Effects of US 1 Project on Florida Key Deer Mortality

ABSTRACT Approximately 26% of annual mortality for the endangered Florida Key deer (Odocoileus virginianus clavium) occurs as deer-vehicle collisions (DVCs) on the 5.6-km section of United States Highway 1 (US 1) on Big Pine Key (BPK), but extensive urban development adjacent to sections of US 1 complicates efforts to reduce DVCs. Our objective was to evaluate the effectiveness of the US 1 Project (continuous 2.6-km system of 2.4-m fencing, 2 underpasses, and 4 experimental deer guards constructed on US 1 on BPK) in reducing DVCs along US 1. Deer used the underpasses all 3 postproject years (2003–2005); however, we observed higher underpass use in 2004 and 2005 compared to 2003. Exclusion fencing reduced deer intrusions onto the fenced section of US 1 during the 3-year period (2003, n = 7 deer; 2004, n = 4; 2005, n = 12). With a reduction of deer intrusions onto this section of US 1, DVCs decreased in the fenced area by 73–100%; however, US 1 DVCs within the unfenced sections of US 1 also increased (40%) as expected. In controlling for effects of increasing deer density and traffic volume, study results suggest that highway improvements have decreased the net risk of DVCs along US 1, which indicates that use of deer fencing, deer guards, and underpasses is applicable in other urban communities experiencing unacceptable levels of DVCs.     

Identifying Sites for Elk Restoration in Arkansas

Abstract: We used spatial data to identify potential areas for elk (Cervus elaphus) restoration in Arkansas. To assess habitat, we used locations of 239 elk groups collected from helicopter surveys in the Buffalo National River area of northwestern Arkansas, USA, from 1992 to 2002. We calculated the Mahalanobis distance (D²) statistic based on the relationship between those elk-group locations and a suite of 9 landscape variables to evaluate winter habitat in Arkansas. We tested model performance in the Buffalo National River area by comparing the D² values of pixels representing areas with and without elk pellets along 19 fixed-width transects surveyed in March 2002. Pixels with elk scat had lower D² values than pixels in which we found no pellets (logistic regression: Wald χ² = 24.37, P < 0.001), indicating that habitat characteristics were similar to those selected by the aerially surveyed elk. Our D² model indicated that the best elk habitat primarily occurred in northern and western Arkansas and was associated with areas of high landscape heterogeneity, heavy forest cover, gently sloping ridge tops and valleys, low human population density, and low road densities. To assess the potential for elk-human conflicts in Arkansas, we used the analytical hierarchy process to rank the importance of 8 criteria based on expert opinion from biologists involved in elk management. The biologists ranked availability of forage on public lands as having the strongest influence on the potential for elk-human conflict (33%), followed by human population growth rate (22%) and the amount of private land in row crops (18%). We then applied those rankings in a weighted linear summation to map the relative potential for elk-human conflict. Finally, we used white-tailed deer (Odocoileus virginianus) densities to identify areas where success of elk restoration may be hampered due to meningeal worm (Parelaphostrongylus tenuis) transmission. By combining results of the 3 spatial data layers (i.e., habitat model, elk-human conflict model, deer density), our model indicated that restoration sites located in west-central and north-central Arkansas were most favorable for reintroduction.     

Identifying threshold densities for wild deer in the UK above which negative impacts may occur

• 1 At high densities, deer populations may have adverse effects upon and within their environment. In this review we explore published and unpublished information to derive density thresholds for deer species in relation to impacts upon agriculture, forestry, conservation habitats, road traffic, and human and livestock health in the UK. Impact levels are affected by many factors other than absolute density. We therefore seek to establish the range of densities within which negative impacts might start to occur and which should trigger objective monitoring of actual impacts.
• 2 In commercial forestry, a threshold of 4 deer per 100ha has been suggested. Unfenced native woodlands seem to regenerate naturally if there are fewer than 4–5 large deer or fewer than 25 roe deer Capreolus capreolus per 100ha; open habitats may suffer only light or moderate impacts from red deer Cervus elaphus at landscape densities of 7–8 per 100ha.
• 3 Woodland bird species may have declined where deer densities are high but absolute thresholds seem impossible to establish. One study suggests maximum diversity at about 8 white‐tailed deer Odocoileus virginianus per 100ha.
• 4 Deer–vehicle collisions are affected by various factors in addition to deer density, but British and American studies suggest that accident frequencies decline at densities below 7–8 per 100ha.
• 5 Fallow deer Dama dama populations may maintain bovine TB (bTB) infection at much lower densities (25/100ha) than red or roe deer (91/100ha and 200/100ha, respectively) assuming 100% prevalence. Even at 30% prevalence a density of 75 fallow deer per 100ha could maintain bTB within the population.
• 6 We conclude that deer density alone is unlikely to be a good predictor of impact, and suggest that long‐term management should be based on assessment both of actual impacts and apparent density of deer.

     

Overabundance of Black-Tailed Deer in Urbanized Coastal California

Abundance of mule deer (Odocoileus hemionus) in western North America is often considered lower than desirable for hunting. Some coastal populations of Columbian black-tailed deer (O. h. columbianus) in California, USA, near urban development, however, are perceived as a nuisance and may be overabundant. To determine the density of a potential nuisance population in Marin County, California, we used a combination of fecal DNA surveys, camera stations, and 2 sources of ancillary data on wildlife observations. We estimated an average density of 18.3 deer/km² (90% CI = 15.8–20.7) throughout Marin County during late summer and early fall, 2015 and 2016. Within the county, areas with intermediate human density (885 people/km², 90% CI = 125–1,646) were associated with the highest deer densities (25–44/km²). Our estimate of average deer density was 1.7–6.1 times higher than published density estimates for deer from elsewhere in California and on the low end of densities reported for mule and white-tailed (O. virginianus) deer in regions where they routinely cause a nuisance to humans. High black-tailed deer densities in Marin County may be partially attributed to a paucity of large predators, but more investigation is warranted to evaluate the effects of a recent increase in coyotes (Canis latrans) on the deer population. Analyses of highway road kill rates and citizen science surveys suggest that the deer population in Marin County has been stable over the past 10 years. Our results demonstrate how robust estimation of deer density can inform human–wildlife conflict issues, not just managed hunting. © 2020 The Wildlife Society.     

Enhancing the Perceived Threat of Vehicle Approach to Deer

ABSTRACT In North America and Europe, deer (Cervidae)—vehicle collisions (DVCs) are common and result not only in injury and death to the animals involved, but also human injury and property damage. Given that most DVCs occur during crepuscular periods, we questioned whether the perceived threat to deer posed by vehicle approach could be enhanced. We hypothesized that a vehicle-based lighting system that better complements peak visual capabilities of deer at night relative to standard tungsten-halogen (TH) lighting alone would elicit a greater flight-initiation distance (FID) by free-ranging white-tailed deer (Odocoileus virginianus). Our lighting system comprised 2 TH lamps and one Xenarc high-intensity discharge (HID) lamp. We defined an a priori logistic model comprising 4 variables potentially explaining deer FID relative to vehicle approach: 1) starting distance of the approach, 2) lighting treatment, 3) season, and 4) deer group size. Deer exposed to the combination of TH lamps and constant illumination of the HID lamp exhibited a mean (SD) FID of 136 (127) m. In contrast, deer exposed to TH lamps only initiated flight on average at 116 (127) m, and those exposed to the combination of TH lamps and the HID lamp pulsed at 2 Hz exhibited a mean FID of 89 (98) m. We contend that the pulsing of the HID lamp while TH lamps were illuminated resulted in consistent loss (over approx. 0.5-sec intervals) of a portion of the image on approach, possibly interfering with sensory information relative to the position of the potential threat. In contrast, the combination of TH lamps and constant illumination of the HID lamp contributed (P = 0.033) to the probability of a FID ≥94 m. We suggest, therefore, that deer FID can be increased by combining currently available TH and HID lamps, or use of HID lamps alone, to enhance detection of an approaching vehicle at night. Also, we encourage research into new lamp designs to better complement deer visual capabilities as well as continued research to quantify deer FID in response to vehicle approach at night and lamp-specific properties that can enhance deer detection of the vehicle.     

Genetic diversity and population structure in urban white-tailed deer

Habitat fragmentation in urban areas has left many species isolated and vulnerable to loss of genetic variation. White-tailed deer (Odocoileus virginianus), however, thrive in urban areas. We compared genetic diversity and structure among deer in 2 urban metroparks with deer in a fenced reserve and with deer from an open, continuously distributed population to inform urban deer management. If urban deer maintain species' typical matrilineal genetic structure, removal of female groups may effectively reduce local abundance. However, if gene flow in urban areas is high, dispersal may impede efforts to reduce abundance. Although genetic diversity was high and mean relatedness was near zero in all locations, distributions of pairwise relatedness in urban metroparks and the fenced reserve contained greater proportions of closely and distantly related deer than the open locations, likely attributable to matrilineal structure. In addition, deer from the metroparks (approx. 65 km apart) were moderately differentiated (F_st = 0.092) indicating gene flow in urban areas may be less than in other landscapes. Our results indicate that removal of matrilineal groups may reduce local urban deer abundance without inducing immigration from surrounding areas. © The Wildlife Society, 2012     

Methodology matters when estimating deer abundance: a global systematic review and recommendations for improvements

Deer (Cervidae) are key components of many ecosystems and estimating deer abundance or density is important to understanding these roles. Many field methods have been used to estimate deer abundance and density, but the factors determining where, when, and why a method was used, and its usefulness, have not been investigated. We systematically reviewed journal articles published during 2004–2018 to evaluate spatio-temporal trends in study objectives, methodologies, and deer abundance and density estimates, and determine how they varied with biophysical and anthropogenic attributes. We also reviewed the precision and bias of deer abundance estimation methods. We found 3,870 deer abundance and density estimates. Most estimates (58%) were for white-tailed deer (Odocoileus virginianus), red deer (Cervus elaphus), and roe deer (Capreolus capreolus). The 6 key methods used to estimate abundance and density were pedestrian sign (track or fecal) counts, pedestrian direct counts, vehicular direct counts, aerial direct counts, motion-sensitive cameras, and harvest data. There were regional differences in the use of these methods, but a general pattern was a temporal shift from using harvest data, pedestrian direct counts, and aerial direct counts to using pedestrian sign counts and motion-sensitive cameras. Only 32% of estimates were accompanied by a measure of precision. The most precise estimates were from vehicular spotlight counts and from capture–recapture analysis of images from motion-sensitive cameras. For aerial direct counts, capture–recapture methods provided the most precise estimates. Bias was robustly assessed in only 16 studies. Most abundance estimates were negatively biased, but capture–recapture methods were the least biased. The usefulness of deer abundance and density estimates would be substantially improved by 1) reporting key methodological details, 2) robustly assessing bias, 3) reporting the precision of estimates, 4) using methods that increase and estimate detection probability, and 5) staying up to date on new methods. The automation of image analysis using machine learning should increase the accuracy and precision of abundance estimates from direct aerial counts (visible and thermal infrared, including from unmanned aerial vehicles [drones]) and motion-sensitive cameras, and substantially reduce the time and cost burdens of manual image analysis.     

Predator densities and white-tailed deer fawn survival

Predation is the dominant source of mortality for white-tailed deer (Odocoileus virginianus) <6 months old throughout North America. Yet, few white-tailed deer fawn survival studies have occurred in areas with 4 predator species or have considered concurrent densities of deer and predator species. We monitored survival and cause-specific mortality from birth to 6 months for 100 neonatal fawns during 2013–2015 in the Upper Peninsula of Michigan, USA, while simultaneously estimating population densities of deer, American black bear (Ursus americanus), coyote (Canis latrans), bobcat (Lynx rufus), and gray wolf (Canis lupus). We estimated fawn predation risk in response to sex, birth mass, and date of birth. Six-month fawn survival pooled among years was 36%, and fawn mortality risk was not related to birth mass, date of birth, or sex. Estimated mean annual deer and predator densities were 334 fawns/100 km², 25.9 black bear/100 km², 23.8 coyotes/100 km², 3.8 bobcat/100 km², and 2.8 wolves/100 km². Despite lower estimated per-individual kill rates, coyotes and black bears were the leading sources of fawn mortality because they had greater densities relative to bobcats and wolves. Our results indicate that the presence of more predator species in a system is not entirely additive in its effect on fawn survival. © The Wildlife Society, 2019     

甘肃兴隆山保护区野生马麝分布、数量特征及影响因素

综合采用样线法、粪堆计数法及重复调查法对甘肃省兴隆山国家级自然保护区的野生马麝（Moschus chrysogaster）进行了种群调查,结合生境分析,确定了其种群分布、数量特征及影响因素。结果表明,兴隆山保护区分布有野生马麝（1159±275）头,平均种群密度为（3.51±0.83）头/km²;各植被类型生境中的野生麝种群数量及密度存在差异,灌丛生境分布有70%的野生马麝种群,达（807±170）头,种群密度为（6.49±1.63）头/km²;针叶林种群密度最大,达（8.85±83.25）头/km²,分布有野生麝（123±45）头;针阔混交林分布最少,仅（41±15）头,种群密度为（5.00±1.84）头/km²;人工林生境无野生马麝分布。保护区各植被类型生境中的野生马麝种群分布差异反映了马麝对适宜生境功能的需求,食物、保温和隐蔽性是制约野生马麝冬季分布和种群数量的关键因素。此外,因生境及人为干扰强度的不同,保护区各区域的野生马麝种群分布存在差异。建议通过减少人为干扰、地表植被管理及人工林管理优化等措施增加生境适宜性,促进兴隆山自然保护区野生马麝种群的快速恢复和增长。     

Spleen mass as a measure of immune strength in mammals

• 1 In studies of birds and their pathogens, spleen size has frequently been used to make inferences about immune system strength. However, the use of spleen size in mammals is more complicated because, in addition to having an immune function, the mammalian spleen is also a reservoir for red blood cells.
• 2 To assess the reliability of mammalian spleen mass as an indicator of immune activity, we quantified the white and red pulp mass by histology of spleens from shot red deer Cervus elaphus. We then analysed the relationships among spleen mass, the amounts of white and red pulp, and the deer's body condition relative to faecal counts of the nematode parasite Elaphostrongylus cervi.
• 3 White and red pulp mass were positively correlated so that an increase in spleen mass was a positive function of both components of the spleen. In male deer, which had significantly lower body condition and higher parasite loads than females, parasite counts were negatively correlated with spleen mass, white pulp mass, and red pulp mass.
• 4 Our findings suggest that (i) spleen mass in shot red deer is a reliable measure of white and red pulp content; and (ii) when looking at the red deer life history, which is greatly influenced by sex of the deer, splenic mass and white pulp mass could be used as reflections of immune system strength.
• 5 Future studies of mammalian spleens can contribute to the understanding of evolved strategies of immune response investment in mammals. However, determination of the white and red pulp spleen components using various sampling methods must be made prior to their application.

     

The effect of terrain and female density on survival of neonatal white‐tailed deer and mule deer fawns

Juvenile survival is a highly variable life‐history trait that is critical to population growth. Antipredator tactics, including an animal's use of its physical and social environment, are critical to juvenile survival. Here, we tested the hypothesis that habitat and social characteristics influence coyote (Canis latrans) predation on white‐tailed deer (Odocoileus virginianus) and mule deer (O. hemionus) fawns in similar ways during the neonatal period. This would contrast to winter when the habitat and social characteristics that provide the most safety for each species differ. We monitored seven cohorts of white‐tailed deer and mule deer fawns at a grassland study site in Alberta, Canada. We used logistic regression and a model selection procedure to determine how habitat characteristics, climatic conditions, and female density influenced fawn survival during the first 8 weeks of life. Fawn survival improved after springs with productive vegetation (high integrated Normalized Difference Vegetation Index values). Fawns that used steeper terrain were more likely to survive. Fawns of both species had improved survival in years with higher densities of mule deer females, but not with higher densities of white‐tailed deer females, as predicted if they benefit from protection by mule deer. Our results suggest that topographical variation is a critical resource for neonates of many ungulate species, even species like white‐tailed deer that use more gentle terrain when older. Further, our results raise the possibility that neonatal white‐tailed fawns may benefit from associating with mule deer females, which may contribute to the expansion of white‐tailed deer into areas occupied by mule deer.     

The evolution of nettle resistance to heavy deer browsing

We examined whether heavy browsing by sika deer, Cervus nippon Temminck, changed morphological characteristics of a Japanese nettle, Urtica thunbergiana Sieb. et Zucc., in Nara Park, where a large population of sika deer has been maintained for more than 1,200 years. Wild nettles of Nara Park exhibited smaller leaf area, 11–223 times more stinging hairs per leaf, and 58–630-times higher stinging hair densities than those of other areas where there was no evidence of sika deer browsing. There were no significant differences in stinging hair length between the areas. Nettles from Nara Park that were cultivated from seeds in a greenhouse retained a larger number and higher density of stinging hairs. In the field, nettles of Nara Park were less frequently browsed by sika deer and showed higher survivorship than nettles that were transplanted from an unbrowsed area into Nara Park. These results indicate that: (1) the U. thunbergiana population of Nara Park has an extremely high stinging hair density compared with those of unbrowsed areas; (2) this characteristic has a genetic basis, and (3) stinging hairs serve as a defensive structure against sika deer, contributing to an increase in survivorship. Thus, we conclude that a U. thunbergiana population in Nara Park, with extremely high stinging hair densities, has evolved through natural selection due to heavy browsing by sika deer.     

Migratory strategies, fawn recruitment, and winter habitat use by urban and rural mule deer (Odocoileus hemionus)

We examined the migratory strategies of mule deer (Odocoileus hemionus) using adjacent urban and rural winter ranges in northern Utah in relation to deer demography and patterns of habitat use. Urban deer were more likely to be migratory than rural deer, even though migratory animals from the two herds intermixed on a common, high-elevation summer range. Urban deer exhibited lower fawn recruitment than rural deer; but within each herd, demographic characteristics of migratory and nonmigratory animals suggested that game theory explained the ratios of deer adopting each behavior. Estimates of animal numbers and available habitat did not reveal clearly whether deer densities differed on the two winter ranges. However, patterns of habitat use by urban deer were so clustered around areas of concealment vegetation that animals probably experienced higher local densities than rural animals. In addition, the clustered patterns of habitat use by urban deer resulted in incomplete use of available forage. This may have contributed to the relatively poor fawn recruitment by urban deer, a phenomenon that appeared to be perpetuated by their strong fidelity to winter range.     

Effects of supplemental feeding and density of white-tailed deer on rodents

Spatial distribution, population density, and reproductive success of many wildlife species may be altered by changes in vegetation composition, habitat structure, and availability of food. Altered distributions of key herbivores such as white-tailed deer (Odocoileus virginianus) may impact all of these factors. Our objective was to determine the direct and indirect effects of supplemental feeding of deer on rodent populations in south Texas. We modeled effects of supplemental feeding and habitat change due to deer browsing through surveys of rodents. Rodents have a short generation time and populations respond quickly to change, so they are a suitable indicator of changes in habitat structure brought about by deer browsing pressure. We sampled rodent populations near to and far from deer feeders within twelve 81-ha enclosures containing three different densities of deer with and without supplemental feed. The three deer densities were low (8.1 ha/deer), medium (3.2 ha/deer), and high (2 ha/deer). We conducted rodent trapping during March and April of 2007 and 2008. Abundance of rodents was much higher (P < 0.001) in 2008 than in the previous year due to an increase in rainfall. However, we found little effect of deer density, supplemental feeding of deer, or distance from deer feeders on rodent populations. Thus we conclude that supplemental feeding of deer and deer density had little influence on rodent communities in this environment. Rodent species native to semi-arid environments are probably adapted to large changes in vegetative productivity brought about by the highly variable annual rainfall patterns, therefore they can adapt to the less abrupt habitat changes resulting from changing densities of deer. Conservation concerns that providing supplemental feed to deer in semi-arid rangeland will disrupt the ecology of the land through changes in rodent populations were not supported. © 2011 The Wildlife Society.     

Invading white-tailed deer change wolf–caribou dynamics in northeastern Alberta

Human-caused habitat change has been implicated in current woodland caribou (Rangifer tarandus caribou) population declines across North America. Increased early seral habitat associated with industrial footprint can result in an increase in ungulate densities and subsequently those of their predator, wolves (Canis lupus). Higher wolf densities can result in increased encounters between wolves and caribou and consequently higher caribou mortality. We contrasted changes in moose (Alces alces) and deer (Odocoileus spp.) densities and assessed their effects on wolf–caribou dynamics in northeastern Alberta, Canada, pre (1994–1997) versus post (2005–2009) major industrial expansion in the region. Observable white-tailed deer (O. virginianus) increased 17.5-fold but moose remained unchanged. Wolf numbers also increased from approximately 6–11.5/1,000 km². Coincident with these changes, spatial overlap between wolf pack territories and caribou range was high relative to the mid-1990s. The high number of wolf locations in caribou range suggests that forays were not merely exploratory, but rather represented hunting forays and denning locations. Scat analysis indicated that wolf consumption of moose declined substantively during this time period, whereas use of deer increased markedly and deer replaced moose as the primary prey of wolves. Caribou increased 10-fold in the diet of wolves and caribou population trends in the region changed from stable to declining. Wolf use of beaver (Castor canadensis) increased since the mid-1990s. We suggest that recent declines in woodland caribou populations in the southerly extent of their range have occurred because high deer densities resulted in a numeric response by wolves and consequently higher incidental predation on caribou. Our results indicate that management actions to conserve caribou must now include deer in primary prey and wolf reduction programs. © 2010 The Wildlife Society     

Reduction and Maintenance of a White-Tailed Deer Herd in Central Massachusetts

Abstract: Controlled public hunts have been used in a variety of settings to reduce overabundant white-tailed deer (Odocoileus virginianus) herds. We present the results of a large-scale (160 km²) controlled hunt at Quabbin Reservation (QR) in central Massachusetts, USA. The QR was divided into 5 hunt zones. Hunting was initiated in each zone from 1991 to 1994 and continued through 2004. The management goal was to achieve posthunt deer densities of4 deer/km². Initial estimated deer densities in each zone ranged from 11.4 deer/km² to 27.6 deer/km². The management goals were reached in each zone after 2-4 years of hunting. Posthunt populations were maintained at or below the goal even though total hunter effort was reduced. Hunters were not required to harvest antlerless deer, but antlerless deer comprised 55-83% of the harvest each year. We simulated the effects of 5 years without hunting on deer populations. The simulated deer population exceeded management goals after 2 years. Our results demonstrate that controlled public deer hunts can effectively reduce deer populations and maintain them at desired levels over large areas with minimal hunter restrictions. Managers should prepare stakeholders during the hunt planning process for the need to continue overall harvest rates of >30% during the maintenance phase of a deer management program.     

Space Use and Survival of White-Tailed Deer in an Exurban Landscape

Abstract: Exurban development is nonmetropolitan, residential development characterized by a human population density and average property size intermediate between suburban and rural areas. Although growth in exurban areas is outpacing that of urban, suburban, or rural landscapes, studies of deer (Odocoileus spp.) ecology in exurban areas are nonexistent. During 2003–2005, we studied space use (i.e., seasonal home-range and core-area size and habitat use relative to human dwellings) and survival of 43 female white-tailed deer (O. virginianus) in an exurban setting near Carbondale, Illinois. Deer had larger home ranges than most suburban deer populations and generally smaller home ranges than rural deer populations. When we analytically controlled for habitat use, deer exhibited a subtle avoidance of human dwellings, especially during the fawning season. The annual survival rate was among the highest reported in the literature at 0.872 (SE = 0.048). Only 5 deer (cause-specific mortality rate = 0.091) were harvested by hunters, indicating major obstacles for wildlife managers when attempting to manage deer in exurban areas using traditional hunter harvest.     

A model to test how ticks and louping ill virus can be controlled by treating red grouse with acaricide

Ticks are the most important vectors of disease‐causing pathogens in Europe. In the U.K., Ixodes ricinus L. (Ixodida: Ixodidae) transmits louping ill virus (LIV; Flaviviridae), which kills livestock and red grouse, Lagopus lagopus scoticus Lath. (Galliformes: Phasianidae), a valuable game bird. Tick burdens on grouse have been increasing. One novel method to reduce ticks and LIV in grouse may be acaricide treatment. Here, we use a mathematical model parameterized with empirical data to investigate how the acaricide treatment of grouse might theoretically control ticks and LIV in grouse. Assuming a situation in which ticks and LIV impact on the grouse population, the model predicts that grouse density will depend on deer density because deer maintain the tick population. In low deer densities, no acaricide treatment is predicted to be necessary because abundances of grouse will be high. However, at higher deer densities, the model predicts that grouse densities will increase only if high numbers of grouse are treated, and the efficacy of acaricide is high and lasts 20 weeks. The qualitative model predictions may help to guide decisions on whether to treat grouse or cull deer depending on deer densities and how many grouse can be treated. The model is discussed in terms of practical management implications.     

Roe and fallow deer: are they compatible neighbours?

The analysis of the relationships between population density and habitat features is important to evaluate the ecological needs of a species, its potential impact on ecosystems and its interspecific interactions. We analysed the spatial variation of roe deer Capreolus capreolus and fallow deer Dama dama densities in a Mediterranean area in summer 2007 and winter 2007/2008. Previous research has shown that fallow deer can actively displace and exclude roe deer from natural feeding sites. Here we show that both species have the greatest densities in ecotone habitats between wood and open fields (abandoned olive groves and pastures), but with contrasting geographic patterns. The fallow deer showed the greatest densities in the central northern part of the study area near to local historical release sites. The densities of roe deer were great where fallow deer were rare and low where fallow deer were abundant. Spatial overlap was great at the habitat scale, indicating a high potential for competition, but was low at the plot scale, suggesting that partitioning of space occurred at a fine scale. Supporting great numbers of deer, the ecotone areas are crucial for the management of ecosystems. We suggest that roe deer avoid areas with great densities of fallow deer and that interspecific interference from the latter affects the density and distribution of the former both at a fine and at a large scale.     

Salt licks do not increase local densities of the deer ked,Lipoptena cervi,an abundant ectoparasite of cervids

The deer ked, Lipoptena cervi (Diptera: Hippoboscidae), is a common ectoparasite of the moose, Alces alces (Artiodactyla: Cervidae). Salt licks are widely used to manipulate moose movements to prevent damage to saplings and traffic accidents. They may cause moose to gather in small areas, which could create aggregates of deer ked pupae as the parasite is a short‐distance flyer and its dispersion depends on its hosts. We investigated whether the population density of flying deer keds could be influenced by manipulating salt licks and how environmental variables affect parasite density. Densities were estimated in 40 experimental sites with four treatments (no salt licks, introduced salt licks, removed salt licks, permanent salt licks) in September during 2007–2010. Forest edges, mixed forests on mineral soil and coniferous forests on peat soil were the habitats with high numbers of parasites. The manipulation of salt licks seemed to be ineffective in reducing the density of deer keds as the only factor to show statistical significance with parasite numbers in the mixed‐model analysis was year of determination. Annual deer ked densities correlated with the abundance of moose in the region. Moreover, high spring and summer temperatures seemed to increase the numbers of flying imagos.