- Research article
- Open Access
Tube construction by a tanaidacean crustacean using a novel mucus secretion system involving the anal opening
© The Author(s). 2017
- Received: 5 September 2017
- Accepted: 1 November 2017
- Published: 21 November 2017
Animals in diverse aquatic groups construct tubes using mucus and filaments, and the acquisition of this capability has likely played an important role in the evolution and diversification of small benthic animals. Tanaidacea is a crustacean order that includes tube-constructing species, most of which belong to Tanaidoidea and Paratanaoidea, with a few in Kalliapseudidae (Apseudoidea). Two previously reported systems used in tube construction are the thoracic-gland system, with secretory glands in thoracic segments (pereonites), and the pereopodal-gland system, with glands in pereopods.
Parapseudidae (Apseudoidea) also includes a tube-constructing species, Parapseudes algicola (Shiino, 1952), which lacks large secretory glands in all pereonites and pereopods, but has a pair of acinar glands in the pleotelson, lateral to the gut. Each gland connects to the gut via a short duct, and thence to the exterior via the anal opening. Secretions released from these glands are used to construct tubes, and contain acidic and neutral mucopolysaccharides.
We report in P. algicola a third, novel secretory system, here termed the pleotelsonal-gland system, used for tube construction in Tanaidacea. It is similar to the secretory system in some “thalassinidean” decapods; both systems have secretory glands connecting to the gut and thence to the anal opening as the outlet; however, these gland systems likely evolved independently. Recent discoveries of novel secretory systems for tube construction in Tanaidacea suggest that information from smaller, less well-known groups will be necessary to understand how acquisitions of tube-constructing capability affected diversification in animals.
- Tube dweller
Tube construction with mucus and filaments is known in diverse aquatic animal groups, including cnidarians, annelids, nemerteans, nematodes, and crustaceans . The tubicolous mode of life is advantageous in various ways; a tube can provide shelter, space for copulation, nursery, and enable efficient feeding and respiration (e.g., [2, 3]). The acquisition of tube-constructing capability, especially in small benthic animals under high predation pressure, must thus play an important role in their evolution and diversification.
Tanaidacea is a crustacean order that contains members which inhabit self-constructed tubes. Most tube-constructing tanaidaceans belong to the superfamilies Tanaidoidea and Paratanaoidea. These form tubes in bottom sediments or on substrata, such as seaweeds, marine vertebrates, and abiotic hard surfaces (e.g., [4–8]) using a thoracic-gland secretory system. Kaji et al.  illustrated details of the morphology related to tube construction in the tanaidoid Sinelobus sp., which possesses two types of secretory glands (“tg1” and “tg2” in ) on the pereonites (thoracic segments). Each gland connects to a single duct; two separate ducts run through a single pereopod and then merge at the pereopodal tip before opening to the exterior. The other superfamily known to contain tube constructors is Apseudoidea, in which members of the family Kalliapseudidae construct tubes in bottom sediments [10, 11]. Kalliapseudids use a pereopodal-gland secretory system, which is quite different from the thoracic-gland system. Kakui and Hiruta  found four types of secretory systems in an apseudomorph tanaidacean, all of which have secretory glands within pereopods: Type A in pereopod 1, Type B in pereopods 2 and 3, Type C in pereopods 4 and 5, and Type D in pereopod 6. One (or several) of these systems secretes filaments for tube construction, although it is not clear which.
In observing live tanaidaceans in the laboratory, we noted several individuals of Parapseudes algicola (Shiino, 1952) (Apseudoidea: Parapseudidae) sticking together. This species has a digging-type pereopod 1 (cf. [12, 13]), which indicates a burrowing mode of life, but individuals adhering to one another further suggests that P. algicola may be able to secrete mucus and construct tubes. In the present study, we show that P. algicola does not simply dig tunnels, but is rather a tube constructor, the first case known in Parapseudidae. For tube construction, this species uses a pair of glands in the pleotelson to release mucus via the anal opening, a novel type of system among tanaidaceans that we term the ‘pleotelsonal-gland system’.
Observation of behavior and tubes
Animals were maintained in the laboratory in a small aquarium with coral sand covering the bottom, at room temperature and under ambient light, and fed every 3 days with porphyrized dry feed for crayfish (JAN code 4971618829092; Kyorin, Japan). To observe behavior in situ, two individuals (independently, one at a time) were transferred by pipette to another aquarium under the same conditions and observed with a Leica MZ16 stereomicroscope. Images and digital movies were made using an Olympus OM-D E-M5 camera mounted on the microscope; one of the movies is available in the figshare repository .
Animals were fixed in Bouin’s fluid. Paraffin sections 5 μm thick were prepared and stained with Mayer’s hematoxylin and eosin (HE), Alcian Blue (AB) with nuclear fast red (Kernechtrot) as a counterstain, or AB and Periodic Acid Schiff (PAS) using standard techniques, and observed with an Olympus BX50 light microscope. Digital images were recorded using a Nikon DS-Fil camera.
Scanning electron microscope (SEM) observation
Specimens were fixed in 70% ethanol (for external morphology) or in Bouin’s fluid (for internal morphology) and preserved in 70% ethanol. The specimens for internal morphology were cut sagittally with a hand-held razor in 70% ethanol, or embedded in paraffin, cut with a Leica RM2125 RTS microtome, deparaffinized, and preserved in 70% ethanol. Specimens were dehydrated in an ethanol series, treated with hexamethyldisilazane, sputter coated with gold, and observed at 20 kV accelerating voltage with a Hitachi S-3000 N SEM.
Four circular coverslips 18 mm in diameter (C018001; Matsunami, Japan) were soaked in absolute ethanol for 1 h to remove dust, dried, and placed in a petri dish containing sterile seawater. Four tanaidaceans were placed in the dish for 2 h, and mucus samples were recovered on the coverslips. Non-stained, AB stained, and AB + PAS stained (using the same staining methods as for the paraffin sections) mucus samples were observed with a Leica MZ16 stereomicroscope. Stained mucus samples were dehydrated in an ethanol series, treated with hexamethyldisilazane, sputter coated with gold, and observed at 20 kV accelerating voltage with a Hitachi S-3000 N SEM.
Behavior and tubes of P. algicola
Tube construction by P. algicola. (MP4 5902 kb)
Position and morphology of glands
Secretion from the pleotelsonal gland
The amount of secretion in the glandular cavity was different among individuals, as can be seen from the staining intensity inside the cavity (cf. Fig. 3a–c). SEM observation showed that the cavity contained two types of secretions, barrel shaped particles and filaments (arrow and arrowhead, respectively, in Fig. 4b′). In an HE-stained specimen (Fig. 3a, c), the entire secretion was light or dark bluish-purple. In an AB and Kernechtrot stained sample (Fig. 3d), most secretions were purple, but the region just above the simple columnar cells was light blue. In a section double-stained with AB and PAS (Fig. 3e), secretions were blue and dark blue to mauve.
Through our behavioral and morphological observations, we concluded that P. algicola constructs tubes. This is the first case of tube construction reported in Parapseudidae, making Parapseudidae the second family in Apseudoidea known to have a tubicolous member. The secretory system of P. algicola consists of paired acinar glands, a short duct connecting each gland to the gut, and thence to the anal opening as the exterior outlet. Hair-like structures covering the duct opening (Fig. 4c′) may function as a one-way valve allowing secretions but not feces to pass. Perhaps significantly, the genus Parapseudes is unique among Parapseudidae in lacking pleopod 5, the most posterior pleopod [15–18] (cf. Fig. 4a). In species where it is present, pleopod 5 is very close to the anal opening and may interfere with secretions emerging from the opening. The absence of pleopod 5 in species in Parapseudes may thus be an adaptive character state related to mucus secretion from the anal opening and tube construction.
SEM observation detected two types of secretions in the glandular cavity, barrel-shaped particles and filaments (Fig. 4b′). This was consistent with the histological observations, where two colors were evident in single sections with AB and AB + PAS staining (Fig. 3d′, e′). We did not observe barrel-shaped particles in the mucus samples on cover slips (Fig. 5c–h); perhaps these particles are maintained only in the animal, with amorphous mucus globules stained dark blue to mauve with AB + PAS (Fig. 5b–e) corresponding to clusters of barrel-shaped secretions. Light blue to blue staining by AB is indicative of acidic mucopolysaccharides; red to magenta staining by PAS is indicative of neutral mucopolysaccharides; and dark blue to mauve staining by AB + PAS is indicative of both acidic and neutral mucopolysaccharides, with the color depending on the proportions of the two molecules . Our staining results thus imply that the mucus contains at least acidic and neutral mucopolysaccharides, although the proportions are unclear.
Animals in various taxa have an independent outlet(s) for filament secretion at the posterior end of the body. In spiders  and millipedes , the secretory system(s) is separate from the digestive tract. The most similar secretory system to that in P. algicola is found in some “thalassinidean” decapods such as Upogebia and Lepidophthalmus . In the case of Upogebia species, the secretory system involves a large glandular mass in pleomere 6 and pleon (corresponding to the pleotelson in P. algicola) and an anal opening as the exterior outlet; secretion from the gland mass enters the gut via dense fields of transcuticular pores. Another similar secretory system involves the Malpighian silk glands in insects , where the Malpighian tubule (functioning in excretion and osmoregulation ) produces a secretion that then enters the gut and is released into the environment via the anal opening. Rakitov  reported that cicada nymphs use this secretion to cement the walls of their burrows. In that it involves glands releasing secretions via the gut and anal opening as the outlet to the exterior, the secretory system in P. algicola also resembles the systems by which squids release ink , and by which mammals release odors for defense and marking [28, 29]. All of these analogous systems had different origins; this must be true even for the two systems in malacostracan crustaceans (P. algicola and Upogebia species), as these animals are phylogenetically distant and exhibit difference in their systems (e.g., the connection between gland and gut).
The thoracic-gland system was previously considered to be the only means by which tanaidaceans construct tubes, and only tanaidoid and paratanaoid species were known to do so . The discovery of the pereopodal-gland system in a kalliapseudid , and now the pleotelsonal-gland system in a parapseudid, show that tube construction in tanaidaceans is diverse, both mechanistically and in terms of its taxonomic distribution. Tube construction in crustaceans has received relatively little attention , but recent discoveries of novel systems in Tanaidacea, a tiny crustacean group, indicate many other filament- and mucus-secreting systems and unexpected tube-constructers may be found among crustaceans. Information from crustaceans and other less-well-studied taxa will be necessary to understand how the acquisition of tube construction affected diversification in animals.
We thank Hisanori Kohtsuka and Mamoru Sekifuji for help in sampling; Matthew H. Dick for reviewing and editing the manuscript; two anonymous reviewers for critical comments on the manuscript; and the Japanese Association for Marine Biology (JAMBIO) Coastal Organism Joint Survey for contributing specimens.
This work was supported in part by a KAKENHI grant (JP16K18597) to KK from the Japan Society for Promotion of Science (JSPS).
Availability of data and materials
The data generated and/or analyzed during the current study are available from the corresponding author on reasonable request.
KK conceived and designed the study, collected and reared the animals, did the SEM work, and made observations on behavior and the mucus. CH did the histological work and interpreted the histological data. Both authors wrote the manuscript. Both authors read and approved the final manuscript.
Ethical approval and consent to participate were not required for this work.
Consent for publication
The authors declare that they have no competing interests.
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- Moore PG, Eastman LB. The tube-dwelling lifestyle in crustaceans and its relation to feeding. In: Thiel M, Watling L, editors. The natural history of the Crustacea 2. Lifestyle and feeding biology. Oxford: Oxford University Press; 2015. p. 35–77.Google Scholar
- Johnson SB, Attramadal YG. A functional-morphological model of Tanais cavolinii Milne-Edwards (Crustacea, Tanaidacea) adapted to a tubicolous life-strategy. Sarsia. 1982;67:29–42.View ArticleGoogle Scholar
- Johnson SB, Attramadal YG. Reproductive behaviour and larval development of Tanais cavolinii (Crustacea: Tanaidacea). Mar Biol. 1982;71:11–6.View ArticleGoogle Scholar
- Hassack E, Holdich DM. The tubicolous habit amongst the Tanaidacea (Crustacea, Peracarida) with particular reference to deep-sea species. Zool Scr. 1987;16:223–33.View ArticleGoogle Scholar
- Krasnow LD, Taghon GL. Rate of tube building and sediment particle size selection during tube construction by the tanaid crustacean, Leptochelia dubia. Estuaries. 1997;20:534–46.View ArticleGoogle Scholar
- Desbruyères D, Segonzac M, Bright M, editors. Handbook of deep-sea hydrothermal vent fauna. 2nd completely revised edition. Freistadt: Plöchl-Druck; 2006.Google Scholar
- Morales-Vela B, Suárez-Morales E, Padilla-Saldívar J, Heard RW. The tanaid Hexapleomera robusta (Crustacea: Peracarida) from the Caribbean manatee, with comments on other crustacean epibionts. J Mar Biol Assoc UK. 2008;88:591–6.View ArticleGoogle Scholar
- Kakui K, Hayakawa Y, Katakura H. Difference in size at maturity in annual and overwintering generations in the tanaidacean Zeuxo sp. in Oshoro Bay, Hokkaido, Japan. Zool Sci. 2017;34:129–36.View ArticlePubMedGoogle Scholar
- Kaji T, Kakui K, Miyazaki N, Murata K, Richard PA. Mesoscale morphology at nanoscale resolution: serial block-face scanning electron microscopy reveals fine 3D detail of a novel silk spinneret system in a tube-building tanaid crustacean. Front Zool. 2016;13:14.View ArticlePubMedPubMed CentralGoogle Scholar
- Drumm DT. Comparison of feeding mechanisms, respiration, and cleaning behavior in two kalliapseudids, Kalliapseudes macsweenyi and Psammokalliapseudes granulosus (Peracarida: Tanaidacea). J Crustacean Biol. 2005;25:203–11.View ArticleGoogle Scholar
- Kakui K, Hiruta C. Diverse pereopodal secretory systems implicated in filament production in an apseudomorph tanaidacean crustacean. J Morphol. 2014;275:1041–52.View ArticlePubMedGoogle Scholar
- Shiino SM. A new genus and two new species of the order Tanaidacea found at Seto. Publications of the Seto Marine Biological Laboratory, vol. 2; 1952. p. 53–68.Google Scholar
- Larsen K, Guţu M, Sieg J. Order Tanaidacea Dana, 1849. In: von Vaupel Klein JC, Charmantier-Daures M, Schram FR, editors. The Crustacea. Revised and updated, as well as extended from the Traité de Zoologie 5. Leiden: Brill; 2015. p. 249–329.Google Scholar
- Kakui K, Hiruta C. Tube construction by a tanaidacean Parapseudes algicola (Shiino, 1952). figshare. 2017. https://doi.org/10.6084/m9.figshare.5373928. Accessed 12 Nov 2017.
- Guţu M. A revision of the family Parapseudidae, with description of a new tribe and three genera. The diagnoses and the key of the superspecific taxa (Crustacea: Tanaidacea: Apseudomorpha). Trav Mus Natl Hist Nat Grigore Antipa. 2008;51:43–70.Google Scholar
- Heard RW, Morales-Núñez AG. Akanthoparapseudes alfaroae, a new genus and species of apseudomorphan tanaidacean (Crustacea: malacostraca: Peracarida) from Puerto Rican coastal waters. Zootaxa. 2011;3111:49–63.Google Scholar
- Bamber RN, Chatterjee T, Marshall DJ. Inshore apseudomorph tanaidaceans (Crustacea: Peracarida) from Brunei: new records and new species. Zootaxa. 2012;3520:71–88.Google Scholar
- Bamber RN. Tanaidaceans from Brunei, IV. The families Kalliapseudidae, Pagurapseudopsidae, Parapseudidae and Apseudidae (Crustacea: Peracarida: Tanaidacea: Apseudomorpha), with descriptions of a new genus and six new species. Zootaxa. 2013;3734:401–41.View ArticlePubMedGoogle Scholar
- Kiernan JA. Histological and histochemical methods: theory and practice. 4th ed. Banbury: Scion Publishing; 2008.Google Scholar
- Kakui K, Katoh T, Hiruta SF, Kobayashi N, Kajihara H. Molecular systematics of Tanaidacea (Crustacea: Peracarida) based on 18S sequence data, with an amendment of suborder/superfamily-level classification. Zool Sci. 2011;28:749–57.View ArticlePubMedGoogle Scholar
- Hilbrant M, Damen WGM. The embryonic origin of the ampullate silk glands of the spider Cupiennius salei. Arthropod Struct Dev. 2015;44:280–8.View ArticlePubMedGoogle Scholar
- Shear WA. Spinnerets in the millipede order Polydesmida, and the phylogenetic significance of spinnerets in millipeds (Diplopoda). Int J Myriapod. 2008;2:123–46.View ArticleGoogle Scholar
- Dworschak PC, Felder DL, Tudge CC. Infraorders Axiidea de Saint Laurent, 1979 and Gebiidea de Saint Laurent, 1979 (formerly known collectively as Thalassinidea). In: Schram FR, von Vaupel Klein JC, editors. The Crustacea. Revised and updated, as well as extended from the Traité de Zoologie 9B. Leiden: Brill; 2012. p. 109–219.Google Scholar
- Sutherland TD, Young JH, Weisman S, Hayashi CY, Merritt DJ. Insect silk: one name, many materials. Annu Rev Entomol. 2010;55:171–88.View ArticlePubMedGoogle Scholar
- Brusca RC, Moore W, Shuster SM. Invertebrates. 3rd ed. Sunderland: Sinauer Associates; 2016.Google Scholar
- Rakitov RA. Structure and function of the Malpighian tubules, and related behaviors in juvenile cicadas: evidence of homology with spittlebugs (Hemiptera: Cicadoidea & Cercopoidea). Zool Anz. 2002;241:117–30.View ArticleGoogle Scholar
- Derby CD. Cephalopod ink: production, chemistry, functions and applications. Mar Drugs. 2014;12:2700–30.View ArticlePubMedPubMed CentralGoogle Scholar
- Johnson RP. Scent marking in mammals. Anim Behav. 1973;21:521–35.View ArticleGoogle Scholar
- Wood WF, Sollers BG, Dragoo GA, Gragoo JW. Volatile components in defensive spray of the hooded skunk, Mephitis macroura. J Chem Ecol. 2002;28:1865–70.View ArticlePubMedGoogle Scholar
- Larsen K. Deep-sea Tanaidacea (Peracarida) from the Gulf of Mexico. Leiden: Brill; 2005.Google Scholar