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Where is dinner? The spatiality of the trophic niche of terrestrial mammalian carnivores in Chile, a systematization for their conservation

Abstract

Knowing what the highest-level mammalian carnivores and intermediate levels eat throughout the geography and how human activities may affect their community dynamics is relevant information to focusing and deciding on conservation efforts within a territory. In this review, we characterize geographically the accumulated knowledge about the trophic niche of terrestrial mammalian carnivore species and evaluate the spatial relationship between the species richness distribution and the geographical distribution of their trophic knowledge in Chile. We found 88 peer-reviewed papers that include trophic studies per se, theses, and short notes carried out in Chile, where at least one trophic element was reported for terrestrial mammalian carnivore species. We found a positive relationship between the species richness distribution pattern and the spatial distribution of accumulated trophic knowledge, i.e., most of the papers have been conducted in Central-southern Chile (Central Chile and Temperate Forest ecoregions) responding to the highest co-occurrence of carnivore species within the limits of the biodiversity hotspot, the most threatened area in the country. Despite this general relationship, we recognize gaps in knowledge regarding regions of the country that require more research effort, such as O’Higgins, Maule, and Ñuble regions, as well as focus efforts on certain species with no or almost no knowledge of their trophic ecology, such as Leopardus colocola, Lyncodon patagonicus and Conepatus chinga. Except for the northern Chilean ecosystems, there is a generalized report of high consumption of exotic mammals in the diet of carnivores in the center and south of the country. However, of the 98 localities recognized in the 88 papers, 20.4% correspond to an anthropized environment, while most (79.6%) correspond to a “non-anthropized” environment or protected area. We hope this review allows researchers and decision-makers to consider the knowledge and lack thereof of carnivore trophic interactions as an opportunity to conserve entire natural communities throughout the Chilean territory.

Introduction

Biological communities comprise all sympatric species of different taxa and life histories that can interact at a given locality. However, the difficulty of thoroughly analyzing all their interactions to understand intrinsic relationships inside the system has led researchers to focus the inter-specific questions on restricted groups of species as “assemblage-guilds” [68, 71, 129, 134, 149] or “indicator species” [16, 42]. Here, mammalian carnivores of the order Carnivora play an essential role as they are the highest-level predators in most terrestrial communities. By occupying the top or superior positions of the energy pyramid, the descent or removal of these predators of an environment can generate a trophic cascade that can alter the ecological structure of a community modifying the interactions that regulate predator and prey populations [27, 50, 128, 150] and act as secondary seed dispersers [56]. This environmental sensitivity has earned them the label of "biological indicators", giving them great ecological value because their predation interactions create impacts that can ripple downward through the trophic levels of an ecosystem, having a fundamental role in the preservation of the biodiversity of terrestrial communities [44, 55, 64, 101, 111]. Carnivora includes several primary conservation icon species, many others are considered flagship, umbrella, keystone, and indicator species. However, Gittleman et al. [50] highlighted that carnivore conservation would be more effective if conservation strategies were focused on prioritizing geographical areas or entire ecological communities rather than addressing individual species separately. Feeding, and consequently the prey availability, is a fundamental factor in the life of carnivores and, in many cases, one of the most limiting n-dimensions of their ecological niche [57]. For example, it has been demonstrated that the greatest threat to tiger (Panthera tigris) conservation is the population reduction of tiger prey [81, 82]. In this sense, knowing what the highest-level mammalian carnivores (hypercanivores) and intermediate levels (mesocarnivores to omnivores) eat throughout the geography and how human activities may be affecting their community dynamics is very relevant information to focus and decide on conservation efforts within a territory. Then, studying the trophic relationships of Carnivora predators is an effective approach for detecting the composition of communities. However, studying carnivores is challenging due to their elusive nature, low abundance, and nocturnal habits [64]. As a result, the ecology of many carnivore species and their communities, such as the Andean small cats in Chile, is poorly understood [28].

The study of carnivores' feeding strategies and diet often utilizes non-invasive methods, such as fecal analysis and observation of food availability. This helps determine the species role in the ecosystem, potential interspecific competition, and impact on prey populations [83]. In this sense, the results of diet analyses might have a far-reaching effect on the development of carnivore management plans, especially if economically important or endangered species are involved [48, 83, 84]. This is essential to understand the geographical context of knowledge and identify gaps and fragmented information. This type of study and knowledge becomes even more relevant in an ecosystem of high international priority for biodiversity conservation, such as the Chilean Winter Rainfall-Valdivian Forests (henceforth, Chilean hotspot), characterized as one of the 34 biodiversity hotspots worldwide [2, 103, 106, 143].

Currently, 15 terrestrial native carnivore species of four different families are found in Chile [29], one Mephitidae: Conepatus chinga; three Canidae: Lycalopex culpaeus, Lycalopex griseus, and Lycalopex fulvipes; four Mustelidae: Galictis cuja, Lontra felina, Lontra provocax, and Lyncodon patagonicus; seven Felidae: Leopardus colocola, Leopardus garleppi, Leopardus pajeros, Leopardus jacobita, Leopardus geoffroyi, Leopardus guigna, and Puma concolor. Moreover, in southern Chile, the American mink (Neovison vison) is an exotic and invasive mustelid that has strongly affected and continues to threaten the Patagonian ecosystems [73, 132]. Chile has the highest carnivore species richness and endemism levels in the Chilean hotspot. Therefore, it is crucial to understand their ecological aspects to develop effective conservation strategies. The main goals of this review are: 1) geographically characterize the accumulated knowledge about the trophic niche of terrestrial mammalian carnivore species present in Chile, 2) evaluate the relationship between the geographical distribution of the mammalian carnivore species richness and the geographical distribution of published information on trophic aspects of these species throughout Chile. We hope to find more studies in central-south Chile due to the high number of sympatric species in the global conservation priority area. This also translates into a significant knowledge gap in extreme regions of the country, 3) recognize the gaps in knowledge about species' diets and areas throughout their respective geographic distributions in Chile allows future and urgent conservation efforts to be geographically focused.

Methods

Search of studies/ bibliographic compilation

We reviewed the scientific literature on the diets of 16 terrestrial mammalian carnivore species (15 native + American mink) by searching for keywords and titles in both English and Spanish through Google Scholar, Web of Science, and SCOPUS. We used the following keywords for each search: “scientific binomial name” AND “diet” OR “feeding habits” OR “trophic niche”. We consider the variants and changes of taxonomic names as 1) “Lycalopex, “Pseudalopex” and “Dusicyon” for the South American foxes and 2) Recent taxonomic arrangement as proposed for Leopardus colocola [29, 108]. Original/research articles, short notes, and theses (hereinafter “papers”) that provide detailed information or the report of a particular trophic item were included. The bibliographic review was carried out between July 2023 and April 2024. To provide detailed diet descriptions by species (Supplementary Information), papers from nearby localities in adjacent countries that cover the same ecoregion as the Chilean distribution of the species were considered for species with less than three papers conducted in Chile.

Gathering information / geographic information

To characterize the geographical locality of each paper, we recorded the geographic coordinates of the study locality reported and identified the administrative province and region to which the locality corresponds. In addition, the ecoregion associated with the study locality was identified. For this, six ecoregions within the country were distinguished, following the classification proposed by the Biodiversity Support Program [8] and Dinerstein et al. [30] and updating the limits of these ecoregions according to the zonal vegetation unit presented in “Bioclimatic and Vegetational Synopsis of Chile” [89]. Ecoregions are the Coastal Atacama Desert, Puna, Central Chile (Mediterranean sclerophyllous forest + Andean Steppe), Temperate Forest (Deciduous + Evergreen), Patagonian Steppe, and Subpolar Forest. Then, we quantified the number of papers and study localities per species conducted by political region, province, and ecoregion. In addition, we categorized each study locality as a “non-anthropized” or “anthropized” environment, according to the paper. We recorded the percentage of exotic prey items in the species' diet reported in each study as another factor that accounts for anthropization.

Spatial relationship and statistical analysis

We describe the spatial pattern of species richness in Chile and statistically determine the areas of the country that present a greater (hotspot) and lower (coldspot) number of species than expected by chance through Gi* statistic [49]. Briefly, Gi* identifies spatial concentrations of high or low values of an entity (in this case, species richness per 0.25 × 0.25° cells). To establish statistically significant areas, a feature must have high or low values and be surrounded by other cells with similar values. Consequently, the local sum of an entity and its neighbors is compared proportionally to the sum of all entities. A significant Z score is assigned if the local sum differs from the random expectation. Significant values of Z > 0 provide evidence of significant hotspots, while those of Z < 0 provide evidence of groups of entities with values lower than those expected by chance. The statistical determination of hotspots and coldspots was performed in ArcGIS 10.4.1 software [40]. To evaluate the relationship between species richness and the number of localities by administrative region and ecoregion, spatial (Simultaneous autoregressive, SAR and conditional autoregressive, CAR) and non-spatial (Ordinary Least Squares regression, OLS) regression methods were performed. Both CAR and SAR incorporate spatial autocorrelation using neighborhood matrices, which specify the relationship between the residuals at each location (i) and those at neighboring locations (j) [86]. The model selection approach was applied to search for the model with the best fit [77]. The selection was carried out using the delta AIC (Δi, using the formula Δ AIC = AICi – min AIC, where AICi is the AIC of model i, and min AIC is the AIC value of the “best” model. As a rule, Δi < 2 suggests substantial evidence for the model, values between 3 and 7 indicate that the model has less support, while Δi > 10 indicates that the model is unlikely [13]. Analyzes were performed through the “MuMin” package [7]. Since the models did not reveal significant spatial autocorrelation (Supplementary Information, Table S1), we chose OLS models to study the relationship of species richness versus localities by administrative regions and ecoregions of Chile. Regression analyses were performed with the ncf [9], spdep, and spatialreg [117] packages in R software [122].

Results

We found 88 papers that included original/research articles, theses, and short notes conducted in Chile, where at least one trophic element was reported for terrestrial mammalian carnivore species (Supplementary Information, Table S2). Papers were collected from 1978 [155] to 2024 [158]. The number of papers per year in Chile shows a slight increase over time, with two peaks in 1991 and 2014 (Fig. 1a). The distribution of the number of papers by species shows that the greatest number have been conducted for L. culpaeus and L. griseus and highlights that three species do not present trophic studies in Chile: C. chinga, L. patagonicus and L. pajeros (Table 1 and Fig. 1b). A summary of the diet in Chile for each of the 16 species is available in Supplementary Information. Of the 88 papers, we quantify 98 study localities. The distribution of the number of study localities by ecoregion shows that the greatest number is found in the central-south ecoregions (Central Chile, Temperate Forest, and Subpolar Forest), with a decrease towards the ecoregions of both the northern (Atacama Coastal Desert) and the southern (Patagonian Steppe) extremes (Table 1 and Fig. 1c). When considering the spatial distribution of study localities in the context of the political-administrative division of the country, the 98 localities are grouped in 37 provinces belonging to the 17 administrative regions of the country (Supplementary information, Table S3). The distribution of research per administrative region showed that the majority are in Araucanía, Los Lagos, and Magallanes. In contrast, Antofagasta, O'Higgins, Maule, and Ñuble regions show only one study (Table 2 and Fig. 1d).

Fig. 1
figure 1

a Distribution of the number of papers per species; b Distribution of the number of study localities per ecoregion; c Distribution of the number of study localities per administrative regions; and d) Distribution of the number of papers over time (R.2 = 0.045)

Table 1 Trophic papers conducted in Chile by ecoregion
Table 2 Number of papers and study locations by administrative region

Geography of anthropization

Of the 98 study localities, 20 (20.4%) report being an anthropized environment or with some degree of anthropization, mainly in central-southern Chile. One locality in Puna (Antofagasta region), six localities in Central Chile (four in the Metropolitan region, one in Valparaíso, and one in Maule region), 12 localities in Temperate Forest (four in the Araucanía region, three in Biobío, two in Los Lagos, two in Los Ríos and one in Maule region) and, one in Subpolar Forest (Magallanes region; Fig. 2). By contrast, most study localities (79.6%) correspond to “non-anthropized” environments or protected areas concentrated mainly in the northern and southern extremes of the country (Fig. 2). Furthermore, the 77.3% of the papers reports a study locality in an “anthropized” environment corresponding to research from 2005 to the present. The study locality by species and anthropized environments revealed that L. culpaeus (11 sites) and L. griseus (7 sites) have the greatest number of papers in these environments, while L. garleppi, L. jacobita, and L. geofroyii do not have papers in anthropized environments (Supplementary Information, Table S3). Concerning the exotic prey items reported in the different papers, despite not describing anthropized environments for the Atacama Coastal Desert ecoregion, the presence of exotic rodents Mus musculus and Rattus rattus has been reported in the diet of L. griseus and L. culpaeus in the Tarapacá region [15, 91]. For the Puna ecoregion, there are no reports of exotic prey items in the diet of terrestrial mammalian carnivore species. For Central Chile, several localities, mainly in the Metropolitana region but also in Atacama, Coquimbo, O'Higgins, and Valparaíso regions, report a greater breadth of exotic prey items, highlighting the presence of Oryctolagus cuniculus, Lepus europaeus, and R. rattus in the diet of L. griseus, L. culpaeus, P. concolor and G. cuja [34, 67, 87, 105, 112, 130, 142, 145, 155, 158]. Eight of the nine species of mammalian carnivores distributed in the Temperate Forest ecoregion show exotic items in their diet. In this ecoregion, exotic prey items are reported in 24 different localities through Maule, Ñuble, Biobío, Araucanía, Los Lagos, and Los Ríos regions. The presence of the exotic fish Salmo trutta in the diet of the semi-aquatic L. provocax and the invasive N. vison in the Los Ríos Region stands out [43, 94], and the presence of exotic rodents and lagomorphs in the diet of all species of terrestrial predators (e.g., [104, 124, 126, 164, 165], Supplementary Information, Table S3). For the Subpolar Forest ecoregion, most of the study localities are in the Torres del Paine National Park and adjacent sites (Magallanes region), where feeding of Ovis aries cattle by P. concolor, L. griseus, and L. culpaeus was reported in several papers [63, 79, 157]. The only research for L. geoffroyi in Chile stands out here. The study shows that this species feeds on the exotic lagomorph Lepus capensis, which has a local high abundance [78]. In addition, in the southern part of Patagonia, at Tierra del Fuego National Park, the invasive N. vison also preys on exotic rodents and lagomorphs [151]. In the Patagonian Steppe ecoregion, the presence of exotic prey items such as cattle and lagomorphs are reported in all study localities (Aysén and Magallanes regions) for the diet of P. concolor, L. griseus and L. culpaeus [3, 37, 70] (Supplementary Information, Table S3).

Fig. 2
figure 2

Spatial distribution of the study localities reported in the 88-papers found. Colored polygons correspond to each ecoregion. Yellow circles correspond to non-anthropized study localities, and red diamonds correspond to anthropized study localities

Spatial analyses

The spatial distribution of mammalian carnivore species richness in Chile shows the highest diversity in the Central Chile ecoregion, with a peak of six species occurring in an area of ~ 27 km2 (0.25° cell). This area corresponds to Valparaíso, Metropolitana, O'Higgins, and Maule regions, while the areas with the lowest species number are in Coastal Atacama Desert and some areas of Patagonia with a minimum of one species (Fig. 3a). Areas with the highest species richness than expected by chance correspond to two areas in the Puna, a great extension in Central Chile + Temperate Forest, and an area in southern Chile that encompasses the Subpolar Forest and Patagonian Steppe ecoregions (Fig. 3b). The OLS model had a better fit than an autoregressive one, showing a positive and significant relationship (with transformed and untransformed data) between the spatial distribution of species richness and the number of localities by ecoregion (R2 = 0.71; p = 0.02), in the same way, the species richness also shows a positive and significant relationship with the number of localities by administrative region (R2 = 0.45; p = 0.002; Table 3, Fig. 4).

Fig. 3
figure 3

Study localities for each species of terrestrial mammalian carnivores. The pale-yellow polygon represents the species' distribution range (Digital Distribution Maps on The IUCN Red List of Threatened Species, UICN [65] and Francisca Zamora-Cornejo). Yellow circles are "non-anthropized" localities and red diamonds are "anthropized" localities

Table 3 Statistical models for the evaluation of the spatial relationship between the distribution of species richness of terrestrial mammalian carnivores in Chile and the number of study localities
Fig. 4
figure 4

a Spatial variability of the mammalian carnivore richness pattern in Chile, b Getis-Ord Gi* Hot Spot Analysis of mammalian carnivore richness across Chile

Discussion

Knowledge—species and knowledge—area relationship

The positive relationship between the species richness distribution pattern of mammalian carnivores and the spatial distribution of accumulated knowledge (measured as the number of papers) about the trophic relationships allows us a first general and encouraging interpretation that most of the studies have been conducted in Central-southern Chile (Central Chile and Temperate Forest ecoregions) which corresponds in turn to the highest co-occurrence of carnivore species area, being this within the limits of the biodiversity hotspot, the most threatened area in the country [103, 106, 143]. However, despite this general relationship, we can recognize gaps in knowledge regarding areas of the country that require greater research effort and focus efforts on certain species with no knowledge of their trophic ecology. A clear spatial bias that is necessary to consider to address new research projects or conservation efforts is the non-uniform distribution of papers by administrative regions within the Chilean hotspot, with one paper for the regions of O'Higgins [112], Ñuble [19], two for Valparaíso [18, 105] and two for the Maule region [22, 158], being these regions part of most affected by the intense change in land use towards productive activities [58]. Indeed, in these regions, it is necessary to evaluate the effects of this landscape transformation on mammalian community interactions. Conversely, most papers are concentrated in the northern portion of the biodiversity hotspot (Coquimbo and Metropolitana regions) and the southern portion (Biobío, Araucanía, Los Ríos, and Los Lagos regions). In the Chilean hotspot, mammalian carnivore species have been exposed to strong human pressure over the last century due to the accelerated replacement of native forests with productive plantations and human settlements (e.g., [104, 112, 114, 160]). However, the largest number of papers have been conducted in public and private protected areas, where the explicit effect of human pressures and landscape transformation on natural communities is difficult to evaluate. In these areas, sometimes far from human productive activities, the trophic papers reflect in the same way a high presence and abundance of exotic species in the diet, such as lagomorphs and rats, accounting for their wide spatial expansion of these species. Concerning South America, in Chilean territory, wild exotic mammals exhibit their most invasive ranges and where they are present at the highest densities [10, 12, 39, 116, 147, 165]. Therefore, carnivores have shown flexible trophic behavior due to this new food supply in protected and transformed areas. Research in anthropized landscapes supports the idea that species such as L. guigna, P. concolor, G. cuja, and the foxes of the genus Lycalopex may use productive plantations as feeding areas [22, 61, 74, 104, 112, 131, 158]. Another example of the consumption of exotic rodents in anthropized areas is reported for L. provocax [43]. Nevertheless, research is key and urgent for species without trophic information in the pristine and anthropized habitats of the Chilean hotspot. This includes species such as C. chinga, L. patagonicus. Although there are trophic studies for C. chinga in other countries and ecoregions (e.g., [31, 96, 115]) that could give light on its community role in northern and southern Chilean territory, it is relevant to know the role of this insectivorous predator on insect assemblages considering that the diversity of Coleoptera in Central Chile is highly endemic [148, 152]. An example of extreme information deficit is the case of L. patagonicus. It is a species with an unknown natural history in Chile and one of the least known carnivores from southern South America [36, 120, 121]. Thus, research priority is required to confirm its current ecological requirements and understand its role in native and anthropized landscapes. Another species with an almost unknown natural history is Leopardus colocola, endemic of Central Chile. The subspecies L. colocolo colocola has recently been elevated to the category of species [29, 108]. However, until the thesis of Zamora-Cornejo [158] in an Andean foothill range protected area of the Maule Region, there was no explicit knowledge about the colocolo's diet in its distribution range of Central Chile. Here, the diet shows a high proportion of exotic mammals and a small proportion of native mammals.

Concerning the north of the country, all papers in the Puna ecoregion have been conducted in non-anthropized areas (except [85]) and without exotic prey items in the diets of carnivores. Here, the lack of knowledge of the diet of the well-studied (in other latitudes) puma stands out. For this region, Perovic et al. [118] and Napolitano et al. [107] point out a high overlap in the trophic niche of L. garleppi and L. jacobita, highlighting the lack of information for the southern part of their distribution. Knowledge about the trophic ecology of these vulnerable species and their ecological interactions can increase significantly by considering the growing information collected and not published in the context of environmental consulting services for environmental impact studies of the highland mining industry, one of the main threats to the habitat of these cats [45, 80, 88]. For L. jacobita, it has been proposed their presence is not continuous throughout its distribution range [23], with isolated records found up to the Maule region (see Fig. 5) where no paper about its trophic ecology has been published. Regarding southern Chile, more papers are available on different species in the Subpolar Forest than the Patagonian Steppe, despite both areas having the same maximum species richness. Most of papers have been conducted in Torres del Paine and Tierra del Fuego National Park, both in the Magallanes region, highlighting the prevalence of exotic species and livestock in the diet of all carnivores except for the two aquatic species belonging to the genus Lontra. In Patagonia, replacing native prey with introduced species is a widespread phenomenon [109]. The natural diet composition of Patagonian carnivores has been dramatically altered in the last 150 years due to hunting and the widespread overgrazing by livestock. In the northern Patagonian cattle farms, native herbivores are ecologically extinct in their role as prey, and carnivores mainly consume exotic species [115]. Thus, as in the protected and anthropized landscapes of the Chilean hotspot, the change from native to exotic prey seems favorable for mammalian carnivores because exotic prey items are more profitable than most native prey due to their number, body size, and vulnerability. In areas of high livestock density, carrion also provides a widespread and profitable food source [12, 52, 63]. The extensive use of exotic resources by carnivores in Central and South Chile implies a clear conservation opportunity for these species. On the other hand, restoring native ecosystems may involve eradicating profitable prey such as lagomorphs, which are categorized as plague due to their native impact on vegetation [69, 73, 144], and native prey populations [24]. Thus, the primary importance of exotic animals as lagomorphs in the food webs lies in their positive or negative impact on the species with fewer interactions in the community, which could be more vulnerable if these exotic animals were controlled or extirpated [6, 52]. Predators with a narrow dietary range or hypercarnivores, such as Leopardus species, could depend on lagomorph abundance compared to native rodents. The lagomorph elimination plan will likely negatively affect the survival of puma in central Chile because it has become a great alternative in the absence of its native prey, such as Lama guanicoe [112]. Given this background, it is necessary to evaluate throughout the territory whether carnivores, both specialist and generalist, can increase their fitness (survival and reproduction) and become more abundant or less vulnerable in the areas where they can exploit these abundant introduced resources compared to carnivores in regions with a less altered native prey base. For instance, an open question is if Lycalopex foxes in Central Chile and Temperate Forest will show a higher fitness due to the exotic items in their diet compared to the Lycalopex foxes of the Puna and Atacama coastal desert. Several unresolved research questions at individual, populational, and communitarian levels may motivate new research to evaluate the apparent benefits and direct or indirect consequences for predators and their variation across the territory. Finally, studying the spatial patterns of the trophic ecology of the invasive N. vison in areas of the Temperate Forest and Subpolar Forest can aid in developing effective management strategies. Such studies can help identify priority areas for resource allocation and control efforts and help understand predation's impact [26]. There are already successful examples in the Lanín National Park in Argentina, where local birdlife has increased in abundance and richness after mink control [51]. The areas with the highest number of birds, located in regions with a high density of emergent vegetation, should be the primary focus for control efforts. It is important to consider that minks could seriously impact the nesting of solitary species found on the ground or shorelines with rocky outcrops [5, 123, 136].

Fig. 5
figure 5

The spatial relationship between the distribution of species richness of terrestrial mammalian carnivores in Chile and the number of study localities. a Localities by ecoregion and b Localities by administrative region

Cryptic community interactions

Knowledge of the trophic ecology of terrestrial mammalian carnivores is a helpful approach to understanding indirect and difficult-to-detect local relationships, such as cascading effects within a community. It is, therefore, a crucial tool to focus research interest on ecological interactions (e.g., predation, competition, mutualism) rather than individual species, being a more integrative approach to the biological conservation of entire communities. Example 1: L. griseus may influence the vegetation structure of the landscape by restricting the low-scale spatial distribution of Octodon degus, its main native prey in Central Chile, through predation and seed dispersal [14, 155]. Example 2: Given that the larvae of the cantaria (Chiasognathus grantii), a native lucanid beetle protected by the Chilean hunting law, are consumed in a high proportion by the invasive European wild boar (Sus scrofa) in southern Chile, an indirect effect of the predation by pumas on European wild boars would also have beneficial effects on the recovery of populations of these insects [146]. Example 3: In Chiloé, the occasional feeding of Bromeliaceae inflorescences could represent an adaptive and opportunistic behavior for L. fulvipes because thorny leaves surround the fruits in a rosette and are accessible to Darwin's fox only after the coipos (Myocastor coypus) feeding on the roots [38]. Example 4: The dietary study of semiaquatic carnivores can contribute to knowledge of the population status of endangered species or species of commercial interest. L. provocax has shown an important preference for Diplomystes camposensis, an endangered and endemic catfish species with little ecological information [43, 54]. Furthermore, knowing the feeding rate of prey that are also a fishing resource (e.g., Concholepas concholepas, Trachurus murphyi) can help manage the extraction quota responsibly, considering the availability of food for Lontra species [21, 90].

Challenges and opportunities

Although the most knowledge about the trophic ecology of mammalian carnivores in Chile is in the areas with the highest co-occurrence of these species, this review identifies two knowledge gaps. The first type is the null or low number of trophic papers for some species, such as C. chinga, G. cuja, L. patagonicus, L. pajeros, and L. colocola in Chile. This demonstrates a tangible difficulty in developing conservation strategies for their populations. A higher number of trophic studies in the different areas of the Chilean territory would allow us to correctly characterize the breadth of this niche axis to each species and thus have a most evident approach to the potential vulnerability to the change in available prey, to the anthropic effect, and to the particular predatory role of each species in different localities of their distribution. The second gap is the lack of information in specific areas of the country's strongly transformed and highly vulnerable landscapes, such as the Maule, O’Higgins, Valparaíso, and Ñuble regions. In Chile, the Ministerio del Medio Ambiente (MMA) is the organism that entrusts its Natural Resources and Biodiversity Division with the implementation and monitoring of biodiversity and allocates the necessary budget for the different administrative regions of the country. In this sense, we hope that this review contributes to the National Biodiversity Strategy 2017–2030 [102] and allows public entities and researchers to pay attention to knowledge about community dynamics that can be addressed by studying interactions between carnivores in different biogeographic and administrative regions of the territory. Indeed, this information can be vital to research and conservation efforts by focusing on specific administrative regions and indicator species such as mammalian carnivores.

Availability of data and materials

All data generated or analyzed during this study are included in this published article [and its supplementary information files].

References

  1. Altamirano TA, Hernández F, De La Maza M, Bonacic C. Güiña (Leopardus guigna) preys on cavity-nesting nestlings. Revista Chilena de Historia Natural. 2013;86(4):501–4.

    Article  Google Scholar 

  2. Arroyo MT, Marquet P, Marticorena C, Simonetti J, Cavieres L, Squeo F, Rozzi R, Massardo F. El hotspot chileno, prioridad mundial para la conservación. In: Ocho Libros Editores. Biodiversidad de Chile, patrimonio y desafíos. Santiago, Chile; 2008. 90–93 pp.

  3. Atalah AG, Sielfeld W, Venegas C. Antecedentes sobre el nicho trófico de Canis griseus Gray 1836, en Tierra del Fuego. Anales del Instituto de la Patagonia (Punta Arenas, Chile). 1980;11:259–71.

    Google Scholar 

  4. Bank MS, Sarno RJ, Campbell NK, Franklin WL. Predation of guanacos (Lama guanicoe) by southernmost mountain lions (Puma concolor) during a historically severe winter in Torres del Paine National Park. Chile Journal of Zoology. 2002;258(2):215–22.

    Article  Google Scholar 

  5. Banks PB, Nordström M, Ahola M, Salo P, Fey K, Korpimäki E. Impacts of alien mink predation on island vertebrate communities of the Baltic Sea Archipelago: review of a long-term experimental study. Boreal Environ Res. 2008;13:3.

    Google Scholar 

  6. Barbar F, Hiraldo F, Lambertucci SA. Medium-sized exotic prey creates novel food webs: the case of predators and scavengers consuming lagomorphs. PeerJ. 2016;4: e2273.

    Article  PubMed  PubMed Central  Google Scholar 

  7. Barton K. MuMIn: Multi-Model Inference. R package version 1.40.0. https://CRAN.R-project.org/package=MuMIn. 2017.

  8. Biodiversity Support Program, Conservation International, The Nature Conservancy, Wildlife Conservation Society, World Resources Institute, and World Wildlife Fund. A Regional Analysis of Geographic Priorities for Biodiversity Conservation in Latin America and the Caribbean. Biodiversity Support Program, Washington, D.C., USA. 1995; 140 pp.

  9. Bjornstad O. ncf: Spatial Covariance Functions. R package version 1.3–2, https://CRAN.R-project.org/package=ncf. 2022.

  10. Bonino N, Cossíos D, Menegheti J. Dispersal of the European hare, Lepus europaeus in South America. Folia Zool. 2010;59(1):9–15.

    Article  Google Scholar 

  11. Borrero LA, Martín FM, Vargas J. Tafonomía de la interacción entre pumas y guanacos en el Parque Nacional Torres del Paine. Chile Magallania (Punta Arenas). 2005;33(1):95–114.

    Google Scholar 

  12. Buenavista S, Palomares F. The role of exotic mammals in the diet of native carnivores from South America. Mammal Rev. 2018;48(1):37–47.

    Article  Google Scholar 

  13. Burnham KP, Anderson DR. Multimodel inference: understanding AIC and BIC in model selection. Sociological methods & research. 2004; 33(2):261-304.

  14. Campos CM, Ojeda RA. Dispersal and germination of Prosopis flexuosa (Fabaceae) seeds by desert mammals in Argentina. J Arid Environ. 1997;35(4):707–14.

    Article  Google Scholar 

  15. Carevic FS, Carmona ER, Cartes F, Taucare F. Contrasting variations in the diet of the Andean fox Lycalopex culpaeus Molina, 1782 on geographical and environmental scales in the Atacama Desert. Mammalia. 2019;83(5):439–46.

    Article  Google Scholar 

  16. Caro TM, O’Doherty G. On the use of surrogate species in conservation biology. Conserv Biol. 1999;13(4):805–14.

    Article  Google Scholar 

  17. Caro JI. Variación espacio-temporal de la dieta del visón americano Neovison vison, en relación a la presencia de aves y sus poblaciones reproductivas al interior del Santuario de la Naturaleza “Carlos Anwandter”. 2017. Veterinary Medicine Thesis, Universidad de Chile.

  18. Castilla JC, Bahamondes I. Observaciones conductuales y ecológicas sobre Lutra felina (Molina 1782) (Carnivora: Mustelidae) en las zonas central y centro-norte de Chile. Arch Biol Med Exp. 1979;12:119–32.

    Google Scholar 

  19. Castillo-Ravanal B, Vallejos-Garrido P, Rodríguez-Serrano E. Diet of Culpeo fox (Lycalopex culpaeus, Molina 1782): the role of non-native prey in a strongly seasonal environment of south-central Chile. Mammalia. 2021;85(2):123–6.

    Article  Google Scholar 

  20. Córdova O, Rau JR, Suazo CG, Arriagada A. Estudio comparativo de la ecología alimentaria del depredador de alto nivel trófico Lontra felina (Molina, 1782) (Carnivora: Mustelidae) en Chile. Rev Biol Mar Oceanogr. 2009;44(2):429–38.

    Article  Google Scholar 

  21. Córdova O, Rau JR. Interacción entre la pesca artesanal y el depredador de alto nivel trófico Lontra felina en Chile. Rev Biol Mar Oceanogr. 2016;51(3):621–7.

    Article  Google Scholar 

  22. Correa P, Roa A. Relaciones tróficas entre Oncifelis guigna, Lycalopex culpaeus, Lycalopex griseus y Tyto alba en un ambiente fragmentado de la zona central de Chile. Mastozoología Neotropical. 2005;12(1):57–60.

    Google Scholar 

  23. Cossíos ED, Walker RS, Lucherini M, Ruiz-García M, Angers B. Population structure and conservation of a high-altitude specialist, the Andean cat Leopardus jacobita. Endangered Species Research. 2012;16(3):283–94.

    Article  Google Scholar 

  24. Courchamp F, Langlais M, Sugihara G. Rabbits killing birds: modeling the hyperpredation process. J Anim Ecol. 2000;69(1):154–64.

    Article  Google Scholar 

  25. Courtin SL, Pacheco NV, Eldridge WD. Observaciones de alimentación, movimientos y preferencias de hábitat del puma, en el Islote Rupanco. Medio Ambiente. 1980;4(2):50–5.

    Google Scholar 

  26. Crego RD, Jiménez JE, Soto C, Barroso O, Rozzi R. Tendencias poblacionales del visón norteamericano invasor (Neovison vison) y sus principales presas nativas desde su arribo a isla Navarino, Chile. Boletín de la Red Latinoamericana para el Estudio de Especies Invasoras. 2014;4:4–18.

    Google Scholar 

  27. Crooks KR, Soulé ME. Mesopredator release and avifaunal extinctions in a fragmented system. Nature. 1999;400(6744):563.

    Article  CAS  Google Scholar 

  28. Crooks KR. Relative sensitivities of mammalian carnivores to habitat fragmentation. Conserv Biol. 2002;16(2):488–502.

    Article  Google Scholar 

  29. D’Elía G, Canto J, Ossa G, Verde-Arregoitia LD, Bostelmann E, Iriarte A, Amador L, Quiroga-Carmona M, Hurtado N, Cadenillas R, Valdez L. Lista actualizada de los mamíferos vivientes de Chile. Boletín Museo Nacional de Historia Natural. 2020;69(2):67–98.

    Article  Google Scholar 

  30. Dinerstein E, Olson DP, Graham DJ, Webster AL, Primm SA, Bookbinder MP, Ledec GC. A Conservation Assessment of the Terrestrial Ecoregions of Latin America and the Caribbean. Environ Conserv. 1995;23:378–9.

    Google Scholar 

  31. Donadio E, Di Martino S, Aubone M, Novaro AJ. Feeding ecology of the Andean hog-nosed skunk (Conepatus chinga) in areas under different land use in north-western Patagonia. J Arid Environ. 2004;56(4):709–18.

    Article  Google Scholar 

  32. Dunstone N, Freer R, Acosta-Jamett G, Durbin L, Wyllie I, Mazzolli M, Scott D. Uso del hábitat, actividad y dieta de la güiña (Oncifelis guigna) en el Parque Nacional Laguna San Rafael, XI Región, Chile. Boletín del Museo Nacional de Historia Natural (Chile). 2002;51:147–58.

    Article  Google Scholar 

  33. Durán JC, Cattan PE, Yañez JL. Food habits of foxes (Canis sp.) in the Chilean National Chinchilla Reserve. J Mammal. 1987;68(1):179–81.

    Article  Google Scholar 

  34. Ebensperger LA, Mella JE, Simonetti JA. Trophic-niche relationships among Galictis cuja, Dusicyon culpaeus, and Tyto alba in central Chile. J Mammal. 1991;72(4):820–3.

    Article  Google Scholar 

  35. Ebensperger LA, Botto-Mahan C. Use of habitat, size of prey, and food-niche relationships of two sympatric otters in southernmost Chile. J Mammal. 1997;78(1):222–7.

    Article  Google Scholar 

  36. Eisenberg JF, Redford KH. Mammals of the Neotropics, Volume 2: The Southern Cone: Chile, Argentina, Uruguay, Paraguay. University of Chicago Press; 1992.

  37. Elbroch LM, Wittmer HU. The effects of puma prey selection and specialization on less abundant prey in Patagonia. J Mammal. 2013;94(2):259–68.

    Article  Google Scholar 

  38. Elgueta EI, Valenzuela J, Rau JR. New insights into the prey spectrum of Darwin’s fox (Pseudalopex fulvipes Martin, 1837) on Chiloé Island. Chile Mammalian Biology-Zeitschrift für Säugetierkunde. 2007;72(3):179–85.

    Article  Google Scholar 

  39. Escobar A, Jackson D. Presencia de Rattus norvegicus (Rodentia: Muridae) en la dieta de Leopardus guigna (Carnivora: Felidae), en una zona suburbana del sur de Chile. Mammalogy Notes. 2023;9(1):364–364.

    Article  Google Scholar 

  40. ESRI ArcGIS for Desktop 10.4.1. Environmental Systems Research Institute, Redlands. 2016

  41. Figueroa RA, Corales ES, Rau JR. Prey of the güiña (Leopardus guigna) in an Andean mixed southern beech forest, southern Chile. Studies on Neotropical Fauna and Environment. 2018;53(3):211–8.

    Article  Google Scholar 

  42. Fleishman E, Thomson JR, Mac Nally R, Murphy DD, Fay JP. Using indicator species to predict species richness of multiple taxonomic groups. Conserv Biol. 2005;19(4):1125–37.

    Article  Google Scholar 

  43. Franco M, Guevara G, Correa L, Soto-Gamboa M. Trophic interactions of the endangered Southern river otter (Lontra provocax) in a Chilean Ramsar wetland inferred from prey sampling, fecal analysis, and stable isotopes. Naturwissenschaften. 2013;100(4):299–310.

    Article  CAS  PubMed  Google Scholar 

  44. Fretwell SD, Barach AL. The regulation of plant communities by the food chains exploiting them. Perspect Biol Med. 1977;20(2):169–85.

    Article  Google Scholar 

  45. Galende GI, Grigera D, von Thüngen J. Composición de la dieta del chinchillón (Lagidium viscacia, Chinchillidae) en el noroeste de la Patagonia. Mastozoología Neotropical. 1998;5(2):123–8.

    Google Scholar 

  46. Galuppo SE. Diet and activity patterns of Leopardus guigna in relation to prey availability in forest fragments of the Chilean temperate rainforest. Doctoral dissertation, University of Minnesota; 2014.

  47. Garrido PV, Oviedo DM, Silva DJ, Ávila JM. Uso y caracterización de letrinas de gato colocolo Leopardus colocolo (Molina, 1782) en el altiplano de la I Región de Tarapacá, Chile. Boletín Museo Nacional de Historia Natural. 2018;67(2):41–8.

    Article  Google Scholar 

  48. Gese EM. Territorial defense by coyotes (Canis latrans) in Yellowstone National Park, Wyoming: who, how, where, when, and why. Can J Zool. 2001;79(6):980–7.

    Article  Google Scholar 

  49. Getis A, Ord JK. The analysis of spatial association by use of distance statistics. Geogr Anal. 1992;24(3):189–206.

    Article  Google Scholar 

  50. Gittleman JL, Funk SM, MacDonald DW, Wayne, RK. (Eds.). Carnivore conservation (Vol. 5). Cambridge University Press; 2001.

  51. Girini JM, Palacio FX, Prieto C, Ferreyra N, Sanguinetti J, Fasola L, Peris S, Montalti D. Evaluación de impacto y manejo del visón americano, un depredador exótico invasor, en el Parque Nacional Lanín, Neuquén. Actas de las XXVII Jornadas Argentinas de Mastozoología, Esquel, Argentina. 2014.

  52. Gübelin P, Correa-Cuadros JP, Ávila-Thieme MI, Flores-Benner G, Duclos M, Lima M, Jaksić FM. European rabbit invasion in a semi-arid ecosystem of Chile: how relevant is its role in food webs? Life. 2023;13(4):916.

    Article  PubMed  PubMed Central  Google Scholar 

  53. Guzmán-Sandoval J, Sielfeld W, Ferrú M. Dieta de Lycalopex culpaeus (Mammalia: Canidae) en el extremo norte de Chile (Región de Tarapacá). Gayana. 2007;71(1):1–7.

    Google Scholar 

  54. Habit E, Jara A, Colin N, Oyanedel A, Victoriano P, González J, Solis-Lufí K. Threatened fishes of the world: Diplomystes camposensis Arratia, 1987 (Diplomystidae). Environ Biol Fishes. 2009;84(4):393–4.

    Article  Google Scholar 

  55. Hairston NG, Smith FE, Slobodkin LB. Community structure, population control, and competition. Am Nat. 1960;94(879):421–5.

    Article  Google Scholar 

  56. Hämäläinen A, Broadley K, Droghini A, Haines JA, Lamb CT, Boutin S, Gilbert S. The ecological significance of secondary seed dispersal by carnivores. Ecosphere. 2017;8(2): e01685.

    Article  Google Scholar 

  57. Harmsen BJ, Foster RJ, Silver S, Ostro L, Doncaster CP. Differential use of trails by forest mammals and the implications for camera-trap studies: a case study from Belize. Biotropica. 2010;42(1):126–33.

    Article  Google Scholar 

  58. Heilmayr R, Echeverría C, Fuentes R, Lambin EF. A plantation-dominated forest transition in Chile. Appl Geogr. 2016;75:71–82.

    Article  Google Scholar 

  59. Hinojosa-Sáez A, Avendaño I, Paredes J, Rau JR, Sade S. Depredación por zorros culpeos sobre huemules del sur en el Parque Nacional Bernardo O'Higgings, Patagonia Chilena. VI Reunión Binacional Sobre el Huemul. Libro de Resúmenes. 2011;(1):38–9.

  60. Ibarra JT, Fasola L, Macdonald DW, Rozzi R, Bonacic C. Invasive American mink Mustela vison in wetlands of the Cape Horn Biosphere Reserve, southern Chile: what are they eating? Oryx. 2009;43(1):87–90.

    Article  Google Scholar 

  61. Iriarte JA, Jiménez JE, Contreras LC, Jaksić FM. Small-mammal availability and consumption by the fox, Dusicyon culpaeus, in central Chilean scrublands. J Mammal. 1989;70(3):641–5.

    Article  Google Scholar 

  62. Iriarte JA, Franklin WL, Johnson WE, Redford KH. Biogeographic variation of food habits and body size of the American puma. Oecologia. 1990;85(2):185–90.

    Article  PubMed  Google Scholar 

  63. Iriarte JA, Johnson WE, Franklin WL. Feeding ecology of the Patagonia puma in southernmost Chile. Rev Chil Hist Nat. 1991;64:145–56.

    Google Scholar 

  64. Iriarte A, Jaksić FM. Los carnívoros de Chile, segunda edición revisada. Ediciones Flora & Fauna Chile y Centro UC CAPES, Pontífica Universidad Católica de Chile. Santiago de Chile, Chile. 2017; 260 pp.

  65. IUCN. 2024. The IUCN Red List of Threatened Species. Version 2024-1. https://www.iucnredlist.org. Accessed 22 Apr 2024.

  66. Jackson D, Escobar Á. Análisis del contenido alimenticio de una feca de zorro culpeo, Lycalopex culpaeus (Molina, 1782) (Mammalia: Canidae) de la Región de La Araucanía, Chile, con predominancia de Brachysternus patagoniensis Jameson y Smith, 2002 (Coleoptera: Scarabaeidae). Revista Chilena de Entomología. 2023;49(1).

  67. Jaksić FM, Schlatter RP, Yáñez JL. Feeding ecology of central Chilean foxes, Dusicyon culpaeus and Dusicyon griseus. J Mammal. 1980;61(2):254–60.

    Article  Google Scholar 

  68. Jaksić FM, Greene HW, Yáñez JL. The guild structure of a community of predatory vertebrates in central Chile. Oecologia. 1981;49(1):21–8.

    Article  Google Scholar 

  69. Jaksić FM, Fuentes ER. Ecology of a successful invader: the European rabbit in central Chile. Biogeography of Mediterranean Invasions (R.H. Groves and F. di Cstri, eds). Cambridge: Cambridge University Press. 1991; 273–284.

  70. Jaksić FM, Yáñez JL, Rau JR. Trophic relations of the southernmost populations of Dusicyon in Chile. J Mammal. 1983;64(4):693–7.

    Article  Google Scholar 

  71. Jaksić FM, Delibes M. A comparative analysis of food-niche relationships and trophic guild structure in two assemblages of vertebrate predators differing in species richness: causes, correlations, and consequences. Oecologia. 1987;71(3):461–72.

    Article  PubMed  Google Scholar 

  72. Jaksić FM, Jiménez JE, Medel RG, Marquet PA. Habitat and diet of Darwin’s fox (Pseudalopex fulvipes) on the Chilean mainland. J Mammal. 1990;71(2):246–8.

    Article  Google Scholar 

  73. Jaksić FM, Iriarte JA, Jiménez JE, Martínez DR. Invaders without frontiers: cross-border invasions of exotic mammals. Biol Invasions. 2002;4(1–2):157–73.

    Article  Google Scholar 

  74. Jiménez JE, Marquet PA, Medel RG, Jaksić FM. Comparative ecology of Darwin’s fox (Pseudalopex fulvipes) in mainland and island settings of southern Chile. Rev Chil Hist Nat. 1991;63:177–86.

    Google Scholar 

  75. Jiménez JE. Ecology of a coastal population of the critically endangered Darwin’s fox (Pseudalopex fulvipes) on Chiloé Island, southern Chile. J Zool. 2007;271(1):63–77.

    Article  Google Scholar 

  76. Jiménez JE, Crego RD, Soto GE, Román I, Rozzi R, Vergara PM. Potential impact of the alien American mink (Neovison vison) on Magellanic woodpeckers (Campephilus magellanicus) in Navarino Island, southern Chile. Biol Invasions. 2014;16(4):961–6.

    Article  Google Scholar 

  77. Johnson JB, Omland KS. Model selection in ecology and evolution. Trends Ecol Evol. 2004;19:101–8.

    Article  PubMed  Google Scholar 

  78. Johnson WE, Franklin WL. Feeding and spatial ecology of Felis geoffroyi in southern Patagonia. J Mammal. 1991;72(4):815–20.

    Article  Google Scholar 

  79. Johnson WE, Franklin WL. Role of body size in the diets of sympatric gray and culpeo foxes. J Mammal. 1994;75(1):163–74.

    Article  Google Scholar 

  80. Kaiser M, Hernández-Hernández J, Guzmán Marín BC. Gato andino (Leopardus jacobita, Cornalia, 1865) en carretera: nueva amenaza para su conservación. Acta Zoológica Lilloana. 2022;66(1):45–51.

    Google Scholar 

  81. Karanth KU, Stith BM. Importance of prey depletion in driving the Tiger’s decline. In: Seidensticker J, Christie S, Jackson P, editors. Riding the Tiger: Tiger Conservation in Human-Dominated Landscapes. Cambridge University Press, Cambridge: UK; 1999. p. 100–13.

    Google Scholar 

  82. Karanth KU, Nichols JD, Kumar NS, Link WA, Hines JE. Tigers and their prey: predicting carnivore densities from prey abundance. Proc Natl Acad Sci. 2004;101(14):4854–8.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  83. Klare U, Kamler JF, Macdonald DW. A comparison and critique of different scat-analysis methods for determining carnivore diet. Mammal Rev. 2011;41(4):294–312.

    Article  Google Scholar 

  84. Kohn MH, Wayne RK. Facts from feces revisited. Trends Ecol Evol. 1997;12(6):223–7.

    Article  CAS  PubMed  Google Scholar 

  85. Lagos N, Villalobos R, Vianna JA, Espinosa-Miranda C, Rau JR, Iriarte A. The spatial and trophic ecology of culpeo foxes (Lycalopex culpaeus) in the high Andes of northern Chile. Studies on Neotropical Fauna and Environment. 2021;58(3):564–73. https://doi.org/10.1080/01650521.2021.2005393

  86. Lichstein JW, Simons TR, Shriner SA, Franzreb KE. Spatial autocorrelation and autoregressive models in ecology. Ecol Monogr. 2002;72:445–63.

    Article  Google Scholar 

  87. Lobos G, Tapia G, Alzamora A, Rebolledo N, Salinas H, Trujillos JC, Girón G, Ascanio R. Dieta del zorro culpeo Lycalopex culpaeus (molina, 1782) durante la megasequía de chile central: Rol del ganado y evidencia de una alta interacción trófica entre mamíferos carnívoros. Mastozoología Neotropical. 2020;27(2):319–27.

    Article  Google Scholar 

  88. Lucherini M, Merino MJ. Perceptions of human-carnivore conflicts in the high Andes of Argentina. Mt Res Dev. 2008;28(1):81–5.

    Article  Google Scholar 

  89. Luebert F, Pliscoff P. Sinopsis bioclimática y vegetacional de Chile (Vol. 2). Santiago, Chile: Editorial Universitaria. 2017.

  90. Mangel JC, Whitty T, Medina-Vogel G, Alfaro-Shigueto J, Caceres C, Godley BJ. Latitudinal variation in diet and patterns of human interaction in the marine otter. Mar Mamm Sci. 2011;27(2):E14–25.

    Article  Google Scholar 

  91. Marquet PA, Torres-Mura JC. Food habits of Pseudalopex foxes in the Atacama desert, pre-Andean ranges. Mammalia. 1993;57(1).

  92. Martínez DR, Rau JR, Jaksić FM. Respuesta numérica y selectividad dietaria de zorros (Pseudalopex spp.) ante una reducción de sus presas en el norte de Chile. Revista Chilena de Historia Natural. 1993;66:195–202.

    Google Scholar 

  93. Medel RG, Jiménez JE, Jaksić FM, Yánez JL, Armesto JJ. Discovery of a continental population of the rare Darwin’s fox, Dusicyon fulvipes (Martin, 1837) in Chile. Biol Cons. 1990;51(1):71–7.

    Article  Google Scholar 

  94. Medina G. A comparison of the diet and distribution of southern river otter (Lutra provocax) and mink (Mustela vison) in southern Chile. J Zool. 1997;242(2):291–7.

    Article  Google Scholar 

  95. Medina G. Seasonal variations and changes in the diet of southern river otter in different freshwater habitats in Chile. Acta Theriol. 1998;43(3):285–92.

    Article  Google Scholar 

  96. Medina CE, Díaz CV, Delgado FA, Ynga GA, Zela HF. Dieta de Conepatus chinga (Carnivora: Mephitidae) en un bosque de Polylepis del departamento de Arequipa. Perú Revista Peruana de Biología. 2009;16(2):183–6.

    Article  Google Scholar 

  97. Medina-Vogel G, Rodríguez CD, Alvarez RE, Bartheld JL. Feeding ecology of the marine otter (Lutra felina) in a rocky seashore of the south of Chile. Mar Mamm Sci. 2004;20(1):134–44.

    Article  Google Scholar 

  98. Medina-Vogel G, González-Lagos C. Habitat use and diet of endangered southern river otter Lontra provocax in a predominantly palustrine wetland in Chile. Wildl Biol. 2008;14(2):211–20.

    Article  Google Scholar 

  99. Medina-Vogel G, Barros M, Organ JF, Bonesi L. Coexistence between the southern river otter and the alien invasive North American mink in marine habitats of southern Chile. J Zool. 2012;290(1):27–34.

    Article  Google Scholar 

  100. Meserve PL, Shadrick EJ, Kelt DA. Diets and selectivity of two Chilean predators in the northern semi-arid zone. Rev Chil Hist Nat. 1987;60(1):93–9.

    Google Scholar 

  101. Miller B, Dugelby B, Foreman D, Del Río CM, Noss R, Phillips M, Reading R, Soulé ME, Terborgh J, Willcox L. The importance of large carnivores to healthy ecosystems. Endangered Species Update. 2001;18(5):202–10.

    Google Scholar 

  102. Ministerio del Medio Ambiente, Gobierno de Chile. Estrategia Nacional de Biodiversidad 2017–2030. 2017. https://estrategia-aves.mma.gob.cl/wp-content/uploads/2023/03/MMA_2017_Estrategia_Nacional_Biodiversidad_2017-2030.pdf. Accessed 22 Mar 2024.

  103. Mittermeier RA, Turner WR, Larsen FW, Brooks TM, Gascon C. Global biodiversity conservation: the critical role of hotspots. In Biodiversity hotspots: distribution and protection of conservation priority areas (eds F. ZACHOS and J. HABEL). Berlin, Heidelberg: Springer Berlin Heidelberg. 2011; 3–22 pp.

  104. Moreira-Arce D, Vergara PM, Boutin S, Simonetti JA, Briceño C, Acosta-Jamett G. Native Forest replacement by exotic plantations triggers changes in prey selection of mesocarnivores. Biol Cons. 2015;192:258–67.

    Article  Google Scholar 

  105. Muñoz-Pedreros A, Yáñez J, Norambuena HV, Zúñiga A. Diet, dietary selectivity and density of South American grey fox, Lycalopex griseus. Central Chile Integrative Zoology. 2018;13(1):46–57.

    Article  PubMed  Google Scholar 

  106. Myers N, Mittermeier RA, Mittermeier CG, Da Fonseca GA, Kent J. Biodiversity hotspots for conservation priorities. Nature. 2000;403(6772):853.

    Article  CAS  PubMed  Google Scholar 

  107. Napolitano C, Bennett M, Johnson WE, O’Brien SJ, Marquet PA, Barría I, Poulin E, Iriarte A. Ecological and biogeographical inferences on two sympatric and enigmatic Andean cat species using genetic identification of faecal samples. Mol Ecol. 2008;17(2):678–90.

    Article  CAS  PubMed  Google Scholar 

  108. Nascimento FOD, Cheng J, Feijó A. Taxonomic revision of the pampas cat Leopardus colocola complex (Carnivora: Felidae): an integrative approach. Zool J Linn Soc. 2020;191(2):575–611.

    Article  Google Scholar 

  109. Novaro AJ, Funes MC, Walker RS. Ecological extinction of native prey of a carnivore assemblage in Argentine Patagonia. Biological Conservation. 2000; 92(1),:25-33.

  110. Nuñez P. Ecología alimentaria de la nutria marina chungungo (Lontra felina; Molina, 1782) en la Isla Guafo, Región de los Lagos, Chile. 2014. Tesis de Grado, Universidad Austral de Chile, Valdivia, Chile.

  111. Oksanen L, Fretwell SD, Arruda J, Niemela P. Exploitation ecosystems in gradients of primary productivity. Am Nat. 1981;118(2):240–61.

    Article  Google Scholar 

  112. Osorio C, Muñoz A, Guarda N, Bonacic C, Kelly M. Exotic prey facilitate coexistence between Pumas and Culpeo Foxes in the Andes of central Chile. Diversity. 2020;12(9):317.

    Article  Google Scholar 

  113. Ostfeld RS, Ebensperger L, Klosterman LL, Castilla JC. Foraging, Activity Budget, and Social-Behavior of the South-American Marine Otter Lutra felina (Molina 1782). Natl Geogr Res. 1989;5(4):422–38.

    Google Scholar 

  114. Otavo S, Echeverría C. Fragmentación progresiva y pérdida de hábitat de bosques naturales en uno de los hotspot mundiales de biodiversidad. Revista Mexicana de Biodiversidad. 2017;88(4):924–35.

    Article  Google Scholar 

  115. Palacios R, Walker RS, Novaro AJ. Differences in diet and trophic interactions of Patagonian carnivores between areas with mostly native or exotic prey. Mammalian Biology-Zeitschrift für Säugetierkunde. 2012;77(3):183–9.

    Article  Google Scholar 

  116. Pavéz EF, Lobos GA, Jaksić FM. Cambios de largo plazo en el paisaje y los ensambles de micromamíferos y rapaces en Chile central. Rev Chil Hist Nat. 2010;83(1):99–111.

    Article  Google Scholar 

  117. Pebesma E, Bivand R. Spatial Data Science with Applications in R. Chapman & Hall. 2023. https://r-spatial.org/book.

  118. Perovic P, Walker S, Novaro A. New records of the Endangered Andean mountain cat in northern Argentina. Oryx. 2003;37(3):374–7.

    Article  Google Scholar 

  119. Poblete AA, Gorski K, Moscoso J. Estimation of the diet of chungungo Lontra felina (Molina, 1782) in two locations of the coast of the Biobío region, Chile. Gayana. 2019;83(1):1–9.

    Google Scholar 

  120. Prevosti FJ, Pardiñas UFJ. Variaciones corológicas de Lyncodon patagonicus (Carnivora, Mustelidae) durante el Cuaternario. Mastozoología Neotropical. 2001;8(1):21–39.

    Google Scholar 

  121. Prevosti FJ, Teta P, Pardiñas UF. Distribution, natural history, and conservation of the Patagonian Weasel Lyncodon patagonicus. Small Carnivore Conservation. 2009;41:29–34.

    Google Scholar 

  122. R Core Team. R: A language and environment for statistical computing. R Foundation for Statistical Computing, Vienna, Austria. 2023. https://www.R-project.org.

  123. Ratcliffe N, Craik C, Helyar A, Roy S, Scott M. Modelling the benefits of American Mink Mustela vison management options for terns in west Scotland. Ibis. 2008;150:114–21.

    Article  Google Scholar 

  124. Rau JR, Tillería M, Martínez D, Muñoz AH. Dieta de Felis concolor (Carnivora: Felidae) en áreas silvestres protegidas del sur de Chile. Rev Chil Hist Nat. 1991;64:139–44.

    Google Scholar 

  125. Rau JR, Martínez DR, Low JR, Tilleria MS. Depredación por zorros chillas (Pseudalopex griseus) sobre micromamíferos cursoriales, escansoriales y arborícolas en un área silvestre protegida del sur de Chile. Rev Chil Hist Nat. 1995;68:333–40.

    Google Scholar 

  126. Rau JR, Jiménez JE. Dieta otoño-invernal del zorro de Darwin: una comparación en dos hábitats de Chiloé. Chile Gestión Ambiental. 2002;8:57–62.

    Google Scholar 

  127. Rau JR, Jiménez JE. Diet of puma (Puma concolor, Carnivora: Felidae) in coastal and Andean ranges of southern Chile. Studies on Neotropical Fauna and Environment. 2002;37(3):201–5.

    Article  Google Scholar 

  128. Ripple WJ, Estes JA, Beschta RL, Wilmers CC, Ritchie EG, Hebblewhite M, Berger J, Elmhagen B, Letnic M, Nelson MP, Schmitz OJ, Smith DW, Wallach AD, Wirsing AJ. Status and ecological effects of the world’s largest carnivores. Science. 2014;343(6167):1241484.

    Article  PubMed  Google Scholar 

  129. Root RB. The niche exploitation pattern of the blue-gray gnatcatcher. Ecol Monogr. 1967;37(4):317–50.

    Article  Google Scholar 

  130. Rubio AV, Alvarado R, Bonacic C. Introduced European rabbit as main prey of the native carnivore culpeo fox (Lycalopex culpaeus) in disturbed ecosystems of central Chile. Studies on Neotropical Fauna and Environment. 2013;48(2):89–94.

    Article  Google Scholar 

  131. Sade S, Rau JR, Orellana JI. Dieta del quique (Galictis cuja) (Molina 1782) en un remanente de bosque valdiviano fragmentado del sur de Chile. Gayana. 2012;76(2):112–6.

    Google Scholar 

  132. Sandoval R, Bahamonde A, Lagos C, Calderón J. Control de visón (Neovison vison) mediante remoción no selectiva de individuos en Monumento Natural Dos Lagunas: I Informe de Avance. Chile: Informe técnico SAG-CONAF. Región de Aysén; 2014.

    Google Scholar 

  133. Sanino GP, Meza MI. Ecología trófica y simpatría de nutrias (Lontra felina y Lontra provocax) en la reserva Añihué, Patagonia chilena. Boletín Museo Nacional de Historia Natural. 2016;65:279–89.

    Article  Google Scholar 

  134. Schoener TW. Resource partitioning in ecological communities. Science. 1974;185(4145):27–39.

    Article  CAS  PubMed  Google Scholar 

  135. Schüttler E, Cárcamo J, Rozzi R. Diet of the American mink Mustela vison and its potential impact on the native fauna of Navarino Island, Cape Horn Biosphere Reserve. Chile Revista Chilena de Historia Natural. 2008;81(4):585–98.

    Google Scholar 

  136. Schüttler E, Klenke R, McGehee S, Rozzi R, Jax K. Vulnerability of ground-nesting waterbirds to predation by invasive American mink in the Cape Horn Biosphere Reserve. Chile Biological Conservation. 2009;142(7):1450–60.

    Article  Google Scholar 

  137. Sepúlveda MA, Bartheld JL, Meynard C, Benavides M, Astorga C, Parra D, Medina-Vogel G. Landscape features and crustacean prey as predictors of the Southern river otter distribution in Chile. Anim Conserv. 2009;12(6):522–30.

    Article  Google Scholar 

  138. Sielfeld WK. Alimentación de las nutrias L. felina y L. provocax en el medio marino al sur del Canal de Beagle. Resúmenes Primera Reunión de Trabajo de Expertos en Mamíferos Acuáticos de América del Sud. 1984; p.-40, 25–29.

  139. Sielfeld WK. Dieta del chungungo (Lutra felina (Molina, 1782) (Mustelidae, carnivora) en chile Austral. Investigaciones en Ciencia y Tecnología, Serie: Ciencias del Mar. 1990;1:23–9.

    Google Scholar 

  140. Silva SI, Bozinovic F, Jaksić FM. Frugivory and seed dispersal by foxes in relation to mammalian prey abundance in a semiarid thornscrub. Austral Ecol. 2005;30(7):739–46.

    Article  Google Scholar 

  141. Silva-Rodriguez EA. Evaluación de conflictos entre zorros chilla (Pseudalopex griseus) y agricultura de subsistencia en una localidad rural del sur de Chile: ¿mito o realidad?. 2006. Veterinary Medicine Thesis, Universidad Austral de Chile.

  142. Simonetti JA. Human-induced dietary shift in Ducicyon culpaeus. Mammalia. 1986;50:406–8.

    Google Scholar 

  143. Simonetti JA. Diversity and conservation of terrestrial vertebrates. Rev Chil Hist Nat. 1999;72:493–550.

    Google Scholar 

  144. Simonetti JA, Fuentes ER. Shrub preferences of native and introduced Chilean matorral herbivores. Acta oecologica Oecologia Applicata. 1983;4(3):269–72.

    Google Scholar 

  145. Simonetti JA, Poiani A, Raedeke KJ. Food habits of Dusicyon griseus in northern Chile. J Mammal. 1984;65(3):515–7.

    Article  Google Scholar 

  146. Skewes O, Moraga CA, Arriagada P, Rau JR. El jabalí europeo (Sus scrofa): Un invasor biológico como presa reciente del puma (Puma concolor) en el sur de Chile. Rev Chil Hist Nat. 2012;85(2):227–32.

    Article  Google Scholar 

  147. Skewes O, Jaksić FM. History of the introduction and present distribution of the european wild boar (Sus scrofa) in Chile. Mastozoología Neotropical. 2015;22(1):113–24.

    Google Scholar 

  148. Solervicens J. Consideraciones generales sobre los insectos, el estado de su conocimiento y las colecciones. Diversidad Biológica de Chile. 1995; 198–210.

  149. Taper ML, Marquet PA. How do species really divide resources? Am Nat. 1996;147(6):1072–86.

    Article  Google Scholar 

  150. Terborgh J, Winter B. Some causes of extinction. Conserv Biol. 1980;2:402–3.

    Article  Google Scholar 

  151. Valenzuela AE, Rey AR, Fasola L, Schiavini A. Understanding the inter-specific dynamics of two co-existing predators in the Tierra del Fuego Archipelago: the native southern river otter and the exotic American mink. Biol Invasions. 2012;15(3):645–56.

    Article  Google Scholar 

  152. Vergara OE, Jerez V, Parra LE. Diversidad y patrones de distribución de coleópteros en la Región del Biobío, Chile: una aproximación preliminar para la conservación de la diversidad. Rev Chil Hist Nat. 2006;79(3):369–88.

    Article  Google Scholar 

  153. Villegas MJ, Aron A, Ebensperger LA. The influence of wave exposure on the foraging activity of marine otter, Lontra felina (Molina, 1782) (Carnivora: Mustelidae) in northern Chile. J Ethol. 2007;25(3):281–6.

    Article  Google Scholar 

  154. Wilson P. Puma predation on guanacos in Torres del Paine National Park. Chile Mammalia. 1984;48(4):515–22.

    Google Scholar 

  155. Yáñez JL, Jaksić FM. Rol ecológico de los zorros (Dusicyon) en Chile central. Anales del Museo de Historia Natural de Valparaíso. 1978;11:105–12.

    Google Scholar 

  156. Yáñez JL, Rau JR. Dieta estacional de Dusicyon culpaeus (Canidae) en Magallanes. Anales del Museo de Historia Natural de Valparaíso. 1980;13:189–91.

    Google Scholar 

  157. Yáñez JL, Cárdenas JC, Gezelle P, Jaksić FM. Food habits of the southernmost mountain lions (Felis concolor) in South America: natural versus livestocked ranges. J Mammal. 1986;67(3):604–6.

    Article  Google Scholar 

  158. Zamora-Cornejo FA. Niche aspects that allow the coexistence of a carnivore community in different habitats of andean mountain range in central Chile. 2024. Master Thesis, Universidad de Concepción.

  159. Zúñiga AH, Fuenzalida V. Dieta del zorro culpeo (Lycalopex culpaeus Molina 1782) en un área protegida del sur de Chile. Mastozoología Neotropical. 2016;23(1):201–5.

    Google Scholar 

  160. Zúñiga AH, Fuenzalida V, Sandoval R. Diet of the gray fox Lycalopex griseus in an agroecosystem of southern-central Chile. Therya. 2018;9(2):179–83.

    Article  Google Scholar 

  161. Zúñiga AH, Fuenzalida V, Sandoval R, Encina F. Seasonal variation in the diet of two predators in an agroecosystem in southern–central Chile. Anim Biodivers Conserv. 2021;44(1):89–102.

    Article  Google Scholar 

  162. Zúñiga AH, Muñoz-Pedreros A. Hábitos alimentarios de Puma concolor (Carnivora, Felidae) en bosques fragmentados del sur de Chile. Mastozoología Neotropical. 2014;21(1):157–61.

    Google Scholar 

  163. Zúñiga AH, Muñoz-Pedreros A, Fierro A. Dieta de Lycalopex griseus (Gray, 1837) (Mammalia: Canidae) en la depresión intermedia del sur de Chile. Gayana. 2008;72(1):113–6.

    Google Scholar 

  164. Zúñiga AH, Quintana V, Fierro A. Relaciones tróficas entre depredadores en un ambiente fragmentado del sur de Chile. Gestión Ambiental. 2005;11(1):31–42.

    Google Scholar 

  165. Zúñiga AH, Rau JR, Fuenzalida V, Fuentes-Ramírez A. Temporal changes in the diet of two sympatric carnivorous mammals in a protected area of south–central Chile affected by a mixed–severity forest fire. Anim Biodivers Conserv. 2020;43(2):177–86.

    Article  Google Scholar 

  166. Zúñiga AH, Rau JR, Sandoval R, Fuenzalida V. Landscape use and food habits of the chilla fox (Lycalopex griseus, Gray) and domestic dog (Canis lupus familiaris) in a peri-urban environment of south-central Chile. Folia Oecologica. 2022;49(2):159–67.

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Acknowledgements

We acknowledge the enjoyable discussions with various colleagues that have inspired a better approach to the problems for the conservation of the fauna of southern South America. We are deeply grateful for the important insights, comments and discussions made by the reviewers.

Funding

This work was founded by ANID FONDECYT Grants 1201506 and 1220998, and VRID-UdeC Grant VRID220.113.100-INV.

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P. V-G devised the research, conducted the literature search, organized and systematized the spatial data, prepared the results tables, coordinated the collaborations, and wrote the manuscript; F. Z–C cooperated in the literature search, organized and systematized the spatial data, and made Figs. 2 and 3; R.R. performed the statistical and spatial analyzes presented in Figs. 4 and 5; F. C-R helped in updating the literature search and systematizing the information; E. R-S cooperated in the draft of the manuscript and final revision of the document. All authors reviewed the final version of the document.

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Correspondence to Paulo Vallejos-Garrido.

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Vallejos-Garrido, P., Zamora-Cornejo, F., Rivera, R. et al. Where is dinner? The spatiality of the trophic niche of terrestrial mammalian carnivores in Chile, a systematization for their conservation. Rev. Chil. de Hist. Nat. 97, 8 (2024). https://doi.org/10.1186/s40693-024-00131-x

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