Scutellospora arenicola and Glomus trimurales: Two new species in the Endogonaceae
No abstract available.
Geology topics
Source-linked reports with geographic coverage including San Miguel Island.
No abstract available.
Coastal eolian sand ramps (5–130 m elevation) on the northern slope (windward) side of the small San Miguel Island (13 km in W-E length) range in age from late Pleistocene to modern time, though a major hiatus in sand-ramp growth occurred during the early Holocene marine transgression (16–9 ka). The Holocene sand ramps (1–5 m measured thicknesses) currently lack large dune forms, thereby representing deflated erosional remnants, locally covering thicker late Pleistocene sand-ramp deposits. The ramp sand was initially supplied from the adjacent island-shelf platform, extending about 20 km north of the present coastline. The sand-ramp deposits and interbedded loess soils were 14 C dated using 112 samples from 32 archaeological sites and other geologic sections. Latest Pleistocene sand ramps (66–18 ka) were derived from across-shelf eolian sand transport during marine low stands. Shoreward wave transport supplied remobilized late Pleistocene sand from the inner shelf to Holocene beaches, where dominant NW winds supplied sand to the sand ramps. The onset dates of the sand-ramp deposition in San Miguel are 7.2 ± 1.5 ka (sample n = 14). The internal strata dates in the vertically accreting sand ramps are 3.4 ± 1.7 ka ( n = 34). The sand ramps in San Miguel show wide-scale termination of sand supply in the latest Holocene time. The sand-ramp top dates or burial dates are 1.7 ± 0.9 ka ( n = 28). The latest Holocene sand ramps are truncated along most of the island's northern coastline, indicating recent losses of nearshore sand reserves to onshore, alongshore, and, possibly, offshore sand sinks. The truncated sand ramps in San Miguel Island and in other sand-depleted marine coastlines provide warnings about future beach erosion and/or shoreline retreat from accelerated sea-level rise accompanying predicted global warming.
Quaternary vertebrate fossils, most notably mammoth remains, are relatively common on the northern Channel Islands of California. Well-preserved cranial, dental, and appendicular elements of Mammuthus exilis (pygmy mammoth) and Mammuthus columbi (Columbian mammoth) have been recovered from hundreds of localities on the islands during the past half-century or more. Despite this paleontological wealth, the geologic context of the fossils is described in the published literature only briefly or not at all, which has hampered the interpretation of associated 14 C ages and reconstruction of past environmental conditions. We recently discovered a partial tusk, several large bones, and a tooth enamel plate (all likely mammoth) at two sites on the northwest flank of San Miguel Island, California. At both localities, we documented the stratigraphic context of the fossils, described the host sediments in detail, and collected charcoal and terrestrial gastropod shells for radiocarbon dating. The resulting 14 C ages indicate that the mammoths were present on San Miguel Island between ∼20 and 17 ka as well as between ∼14 and 13 ka (thousands of calibrated 14 C years before present), similar to other mammoth sites on San Miguel, Santa Cruz, and Santa Rosa Islands. In addition to documenting the geologic context and ages of the fossils, we present a series of protocols for documenting and reporting geologic and stratigraphic information at fossil sites on the California Channel Islands in general, and in Channel Islands National Park in particular, so that pertinent information is collected prior to excavation of vertebrate materials, thus maximizing their scientific value.
San Miguel Island is the westernmost of the California Channel Islands and one of the windiest areas on the west coast of North America. The majority of the island is covered by coastal sand dunes, which were stripped of vegetation and subsequently mobilized due to droughts and sheep ranching during the late 19th century and early 20th century. Since the removal of grazing animals, vegetation and biological soil crusts have once again stabilized many of the island's dunes. In this study, historical aerial photographs and field surveys were used to develop a chronosequence of the pattern of change in vegetation communities and biological soil crust levels of development (LOD) along a gradient of dune stabilization. Historical aerial photographs from 1929, 1954, 1977, and 2009 were georeferenced and used to delineate changes in vegetation canopy cover and active (unvegetated) dune extent among 5 historical periods (pre-1929, 1929–1954, 1954–1977, 1977–2009, and 2009–2011). During fieldwork, vegetation and biological soil crust communities were mapped along transects distributed throughout San Miguel Island's central dune field on land forms that had stabilized during the 5 time periods of interest. Analyses in a geographic information system (GIS) quantified the pattern of changes that vegetation and biological soil crust communities have exhibited on the San Miguel Island dunes over the past 80 years. Results revealed that a continuing increase in total vegetation cover and a complex pattern of change in vegetation communities have taken place on the San Miguel Island dunes since the removal of grazing animals. The highly specialized native vascular vegetation (sea rocket, dunedelion, beach-bur, and locoweed) are the pioneer stabilizers of the dunes. This pioneer community is replaced in later stages by communities that are dominated by native shrubs (coastal goldenbush, silver lupine, coyote-brush, and giant coreopsis), with apparently overlapping or cyclical succession pathways. Many of the dunes that have been stabilized the longest (since before 1929) are dominated by exotic grasses. Stands of biological soil crusts (cyanobacteria) are found only on dunes where vascular vegetation is already present. Biological soil crusts are not found on dunes exhibiting a closed vascular plant canopy, which may indicate that the role of soil crusts in dune stabilization on the island is transitory. Particle-size analyses of soil samples from the study area reveal that higher biological soil crust LOD is positively correlated with increasing fine grain content. The findings indicate that changes in vegetation communities may be the most rapid at earlier and later stages of dune stabilization and that regular monitoring of dunes may help to identify the interactions between vegetation and soil crusts, as well as the potential transitions between native and exotic plant communities.
The attendance patterns of California sea lions were studied during the non-breeding seasons from 1991 to 1994. Lactating females frequented the rookery to nurse their pups until weaning; most non-lactating females left the rookery for the season. Females spent over 70% of their time at sea except in 1993 when they spent 59% of their time at sea. The mean foraging trip length in the winter and spring ranged from 3.3 to 4.6 d; the mean nursing visit ranged from 1.2 to 1.4 d. The duration of foraging trips and nursing visits was variable over the season for individuals but no pattern of change was detected. Interannual and seasonal differences were not significant for time at sea, visits ashore, or foraging-trip duration before, during, or after the 1992-1993 El Nino event. Pups spent an average of 66.6% of their time ashore and up to three days away from the rookery during their mother's absence. Most females and pups stayed associated until April or May. The results suggest that seasonal movement of prey is more important in determining attendance patterns late in the lactation period than increasing energy demands of the pup.
Nests and nest sites of the San Miguel Island ( SMI ) Song Sparrow ( Melospiza melodia micronyx ) are described; nests are compared with those of 16 other races of Song Sparrows. Bush lupins ( Lupinus albifrons ), coyote brush ( Baccharis pilularis ) and golden bush ( Haplopappus venetus ) were the shrubs used most commonly as nest sites by Song Sparrows on SMI. As a result of its location, the nest was effectively concealed from gray foxes ( Urocyon littoralis ), the major predator of this sparrow. Nest and nest site also moderated the combined chilling effects of cool air temperatures and strong northwesterly winds on the eggs and nestlings. Even in the absence of these moderating effects of the nest site, the energetic cost of incubation, estimated at 41-53% of the sparrow's resting metabolic rate, was modest. Twenty-nine percent of the canopy above the nest was open and as much as 73% of the nest cup was in the sun at midday, a time when surface temperatures of foliage, nest and nestlings sometimes exceeded 40 C. Whereas this exposure did not apparently reduce fledging success, it may explain why the incidence of addled eggs was so high in this population of Song Sparrows compared to others. Significant differences existed among races of Song Sparrows in the size, porosity and insulation of the nest. In most cases, these differences were not related to the latitude of the races' nesting areas.
Patterns of growth (reviewed by Ricklefs 1968, 1969; O'Connor 1984) and the development of endothermy (reviewed by Dawson and Hudson 1970, Dunn 1975, Hill and Beaver 1982) have been well-studied in altricial wild birds, especially passerines. But few studies compare grown and thermogenesis in separate populations of the same species. Results of such studies with emberizids varied among species. King and Hubbard (1981), for example, found that nestlings from subarctic, subalpine, and low-altitude montane populations of White-crowned Sparrows ( Zonotrichia leucophrys gambelii ) grew at similar rates. In contrast, Rogers (1985) reported that the growth rates of nestlings in different populations of Savannah Sparrows ( Passerculus sandwichensis ) varied in response to the different environmental constraints of the localities in which they were reared. Nice (1937) and Smith et al. (1982) documented patterns of nestling growth in mainland (Ohio) and insular (Mandarte Island, British Columbia, Canada) populations of Song Sparrows ( Melospiza melodia ), respectively, and found that they were similar to those reported for most other passerines by Ricklefs (1968, 1969) and O'Connor (1984). In 1985-1986, we had the opportunity to examine the growth of nestlings from a third race of Song Sparrows, M. m. micronyx , which is endemic to San Miguel Island near Santa Barbara, California. We also studied the development of endothermy in these young birds, a process not hitherto described for nestling Song Sparrows. We report both in this paper.
The water-vapor pressure (P N ) in nests of the San Miguel Island race of Song Sparrows ( Melospiza melodia micronyx ) averaged 16 torr, but varied considerable between nests and within individual nests during successive days of incubation. Large daily fluctuations occurred throughout the incubation period and did not parallel concurrent changes in ambien vapor pressure (P 1 ). Daily rates of water loss from nest eggs (M H 2 O ) averaged 28 mg day -1 , but also varied considerable within and between nests and did not correlate with changes in P 1 . M H 2 O increased 6-33% after the third day of incubation. P N was significantly higher and M H 2 O significantly lower in nests located in sheltered gullies than in nests from a windswept slope. These data suggest that Song Sparrows do not regulate P N to achieve hatching success.