Category Archives: NorBOL

Door #10: Siphonophores

Today, I thought I’d introduce to you to a cool group of animals that is ubiquitous in the oceans (including the Norwegian seas), but unfamiliar to most people. Siphonophores (“kolonimaneter” in Norwegian) belong to cnidarians, a group that includes corals, anemones, hydroids and jellyfish, and is characterized by the presence of stinging cells used in prey capture. All siphonophores are predatory, and use their stinging tentacles to catch small crustaceans or, in the case of some species, even small fish.

The most (or only) familiar siphonophore for the majority of people is probably the highly venomous Portuguese Man O’War (Physalia physalis), which can be spotted floating on the surface of the ocean or stranded on beaches. However, it is not really representative of the group as a whole, as most siphonophores live in the water column of the open ocean rather than its surface. There are around 200 described species of siphonophores.

The most fascinating feature of siphonophores is their peculiar body plan. While siphonophores may appear to be a single animal, they are in fact a colony of physiologically connected and genetically identical but morphologically diverse individuals called zooids that have specialized to carry out different tasks for the colony. Siphonophores belong to the class Hydrozoa (“polyppdyr” in Norwegian), which covers two basic body plans: the polyp/hydroid and the medusa.

Schematic of a physonect siphonophore. From http://www.siphonophores.org (CC-by-nc-sa)

The various zooids comprising a siphonophore colony can also be divided into these main groups. For example, the zooids used for swimming, called nectophores, are medusoid, while the feeding zooids, or gastrozooids, are polyp-like. The siphonophore colony can also include specialized defensive, protective and reproductive zooids. All the zooids forming a colony arise by budding from a single fertilized egg. The different zooids are specialized to the degree that they cannot function as individual animals any more, and are only able to perform their specific tasks as parts of the siphonophore colony.

Anterior nectophore, posterior nectophore and eudoxid of the calycophoran siphonophore Dimophyes arctica – a common species in Norwegian waters. Photos by Aino Hosia (cc-by-sa)

The zooids, for example the swimming nectophores, vary in appearance between species, and can be used for species identification. In addition, the various types of zooids in the colony are arranged in a strict species specific pattern, providing the intact colonies of each species with their particular appearance. While the individual zooids are generally small, millimeters to centimeters in size, some siphonophore species, like Praya dubia, may have colonies that reach 40 m in length! Siphonophore colonies generally have a zone of one or more (up to several dozen) swimming nectophores at the front, used to pull the colony through water. Behind this nectosome is the siphosome, which contains the feeding, reproductive and other zooids in a repeating pattern, each iteration of which is called a cormidium. In some species (suborder Calycophorae), these cormidia are released as small free-living reproductive colonies called eudoxids. Unfortunately, siphonophore colonies are extremely fragile and tend to fall apart during standard plankton sampling with nets, leaving behind a bewildering array of small bits and pieces – part of the reason they are relatively poorly known to most people.

Colony of physonect siphonophore Physophora hydrostatica, aka hula skirt siphonophore. Photo by Aino Hosia (cc-by-sa)

Intact siphonophore colonies are beautiful, but often utterly alien in appearance. It is interesting to consider where to draw the line between an individual and a colony. While we as individuals have specialized organs to carry out our various bodily functions, siphonophore colonies are made up of specialized interdependent individuals or zooids similarly carrying out their specific tasks.

As part of project HYPNO we are charting the diversity of pelagic hydrozoans, including siphonophores, in Norway. There are ~15 species observed in Norwegian waters, and some, particularly Dimophyes arctica, Lensia conoidea and Nanomia sp. are extremely common components of marine plankton. However, siphonophores are primarily noticed when they become a nuisance: For example, mass occurrences of Muggiaea atlantica and Apolemia uvaria have in the past killed large numbers of farmed fish in Norway, with resulting losses to aquaculture companies.

– Aino (HYPNO)

Intrigued by siphonophores? For more information, visit e.g. http://www.siphonophores.org/ by Casey Dunn.

Door # 6: Stuffed Syllid

Todays calendar critter is a Trypanosyllis sp. – a undescribed species from the genera Trypanosyllis in the family Syllidae. It most closely resembles a species described from the Mediterranean Sea. The Norwegian species is common in coral rubble, and has been assumed to be the same species as the one described from the Mediterranean. Genetic work reveals that these two are in fact separate species, and thus the Norwegian one is a new species awaiting formal description and naming. (If you read Norwegian, you can learn more about how species are described and named here: Slik gir vi navn til nye arter).

A new species of Trypanosyllis, collected in Sletvik, Norway. Photo by Arne Nygren. CC-by-sa

This specimen was collected, identified and photographed by Arne Nygren during our field work in Sletvik as part of his work on cryptic polychate species in Norway.

Syllids have opted for a rather fascinating way of ensuring high fertilization rates; something called epitoky: they asexually produce a special individual – the epitokous individual – from their bodies, and release this to go swimming in search of a mate. In the photo you can see that the female reproductive body (epitoke) is filled with orange eggs and has its own set of eyes, close to the middle of the animal. This section will break away from the mother animal and swim away in search of a male reproductive body to reproduce with. The mother animal will then grow a new female reproductive body.

-Arne & Katrine

Door #4: A spindly Sunday

One of the cool things with the NorBOL-project is that it allows us spotlight animal groups that we don’t normally get to do much with. One such group is the sea spiders, or Pycnogonida. These spider-like critters wander around on the seafloor looking for other invertebrates to snack on (some also live on detritus and algae), and (presumably) for love. I certainly find a lot of them carrying egg sacks and young ones, so they must succeed every now and then! In the Pycnogonida, it is the males who care for the laid eggs and the young, rolling the eggs into one or several balls that he carries around on his ovigers.

: Nymphon hirtipes with eggs. It was collected at Spitsbergen

: Nymphon hirtum from the Arctic

: Nymphon grossipes collected by MAREANO

: Many, many juveniles on this Nymphon hirtum

The ones I photographed ranged from tiny to over 30 cm:

Colossendeis angusta, collected by MAREANO – this is bigger than a handful

Ammothea echinata from the day when we joined the local student dive club – the animal is only a few mm

Anatomy of a pycnogonid: A: head; B: thorax; C: abdomen 1: proboscis; 2: chelifores; 3: palps; 4: ovigers; 5: egg sacs; 6a–6d: four pairs of legs Sars, G. O. (1895). An account of the Crustacea of Norway, with short descriptions and figures of all the species. Christiania, Copenhagen, A. Cammermeyer. L. Fdez (LP) – digitization and colouration. - Own work External anatomy of Nymphon sea spider. After G. O. Sars (1895).

Anatomy of a pycnogonid: A: head; B: thorax; C: abdomen 1: proboscis; 2: chelifores; 3: palps; 4: ovigers; 5: egg sacs; 6a–6d: four pairs of legs L. Fdez (LP) – digitization and colouration. – Own work based on External anatomy of Nymphon sea spider. After G. O. Sars (1895).

At first glance they look a lot like the spiders we find on land, but they are really a very different class of animals (literally!); The sea spiders are found within Animalia (Kingdom) > Arthropoda (Phylum) > Chelicerata (Subphylum) > Pycnogonida (Class) (from WoRMS), whilst “land spiders” are found within the order Aranea in the class Arachnida.

Extant (now-living) members of the Pycnogonida are found within the order Pantopoda, which translates into “all legs”, which describes them quite well! They have even moved most of their internal organs (of which they have rather few; respiration is done across the body surface, so no gills) into the legs.

The more I look at them, the funnier they look – but that may be in the eye of the beholder, as a few arachnophobes passing by the camera have declared loudly that there is nothing charming to find here – I beg to disagree!

Goofy looking Nymphon stroemi (note the cheliphores/claws)

Goofy looking Nymphon stroemi (note the chelipores/claws) and the eyes on a tubercle on the head – they have eyes facing both forwards and backwards

Pycnogonum litorale

Some species, like this Nymphon gracile, can also swim: “…the swimming motions are the same as those used in walking, but more vigorously executed” King 1974

Nymphon hirtipes with hitchikers

Pseudopallene circularis from Spitsbergen

They are usually slow movers: Hover over the image to see a pycnogonid walking on the sea floor

To fill a plate with tissue samples from 95 specimens (1 animal = 1 specimen) of pycnogonida doesn’t sound too complicated, does it? Well, it turned out to be a bit of an adventure to gather enough animals that had been preserved in such a way that we could get DNA out of them (older material is usually fixated in Formaldehyde, which makes it unsuited for genetic work), and that was identified (had a name to them). Since we are in the process of building up the national (and international) reference library (the BOLD database) that the short DNA-segments (the “barcodes”) are to be matched up to later when someone wants to know which species “Animal X” belongs to, we need to know which species we are submitting for sequencing.

Our collection of barcode-compatible identified pycnogonids received a welcome boost when the shipment of processed material (identified, and measured for biomass) from MAREANO‘s beamtrals collected in 2013 arrived, as these had been fixated in ethanol – and identified by researchers who have worked extensively with the group.

Even so, I couldn’t fill a whole plate with only those specimens. Thankfully, I have skilled collegues that were able to put species names to almost all of the critters I could hunt down in our collections, and so now we have 95 animals ready from 26 different species! We also have some bona fide mysteries that we hope the BOLD-database will help us solve as well; animals that does not comply with any of the identification keys…!

Fingers crossed for a very successful sequence run and a lot of new information about the Pycnogonida of Norway!

Pseudopallene longicollis, collected by MAREANO

Info:
King, P.E. 1974: British Sea Spiders, synopses of the British Fauna (New Series) No. 5

Door #3: a week in the field

We spent a lovely week in October collecting animals at the field station of NTNU in Agdenes in central Norway.

: Not too far from Trondheim…

: ..here!

: You’ll find the field station of Sletvik

About 15 researchers and collection curators were gathered for a week of sampling with gear ranging from grabs and trawls deployed from the research vessel Gunnerus to buckets and shovels on the beach. As you may be able to tell, a good time was had by all!

The field work was arranged by the our colleagues at NTNU University Museum, and served multiple purposes:

We collected ultra-fresh material for barcoding through the norwegian Barcode of Live project (NorBOL) – several plates were initiated during the week and then brought back to Bergen where we will continue filling them with material from our collections – each plate needs to be filled with 95 samples that can be run with the same primer, so we need to select our material carefully.
The marine collections of NTNU got a substantial boost
Fresh material was collected for teaching faunistics
Photodocumenting live specimens (we have some fantastic polychaete photos from this coming up later in our calendar)
Four Norwegian Species Initiative funded projects were participating, collecting material for their projects – as were people from the EU-project SponGES.
We at UM also relished the chance to sample in the littoral zone, which is a undersampled habitat in our collections

We are working on the material now, and some of it is scheduled to make an apperance on the blog over the next couple of weeks – so stay tuned!

Door #2: The head of the Medusa

Medusa by Carvaggio (Wikimedia)

Today we go mythological, and visit the Greek pantheon.

Medusa was one of three Gorgon sisters who all had snakes for hair according to the mythology – and one can certainly understand how the British zoologist Leach (1791-1836) came to think of the name when he formally described the genus Gorgonocephalus (Literally ” Gorgon’s head”) in 1815. They are found within the echinoderm class of Ophiuroidea (brittle stars).

In English they are known as basket stars, whilst Norwegians know them as “Medusahode” – head of the Medusa.

The English name refers to how they feed: basket stars are predators, and raise their bifurcated arms covered with tiny hooks, spines and grooves up into the current forming a basket to sift and entrap plankton and other small critters from the water as it streams past – then they use their arm branches (possibly aided by the tube feet) to guide the trapped food to their mouths, which is on the underside (like in starfish).

Gorgonocephalus lamarcki, photo by K.Kongshavn

This specimen was collected in Svalbard in 2009 (way up at 80ºN) during a student course at UNIS, and has been barcoded through the Norwegian Barcode of Life (NorBOL) project.

Hover your cursor over the image below to see a basket star move

-Katrine

A week of worms in Wales!

Does that not sound appealing?
It was actually a lovely event!

The IPC2016 logo © National Museum Wales

The 12^th International Polychaete Conference took place in Cardiff, Wales during the first week of August. These events have been taking place every third year since 1981, and the previous one was in Sydney, Australia in 2013.

Polychaetologists assembled on the steps of the National Museum Cardiff (c) IPC2016

Polychaetologists anno 2016 assembled on the steps of the National Museum Cardiff © National Museum Wales

During an intensive week of presentations and posters spanning topics within Systematics, Phylogeny, Ecology, Methodologies, Biodiversity, Biodiversity and Ecology, Morphology, Reproduction & Larval Ecology, Development, and Polychaete studies, people had the chance to showcase their work, and learn more about what others are working on. The local organising committee invited us to “Have a happy conference, re-connecting with those already known, meeting correspondents for the first time, ans making new connections and new friends” – and I think we can safely say that the mission was accomplished!

Cardiff – and the National Museum Wales – was an excellent venue for “polychaetologists” from all over the globe.

Snapshots of Cardiff (photos: K.Kongshavn)

In all we were 190 attendees from about 30 countries present – including a sizeable Norwegian group! Some of us (below) gave talks, and most were also involved in posters. Results and material from large projects and surveys such as PolyNor (Polychaete diversity in Nordic Seas), MAREANO (Marine AREA database for NOrwegian waters), NorBOL (The Norwegian Barcode of Life), and MIWA (Marine Invertebrates of West Africa) were all well incorporated in the Norwegian contributions.

: Torkild

: Nataliya

: Martin

: Katrine

There were in fact a lot of contributions involving one or more collaborators from a Norwegian institution (UM, NTNU, NIVA, The SARS center, NHM Oslo, Akvaplan-NIVA ++) being presented during the conference. It is really nice to see that the community is growing through recruitment of both students and international researchers.

Norwegian delegates lining up in the City Hall before the start of the banquet

As Torkild said in his excellent blog post (in Norwegian, translation by me):

Pins marking where participants come from – this was not quite completed when the photo was taken, but none the less..well represented!

With so many active participants in the field, a lot of exciting research is being carried out in Norway. Not only do we have many projects – large and small – running at our institutions involving our “regular” Norwegian collaborators; there is also a significant proportion of international participation in these projects.

Furthermore, our activities enable researchers from all over the world to visit or loan from our scientific collections, and study the substantial (new) material that the projects are generating. It is nice to see that our efforts are being recognized in the international community! The recent flurry of activities has been well aided by the Norwegian Species Initiative (Artsprosjektet) (and the MIWA-project at UM).

The majority of our research is based on, or incorporates, museum material from our collections. The collections have been built over years, decades and even centuries, and continue to increase in scientific value as new science is added.

It is gratifying to see the material being used, and we hope it will gain even more attention in the aftermath of the conference.

From the poster session – these are some (!) of the posters we were involved in (photos: K.Kongshavn)

The University Museum was well represented, both in attendance, and in contributions. Below is a list of what we (co-)authored, presenting author is in bold, and University Museum people are in italics. We plan on posting some of the posters here, so stay tuned for that!

Presentations:

Giants vs pygmies: two strategies in the evolution of deep-sea quill worms (Onuphidae, Annelida)
Nataliya Budaeva, Hannelore Paxton, Pedro Ribeiro, Pilar Haye, Dmitry Schepetov, Javier Sellanes, Endre Willassen
DNA barcoding contributing to new knowledge on diversity and distribution of Polychaeta (Annelida) in Norwegian and adjacent waters
Torkild Bakken, Jon A. Kongsrud, Katrine Kongshavn, Eivind Oug, Tom Alvestad, Nataliya Budaeva, Arne Nygren, Endre Willassen
Diversity and phylogeny of Diopatra bristle worms (Onuphidae, Annelida) from West Africa
Martin Hektoen, Nataliya Budaeva
Experiences after three years of automated DNA barcoding of Polychaeta
Katrine Kongshavn, Jon Anders Kongsrud, Torkild Bakken, Tom Alvestad, Eivind Oug, Arne Nygren, Nataliya Budaeva, Endre Willassen

Posters

Diversity and species distributions of Glyceriformia in shelf areas off western Africa
Lloyd Allotey, Akanbi Bamikole Williams, Jon Anders Kongsrud, Tom Alvestad, Katrine Kongshavn, Endre Willassen
Eclysippe Eliason, 1955 (Annelida, Ampharetidae) from the North Atlantic with the description of a new species from Norwegian waters
Tom Alvestad, Jon Anders Kongsrud, Katrine Kongshavn
Phylogeny of Ampharetidae
Mari Heggernes Eilertsen, Tom Alvestad, Hans Tore Rapp, Jon Anders Kongsrud
Ophelina (Polychaeta, Opheliidae) in Norwegian waters and adjacent areas – taxonomy, identification and species distributions
Jon Anders Kongsrud, Eivind Oug, Torkild Bakken, Arne Nygren, Katrine Kongshavn
Pista Malmgren, 1866 (Terebellidae) from Norway and adjacent areas
Mario H. Londoño-Mesa, Arne Nygren, Jon Anders Kongsrud
Lumbrineridae (Annelida, Polychaeta) from Norwegian and adjacent waters with the description of a new deep-water species of Abyssoninoe
Eivind Oug, Katrine Kongshavn, Jon Anders Kongsrud
Nephtyidae (Polychaeta, Phyllodocida) of West African shelf areas
Ascensão Ravara, Jon Anders Kongsrud, Tom Alvestad
Phylogeny of the family Maldanidae based on molecular data
Morten Stokkan, Jon Anders Kongsrud, Endre Willassen

We had a mid-week excursion where we got to see a bit more of our hosting country; namely the impressive Caerphilly Castle constructed in the 13th century and still looking magnificent today, and a lovely lunch at the Llanerch wineyard with time for informal mingling and catching up.

Caerphilly Castle (photo: K.Kongshavn)

Note the red dragon in the Castle wall; this is the dragon of the Welsh flag. The story goes something like this (according to Wikipedia, at least!): From the Historia Brittonum,^[2] written around 830 a text describes a struggle between two serpents deep underground, which prevents King Vortigern from building a stronghold. This story was later adapted into a prophecy made by the wizard Myrddin (or Merlin) of a long fight between a red dragon and a white dragon. According to the prophecy, the white dragon, representing the Saxons, would at first dominate but eventually the red dragon, symbolising the Britons, would be victorious.

Being museum people (er..? People employed at a museum, I mean!) ourselves, we made sure to visit the exhibitions as well, and especially the new “Wriggle!” exhibition, which is all about..worms! Lots of fun, and a*a lot* of information packed in. Make sure to visit it, if you get the chance!

Visiting the “Wriggle!” exhibition during the Ice Breaker event

The attendants have also been busy on Twitter, visit @IPC2016 or check #IPC12Cardiff for loads of photos and on-the-spot-commentaries

Finally, we would like to extend our heartfelt thanks to the arranging committee – DIOLCH!

Cheers, Katrine

ps: Dw i’n hoffi mwydod!

Seaweeds continued

An alternate world?

The week flew by in a flurry of Latin names, literature and sea water – today is the day for unpacking, making sure that everything is stored safely, and revising lists.

An impressive collection of species on the final day!

A voucher, neatly laid out and ready to be pressed.

Pressing voucher specimens

Tissue samples

In total we collected 88 samples of 76 different species, most of which are not in the BOLD database for Norway yet. It will be exciting to see what results we get!

: Pelvetia canaliculata

: Ceramium cf virgatum

: Ulva lactua

: Fucus serratus

: Chaetomorpha aerea/linum

: Chylocladia verticilliata

: Delesseria sanguinea

: Plocamium lyngbyanum

: Stealth zoology; Aplysia punctata

The tissue samples will be sent to the Saunders lab, as they have kindly offered collaborate on this collection and help us with the sequencing as our go-to lab in NorBOL is not optimally set up to deal with algae.

Thank you so much to all the students and teachers for being so welcoming, and for being good sports about me spiriting away your specimens!

Guest researchers: Mario

We started early with visitors for 2016; Mario arrived already on the 4th of January!

Mario, on his temporary spot in the lab, studying spaghetti worms.

Mario’s home institution is the University of Antioquia, in Medellin, Colombia, and the contrast to snow covered (and/or rain swept) Bergen has been great; this was his first time having snow beneath his shoes.

Arne

Another of our polychaete collaborators, Arne Nygren from Sjöfartsmuseet Akvariet in Gothenburg (Artsprosjekt can be found here (NO)) seized the chance to visit as well, and together with the resident polychaetologists (Jon, Tom and Nataliya) it meant that we suddenly had an impromptu polychaete workshop on our hands 🙂

Being able to meet in person makes the work flow smoother all around, as work was delegated and plans concretized. 2016 is likely to be a year with much focus on the Polychaeta, as it is both the final year of the PolyNor project (ends in spring), and the year of the 12^th International Polychaete Conference, which will be held in Cardiff, Wales.

During Mario’s month-long stay he was examining the collection of terebellids from West Africa and the museum’s collection of the bristle worm genus Pista, much of which will later be barcoded through NorBOL (for the Norwegian material) and MIWA (for our West African samples).

Pista cristata identified by Dr. T. Holthe, one of the most important experts on spaghetti worms, from University of Bergen. RCP. Photo: MHL

In his own words:

Eupolymnia nebulosa after one collecting trip to Lysefjord close to Bergen. Photo: MHL

Eupolymnia nebulosa after a collecting trip to Lysefjorden close to Bergen. Photo: MHL

I usually work on the morphology of just one of the several families of polychaetes, the Terebellidae, or spaghetti worms. This visit has been very important since we have been able to separate four Pista species from the North Sea, using both morphological and molecular tools. “The combination of these two different methods has been superb”.

Jon, Arne and I began this study during August 2014, but this undertaking seems like it will never end because we keep adding more material. The recent findings have been the significance of some characters that did not have taxonomical importance in the past. Now, they are the clues for splitting very close species.

But this is not enough; it was possible to identify 43 species of terebellids belonging to 16 different genera, from material collected along the West African coasts.

This is a high polychaete diversity in only one family. For example, we found three Lysilla species, in a region with only one recorded species. New species? Highly possible. One can only wonder what the diversity of the remaining families is?

Verticilate chaetae (bristles) from one of the polycirrinae species photographed through a microscope. Photo: MHL

Methyl-green staining pattern of one of Pista species. Photo: MHL

All this was accompanied with a perfect view through the window, seeing it snow some days, or watching the Sun on the mountains in front; some times with white top mountains, some times with deep blue sky. A landscape like that never could be my company in my tropical city.

Snowy view from the lab window Photo: MHL

Thank you for visiting, it was very nice having you here – we wish you the best of luck with your next adventure in Antarctica!

Biodiversity Valentines

This gorgeous polychaete (Bristle worm) is from the family Serpulidae, it was identfied as a Pomatoceros triquetes during the students' course in marine faunistics

This gorgeous polychaete (bristle worm) is from the family Serpulidae, it was identified as a Pomatoceros triquetes during the students’ course in marine faunistics (Photo: K.Kongshavn)

~~Release the Kraken!~~

Oh, dear… this challenge:

Please share your love of biodiversity this Valentine’s Day with the hashtag #bdvalentine.

Have fun and help raise awareness of biodiversity and conservation!

We’ll be on Twitter and Facebook celebrating all day on Friday, February 12th with “Biodiversity Valentines.” Tweet your best biodiversity-themed Valentine message with the hashtag #bdvalentine. You can borrow from our growing Facebook gallery of #bdvalentine images here: https://goo.gl/dZkQdS .

Get your creative juices flowing (and your creative and communications folks brainstorming)! We’ll retweet and create a gallery of your images all day on Friday, February 12th.

At JRS, we’re working to increase the use of biodiversity data and information services for conservation and sustainable development in Africa. We love biodiversity data. Join in with your #bdvalentine!

ticked into our in-box from the JRS Biodiversity Foundation a couple of days ago, and we decided to give it a spin.

Now, biologists seem to gravitate towards punny (and occasionally funny) humour, and there’s been an avalanche of submissions and suggestions on what we could post.

Here’s a selection of submissions from the Invertebrate collections, we hope you’ll enjoy them!

Interspecies <3 between Laonice sarsi and L. bahusiensis (photo:T. Alvestad)

This little Cephalopod was collected by MAREANO. (Photo: K.Kongshavn)

This cuttlefish was encountered in an Aquarium, and thus does not reside in our collections! They belong to the class Cephalopoda, which also includes squid, octopodes, and nautiluses. Cuttlefish have a unique internal shell, the cuttlebone. Despite their name, cuttlefish are not fish but molluscs. (Photo: K.Kongshavn)

Not a local species! Jelly fish do not have a independent circulatory system, nor do they have structured organ systems, brain, or breathing apparatus.

A friendly (?) Isopod from the Cirolanidae family.

Uncini bristles from a Euclymene (Maldanidae) polychaete. The picture is taken with an Scanning Electron Microscope (SEM) at our local SEM lab. The scale bar is 2 µm, or 0.002 mm, so these are truly TINY structures.

Here’s an Ebalia sp. that we have barcoded through NorBOL.

Here’s a Urticina eques (Photo: K.Kongshavn)

A Crossaster papposus collected for NorBOL together with the local student dive club SUB (Photo: K.Kongshavn)

A marine snail in the family Naticidae (Photo: K.Kongshavn)

A marine snail in the family Naticidae, also known as moon snails or necklace shells. These snails are predators, mainly feeding on Bivalves (Photo: K.Kongshavn)

We could not resist, even though it's a vertebrate (Photo: K.Kongshavn)

Look at that face! We could not resist including him(?), even though it’s a vertebrate (Photo: K.Kongshavn)

apologies for the ear worm!

Well, we sure had fun – we hope you did too!

Make sure to check out other contributions to the hashtag #bdvalentine on Twitter and Facebook.

Berthella sideralis, a rarity finally documented alive and barcoded!

The Pleurobranchidae sea slug species Berthella sideralis was described by the Swedish malacologist Sven Ludvig Lovén in 1846 based on specimens collect at Bohuslän, in southern Sweden not far from the city of Gothenburg. This species has hardly been mentioned in the literature after its original description, and no images of life species are to our best knowledge available in books, research papers or even web platforms – until now!

A synthesis of the morphological features of B. sideralis can be found in Cervera et al. (2010) who studied in detail two specimens collected during 1930’s in Trondheimfjord as part of a phylogenetic study of the genus Berthella.

Recently, in late November 2015 during a Museum scientific cruise – there is a blog post about this day of field work here – we collected one specimen in Hjeltefjorden (around Bergen) at 220 meters depth using an RP-sledge. This specimen is here documented and was recently genetically barcoded as part of our effort to barcode the Norwegian marine fauna through the NorBOL project.

A live specimen of Berthella sideralis. Ths scale bar i 5 mm. Photo: K. Kongshavn

A live specimen of Berthella sideralis. The scale bar i 5 mm. Photo: K. Kongshavn

Berthella sideralis is only known from Sweden and Norway. In Norway it has been reported between Bergen and Finnmark.

Reference: Cervera, J L., Gosliner, T. M., García-Gómez, J. C., & Ortea, J. A. 2010. A new species of Berthella Blainville, 1824 (Opisthobranchia, Notaspidea) from the Canary Island (Eastern Atlantic Ocean), with a re-examination of the phylogenetic relationships of the Notaspidea. Journal of Molluscan Studies, 66: 301–311.

-Manuel & Katrine

The Invertebrate Collections

The University Museum of Bergen