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John N. Baldwin

Publications and source records attributed to John N. Baldwin.

5 recordsLinked to original sources

Diet of diamondback terrapins (Malaclemys terrapin) in subtropical mangrove habitats in South Florida

Unique among turtles as the only exclusively estuarine species, the diamondback terrapin’s (Malaclemys terrapin) life history predisposes it to impacts from humans both on land and in the near-shore environment. Terrapins are found in salt marshes and mangroves along the Atlantic and Gulf coasts from Massachusetts to Texas. Whereas previous dietary studies have elucidated terrapins’ role in temperate salt marsh food webs, food resources for terrapins inhabiting subtropical mangrove habitats have not been studied. We examined dietary resource use for diamondback terrapins in subtropical mangrove creek and island habitats within Everglades National Park, Florida, to determine foraging strategies of terrapins inhabiting south Florida (SF) mangrove systems. Fecal analysis revealed 6 categories of food items, with gastropods, crabs, and bivalves being the dominant food items. Multivariate analysis revealed differences in food sources based on habitat more so than by terrapin size class. Our results revealed that like their counterparts in temperate salt marshes, SF terrapins consume similar prey categories but with different species and abundances comprising each category.

Florida

Malaclemys terrapin rhizophorarum (mangrove diamond-backed terrapin)

MALACLEMYS TERRAPIN RHIZOPHORARUM (Mangrove Diamond-backed Terrapin). DIET. Malaclemys terrapin rhizophorarum, one of seven subspecies of M. terrapin, inhabits subtropical mangrove habitats in South Florida, USA. In temperate climates M. terrapin is largely carnivorous, feeding primarily on gastropods, bivalves, and decapod crustaceans (Tucker et. al. 1995. Herpetologica 51:167–181; Butler et. al. 2012. Chelon. Conserv. Biol. 11:124–128). In addition to its preferred prey, M. t. rhizophorarum has also been reported to consume barnacles, fish, and vegetation (Tucker et. al. 1995, op. cit.; Butler et. al. 2012, op. cit.; Tulipani 2013. Ph.D. Dissertation. The College of William and Mary, Williamsburg, Virginia. 224 pp.). Herein, we report observations regarding the diet of M. t. rhizophorarum from the southernmost extent of their range in the Florida Keys, USA.

Herpetological Review

The earthquake cycle in the San Francisco Bay region: A.D. 1600–2012

Stress changes produced by the 1906 San Francisco earthquake had a profound effect on the seismicity of the San Francisco Bay region (SFBR), dramatically reducing it in the twentieth century. Whether the SFBR is still within or has emerged from this seismic quiescence is an issue of debate with implications for earthquake mechanics and seismic hazards. Historically, the SFBR has not experienced one complete earthquake cycle (i.e., the accumulation of stress, its release primarily as coseismic slip during surface‐faulting earthquakes, its re‐accumulation in the interval following, and its subsequent rerelease). The historical record of earthquake occurrence in the SFBR appears to be complete at about M 5.5 back to 1850 ( Bakun, 1999 ). For large events, the record may be complete back to 1776, which represents about half a cycle. Paleoseismic data provide a more complete view of the most recent pre‐1906 SFBR earthquake cycle, extending it back to about 1600. Using these, we have developed estimates of magnitude and seismic moment for alternative sequences of surface‐faulting paleoearthquakes occurring between 1600 and 1776 on the region’s major faults. From these we calculate seismic moment and moment release rates for different time intervals between 1600 and 2012. These show the variability in moment release and suggest that, in the SFBR regional plate boundary, stress can be released on a single fault in great earthquakes such as that in 1906 and in multiple ruptures distributed on the regional plate boundary fault system on a decadal time scale.

California

A record of large earthquakes during the past two millennia on the southern Green Valley Fault, California

We document evidence for surface-rupturing earthquakes (events) at two trench sites on the southern Green Valley fault, California (SGVF). The 75-80-km long dextral SGVF creeps ~1-4 mm/yr. We identify stratigraphic horizons disrupted by upward-flowering shears and in-filled fissures unlikely to have formed from creep alone. The Mason Rd site exhibits four events from ~1013 CE to the Present. The Lopes Ranch site (LR, 12 km to the south) exhibits three events from 18 BCE to Present including the most recent event (MRE), 1610 ±52 yr CE (1σ) and a two-event interval (18 BCE-238 CE) isolated by a millennium of low deposition. Using Oxcal to model the timing of the 4-event earthquake sequence from radiocarbon data and the LR MRE yields a mean recurrence interval (RI or μ) of 199 ±82 yr (1σ) and ±35 yr (standard error of the mean), the first based on geologic data. The time since the most recent earthquake (open window since MRE) is 402 yr ±52 yr, well past μ~200 yr. The shape of the probability density function (pdf) of the average RI from Oxcal resembles a Brownian Passage Time (BPT) pdf (i.e., rather than normal) that permits rarer longer ruptures potentially involving the Berryessa and Hunting Creek sections of the northernmost GVF. The model coefficient of variation (cv, σ/μ) is 0.41, but a larger value (cv ~0.6) fits better when using BPT. A BPT pdf with μ of 250 yr and cv of 0.6 yields 30-yr rupture probabilities of 20-25% versus a Poisson probability of 11-17%.

California

Photomosaics and logs of trenches on the San Andreas Fault at Arano Flat near Watsonville, California

We present photomosaics and logs of the walls of trenches excavated for a paleoseismic study at Arano Flat, one of two sites along the San Andreas fault in the Santa Cruz Mountains on the Kelley-Thompson Ranch. At this location, the fault consists of a narrow zone along the northeast side of a low ridge adjacent to a possible sag pond and extends about 60-70 meters across a broad alluvial flat. This site was a part of Rancho Salsipuedes beginning in 1834 and was purchased by the present owner’s family in 1851.

California