58
G. Benckiser
212. Shestakov, S.V., Karbysheva, E.A.: The role of viruses in the evolution of cyanobacteria. Biol.
Bull. Rev. 5, 527–537 (2015). https://doi.org/10.1134/s2079086415060079
213. Sikorski, J.: The prokaryotic biology of soil. Soil Organ. 87, 1–28 (2015)
214. Silpe, J.E., Bassler, B.L.: A host-produced quorum-sensing autoinducer controls a phage
lysis-lysogeny decision. Cell 176, 268–280 (2019). https://doi.org/10.1016/j.cell.2018.10.059
215. Sime-Ngando, T.: Environmental bacteriophages: viruses of microbes in aquatic ecosystems.
Front. Microbiol. (2014). https://doi.org/10.3389/fmicb.2014.00355
216. Simpson, A., Slamovits, C., Archibald, J.M.: Protist diversity and eukaryote phylogeny. In:
Archibald, J., Simpson, A., Slamovits, C. (eds.) Handbook of the Protists. Springer, Cham
(2017). https://doi.org/10.1007/978-3-319-28149-0_45
217. Sochorec, M., Jandák, J., Raus, J., Kvasnovský, M., Hejduk, S., Knot, P.: Influence of different
grassland management on water infiltration and soil physical properties Bulgarian. J. Agricult.
Sci. 21, 573–578 (2015)
218. Song, W., Xiaojuan, T., Jinsong, Z., Meng, P., Jun, L.: Autotrophic and heterotrophic components of soil respiration caused by rhizosphere priming effects in a plantation. Plant. Soil.
Environ. 63, 295–299 (2017). https://doi.org/10.17221/233/2017-PSE
219. Srinivasiah, S., Lovett, J., Polson, S., Bhavsar, S., Ghosh, D., Roy, K., Fuhrmann, J.J., Radosevich, M., Wommack, K.: Direct assessment of viral diversity in soils by random PCR amplification of polymorphic DNA. Appl. Environ. Microbiol. 79, 5450–5457 (2013). https://doi.
org/10.1128/AEM.00268-13
220. Staege, M.S., Emmer, A.: Endogenous viral elements—links between autoimmunity and
cancer? Front. Microbiol. (2018). https://doi.org/10 3389/fmicb.201801371
221. Stahl, A., Vollrath, P., Samans, B., Frisch, M., Wittkop, B., Snowdon, R.J.: Effect of breeding
on nitrogen use efficiency-associated traits in oilseed rape. J. Exp. Bot. 70, 1969–1986 (2019).
https://doi.org/10.1093/jxb/erz044 https://doi.org/10.1080/1343943X.2019.1617638
222. Steen, A.D., Crits-Christoph, A., Carini, P., DeAngelis, K.M., Fierer, N., Lloyd, K.G.,
Cameron Thrash, J.: High proportions of bacteria and archaea across most biomes remain
uncultured. ISME J. (2019). https://doi.org/10.1038/s41396-019-0484-y
223. Steidinger, B.S., Crowther, T.W., Liang, J., Van Nuland, M.E., Werner, G.D.A.., Reich, P.B.,
Nabuurs, G., de-Miguel, S., Zhou, M., Picard, N., Herault, B., Zhao, X., Zhang, C., Routh, D.,
Peay, K.G.: Climatic controls of decomposition drive the global biogeography of forest-tree
symbioses. Nature 569, 404–408 (2019). https://doi.org/10.1038/s41586-019-1128-0
224. Stewart, F.M., Levin, B.R.: The population biology of bacterial viruses: why be temperate.
Theor. Popul. Biol. 26, 93–117 (1984)
225. Stewart, P.S., Franklin, M.J.: Physiological heterogeneity in biofilms. Nat. Rev. Microbiol. 6,
99–210 (2008). https://doi.org/10.1038/nrmicro1838
226. Strous, M., Pelletier, E., Mangenot, S., Rattei, T., Lehner, A., Taylor, M., Horn, M., Daims,
H., Bartol-Mavel, D., Wincker, P., Barbe, V., Fonknechten, N., Vallenet, D., Segurens, B.,
Schenowitz-Truong, C., Médigue, C., Collingro, A., Snel, B., Dutilh, B.E., Op den Camp,
H.J.M., van der Drift, C., Cirpus, I., van de Pas-Schoonen, K.T., Harhangi, H.R., van Niftrik,
L., Schmid, M., Keltjens, J., van de Vossenberg, J., Kartal, B., Meier, H., Dj, Frishman,
Huynen, M.A., Mewes, H.-W., Weissenbach, J., Jetten, M.S.M., Wagner, M., Le Paslier, D.:
Deciphering the evolution and metabolism of an anammox bacterium from a community
genome. Nature 440, 790–794 (2006). https://doi.org/10.1038/nature04647
227. Tebbe, C.C., Schloter, M.: Discerning the diversity of soil prokaryotes (bacteriaand archaea)
and their impact on agriculture. In: Benckiser, G., Schnell, S. (eds.) Biodiversity in Agricultural
Production Systems, pp. 81–100. Taylor and Francis, Boca Raton pp (2007)
228. Tennant, P., Fermin, G., Foster, J.E. (eds.): Viruses: Molecular Biology, Host Interactions,
and Applications to Biotechnology, p. 224. Academic Press, London (2018)
229. Thomas, R., Berdjeb, L., Sime-Ngando, T., Jacquet, S.: Viral abundance, production, decay
rates and life strategies (lysogeny versus lysis) in Lake Bourget (France). Envron. Microbiol.
13, 616–630 (2011). https://doi.org/10.1111/j.1462-2920.2010.02364.x
230. Thompson, L.R., Zeng, Q., Kelly, L., et al.: Phage auxiliary metabolic genes and the redirection
of cyanobacterial host carbon metabolism. PNAS 108, 757–764 (2011). https://doi.org/10.
1073/pnas.110216410810
G. Benckiser
212. Shestakov, S.V., Karbysheva, E.A.: The role of viruses in the evolution of cyanobacteria. Biol.
Bull. Rev. 5, 527–537 (2015). https://doi.org/10.1134/s2079086415060079
213. Sikorski, J.: The prokaryotic biology of soil. Soil Organ. 87, 1–28 (2015)
214. Silpe, J.E., Bassler, B.L.: A host-produced quorum-sensing autoinducer controls a phage
lysis-lysogeny decision. Cell 176, 268–280 (2019). https://doi.org/10.1016/j.cell.2018.10.059
215. Sime-Ngando, T.: Environmental bacteriophages: viruses of microbes in aquatic ecosystems.
Front. Microbiol. (2014). https://doi.org/10.3389/fmicb.2014.00355
216. Simpson, A., Slamovits, C., Archibald, J.M.: Protist diversity and eukaryote phylogeny. In:
Archibald, J., Simpson, A., Slamovits, C. (eds.) Handbook of the Protists. Springer, Cham
(2017). https://doi.org/10.1007/978-3-319-28149-0_45
217. Sochorec, M., Jandák, J., Raus, J., Kvasnovský, M., Hejduk, S., Knot, P.: Influence of different
grassland management on water infiltration and soil physical properties Bulgarian. J. Agricult.
Sci. 21, 573–578 (2015)
218. Song, W., Xiaojuan, T., Jinsong, Z., Meng, P., Jun, L.: Autotrophic and heterotrophic components of soil respiration caused by rhizosphere priming effects in a plantation. Plant. Soil.
Environ. 63, 295–299 (2017). https://doi.org/10.17221/233/2017-PSE
219. Srinivasiah, S., Lovett, J., Polson, S., Bhavsar, S., Ghosh, D., Roy, K., Fuhrmann, J.J., Radosevich, M., Wommack, K.: Direct assessment of viral diversity in soils by random PCR amplification of polymorphic DNA. Appl. Environ. Microbiol. 79, 5450–5457 (2013). https://doi.
org/10.1128/AEM.00268-13
220. Staege, M.S., Emmer, A.: Endogenous viral elements—links between autoimmunity and
cancer? Front. Microbiol. (2018). https://doi.org/10 3389/fmicb.201801371
221. Stahl, A., Vollrath, P., Samans, B., Frisch, M., Wittkop, B., Snowdon, R.J.: Effect of breeding
on nitrogen use efficiency-associated traits in oilseed rape. J. Exp. Bot. 70, 1969–1986 (2019).
https://doi.org/10.1093/jxb/erz044 https://doi.org/10.1080/1343943X.2019.1617638
222. Steen, A.D., Crits-Christoph, A., Carini, P., DeAngelis, K.M., Fierer, N., Lloyd, K.G.,
Cameron Thrash, J.: High proportions of bacteria and archaea across most biomes remain
uncultured. ISME J. (2019). https://doi.org/10.1038/s41396-019-0484-y
223. Steidinger, B.S., Crowther, T.W., Liang, J., Van Nuland, M.E., Werner, G.D.A.., Reich, P.B.,
Nabuurs, G., de-Miguel, S., Zhou, M., Picard, N., Herault, B., Zhao, X., Zhang, C., Routh, D.,
Peay, K.G.: Climatic controls of decomposition drive the global biogeography of forest-tree
symbioses. Nature 569, 404–408 (2019). https://doi.org/10.1038/s41586-019-1128-0
224. Stewart, F.M., Levin, B.R.: The population biology of bacterial viruses: why be temperate.
Theor. Popul. Biol. 26, 93–117 (1984)
225. Stewart, P.S., Franklin, M.J.: Physiological heterogeneity in biofilms. Nat. Rev. Microbiol. 6,
99–210 (2008). https://doi.org/10.1038/nrmicro1838
226. Strous, M., Pelletier, E., Mangenot, S., Rattei, T., Lehner, A., Taylor, M., Horn, M., Daims,
H., Bartol-Mavel, D., Wincker, P., Barbe, V., Fonknechten, N., Vallenet, D., Segurens, B.,
Schenowitz-Truong, C., Médigue, C., Collingro, A., Snel, B., Dutilh, B.E., Op den Camp,
H.J.M., van der Drift, C., Cirpus, I., van de Pas-Schoonen, K.T., Harhangi, H.R., van Niftrik,
L., Schmid, M., Keltjens, J., van de Vossenberg, J., Kartal, B., Meier, H., Dj, Frishman,
Huynen, M.A., Mewes, H.-W., Weissenbach, J., Jetten, M.S.M., Wagner, M., Le Paslier, D.:
Deciphering the evolution and metabolism of an anammox bacterium from a community
genome. Nature 440, 790–794 (2006). https://doi.org/10.1038/nature04647
227. Tebbe, C.C., Schloter, M.: Discerning the diversity of soil prokaryotes (bacteriaand archaea)
and their impact on agriculture. In: Benckiser, G., Schnell, S. (eds.) Biodiversity in Agricultural
Production Systems, pp. 81–100. Taylor and Francis, Boca Raton pp (2007)
228. Tennant, P., Fermin, G., Foster, J.E. (eds.): Viruses: Molecular Biology, Host Interactions,
and Applications to Biotechnology, p. 224. Academic Press, London (2018)
229. Thomas, R., Berdjeb, L., Sime-Ngando, T., Jacquet, S.: Viral abundance, production, decay
rates and life strategies (lysogeny versus lysis) in Lake Bourget (France). Envron. Microbiol.
13, 616–630 (2011). https://doi.org/10.1111/j.1462-2920.2010.02364.x
230. Thompson, L.R., Zeng, Q., Kelly, L., et al.: Phage auxiliary metabolic genes and the redirection
of cyanobacterial host carbon metabolism. PNAS 108, 757–764 (2011). https://doi.org/10.
1073/pnas.110216410810
