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Declining soil Crustacea in a World Heritage Site caused by land nemertean

Scientific Reportsvolume 7, Article number: 12400 (2017) | Download Citation

Abstract

Invasive non-native species are of great concern throughout the world. Potential severity of the impacts of non-native species is assessed for effective conservation managements. However, such risk assessment is often difficult, and underestimating possible harm can cause substantial issues. Here, we document catastrophic decline of a soil ecosystem in the Ogasawara Islands, a UNESCO World Heritage site, due to predation by non-native land nemertine Geonemertes pelaensis of which harm has been previously unnoticed. This nemertine is widely distributed in tropical regions, and no study has shown that it feeds on arthropods. However, we experimentally confirmed that G. pelaensis predates various arthropod groups. Soil fauna of Ogasawara was originally dominated by isopods and amphipods, but our surveys in the southern parts of Hahajima Island showed that these became extremely scarce in the areas invaded by G. pelaensis. Carnivorous arthropods decreased by indirect effects of its predation. Radical decline of soil arthropods since the 1980s on Chichijima Island was also caused by G. pelaensis and was first recorded in 1981. Thus, the soil ecosystem was already seriously damaged in Ogasawara by the nemertine. The present findings raise an issue and limitation in recognizing threats of non-native species.

Introduction

Invasive non-native species transported by human activities have caused serious impacts on native ecosystems1,2,3. Accurate risk assessment of the non-native species is essential for successful ecosystem management2, because not all non-native species cause harm to ecosystems, and only a fraction established have an effect that is considered harmful3,4. Black, grey and white lists are used for simplifying the processes to address this issue5. A black list is useful to anticipate threats of particular non-native species and to prevent their extension. In contrast, species that are not on the black list are generally perceived as not being threats or at least less threatening. Therefore, underestimation of potential impact may be seriously detrimental in ecosystems by delaying conservation responses or allowing spreads of the harmful invasive species. We provide here a case study providing an insight on this issue.

Non-native species are particularly of concern on islands, because invasive non-native species often cause serious decline of island ecosystems6,7,8,9. Like other oceanic islands, a number of non-native species have been introduced to the Ogasawara archipelagos in the western Pacific ocean (Fig. 1). The Ogasawara archipelagos are registered as a UNESCO World Heritage Site (WHS) because of their unique ecosystems10. Conservation programs have been carried out to control the invasive species that have impacted the ecosystem of Ogasawara11, such as Pheidole megacephala 12, Bufo marinus 13, Anolis carolinensis 14, Achatina fulica 15, Rattus rattus 16 and Platydemus manokwari 17. In Japan, potential invasiveness was screened for all of the recorded non-native species. The Invasive Alien Species Act, adopted in 2004, specifies that species that are designated as “invasive alien species” (IASs) by the Japan Ministry of the Environment are subject to strict monitoring and that trade in these species is prohibited18. Therefore, invaded IASs in Ogasawara have been monitored, eradicated and/or their further spread has been prevented within the islands. For example, Bufo marinus, which was introduced to Ogasawara in 1949, has been controlled, because this toad is listed as an IAS and has been believed to have caused serious decline of soil arthropods in Ogasawara19,20. Soil animals of Ogasawara were originally composed by arthropods and land snails and particularly dominated by isopods and amphipods21,22. On the Chichijima Island, these land crustaceans have radically decreased since the 1980s, and currently they are mostly absent on the island23,24. Subsequently, a similar decrease of soil arthropods has occurred on Hahajima Island, and currently isopods and amphipods are abundant only in the southernmost part of the island25. However, recent eradication of B. marinus on the southern parts of Hahajima resulted in no increases of isopods, but instead, the range of the isopods has continued to contract in the north-to-south direction25,26,27. Thus, B. marinus appears not to be a main factor causing the decline of the soil arthropods in Ogasawara27.

Figure 1
Figure 1

Maps of study site and distributions of G. pelaensis and arthropod taxa. (a) Location of Ogasawara Islands. (b) Location of Hahajima-Island. (c) Maps of Minamizaki and study sites. (d) Distribution areas of G. pelaensis indicated by squares. (e,f) Occurrence and density of Isopoda (e), Amphipoda (f). Density is shown in size of circles. Figure 1 was created using the QGIS ver 2.16. Copyright © (1974–2014) National Land Information Division, National Spatial Planning and Regional Policy Bureau, MLIT of Japan. Figure was created and modified by authors based on coastline data of National Land Numerical Information with permission of National Land Information Division, National Spatial Planning and Regional Policy Bureau, MLIT of Japan.

Recently, invasive African big-headed ants Pheidole megacephala were found on Hahajima, and their impacts on land snails were detected12. However, the ranges of P. megacephala are limited, and these ants are unlikely to be a major cause of the decline of soil arthropods, though surveys are needed to estimate their impacts.

Because of the limitation of resources that can be provided for conservation in Ogasawara, all efforts to control non-native species are focused on the species listed as IASs or those with records of exhibiting invasiveness in other regions, and few surveys are provided for other non-native species. The land nemertine distributed on the Ogasawara Islands is such an example. The land nemertine occurred from the Ogasawara Islands was described as Geonemertes pelaensis by Kawakatsu28, Okochi29 and Kajihara30. Several researchers have studied taxonomy and distribution of land nemertine in Ogasawara since 1990s28,29,30,31,32. This species is widely distributed in tropical regions as a non-native species, particularly on islands33,34,35. There is no record of impacts on ecosystems caused by G. pelaensis. In Ogasawara, this species was first recorded on Chichijima in 198128 and on Hahajima in 1995, and the species is currently distributed in entire parts of Chichijima31. A previous study experimentally showed that G. pelaensis is malacophagous and does not feed on arthropods36. However, in Ogasawara, G. pelaensis was not an effective predator on land snails29. Hence, this non-native nemertine has been recognized as a species that causes no harm to the ecosystem. However, we speculate that, in fact, this nemertine might be a predator that has caused the catastrophic decline of soil arthropod fauna in Ogasawara. In the present study, we test this hypothesis using feeding experiments and field surveys.

Results

Soil arthropod communities

The Ogasawara archipelagos are composed of the Chichijima, Hahajima (Fig. 1b) and Mukojima Islands. The study area was in Minamizaki, which was in the southern part of Hahajima (Fig. 1b,c). Surveys in previous studies29 and our preliminary surveys documented that the land nemertine Geonemertes pelaensis is distributed throughout mostly all parts of the north and central Hahajima. In the present study, we found that land nemertine is not distributed in the southern part of Minamizaki. In the northern part of Minamizaki, G. pelaensis occurred throughout except for a few sites in the central and western parts. The distributional area of G. pelaensis did not overlap with the distributional area of the African big-headed ant P. megacephala. Among the sites surveyed, G. pelaensis existed at 12 sites, and P. megacephala were found at 7 sites. Both of G. pelaensis and P. megacephala were not found at 14 sites.

The most dominant order among the soil arthropods in the Minamizaki area was Isopoda (5174 individuals in total, occupying 53.5% of the whole individuals). The average density of Isopoda at the sites where both G. pelaensis and P. megacephala were absent (1232.8 individuals/m2) was mostly equal compared to the average density at the sites where P. megacephala were found (1237.3 individuals/m2). In contrast, the average density of Isopoda at the sites where G. pelaensis were found was only approximately one-tenth of that at the sites where no G. pelaensis were found (139.6 individuals/m2) (Fig. 2). The ranges of Isopoda with high density were restricted to the areas where G. pelaensis was absent (Fig. 1). Especially, the endemic species of Spherillo, which dominated in the isopod community of the southern parts of Minamizaki, was absent in most of the sites where G. pelaensis was found (Fig. 1). The selected GLMM showed that existence of G. pelaensis negatively affected the density of Isopoda (P = 7.68 × 10−6) (Supplementary Table S1).

Figure 2
Figure 2

(aj) Box plots showing changes in density of each of nine arthropod taxa at the sites where G. pelaensis exsit (white), those where P. megacephala exist (grey), and those where both G. pelaensis and P. megacephala are absent (black). Whiskers indicate the minimum and maximum density at each site. Horizontal lines of the box except for thick line indicate 25% and 75% quantile. A thick line indicates mean value. (km) Composition of the arthropod fauna at the sites where G. pelaensis exsit (k), those where P. megacephala exist (l), and those where both G. pelaensis and P. megacephala are absent (m). Numbers in pie charts correspond to each taxonomies; Isopoda, 1, Hymenoptera, 2, Araneae, 3, Diplopoda, 4, Amphipoda, 5, Lepidoptera, 6, Collembola, 7, Coleoptera, 8, Diplura, 9, Hemiptera, 10, Scizomida, 11, Chilopoda, 12, Others, 13.

Amphipoda was mostly absent at the sites where G. pelaensis was found (Fig. 1). The average density of Amphipoda at the sites where G. pelaensis was absent was 40.4 individuals/m2 (P. megacephala absent) and 185.9 individuals/m2 (P. megacephala present), whereas it was 0.9 individuals/m2 at the sites where G. pelaensis was found (Fig. 2). The selected GLMM showed that existence of G. pelaensis negatively affected the density of Amphipoda (P = 3.35 × 10−6) (Supplementary Table S1).

Effects of G. pelaensis on the density of other orders detected in GLMM analyses are shown in Supplementary Table S1. In Chilopoda, density was also negatively affected by the presence of G. pelaensis in selected GLMM (P = 3.01 × 10−2). In Hemiptera, presence of G. pelaensis was not included in selected GLMM, but Nerthra macrothorax, which occupied more than 80% of individuals of Hemiptera collected, was affected by presence of G. pelaensis (P = 7.10 × 10−3) (Supplementary Table S1). Indeed, N. macrothorax was mostly absent at the sites where G. pelaensis was found (Fig. 1). In other orders such as Diplopoda, Araneae and Hymenoptera, no negative effects of G. pelaensis was detected in the GLMM analyses.

Negative impacts of P. megacephala on the density of soil arthropods were less obvious than those of G. pelaensis (Fig. 2). On the basis of the GLMM analyses, P. megacephala provided negative effects on Schizomida (P = 1.24 × 10−2) (Supplementary Table S1).

Total biomass represented by total numbers of individuals at the sites where G. pelaensis existed was approximately 40% of those at the sites where no G. pelaensis was found. Radical differences in the composition of soil arthropod fauna were found between the sites where G. pelaensis existed and those where it did not. These findings suggest that G. pelaensis has a serious impact on the soil fauna of Ogasawara.

Feeding habits of Geonemertes pelaensis

Based on our observation of feeding behavior, the nemertine G. pelaensis extrudes its proboscis when it catches prey and/or is stimulated from the outside—like most other groups of nemertines. In the feeding experiments, Burmoniscus okinawaensis (Isopoda), Spherillo boninensis (Isopoda) and Talitridae sp. (Amphipoda) were predated by G. pelaensis, and 2, 4 and 7 individuals were consumed, respectively. In our experiments, we could not identify which individual nemertine consumed each prey item. When G. pelaensis preyed on B. okinawaensis and S. boninensis, it sucked out the internal parts of the victim’s body, resulting in a change of colour from dark grey to white in the victims and from white to dark grey in G. pelaensis (Fig. 3). In contrast, Nerthra macrothorax (Hemiptera) and Japanioiulus lobatus (Diplopoda) were not predated by G. pelaensis.

Figure 3
Figure 3

Photographs showing that G. pelaensis preys on Isopoda sp. Body color of G. pelaensis changed from white (a) to grey (b), because body contents of Isopoda sp. moved to G. pelaensis by predation.

We did not use Araneae and Diptera for the present feeding experiments, because it seemed unlikely that the nemertine could capture animals like these quickly moving animals. However, in our additional experiments, we observed that G. pelaensis preyed on a spider (see Supplementary Video S1), Drosophila, Cicadoidea and Lepidoptera (See Supplementary Fig. S1).

Discussion

The present study documents that the land nemertine Geonemertes pelaensis is a predator of arthropods and caused serious declines of Isopoda and Amphipoda in Ogasawara. The decline of arthropod fauna, particularly the disappearance of Isopoda and Amphipoda, that has occurred on Chichijima since the 1980s are results of predation by this non-native nemertine. Similar decreases in land crustaceas formerly recorded in the north and central parts of Hahajima are also caused by predation of this nemertine. These conclusions are supported by our field surveys and feeding experiments. In Ogasawara, Isopoda and Amphipoda are the dominant components of the original soil fauna, and all of the species that belong to Isopoda and Amphipoda are native21,37. Approximately 80% of isopod species in Ogasawara are endemic21. Amphipoda also includes many endemic species, though the taxonomy of amphipods in Ogasawara remains unclear. These imply that predation by non-native nemertine is a serious conservation issue.

Other orders such as Diplopoda show no decline in the areas where G. pelaensis exists, suggesting that G. pelaensis does not feed on these groups. The result of our feeding experiment on Diplopoda is consistent with this conclusion. In contrast, Nerthra macrothorax, which showed a decline of density in nature but were not predated in the laboratory, reveals an incongruence. It is most likely that the decline of Nerthra macrothorax is due to indirect effects of predation by G. pelaensis. Nerthra macrothorax is carnivorous insect and preys on mainly isopods38,39. Therefore, radical decline of isopods caused by the nemertine’s predation subsequently results in declines of Nerthra macrothorax because of scarcity of its diet. Declines of carnivorous Chilopoda at the sites where G. pelaensis exists also appear to be the result of indirect effects of predation by G. pelaensis. Although Chilopoda was not used in the feeding experiments, Chilopoda is unlikely to be predated by G. pelaensis, considering the result of the feeding experiment on Diplopoda. Araneae, which is predated by G. pelaensis, may have some resistance against predation by G. pelaensis, because it is mainly composed of non-native species. In addition, the main diet of Araneae in Minamizaki consists of microorganisms such as Collembola and mites, which are unlikely to be consumed by G. pelaensis.

Hence, predation by G. pelaensis causes not only serious decreases in the density of Isopods, but it also causes cascade effects on the food webs in the soil ecosystems of Ogasawara. As a result of the nemertine’s predation, biomass of soil fauna radically decreases in Ogasawara, and ecological function of the soil ecosystem is seriously damaged.

The contraction of the distribution of Isopoda from north to south in Minamizaki, which has been reported in the previous studies27, appears to reflect the spread of the distribution of G. pelaensis from north to south in this area. In our preliminary survey conducted in January, G. pelaensis was not recorded in site 4, whereas G. pelaensis was recorded at this site in our survey in September, suggesting expansion of the distribution of G. pelaensis toward the south.

Distributions of G. pelaensis in Ogasawara remain unclear except for the islands of Chichijima, Hahajima and Nishijima. Our preliminary surveys documented that no G. pelaensis occurs on the Nishijima Island, which has rich soil arthropod fauna dominated by isopods and amphipods. Further surveys of the distribution of G. pelaensis and status of soil fauna are required in other islands of Ogasawara. The development of a quarantine program is required to prevent further spread of G. pelaensis to the islands like Nishijima that are not invaded by G. pelaensis.

There is a striking contrast in terms of feeding habits of G. pelaensis between our findings and a previous study that showed that G. pelaensis is malacophagous and does prey on arthropods on the basis of feeding experiments. This inconsistency may imply that G. pelaensis includes different cryptic species with different feeding habits. Further taxonomic studies of this land nemertine are required to address this issue. As an alternative hypothesis, shifts in feeding habits have occurred in the populations of Ogasawara, and levels of invasiveness would be different among different ecosystems12. Further surveys of the feeding habits of G. pelaensis in other regions are needed to clarify this issue. In addition, it is urgently needed to assess the impacts of G. pelaensis on native arthropod fauna in other tropical islands where this nemertine has already invaded. Like the case of Ogasawara, unnoticed decline of soil fauna may have already occurred. Furthermore, it is very crucial to prevent further spread of G. pelaensis to other regions. This nemertine has expanded its distribution to tropical regions via transport with crops40. However, identification of this nemertine is difficult, and this nemertine is easily overlooked. It would be rather efficient and important to develop a system to prevent invasion of any non-native species through transportation of agricultural crops.

The present findings raise an issue and point to a limitation relative to the use of an official black list of invasive species, such as Japan’s IAS list, to anticipate threats of particular non-native species and to prevent their spread. The government generally has no responsibility to monitor IAS risk or to prevent the spread of non-native species that are not on the official invasive species list, particularly if there is no evidence that it potentially exhibits serious risks. In Ogasawara, this caused a substantial delay in recognizing the threats of G. pelaensis. The decline of soil arthropods, particularly of isopods and amphipods, has been long believed to be a result of predation by the invasive toad Bufo marinus. However, the impact of G. pelaensis on the soil arthropod fauna in Ogasawara is far more serious than that of Bufo marinus and African big-headed ants Pheidole megacephala, both of which are on the list of “100 of the World’s Worst Invasive Alien Species” by IUCN41. Any stakeholders using the official list of invasive species to develop conservation programs should recognize that there are always unknown risks related to the invasion of non-native species and that they have information of only a small fraction of non-native species.

Methods

Field surveys

The forest at Minamizaki are dominated by Planchonella obovata, Rhaphiolepis wrightiana, Calophyllum inophyllum, Terminalia catappa, Livistona chinensis and Pandanus boninensis. We conducted a soil fauna investigation and survey of the distribution of Geonemertes pelaensis during July 4–11 and August 19 to September 17 in 2016. Preliminary surveys of G. pelaensis were conducted in January 2016.

Soil arthropod fauna were investigated at 33 sites (Fig. 1c) (9 sites in July, 24 sites in August and September). The study sites were placed so as to cover the entire area of Minamizaki. Each site was 10 m × 10 m in area and placed on the forest floor. Three quadrates (25 cm × 25 cm each) were placed at random within each site. The litter layer and topsoil (up to 5 cm) were collected from each quadrate. Soil animals were collected by hand-sorting them from the collected soil and litter. We excluded mites from subject organisms because they were too small to collect by hand-sorting. The collected animals were preserved by 80% ethanol and were identified under a stereomicroscope. The soil water content was also measured by a meter (model PMS-714, FUSO) in each quadrate.

A survey of the distribution of G. pelaensis was conducted at the same 33 sites during the daytime. At each site, we searched for G. pelaensis 15 minutes by looking under rotten log, fallen leaves of Livistona chinensis and the base of the leaves of Pandanus boninensis, and we recorded whether nemertine was distributed. All of these materials of land nemertine were identified as Geonemertes pelaensis (Fig. 1), because there was no records of other species of land nemertine in Ogasawara30.


Feeding experiments of Geonemertes pelaensis

We conducted feeding experiments of G. pelaensis at the Ogasawara Environmental Planning Laboratory, Hahajima. The individuals of G. pelaensis were collected from the survey sites of Minamizaki and carried to the laboratory. Five individuals were kept in each plastic box (about 10 cm × 10 cm × 5 cm) for one week with five prey items. The individuals of G. pelaensis that were used for the experiment were 2~3 cm length. Burmoniscus okinawaensis, Spherillo boninensis, Nerthra macrothorax, Talitridae sp and Japanioiulus lobatus were selected for prey items; their lengths were 5 mm, 5 mm, 5 mm, 10 mm and 15~20 mm, respectively. All these prey items were collected from Minamizaki and carried to the laboratory. A wet-paper layer was laid on the bottom of the boxes to prevent desiccation. We counted the number of prey items eaten by the nemertine every day; if organisms were consumed, we added new individuals equal to the consumed number of individuals. This experiment was conducted only for investigating whether G. pelaensis can eat arthropods, and so preference of different diets and consumption rate was not surveyed.


Statistical analysis

The species identified were grouped into orders or classes. To evaluate the impact of G. pelaensis on soil fauna, generalized liner mixed models (GLMM) were created using the R library lme442. The number of individuals of each taxa collected from each quadrate was used as the dependent variables (n = 99). The taxa of which the total number of individuals found were less than 50 were not used for GLMM. The taxa used for GLMM included Isopoda, Amphipoda, Diplopoda, Chilopoda, Araneae, Schizomida, Hymenoptera, Coleoptera, Collembola, Diplura, Lepidoptera and Nerthra macrothorax (represented Hemiptera). Elevation and water content in each quadrate were used as independent variables. Pheidole megacephala is narrowly distributed within the central part of Minamizaki12. In order to evaluate its influence separately, presence or absence of this ant was also included as an independent variable. In the analysis of Hymenoptera, presence or absence of P. megacephala was not treated as an independent variable because P. megacephala was included in the collected samples of Hymenoptera. The presence or absence of G. pelaensis and P. megacephala was treated as binary data (1: presence, 0: absence). The dependent variable is assumed to have a Negative binomial error distribution. This error distribution has been used to describe over-dispersed datasets or count data of soil animals43,44,45. All GLMMs included individuals across the sites, and the difference of the quadrates was treated as random effects. Stepwise backward selection method was used to determine selected model. Non-significant independent variables (P > 0.05) were removed from full model one at a time. P-values from GLMMs were obtained by model comparisons (Chi-squared test).

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Acknowledgements

I am sincerely grateful to K. Akiyama, K. Hayama, T. Kojima and Y. Sakairi for their help in our field surveys. I also thank Y. Nakahara, T. Ohbayashi, H. Karube, K. Eguchi, K. Goka, and T. Sasaki for their helpful comments and the information and the Kanto Regional Environment Office, the Japan Ministry of the Environment, and the Ogasawara Branch of the Tokyo Metropolitan Office for supporting my field surveys. This research was supported by Sumitomo Foundation and the Environment Research and Technology Development Fund (4–1402) of the Japan Ministry of the Environment.

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Affiliations

  1. Graduate School of Life Science & Center for Northeast Asian Studies, Tohoku University, 41 Kawauchi, Aoba-ku, Sendai, Miyagi, 980–8576, Japan

    • Shotaro Shinobe
    • , Shota Uchida
    •  & Satoshi Chiba
  2. Japan Wildlife Research Center, 3-3-7, Kotobashi, Sumida, Tokyo, 130–8606, Japan

    • Hideaki Mori
  3. Japan Forest Technology Association, 7, Rokubancho, Chiyoda-ku, Tokyo, 102-0085, Japan

    • Isamu Okochi

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Contributions

S.C., H.M. and I.O. designed research. S.S. and S.U. conducted survey and experiment, and analyzed data. S.C. supervised the project. All authors discussed results and wrote the manuscript text.

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The authors declare that they have no competing interests.

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Correspondence to Shotaro Shinobe.

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https://doi.org/10.1038/s41598-017-12653-4

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