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      Flatworm mucus as the base of a food web

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          Abstract

          Background

          By altering their habitats, engineering species can improve their own fitness. However, the effect of this strategy on the fitness of coexisting species or on the structure of the respective food web is poorly understood. In this study, bacteria and bacterivorous nematodes with short ( Caenorhabditis elegans) and long ( Plectus acuminatus) life cycles were exposed to the mucus secreted by the freshwater flatworm Polycelis tenuis. The growth, reproduction, and feeding preferences of the nematodes in the presence/absence of the mucus were then determined. In addition, confocal laser scanning microscopy (CLSM) was used to examine the structural footprint of the mucus and the mucus colonization dynamics of bacteria and protozoans.

          Results

          Mucus exposure resulted in a greater reproductive output in P. acuminatus than in C. elegans. In a cafeteria experiment, both nematode species were attracted by bacteria-rich patches and were not deterred by mucus. CLSM showed that the flatworms spread a layer of polysaccharide-rich mucus ca. 15 µm thick from their tails. Subsequent colonization of the mucus by bacteria and protozoans resulted in an architecture that progressively resembled a complex biofilm. The presence of protozoans reduced nematode reproduction, presumably due to competition for their bacterial food supply.

          Conclusion

          Animal secretions such as mucus may have broader, community-level consequences and contribute to fueling microbial food webs.

          Electronic supplementary material

          The online version of this article (10.1186/s12898-019-0231-2) contains supplementary material, which is available to authorized users.

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          Most cited references21

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          Niche construction, biological evolution, and cultural change.

          We propose a conceptual model that maps the causal pathways relating biological evolution to cultural change. It builds on conventional evolutionary theory by placing emphasis on the capacity of organisms to modify sources of natural selection in their environment (niche construction) and by broadening the evolutionary dynamic to incorporate ontogenetic and cultural processes. In this model, phenotypes have a much more active role in evolution than generally conceived. This sheds light on hominid evolution, on the evolution of culture, and on altruism and cooperation. Culture amplifies the capacity of human beings to modify sources of natural selection in their environments to the point where that capacity raises some new questions about the processes of human adaptation.
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            Ecological drivers of the Ediacaran-Cambrian diversification of Metazoa

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              Life cycle and population growth rate of Caenorhabditis elegans studied by a new method

              Background The free-living nematode Caenorhabditis elegans is the predominant model organism in biological research, being used by a huge number of laboratories worldwide. Many researchers have evaluated life-history traits of C. elegans in investigations covering quite different aspects such as ecotoxicology, inbreeding depression and heterosis, dietary restriction/supplement, mutations, and ageing. Such traits include juvenile growth rates, age at sexual maturity, adult body size, age-specific fecundity/mortality, total reproduction, mean and maximum lifespan, and intrinsic population growth rates. However, we found that in life-cycle experiments care is needed regarding protocol design. Here, we test a recently developed method that overcomes some problems associated with traditional cultivation techniques. In this fast and yet precise approach, single individuals are maintained within hanging drops of semi-fluid culture medium, allowing the simultaneous investigation of various life-history traits at any desired degree of accuracy. Here, the life cycles of wild-type C. elegans strains N2 (Bristol, UK) and MY6 (Münster, Germany) were compared at 20°C with 5 × 109 Escherichia coli ml-1 as food source. Results High-resolution life tables and fecundity schedules of the two strains are presented. Though isolated 700 km and 60 years apart from each other, the two strains barely differed in life-cycle parameters. For strain N2 (n = 69), the intrinsic rate of natural increase (r md-1), calculated according to the Lotka equation, was 1.375, the net reproductive rate (R 0) 291, the mean generation time (T) 90 h, and the minimum generation time (T min) 73.0 h. The corresponding values for strain MY6 (n = 72) were r m = 1.460, R 0 = 289, T = 84 h, and T min = 67.3 h. Peak egg-laying rates in both strains exceeded 140 eggs d-1. Juvenile and early adulthood mortality was negligible. Strain N2 lived, on average, for 16.7 d, while strain MY6 died 2 days earlier; however, differences in survivorship curves were statistically non-significant. Conclusion We found no evidence that adaptation to the laboratory altered the life history traits of C. elegans strain N2. Our results, discussed in the light of earlier studies on C. elegans, demonstrate certain advantages of the hanging drop method in investigations of nematode life cycles. Assuming that its reproducibility is validated in further studies, the method will reduce the inter-laboratory variability of life-history estimates and may ultimately prove to be more convenient than the current standard methods used by C. elegans researchers.
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                Author and article information

                Contributors
                benjamin.wilden@uni-bielefeld.de
                nabil.majdi@uni-bielefeld.de
                ute.kuhlicke@ufz.de
                thomas.neu@ufz.de
                traunspurger@uni-bielefeld.de
                Journal
                BMC Ecol
                BMC Ecol
                BMC Ecology
                BioMed Central (London )
                1472-6785
                29 March 2019
                29 March 2019
                2019
                : 19
                : 15
                Affiliations
                [1 ]ISNI 0000 0001 0944 9128, GRID grid.7491.b, Department of Animal Ecology, , University of Bielefeld, ; Konsequenz 45, 33615 Bielefeld, Germany
                [2 ]ISNI 0000 0001 2353 1689, GRID grid.11417.32, EcoLab, UMR 5245, CNRS, INP, UPS, ENSAT, , Université de Toulouse, ; 118 route de Narbonne, 31062 Toulouse, France
                [3 ]ISNI 0000 0004 0492 3830, GRID grid.7492.8, Department River Ecology, , Helmholtz Centre of Environmental Research, ; Brückstr. 3a, 39114 Magdeburg, Germany
                Author information
                http://orcid.org/0000-0003-4334-0286
                Article
                231
                10.1186/s12898-019-0231-2
                6441204
                30925873
                2a47cd58-ba5f-4e60-9801-056d06682263
                © The Author(s) 2019

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

                History
                : 26 May 2018
                : 23 March 2019
                Categories
                Research Article
                Custom metadata
                © The Author(s) 2019

                Ecology
                ecological engineering,mucus structure,confocal microscopy,aquatic ecology,niche construction

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