Are latrine sites an accurate predictor of seasonal habitat selection by river otters (<Emphasis Type="Italic">Lontra canadensis</Emphasis>) in freshwater systems?

Temporal variation in the availability of food resources is a likely driving factor influencing the distribution and habitat use of river otters (Lontra canadensis). Although latrine sites are commonly used to determine habitat selection, it is unclear if latrine sites are an accurate predictor or even a useful indicator of the seasonal habitat use and distribution of river otters. We apply resource selection functions (RSF) to both latrine and telemetry locations to investigate whether latrine sites identified along lake shorelines during the ice-free season are appropriate predictors of otter habitat selection along shorelines during the ice-free and ice-cover seasons in central British Columbia, Canada. We found that the top models describing otter latrine sites and telemetry locations during the ice-free season were similar. The top RSF models and associated coefficients for the ice-cover season differed, however, with otter presence being positively influenced by shallower water depths. For the spatial extrapolation of averaged RSF coefficients, we found that 21.4 and 69.3 % of predicted latrine habitat along lake shorelines overlapped with ice-cover and ice-free habitat generated from telemetry locations, respectively. The location and activity at latrine sites appear to be a useful method for monitoring otter distribution and habitat use during the ice-free, but not during the ice-cover season. The results of our RSF analyses as well as home range measurements of otters in our study area suggest that cold temperatures and ice cover may be a limiting factor for the distribution of otter populations at northern latitudes.     

Unveiling the Limitations of Scat Surveys to Monitor Social Species: A Case Study on River Otters

Abstract: We examined the relationship between the production of sites with feces (i.e., latrines) and river otter (Lontra canadensis) abundance to determine whether scat surveys were adequate for monitoring relative population size for species leaving activity signs in a clumped distribution on the landscape. We conducted winter riparian transects to simultaneously monitor otter abundance via snow tracks and latrine sites along the rivers of Kouchibouguac National Park and surrounding area in New Brunswick, Canada. Our data showed that latrine abundance poorly reflected otter abundance for given stretches of rivers because the relationship was nonlinear and reached a plateau. The number of latrine sites was not related to the time period since last snowfall, which indicated that otters repetitively defecated at the same sites. Individual otters and groups did not produce activity signs over larger distances as a function of time, which indicated that they tend to stay in their home ranges in winter. We discuss why scat survey protocols based on determining presence—absence of a species at predetermined search sites may poorly reflect population size, as well as population fluctuations in time. Caution is advised when interpreting data from such surveys for species for which feces or other activity signs surveyed play a role in intraspecific communication and tend to be in a clumped distribution on the landscape.     

Why do river otters scent-mark? An experimental test of several hypotheses

We tested several alternative hypotheses about the function of scent marking by the North American river otter, Lontra canadensis. Otters may mark at latrine sites with spraints (faeces) to (1) signal species identity, (2) advertise their reproductive status, (3) establish and maintain territories, and (4) communicate social status and identity to group members. Olfactory preference tests were conducted at the Alaska Sealife Center in Seward, Alaska, on a group of 15 wild-caught male otters in February 1999. We found that male otters investigated otter scent more than sealion faeces. The male otters also showed a preference for male scent over the scent of anoestrous females. No preference for the scent of unfamiliar males, compared with the scent of familiar males, was observed, and no preference for the scent of close kin was detected. However, an investigation of dominant relationships of the captive otters showed that dominant males spent more time investigating male scent than did subordinate males. Thus, spraints deposited at latrine sites may function to communicate social status of males.     

River otter population size estimation using noninvasive latrine surveys

Across much of North America, river otter (Lontra canadensis) populations were extirpated or greatly reduced by the early 20th century. More recently, reintroductions have resulted in restored populations and the recommencement of managed trapping. Perhaps the best example of these river otter reintroductions occurred in Missouri, regarded as one of the most successful carnivore recovery programs in history. However, abundance estimates for river otter populations are difficult to obtain and often contentious when used to underpin management activities. We assessed the value of latrine site monitoring as a mechanism for quantifying river otter abundance. Analyses of fecal DNA to identify individual animals may result in an improved population estimate and have been used for a variety of mammal species. We optimized laboratory protocols, redesigned existing microsatellite primers, and calculated genotyping error rates to enhance genotyping success for a large quantity of river otter scat samples. We also developed a method for molecular sexing. We then extracted DNA from 1,421 scat samples and anal sac secretions (anal jelly) collected during latrine site counts along 22–34-km stretches representing 8–77% of 8 rivers in southern Missouri in 2009. Error rates were low for the redesigned microsatellites. We obtained genotypes at 7–10 microsatellite loci for 24% of samples, observing highest success for anal jelly samples (71%) and lowest for fresh samples (collected within 1 day of defecation). We identified 63 otters (41 M, 22 F) in the 8 rivers, ranging from 2 to 14 otters per river. Analyses using program CAPWIRE resulted in population estimates similar to the minimum genotyping estimate. Density estimates averaged 0.24 otters/km. We used linear regression to develop and contrast models predicting population size based on latrine site and scat count indices, which are easily collected in the field. Population size was best predicted by a combination of scats per latrine and latrines per kilometer. Our results provide methodological approaches to guide wildlife managers seeking to initiate similar river otter fecal genotyping studies, as well as to estimate and monitor river otter population sizes. © 2011 The Wildlife Society.     

Comparing direct and indirect methods to estimate detection rates and site use of a cryptic semi-aquatic carnivore

Monitoring animal populations can be challenging, particularly when working with species that are cryptic, rare, or occur at low densities. The northern river otter (Lontra canadensis) is a cryptic, semi-aquatic carnivore that has been intensively studied in recent decades, yet much of what is known about its ecology is a result of studies that have employed indirect methods of detection and monitoring. These indirect methods, such as latrine or other sign surveys, have been the primary approach used for studying distribution, abundance, and habitat use of otters, with minimal representation of direct methods. In this study, we compared direct (camera traps) and indirect (scat count surveys) methods of evaluating detection probabilities and site use patterns of otters at latrines. We found that the direct method produced a significantly greater monthly detection probability than the indirect method and that camera surveys resulted in fewer occurrences of false negatives than scat surveys. However, the number of scats deposited at a site was positively correlated with number of visits by otters at a site (Tau-b = 0.675). Thus, while cameras outperformed scat counts in terms of detection, the two methods were comparable in determining intensity of site use. We conclude that, depending on the parameter of interest, scat counts may be an acceptable surrogate for more direct methods of monitoring otters and other cryptic species. We caution, however, that in the absence of comparative methodological data, direct methods such as camera trapping should be preferred when making inferences about animal distribution, abundance, or habitat use.     

A Pragmatic Approach for Determining Otter Distribution from Disparate Occurrence Records

Opportunistic records of animal occurrence may be problematic for inferring species distribution and habitat requirements because of unknown and uncontrolled sources of sampling variance. In this study, we used occurrence records for river otters (Lontra canadensis) derived from sign surveys, road kills, trapper bycatch, and opportunistic sightings (n = 185 records collected 2001–2012) to assess the potential distribution and habitat relationships of otters across central and western New York, USA. To mitigate for obvious observation biases, we standardized observation intensity across regions a priori and restricted inference to readily accessible areas (i.e., ≤700 m from the nearest road). Model selection, and the direction of covariate effects, proved robust to these sampling biases although effect sizes varied −7.1% to +48.0% after bias correction, with the coefficient for the proportion of available shoreline being the most unstable. Ultimately, the top bias-corrected model proved a reliable index for otter probability of occurrence given a strong, positive, and linear relationship with a withheld set of standardized survey records for otters collected in winter 2016–2017 (n = 57; R² = 0.90). This model indicated that approximately 20% of the study area represented high probability of otter occurrence. We demonstrated that reliable inference on wildlife habitat requirements can be obtained from disparate records of animal occurrence provided that data biases are known and effectively mitigated. © 2020 The Wildlife Society.     

Enhancing tourist opportunities to view spotted‐necked otters (Lutra maculicollis) at Rubondo Island National Park: can the apriori location of latrines simplify identifying best viewing areas?

We observed spotted‐necked otters (Lutra maculicollis) along a 5.17‐km section of shoreline at Rubondo Island National Park, Tanzania, during May 2008 and February, June–August 2009 to determine whether their activity areas were associated with latrine site (places along the shoreline where spotted‐necked otters scent mark by depositing scats and urine) as part of an assessment to determine how tourists or researchers can best view the species. For this assessment, we compared the distance of spotted‐necked otters sightings associated with the shoreline (n = 207) with the distance between an equal number of geographical information system (GIS)‐generated random points to the nearest latrine for each of the respective points. The mean distances for locations of spotted‐necked otter sightings to the nearest latrine differed from the mean distance of random points to latrines [171.9 m (SE = 11.30) and 66.1 m (SE = 8.16), respectively; t = ?9.23, df = 412, P < 0.001]. Sightings also were much (2.6 times) closer to latrines that occurred in groups than those that were isolated (single). Establishing viewing sites at or near latrines (particularly those occurring in clusters) would thus seem an effective way to maximize opportunities to see spotted‐necked otters.     

Invasive species and climate change: <Emphasis Type="Italic">Conyza canadensis</Emphasis> (L.) Cronquist as a tool for assessing the invasibility of natural plant communities along an aridity gradient

The predicted reduction in precipitation in the eastern Mediterranean due to climate change may expose the natural plant communities to invasive species. We assessed whether natural plant communities along an aridity gradient in Israel were resistant to invasion by considering differences in abiotic conditions and community characteristics in these regions. We considered Conyza canadensis as a model plant as it is a common invader in the region. We examined the mechanisms and functional traits of both the plant communities and C. canadensis that promote or discourage invasion. Study sites represented a rainfall gradient with four ecosystem types: mesic Mediterranean, Mediterranean, semiarid and arid. Our results showed that the mechanisms of community invasion resistance varied along the aridity gradient. At the arid and semiarid sites, water deficiency impaired the establishment of C. canadensis. At the mesic Mediterranean site, plant competition had a negative effect on C. canadensis performance, thus greatly reducing the likelihood of its establishment. We conclude that a decrease in regional precipitation due to climate change may not affect intrinsic resistance characteristics of natural plant communities to invasion in the area.     

Influence of occupation history and habitat on Washington sea otter diet

Habitat characteristics are primary determinants of nearshore marine communities. However, biological drivers like predation can also be important for community composition. Sea otters (Enhydra lutris ssp.) are a salient example of a keystone species exerting top‐down control on ecosystem community structure. The translocation and subsequent population growth and range expansion of the northern sea otter (Enhydra lutris kenyoni) in Washington State over the last five decades has created a spatio‐temporal gradient in sea otter occupation time and density, and acts as a natural experiment to quantify how sea otter population status and habitat type influence sea otter diet. We collected focal observations of sea otters foraging at sites across the gradient in varying habitat types between 2010 and 2017. We quantified sea otter diet composition and diversity, and long‐term rates of energy gain across the gradient. We found that sea otter diet diversity was positively correlated with cumulative sea otter density, while rate of energy gain was negatively correlated with cumulative density. Additionally, we found that habitat type explained 1.77 times more variance in sea otter diet composition than sea otter cumulative density. Long‐term diet studies can provide a broader picture of sea otter population status in Washington State.     

The influence of wave exposure on the foraging activity of marine otter, <Emphasis Type="Italic">Lontra felina</Emphasis> (Molina, 1782) (Carnivora: Mustelidae) in northern Chile

The marine otter Lontra felina has been said to prefer wave-exposed habitats over more protected sites in response to a greater prey abundance in exposed habitat. We examined how the foraging activity of L. felina is affected by the regime of wave exposure and prey availability at Isla Choros, northern Chile. Through focal sampling we recorded time spent by otters in foraging, the duration of dives, and the hunting success on a wave-exposed and a wave-protected site on the island. In addition, we quantified the abundance of prey in both habitats. Marine otters spent more time foraging in the wave-protected site compared with the wave-exposed habitat. Successful dives reached 26.9% in the wave-exposed habitats, and 38.2% in the wave-protected habitat. Foraging dives were 18% shorter in wave-exposed as compared with wave-protected habitat. Numerically, available prey did not differ significantly with habitat. Our results are more consistent with the hypothesis that wave-exposed habitats represent a sub-optimal habitat to foraging marine otters. Marine otters’ use of wave-exposed patches through northern and central Chile coastal areas probably reflects a low availability of suitable protected areas and greater human disturbance of more protected habitat.     

Improved genotyping and sequencing success rates for North American river otter (<Emphasis Type="Italic">Lontra canadensis</Emphasis>)

Genetic analysis of non-invasively collected fecal samples has become an important monitoring tool in wildlife management and population and conservation genetics. However, these samples are often difficult to obtain for bioindicator species such as river otters (Lontra canadensis). Moreover, DNA extraction and genotyping success rates have often been low in this species. In this technical note, alternate means of collecting fecal DNA samples at river otter latrine sites are described. Using a modified fecal swabbing protocol and a DNA lysis buffer solution, we were able to increase genotyping success rates to ≥?69% at 9/11 loci. The increased success rate now renders this protocol a more cost-efficient and reliable method for generating population level data in this species.     

Patterns of otter Lutra lutra road mortality in a landscape abundant in lakes

In order to reduce otter (Lutra lutra) road mortality and to predict accident sites, we assessed the localities of traffic accidents involving otters in the Uckermark County, Brandenburg, Northeast Germany. Eighty-eight otter accident sites from the years 1990 to 2003—as recorded by the Naturschutzstation Zippelsförde des Landesumweltamtes Brandenburg (Brandenburg State Office for Environment)—were categorised according to traffic and road patterns, otter habitat suitability, as well as presence and type of watercourse crossings. From these numerical data, we compiled a list of characteristics to identify other potentially dangerous sites where otter road traffic accidents are likely to occur using a geographic information system. With a principal component analysis, we categorised three groups of accident sites. Firstly, most otter road accidents were located close to either one or two lakes. Secondly, otters were frequently killed at places where no body of water occurred within a distance of 200 m to the road. Thirdly, and in contrast to other locations, in the Uckermark County, fewest accidents happened where a road crossed a watercourse. Mitigation measures were suggested and discussed for the recorded and potential accident sites.

     

Applying social and ecological approaches to evaluate factors influencing river otter (<Emphasis Type="Italic">Lontra canadensis</Emphasis>) visitation to fish-rearing facilities in Pennsylvania

In Pennsylvania the production of game and other fish species is a $1.6 billion industry, and loss from depredation can take a serious toll on fish stocks and associated revenues. Following a reintroduction project and natural expansion of native populations, river otters (Lontra canadensis) are now widely distributed throughout Pennsylvania. To determine occurrence and extent of depredation by river otters, we conducted telephone or mail surveys with 156 (80%) of Pennsylvania’s 196 fish-rearing facilities. River otters were reported in the vicinity of 50 (32%) facilities, of which 23 (46%) reported river otter visitation. Of the facilities that reported river otter visitation, most (87%) reported losing <5% of fish stock to otters and 91% reported an annual economic loss of <$500 from river otter depredation. Binary logistic regression determined that greater amounts of tree cover (%), facilities that reared >100,000 fish annually, and private facilities were more likely to experience visitation by river otters. Our results demonstrate that the existence of river otter populations in Pennsylvania does not appear to be a significant economic threat to fish-rearing facilities and physical and landscape characteristics of the facilities are important in determining the likelihood of river otter visitation.     

Reductions in the dietary niche of southern sea otters (Enhydra lutris nereis) from the Holocene to the Anthropocene

The sea otter (Enhydra lutris) is a marine mammal hunted to near extinction during the 1800s. Despite their well‐known modern importance as a keystone species, we know little about historical sea otter ecology. Here, we characterize the ecological niche of ancient southern sea otters (E. lutris nereis) using δ¹³C analysis and δ¹⁵N analysis of bones recovered from archaeological sites spanning ~7,000 to 350 years before present (N = 112 individuals) at five regions along the coast of California. These data are compared with previously published data on modern animals (N = 165) and potential modern prey items. In addition, we analyze the δ¹⁵N of individual amino acids for 23 individuals to test for differences in sea otter trophic ecology through time. After correcting for tissue‐specific and temporal isotopic effects, we employ nonparametric statistics and Bayesian niche models to quantify differences among ancient and modern animals. We find ancient otters occupied a larger isotopic niche than nearly all modern localities; likely reflecting broader habitat and prey use in prefur trade populations. In addition, ancient sea otters at the most southerly sites occupied an isotopic niche that was more than twice as large as ancient otters from northerly regions. This likely reflects greater invertebrate prey diversity in southern California relative to northern California. Thus, we suggest the potential dietary niche of sea otters in southern California could be larger than in central and northern California. At two sites, Año Nuevo and Monterey Bay, ancient otters had significantly higher δ¹⁵N values than modern populations. Amino acid δ¹⁵N data indicated this resulted from shifting baseline isotope values, rather than a change in sea otter trophic ecology. Our results help in better understanding the contemporary ecological role of sea otters and exemplify the strength of combing zooarchaeological and biological information to provide baseline data for conservation efforts.     

Estimating Carrying Capacity for Sea Otters in British Columbia

ABSTRACT We estimated carrying capacity for sea otters (Enhydra lutris) in the coastal waters of British Columbia, Canada, by characterizing habitat according to the complexity of nearshore intertidal and sub-tidal contours. We modeled the total area of complex habitat on the west coast of Vancouver Island by first calculating the complexity of the Checleset Bay-Kyuquot Sound (CB-KS) region, where sea otters have been at equilibrium since the mid-1990s. We then identified similarly complex areas on the west coast of Vancouver Island (WCVI model), and adapted the model to identify areas of similar complexity along the entire British Columbia coast (BC model). Using survey data from the CB-KS region, we calculated otter densities for the habitat predicted by the 2 models. The density estimates for CB-KS were 3.93 otters/km² and 2.53 otters/km² for the WCVI and BC models, respectively, and the resulting 2 estimates of west coast of Vancouver Island complex habitat carrying capacity were not significantly different (WCVI model: 5,123, 95% CI = 3,337–7,104; BC model: 4,883, 95% CI = 3,223–6,832). The BC model identified the region presently occupied by otters on the central British Columbia coast, but the amount of coast-wide habitat it predicted (5,862 km²) was relatively small, and the associated carrying capacity estimate (14,831, 95% CI = 9,790–20,751) was low compared to historical accounts. We suggest that our model captured a type of high-quality or optimum habitat prevalent on the west coast of Vancouver Island, typified by the CB-KS region, and that suitable sea otter habitat elsewhere on the coast must include other habitat characteristics. We therefore calculated a linear, coast-wide carrying capacity of 52,459 sea otters (95% CI = 34,264–73,489)—a more realistic upper limit to sea otters in British Columbia. Our carrying capacity estimates are helping set population recovery targets for sea otters in Canada, and our habitat predictions represent a first step in Critical Habitat identification. This habitat-based approach to estimating carrying capacity is likely suitable for other nonmigratory, density-dependent species.     

Fecal genotyping reveals demographic variation in river otters inhabiting a contaminated environment

The deposition and accumulation of persistent contaminants into coastal systems can have lingering negative consequences for wildlife populations and their habitats. Using multi-locus genotyping of non-invasively collected feces, we assessed the effects of such pollution on reproduction, survival, genetic variability, and abundance of river otters (Lontra canadensis) along a gradient of urban–industrial development on southern Vancouver Island, British Columbia, Canada. Genetic analyses indicated a pattern consistent with small-scale structuring, with individuals partitioned into 2 local subpopulations—those identified in the contaminated harbors of southern Vancouver Island and points west (Colwood/Harbors), and those inhabiting uncontaminated habitat east of the harbors (Oak Bay). Genetic and demographic analyses for the 2 clusters provide strong support for the conclusion that, despite contamination concerns, Colwood/Harbors river otters exhibited acceptable levels of survival and successfully reproduced (i.e., high levels of relatedness, high self-recruitment, and high emigration). However, our data indicate that the Colwood/Harbors area constitutes lower quality habitat supporting lower densities of otters, especially during winter, and excess individuals produced in that region emigrate to other areas. Immigration into Colwood/Harbors, however, seems limited, possibly because of behavioral aversion of non-habituated otters to anthropogenic disturbance associated with the harbors and limited optimal otter habitat. Our findings suggest that the effects of chronic contaminant exposure at the population level may be inadvertently mitigated through the behavioral decisions of individuals to avoid poor quality habitats. We conclude that populations of river otters can persist in and around locally contaminated sites if relatively less disturbed and contaminated habitats remain in the vicinity of the affected areas. © 2012 The Wildlife Society.     

Insights into marine otter (Lontra felina) distribution along the Peru coastline

The marine otter (Lontra felina) has a patchy distribution associated with rocky coastlines along the Pacific coast of South America. In Peru marine otters are found from La Libertad (8°04′S) to Tacna (18°09′S), however, few studies have assessed its population and conservation status. To assess marine otters' current distribution along the Peru coastline, we conducted visual surveys and collected environmental characteristics such as human presence and habitat type. We surveyed 20 locations from five regions where otter presence was based on signs of detection (spraints, food leftovers, tracks, or direct observations). In addition, data on human presence, habitat type, and geographic location were also collected. Across the 20 locations, 268 sections were scanned, and marine otters were detected in 90% (n = 18) of locations and in 19% (n = 52) of sections. Spraints were the most frequent sign detected while direct observations occurred only in seven locations. Our analysis indicates habitat features play an important role in marine otter presence, with habitats with large rocks providing preferred conditions. Our study provides information on marine otter distribution along the Peru coastline that can assist in the identification of locations for focused conservation initiatives and strategies, which should be coordinated among regions to strengthen their design and implementation.     

Using videotaping to validate the use of spraints as an index of Eurasian otter (Lutra lutra) activity

Eurasian Otter (Lutra lutra) surveys are commonly based on spraints (otter faeces) as an index of use intensity, habitat preference, and to a certain degree, population density. We were interested to know: (1) Does the number of fresh spraints correlate to the number of visits? (2) Can spraints be indicative of activity levels? (3) Is the absence of fresh spraints indicative of no visits? We used videotaping that provided a true picture of otter nocturnal activity at marking sites and compared our findings with the number of fresh spraints the following morning. This enabled us to correlate the number of spraints with the number of otter visits during the night and assess the validity of spraints as an activity index. We carried out a total of 59 videotaping nights and counted spraints in 29 sprainting sites between September 2002 and March 2004. We found a positive correlation between the proportion of nights a latrine was visited and the proportion of nights fresh spraints were deposited. The number of fresh spraints/night/site was positively correlated with the number of otter visits/night/site. Latrines visited on more nights had a higher number of fresh spraints per night visited. However, in about half the nights where no spraints were found, visits were recorded. Spraints are generally a good indicator of use intensity of a specific latrine and consequently a possible indicator of activity level and habitat preference. Understanding what determines scent-marking behaviour and its relationship to actual activity and presence can improve our ability to assess otter populations and design management protocols.     

A Survey of Abnormal Repetitive Behaviors in North American River Otters Housed in Zoos

Stereotypic behaviors, indicating poor welfare and studied in a variety of species (especially carnivores), appear related to characteristics of current and past environments. Although North American river otters (Lontra canadensis) often develop abnormal, repetitive, possibly stereotypic behaviors, no published reports describe otter housing and management or characterize how these variables relate to abnormal repetitive behavior (ARB) occurrence. The first author developed surveys to gather data on housing, individual history, management, and the prevalence of ARBs in otters housed in facilities accredited by the Association of Zoos and Aquariums. Consistent with anecdotal evidence that otters are prone to ARBs, 46% of river otters in the study exhibit them. ARBs were mostly locomotor and often preceded feeding. Exhibits where otters were fed and trained housed a greater percentage of nonhuman animals with ARBs. This study supports the Tarou, Bloomsmith, and Maple (2005) report that more hands-on management is associated with higher levels of ARBs because management efforts are only for animals with ARBs. Escape motivation, breeding season, feeding cues, and ability to forage may affect ARBs in river otters and should be investigated.     

Habitat correlates of the Eurasian otter Lutra lutra recolonizing Central Poland

The increase in Eurasian otter Lutra lutra populations in their natural range and recolonization processes are recently observed in several European countries. We address the process of otter recolonization and habitat utilization in Central Poland over 14 years. Field surveys in 1998 and 2007 documented increase in occurrence of the species. The frequency of positive sites denoted 15 % in 1993, 38 % in 1998, and 89 % in 2007. Otter occurrence at study sites was positively affected by river width while negatively affected by presence of buildings at the site and river regulation. During the most intensive colonization process in the 1990s, the habitat preferences of the otter did not change. However, the sites inhabited by otters after 1998 were characterized by lower river width and tree cover and were more often located on regulated river sections, suggesting change in habitat tolerance during expansion. The otter abundance in transformed habitats is a result of increasing population numbers and the necessity to inhabit suboptimal sections of watercourses. Thus, it seems that presence–absence data for otter populations cannot be considered a reliable indicator of habitat quality, being depended of the population density.