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Block course structure

Block structure (b). Perhaps the strongest of these alternatives is the block structure in which the time and content allotted to two courses is combined into one course (Fig. 4.5b). Either one instructor teaches an integrated course, or more [Pg.100]

Linked or merged structures (c). The linked or merged structure allows a disciplinary connection that is almost as strong as the block structure (Fig. 4.5c). In this structure, two instructors start the term teaching independently, but at some point, the two courses flow together and work in common. This is most effective when the cormnon work is associated with a design project or end-of-term problem that requires the integration of content from both courses. [Pg.101]

Simultaneous structure (0. Hie weakest linkage is found in the simultaneous structure (Fig. 4.5f). In this structure, two instructors teach two separate, parallel courses. Through good communication and cooperation, they point out, in teal time, how learning in one of the courses can influence that in the other. In addition, they individually create exercises that require knowledge and apphcation from both courses. [Pg.101]

Depending on pre-existing conditions and choices of organizing principle, integration plan and block structures, a concept for the structure of the integrated curriculum will have evolved. Below, four types of elements are discussed in relation [Pg.101]

Engineering core various innovative curricular structures to carry skills as a part of the regular curriculum [Pg.102]


The eigenvalue E like the eigenfunction xp will, of course, depend on the parameter c. In view of the 2 x 2 block-matrix structure of (96) we write... [Pg.70]

The nature of the association maintains a locally effective shielding of the sulfonate anions within the aggregate and preservation of the clustered structure. This suggests that for these block polymer structures, the energetics of maintaining hydrophobic association are more favorable than monomer dispersion due to ionic repulsion. This was further demonstrasted by the extreme salt sensitivity of these polymers to solution ionic strength. Small amounts of sodium chloride resulted in polymer precipitation and of course loss of viscosification. This precludes the use of these particular polymers for chemically enhanced oil recovery and indicates the need for nonionic functionality to provide water solubility. To further pursue this approach acrylamide based polymers were studied. [Pg.155]

Of course, there is no problem at all in principle. Structure is itself an electronic property, in that it must be determined by the Coulomb forces of the electrons (and nuclei) of the system and should be derivable from the Hamiltonian. The troublesome needle-inhaystack aspect of structure determination is often a nuisance here, but even if we are lucky enough to be faced with a choice between a few reasonable structures (as in the impurity problem), the fact is that the description of the cohesive forces of solids is a difficult and delicate business. Perhaps the stumbling-block of structure determination has been overemphasized here, but there does not seem to be a wide realization of the problem and its importance to future progress. [Pg.44]

Polynuclear complexes based on octahedral building blocks may be structurally not well defined because of stereogenic problems [8]. However, clever synthetic strategies have recently been devised to obtain chirally pure species [61-65]. Synthesis and, of course, photophysical and photochemical studies of stereochemically pure metal-based dendrimers are still in their infancy. [Pg.233]

It also seems likely that some mental disorders (perhaps major depressive disorder) in their present form will fail to show evidence of taxonicity, but definitional refinement would help elucidate underlying taxa (e.g., melancholia). Thus, taxometrics may be able to serve as an impetus and a guide for revising the diagnostic system. Of course, taxometric methods alone are not sufficient to tackle this task and should be used in conjunction with dimensional methods, such as exploratory factor analysis. Dimensions provide the building blocks for construction of taxa, and research on the structure of psychopathology should integrate dimensional and taxometric methods. [Pg.175]

The micellar structure depicted in Fig. 2 is of course only valid for simple AB diblock copolymers. The situation can be much more complex for micelles prepared from block copolymers with complex architectures, as will be discussed later. [Pg.88]

Of course, all these achievements imply to meet a strict and difficult requirement, i.e. to be able to control precisely and simultaneously, both the structural and molecular characteristics of the block polymers involved it is the role (maybe too often underestimated) of synthetic polymer chemistry, to meet these challenges. [Pg.308]

The principle of this simple combinatorial game is obvious by now it can be easily extended using other hydrocarbon building blocks. The three-membered ring, for example, can be enlarged and also be anchored to other positions of the allene element, of course, thus yielding ring structures such as 36-39. However, these will not be discussed comprehensively in this Chapter to keep its limits acceptable. Besides, cycloallenes (36) are dealt with separately in Chapter 6. [Pg.188]

There is another point about the thermodynamic stability of prebiotic compounds. This is the fact that a series of thermodynamically very stable molecules seem to have been ignored in the course of prebiotic molecular evolution as building blocks of living structures. Take sugars, for example six-membered rings have not been used for the construction of nucleic acids, where only o-ribose takes the stage. Furthermore, only two types of purine and only two of the pyrimidine bases have been utilized among the many possible nucleic acids. Actually one could make a... [Pg.50]

Fig. 8.7. Structure of the catalytic domain of the insulin receptor. The crystal structure of the tyrosine kinase domain of the insulin receptor (Hubbard et al., 1994) has a two-lobe structure that is very similar to the structure of the Ser/Thr-specific protein kinases. Structural elements of catalytic and regulatory importance are shown. The P loop mediates binding of the phosphate residue of ATP the catalytic loop contains a catalytically essential Asp and Asn residue, found in equivalent positions as conserved residues in many Ser/Thr-specific and Tyr-specific protein kinases. Access to the active center is blocked by a regulatory loop containing three Tyr residues (Tyrll58, Tyrll62 and Tyrll63). Tyrll62 undergoes autophosphorylation in the course of activation of the insulin receptor. MOLSKRIPT representation according to Kraulis, (1991). Fig. 8.7. Structure of the catalytic domain of the insulin receptor. The crystal structure of the tyrosine kinase domain of the insulin receptor (Hubbard et al., 1994) has a two-lobe structure that is very similar to the structure of the Ser/Thr-specific protein kinases. Structural elements of catalytic and regulatory importance are shown. The P loop mediates binding of the phosphate residue of ATP the catalytic loop contains a catalytically essential Asp and Asn residue, found in equivalent positions as conserved residues in many Ser/Thr-specific and Tyr-specific protein kinases. Access to the active center is blocked by a regulatory loop containing three Tyr residues (Tyrll58, Tyrll62 and Tyrll63). Tyrll62 undergoes autophosphorylation in the course of activation of the insulin receptor. MOLSKRIPT representation according to Kraulis, (1991).

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