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5. Telecouplings in water management: Effects of long-distance water transfers, international tourists and international trade on local water resources and consumption

Author

Luetkemeier, R., Söller, L., and Huber, I.

Abstract

Water managers usually consider the hydrological boundaries as relevant entities in which water needs to be managed to fulfill ecological and societal demands. However, despite this recognition, challenges remain in ensuring water of good quality and quantity, which became particularly evident in recent drought years in Europe. Against this background, we consider long-distance effects – so-called telecouplings – as relevant processes that have an effect on local water resources and consumption patterns. In this study, we explore the effects of three distinct telecoupling flows: (i) long-distance water transfers, (ii) international tourists and (iii) international trade that carries virtual water volumes. We investigate the mechanisms of how telecoupling flows alter local water balances and consumption patterns in three case studies of Germany, Croatia and Spain. We make use of water consumption statistics, groundwater recharge estimates and trade statistics to quantify the telecoupling flows. The results suggest that telecouplings can have positive effects by balancing water-deficit and surplus areas as in the case of long-distance water transfers. However, negative consequences on water availability can occur by international tourists, who translocate their water consumption habits to dry regions and increase local water consumption at their destinations. In a similar manner, food consumption patterns impact on groundwater resources in regions of agricultural production that strongly rely on irrigation.We see the necessity to incorporate respective telecoupling effects into water management strategies by explicitly targeting certain entry points to adjust telecoupling flows, which likely goes beyond the hydrological boundaries that are usually considered as system boundaries., The 28th IUGG General Assembly (IUGG2023) (Berlin 2023)

Published
2023
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18. Abstracts, 50th Annual Meeting, Eastern Branch Entomological Society of America

Author

Abdel-Monem, A H, Cameron, E A, Mumma, R O, Ahmad, S, Andaloro, J T, Peters, T M, Alicandro, A J, Ba-Angood, S A, Barnes, J K, Bell, R A, Shapiro, M, Owens, C, Bellinger, R G, Dively, G P, Bode, W M, Boobar, L R, Granett, J, Bowers, M D, Brown, M W, Rutschky, C W, Caron, D M, Waller, G D, Chabora, P C, Smolin, S J, Coggin, D L, Crnjar, R M, Prokopy, R J, Dethier, V G, Daoust, R A, Gunner, H B, Mccully, J E, Dubois, N R, Fein, B L, Reissig, W H, Roelofs, W L, Fell, R D, Forgash, A J, Respicio, N C, Khoo, B K, Franklin, E R, Kunz, T H, Fryauff, D J, Sutherland, D J, Gagne, R J, Geden, C J, Stoffolano, J G, Gotwald, H W, Grant, S T, Grippo, R S, Huber, I, Hare, J D, Dodds, J A, Harrison, F P, Richardson, J C, Bean, R A, Qawiyy, O J, Hefetz, A, Batra, S W T, Helgesen, R G, Baxendale, F, Hendrickson, R M, Henry, C S, Hill, A S, Hislop, R G, Alves, N, Hofmaster, R N, Francis, J, Horsburgh, R L, Hower, A A, Jones, J C, Ruschell, R J, Jubb, G L, Obourn, T H, Petersen, D H, Kapin, M A, Keil, C B, Ramaswamy, S B, Kopelman, A, Kraft, S K, Denno, R F, Lautenschlager, R A, Podgwaite, J D, Rothenbacher, H, Lienk, S E, Chapman, P J, Lord, W D, Roth, R R, Mack, T P, Smilowitz, Z, Magnarelli, L A, Mague, D L, Streu, H T, Maier, C T, May, Michael L., Mccaffrey, J P, Mcclure, M S, Mellors, W K, Morales, J, Newhart, A T, Novak, M A, O'callaghan, D P, Gallagher, E M, Lanier, G N, Parrella, M P, Patterson, J W, Vannote, R L, Pollack, E H, Powell, P K, Robinson, W H, Rajotte, E G, Roberts, R B, Gupta, A P, Roberts, J E, Snider, M T, Salbert, P, Elliott, N, Schauff, M E, Schneider, J C, Schults, J C, Nothnagle, P J, Holmes, R T, Schultz, P B, Semtner, P J, Owens, C D, Whalon, M E, Martinka, C A, Nolan, E S, Smith, J H, Yendol, W G, Stephens, G R, Surles, W W, Ekins, W L, Turner, E C, Versoi, P L, Wallner, W E, Gregory, R A, Weseloh, R M, Bajusz, B A, Willson, H R, Wraight, S P, Singer, S, Jamnback, H, Zimmerman, R H, Morris, C D, and BioStor

Published
1978

21. Development, behaviour and sensory processing in Marshall–Smith syndrome and Malan syndrome: phenotype comparison in two related syndromes

Author

Mulder, P. A., primary, Balkom, I. D. C., additional, Landlust, A. M., additional, Priolo, M., additional, Menke, L. A., additional, Acero, I. H., additional, Alkuraya, F. S., additional, Arias, P., additional, Bernardini, L., additional, Bijlsma, E. K., additional, Cole, T., additional, Coubes, C., additional, Dapia, I., additional, Davies, S., additional, Di Donato, N., additional, Elcioglu, N. H., additional, Fahrner, J. A., additional, Foster, A., additional, González, N. G., additional, Huber, I., additional, Iascone, M., additional, Kaiser, A.‐S., additional, Kamath, A., additional, Kooblall, K., additional, Lapunzina, P., additional, Liebelt, J., additional, Lynch, S. A., additional, Maas, S. M., additional, Mammì, C., additional, Mathijssen, I. B., additional, McKee, S., additional, Mirzaa, G. M., additional, Montgomery, T., additional, Neubauer, D., additional, Neumann, T. E., additional, Pintomalli, L., additional, Pisanti, M. A., additional, Plomp, A. S., additional, Price, S., additional, Salter, C., additional, Santos‐Simarro, F., additional, Sarda, P., additional, Schanze, D., additional, Segovia, M., additional, Shaw‐Smith, C., additional, Smithson, S., additional, Suri, M., additional, Tatton‐Brown, K., additional, Tenorio, J., additional, Thakker, R. V., additional, Valdez, R. M., additional, Van Haeringen, A., additional, Van Hagen, J. M., additional, Zenker, M., additional, Zollino, M., additional, Dunn, W. W., additional, Piening, S., additional, and Hennekam, R. C., additional

Published
2020
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24. Development, behaviour and sensory processing in Marshall–Smith syndrome and Malan syndrome: phenotype comparison in two related syndromes

Author

Mulder, P. A., van Balkom, I. D. C., Landlust, A. M., Priolo, M., Menke, L. A., Acero, I. H., Alkuraya, F. S., Arias, P., Bernardini, L., Bijlsma, E. K., Cole, T., Coubes, C., Dapia, I., Davies, S., Di Donato, N., Elcioglu, N. H., Fahrner, J. A., Foster, A., Gonzalez, N. G., Huber, I., Iascone, M., Kaiser, A. -S., Kamath, A., Kooblall, K., Lapunzina, P., Liebelt, J., Lynch, S. A., Maas, S. M., Mammi, C., Mathijssen, I. B., Mckee, S., Mirzaa, G. M., Montgomery, T., Neubauer, D., Neumann, T. E., Pintomalli, L., Pisanti, M. A., Plomp, A. S., Price, S., Salter, C., Santos-Simarro, F., Sarda, P., Schanze, D., Segovia, M., Shaw-Smith, C., Smithson, S., Suri, M., Tatton-Brown, K., Tenorio, J., Thakker, R. V., Valdez, R. M., Van Haeringen, A., Van Hagen, J. M., Zenker, M., Zollino, Marcella, Dunn, W. W., Piening, S., Hennekam, R. C., Zollino M. (ORCID:0000-0003-4871-9519), Mulder, P. A., van Balkom, I. D. C., Landlust, A. M., Priolo, M., Menke, L. A., Acero, I. H., Alkuraya, F. S., Arias, P., Bernardini, L., Bijlsma, E. K., Cole, T., Coubes, C., Dapia, I., Davies, S., Di Donato, N., Elcioglu, N. H., Fahrner, J. A., Foster, A., Gonzalez, N. G., Huber, I., Iascone, M., Kaiser, A. -S., Kamath, A., Kooblall, K., Lapunzina, P., Liebelt, J., Lynch, S. A., Maas, S. M., Mammi, C., Mathijssen, I. B., Mckee, S., Mirzaa, G. M., Montgomery, T., Neubauer, D., Neumann, T. E., Pintomalli, L., Pisanti, M. A., Plomp, A. S., Price, S., Salter, C., Santos-Simarro, F., Sarda, P., Schanze, D., Segovia, M., Shaw-Smith, C., Smithson, S., Suri, M., Tatton-Brown, K., Tenorio, J., Thakker, R. V., Valdez, R. M., Van Haeringen, A., Van Hagen, J. M., Zenker, M., Zollino, Marcella, Dunn, W. W., Piening, S., Hennekam, R. C., and Zollino M. (ORCID:0000-0003-4871-9519)

Abstract

Background: Ultrarare Marshall–Smith and Malan syndromes, caused by changes of the gene nuclear factor I X (NFIX), are characterised by intellectual disability (ID) and behavioural problems, although questions remain. Here, development and behaviour are studied and compared in a cross-sectional study, and results are presented with genetic findings. Methods: Behavioural phenotypes are compared of eight individuals with Marshall-Smith syndrome (three male individuals) and seven with Malan syndrome (four male individuals). Long-term follow-up assessment of cognition and adaptive behaviour was possible in three individuals with Marshall–Smith syndrome. Results: Marshall–Smith syndrome individuals have more severe ID, less adaptive behaviour, more impaired speech and less reciprocal interaction compared with individuals with Malan syndrome. Sensory processing difficulties occur in both syndromes. Follow-up measurement of cognition and adaptive behaviour in Marshall–Smith syndrome shows different individual learning curves over time. Conclusions: Results show significant between and within syndrome variability. Different NFIX variants underlie distinct clinical phenotypes leading to separate entities. Cognitive, adaptive and sensory impairments are common in both syndromes and increase the risk of challenging behaviour. This study highlights the value of considering behaviour within developmental and environmental context. To improve quality of life, adaptations to environment and treatment are suggested to create a better person-environment fit.

Published
2020

34. Abstracts, 50th Annual Meeting, Eastern Branch Entomological Society of America

Author

Abdel-Monem, A. H., Cameron, E. A., Mumma, R. O., Ahmad, S., Andaloro, J. T., Peters, T. M., Alicandro, A. J., Ba-Angood, S. A., Barnes, J. K., Bell, R. A., Shapiro, M., Owens, C., Bellinger, R. G., Dively, G. P., Bode, W. M., Boobar, L. R., Granett, J., Bowers, M. D., Brown, M. W., Rutschky, C. W., Caron, D. M., Waller, G. D., Chabora, P. C., Smolin, S. J., Coggin, D. L., Crnjar, R. M., Prokopy, R. J., Dethier, V. G., Daoust, R. A., Gunner, H. B., Dively,, G. P., McCully, J. E., Dubois, N. R., Fein, B. L., Reissig, W. H., Roelofs, W. L., Fell, R. D., Forgash, A. J., Respicio, N. C., Khoo, B. K., Franklin, E. R., Kunz, T. H., Fryauff, D. J., Sutherland, D. J., Gagné, R. J., Geden, C. J., Stoffolano,, J. G., Gotwald,, H. W., Grant, S. T., Grippo, R. S., Huber, I., Hare, J. D., Dodds, J. A., Harrison, F. P., Richardson, J. C., Bean, R. A., Qawiyy, O. J., Hefetz, A., Batra, S. W. T., Helgesen, R. G., Baxendale, F., Hendrickson,, R. M., Henry, C. S., Hill, A. S., Hislop, R. G., Alves, N., Hofmaster, R. N., Francis, J., Horsburgh, R. L., Hower, A. A., Jones, J. C., Ruschell, R. J., Jubb,, G. L., Obourn, T. H., Petersen, D. H., Kapin, M. A., Keil, C. B., Ramaswamy, S. B., Kopelman, A., Kraft, S. K., Denno, R. F., Lautenschlager, R. A., Podgwaite, J. D., Rothenbacher, H., Lienk, S. E., Chapman, P. J., Lord, W. D., Roth, R. R., Mack, T. P., Smilowitz, Z., Magnarelli, L. A., Mague, D. L., Streu, H. T., Maier, C. T., May, M. L., McCaffrey, J. P., McClure, M. S., Mellors, W. K., Morales, J., Newhart, A. T., Novak, M. A., O'Callaghan, D. P., Gallagher, E. M., Lanier, G. N., Parrella, M. P., Patterson, J. W., Vannote, R. L., Pollack, E. H., Powell, P. K., Robinson, W. H., Rajotte, E. G., Roberts, R. B., Gupta, A. P., Roberts, J. E., Snider, M. T., Salbert, P., Elliott, N., Schauff, M. E., Schneider, J. C., Schults, J. C., Nothnagle, P. J., Holmes, R. T., Schultz, P. B., Semtner, P. J., Sr., J. E. Roberts,, Owens, C. D., Whalon, M. E., Martinka, C. A., Nolan, E. S., Smith, J. H., Yendol, W. G., Stephens, G. R., Surles, W. W., Ekins, W. L., Turner,, E. C., Versoi, P. L., Wallner, W. E., Gregory, R. A., Weseloh, R. M., Bajusz, B. A., Willson, H. R., Wraight, S. P., Singer, S., Jamnback, H., Zimmerman, R. H., and Morris, C. D.

Published
1978

37. Yeast artificial chromosome cloning of the Xq13.3-q21.31 region and fine mapping of a deletion associated with choroideremia and nonspecific mental retardation

Author

van der Maarel, SM, Scholten, IH, Maat-Kievit, JA, Huber, I, de Kok, YJ, de Wijs, I, van de Pol, TJ, van Bokhoven, H, den Dunnen, JT, and van Ommen, GJ

Abstract

Microscopically detectable deletions and X;autosome translocations have previously facilitated the construction of a high-resolution interval map of the Xq21 region. Here, we have generated three yeast artificial chromosome contigs spanning approximately 7 megabases of the Xq13.3-q21.31 region. In addition, a novel deletion associated with choroideremia and mental retardation was identified and mapped in detail. The proximal deletion endpoint was positioned between the loci DXS995 and DXS232, which enabled us to confirm the critical region for a locus involved in mental retardation. The distal deletion endpoint is situated in the Xq21.33 band, which allowed us to refine the order of several markers in this region.

Published
2016

40. Patents and literature: Immobilized Biocatalysts

Author

Linhardt, Robert J., Amotz S., Rugh S., Markussen E. K., Thomsen K., Bigwood M. P., Naples J. O., Blattler W. A., Lambert J. M., Senter P. D., Boross L. E., Szaj E., Kovacs K., Dar E., Ivony K. K., Seres G. E., Szanj E., Szejtli J. E., Bozzelli J. W., Cheng R. C., Calvo L. C., Campbell D. N., Schmidt J. C., Cannon J. J., Chibata I., Tosa T., Takamatsu S., Degelaen J., Loffet A., Durieux J. P., Freedman H. H., Gardner D. L., Hafner E. W., Jackson D. M., Hagerdal B. G. R., Mosbach K. H., Ho G. -H., Liao C. -C., Ikeda M., Sakamoto S., Suzuki K., Jao Y. -C., Good I. C., Jarvis A. P., Lim F., Karasawa Y., Takata Y., Kasahara Y., Suzuki H., Ashihara Y., Katz E., Benedicktus J. J., Knarr E. L., Scallet B. L., Keyes M. H., Vasan S., Kuu W. Y., Malloy T. P., DeFilippi L. J., Manecke G., Klussmann U., Metcalfe L. D., Frank D., Meyers W. E., Beck L. R., Miyashiro Y., Ogawa M., Yamazaki Y., Igarasi S., Miyata T., Namiki S., Nees S., Niiyama Y., Mori J., Sugahara K., Noll L. A., Pierce P. J., Pinnavaia T. J., Mortland M. M., Boyd S. A., Reischl A., Rembaum A., Yen R. C. K., Robertson J. S., LiPuma M. M., Gross S. E., Rohrbach R. P., Maliarik M. J., Roland J. F., Rosevear A., Lambe C. A., Sakata C., Imai H., Kiss J. E., Ivony J. E., Huber I. E., Boros L. E., Tennent D. L., Sharma B. P., Turkov E., Stamberg J. E., von Blucher H., de Ruiter E., Wolfe S., Westlake D., Jensen S., Wood L. L., Calton G. J., Yoshioka T., Teramoto K., and Shimamura M.

Published
1987
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