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Nutrient and herbivore alterations cause uncoupled changes in producer diversity, biomass and ecosystem function, but not in overall multifunctionality.

Scientific reports

Alberti J, Cebrian J, Alvarez F, Escapa M, Esquius KS, Fanjul E, Sparks EL, Mortazavi B, Iribarne O.
PMID: 28572596
Sci Rep. 2017 Jun 01;7(1):2639. doi: 10.1038/s41598-017-02764-3.

Altered nutrient cycles and consumer populations are among the top anthropogenic influences on ecosystems. However, studies on the simultaneous impacts of human-driven environmental alterations on ecosystem functions, and the overall change in system multifunctionality are scarce. We used estuarine...

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Alberti J, Cebrian J, Alvarez F, et al. Nutrient and herbivore alterations cause uncoupled changes in producer diversity, biomass and ecosystem function, but not in overall multifunctionality. Sci Rep. 2017;7(1):2639doi: 10.1038/s41598-017-02764-3.
Alberti, J., Cebrian, J., Alvarez, F., Escapa, M., Esquius, K. S., Fanjul, E., Sparks, E. L., Mortazavi, B., & Iribarne, O. (2017). Nutrient and herbivore alterations cause uncoupled changes in producer diversity, biomass and ecosystem function, but not in overall multifunctionality. Scientific reports, 7(1), 2639. https://doi.org/10.1038/s41598-017-02764-3
Alberti, J, et al. "Nutrient and herbivore alterations cause uncoupled changes in producer diversity, biomass and ecosystem function, but not in overall multifunctionality." Scientific reports vol. 7,1 (2017): 2639. doi: https://doi.org/10.1038/s41598-017-02764-3
Alberti J, Cebrian J, Alvarez F, Escapa M, Esquius KS, Fanjul E, Sparks EL, Mortazavi B, Iribarne O. Nutrient and herbivore alterations cause uncoupled changes in producer diversity, biomass and ecosystem function, but not in overall multifunctionality. Sci Rep. 2017 Jun 01;7(1):2639. doi: 10.1038/s41598-017-02764-3. PMID: 28572596; PMCID: PMC5454014.
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Bis[mu-4-(ethylammoniomethyl)-3,5-dimethylpyrazolato-kappa2N1:N2]bis[(eta4-1,5-cyclooctadiene)rhodium(I)] dichloride dichloromethane methanol solvate.

Acta crystallographica. Section C, Crystal structure communications

Esquius G, Pons J, Yáñez R, Ros J, Solans X, Font-Bardia M.
PMID: 11828104
Acta Crystallogr C. 2002 Feb;58:m133-4. doi: 10.1107/s0108270101020017. Epub 2002 Jan 31.

In the title compound, [Rh(2)(C(8)H(15)N(3))(2)(C(8)H(12))(2)]Cl(2).CH(2)Cl(2).CH(3)OH, the dinuclear Rh(I) complex has C(2) symmetry and the two pyrazolato ligands act as mu-bridges. The coordination of each Rh(I) cation is completed by one cyclooctadiene (COD) ligand. It is shown that the average...

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Esquius G, Pons J, Yáñez R, et al. Bis[mu-4-(ethylammoniomethyl)-3,5-dimethylpyrazolato-kappa2N1:N2]bis[(eta4-1,5-cyclooctadiene)rhodium(I)] dichloride dichloromethane methanol solvate. Acta Crystallogr C. 2002;58:m133-4doi: 10.1107/s0108270101020017.
Esquius, G., Pons, J., Yáñez, R., Ros, J., Solans, X., & Font-Bardia, M. (2002). Bis[mu-4-(ethylammoniomethyl)-3,5-dimethylpyrazolato-kappa2N1:N2]bis[(eta4-1,5-cyclooctadiene)rhodium(I)] dichloride dichloromethane methanol solvate. Acta crystallographica. Section C, Crystal structure communications, 58m133-4. https://doi.org/10.1107/s0108270101020017
Esquius, Glòria, et al. "Bis[mu-4-(ethylammoniomethyl)-3,5-dimethylpyrazolato-kappa2N1:N2]bis[(eta4-1,5-cyclooctadiene)rhodium(I)] dichloride dichloromethane methanol solvate." Acta crystallographica. Section C, Crystal structure communications vol. 58 (2002): m133-4. doi: https://doi.org/10.1107/s0108270101020017
Esquius G, Pons J, Yáñez R, Ros J, Solans X, Font-Bardia M. Bis[mu-4-(ethylammoniomethyl)-3,5-dimethylpyrazolato-kappa2N1:N2]bis[(eta4-1,5-cyclooctadiene)rhodium(I)] dichloride dichloromethane methanol solvate. Acta Crystallogr C. 2002 Feb;58:m133-4. doi: 10.1107/s0108270101020017. Epub 2002 Jan 31. PMID: 11828104.
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Solvent Free Synthesis of PdZn/TiO.

Topics in catalysis

Bahruji H, Esquius JR, Bowker M, Hutchings G, Armstrong RD, Jones W.
PMID: 30930591
Top Catal. 2018;61(3):144-153. doi: 10.1007/s11244-018-0885-6. Epub 2018 Jan 12.

Catalytic upgrading of CO

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Bahruji H, Esquius JR, Bowker M, et al. Solvent Free Synthesis of PdZn/TiO. Top Catal. 2018;61(3):144-153doi: 10.1007/s11244-018-0885-6.
Bahruji, H., Esquius, J. R., Bowker, M., Hutchings, G., Armstrong, R. D., & Jones, W. (2018). Solvent Free Synthesis of PdZn/TiO. Topics in catalysis, 61(3), 144-153. https://doi.org/10.1007/s11244-018-0885-6
Bahruji, Hasliza, et al. "Solvent Free Synthesis of PdZn/TiO." Topics in catalysis vol. 61,3 (2018): 144-153. doi: https://doi.org/10.1007/s11244-018-0885-6
Bahruji H, Esquius JR, Bowker M, Hutchings G, Armstrong RD, Jones W. Solvent Free Synthesis of PdZn/TiO. Top Catal. 2018;61(3):144-153. doi: 10.1007/s11244-018-0885-6. Epub 2018 Jan 12. PMID: 30930591; PMCID: PMC6405179.
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