Assessing freshwater fish biodiversity of Kumbe River, Papua (Indonesia) through environmental DNA metabarcoding
Arif Wibowo A * , Kurniawan Kurniawan A , Dwi Atminarso A B , Tri Heru Prihadi C , Lee J. Baumgartner B , Meaghan L. Rourke B D , Satoshi Nagai E , Nicolas Hubert F and Anti Vasemagi G HA Research Center for Conservation of Marine and Inland Water Resources, National Research and Innovation Agency, Jalan Raya Jakarta-Bogor Km. 48 Cibinong, Bogor, West Java 16911, Indonesia.
B Gulbali Institute for Agriculture, Water and Environment, Charles Sturt University, PO Box 789, Albury, NSW 2640, Australia.
C Research Center for Fisheries, National Research and Innovation Agency, Jalan Raya Jakarta-Bogor Km. 48 Cibinong, Bogor, West Java 16911, Indonesia.
D New South Wales Department of Primary Industries, Narrandera Fisheries Centre, Narrandera, NSW 2700, Australia.
E Japan Fisheries Research and Education Agency, Fisheries Resources Institute, Fisheries Stock Assessment Center, Yokohama, Japan.
F Université Montpellier (UMR) 5554 Institut des sciences de l’évolution de Montpellier (ISEM) (IRD, UM, CNRS, EPHE), Université de Montpellier, Place Eugène Bataillon, Montpellier cedex 05 34095, France.
G Department of Aquatic Resources, Institute of Freshwater Research, Swedish University of Agricultural Sciences, Drottningholm, Sweden.
H Estonian University of Life Sciences, Institute of Veterinary Medicine and Animal Sciences, Tartu, Estonia.
Pacific Conservation Biology 29(4) 340-350 https://doi.org/10.1071/PC21078
Submitted: 25 December 2021 Accepted: 29 July 2022 Published: 25 August 2022
© 2023 The Author(s) (or their employer(s)). Published by CSIRO Publishing. This is an open access article distributed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (CC BY-NC-ND)
Abstract
Context: The ability to accurately assess biodiversity is a critical first step towards effective conservation and management. However, assessment of biodiversity using conventional monitoring programs is often constrained by high cost and a lack of taxonomic expertise. Environmental DNA (eDNA) metabarcoding may be a useful tool to efficiently catalogue biodiversity in areas that cannot be easily assessed using other methods.
Aims: Here, we evaluated the potential of eDNA metabarcoding for assessing fish biodiversity and distribution in the Kumbe River, Papua Province, Indonesia.
Methods: We selected four sampling locations and collected seven eDNA samples from each location. We used eDNA metabarcoding of the Cytochrome-b gene to characterise the fish community.
Key results: A total of 23 species were detected, three of which comprised 92% of sequence reads detected: Melanotaenia goldiei (32%), Craterocephalus randi (31%), and the invasive tilapia Oreochromis niloticus (29%). Only five species that were previously detected using conventional methods were detected by metabarcoding: M. goldiei, Craterocephalus stercusmuscarum, O. niloticus, Neoarius graeffei, and Arius arius. We detected 18 species (70% native) that have never been recorded from the Kumbe River.
Conclusions: This work has demonstrated that fish biodiversity is substantially underestimated in the Kumbe River. Environmental DNA metabarcoding is a promising rapid, non-invasive and cost-effective method for assessing fish biodiversity in Papua.
Implications: The findings support future investment in eDNA metabarcoding to characterise the fish biodiversity in Papua. This will assist in allocating the limited resources for conservation and management to areas most at risk from anthropogenic impacts.
Keywords: biodiversity, eDNA, freshwater fish, Indonesia, metabarcoding, Papua, river, tropical.
References
Anonymous (2010) Inventarisation of river in Papua, Indonesia in 2010. Available at https://lingkunganhidup.papua.go.id/gi/fckimage/file/SLHD/Tabel%20SD-11.pdfAustin, KG, Schwantes, A, Gu, Y, and Kasibhatla, PS (2019). What causes deforestation in Indonesia? Environmental Research Letters 14, 024007.
| What causes deforestation in Indonesia?Crossref | GoogleScholarGoogle Scholar |
Bartkowski, B, Lienhoop, N, and Hansjürgens, B (2015). Capturing the complexity of biodiversity: a critical review of economic valuation studies of biological diversity. Ecological Economics 113, 1–14.
| Capturing the complexity of biodiversity: a critical review of economic valuation studies of biological diversity.Crossref | GoogleScholarGoogle Scholar |
Bessey, C, Jarman, SN, Berry, O, Olsen, YS, Bunce, M, Simpson, T, Power, M, McLaughlin, J, Edgar, GJ, and Keesing, J (2020). Maximizing fish detection with eDNA metabarcoding. Environmental DNA 2, 493–504.
| Maximizing fish detection with eDNA metabarcoding.Crossref | GoogleScholarGoogle Scholar |
Burian, A, Mauvisseau, Q, Bulling, M, Domisch, S, Qian, S, and Sweet, M (2021). Improving the reliability of eDNA data interpretation. Molecular Ecology Resources 21, 1422–1433.
| Improving the reliability of eDNA data interpretation.Crossref | GoogleScholarGoogle Scholar |
Bylemans, J, Gleeson, DM, Duncan, RP, Hardy, CM, and Furlan, EM (2019). A performance evaluation of targeted eDNA and eDNA metabarcoding analyses for freshwater fishes. Environmental DNA 1, 402–414.
| A performance evaluation of targeted eDNA and eDNA metabarcoding analyses for freshwater fishes.Crossref | GoogleScholarGoogle Scholar |
Carraro, L, Hartikainen, H, Jokela, J, Bertuzzo, E, and Rinaldo, A (2018). Estimating species distribution and abundance in river networks using environmental DNA. Proceedings of the National Academy of Sciences 115, 11724–11729.
| Estimating species distribution and abundance in river networks using environmental DNA.Crossref | GoogleScholarGoogle Scholar |
Cilleros, K, Valentini, A, Allard, L, Dejean, T, Etienne, R, Grenouillet, G, Iribar, A, Taberlet, P, Vigouroux, R, and Brosse, S (2019). Unlocking biodiversity and conservation studies in high-diversity environments using environmental DNA (eDNA): a test with Guianese freshwater fishes. Molecular Ecology Resources 19, 27–46.
| Unlocking biodiversity and conservation studies in high-diversity environments using environmental DNA (eDNA): a test with Guianese freshwater fishes.Crossref | GoogleScholarGoogle Scholar |
Cleary DFR, DeVantier L (2011) Indonesia: threats to the country’s biodiversity. In ‘Encyclopedia of environmental health’. (Ed. JO Nriagu) pp. 187–197. (Elsevier)
Dahruddin, H, Hutama, A, Busson, F, Sauri, S, Hanner, R, Keith, P, Hadiaty, R, and Hubert, N (2017). Revisiting the ichthyodiversity of Java and Bali through DNA barcodes: taxonomic coverage, identification accuracy, cryptic diversity and identification of exotic species. Molecular Ecology Resources 17, 288–299.
| Revisiting the ichthyodiversity of Java and Bali through DNA barcodes: taxonomic coverage, identification accuracy, cryptic diversity and identification of exotic species.Crossref | GoogleScholarGoogle Scholar |
de Bruyn, M, Rüber, L, Nylinder, S, Stelbrink, B, Lovejoy, NR, Lavoué, S, Tan, HH, Nugroho, E, Wowor, D, Ng, PKL, Siti Azizah, MN, Von Rintelen, T, Hall, R, and Carvalho, GR (2013). Paleo-drainage basin connectivity predicts evolutionary relationships across three Southeast Asian biodiversity hotspots. Systematic Biology 62, 398–410.
| Paleo-drainage basin connectivity predicts evolutionary relationships across three Southeast Asian biodiversity hotspots.Crossref | GoogleScholarGoogle Scholar |
de Bruyn, M, Stelbrink, B, Morley, RJ, Hall, R, Carvalho, GR, Cannon, CH, van den Bergh, G, Meijaard, E, Metcalfe, I, Boitani, L, Maiorano, L, Shoup, R, and von Rintelen, T (2014). Borneo and Indochina are major evolutionary hotspots for Southeast Asian biodiversity. Systematic Biology 63, 879–901.
| Borneo and Indochina are major evolutionary hotspots for Southeast Asian biodiversity.Crossref | GoogleScholarGoogle Scholar |
Deiner, K, Bik, HM, Mächler, E, Seymour, M, Lacoursière-Roussel, A, Altermatt, F, Creer, S, Bista, I, Lodge, DM, de Vere, N, Pfrender, ME, and Bernatchez, L (2017). Environmental DNA metabarcoding: transforming how we survey animal and plant communities. Molecular Ecology 26, 5872–5895.
| Environmental DNA metabarcoding: transforming how we survey animal and plant communities.Crossref | GoogleScholarGoogle Scholar |
Ditya, YC, Wibowo, A, and Husnah, H (2018). Spatial and temporal distribution of fish in the floodplain of Kumbe River. Papua. Indonesian Fisheries Research Journal 24, 69–81.
| Spatial and temporal distribution of fish in the floodplain of Kumbe River. Papua.Crossref | GoogleScholarGoogle Scholar |
Djalil, VN, Farajallah, A, and Wardiyatno, Y (2018). Application of environmental DNA (eDNA) for detection of Cherax quadricarinatus (Von Martens 1868) using water sample. Jurnal Biologi Tropis 18, 134–140.
| Application of environmental DNA (eDNA) for detection of Cherax quadricarinatus (Von Martens 1868) using water sample.Crossref | GoogleScholarGoogle Scholar |
Duda, JJ, Hoy, MS, Chase, DM, Pess, GR, Brenkman, SJ, McHenry, MM, and Ostberg, CO (2021). Environmental DNA is an effective tool to track recolonizing migratory fish following large-scale dam removal. Environmental DNA 3, 121–141.
| Environmental DNA is an effective tool to track recolonizing migratory fish following large-scale dam removal.Crossref | GoogleScholarGoogle Scholar |
Dunker, KJ, Sepulveda, AJ, Massengill, RL, Olsen, JB, Russ, OL, Wenburg, JK, and Antonovich, A (2016). Potential of environmental DNA to evaluate Northern Pike (Esox lucius) eradication efforts: an experimental test and case study. PLoS ONE 11, e0162277.
| Potential of environmental DNA to evaluate Northern Pike (Esox lucius) eradication efforts: an experimental test and case study.Crossref | GoogleScholarGoogle Scholar |
Ficetola, GF, Miaud, C, Pompanon, F, and Taberlet, P (2008). Species detection using environmental DNA from water samples. Biology Letters 4, 423–425.
| Species detection using environmental DNA from water samples.Crossref | GoogleScholarGoogle Scholar |
Ficetola, GF, Pansu, J, Bonin, A, Coissac, E, Giguet-Covex, C, De Barba, M, Gielly, L, Lopes, CM, Boyer, F, Pompanon, F, Raye, G, and Taberlet, P (2015). Replication levels, false presences and the estimation of the presence/absence from eDNA metabarcoding data. Molecular Ecology Resources 15, 543–556.
| Replication levels, false presences and the estimation of the presence/absence from eDNA metabarcoding data.Crossref | GoogleScholarGoogle Scholar |
Fujii, K, Doi, H, Matsuoka, S, Nagano, M, Sato, H, and Yamanaka, H (2019). Environmental DNA metabarcoding for fish community analysis in backwater lakes: a comparison of capture methods. PLoS ONE 14, e0210357.
| Environmental DNA metabarcoding for fish community analysis in backwater lakes: a comparison of capture methods.Crossref | GoogleScholarGoogle Scholar |
Garg, T, Hamilton, SE, Hochard, JP, Kresch, EP, and Talbot, J (2018). (Not so) gently down the stream: river pollution and health in Indonesia. Journal of Environmental Economics and Management 92, 35–53.
| (Not so) gently down the stream: river pollution and health in Indonesia.Crossref | GoogleScholarGoogle Scholar |
Goldberg, CS, Turner, CR, Deiner, K, Klymus, KE, Thomsen, PF, Murphy, MA, Spear, SF, McKee, A, Oyler-McCance, SJ, Cornman, RS, Laramie, MB, Mahon, AR, Lance, RF, Pilliod, DS, Strickler, KM, Waits, LP, Fremier, AK, Takahara, T, Herder, JE, Taberlet, P, and Gilbert, M (2016). Critical considerations for the application of environmental DNA methods to detect aquatic species. Methods in Ecology and Evolution 7, 1299–1307.
| Critical considerations for the application of environmental DNA methods to detect aquatic species.Crossref | GoogleScholarGoogle Scholar |
Gustiano, R, Kurniawan, K, and Haryono, H (2021). Optimizing the utilization of genetic resources of Indonesian native freshwater fish. Asian Journal of Conservation Biology 10, 189–196.
| Optimizing the utilization of genetic resources of Indonesian native freshwater fish.Crossref | GoogleScholarGoogle Scholar |
Hänfling, B, Lawson Handley, L, Read, DS, Hahn, C, Li, J, Nichols, P, Blackman, RC, Oliver, A, and Winfield, IJ (2016). Environmental DNA metabarcoding of lake fish communities reflects long-term data from established survey methods. Molecular Ecology 25, 3101–3119.
| Environmental DNA metabarcoding of lake fish communities reflects long-term data from established survey methods.Crossref | GoogleScholarGoogle Scholar |
Hansen, BK, Bekkevold, D, Clausen, LW, and Nielsen, EE (2018). The sceptical optimist: challenges and perspectives for the application of environmental DNA in marine fisheries. Fish and Fisheries 19, 751–768.
| The sceptical optimist: challenges and perspectives for the application of environmental DNA in marine fisheries.Crossref | GoogleScholarGoogle Scholar |
Herder, F, Schliewen, UK, Geiger, MF, Hadiaty, RK, Gray, SM, McKinnon, JS, Walter, RP, and Pfaender, J (2012). Alien invasion in Wallace’s dreamponds: records of the hybridogenic “flowerhorn” cichlid in Lake Matano, with an annotated checklist of fish species introduced to the Malili Lakes system in Sulawesi. Aquatic Invasions 7, 521–535.
| Alien invasion in Wallace’s dreamponds: records of the hybridogenic “flowerhorn” cichlid in Lake Matano, with an annotated checklist of fish species introduced to the Malili Lakes system in Sulawesi.Crossref | GoogleScholarGoogle Scholar |
Hubert, N, Kadarusman, , Wibowo, A, Busson, F, Caruso, D, Sulandari, S, Nafiqoh, N, Pouyaud, L, Rüber, L, Avarre, J-C, Herder, F, Hanner, R, Keith, P, and Hadiaty, RK (2015). DNA barcoding Indonesian freshwater fishes: challenges and prospects. DNA Barcodes 3, 144–169.
| DNA barcoding Indonesian freshwater fishes: challenges and prospects.Crossref | GoogleScholarGoogle Scholar |
Hubert, N, Lumbantobing, D, Sholihah, A, Dahruddin, H, Delrieu-Trottin, E, Busson, F, Sauri, S, Hadiaty, R, and Keith, P (2019). Revisiting species boundaries and distribution ranges of Nemacheilus spp. (Cypriniformes: Nemacheilidae) and Rasbora spp. (Cypriniformes: Cyprinidae) in Java, Bali and Lombok through DNA barcodes: implications for conservation in a biodiversity hotspot. Conservation Genetics 20, 517–529.
| Revisiting species boundaries and distribution ranges of Nemacheilus spp. (Cypriniformes: Nemacheilidae) and Rasbora spp. (Cypriniformes: Cyprinidae) in Java, Bali and Lombok through DNA barcodes: implications for conservation in a biodiversity hotspot.Crossref | GoogleScholarGoogle Scholar |
Huson, DH, Auch, AF, Qi, J, and Schuster, SC (2007). MEGAN analysis of metagenomic data. Genome Research 17, 377–386.
| MEGAN analysis of metagenomic data.Crossref | GoogleScholarGoogle Scholar |
Imai, N, Furukawa, T, Tsujino, R, Kitamura, S, and Yumoto, T (2018). Factors affecting forest area change in Southeast Asia during 1980–2010. PLoS ONE 13, e0197391.
| Factors affecting forest area change in Southeast Asia during 1980–2010.Crossref | GoogleScholarGoogle Scholar |
Itakura, H, Wakiya, R, Yamamoto, S, Kaifu, K, Sato, T, and Minamoto, T (2019). Environmental DNA analysis reveals the spatial distribution, abundance, and biomass of Japanese eels at the river-basin scale. Aquatic Conservation: Marine and Freshwater Ecosystems 29, 361–373.
| Environmental DNA analysis reveals the spatial distribution, abundance, and biomass of Japanese eels at the river-basin scale.Crossref | GoogleScholarGoogle Scholar |
Janosik, AM, and Johnston, CE (2015). Environmental DNA as an effective tool for detection of imperiled fishes. Environmental Biology of Fishes 98, 1889–1893.
| Environmental DNA as an effective tool for detection of imperiled fishes.Crossref | GoogleScholarGoogle Scholar |
Jellyman, PG, Bauld, JT, and Crow, SK (2017). The effect of ramp slope and surface type on the climbing success of shortfin eel (Anguilla australis) elvers. Marine and Freshwater Research 68, 1317–1324.
| The effect of ramp slope and surface type on the climbing success of shortfin eel (Anguilla australis) elvers.Crossref | GoogleScholarGoogle Scholar |
Kadarusman, , Hubert, N, Hadiaty, RK, Sudarto, , Paradis, E, and Pouyaud, L (2012). Cryptic diversity in Indo-Australian rainbowfishes revealed by DNA barcoding: implications for conservation in a biodiversity hotspot candidate. PLoS ONE 7, e40627.
| Cryptic diversity in Indo-Australian rainbowfishes revealed by DNA barcoding: implications for conservation in a biodiversity hotspot candidate.Crossref | GoogleScholarGoogle Scholar |
Koh LP, Kettle CJ, Sheil D, Lee TM, Giam X, Gibson L, Clements GR (2013) Biodiversity state and trends in Southeast Asia. In ‘Encyclopedia of biodiversity’. (Ed. SA Levin) pp. 509–527. (Academic Press)
Kottelat M, Whitten T (1996) Freshwater biodiversity in Asia with special reference to fish. World Bank Technical paper. (World Bank)
Kurniawan, K, Gustiano, R, Kusmini, II, and Prakoso, VA (2021). Genetic resources preservation and utilization of Indonesian native freshwater fish consumption. Ecology, Environment and Conservation 27, 227–233.
Lasmana, Y, Simanungkalit, P, Gifariyono, M, Sotyadarpita, G, and Triadi, LB (2018). Potential of tidal lowland for irrigation development in Merauke Regency using hydrodynamic modelling 1D2D. Jurnal Teknik Hidraulik 9, 17–32.
| Potential of tidal lowland for irrigation development in Merauke Regency using hydrodynamic modelling 1D2D.Crossref | GoogleScholarGoogle Scholar |
Lecaudey, LA, Schletterer, M, Kuzovlev, VV, Hahn, C, and Weiss, SJ (2019). Fish diversity assessment in the headwaters of the Volga River using environmental DNA metabarcoding. Aquatic Conservation: Marine and Freshwater Ecosystems 29, 1785–1800.
| Fish diversity assessment in the headwaters of the Volga River using environmental DNA metabarcoding.Crossref | GoogleScholarGoogle Scholar |
Ligtvoet, W, Witte, F, Goldschmidt, T, van Oijen, MJP, Wanink, JH, and Goudswaard, PC (1991). Species extinction and concomitant ecological changes in Lake Victoria. Netherlands Journal of Zoology 42, 214–232.
| Species extinction and concomitant ecological changes in Lake Victoria.Crossref | GoogleScholarGoogle Scholar |
Mace, GM, Norris, K, and Fitter, AH (2012). Biodiversity and ecosystem services: a multilayered relationship. Trends in Ecology & Evolution 27, 19–26.
| Biodiversity and ecosystem services: a multilayered relationship.Crossref | GoogleScholarGoogle Scholar |
Majaneva, M, Diserud, OH, Eagle, SHC, Bostrom, E, Hajibabaei, M, and Ekrem, T (2018). Environmental DNA filtration techniques affect recovered biodiversity. Scientific Reports 8, 4682.
| Environmental DNA filtration techniques affect recovered biodiversity.Crossref | GoogleScholarGoogle Scholar |
McElroy, ME, Dressler, TL, Titcomb, GC, Wilson, EA, Deiner, K, Dudley, TL, Eliason, EJ, Evans, NT, Gaines, SD, Lafferty, KD, Lamberti, GA, Li, Y, Lodge, DM, Love, MS, Mahon, AR, Pfrender, ME, Renshaw, MA, Selkoe, KA, and Jerde, CL (2020). Calibrating environmental DNA metabarcoding to conventional surveys for measuring fish species richness. Frontiers in Ecology and Evolution 8, 276.
| Calibrating environmental DNA metabarcoding to conventional surveys for measuring fish species richness.Crossref | GoogleScholarGoogle Scholar |
Meyer, M, and Kircher, M (2010). Illumina sequencing library preparation for highly multiplexed target capture and sequencing. Cold Spring Harbour Protocols 6, 1–10.
Nathan, LR, Jerde, CL, Budny, ML, and Mahon, AR (2015). The use of environmental DNA in invasive species surveillance of the Great Lakes commercial bait trade. Conservation Biology 29, 430–439.
| The use of environmental DNA in invasive species surveillance of the Great Lakes commercial bait trade.Crossref | GoogleScholarGoogle Scholar |
Nugraha, MFI, Pouyaud, L, Carman, O, Widyastuti, U, Junior, MZ, Kadarusman, , and Avarre, J-C (2015). Genetic diversity of Boeseman’s rainbowfish (Melanotaenia boesemani) reared in Indonesian farms compared to endangered natural populations. Tropical Conservation Science 8, 796–812.
| Genetic diversity of Boeseman’s rainbowfish (Melanotaenia boesemani) reared in Indonesian farms compared to endangered natural populations.Crossref | GoogleScholarGoogle Scholar |
Ogutu-Ohwayo, R (1990). The decline of native fishes of Lake Victoria and Kyoga (East Africa) and the impact of the introduced species, other environmental characteristics on amphibian distribution and abundance in mountain lakes of Northern Spain. Animal Conservation 9, 171–178.
Olds, BP, Jerde, CL, Renshaw, MA, Li, Y, Evans, NT, Turner, CR, Deiner, K, Mahon, AR, Brueseke, MA, Shirey, PD, Pfrender, ME, Lodge, DM, and Lamberti, GA (2016). Estimating species richness using environmental DNA. Ecology and Evolution 6, 4214–4226.
| Estimating species richness using environmental DNA.Crossref | GoogleScholarGoogle Scholar |
Pauchard, N (2017). Access and benefit sharing under the convention on biological diversity and its protocol: what can some numbers tell us about the effectiveness of the regulatory regime? Resources 6, 11.
| Access and benefit sharing under the convention on biological diversity and its protocol: what can some numbers tell us about the effectiveness of the regulatory regime?Crossref | GoogleScholarGoogle Scholar |
Peel, MC, Finlayson, BL, and McMahon, TA (2007). Updated world map of the Köppen-Geiger climate classification. Hydrology and Earth System Sciences 11, 1633–1644.
| Updated world map of the Köppen-Geiger climate classification.Crossref | GoogleScholarGoogle Scholar |
Pereira, HM, Ferrier, S, Walters, M, Geller, GN, Jongman, RHG, Scholes, RJ, Bruford, MW, Brummitt, N, Butchart, SHM, Cardoso, AC, Coops, NC, Dulloo, E, Faith, DP, Freyhof, J, Gregory, RD, Heip, C, Höft, R, Hurtt, G, Jetz, W, Karp, DS, McGeoch, MA, Obura, D, Onoda, Y, Pettorelli, N, Reyers, B, Sayre, R, Scharlemann, JPW, Stuart, SN, Turak, E, Walpole, M, and Wegmann, M (2013). Essential biodiversity variables. Science 339, 277–278.
| Essential biodiversity variables.Crossref | GoogleScholarGoogle Scholar |
Pont, D, Rocle, M, Valentini, A, Civade, R, Jean, P, Maire, A, Roset, N, Schabuss, M, Zornig, H, and Dejean, T (2018). Environmental DNA reveals quantitative patterns of fish biodiversity in large rivers despite its downstream transportation. Scientific Reports 8, 10361.
| Environmental DNA reveals quantitative patterns of fish biodiversity in large rivers despite its downstream transportation.Crossref | GoogleScholarGoogle Scholar |
Rees, HC, Maddison, BC, Middleditch, DJ, Patmore, JRM, and Gough, KC (2014). REVIEW: the detection of aquatic animal species using environmental DNA – a review of eDNA as a survey tool in ecology. Journal of Applied Ecology 51, 1450–1459.
| REVIEW: the detection of aquatic animal species using environmental DNA – a review of eDNA as a survey tool in ecology.Crossref | GoogleScholarGoogle Scholar |
Rice, CJ, Larson, ER, and Taylor, CA (2018). Environmental DNA detects a rare large river crayfish but with little relation to local abundance. Freshwater Biology 63, 443–455.
| Environmental DNA detects a rare large river crayfish but with little relation to local abundance.Crossref | GoogleScholarGoogle Scholar |
Roesma, DI, Djong, HT, Janra, MN, and Aidil, DR (2021). Freshwater vertebrates monitoring in Maninjau Lake, West Sumatra, Indonesia using environmental DNA. Biodiversitas Journal of Biological Diversity 22, 2794–2802.
| Freshwater vertebrates monitoring in Maninjau Lake, West Sumatra, Indonesia using environmental DNA.Crossref | GoogleScholarGoogle Scholar |
Rojahn, J, Gleeson, DM, Furlan, E, Haeusler, T, and Bylemans, J (2021). Improving the detection of rare native fish species in environmental DNA metabarcoding surveys. Aquatic Conservation: Marine and Freshwater Ecosystems 31, 990–997.
| Improving the detection of rare native fish species in environmental DNA metabarcoding surveys.Crossref | GoogleScholarGoogle Scholar |
Sato, H, Sogo, Y, Doi, H, and Yamanaka, H (2017). Usefulness and limitations of sample pooling for environmental DNA metabarcoding of freshwater fish communities. Scientific Reports 7, 14860.
| Usefulness and limitations of sample pooling for environmental DNA metabarcoding of freshwater fish communities.Crossref | GoogleScholarGoogle Scholar |
Schenekar, T, Schletterer, M, Lecaudey, LA, and Weiss, SJ (2020). Reference databases, primer choice, and assay sensitivity for environmental metabarcoding: lessons learnt from a re-evaluation of an eDNA fish assessment in the Volga headwaters. River Research and Applications 36, 1004–1013.
| Reference databases, primer choice, and assay sensitivity for environmental metabarcoding: lessons learnt from a re-evaluation of an eDNA fish assessment in the Volga headwaters.Crossref | GoogleScholarGoogle Scholar |
Seymour, M (2019). Rapid progression and future of environmental DNA research. Communications Biology 2, 80.
| Rapid progression and future of environmental DNA research.Crossref | GoogleScholarGoogle Scholar |
Sholihah, A, Delrieu-Trottin, E, Sukmono, T, Dahruddin, H, Risdawati, R, Elvyra, R, Wibowo, A, Kustiati, K, Busson, F, Sauri, S, Nurhaman, U, Dounias, E, Zein, MSA, Fitriana, Y, Utama, IV, Muchlisin, ZA, Agnèse, J-F, Hanner, R, Wowor, D, Steinke, D, Keith, P, Rüber, L, and Hubert, N (2020). Disentangling the taxonomy of the subfamily Rasborinae (Cypriniformes, Danionidae) in Sundaland using DNA barcodes. Scientific Reports 10, 2818.
| Disentangling the taxonomy of the subfamily Rasborinae (Cypriniformes, Danionidae) in Sundaland using DNA barcodes.Crossref | GoogleScholarGoogle Scholar |
Sholihah, A, Delrieu-Trottin, E, Condamine, FL, Wowor, D, Rüber, L, Pouyaud, L, Agnèse, J-F, and Hubert, N (2021a). Impact of pleistocene eustatic fluctuations on evolutionary dynamics in southeast asian biodiversity hotspots. Systematic Biology 70, 940–960.
| Impact of pleistocene eustatic fluctuations on evolutionary dynamics in southeast asian biodiversity hotspots.Crossref | GoogleScholarGoogle Scholar |
Sholihah, A, Delrieu-Trottin, E, Sukmono, T, Dahruddin, H, Pouzadoux, J, Tilak, M-K, Fitriana, Y, Agnèse, J-F, Condamine, FL, Wowor, D, Rüber, L, and Hubert, N (2021b). Limited dispersal and in situ diversification drive the evolutionary history of Rasborinae fishes in Sundaland. Journal of Biogeography 48, 2153–2173.
| Limited dispersal and in situ diversification drive the evolutionary history of Rasborinae fishes in Sundaland.Crossref | GoogleScholarGoogle Scholar |
Shu, L, Ludwig, A, and Peng, Z (2021). Environmental DNA metabarcoding primers for freshwater fish detection and quantification: in silico and in tanks. Ecology and Evolution 11, 8281–8294.
| Environmental DNA metabarcoding primers for freshwater fish detection and quantification: in silico and in tanks.Crossref | GoogleScholarGoogle Scholar |
Sigsgaard, EE, Carl, H, Møller, PR, and Thomsen, PF (2015). Monitoring the near-extinct European weather loach in Denmark based on environmental DNA from water samples. Biological Conservation 183, 46–52.
| Monitoring the near-extinct European weather loach in Denmark based on environmental DNA from water samples.Crossref | GoogleScholarGoogle Scholar |
Sigsgaard, EE, Jensen, MR, Winkelmann, IE, Møller, PR, Hansen, MM, and Thomsen, PF (2020). Population-level inferences from environmental DNA – current status and future perspectives. Evolutionary Applications 13, 245–262.
| Population-level inferences from environmental DNA – current status and future perspectives.Crossref | GoogleScholarGoogle Scholar |
Simpfendorfer, CA, Kyne, PM, Noble, TH, Goldsbury, J, Basiita, RK, Lindsay, R, Shields, A, Perry, C, and Jerry, DR (2016). Environmental DNA detects critically endangered largetooth sawfish in the wild. Endangered Species Research 30, 109–116.
| Environmental DNA detects critically endangered largetooth sawfish in the wild.Crossref | GoogleScholarGoogle Scholar |
Stewart, KA (2019). Understanding the effects of biotic and abiotic factors on sources of aquatic environmental DNA. Biodiversity and Conservation 28, 983–1001.
| Understanding the effects of biotic and abiotic factors on sources of aquatic environmental DNA.Crossref | GoogleScholarGoogle Scholar |
Taberlet, P, Coissac, E, Pompanon, F, Brochmann, C, and Willerslev, E (2012). Towards next-generation biodiversity assessment using DNA metabarcoding. Molecular Ecology 21, 2045–2050.
| Towards next-generation biodiversity assessment using DNA metabarcoding.Crossref | GoogleScholarGoogle Scholar |
Thalinger, B, Wolf, E, Traugott, M, and Wanzenböck, J (2019). Monitoring spawning migrations of potamodromous fish species via eDNA. Scientific Reports 9, 15388.
| Monitoring spawning migrations of potamodromous fish species via eDNA.Crossref | GoogleScholarGoogle Scholar |
Trebitz, AS, Hoffman, JC, Darling, JA, Pilgrim, EM, Kelly, JR, Brown, EA, Chadderton, WL, Egan, SP, Grey, EK, Hashsham, SA, Klymus, KE, Mahon, AR, Ram, JL, Schultz, MT, Stepien, CA, and Schardt, JC (2017). Early detection monitoring for aquatic non-indigenous species: optimizing surveillance, incorporating advanced technologies, and identifying research needs. Journal of Environmental Management 202, 299–310.
| Early detection monitoring for aquatic non-indigenous species: optimizing surveillance, incorporating advanced technologies, and identifying research needs.Crossref | GoogleScholarGoogle Scholar |
Turner, CR, Uy, KL, and Everhart, RC (2015). Fish environmental DNA is more concentrated in aquatic sediments than surface water. Biological Conservation 183, 93–102.
| Fish environmental DNA is more concentrated in aquatic sediments than surface water.Crossref | GoogleScholarGoogle Scholar |
Ulayya, N, Andayani, N, and Maryanto, AE (2020). Development of environmental DNA approaches to detect alligator gar (Atractosteus spatula) from water samples. IOP Conference Series: Earth and Environmental Science 481, 012013.
| Development of environmental DNA approaches to detect alligator gar (Atractosteus spatula) from water samples.Crossref | GoogleScholarGoogle Scholar |
Valiere, N, and Taberlet, P (2000). Urine collected in the field as a source of DNA for species and individual identification. Molecular Ecology 9, 2150–2152.
Wibowo, A, Wahlberg, N, and Vasemägi, A (2017). DNA barcoding of fish larvae reveals uncharacterised biodiversity in tropical peat swamps of New Guinea, Indonesia. Marine and Freshwater Research 68, 1079–1087.
| DNA barcoding of fish larvae reveals uncharacterised biodiversity in tropical peat swamps of New Guinea, Indonesia.Crossref | GoogleScholarGoogle Scholar |
Wibowo, A, Shibuno, T, and Sulit, VT (2018). The making of a center of excellence in science and technology on inland fisheries management: the SEAFDEC/IFRDMD. Fish for the People 16, 28–33.
Xiao, Y, Ouyang, Z, Xu, W, Xiao, Y, Zheng, H, and Xian, C (2016). Optimizing hotspot areas for ecological planning and management based on biodiversity and ecosystem services. Chinese Geographical Science 26, 256–269.
| Optimizing hotspot areas for ecological planning and management based on biodiversity and ecosystem services.Crossref | GoogleScholarGoogle Scholar |
Xiong, F, Shu, L, Zeng, H, Gan, X, He, S, and Peng, Z (2022). Methodology for fish biodiversity monitoring with environmental DNA metabarcoding: the primers, databases and bioinformatic pipelines. Water Biology and Security 1, 100007.
| Methodology for fish biodiversity monitoring with environmental DNA metabarcoding: the primers, databases and bioinformatic pipelines.Crossref | GoogleScholarGoogle Scholar |
Yachi, S, and Loreau, M (1999). Biodiversity and ecosystem productivity in a fluctuating environment: the insurance hypothesis. Proceedings of the National Academy of Sciences 96, 1463–1468.
| Biodiversity and ecosystem productivity in a fluctuating environment: the insurance hypothesis.Crossref | GoogleScholarGoogle Scholar |
Yamanaka, H, and Minamoto, T (2016). The use of environmental DNA of fishes as an efficient method of determining habitat connectivity. Ecological Indicators 62, 147–153.
| The use of environmental DNA of fishes as an efficient method of determining habitat connectivity.Crossref | GoogleScholarGoogle Scholar |
Zhang, S, Zhao, J, and Yao, M (2020). A comprehensive and comparative evaluation of primers for metabarcoding eDNA from fish. Methods in Ecology and Evolution 11, 1609–1625.
| A comprehensive and comparative evaluation of primers for metabarcoding eDNA from fish.Crossref | GoogleScholarGoogle Scholar |