Thomas G. Dahlgren’s research while affiliated with University of Gothenburg and other places

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Publications (205)


A new species of Erinaceusyllis (Annelida: Syllidae) discovered at a wood-fall in the eastern Clarion-Clipperton Zone, central Pacific Ocean.
  • Article

November 2024

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17 Reads

Deep Sea Research Part I Oceanographic Research Papers

Christian L. Nilsson

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Helena Wiklund

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Adrian G. Glover

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[...]

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Thomas G. Dahlgren

Diversity and phylogeny of demosponge fauna in the abyssal nodule fields of the eastern Clarion‐Clipperton Zone, Pacific Ocean

July 2024

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78 Reads

Zoologica Scripta

More than 7000 demosponge species have been described to date globally but <2% are known from the abyssal plains, which occupy some 50% of the Earth's surface. The demosponge fauna in the abyssal nodule fields at Clarion‐Clipperton Zone (CCZ) in the Pacific Ocean, a region being explored for potential deep‐sea mining, is a case in point. A total of 21 species belonging to 13 genera in nine families and seven orders were identified from the eastern region of the CCZ, of which most are new to science. They are small in size (<5 mm), with simple skeletons and poor spicule diversity. All ordinal representatives of Demospongiae were utilized to determine taxonomic position of the highly homoplasious tiny demosponges in our molecular phylogenetic analyses. Our results indicated Plenaster craigi , the most common and abundant species in the eastern CCZ, represents a new family, and possibly in a new order. Interestingly, P. craigi and members of the families Polymastiidae and Hamacanthidae, all filter‐feeding demosponge species, are far more abundant in nodule fields than the carnivorous sponges (Cladorhizidae) which were widely known to be the most dominant demosponge group in the abyssal depths. Lastly, it is highly likely that such tiny demosponges are present in other habitats. They might have been overlooked and/or ignored by sponge researchers in the past due to their tiny size and nondescript habitus. These demosponges could be distinct new species, not juveniles or indeterminates and warrant full taxonomic treatment.


Sampling sites for eDNA, BRUV recordings and fishing effort. All sites, number of eDNA samples N = 4, except for reference points where N = 3.
Monitoring of the invasive round goby in an estuarine seascape based on eDNA
  • Preprint
  • File available

May 2024

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34 Reads

Non-indigenous species (NIS) is one of the five most global concerns when it comes to ecosystem services and threats to native biodiversity. This is especially true in aquatic environments which are harder to monitor than terrestrial environments, and NIS are often found first when they are fully established and basically impossible to eradicate. In marine environments, this is further complicated due to the connectivity and difficulty of eradication. The development and implementation of effective monitoring methods for marine NIS are therefore crucial to enable early detection useful for management strategies. In this study, we develop and evaluate environmental DNA monitoring using quantitative (q)PCR as a means to assess presence of the euryhaline round goby fish (Neogobius melanostomus) in a seascape environment close to Scandinavia's largest shipping port. We developed a dPCR assay for the species, targeting a region of 12S gene, and verified its specificity compared to other common species from the gobiid-family in the region. We also experimentally determined the decaying rate of round goby DNA in water to a half-life of 9.8 hours in 15 PSU and 15 dC with live fish in captivity. Finally, we sampled 10 sites within a 400 km2 area for eDNA and presence of the species using fyke-nets and baited remote video to validate the accuracy of the water samples to predict presence, and abundance. We found that the number of DNA copies extracted from the water samples varied strongly at sites where round gobies were caught in nets or on video, but that the average value from four water samples significantly correlated with an average value from four video samples, and also with the total catch at each site. The eDNA assay also detected signals from the species at sites where no fish were caught by fishing or on video. These results show that this method is highly sensitive for the species even in low abundance, and with sufficient amounts of replicates, it can be possible to determine the relative abundance between sites.

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Fig. 1. Map of the North Sea, Skagerrak and Kattegat. Modified from ICES (2019).
Productivity attributes and cut-offs for low, medium, and high-risk scores.
Data quality tracking used, based on Patrick et al. (2010).
Ecological risk assessment of invertebrates caught in Swedish west-coast fisheries

February 2024

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45 Reads

Fisheries Research

Ecological risk assessments are important as scientific support for the implementation of ecosystem-based fisheries management. Marine invertebrates are important to ecosystem structure and function and may be sensitive to fishing pressure. Some are also of increasing commercial value-but have hitherto not been paid much attention to in ecological risk assessments. Here, catches of invertebrates in Swedish west-coast fisheries with demersal trawls and creels are examined from an ecological risk assessment perspective. It is found that few non-commercial invertebrate species have been regularly recorded in onboard observer programs. Furthermore, for being a comparatively well-studied area, it is striking to find that out of the 93 species included, 56% could be classified as data deficient in terms of known attributes needed to perform basic ecological risk assessments. This implies that there is little or no available information on the basic life history traits important for estimating productivity. Additionally, onboard observer data for invertebrates are inadequate beyond targeted commercial species for robust statistical analysis on volumes generated over time and between fisheries. However, over 18% of the studied species are categorized as red-listed on the Swedish IUCN Red List. Combined with the few records available in observer data programs, the study illustrates the need to pay more attention to marine invertebrates in fisheries monitoring programs and research, especially bycaught and non-commercial invertebrate species.



Checklist of newly-vouchered annelid taxa from the Clarion-Clipperton Zone, central Pacific Ocean, based on morphology and genetic delimitation

September 2023

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258 Reads

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2 Citations

We present a checklist of annelids from recent United Kingdom Seabed Resources (UKSR) expeditions (Abyssal Baseline - ABYSSLINE project) to the eastern abyssal Pacific Clarion-Clipperton Zone (CCZ) polymetallic nodule fields, based on DNA species delimitation, including imagery of voucher specimens, Darwin Core (DwC) data and links to vouchered specimen material and new GenBank sequence records. This paper includes genetic and imagery data for 129 species of annelids from 339 records and is restricted to material that is, in general, in too poor a condition to describe formally at this time, but likely contains many species new to science. We make these data available both to aid future taxonomic studies in the CCZ that will be able to link back to these genetic data and specimens and to better underpin ongoing ecological studies of potential deep-sea mining impacts using the principles of FAIR (Findable, Accessible, Interoperable, Reusuable) data and specimens that will be available for all. We include genetic, imagery and all associated metadata in Darwin Core format for 129 species of annelids from the Clarion-Clipperton Zone, eastern abyssal Pacific, with 339 records.


Taxonomy, phylogeny, and biodiversity of Lumbrineridae (Annelida, Polychaeta) from the Central Pacific Clarion-Clipperton Zone

July 2023

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244 Reads

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1 Citation

The DNA taxonomy of six species of the annelid family Lumbrineridae collected from the Clarion-Clipperton Zone (CCZ) in the Central Pacific, an area of potential mining interest for polymetallic nodules, is presented. Lumbrinerids are an ecologically important and understudied annelid family within the deep sea, with many species still undescribed. This study aims to document the taxonomy and biodiversity of the CCZ using specimens collected from the UK-1, OMS, and NORI-D exploration contract areas and Areas of Particular Environmental Interest. Species were identified through a combination of morphological and molecular phylogenetic analysis. We present informal species descriptions associated with voucher specimens, accessible through the Natural History Museum (London) collections, to improve future taxonomic and biodiversity studies of this region. Five taxa in this study had no morphological or genetic matches within the literature and therefore are possibly new to science, but their suboptimal morphological preservation prevented the formalisation of new species. The most abundant taxon Lumbrinerides cf. laubieri (NHM_0020) was compared with the holotype of Lumbrinerides laubieri Miura, 1980 from the deep Northeast Atlantic. Currently no reliable morphological characters separating the Pacific and Atlantic specimens have been found and molecular data from the Atlantic specimens was not available.


Study region in the northeast Pacific basin and examples of abyssal benthic megafauna typically encountered at different depth ranges
a, Map of study locations surveyed using deep-sea robots (ROVs and AUVs). Points indicate locations (depths 3,900–5,300 m) where data from seabed imagery studies were collated from, aligned and reanalysed using standardized methodology for homogenous detectability and taxonomic identification of invertebrate benthic megafauna (animals >10 mm). The colour of the points follows a consistent scheme used to differentiate each site in the other figures. b–p, Examples of abyssal Pacific metazoan megafauna morphotypes (including depth, site and code in standardized catalogue), ordered by depth. b, Relicanthus daphneae sp. inc. (3,914 m, APEI-12, REL_001). c, Bathystylodactylus echninus (4,005 m, APEI-6. DEC_009). d, Leptochiton sp. indet. (4,205 m, NORI-D, MOL_002). e, Bathygorgia profunda sp. inc. (4,050 m, APEI-6, ALC_004), growing attached to a fossilized Otodus megalodon shark tooth. f, Sicyonidae gen. indet. (4,247 m, BGR-E, ACT_002). g, Thenea sp. indet. (4,190 m, NORI-D, DES_021). h, Ophiosphalma glabrum sp. inc. (4,621 m, TOML-D, OPH_010). i, Bifaxariidae gen. indet. (4,210 m. BGR-E, BRY_012). j, Hyalonema clarioni sp. inc. (4,848 m, TOML-C, HEX_002). k, Grimpoteuthis sp. indet. (4,959 m, TOML-C, MOL_008). l, Abyssopathes lyra (4,770 m, TOML-B, ANT_002). m, Tergivelum sp. indet. (5,019 m, KODOS, HEM_005). n, Psychropotes sp. indet. (5,007 m, APEI-4, HOL_047). o, Kamptosoma abyssale sp. inc. (5,240 m. APEI-1, URC_010). p, Actinostolidae gen. indet. (4,620 m, APEI-9, ACT_088).
Variations in the taxonomic composition of invertebrate megafaunal communities demarking biogeographic provinces within the northeast Pacific abyss
a,b, Two-dimensional representation of multidimensional scaling analyses, depicting assemblage Bray–Curtis dissimilarity rates (distance) calculated between 161 independent community samples (containing 200 specimens identified to morphotype level per sample) across 28 geographical locations. a,b, Sample point colour coding: study site of each sample location (a) or mean depth at sample location (b). Arrow depicting the spatial extent of the carbonate compensation depth (CCD) across the northeast Pacific. Isotropic contour lines (fitted using GAMs) represent rough approximates of depth-range bins to aid visualization of patterns. c, Ridgeline plots outlining the geometric distribution of total abundance along depth for the dominant taxonomic groups in the abyssal CCZ megabenthos. On the y axis, frequency distribution relative to all the specimen occurrences sampled per group; colour, depth range (as depicted in b). d, Top four dominant taxonomic groups within the communities of different depth ranges (background seabed illustrating depth variation exaggerated across the region). ACT, Actiniaria; HOL, Holothuroidea; HEX, Hexactinellida; ANT, Antipatharia; ALC, Alcyonacea; OPH, Ophiuroidea; BRY, Bryozoa; and DEM, Demospongia. Note that depth was plotted decreasing from left to right, that is, west to east, to mirror the approximate spatial pattern across the CCZ.
Standing stocks were substantially larger in the shallow than in the deep-abyssal province while biodiversity rates were similar, although slightly increasing with depth, across the northeast Pacific abyss
a,b, Faunal densities calculated in 84 independent community samples (containing 400–500 specimens) extending across 23 geographical locations. a,b, Variations in faunal density: between abyssal provinces (n = 41 samples in shallow, 27 in transition and 16 in the deep province) (a); and across the depth range (F1,82 = 51.61, P = 0.001, 2.81 × 10⁻¹⁰) (b). c–f, Diversity estimates calculated in 161 independent community samples (containing 200 specimens identified to morphotype level per sample) extending across 28 geographical locations. c,d, Variations in morphotype richness (S): between abyssal provinces (n = 81 samples in shallow, 39 in transition and 41 in the deep province) (c); and across the depth range (F1,159 = 115.4, P = 2.2 × 10⁻¹⁶) (d). e,f, Variations in the exponential form of Shannon’s diversity index (expH’): between abyssal provinces (n = 81 samples in shallow, 39 in transition and 41 in the deep province) (e); and across the depth range (F1,159 = 94.09, P = 2.2 × 10⁻¹⁶) (f). g,h, Morphotype accumulation curves, showing variations in the total richness sampled: between provinces (dash-line: all data combined) (g); and between different sites (including only sites with more than three community samples) (h). a,d,e, Mean values (bars) and 95% confidence intervals (error bars) across all the samples in each province. b,d,f, Values calculated for each independent sample (points) and results of linear regression; mean (dashed-line) and 95% confidence intervals (shallowing). g,h, Mean values across 100 randomizations (lines) and 95% confidence intervals (shallowing). Note depth was plotted throughout decreasing from left to right, west to east, to mirror the approximate spatial pattern across the CCZ.
Carbonate compensation depth drives abyssal biogeography in the northeast Pacific

July 2023

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544 Reads

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6 Citations

Nature Ecology & Evolution

Abyssal seafloor communities cover more than 60% of Earth’s surface. Despite their great size, abyssal plains extend across modest environmental gradients compared to other marine ecosystems. However, little is known about the patterns and processes regulating biodiversity or potentially delimiting biogeographical boundaries at regional scales in the abyss. Improved macroecological understanding of remote abyssal environments is urgent as threats of widespread anthropogenic disturbance grow in the deep ocean. Here, we use a new, basin-scale dataset to show the existence of clear regional zonation in abyssal communities across the 5,000 km span of the Clarion–Clipperton Zone (northeast Pacific), an area targeted for deep-sea mining. We found two pronounced biogeographic provinces, deep and shallow-abyssal, separated by a transition zone between 4,300 and 4,800 m depth. Surprisingly, species richness was maintained across this boundary by phylum-level taxonomic replacements. These regional transitions are probably related to calcium carbonate saturation boundaries as taxa dependent on calcium carbonate structures, such as shelled molluscs, appear restricted to the shallower province. Our results suggest geochemical and climatic forcing on distributions of abyssal populations over large spatial scales and provide a potential paradigm for deep-sea macroecology, opening a new basis for regional-scale biodiversity research and conservation strategies in Earth’s largest biome.


Environmental DNA reveals spatial patterns of fish and plankton diversity at a floating offshore wind farm

July 2023

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125 Reads

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5 Citations

In this study, we collected water eDNA from sampling stations at the first full scale floating offshore wind farm (OWF), the Hywind Pilot Park, east of Peterhead, UK, and a nearby reference area. We combined targeted droplet digital PCR (ddPCR) quantification of two commercially important species, Atlantic mackerel ( Scombrus scombrus ) and Atlantic herring ( Clupea harengus ), with metabarcoding of fish and plankton communities. The goal of this study was to assess the performance of eDNA data to characterize pelagic communities and its use for environmental monitoring. The metabarcoding recovered 26 fish species including both pelagic and demersal taxa. The plankton data were dominated by dinoflagellates ( Karenia ) and calanoid copepods. We found that both specific quantification of eDNA from mackerel and herring and eDNA metabarcoding of fish communities were able to reveal spatial patterns: Mackerel was most abundant in the surface across both OWF and reference sites; herring was present at a wider depth range. While ddPCR and metabarcoding data for these two species were broadly congruent, we observed detection/non‐detection mismatches for both methods, highlighting the need for robust sampling design. There was no consistent OWF versus reference area pattern in the demersal fraction of fish assemblages. We interpret our findings as representing a snapshot of fish school location around the time of sampling, and do not consider the single timepoint data from this pilot study to be sufficient to attribute any effects to the OWF itself. As a non‐invasive tool, we conclude that eDNA has a high potential in future environmental monitoring of OWFs. We recommend further ground‐truthing and biomass correlation of eDNA data with catch data and establishing eDNA time series as next steps towards implementation of eDNA in OWF environmental monitoring.



Citations (46)


... Sessile (Porifera, top left) and motile fauna (Arthropoda, bottom right) are shown within the black inset in (d). The fauna annotation was based on the standardized taxonomic field guide presented bySimon-Lledó et al. (2023). (e) The outer crater shows low-to-no nodule coverage and angular rocks as seafloor pavement. ...

Reference:

An Interpretable Multi-Model Machine Learning Approach for Spatial Mapping of Deep-Sea Polymetallic Nodule Occurrences
Carbonate compensation depth drives abyssal biogeography in the northeast Pacific

Nature Ecology & Evolution

... However, these vertical patterns were observed in stratified open ocean waters or in areas where a pronounced halocline or thermocline is present; hence the eDNA dispersal between water masses was limited. For example, a study conducted at the Hywind Pilot Offshore Windfarm in Scotland, where the study area had a depth of approximately 110 m and a thermocline was detected at 20 m depth, revealed a vertical eDNA pattern of fish communities that correspond with their habitat preferences 30 . These studies demonstrate the strength of eDNA metabarcoding to determine community patterns for a wide range of spatial scales. ...

Environmental DNA reveals spatial patterns of fish and plankton diversity at a floating offshore wind farm

... The broader depth range from which FeMn crusts were collected likely contributed to capturing a greater diversity (Fig. 10). This mirrors the high diversity recently reported for fauna in the polymetallic nodule fields in the Clarion Clipperton Zone (Rabone et al., 2023). ...

How many metazoan species live in the world’s largest mineral exploration region?

Current Biology

... Of course, today DNA offers a fast way to delineate "species" and try to understand some ecological processes (e.g. Janssen et al. 2015;Stewart et al. 2023). However, beyond thousands of sequences in a database representing potential species (termed "dark taxa" by Page 2016), there is little information about these species such as their ecological role, their relationships to other species or their natural history. ...

Biodiversity, biogeography, and connectivity of polychaetes in the world's largest marine minerals exploration frontier

... Thus, a range of sampling methods may be required for gaining a complete perspective, including passive and active acoustic monitoring, telemetry arrays, aerial surveillance, unmanned or remote guided drones, boat based and underwater imagery/video surveys, as well as newer methods such as environmental DNA (Dahlgren et al., 2023;Hemery et al., 2022;Sanderson et al., 2023;Williamson et al., 2018). ...

The Use of eDNA to Monitor Pelagic Fish in Offshore Floating Wind Farms

Oceanography

... Knowledge of macrofauna (≥300 μm in deep sea) in these areas, is limited to older, non-chemosynthetic studies such as those made by Hartman (1967) and Orensanz (1990) on the polychaete fauna from Malvinas Basin. As seep communities provide critical ecosystem services , have low resilience to disturbance (Baco et al., 2010), and high conservation value (Amon et al., 2017), their detection and exclusion from areas targeted for exploratory drilling activities is urgently needed (Cordes et al., 2016;Bravo et al., 2023). ...

Insights from the management of offshore energy resources: Toward an ecosystem-services based management approach for deep-ocean industries

... The last global review of described abyssal polychaete species (Paterson et al. 2009) reported 276 species records at depths between 4000 and 5000 m, showcasing that little is known for the abyssal polychaetes in general. In the CCZ, the last decade has seen significant taxonomic progress with a number of species descriptions (Table 3) including 17 new polynoids (Bonifácio and Menot 2018); 12 new cirratulids (Blake 2016(Blake , 2019, 12 new species belonging to Opheliidae, Scalibregmatidae and Travisiidae (Wiklund et al. 2019); three new euphrosinids (Neal et al. 2022b); two new syllids (Maciolek 2020); two new orbiniids (Blake 2017(Blake , 2019; three new species belonging to Spionidae and Poecilochaetidae (Paterson et al. 2016;Neal et al. 2022a); and one new nereidid (Drennan et al. 2021). These are the first polychaete species described during the ~ 50 years of studies in the CCZ. ...

Abyssal fauna of polymetallic nodule exploration areas, eastern Clarion-Clipperton Zone, central Pacific Ocean: Amphinomidae and Euphrosinidae (Annelida, Amphinomida)

... Data mapping to DwC would also allow for publishing of legacy datasets. This is particularly important given the lack of legacy data available, with very few CCZ studies for example published prior to 2000, as ascertained in the parallel study (39;Rabone et al.,Accepted). Although data quality can be highly variable in legacy data, here Deep-Data could draw on lessons from natural history collections, publishing data with data quality/data completeness flags as done in GBIF for example. ...

First Synthesis of Metazoan Biodiversity in the World's Largest Mineral Exploration Frontier

SSRN Electronic Journal

... Part of this research focuses on developing extraction strategies for these ores and is conducted under contracts with the International Seabed Authority (ISA) -a UN body that has exclusive rights to grant exploration licences in the Area. Extensive research is being conducted, including studies on various technologies for nodule exploration [2] and extraction [3], as well as taxonomic and ecological research of species inhabiting the Area [4][5][6][7] and the impact of mining on deep-sea ecosystems (e.g. [8,9]). ...

Abyssal fauna of polymetallic nodule exploration areas, eastern Clarion-Clipperton Zone, central Pacific Ocean: Annelida: Spionidae and Poecilochaetidae

Marine Biodiversity

... References. AFD (2024), ALA (2024), Bribiesca-Contreras et al. (2022), Clark (1920), Hansen (1975), Kremenetskaia et al. (2021), Ludwig (1894), Théel (1882). Table S1, Figure S1 Material examined. ...

Benthic megafauna of the western Clarion-Clipperton Zone, Pacific Ocean