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uted to differences in the extent of troponin-T proteolysis in excised beef semitendinosus muscle from 2 to 10 days postmortem (Weaver et al. 2008). Using an in vitro model, in which myo brils with varying sarcomere lengths were digested with exogenous calpain, it was observed that sarcomere length in uenced the rate and extent of troponin-T degradation (Weaver et al. 2009). In both of these studies, less proteolysis was observed in samples with shorter sarcomeres. The limited protein degradation with shorter sarcomeres was hypothesized to be a function of limited substrate availability (Weaver et al. 2008, 2009), but more data is required to elucidate this mechanism. It is also unclear from these studies if the range in sarcomere lengths that resulted in proteolytic differences is indicative of the natural variation in sarcomere length that exists in muscles from commercially processed beef. Nevertheless, these studies indicate that besides having a direct effect on tenderness, large differences in sarcomere length may also impact the postmortem proteolysis responsible for the aging tenderization of meat.

Serializability in Replicated Databases To consider mutual consistency in a replicated database, we need to extend the local serializability de nition. In a replicated database, schedule S is globally serializable if and only if all local schedules are serializable and the order of commitment for two con icting transactions is the same at every site where the two transactions run. Applying these requirements to our example, we see that for con icting transactions T1 and T2, at the LA site the commitment order is T1 T2 but in NY, the commitment order is T2 T1. Since the two transactions do not commit in the same order across both sites, they leave the database copies in an inconsistent state. 5.2.4.3 Con ict Serializable Schedules The serializability concept we have discussed so far is known as con ict serializability, which was rst discussed in [Eswaran76]. Although it is true that con ict serializable schedules produce a consistent database, they are not the only schedules that do so. 5.2.4.4 View Serializable Schedules Consider schedule S = R1(X), W2(X), W1(X), W3(X). This schedule is not con ict serializable since it implies the PCOs T1 T2, T1 T3, T2 T1, and T2 T3, which cannot all be satis ed the total order graph is not acyclic. After a closer look, however, we notice that this schedule produces the same result as the following two schedules:

The above rule indicates when the closed neighbor set of v is covered by the one of u, vertex v can be removed from G if the EL of v is smaller than that of u ID is used to break a tie when el(v) = el(u) In Figure 204 (a), since N[v] N[u], node v is removed from G if el(v) < el(u) and node u is the only dominating node in the graph In Figure 204 (b), since N[v] = N[u], either v or u can be removed from G To ensure that one and only one node is removed, we pick the one with a smaller EL Rule 2b: Assume that u and w are two marked neighbors of marked vertex v in G The marker of v is changed to F if one of the following conditions holds: 1.

Illustrated TCP/IP by Matthew G. Naugle Wiley Computer Publishing, John Wiley & Sons, Inc. ISBN: 0471196568 Pub Date: 11/01/98

coordination in rowing. Paper presented at the 31st Australasian Experimental Psychology Conference, Dunedin, New Zealand. Staddon, J. E. R., & Hinson, J. M. (1983). Optimization: A result or mechanism Science, 221, 976 977. Starkes, J., Helsen, W., & Jack, R. (2001). Expert performance in sport and dance. In R. N. Singer, H. A. Hausenblas, & C. M. Janelle (Eds.), Handbook of sport psychology (2nd ed., pp. 174 201). New York: Wiley. Swinnen, S. (2002). Intermanual coordination: From behavioral principles to neural network interactions. Nature Reviews Neuroscience, 3, 348 359. Tayler, M. T. (2002). Bimanual coordination in catching behavior. In K. Davids, G. J. P. Savelsbergh, S. J. Bennett, & J. van der Kamp (Eds.), Interceptive actions in sport (pp. 242 258). London: Routledge, Taylor & Francis. Tayler, M. A., & Davids, K. (1997). Catching with both hands: An evaluation of neural cross-talk and coordinative structure models of bimanual coordination. Journal of Motor Behavior, 29, 254 262. Todd, J. T. (1981). Visual information about moving objects. Journal of Experimental Psychology: Human Perception, 7, 795 810. Tononi, G., Sporns, O., & Edelman, G. M. (1999). Measures of degeneracy and redundancy in biological networks. Proceedings of the National Academy of Science, 96, 3257 3262.