Sediment Distribution Around Glacially Abraded Bedrock Landforms (Whalebacks) at Lago Tranquilo, Chile

Whalebacks are convex landforms created by the smoothing of bedrock by glacial processes. Their formation is attributed to glacial abrasion either by bodies of subglacial sediment sliding over bedrock or by individual clasts contained within ice. This paper reports field measurements of sediment depth around two whaleback landforms in order to investigate the relationship between glacigenic deposits and whaleback formation. The study site, at Lago Tranquilo in Chilean Patagonia, is situated within the Last Glacial Maximum (LGM) ice limits. The two whalebacks are separated by intervening depressions in which sediment depths are generally 0.2 to 0.3 m. Two facies occur on and around the whalebacks. These facies are: (1) angular gravel found only on the surface of the whalebacks, interpreted as bedrock fracturing in response to unloading of the rock following pressure release after ice recession, and (2) sandy boulder‐gravel in the sediment‐filled depressions between the two whalebacks, interpreted as an ice‐marginal deposit, with a mixture of sediment types including basal glacial and glaciofluvial sediment. Since the whalebacks have heavily abraded and striated surfaces but are surrounded by only a patchy and discontinuous layer of sediment, the implication is that surface abrasion of the whalebacks was achieved primarily by clasts entrained in basal ice, not by subglacial till sliding.     

Vegetation changes in the Jornada Basin from 1858 to 1998

Notes made by land surveyors in 1858 were utilized to estimate cover of grasses and shrubs on the Jornada Experimental Range (JER) and the Chihuahuan Desert Range Research Center (CDRRC) in the northern Chihuahuan Desert in southern New Mexico, USA. Portions of these areas have been previously assessed for historical vegetation dynamics but the entire 84,271 ha assessed in the 19th century has not been examined in total. In 1858, fair to very good grass cover occurred on 98% and 67% of the JER and CDRRC, respectively. Shrubs were present throughout both properties but 45% of the JER and 18% of the CDRRC were shrub free. Reconnaissance surveys, made to determine carrying capacity for livestock were made in 1915–1916 and 1928–1929 on the JER and in 1938 on the CDRRC, show that shrubs had made large increases in area occupied at the time of the surveys. Vegetation type maps were made of both properties in 1998. Mesquite (Prosopis glandulosa) was the primary dominant on 59% of the JER in 1998 and creosotebush (Larrea tridentata) was the primary dominant on 27% of the area. On the CDRRC mesquite and creosotebush were primary dominants on 37% and 46% of the area, respectively. Grass cover has decreased greatly with the increase in shrubs and only shrub control efforts have maintained the once abundant black grama (Bouteloua eriopoda) as a primary dominant on 1% or less of the area on both properties.     

Climatic response of thick leaf spruce (Picea crassifolia) tree-ring width at different elevations over Qilian Mountains, northwestern China

Tree-ring cores of thick leaf spruce (Picea crassifolia) taken from four sites at different elevations, in the middle of the Qilian Mountains, in the arid and semi-arid region of northwestern China, were used to develop four tree-ring width chronologies using standard dendrochronological methods. Results indicate that with increasing altitude the chronologies’ year-to-year variations decreased. Hence, the sensitivity of the tree-ring chronologies to climate decreases with altitude. Further analysis showed that the significant limiting factor on tree growth is spring precipitation. Measurements of stomata density and leaf dry weight suggest the species’ ecological adaptation strategy changes with elevation. At high elevation the metabolic rate of thick leaf spruce decreases, thus showing the effect of the climate.