural intensification in grasslands has led to the decline of meadow bird populations in The Netherlands in the last 60 years. Habitat for meadow bird chicks has declined in quality and... Show moreAgricultural intensification in grasslands has led to the decline of meadow bird populations in The Netherlands in the last 60 years. Habitat for meadow bird chicks has declined in quality and quantity, thereby reducing food availability. Agri-environment schemes (AES) to halt the decline in meadow bird numbers have thus far been insufficient. These AES are on the level of entire fields, but recent research suggests that margins of fields may be more suitable chick habitat than centres of fields. Therefore, it could be productive to specifically target grass field margins as part of meadow bird AES. Our study examined the differences in food availability for meadow bird families in different portions of a grass field. Invertebrates were sampled in different locations on the field and results were compared to known dietary preferences of four species of meadow bird chicks. We show strong differences in food availability within fields, depending on meadow bird species. The preferred prey species of chicks of Black-tailed Godwit Limosa limosa and Redshank Tringa totanuspredominantly occurred in field margins, whereas those of Oystercatcher Haematopus ostraleguschicks were found mostly in the main part of the field. The prey species of Northern LapwingVanellus vanellus chicks showed no clear pattern within fields. We conclude that food availability within a field differs spatially between meadow bird species. Particularly for Black-tailed Godwit and Redshank, grass field margins constitute an important part of the field. Therefore, specific management to further enhance food availability in these margins may constitute an important addition to the existing mosaic approach. Show less
