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J. M. Wilson

Publications and source records attributed to J. M. Wilson.

3 recordsLinked to original sources

An axial view of a metamorphic core complex: Crustal structure of the Whipple and Chemehuevi Mountains, southeastern California

A 135‐km‐long, NW‐SE trending, seismic refraction/wide‐angle reflection profile provides a unique along‐strike view of the crustal structure of a belt of metamorphic core complexes in southeastern California: the Whipple, Chemehuevi, and Sacramento mountains metamorphic core complexes. Interpretation of the seismic data was done by two‐dimensional forward modeling of travel times and amplitudes. The final model consists of (1) a thin (< 1.5 km) veneer of upper plate and fractured lower plate rocks (velocities of 1.5–5.3 km s −1 ) overlying a fairly homogeneous basement with velocities of 6.0 km s −1 ; (2) a localized, high‐velocity (6.4 km s −1 ) body, situated directly beneath the Whipple Mountains; (3) a 6.3–6.4 km s −1 middle crust that is thickest beneath the core complexes; (4) a 6.65±0.15 km s −1 lower crust; (5) crustal thickness of 27 km with a deeper crustal root (3 km) beneath the Whipple Mountains metamorphic core complex; and (6) a P n velocity of 8.0±0.10 km s −1 . The crustal structure that underlies the belt of metamorphic core complexes provides new insights into the processes that control extension in the deep crust. Upper crustal velocities are higher beneath the Whipple Mountains (where velocities increase to 6.4 km s −1 at ∼5 km depth) than beneath the Chemehuevi and Sacramento mountains. In addition, midcrustal discontinuities rise 2–5 km beneath the Whipple complex compared to the other complexes. These observations support greater uplift and a slightly deeper midcrustal origin for the rocks now exposed in the core of the Whipple Mountains compared to rocks in the Chemehuevi and Sacramento mountains. Despite the enhanced uplift and extension in the Whipple Mountains, the crust is thicker here (30 km) than anywhere else along the Colorado River extensional corridor. This may be in part a relic of compressional and magmatic thickening during the Mesozoic. However, we suggest that inflation of the crust during Tertiary extension was the dominant mechanism. Both mantle‐derived magmatism and lateral ductile inflow in the crust are proposed.

Arizona, California

Ionoregulatory changes during metamorphosis and salinity exposure of juvenile sea lamprey (Petromyzon marinus L.)

Ammocoetes of the anadromous sea lamprey Petromyzon marinus L. spend many years in freshwater before metamorphosing and migrating to sea. Metamorphosis involves the radical transformation from a substrate-dwelling, filter feeder into a free-swimming, parasitic feeder. In the present work we examined osmoregulatory differences between ammocoetes and transformers (metamorphic juveniles), and the effects of salinity acclimation. We measured the expression of key ion-transporting proteins [Na+/K+-ATPase, vacuolar (V)-type H+-ATPase and carbonic anhydrase (CA)] as well as a number of relevant blood parameters (hematocrit, [Na+] and [Cl -]). In addition, immunofluorescence microscopy was used to identify and characterize the distributions of Na+/K+-ATPase, V-type H+-ATPase and CA immunoreactive cells in the gill. Ammocoetes did not survive in the experiments with salinities greater than 10???, whereas survival in high salinity (???25-35???) increased with increased degree of metamorphosis in transformers. Plasma [Na+] and [Cl -] of ammocoetes in freshwater was lower than transformers and increased markedly at 10???. In transformers, plasma ions increased only at high salinity (>25???). Branchial Na+/K+-ATPase levels were ??? tenfold higher in transformers compared to ammocoetes and salinity did not affect expression in either group. However, branchial H +-ATPase expression showed a negative correlation with salinity in both groups. Na+/K+-ATPase immunoreactivity was strongest in transformers and associated with clusters of cells in the interlamellar spaces. H+-ATPase (B subunit) immunoreactivity was localized to epithelial cells not expressing high Na+/K+-ATPase immunoreactivity and having a similar tissue distribution as carbonic anhydrase. The results indicate that branchial Na+/K+-ATPase and salinity tolerance increase in metamorphosing lampreys, and that branchial H+-ATPase is downregulated by salinity.

Journal of Experimental Biology