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The garden dormouse is a European mammal whose range has shrunk rapidly within the last 40-50 years, disappearing from large parts of Central and Eastern Europe. This ongoing decline is worrying, especially because the underlying reasons are poorly understood. Since 2018, the German-wide project 'In Search of the Garden Dormouse' aims to reveal and investigate causes for this drastic decline. The current garden dormouse distribution has been assessed using a large-scale citizen science approach. Dormouse records were gathered via an online reporting tool and systematically by biologists and citizen science volunteers with different methods. The current garden dormouse distribution in Germany is divided into several isolated areas. The species is currently common in central and southwestern parts of Germany but has declined or is even locally extinct in several regions. A range loss of ca. 35 % since 2 Büchner S. et al. 1970 could be calculated. The observations in some urban areas are so numerous that vital populations can be assumed for this part of the range, in contrast to a decline in several low mountainous areas. The project provides insights into the biology and ecology of an endangered and understudied species; it has shown that a small mammal can become a flagship species. It successfully raised awareness of dormouse conservation needs with the public.
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*Corresponding author: muscardinus@gmx.net
ACTA ZOOLOGICA BULGARICA
The Garden Dormouse as a Research and Conservation
Priority in a German Large-Scale Citizen Science Project
Sven Büchner1*, Johannes Lang1, Holger U. Meinig1, Teresa F. Nava1, Katharina Zistl1,
Alina von Thaden2,3, Carsten Nowak2,3, Tobias E. Reiners2, Harald Brünner4, Franz Langer4,
Andrea Andersen5, Uwe Friedel11, Anita Giermann12, Eckardt Kasch6, Mechthild Klocke5,
Andrea Krug13, Jenny Kupfer5, Thomas Mölich12, Hartmut Schmid7, Jutta Schreiner14,
Susanne Steib15, Christine Thiel-Bender16, Nicola Moczek8, Joanna Fietz9 & Christelle Nowack10
1 Justus-Liebig-University Giessen, Clinic for Birds, Reptiles, Amphibians and Fish, Working Group for Wildlife Research, Frankfurter
Strasse 114, D-35392 Giessen, Germany; E-mails: muscardinus@gmx.net, johannes.lang@vetmed.uni-giessen.de,
holger.meinig@t-online.de, Teresa.Nava@vetmed.uni-giessen.de, katharina.zistl@gmail.com
2 Conservation Genetics Group, Senckenberg Research Institute and Natural History Museum Frankfurt, Clamecystrasse 12, D-63571
Gelnhausen, Germany; E-mails: vonthaden.research@gmail.com, Carsten.Nowak@senckenberg.de, Tobias.Reiners@Senckenberg.de
3 LOEWE Centre for Translational Biodiversity Genomics (LOEWE-TBG), Senckenberganlage 25, D-60325 Frankfurt am Main,
Germany
4 Arbeitsgruppe Wildlebende Säugetiere Baden-Württemberg e.V., Birkenstraße 9, D-72072 Tübingen, Germany;
E-mail: Kontakt@agws-bw.de
5 BUND Bund für Umwelt und Naturschutz Deutschland e. V. (BUND Friends of the Earth Germany, Kaiserin-Augusta-Allee 5,
D-10553 Berlin, Germany; E-mails: Andrea.Andersen@bund.net, Mechthild.Klocke@bund.net, Jenny.Kupfer@bund.net
6 Wörth 4, D-82389 Böbing, Germany; E-mails: eckardtkasch@yahoo.de
7 Prüllstr. 56, D-93093 Donaustauf, Germany; E-mail: hart.schmid@t-online.de
8 PSY:PLAN Institut für Architektur- und Umweltpsychologie, Libauer Str. 14, D-10245 Berlin, Germany; E-mail: moczek@psyplan.de
9 
E-mail: Joanna.Fietz@uni-hohenheim.de
10 Bundesprogramm Biologische Vielfalt, DLR Projektträger, Heinrich-Konen-Str. 1, 53227 Bonn, Germany; E-mail: Christelle.
Nowack@dlr.de
11 BUND Naturschutz Bayern, Hessestraße 4, D-90443 Nürnberg, Germany; E-mail: Uwe.Friedel@bund-naturschutz.de
12
13 BUND Niedersachsen, Goebenstraße 3a, D-30161 Hannover, Germany; E-mails: Andrea.Krug@nds.bund.net
14 BUND Rheinland-Pfalz, Hindenburgplatz 3, D-55118 Mainz, Germany; E-mail: Jutta.Schreiner@bund-rlp.de
15 BUND Hessen, Geleitsstraße 14, D-60599 Frankfurt am Main, Germany; E-mail: susanne.steib@bund-hessen.de
16 BUND NRW, Merowingerstraße 88, D-40225 Düsseldorf, Germany; E-mail: christine.thiel-bender@bund-nrw.de
Abstract: The garden dormouse is a European mammal whose range has shrunk rapidly within the last 40–50
years, disappearing from large parts of Central and Eastern Europe. This ongoing decline is worrying,
especially because the underlying reasons are poorly understood. Since 2018, the German-wide project
‘In Search of the Garden Dormouse’ aims to reveal and investigate causes for this drastic decline. The
current garden dormouse distribution has been assessed using a large-scale citizen science approach.
Dormouse records were gathered via an online reporting tool and systematically by biologists and citi-

divided into several isolated areas. The species is currently common in central and southwestern parts
of Germany but has declined or is even locally extinct in several regions. A range loss of ca. 35 % since
Research Article
Acta Zool. Bulg., Supplement 19, Published online 29 December 2023
Proceedings, 11th International Dormouse Conference
Svilengrad, Bulgaria, 9-13 May 2022
https://www.acta-zoologica-bulgarica.eu/2023/Suppl_19_02
2
Büchner S. et al.
1970 could be calculated. The observations in some urban areas are so numerous that vital populations
can be assumed for this part of the range, in contrast to a decline in several low mountainous areas. The
project provides insights into the biology and ecology of an endangered and understudied species; it has

conservation needs with the public.
Key words: In Search of the Garden Dormouse, geographic range, ecology, conservation, Eliomys quercinus
Introduction
As the earth is losing species at an alarming rate
( et al. 2011), adequate data on geographic
distribution and species’ conservation status become
essential for a conservation strategy. Data on species
distribution are generally collected by continuous
 et al. 2007, -
 et al. 2018, ).
Key principles include an appropriate monitoring
design and its integration into management actions,
involvement of people and organizations, sound
data management and public outreach ( et
al. 2018). At the same time, attributes such as rar-
ity, low detectability, a cryptic lifestyle, and narrow
habitat niches present particular challenges associ-
ated with monitoring of threatened taxa ( et
al. 2007). This is why data collected on threatened
species often focus on geographic distribution and
trends ( 2021). Distribu-
tion maps based on reliable observations represent
-
ing conservation strategies.
The garden dormouse is a European mammal
whose range has shrunk rapidly within the last 40–
50 years, disappearing from large parts of Central
and Eastern Europe ( 2017). This ongo-
ing decline is worrying, especially because the un-
derlying reasons are poorly understood (
2017). Although various hypotheses were discussed
among dormice experts – such as during some of
the previous International Dormouse Conferences
( 2003) - no conspicuous drivers for the
     -
trasting habitats occupied by garden dormice. In
Germany, for example, habitats range from vine-
yards, gardens and settlements in the warmest re-
gions, to predominantly cold and damp areas such as
spruce forests and boulders in low mountain ranges
( 2012). Based on this diversity,
garden dormice appear adaptable in terms of habitat.
-
tive conservation strategy look like?
Despite the urgent need for accurate data on the
species’ distribution and its ecology for developing
conservation measures, the garden dormouse has
rarely been in the focus of current research until re-
cently ( et al. 2022). Since 2018, the German-
wide project ‘In Search of the Garden Dormouse’
aims to investigate causes for this drastic decline.

strategy is being developed and will be implement-
ed. In particular, the project encompasses research
on the current versus previous garden dormouse
distribution in Germany; genetic diversity; phenol-
ogy, such as daily activity, timing of hibernation and
     
feeding ecology and spatial variation in diet com-
position; as well as causes of mortality, diseases
and parasite load. This broad research approach is
realised as a joint project, involving the Friends of
the Earth Germany (BUND), the Conservation Ge-
netics Group at Senckenberg Research Institute, the
Justus-Liebig-University Giessen and several part-
ners as well as hundreds of citizen scientists. The
project is funded within the Federal Programme for
Biological Diversity by the German Federal Agency
for Nature Conservation. Here, we describe the re-
sults of the current garden dormouse distribution in
Germany, representing the basis for all subsequent
conservation measures.
Materials and Methods
The project is the joint work of biologists, students
      
levels of involvement. A crowd science approach
was chosen to map the distribution of the garden dor-
mouse in Germany. A reporting tool on the project
website was installed (https://www.gartenschlaefer.
de/en/reporting-tool/). One challenge to this approach

some other projects, the ratio of data sets submitted
by volunteers to usable data sets was criticised as low
(Hunter et al. 2012). Limited training, background
knowledge and expertise of CSV can potentially lead
to poor quality or misleading data being submitted
  
was invested to train volunteers in this project. The
reporting tool collects data on the observed dormouse
species: all four species occurring in Germany could
be reported: garden dormouse (Eliomys quercinus),
The Garden Dormouse as a Research and Conservation Priority in a German Large-Scale Citizen Science
3
edible dormouse (Glis glis), hazel dormouse (Mus-
cardinus avellanarius) and forest dormouse (Dryo-
mys nitedula). Respective observation date and lo-
cation (a map application was developed to allow to
mark the point and get geographic coordinates) and
the type of observation are to be added. The reporting
tool also allows adding remarks. Observers are fur-
ther requested to upload images, videos or recorded
      

Evaluation Criteria (SMEC) (Table 1), which were
      
2021,  et al. 2023).
The online reporting tool is available online
since April 2019. It was promoted and supported
by ongoing public relations work within the project,
consisting of approx. 12,500 media articles (TV, ra-
dio, newspapers and journals until the end of 2021
resulting in 2 billion reads) and social media (about
250,000 post shares p.a.). The project’s actions were
        -
tary about the project, a cooperation with Museum
Wiesbaden for a new exhibition entitled Germany’s
Panda – The Garden Dormouse (https://museum-
wiesbaden.de/deutschlands-panda-der-garten-
      
Citizen Science Forum (https://www.buergerschaf-
fenwissen.de/projekt/spurensuche-gartenschlaefer)
or Environmental Week (hosted by the Federal Pres-
ident of Germany, https://www.woche-der-umwelt.
de/ausstellerKonkret/1587) as well as national and
regional garden dormouse conferences.
Until 15th of December 2022, approx. 5,000
persons reported their observations at the online
    
done by some of the authors (SB, HM, JL, KZ, TN,
AA) and, since 2022, also supported by special
trained volunteers.
A more labour-intensive involvement for vol-
unteers (more than 450 persons) was taking part in
an active search for the garden dormouse. Methods
used for an active search were footprint tunnels
(  et al. 2018, -
 et al. 2020), camera traps ( et al. 2016,
 2016) and checking of nest-
boxes ( et al. 2020). Active searches were
coordinated by the regional chapters of the BUND
in consultation with the whole project team. The
main focus of the active search were 10 km raster
cells of the European Environment Agency (EEA)-
Table 1. Small Mammal Evaluation Criteria (SMEC) used for evaluating garden dormouse reports (from  2021,

Category Denition
C1 Absolutely unambiguous: The report represents positive evidence. The evidence is substantiated by photos, videos,

C2 Very likely: The report comes from an expert. The report cannot be re-checked; it cannot be re-determined. This
observation is also counted as evidence.
C3 Uncertain: The report cannot be counted as evidence.
C3a
Promising
species are described (e.g., eye mask for the garden dormouse). A longer observation time, e.g., over several min-


C3b Possible: The report is not typical, cannot be clearly assigned to the target species, or there is not enough informa-
tion to assign the report to a higher category.
C4 False report: The report is demonstrably not the target species or the report is obviously incorrectly located (con-

C5
Translocated: This level is particularly important. Strictly speaking, the level translocated is also a sub-level of “ab-
-
tive detection, categories C1 or C2), but the animal did not arrive at the site by natural dispersal but was passively
moved to the site for other reasons. One of the following statements applies to this: The site of discovery is outside
the species area. The site of discovery does not represent a suitable habitat for a population capable of reproducing,


habitats are not considered as category C5.
C6 No assessment possible

C0 Active search without result (so called zero counts, used additionally for the project work, not used in the online
reporting tool)
4
Büchner S. et al.
grid without records so far, and with either (i) old
records, or (ii) close by known populations, or (iii)
several C3a reports from the online reporting tool.
Detailed information was provided to volun-
teers on where and how to use the methods. For
each plot, a consecutive protocol with date, place,
observer and remarks was kept.
Footprint tunnels (7,542 in total) were placed
in transects of 25 tunnels, reduced to 12 tunnels at
some places in 2021. Distances between the tunnels
were 20–25 m. During the active garden dormouse
season, the tunnels were checked every fortnight, the
tracking cards were replaced and the ink refreshed.

key for the footprints. Cards with prints were stored,

soon as a garden dormouse could be reported, the
tunnels were moved to the next transect.
In total, 567 camera traps were used (Minox
DTC 550, Minox GmbH, Isny, Germany). The cam-
era traps were put up at 50–70 cm height from the
ground on a tree trunk. Bait was placed (a sponge
with nut oil or apple juice) at a distance of approxi-
mately 1.5 m. The cameras were checked at least
monthly when batteries and memory cards were ex-
changed. Data on memory cards were uploaded to a

found, the camera was transferred to a new site.
Nestboxes, deployed in 24 transects, played
only a minor role for the search of garden dormouse
presence. A total of 500 wooden boxes measuring
20x20x21 cm were used, sited with the entrance
hole (diameter 32 mm) facing the tree trunk. Vol-
unteers also collected garden dormouse carcasses
( et al. 2023) and DNA samples
and provided them for research.
In addition, we conducted surveys for garden
 
et al., in press), checked samples in museums in
Germany and the monitoring databases of the Ger-
man Federal States.
All collected data were combined in a central
project database that will be maintained long-term
and available beyond the end of the project. The to-
tal surface area (in km²) of the current range was
calculated according to the guidelines for reporting
the range of a species under the European Habitats
      DG
 2017,   
2010). A ‘gap distance’ of 20 km was used as the
distance between two distribution grids that will not
be joined together to form a single range polygon
but will be shown as discontinuities in a range (DG
2017).
The project has been supported and still is sup-
ported by accompanying social research. The focus
is on the experiences of the CSV in the collaborative
research project and therefore several surveys are
carried out ( 2020).
Results
In total, 16,557 data are included in the database
by December 15th 2022. The majority consists of
records on the garden dormouse (not exclusively
from Germany), followed by C3 reports, records of
edible and hazel dormice, reports of the categories
C4-6 and zero counts (C0). Most of the collected
evidence comes from observations registered on the
online reporting tool (Table 2). Reports of dormice
via this tool were sent in almost daily, with peaks
during the summer months of more than 10 new re-
ports per day.
Garden dormice are currently common in the
central part of Rhineland-Palatinate (RP), south-
ern Hesse (HE) and North Rhine-Westphalia (NW)
along river Rhine. The species also occurs in clus-
ters in the mountains of Harz, Thuringian Schief-
ergebirge and Bavarian Frankenwald and Fichtel-
gebirge as well as the Black Forest (Fig. 1). Some
isolated populations could be documented, which
are leftovers of a formerly larger range. The recent
distribution covers an area of approx. 36,917 km².
Comparing old and recent records (Fig. 1), a
decline or even local extinction can be document-
Table 2. Numbers of records of garden dormice and ori-
gin in the data base of the project “In the search for the
Garden Dormouse”.
Method Number of C1 and C2
evidences
Opportunistic
Online reporting tool 4,681
Reports directly to the team 1,508
Collected carcasses 501
Active search
Footprint tunnels 77
Camera traps* 251
Nest boxes 117
Genetic samples 1,751
Existing data
Data bases of federal states 498
Museum samples 1,523
Total: 10,907
* Excluding images of long-term observations from
special sites
The Garden Dormouse as a Research and Conservation Priority in a German Large-Scale Citizen Science
5
ed for Saxony (SN), parts of Thuringia (TH) and
Hesse, the eastern part of Bavaria (BY) (along the
border to Czech Republic) and the eastern part of
North Rhine-Westphalia. The habitat loss amounts
to approx. 223,022 km² (35.2 %) since 1970.
Concerning the translocated garden dormice,
67 cases of have been documented. These include
individuals trapped at a military air base, at a con-
         
from known garden dormouse populations. In some
of these cases, it was possible to collect hair or fae-
ces and the region of origin (partly several 100 km
away) could be determined via genetic analysis.
Discussion
Through a multidisciplinary approach including
research institutions, NGOs and a professional in-
volvement of hundreds of citizen scientists, it was
possible to generate comprehensive large-scale sci-

This data now provides a much clearer picture of the
current garden dormouse distribution in Germany.
They also allow deep insights into the biology and
ecology of an endangered species, which will be the
     
further studies.
    
Germany by  (2012) was based
mainly on expert assessment. Now, with more than
10,000 records, it is possible to describe the distri-
bution of garden dormice in Germany in much more
  
future distribution trends.
The data quality of the online reports was very
high. We attribute this to the intensive professional
public relations work, which, among other things,
    -
tures of the garden dormouse and the (preliminary)

   
laypersons. The newly developed evaluation crite-
ria SMEC proved themselves very useful in practice
for the database and were helpful in the feedback to
reporting persons.
In total, 66.8 % of the online reports contained
evidence of dormice such as photos (Fig. 2), videos
or recorded calls. The availability of smartphones
with the ability to take high quality photos/videos
even in low light conditions or sound recordings was
very helpful for the project. In addition, many peo-
ple use camera traps in their gardens or on the balco-
ny and were willing to share their observations. Nu-
merous messages accompanying the reports asked
for information about the observed wildlife in the
immediate vicinity. This shows the interest in ani-
mals in general, the lack of knowledge about small
mammals, and at the same time the potential for citi-
zen science projects. It is particularly gratifying that
even carcasses were collected and made available
for further investigations. We therefore conclude
that citizen science can be an extremely powerful
and robust method for mapping small mammal dis-
tributions. We suggest that cautious combination of
citizen science data with long-term expert survey-
ing could be a highly reliable method for monitor-
ing biodiversity. In order to learn systematically
from this experience, a large-scale survey with 4138
CSVs was conducted in September 2022 (
, in preparation).
Even if it is still ongoing, the project has al-
ready yielded the largest data set on Garden dormice
known to us to date. Particularly helpful in the eval-
uation of the data were the targeted active searches
Fig. 1. Records of Garden dormice in Germany and
neighbouring countries between 1970 and 2022
provided as part of the project “In search for the Garden
Dormouse”. Grey squares = 10x10 km raster cell with
Garden dormouse presence between 1970 and 2017;
Black squares = 10x10 km raster cell with Garden
dormouse presence between 2018 and 2022; white circle
= translocated individual.
6
Büchner S. et al.

citizen scientists were keen and happy to detect gar-
den dormice. Fortunately, it was possible to convey
that zero counts were just as important as detections
of garden dormice. The active searches contributed
  
-
tured the general distribution pattern of the garden
dormouse in Germany and that only individual small
and isolated populations may have been overlooked.
The garden dormouse range in Germany is di-
vided into several isolated parts. The observations
in the urban areas along river Rhine are so numer-
ous that a vital population (or vital populations) can
be assumed for this part of the range, even taking
into account the bias in the number of records due
to more contact between humans and garden dor-
mice in settlements. Occurrences in cities and vil-
lages were known for decades (e.g.,  1916,
 1922,    1969).
Urban areas can provide good habitats for the gar-
den dormouse and the species has adapted to this
environment like other species, e.g., the Blackbird
(Turdus merula) or the Black Redstart (Phoenicu-
rus ochruros). It remains unclear so far why garden
dormice do not occur in cities along the river Rhine
south and north of the known range or in the eastern
parts of Germany. However, in comparison to older
records, there is no distribution decline in this habi-
tat type, but even a slight spreading of the species
southwards into the city of Mannheim during the
last 30 years. Nevertheless, it must be emphasised
this does not mean there are no threats to the species
in urban areas (see  et al. 2023).
Frequent reports of active garden dormice dur-
ing the winter months or individuals found in torpor
in nestboxes during frost periods instead of hiber-
nating in the ground indicate an adaption of the ani-
mals to the urban habitats where food is available
nearly all the year round. Garden dormice in the cit-
ies used bird feeders or directly fed with seeds and
fruits.    (1969) previ-

conditions in urban areas with prolonged active sea-
son and consequently having a second litter because
of a better food supply.
In contrast to urban areas, there is a clear and,
in some cases, rapid decline in the low mountain
ranges. For some parts, this is well documented,
such as in the Bavarian Forest where garden dor-
mice have been frequently reported until the 1990s
( 1988,  1996) but could not
-
ony where the decline already started in the 1920s
Fig. 2. Garden dormouse photo as proof for an online report of observation. Photo Jochen Pulch.
The Garden Dormouse as a Research and Conservation Priority in a German Large-Scale Citizen Science
7
and extinction is very likely ( 2009). There
are fewer old data for other parts of Germany, which
      
general, it can be stated that the decline was greater
in the eastern and central parts of Germany where
the garden dormouse mainly inhabited forests domi-
nated by spruce (Picea abies). However, there are
still populations in such habitats, which is why the
garden dormouse must also be considered a typical
forest species. Consequently, conservation measures
should also be focused on this type of habitat. Bark
beetle (Ips typographus) calamities or the associated
forest treatments with clearing of large areas using
big machinery in response to the calamity are cur-
rently putting these habitats under particular pres-
sure. Therefore, conservation strategies must be
developed and implemented together with the for-
estry sector urgently. Climate change is thought to
impact garden dormouse populations in the south of
its range ( et al. 2017). However, milder
winters and poorer hibernation conditions could
also pose a threat to the species in the low mountain
regions in Germany.
Comparing the distribution of the species over
the time should also take into account that the garden
dormouse is vulnerable to translocations. Its ability to
enter torpor and its adaptability to urban areas may re-
sult in (unintended) transportation in association with
food or other goods. We can assume that at least some
single old observations or museum specimens do not
represent a former permanent occurrence. However,
    
estimate of a distribution loss of approximately 35 %
since 1970 is therefore very conservative, as all iso-
lated individual specimens were excluded from the
calculation of the former range. Consequently, a
considerable range loss has to be assumed also for
Germany, as is described for the whole species’ range
( 2017). On the other hand, the stable oc-
currences along river Rhine invalidate the assumption
of low habitat suitability for garden dormice in Ger-
many by  (2021).
Large mammals seem to have a higher extinc-
tion risk compared to small ones ( et al. 2003,
 et al. 2015). However, the recent extinc-
tion rates of all mammals are higher than expected
from the fossil records ( et al. 2011), and
small mammals are as threatened as large mammals
(  2007). In contrast to the charis-
       
publicity for small mammals and only little attention
has been directed to their conservation. Our garden
dormouse project has shown that a small mammal
        -
fully raised awareness on dormouse conservation
needs among the public.
Acknowledgments: Holger Sticht (Cologne) had the initial
idea for a garden dormouse project. His commitment to the spe-
cies and his great enthusiasm eventually led to this joint work.
The project would not have been possible without the support
of several hundred volunteers. We are very thankful for their
contribution. Götz Ellwanger (Federal Agency for Nature Con-
servation) kindly helped us to calculate the garden dormouse
range. Special thanks go to BUND colleagues Christiane Bohn,
Christin Leiberg, Judith Gerick, Jochen Behrmann, Thomas
Norgall, Sina Schröder, Nora Albers, Kai Frobel, Siglinde
Gramoll, Ines Leonhardt, Julia Dreyer and Maren Goschke. The
director of the Clinic for Birds, Reptiles, Amphibians and Fish
at the Justus-Liebig-University Michael Lierz and the team at
the university (Nicolle Bräsel, Eva Marie Famira-Parcsetich,
Christine Jelinek, Franziska Sommer and Irmhild Wolz) are also
acknowledges. We are also grateful to all the students dedicat-
ing their work for the Garden dormouse.
Funding: This project is being funded by the German Federal
Agency for Nature Conservation with resources from the Ger-
man Federal Ministry for the Environment, Nature Conserva-
tion, Nuclear Safety and Consumer Protection. It is included in
the in the Federal Programme for Biological Diversity.
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... As this forest landscape is also known for its garden dormouse population, it is of conservation importance to monitor the species, explore its habitat associations and determine appropriate forestry management practices. In this study, we aim to address the habitat requirements of that garden dormouse population as part of the German-wide project 'In Search of the Garden dormouse' (Büchner et al., 2024). ...
... In such instances, we either conducted the transect on the opposite side of the road or initiated an additional transect further along the road ( Figure 1). To adequately cover the activity range of the garden dormouse, we deployed the tunnels at regular intervals of 20 m from each other (Büchner et al., 2024;Melcore et al., 2020). Of all the footprint tunnels, 7% were located in deforested areas, 13% in forest strips, 30% in areas with succession and 50% in reforested areas, of which 8% were classified as old-growth forest. ...
... We identified the footprints of the garden dormouse and distinguished them from other animal traces (Büchner et al., 2024). ...
Article
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The garden dormouse (Eliomys quercinus) is an understudied mammal species endemic to Europe. Once distributed widely across the continent, its eastern populations have significantly declined, with the species now found in only 50% of its former range. In Germany, it also occurs in spruce forests in low mountain ranges. However, this habitat has recently been lost due to bark beetle infestation following a prolonged period of drought. In some places, not only the dead trees are removed, but also all the branches and topsoil. We assessed habitat requirements of a garden dormouse population in such a changing habitat in the Harz Mountains, Germany. To assess garden dormouse occupancy, we conducted transect surveys using footprint tunnels during July and October 2022 for the presence of garden dormice. Additionally, we measured covariates such as coverage of tree, shrub and herb layers, as well as deadwood, soil characteristics and reforestation. Using single‐season occupancy modelling, we evaluated the effects of these habitat covariates on the occupancy of the garden dormouse. Our results indicated that garden dormouse occupancy was negatively affected by herb cover but positively associated with plant successional stages. Furthermore, occupancy of the garden dormouse was positively coupled with the occurrence of the hazel dormouse (Muscardinus avellanarius). Detection probability increased with higher weekly minimum temperatures. Practical implications: For the conservation of garden dormice in low mountain ranges like the Harz, practical measures should include establishing interconnected forest edges and strips. Moreover, we suggest adopting a dynamic, mosaic approach to felling, avoiding topsoil removal and promoting regeneration that fosters semi‐open successional habitats as essential strategies.
... Changing climate and intensification of land use have been suggested as possible influences; however, the demographic shift appears to have started before major 20th century landscape-level changes (Meinig and Büchner 2012;Bertolino 2017). Despite this possible influence of habitat loss, the garden dormouse also shows signs of being a habitat generalist, and this forest species has also adapted well to urban areas in some parts of its range while essentially vanishing from others (Meinig and Büchner 2012;Büchner et al. 2024), making its decline an ongoing mystery. ...
... Population genetic analysis has been identified as a major research need in garden dormouse conservation (Meinig and Büchner 2012;Büchner et al. 2024), as genetic data could aid in understanding patterns of connectivity and gene flow between regions and uncover past population processes that may help explain current declines. Prior karyotyping and mitochondrial DNA analyses suggested the existence of four genetically distinct clades within Europe (Libois et al. 2012;Perez et al. 2013), although the existence of hybrid individuals indicated gene flow between clades (Perez et al. 2013). ...
... By generating a long-read-based high-quality reference genome for the garden dormouse, our study provides a genetic resource that can be used to aid conservation efforts of small mammals in Europe. This study was performed in the frame of the citizenscience-focused project Spurensuche Gartenschläfer (In Search of the Garden Dormouse), which is the first national conservation and research project for this species in Germany (Büchner et al. 2024). The project aims to restore garden dormouse populations, as the species continues to decline across much of its range (Lang et al. 2022). ...
Article
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Genomic resources are important for evaluating genetic diversity and supporting conservation efforts. The garden dormouse ( Eliomys quercinus ) is a small rodent that has experienced one of the most severe modern population declines in Europe. We present a high-quality haplotype-resolved reference genome for the garden dormouse, and combine comprehensive short and long-read transcriptomics data sets with homology-based methods to generate a highly complete gene annotation. Demographic history analysis of the genome reveal a sharp population decline since the last interglacial, indicating an association between colder climates and population declines before anthropogenic influence. Using our genome and genetic data from 100 individuals, largely sampled in a citizen-science project across the contemporary range, we conduct the first population genomic analysis for this species. We find clear evidence for population structure across the species’ core Central European range. Notably, our data show that the Alpine population, characterized by strong differentiation and reduced genetic diversity, is reproductively isolated from other regions and likely represents a differentiated evolutionary significant unit (ESU). The predominantly declining Eastern European populations also show signs of recent isolation, a pattern consistent with a range expansion from Western to Eastern Europe during the Holocene, leaving relict populations now facing local extinction. Overall, our findings suggest that garden dormouse conservation may be enhanced in Europe through the designation of ESUs.
... Specifically, we asked the following questions: To answer these questions, we analyzed data from capturemark-recapture studies conducted in the Northern Black Forest during 2003-2005 and 2018-2021. The Black Forest is one of the last distribution areas of garden dormice within mountainous, coniferous-rich forests in Germany (Büchner et al. 2024). ...
... This is consistent with our finding that no garden dormice were captured in Period 2 at the ME study site, indicating that they no longer occur there. These findings are even more worrying as we were studying a population of garden dormice that is regarded to be thriving and seems so far unaffected by the dramatic decline of this species (Büchner et al. 2024). However, even though our study sites were located within a strictly protected area (since 2014) in which the use of pesticides is prohibited, it is likely that pesticide pollution can affect local insect populations. ...
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Biodiversity is decreasing worldwide, and early indicators are needed to identify endangered populations before they start to decline in abundance. In mammals, body mass (BM) is regarded as an indicator of fitness, and its loss is used as an early warning signal preceding population decline. The garden dormouse (Eliomys quercinus, Gliridae, BM: 60–110 g) is a small mammalian hibernator that has disappeared from over 50% of its former range in the last decades. The aim of this study was to investigate whether garden dormice from a presumably thriving and stable population already show early warning signals, which may precede a population decline. We therefore conducted capture‐mark‐recapture studies during 2003–2005 (Period 1) and 2018–2021 (Period 2) in the Northern Black Forest, one of its last natural distribution areas in Germany. We collected fecal samples, measured BM, and tibia length as a proxy for size and age. Results revealed that in Period 2 adult dormice had a significantly lower (12%) pre‐hibernation BM, corrected for body size, and juveniles showed a significantly lower BM gain after weaning than nearly two decades ago. Fecal samples collected in Period 2 showed that arthropods represented the main food residues in fecal samples during juvenile growth and pre‐hibernation fattening. Ambient temperature during hibernation showed no correlation with BM at emergence. We could not detect a phenological time shift in reproduction; however, we found only one birth peak in Period 2, compared with two birth peaks in Period 1. Observed changes in BM and reproduction pattern represent early warning signals, as they point to an insufficient availability of high‐quality food, which prevents dormice from meeting their nutritional requirements, with potentially serious consequences for their reproductive success and survival. As arthropods are the dominant food resource, their decline may at least partly explain this phenomenon.
... " The reasons for the accelerating declines in large parts of its range remain unknown, and therefore no specific risk factor can be identified [3]. To investigate possible reasons of such decline in the region, a project "In Search of the Garden Dormouse" was launched in Germany in 2018 [4]. Numerous dormouse carcasses were collected by volunteers (citizen scientists) and examined. ...
Article
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Background The garden dormouse (Eliomys quercinus) has experienced a significant population decline across Europe in recent decades. While habitat loss and climate change are often cited as primary factors, pathogen exposure, either to novel or to previously known, may play a role in such a decline. This study aimed to investigate the presence of polyomaviruses in garden dormice, given that these viruses are highly prevalent and can cause disease, particularly in immunocompromised individuals. Methods The carcasses of garden dormice (n = 89) were collected throughout Germany. Kidney samples were tested for the presence of polyomavirus DNA using nested degenerate and specific diagnostic PCRs. Seroprevalence was assessed from chest cavity fluid samples through an enzyme-linked immunosorbent assay using polyomavirus VP1 virus-like particles produced in yeast. Results A new polyomavirus, related to chimpanzee (Pan troglodytes) polyomaviruses 4 and 5 and human Merkel cell polyomavirus, was identified in the garden dormouse. Two 5,380 bp-length complete viral genomes were sequenced from dormice kidney samples (sequences PQ246041 and PQ246042). Genes encoding the putative structural proteins VP1, VP2, and VP3, as well as the Large, Middle, and small T antigens, containing conserved functional domains were identified. Polyomavirus DNA was detected in 2 of 74 dormice (2.7%, 95% confidence interval: 0-6.4%) through PCR, while 12 of 69 animals (17.4%, 95% confidence interval: 8.4-26.3%) tested positive for polyomavirus-specific antibodies. Conclusions In conclusion, here we describe a novel polyomavirus in the garden dormouse with molecular and serological detection. Pairwise sequence comparison and phylogenetic analysis suggest that this novel virus may represent a novel species within the genus Alphapolyomavirus. Future work should examine if this virus is garden dormouse-specific and whether it is associated with disease in dormice.
... Its geographical range has shrunk significantly by 50% since 1978 and by another third since 2008 (Temple & Terry 2007;Bertolino 2017). While dormice are common and widely distributed in South-western Europe (Portugal, Spain, France and Italy), North-western, Central and Eastern Europe have witnessed a sharp decline (Germany, Belgium, Ukraine, Czech Republic, Romania, and Croatia) or even total disappearance (Lithuania, Latvia, Estonia, Poland, Finland, and Slovakia), emphasizing the urgent need for targeted conservation efforts in these specific areas (Bertolino et al. 2008;Cortens & Verbeylen 2009;Meinig & Büchner 2012;Bertolino 2017;Bennett & Richard 2021;Verbeylen 2022;Pilāts et al. 2023;Büchner et al. 2023;Cichocki et al. 2024). ...
Article
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The garden dormouse (Eliomys quercinus) faces significant population declines across Europe, prompting urgent conservation measures. A critical aspect of these efforts is understanding the species’ dietary composition and preferences within specific areas and how this changes throughout the year. We compared garden dormouse diets between two habitats in West Flanders, Belgium with faecal analysis from May to October, covering almost their entire active phase. Our findings revealed a diverse diet of both plant and animal matter, with notable variations between habitats and seasons. Blackberries and other fruits, leaves, and to a lesser extent flowers, were the predominant plant-based food sources in both study areas, with seasonal fluctuations indicating a dietary shift throughout the dormice’s active period. Spring diets consisted primarily of young leaves and flowers, changing to increased fruit consumption in summer. Beetles emerged as a main animal food source throughout the entire active period. Snails were prominently eaten in the woody area, while millipedes prevailed in the diet in the dune environment, both more in spring than later in the active season. These insights highlight the importance of maintaining diverse fruit sources and preserving beetle, snail, and millipede populations for garden dormouse conservation. This study provides valuable insights into dormouse dietary preferences and thus contributes to targeted conservation strategies being essential for the survival of the dormouse.
... The garden dormouse is a small (33-63 g; Holden-Musser et al. 2016) hibernating rodent endemic to Europe. It shows a surprising adaptability to different environmental conditions, ranging from cold and wet forests to warm and dry plains, from Mediterranean habitats up to the tree line in the Alps and from natural habitats to the centres of cities (Amori et al. 2016;Bertolino 2017;Bertolino et al. 2008;Büchner et al. 2024;Nava et al. 2024). Garden dormouse populations are declining throughout its range and the species is currently listed as near threatened on the redlist of the International Union for the Conservation of Nature (IUCN) (Bertolino 2017;Bertolino et al. 2008). ...
Article
Nesting is a central topic in the behavioural ecology of many species, but data on the materials used to construct mammal nests are rarely reported. This paper describes the most commonly used components from 25 summer nests of the garden dormouse, a small threatened rodent endemic to Europe. Median nest dry weight of 25 nests was 15.5 g (10.3–21.1 g) and moss was the most common material (78 %), followed by leaves (9 %). Mosses were also the most frequently used material, with Hypnum cupressiforme being the most frequently used taxon in 11 out of 25 nests.
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Flea parasitism can affect the fitness of the host. Whether ectoparasites and diseases play a role in the decline of the garden dormouse (Eliomys quercinus) was one of the questions investigated in a project on the species. We searched for fleas in garden dormouse summer nests and on 24 specimens in Germany. In 50 nests, 3,289 fleas from seven species were identified. Prevailing species in nests were Ceratophyllus sciurorum (1,282 / 44 nests), Ceratophyllus gallinae (1,973 / 23 nests) and Nosopsyllus fasciatus. Myoxopsylla laverani, was quite uncommon in nests. On the garden dormice themselves 76 (between 1 and 18 fleas) from seven species were collected and identified: M. laverani was the most common (38 fleas from 9 dormice), followed by C. sciurorum and N. fasciatus. It appears that the flea community of the garden dormouse in Germany is similar to what is already known from other parts of its range: predominance of the squirrel flea, abundance of bird fleas and several small mammal fleas including the northern rat flea. So far, the distribution area of M. laverani was thought to be limited to special thermal conditions. However, this species also occurs in the northeastern part of the garden dormouse range in Germany. Sharing some flea species with rats (Rattus norvegicus) and house mice (Mus musculus) in urban areas make garden dormice vulnerable to different infections. Consequently, ecological rat and house mouse control in urban areas should therefore be recognised as a conservation measure for the threatened garden dormouse.
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The Forest Dormouse ( Dryomys nitedula ) shows a large albeit heavily fragmented distribution across Europe and Asia. Austrian populations belong to the distinct subspecies D. nitedula intermedius, which has only been found in the eastern Alpine region. Information on the occurrence of this subspecies is very rare and at the outset of this study most records dated back several decades. The aim of this research was to collect and critically analyse all published records on D.n.intermedius in Austria and revise its distribution range combining data research, field work and citizen science. The species’ current distribution was assessed via a nest box study and a nationwide citizen science program. A total of 168 records could be obtained, with 78 recent detections (2020-2024) from the project. Citizen science proved to be a highly efficient method to obtain records, whereas next box occupancy was low even in the core area of the species’ confirmed range. While a suspected decline of D. n. intermedius in the Alpine foothills was reaffirmed, new occurrences in the south could be documented. The main area of the current Austrian forest dormouse distribution is located in the Central Alps.
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Understanding habitat use and requirements is essential for the conservation of endangered species, such as the garden dormouse (Eliomys quercinus). Therefore, we radio-tracked garden dormice (n = 39) in the Black Forest National Park (Germany) between 2019 and 2021, determined home range size by calculating autocorrelated kernel density estimates, located resting sites during the day, and analyzed their resting behavior. Furthermore, we investigated their crossing behavior across paths varying in width, in the degree of canopy closure, and understory. Median home range size was 3.8 ha (Q25 = 2.3 ha, Q75 = 6.6 ha) in adults and 1.9 ha in juveniles. Adult males increased their home range sizes during reproduction. In September, shortly before hibernation, adults used smaller home ranges, likely to save energy. During the day, garden dormice used nest boxes and natural nests under the ground as resting sites. Ground holes were an important resource as they were most frequently used by reproductive individuals and also at low ambient temperatures (0.1–14.7 °C). In contrast, nest boxes were used only at higher ambient temperatures (> 5.9 °C). Forest trails with tree cover and/or undergrowth were frequently crossed by adults, while 4 m wide forest paths without tree cover or undergrowth were rarely crossed. The results of our study show that the preservation of natural resting sites, the restoration of forest trails, or the installation of crossing structures are important conservation measures for the garden dormouse, facilitating migration and colonization of new habitats and reducing the risk to lose genetic variability.
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The garden dormouse shows an ongoing decline all over Europe. Glirids are difficult to monitor due to their nocturnal activity and their relatively low densities. In this study, we used a very simple and easy detection method in the city of Wiesbaden (Germany), which has a stable garden dormouse population. In the summer 2019, characteristic vocalizations of the animals were used to map the occurrence of the species. Within 20 summer nights, 128 acoustic detections of garden dormice were obtained, which resulted in records for 55 out of 61 investigated km² grids. The species was found almost all over the area, mainly in semi-open areas like gardens and allotments but also in highly built-up and cultivated areas. Our study showed that using a simple, cost-effective and non-invasive method, in combination with citizen science projects, could provide valuable data for dormice monitoring.
Article
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The garden dormouse shows an ongoing decline all over Europe. Glirids are difficult to monitor due to their nocturnal activity and their relatively low densities. In this study, we used a very simple and easy detection method in the city of Wiesbaden (Germany), which has a stable garden dormouse population. In the summer 2019, characteristic vocalizations of the animals were used to map the occurrence of the species. Within 20 summer nights, 128 acoustic detections of garden dormice were obtained, which resulted in records for 55 out of 61 investigated km² grids. The species was found almost all over the area, mainly in semi-open areas like gardens and allotments but also in highly built-up and cultivated areas. Our study showed that using a simple, cost-effective and non-invasive method, in combination with citizen science projects, could provide valuable data for dormice monitoring.
Article
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In 2018, a six-year project was started to investigate the current distribution of the garden dormouse (Eliomys quercinus) in Germany, as well as to elucidate reasons for its drastic population declines across Europe. The joint project by the German Federation for the Environment and Nature Conservation (BUND), the Justus Liebig University Giessen and the Senckenberg Society for Nature Research is funded by the German Federal Biological Diversity Programme and is designed as an interdisciplinary citizen science project. Among other activities, volunteers get involved through the reporting of dormouse observations via an online tool, which are verified according to newly developed and standardised criteria. In addition, various field methods were employed in an active search. Further, during the first phase of the project, active tracking was carried out using various methods with the support of volunteers, and the species' use of space and resources was investigated by telemetry. Following three years of research, we present first results in this paper, including the current distribution and an identification of possible threats. In the second project phase, a nationwide species protection project will be developed and individual measures will begin to be implemented regionally. Finally, the joint project has inspired similar efforts in neighbouring countries that are likewise seeking to develop conservation strategies for dormice.
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There are differences regarding distribution, conservation status and protection according to national and European laws and directives between the four dormouse species (Gliridae) native to Central Europe. We question the coherence between scientific knowledge and conservation status of dormice in Europe and hypothesize that the species included in the Habitats Directive have been the subject of considerable research, while those not included have been neglected, despite having an unfavourable conservation status. We did a review of the research presented at the International Conferences on Dormice from 1990–2017 and published in the scientific literature since 1950 to see for which species the most research was done and whether the Habitats Directive had an impact. The number of presentations increased over time for the Hazel (Muscardinus avellanarius, N = 200) and the Edible dormouse (Glis glis, N = 150), while those on the Garden dormouse (Eliomys quercinus, N = 46) decreased until 2014 with an apparent increase only in 2017; the Forest dormouse (Dryomys nitedula, N = 67) does not show any trends. The number of published articles increased for all species except for the Garden dormouse. This focus does not adequately address the current threats of the species. The results can serve as a guide for the re-evaluation of future research priorities and conservation strategies as well as the implementation of new monitoring projects and ecological studies.
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The garden dormouse Eliomys quercinus has been declining in both abundance and range since the mid-twentieth century. The eastern edge of its range has contracted from the Ural Mountains to eastern Germany. Habitat loss and fragmentation has been the most supported theory to explain the observed decline. Climate change has been implicated in declines of other terrestrial mammals, but not investigated for E. quercinus . To better understand the factors influencing the distribution of this species and to map habitat suitability for E. quercinus across Europe, we created a Maxent species distribution model. Among the main environmental variables used for the modelling, two novel climate change indicator variables were produced to indicate the degree of climate change between the early twentieth century and the present. Areas of high suitability were mapped, and variable importance estimated using jackknife tests and variable contribution metrics. The climate change indicators outperformed many conventional variables, which could indicate that climate change is a factor behind the current distribution of E. quercinus . We also analysed the land use types where presence points of E. quercinus were located and whether they were in areas of “high nature value farmland”. Over 30% of all spatially filtered presence points corresponded to high nature value farmland areas. Our results could indicate a role for changing climate (particularly in temperature) in the range decline E. quercinus , and for high nature value farmland practices in conserving this species. Field studies and improved monitoring for this species are recommended to confirm both possible findings.
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Monitoring is essential for effective conservation and management of threatened species and ecological communities. However, more often than not, threatened species monitoring is poorly implemented, meaning that conservation decisions are not informed by the best available knowledge. We outline challenges and provide best‐practice guidelines for threatened species monitoring, informed by the diverse perspectives of 26 conservation managers and scientists from a range of organisations with expertise across Australian species and ecosystems. Our collective expertise synthesised five key principles that aim to enhance the design, implementation and outcomes of threatened species monitoring. These principles are (i) integrate monitoring with management; (ii) design fit‐for‐purpose monitoring programs; (iii) engage people and organisations; (iv) ensure good data management; and (v) communicate the value of monitoring. We describe how to incorporate these principles into existing frameworks to improve current and future monitoring programs. Effective monitoring is essential to inform appropriate management and enable better conservation outcomes for our most vulnerable species and ecological communities.
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Climate change affects distribution and persistence of species. However, forecasting species’ responses to these changes requires long-term data series that are often lacking in ecological studies. We used 15 years of small mammal trapping data collected between 1978 and 2015 in 3 areas at Doñana National Park (southwest Spain) to (i) describe changes in species composition and (ii) test the association between local climate conditions and size of small mammal populations. Overall, 5 species were captured: wood mouse Apodemus sylvaticus, algerian mouse Mus spretus, greater white-toothed shrew Crocidura russula, garden dormouse Eliomys quercinus, and black rat Rattus rattus. The temporal pattern in the proportion of captures of each species suggests that the small mammal diversity declined with time. Although the larger species (e.g., E. quercinus), better adapted to colder climate, have disappeared from our trapping records, M. spretus, a small species inhabiting southwest Europe and the Mediterranean coast of Africa, currently is almost the only trapped species. We used 2-level hierarchical models to separate changes in abundance from changes in probability of capture using records of A. sylvaticus in all 3 areas and of M. spretus in 1. We found that heavy rainfall and low temperatures were positively related to abundance of A. sylvaticus, and that the number of extremely hot days was negatively related to abundance of M. spretus. Despite other mechanisms are likely to be involved, our findings support the importance of climate for the distribution and persistence of these species and raise conservation concerns about potential cascading effects in the Doñana ecosystem.
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A comparison of historical data on the occurrence of Eliomys quercinus in Germany until 1987 with available data from 1990 until today for many regions shows a decline of the species and in some parts of its former range in the East an extinction. In general the knowledge on the actual range of the garden dormouse in Germany and the development of its populations on a regional scale are unsatisfactory. There is urgent need for an actual mapping of the species and research on its habitat requirements as Germany carries a high degree of responsibility for the conservation of Eliomys quercinus.
Article
Glirids are arboreal rodents that are difficult to monitor due to their nocturnal activity and their relatively low density. We compared results from footprint tunnels with those from two other monitoring methods (nest boxes and nesting tubes) for three dormouse species in an occupancy framework. Footprint tunnels performed better than the other two methods for the hazel dormouse Muscardinus avellanarius and the edible dormouse Glis glis, and were the only method which detected the garden dormouse Eliomys quercinus. Our findings provide evidence to support the effectiveness of footprint tunnels in monitoring the occurrence of dormouse species in comparison with other methods. Glirids are arboreal species that are difficult to monitor due to their nocturnal activity and their relatively low density. We compared the effectiveness of footprint tunnels, nest boxes, and nesting tubes for monitoring Muscardinus avellanarius, Glis glis, and Eliomys quercinus, within the framework of occupancy models in order to take into account imperfect detection. Footprint tunnels outperformed nest boxes and nesting tubes, returning an occupancy rate nearly five times higher for hazel and edible dormice, while the garden dormouse was recorded only with footprint tunnels. Therefore, we propose the use of footprint tunnels as a standard method for monitoring these species. The image represents a footprint tunnel on a branch used to sample dormice and footprints left by the three species.
Article
The garden dormouse Eliomys quercinus , a native European rodent species, suffered a significant contraction in its geographical range in the last few decades. The species has disappeared from large parts of central and eastern Europe and is considered extinct in some countries. I reviewed the information available on the occurrence and distribution of the species in 26 countries where it was previously reported. Present and past introductions outside its native range were also summarised. The garden dormouse is considered extinct in Lithuania, Finland, and Slovakia, probably extinct in Belarus, and present with single populations in the Netherlands, Poland, and Slovenia; in Slovakia, however, monitoring is necessary to verify recent records. The species is rare and localised in Austria, Ukraine, Romania, and Croatia and is in regression in Germany, Flanders (Belgium), Czech Republic, Latvia, and Estonia. In 2015, the garden dormouse occupied 49% of its 1978 geographical range and 67% of its 2008 range. South‐western Europe is the stronghold of the species; it is still common in large parts of Portugal, Spain, France, and Italy. However, there are indications that also in these countries, the species is locally declining. Present knowledge cannot explain the extensive regression of the garden dormouse's range in central and eastern Europe. Probably, it is the result of the interaction of different factors, acting locally and at a large scale, and related to specific ecological requirements of the species. There is a strong need for research to determine the reasons for the dramatic population and geographical range contraction of the garden dormouse. Meanwhile, it is important to monitor this species and to identify appropriate conservation measures.