Biodiversity Data Journal : Data Paper (Biosciences)
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Data Paper (Biosciences)
Resampling a carrion beetle fauna after 40 years (Coleoptera, Staphylinidae, Silphinae, and Leiodidae, Cholevinae)
expand article infoMenno Schilthuizen‡,§,|,, Teun van der Sterren#, Isabel Kersten#, Mike Groenhof|,¤, Henk van der Meulen|,«, Leonie Wezendonk#
‡ Taxon Expeditions B.V., Leiden, Netherlands
§ Leiden University, Leiden, Netherlands
| Taxon Foundation, Leiden, Netherlands
¶ Naturalis Biodiversity Center, Leiden, Netherlands
# Thomas a Kempis College, Arnhem, Netherlands
¤ Institute for Biology Leiden, Leiden, Netherlands
« GELIFES, Groningen University, Groningen, Netherlands
Open Access

Abstract

Background

From 29 May until 5 June 1982, the first author placed baited pitfall traps to sample the Staphylinidae, Silphinae and Leiodidae, Cholevinae (Coleoptera) fauna in a mixed forest in the Netherlands. Exactly 40 years later (29 May until 5 June 2022), as a project on insect declines with high school students at a nearby school, a resampling was carried out.

New information

We report the silphine and cholevine specimens recorded both in 1982 and 2022. We found that total species richness and biomass had not noticeably changed, but there were some distinct appearances and disappearances of species. In addition, the species abundance distribution has become more skewed in favour of locally common species, such as Sciodrepoides watsoni and Fissocatops westi. We discuss our results in the context of insect declines worldwide.

Keywords

carrion trapping, insect declines, Staphylinidae, Leiodidae, education

Introduction

In recent years, many studies have appeared that investigate the rate of decline in insect densities and diversities (e.g. Hallmann et al. (2017), Van Klink et al. (2020)). These studies essentially depend on the availability of long-term surveys in the same area using standardised sampling techniques. While studies with temporally dense sampling (continuous, annual or with regular longer intervals) are obviously most valuable, comparisons between two time-points (e.g. Cuesta and Lobo (2019), Opito et al. (2023)) can also add important data to the study of long-term trends in entomofauna.

In 1982, the first author (M.S.), as high school student and encouraged by his biology teacher, Daan Vestergaard, conducted a one-week inventory of carrion-visiting beetles (Silphinae and Cholevinae) with baited pitfall traps in the Lichtenbeek Estate near Oosterbeek, the Netherlands. In this paper, we describe the results of a resampling, using exactly the same inventory technique, precisely 40 years later by a student-teacher team from a nearby school, in the context of understanding environmental change and insect declines.

Our study showed no noticeable differences in species richness, total abundance and biomass between the two sampling years. However, in 2022, the species abundance distribution had a lower evenness and a more hollow shape than in 1982: a few very abundant species, many very rare species and very few species with intermediate abundances. Furthermore, there are several striking differences in the abundance of specific species, most of which are species that have declined compared to 1982, but also some that have increased.

For some species that showed conspicuous changes in abundance, it is possible to speculate on the causes. For example, Nicrophorus humator is a common forest species with two discrete abundance peaks, in April-May and in August (Schilthuizen and Vallenduuk 1998, Colijn and Heijerman 2020). The fact that we found 130 individuals in 1982 and only four in 2022 could be the result of a shift in the phenology. The biological onset of spring has advanced by over two weeks in the past few decades in the Netherlands (Van Vliet et al. 2014), so it is possible that the 1982 sampling fell within the spring peak of N. humator, whereas during the 2022 sampling, the peak was already over. For other species, for example, Oiceoptoma thoracicum, which has been more frequently reported in the past decades and Catops subfuscus, for which records appear to have declined (Schilthuizen, pers. obs.), the changes may reflect true changes in the nationwide population density of these species.

The data we present describe a comparison in Silphinae and Cholevinae communities at two time points exactly 40 years apart. While the limited scope of the comparison precludes any far-reaching interpretation, the patterns we found (no declines in species richness, total abundance and biomass, but distinctly reduced evenness) might point to a general trend and the data could be used for ongoing meta-analyses on insect declines. A note of caution is, however, warranted, because of changes in the sampling set-up (for example, ethanol vs. salt water as preservative), the weather and the habitat.

Project description

Title: 

Resampling the carrion beetles of Lichtenbeek Estate 40 years later

Study area description: 

The 89 ha Lichtenbeek Estate (52.00°N 05.84°E) is a mixed forest near Arnhem, the Netherlands. It is located partly within the Municipality of Arnhem, partly in that of Renkum. On the north, it is bordered by the N224 provincial road, on the west by a smaller road, the Dreijenseweg. On the east and southeast, the forest is adjoined by pasture and arable land and on the south by a residential area in the northern part of the town of Oosterbeek. We also included the western portion of the smaller forest of Vijverberg, located to the north of the N224, which holds the springs that used to feed the brook after which Lichtenbeek was named. The forest is located at ca. 50 m elevation on the south-exposed slope of the glacial moraine north of the Rhine and has a podzol soil of fine to coarse sand. Its vegetation is composed of separated stands, some of which contain primarily deciduous trees (Fagus sylvatica, Quercus sp.), others coniferous trees (e.g. Pseudotsuga menziesii). As no major changes have taken place in the layout or tree vegetation of the forest over the past 40 years, we cannot rule out that, although some plots may have been logged and regrown, others may have matured. Permission to conduct this study was granted by Stichting Geldersch Landschap & Kastelen (through Mr. Bram de Jong).

Design description: 

In the week of 29.v. - 5.vi.1982, one of us (M.S.) used 1 litre cans with a 10 cm diameter opening as pitfall traps. These were dug in so that the top was flush with the soil surface and baited with 100 g each of horse meat (16 traps), mushrooms (2 traps), Dutch old cheese (3 traps) and apple (1 trap); see Fig. 1 for a map of the trap positions. A square of chicken wire was placed over each trap and secured with tent pegs; from the chicken wire, the bait was suspended. As preservative in the traps, 70% ethanol was used. The traps were emptied once, at the end of the sampling week and were then removed. All collected material of Silphinae and Cholevinae was identified by M.S. to species level, where necessary using genital dissection and is currently in the collection of Naturalis Biodiversity Center, Leiden, the Netherlands; small numbers of duplicates are retained in the collection of Taxon Foundation, Leiden, the Netherlands. The data were reported on in a different context in Schilthuizen (2022). The local weather during the 1982 sampling week (at weather station Deelen, 8 km NNE of Lichtenbeek; obtained from https://daggegevens.knmi.nl) was very warm (daily mean temperature 20.5°C), very little wind (daily mean wind speed 2.9 m/s), sunny (daily mean sunshine duration 11.4 h) and mostly dry (two days with rain, 0.3 and 1.7 mm, respectively).

Figure 1.  

Map of the Lichtenbeek Estate (satellite image provided by Google Earth) and the positions of the traps. Colours of the numbers indicate the bait type used: white, meat; orange, cheese; blue, mushrooms; green, apple.

In the week of 29.v. – 5.vi.2022, using 1982 sketch maps and notes kept by M.S., we replicated the trapping procedure of 1982, with the following exceptions: we used 1 litre plastic yoghurt tubs with, as preservative, a saturated sodium chloride (NaCl) solution and a drop of dishwashing detergent; horse meat was replaced by beef. One trap (No. 12) was lost, so we removed the catch from this trap also from the 1982 dataset. All collected material of Silphinae was sorted by T.v.d.S. and I.K., identified by T.v.d.S and checked by M.S. The Cholevinae were sorted by T.v.d.S., I.K. and M.S. and identified by M.S. One badly damaged female Choleva could not be identified to species. All specimens were deposited into the collection of Taxon Foundation, Leiden, the Netherlands, except for a small number of Silphinae duplicates (two specimens per species), which were kept in the private collection of T.v.d.S. The local weather (Deelen data) during the 2022 sampling week was cooler than in 1982 (daily mean temperature 13.7°C), there was also very little wind (daily mean wind speed 3.3 m/s), it was less sunny (daily mean sunshine duration 6.3 h) and wetter (four days with rain, 0.9, 2.0, 2.6 and 27.1 mm, respectively).

All specimens of all Silphinae and Cholevinae species were counted, tabulated and compared in PAST 4.11 (Hammer et al. 2001). To estimate biomass, based on Schilthuizen and Vallenduuk (1998) and an assumed specific weight similar to that of water, we used an average volume of Silphinae of 3 x 4 x 12 mm = 144 mg and of Cholevinae of 1.5 x 2 x 4 mm = 12 mg.

In 1982 and 2022, we collected 1151 and 1523 individuals, respectively, from a total of nine Silphinae and 16 Cholevinae species. Not all species were found in both years. In 1982 (21 species found), one silphine (Silpha tristis) and three cholevines (Catops chrysomeloides, Catops kirbyi and Catops subfuscus) were found that were not found in 2022 and, in 2022 (20 species found), two silphines (Silpha obscura and Oiceoptoma thoracicum) and three cholevines (Catops neglectus, Choleva sp., and Ptomaphagus subvillosus) were found that were not found in 1982. Margalef’s species diversity index (Clifford and Stephenson 1975) was 2.696 in 1982 and 2.729 in 2022 and Buzas & Gibson’s evenness (Buzas and Gibson 1969) was 0.444 and 0.213 in 1982 and 2022, respectively. The estimated biomass was 86.412 g and 82.824 g in 1982 and 2022, respectively.

All data have been uploaded to GBIF, and summarised in Fig. 2 and Tables 1, 2. We found a significant difference in species composition between the two sampling years (Chi-squared = 815.87, d.f. = 24, p < 0.000001). In particular, strong differences of an order of magnitude or more were found in the abundances of Nicrophorus humator, Silpha tristis, Oiceoptoma thoracicum, Catops picipes, Catops subfuscus, Catops tristis, Fissocatops westi, Nargus velox and Ptomaphagus medius. Of these species, six declined and three rose in abundance (see Table 1).

Table 1.

Numbers of individuals found for all species, pooled per sampling period for all traps.

Family

Species

N (1982)

N (2022)

Staphylinidae

Nicrophorus humator

130

4

Staphylinidae

Nicrophorus vespillo

18

21

Staphylinidae

Nicrophorus vespilloides

254

117

Staphylinidae

Phosphuga atrata

1

4

Staphylinidae

Silpha carinata

132

322

Staphylinidae

Silpha obscura

0

2

Staphylinidae

Silpha tristis

13

0

Staphylinidae

Oiceoptoma thoracicum

0

14

Staphylinidae

Thanatophilus sinuatus

2

5

Leiodidae

Catops chrysomeloides

1

0

Leiodidae

Catops coracinus

88

13

Leiodidae

Catops fuliginosus

6

5

Leiodidae

Catops kirbyi

1

0

Leiodidae

Catops neglectus

0

4

Leiodidae

Catops nigricans

1

3

Leiodidae

Catops picipes

34

5

Leiodidae

Catops subfuscus

24

0

Leiodidae

Catops tristis

65

6

Leiodidae

Choleva sp.

0

1

Leiodidae

Fissocatops westi

15

161

Leiodidae

Nargus velox

23

1

Leiodidae

Ptomaphagus medius

1

15

Leiodidae

Ptomaphagus subvillosus

0

1

Leiodidae

Sciodrepoides fumatus

50

15

Leiodidae

Sciodrepoides watsoni

292

804

total

1151

1523

Table 2.

Summary statistics for the two sampling periods.

1982

2022

Species richness

21

20

Number of specimens

1151

1523

Margalef's diversity

2.696

2.729

Biomass (g)

86.412

82.824

Evenness (95% C.I.)

Shannon's H

1/D (Simpson)

0.444 (0.432 - 0.551)

2.184

6.562

0.213 (0.204 - 0.252)

1.501

2.936

Figure 2.  

Species abundance distributions, organised from most common on the left to rarest on the right, across all traps and all species for both sampling periods (one species per column).

Funding: 

This study was supported by the Prins Bernhard Cultuurfonds (Gelderland) and the Suzanne Hovinga Stichting.

Geographic coverage

Description: 

The study was conducted on the Lichtenbeek Estate near Oosterbeek, Province of Gelderland, the Netherlands.

Coordinates: 

51.9978 and 52.0065 Latitude; 5.844 and 5.8551 Longitude.

Taxonomic coverage

Description: 

Coleoptera, Staphylinidae, Silphinae (carrion beetles).

Coleoptera, Leiodidae, Cholevinae (round fungus beetles).

Taxa included:
Rank Scientific Name Common Name
subfamily Cholevinae round fungus beetles
subfamily Silphinae carrion beetles

Temporal coverage

Data range: 
1982-5-29 - 2022-6-05.

Collection data

Collection name: 
Taxon Expeditions
Collection identifier: 
TXEX
Specimen preservation method: 
dry and in ethanol

Usage licence

Usage licence: 
Creative Commons Public Domain Waiver (CC-Zero)

Data resources

Data package title: 
Carrion beetles Lichtenbeek
Number of data sets: 
2
Data set name: 
Data Resources 1 (sampling events)
Description: 

This dataset describes the sampling events with baited pitfall traps in Lichtenbeek Estate, Oosterbeek, the Netherlands, on two occasions: 1982 and 2022. These have been uploaded to GBIF.

Column label Column description
eventID Code for each pitfall collection event.
samplingProtocol Type of sampling method.
samplingEffort The duration of the sampling.
sampleSizeValue The value of the trap volume.
sampleSizeUnit The unit of measurement for sampling size.
eventDate The time-span covered by the sampling event.
country The country where the sampling event took place.
countryCode The code for the country where the sampling event took place.
locality The name of the locality where the sampling event took place.
locationID An identification code for the location of the sampling event.
decimalLatitude The latitude of the location of the sampling event in decimal degrees.
decimalLongitude The longitude of the location of the sampling event in decimal degrees.
geodeticDatum The geodetic datum for the longitude and latitude locator used.
coordinateUncertaintyInMetres The uncertainty in metres about the coordinates.
type type
ownerInstitutionCode The institution where the samples are held.
Data set name: 
Data Resources 2 (occurrences)
Description: 

Specimens recorded for each sampling event.

Column label Column description
eventID Code for each pitfall collection event.
occurrenceID Code for each set of specimens recorded per sampling event.
basisOfRecord The basis on which the record was made.
organismQuantity The number of individuals aggregated into the record.
organismQuantityType Qualifier for the types of organisms recorded.
occurrenceStatus Present or absent.
scientificName The scientific name of the taxon recorded.
kingdom The kingdom to which the taxon belongs.
phylum The phylum to which the taxon belongs.
class The class to which the taxon belongs.
order The order to which the taxon belongs.
family The family to which the taxon belongs.
taxonRank The taxonomic rank of the taxon.
identifiedBy The name of the authority responsible for the identification.
recordedBy The organisation responsible for the record.
type type of record.
ownerInstitutionCode The organisation or person owning the data.

Acknowledgements

We are grateful to board members Aglaia Bouma and Norbert Peeters of Taxon Foundation for guiding this project and to the biology section of the Thomas a Kempis College for general support, in particular Krista Voskuil for collecting the empty jars and all the other materials for the traps. Daphne Suijker kindly supported the specimen processing work in the LiveScience hall of Naturalis Biodiversity Center. We would like to thank Geldersch Landschap en Kastelen for allowing us to work in Lichtenbeek. Roel van Klink, Gijs Gerrits, Theodoor Heijerman and Ed Colijn provided valuable input.

References

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