Geology topics

John Fieberg

Publications and source records attributed to John Fieberg.

9 recordsLinked to original sources

USGS2022

Sandhill crane colt survival in Minnesota

Age-structured population models require reliable estimates of cohort-specific survival rates, yet vital rates of younger age classes are often difficult to estimate because of the logistical challenges of monitoring young animals. As part of a study of sandhill cranes Antigone canadensis in the zone of contact between breeding distributions of the Eastern Population and Midcontinent Population in Minnesota, we monitored first summer survival of 34 sandhill cranes (hereafter colts) by using very-high-frequency and global positioning system–global system for mobile communications transmitters. We estimated daily survival probabilities from 19 to 120 d posthatch by using a generalized linear model accounting for interval censoring, resulting in an estimated period survival rate of 0.52 (90% CI, 0.36–0.71) over summer (100 d). Estimated daily probabilities of survival increased as colts became older and fledged (at 70–75 d posthatch), when they presumably became less vulnerable to predation. Causes of mortality were mostly unknown aside from one case of a collision with a vehicle. There is a scarcity of published colt survival rate estimates for sandhill cranes, and what is available varies widely by study site. Region-specific sandhill crane colt survival rate estimates can inform future management efforts and inform population dynamics research and overall natural history knowledge of sandhill cranes.

Minnesota↗

USGS2020

Habitat use by tiger prey in Thailand’s Western Forest Complex: What will it take to fill a half-full tiger landscape?

Tiger populations are declining globally, and depletion of major ungulate prey is an important contributing factor. To better understand factors affecting prey distribution in Thailand’s Western Forest Complex (WEFCOM), we conducted sign surveys for gaur (Bos gaurus ), banteng ( Bos javanicus ), and sambar ( Rusa unicolor ) along 3517 1-km transects and used occupancy models to identify important covariates associated with habitat use by each species. Habitat use by both gaur and sambar was lowest in areas closest to human settlements, although sambar preferred lower slopes near streams whereas gaur preferred steeper slopes at higher elevations. Banteng were found in only one of 17 protected areas (Huai Kha Khaeng [HKK] Wildlife Sanctuary), where they used low elevations and low slopes. We used these modeled relationships to predict occurrence of gaur, sambar, and banteng across each square km of the 19,000 km 2 WEFCOM landscape, using > 60 % occupancy probability to define suitable habitat use for each species. Based on this criterion, gaur and sambar occupied 28 and 50 % of suitable habitat in WEFCOM, and banteng occupied 57 % of suitable habitat in HKK. We used our models to assess the effectiveness of two hypothetical conservation initiatives. First, we modeled the impact of decreasing human activities around nine villages in the core of WEFCOM, which increased predicted suitable habitat in WEFCOM to 68 and 75 % for guar and sambar. We also modeled the extent of potential banteng habitat that still remains in the other 16 protected areas. This could result in a 4-fold increase in banteng suitable habitat in WEFCOM. This is the first study to use occupancy surveys to determine where large prey species can be restored to support management to increase the distribution of tigers, and potentially fill a half-full tiger landscape.

Journal for Nature Conservation↗

USGS2019

Impact of prey occupancy and other ecological and anthropogenic factors on Tiger distribution in Thailand’s Western Forest Complex

Despite conservation efforts, large mammals such as tigers (Panthera tigris) and their main prey, gaur (Bos gaurus), banteng (Bos javanicus), and sambar (Rusa unicolor), are highly threatened and declining across their entire range. The only large viable source population of tigers in mainland Southeast Asia occurs in Thailand's Western Forest Complex (WEFCOM), an approximately 19,000 km 2 landscape of 17 contiguous protected areas. We used an occupancy modeling framework, which accounts for imperfect detection, to identify the factors that affect tiger distribution at the approximate scale of a female tiger's home range, 64 km 2 , and site use at a scale of 1-km 2 . At the larger scale, we estimated the proportion of sites at WEFCOM that were occupied by tigers; at the finer scale, we identified the key variables that influence site-use and developed a predictive distribution map. At both scales, we examined key anthropogenic and ecological factors that help explain tiger distribution and habitat use, including probabilities of gaur, banteng, and sambar occurrence from a companion study. Occupancy estimated at the 64-km 2 scale was primarily influenced by the combined presence of all three large prey species, and 37% or 5,858 km 2 of the landscape was predicted to be occupied by tigers. In contrast, site use estimated at the scale of 1 km 2 was most strongly influenced by the presence of sambar. By modeling occupancy while accounting for imperfect probability of detection, we established reliable benchmark data on the distribution of tigers in WEFCOM. This study also identified factors that limit tiger distributions; which managers can then target to expand tiger distribution and guide recovery elsewhere in Southeast Asia.

Ecology and Evolution↗

USGS2018

An historical overview and update of wolf-moose interactions in northeastern Minnesota

Wolf (Canis lupus) and moose (Alces americanus) populations in northeastern Minnesota, USA, have fluctuated for decades and, based on helicopter counts, moose numbers declined to a new low from 2006 to about 2012. Other steep declines were found in 1991 and 1998 during periods when moose counts were done with ®xed-wing aircraft; these declines also appeared to be real. Winter wolf numbers, monitored in part of the moose range, had been increasing since about 2002 to the highest population in decades in 2009. However, from 2009 to 2016, wolves decreased precipitously, and the moose-population decline leveled off from 2012 to 2017. Calf:population ratios from 1985 to 1997 and from 2005 to 2016 were inversely related to wolf numbers in the wolf-study area the previous winter both as wolves increased and decreased in abundance. Similarly, log annual growth rates of moose numbers were negatively correlated with counts of wolves in the prior year. Other factors such as nutrition and parasites, and possibly climate change, likely have been involved in the recent moose decline. However, wolves, as in other areas, appear to have contributed to the decline in the northeastern Minnesota moose population at least in part through predation on calves, supporting earlier reports. Published 2018. This article is a U.S. Government work and is in the public domain in the USA.

Minnesota↗

USGS2018

Factors affecting gray wolf (Canis lupus) encounter rate with elk (Cervus elaphus) in Yellowstone National Park

Despite encounter rates being a key component of kill rate, few studies of large carnivore predation have quantified encounter rates with prey, the factors that influence them, and the relationship between encounter rate and kill rate. The study’s primary motivation was to determine the relationship between prey density and encounter rate in understanding the mechanism behind the functional response. Elk (Cervus elaphus Linnaeus, 1758) population decline and variable weather in northern Yellowstone National Park provided an opportunity to examine how these factors influenced wolf (Canis lupus Linnaeus, 1758) encounter rates with elk. We explored how factors associated with wolf kill rate and encounter rate in other systems (season, elk density, elk group density, average elk group size, snow depth, wolf pack size, and territory size) influenced wolf–elk encounter rate in Yellowstone National Park. Elk density was the only factor significantly correlated with wolf–elk encounter rate, and we found a nonlinear density-dependent relationship that may be a mechanism for a functional response in this system. Encounter rate was correlated with number of elk killed during early winter but not late winter. Weak effects of snow depth and elk group size on encounter rate suggest that these factors influence kill rate via hunting success because kill rate is the product of hunting success and encounter rate.

Wyoming↗

USGS2015

Growth rates and variances of unexploited wolf populations in dynamic equilibria

Several states have begun harvesting gray wolves ( Canis lupus ), and these states and various European countries are closely monitoring their wolf populations. To provide appropriate perspective for determining unusual or extreme fluctuations in their managed wolf populations, we analyzed natural, long-term, wolf-population-density trajectories totaling 130 years of data from 3 areas: Isle Royale National Park in Lake Superior, Michigan, USA; the east-central Superior National Forest in northeastern Minnesota, USA; and Denali National Park, Alaska, USA. Ratios between minimum and maximum annual sizes for 2 mainland populations ( n  = 28 and 46 yr) varied from 2.5–2.8, whereas for Isle Royale ( n  = 56 yr), the ratio was 6.3. The interquartile range (25th percentile, 75th percentile) for annual growth rates, N t +1 / N t , was (0.88, 1.14), (0.92, 1.11), and (0.86, 1.12) for Denali, Superior National Forest, and Isle Royale respectively. We fit a density-independent model and a Ricker model to each time series, and in both cases we considered the potential for observation error. Mean growth rates from the density-independent model were close to 0 for all 3 populations, with 95% credible intervals including 0. We view the estimated model parameters, including those describing annual variability or process variance, as providing useful summaries of the trajectories of these populations. The estimates of these natural wolf population parameters can serve as benchmarks for comparison with those of recovering wolf populations. Because our study populations were all from circumscribed areas, fluctuations in them represent fluctuations in densities (i.e., changes in numbers are not confounded by changes in occupied area as would be the case with populations expanding their range, as are wolf populations in many states).

Alaska, Michigan, Minnesota↗

USGS2014

Re-evaluating the northeastern Minnesota moose decline and the role of wolves

We re-evaluated findings from Lenarz et al. (2009) that adult moose ( Alces alces ) survival in northeastern Minnesota was related to high January temperatures and that predation by wolves ( Canis lupus ) played a minor role. We found significant inverse relationships between annual wolf numbers in part of the moose range and various moose demographics from 2003 to 2013 that suggested a stronger role of wolves than heretofore believed. To re-evaluate the temperature findings, we conducted a simulation study, mimicking the approach taken by Lenarz et al. (2009), to explore the potential for concluding a significant relationship exists between temperature and survival, when no association exists. We found that the high R 2 s and low probabilities associated with the regression models in Lenarz et al. (2009) should be viewed cautiously in light of the large number of fitted models (m = 45) and few observations (n = 6 for each of 5 response variables).

Minnesota↗

USGS2012

Recent population trends of mountain goats in the Olympic Mountains, Washington

Mountain goats ( Oreamnos americanus ) were introduced in Washington's Olympic Mountains during the 1920s. The population subsequently increased in numbers and expanded in range, leading to concerns by the 1970s over the potential effects of non-native mountain goats on high-elevation plant communities in Olympic National Park. The National Park Service (NPS) transplanted mountain goats from the Olympic Mountains to other ranges between 1981 and 1989 as a means to manage overabundant populations, and began monitoring population trends of mountain goats in 1983. We estimated population abundance of mountain goats during 18–25 July 2011, the sixth survey of the time series, to assess current population status and responses of the population to past management. We surveyed 39 sample units, comprising 39% of the 59,615-ha survey area. We estimated a population of 344 ± 72 (90% confidence interval [CI]) mountain goats in the survey area. Retrospective analysis of the 2004 survey, accounting for differences in survey area boundaries and methods of estimating aerial detection biases, indicated that the population increased at an average annual rate of 4.9% since the last survey. That is the first population growth observed since the cessation of population control measures in 1990. We postulate that differences in population trends observed in western, eastern, and southern sections of the survey zone reflected, in part, a variable influence of climate change across the precipitation gradient in the Olympic Mountains.

Washington↗

USGS2010

Design and analysis of simple choice surveys for natural resource management

We used a simple yet powerful method for judging public support for management actions from randomized surveys. We asked respondents to rank choices (representing management regulations under consideration) according to their preference, and we then used discrete choice models to estimate probability of choosing among options (conditional on the set of options presented to respondents). Because choices may share similar unmodeled characteristics, the multinomial logit model, commonly applied to discrete choice data, may not be appropriate. We introduced the nested logit model, which offers a simple approach for incorporating correlation among choices. This forced choice survey approach provides a useful method of gathering public input; it is relatively easy to apply in practice, and the data are likely to be more informative than asking constituents to rate attractiveness of each option separately.

Journal of Wildlife Management↗