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Phyllodocida

Phyllodocida is an order of errantian polychaete annelids characterized by a muscular, axial proboscis, ventral sensory palps, enlarged anterior cirri, compound chaetae with a single ligament, and the absence of dorsolateral folds.^[1] Established by Dales in 1962, it encompasses over 4,600 valid species across 27 families, representing more than 6,600 nominal taxa, making it one of the most diverse groups within Polychaeta.^[2]^[1] The order is divided into four main suborders—Aphroditiformia, Glyceriformia, Nereidiformia, and Phyllodociformia—along with some taxa of uncertain placement, supported by both molecular and morphological evidence.^[2]^[1] These polychaetes exhibit a protrusible proboscis that may be armed with chitinous jaws, teeth, or papillae, enabling diverse feeding strategies such as predation on invertebrates or scavenging.^[3] Species range in size from several millimeters to over a meter, with segmented bodies bearing parapodia for locomotion and often well-developed eyes for sensory perception.^[1] Phyllodocida species are predominantly marine and benthic, inhabiting environments from intertidal zones to abyssal depths exceeding 10,000 meters, including sandy or muddy substrates, hard bottoms, and extreme settings like hydrothermal vents and methane seeps.^[3]^[1] While most are bottom-dwellers, some lineages are holoplanktonic, free-living in the water column, and others occur in brackish, freshwater, or even terrestrial habitats, demonstrating remarkable ecological versatility.^[2] Ecologically, they play key roles as predators or associates, with notable symbiotic relationships—such as polynoids living on echinoderms or cnidarians—and contributions to nutrient cycling in marine ecosystems worldwide.^[3]^[1] Fossil records trace the group back to the Devonian period, with most families emerging by the Carboniferous, highlighting their evolutionary persistence.^[1] Ongoing molecular studies, including DNA barcoding, continue to uncover cryptic diversity and refine taxonomic boundaries within this clade.^[1]

Taxonomy and Phylogeny

Classification

Phyllodocida is classified as an order within the subclass Errantia of the class Polychaeta in the phylum Annelida.^[4] This placement situates it among the errantian polychaetes, characterized by their mobile lifestyles and well-developed parapodia.^[1] The order is currently divided into four suborders: Aphroditiformia, Glyceriformia, Nereidiformia, and Phyllodociformia.^[1] Phyllodocida is further positioned within the clade Aciculata, a major subgroup of Errantia that also encompasses Eunicida, distinguished by the presence of acicular chaetae.^[5] The taxonomic framework of Phyllodocida was first established as a monophyletic order by Dales in 1962, based on shared morphological features such as the axial muscular pharynx.^[4] Prior to this, polychaete classifications were more fragmented, with families scattered across various errantian groups; however, post-2000s analyses integrating molecular and morphological data have confirmed its monophyly and refined subordinal boundaries, resolving earlier paraphyletic interpretations.^[1] As of a 2021 diversity assessment, the order comprises over 4,600 accepted nominal species across 27 families.^[1]

Phylogenetic Relationships

Phyllodocida is widely recognized as a monophyletic clade within Annelida, primarily supported by the presence of an axial muscular pharynx as a defining synapomorphy. This structure, characterized by a symmetrical, protrusible pharynx with strong musculature, distinguishes Phyllodocida from other polychaete groups and has been consistently identified in morphological studies as a key evolutionary innovation.^[6] Within the subclass Errantia, Phyllodocida forms part of the larger Aciculata clade alongside Eunicida, with this grouping positioned as sister to the orbinioid-parergodrilid complex, which includes Orbiniida.^[7] A seminal 2009 total-evidence analysis combining morphology and sequence data from six genes across 87 annelid terminals robustly confirmed this placement, resolving Phyllodocida as monophyletic and highlighting shared features like aciculae homology with Eunicida.^[7] Subsequent studies, such as a 2015 cladistic analysis of Sphaerodoridae incorporating 33 terminals from five genera, further corroborated the monophyly of the family within Phyllodocida using both molecular and morphological data.^[8] More recently, a 2021 assessment of Phyllodocida diversity expanded the recognized family count to 27 morphologically homogeneous clades, encompassing over 4,600 nominal species, while integrating phylogenomic insights to refine internal relationships.^[1] Despite these advances, phylogenetic uncertainties persist, particularly regarding the suborder Nereidiformia, which lacks unambiguous synapomorphies and shows variable support in molecular datasets.^[7] Ongoing debates also surround incertae sedis families like Tomopteridae, whose holoplanktonic members exhibit long-branch attraction in analyses and uncertain affinities, potentially aligning closer to Glyceriformia or even outside core Phyllodocida.^[1] On a broader scale, Phyllodocida, as a constituent of Annelida, is embedded within the lophotrochozoan superphylum, with total-evidence phylogenies consistently placing Annelida as a derived clade alongside molluscs and other spiralians based on shared trochophore larvae and molecular markers.^[7]

Fossil Record

The fossil record of Phyllodocida extends from the Early Ordovician to the present, with the earliest unambiguous body fossils represented by plumulitid machaeridians from deposits in Morocco, dating to approximately 485 million years ago.^[9] These armored annelids, such as Plumulites bengtsoni, exhibit sclerites and parapodia suggestive of early errantian morphology, placing them within the crown group of Phyllodocida as total-group Aphroditiformia.^[10] Scolecodonts, the mineralized jaw apparatuses of jawed polychaetes, provide additional early evidence, with Ordovician occurrences primarily attributed to the sister order Eunicida, though some morphologies hint at phyllodocidan affinities.^[11] Definitive phyllodocidan scolecodonts and body fossils become more common in the Silurian and Devonian, marking the onset of broader diversification during the Paleozoic.^[12] Key fossil taxa include lepidocoleid machaeridians from the Devonian, such as pyritized specimens from the Arkona Shale in Ontario, which preserve soft tissues like parapodia and chaetae, offering insights into locomotion and sclerite arrangement.^[13] Scolecodonts attributed to phyllodocidans, such as those from the Middle Devonian, display diverse jaw morphologies, including paired lateral jaws that are plesiomorphic for the clade.^[14] By the Carboniferous, representatives of modern families like Glyceridae and Nereididae appear in lagerstätten such as Mazon Creek, indicating early establishment of extant lineages.^[15] These fossils document a Paleozoic diversification, with phyllodocidans adapting to expanding shallow marine environments.^[16] The fossil record of Phyllodocida is incomplete due to the poor preservation of soft tissues in most polychaetes, which decay rapidly through stages including loss of body integrity and gut support, leaving only durable elements like jaws and setae.^[17] Exceptional preservations, such as those in Silurian Herefordshire or Devonian pyritized forms, are rare and provide glimpses of internal anatomy, but behavioral inferences often rely on trace fossils like burrows.^[18] This taphonomic bias underestimates early diversity.^[1] Evolutionary radiation accelerated in the Mesozoic, linked to ecosystem restructuring during the Mesozoic Marine Revolution, including intensified predation and habitat shifts that favored mobile errantians.^[19] Mesozoic scolecodonts reflect a modern aspect, with increased family-level diversity paralleling broader marine biotic turnover.^[20]

Morphology and Anatomy

External Morphology

Phyllodocida exhibit an elongated, segmented body plan typical of errant polychaetes, consisting of a prostomium, peristomium, and numerous chaetigers that can number from fewer than 20 to over 200, depending on the family. The body is generally cylindrical or fusiform, though some suborders show modifications such as dorsoventral flattening in Aphroditiformia or a slender, transparent form in pelagic groups like Alciopidae. Overall length varies widely, from as small as 1-3 mm in diminutive forms like certain syllids to over 1 m in larger species such as those in Goniadidae or Nereididae.^[21]^[1]^[22] The prostomium is distinct and pre-segmental, often bearing 1-6 antennae, paired palps, and in many taxa, simple or compound eyes arranged in various configurations. Its shape ranges from quadrangular or conical in Phyllodociformia to heart-shaped or trapezoidal in other groups, with additional features like a nuchal papilla or epaulettes present in families such as Phyllodocidae. In Aphroditiformia, the prostomium remains unfused to the first setiger, enhancing mobility.^[21] Parapodia are prominent, typically biramous with distinct notopodia and neuropodia, though uniramous forms occur in some families like Phyllodocidae and Iospilidae. They bear chaetae, including capillary setae, composite hooded hooks, or acicular spines, which aid in locomotion and burrowing; for example, neurochaetae are often composite falcigers or compound blades in Nereidiformia. In suborder Aphroditiformia, such as Polynoidae, dorsal elytra—scale-like structures—alternate with dorsal cirri, providing protection and sometimes a felted texture from notosetae. Parapodia may include additional lobes or cirri, with orientation varying, such as forward-directed in some aphroditiformians.^[21] The proboscis is eversible and muscular, serving as the primary feeding apparatus, and is supported internally by the pharynx (detailed further in internal anatomy). It ranges from unarmed and smooth in taxa like Lacydoniidae to armed with jaws, papillae, or hooks; for instance, Glyceriformia feature four robust jaws, while Nereidiformia have paragnaths or simple papillae. In some cases, it forms a scoop-like structure for sediment ingestion.^[21] Coloration and pigmentation in Phyllodocida are diverse and often species-specific, ranging from translucent in pelagic forms to opaque patterns in benthic taxa, though pigments typically fade after preservation. Many exhibit iridescence due to structural coloration in scales or integument, particularly in polynoids where elytra display metallic sheens in hues like gold, pink, or blue, resulting from light reflection within scale microstructures rather than pigments.^[21]^[23]

Internal Anatomy

The internal anatomy of Phyllodocida reveals a suite of organ systems adapted for an active, errant lifestyle, with features that distinguish this clade within Errantia. The digestive system is characterized by an axial pharynx, a key synapomorphy for Phyllodocida, which is muscular and typically protrusible or eversible, allowing for effective prey capture and ingestion.^[6] This pharynx is followed by a short esophagus that transitions into a straight or slightly coiled intestine, often featuring a dorsal typhlosole—a longitudinal fold that increases the absorptive surface area for nutrient uptake.^[24] In representatives like Syllis gracilis (Syllidae), the intestine includes a non-muscular ventricle with paired caeca for initial digestion, emphasizing the system's efficiency in processing varied diets.^[25] The nervous system follows the typical annelid pattern but shows refinements suited to sensory integration in mobile species. A dorsal brain, or supraesophageal ganglion, lies within the prostomium, connected via circumesophageal connectives to subesophageal ganglia, which link to a double ventral nerve cord bearing segmental ganglia and lateral nerves for motor control.^[24] This configuration supports coordinated locomotion and environmental response, as seen in detailed reconstructions of Syllis gracilis where the ventral cord's ganglia are distinctly metameric.^[25] Circulation in Phyllodocida is mediated by a closed vascular system, comprising a dorsal longitudinal vessel that conveys blood anteriorly and a ventral vessel for posterior flow, with peristaltic contractions in the dorsal vessel often serving a heart-like function.^[24] Some taxa, such as certain nereidids, possess additional lateral vessels or enlarged segments acting as accessory pumps, enhancing oxygen delivery to active tissues, though highly muscularized "hearts" are absent in simpler forms like Syllis.^[25]^[26] Excretion occurs via metanephridia, paired tubular organs present in most segments, each featuring a ciliated nephrostome for coelomic fluid intake, a tortuous duct for reabsorption, and a nephridiopore opening externally near the parapodia.^[24] These structures maintain osmotic balance in diverse marine habitats, with their metameric arrangement mirroring the segmental body plan, as observed in micro-CT imaging of syllids.^[25] Sensory capabilities are augmented by nuchal organs, paired ciliated structures positioned posteriorly on the prostomium, functioning primarily as chemoreceptors to detect dissolved substances in the water column.^[27] In phyllodocids and related families, these organs appear as grooved or pit-like formations, integrating with the brain for rapid behavioral responses to chemical cues.^[24]

Ecology and Distribution

Habitats and Distribution

Phyllodocida species are predominantly marine annelids, occurring in benthic, pelagic, and occasionally brackish environments worldwide, with rare instances in freshwater or terrestrial habitats.^[28] They exhibit a cosmopolitan distribution, spanning from polar regions to tropical latitudes across all major ocean basins, including the Arctic, Atlantic, Pacific, Antarctic, Mediterranean, Black, Red, and Indian Seas.^[28] While sampling biases favor well-studied areas like European, North American, and Australian continental shelves, the highest species diversity is reported in Indo-Pacific waters, with additional hotspots in the Caribbean/Gulf of Mexico and Indian Ocean coasts.^[28] Endemism is particularly notable in extreme deep-sea settings, such as hydrothermal vents and cold seeps.^[28] In terms of depth, Phyllodocida inhabit zones from the intertidal to hadal depths exceeding 10,000 m; however, the majority (88.5%) occur in shallow coastal waters between 10 and 100 m.^[28] Benthic forms dominate, favoring soft sediments like mud or sand, mixed substrates, or hard rocky surfaces, while holoplanktonic taxa occupy open ocean waters from the surface to mid-depths.^[28] Suborder Aphroditiformia, including scale worms (Polynoidae), often live symbiotically with invertebrates such as echinoderms, cnidarians, corals, sponges, and deep-sea mussels, associated with shallow rocky habitats such as algal beds and coral reefs but extend to deep-sea environments like cold-water coral aggregations and mud volcanoes. In contrast, Glyceriformia species, such as those in Glyceridae and Goniadidae, are primarily infaunal burrowers in marine sediments, ranging from intertidal mudflats to abyssal plains and even hydrothermal vents.^[28] Adaptations to extreme conditions enable survival in hypoxic or high-pressure deep-sea habitats; for instance, polynoid scale worms in vent communities have evolved specialized tetra-domain hemoglobins for oxygen transport under low-oxygen levels. These physiological traits, combined with structural modifications for pressure tolerance, facilitate their presence in chemosynthetic ecosystems like methane seeps and anchialine caves.^[28]

Feeding and Behavior

Members of Phyllodocida are predominantly carnivorous, preying on small invertebrates such as polychaetes, crustaceans, and mollusks, though some species exhibit scavenging behaviors by consuming carrion or detritus, and a few are omnivorous, incorporating algae or plant material into their diet.^[29] For instance, species in the family Nereididae, like Nereis diversicolor, opportunistically feed on a mix of animal prey, detritus, and algae, adapting to available resources in intertidal zones.^[29] In contrast, families such as Glyceridae actively hunt burrowing prey using chemical cues to track mucous trails.^[29] Feeding primarily involves the eversion of a muscular proboscis or pharynx to capture prey, often aided by jaws in burrowing or sediment-dwelling forms for grasping and tearing.^[29] This mechanism, detailed in internal anatomy sections, allows rapid extension to engulf small organisms, with toxic secretions in some glycerids enhancing immobilization.^[30] Scavengers, such as certain amphinomids, browse on dead organic matter or predigest tissues using an eversible rasping pad.^[29] Locomotion in benthic Phyllodocida relies on crawling facilitated by parapodia, which function as paddles or legs to propel the worm over sediments or through burrows, enabling active foraging.^[29] Pelagic taxa, including the Tomopteridae, employ undulatory swimming combined with metachronal parapodial paddling for efficient propulsion in open water, achieving graceful, rhythmic movement.^[31] Most species exhibit solitary behaviors during foraging, though some, like hesionids in interstitial habitats, show gregarious tendencies for resource partitioning without territorial aggression.^[29] In predator-prey interactions, Phyllodocida employ defensive strategies such as camouflage provided by elytra in polynoids, which mimic surrounding substrates or host surfaces for concealment.^[32] Deep-sea species, particularly in Polynoidae and Tomopteridae, utilize bioluminescence to deter predators, emitting flashes from parapodial glands to confuse or distract attackers during escapes.^[33] Additionally, some phyllodocids, like Phyllodoce mucosa, extrude repulsive mucoid secretions as an antipredation response.^[34]

Reproduction and Development

Reproductive Strategies

Phyllodocida, a diverse clade of errantian annelids, predominantly exhibit dioecious reproductive strategies, with separate sexes in most families including Nereididae, Syllidae, Glyceridae, Polynoidae, and Nephtyidae.^[1] This gonochorism facilitates sexual dimorphism, where males and females develop distinct gametes within coelomic gonads, often maturing seasonally in response to environmental cues like temperature and lunar cycles.^[35] External fertilization is the prevailing mode, with gametes released into the water column to maximize dispersal in marine habitats.^[1] A notable adaptation in several phyllodocid families is epitoky, a metamorphic process transforming benthic atokous individuals into pelagic epitokes specialized for reproduction. In Nereididae, such as species of Hediste and Alitta, epitoky involves profound morphological changes, including enhanced swimming appendages and enlarged gamete stores, culminating in synchronized swarming events for mass spawning.^[36] Epitoky also occurs in Syllidae, where it supports external fertilization alongside the atokous form's routine activities.^[22] Epitoky is also reported in some Glyceridae species, involving swarming and direct gamete shedding through nephridial ducts or body wall rupture, often without the profound morphological changes seen in Nereididae or Syllidae.^[37]^[38] Hermaphroditism is rare within Phyllodocida but documented in select Syllidae, such as Syllis vittata, where simultaneous hermaphrodites possess both ect-aquasperm and oogonia, potentially enabling self-fertilization under isolated conditions.^[39] Asexual reproduction is likewise uncommon but prominent in Syllidae through schizogamy, involving stolonization where posterior body segments detach as reproductive units via architomic fission or paratomy, regenerating complete individuals.^[22] Similar paratomic fission has been observed in some Hesiionidae, allowing clonal propagation in stable environments.^[35] Parental care is minimal across Phyllodocida, with most species abandoning gametes post-release, though brooding occurs in Polynoidae. In genera like Lepidonotus and deep-sea associates, females retain fertilized eggs externally under dorsal elytra or within tubes, protecting juveniles until release without extended provisioning.^[40] Reproductive strategies vary by family: Nereididae and Syllidae emphasize pelagic swarming with larval dispersal, while Glyceridae favor direct gamete broadcast leading to benthic settlement, reflecting adaptations to infaunal lifestyles.^[1]

Life Cycle Stages

The life cycle of Phyllodocida species typically commences with external fertilization, yielding free-swimming trochophore larvae that serve as the initial developmental stage.^[41] These larvae are pear-shaped, equipped with ciliary bands such as the prototroch for locomotion and feeding, and the telotroch posteriorly, enabling planktotrophic nutrition in the plankton.^[41] In representative species like Platynereis dumerilii (Nereididae), the trochophore hatches approximately 24 hours post-fertilization at 18°C, progressing through early, mid, and late substages where eyes, stomodeum, and initial segments form over the next 24-48 hours.^[41] Many Phyllodocida exhibit further larval development into metatrochophore and nectochaete stages, where additional ciliary bands and the first three segments with chaetae emerge.^[41] The nectochaete, a more advanced planktonic form, develops functional parapodia and begins active feeding around 5-7 days post-fertilization, with variable durations influenced by individual rates.^[41] Some taxa, such as certain phyllodocids, display specialized larval morphologies, though trochophore and nectochaete types predominate across the clade.^[42] Metamorphosis marks the transition to benthic life, occurring at the 3-7 segment stage upon settlement, where larval ciliary structures like the prototroch are resorbed, and adult-like features such as antennae and cirri develop.^[41] Segment addition continues posteriorly from a telotroch-derived growth zone, facilitating body elongation during this phase.^[41] Environmental cues, including temperature (accelerating development 2-4 fold per 10°C rise) and salinity (slower rates at lower levels like 23‰), trigger hatching and metamorphosis timing.^[41] Post-metamorphosis growth in Phyllodocida is indeterminate, characterized by continuous segmentation and parapodial elaboration throughout adulthood, allowing adaptation to varying habitats.^[43] Lifespans typically range from 1-2 years in shallow-water forms like Platynereis dumerilii (up to 18 months at 18°C), extending to 3-5 years in some cold-water species due to reduced metabolic rates.^[41]^[43]^[44]

Diversity and Families

Species Diversity

Phyllodocida encompasses over 4,800 valid species distributed across 29 families, representing a substantial portion of annelid biodiversity within the subclass Errantia.^[2] This order's species richness is dominated by a few highly diverse families, with Syllidae being the most speciose, comprising over 1,100 valid species in 79 genera, followed by Polynoidae (approximately 870 species in 154 genera), Nereididae, and Phyllodocidae.^[28] Molecular barcoding efforts have revealed extensive cryptic diversity, indicating that the true number of species likely exceeds 7,000 when accounting for undescribed lineages, particularly in morphologically conservative groups.^[45] Diversity hotspots for Phyllodocida are concentrated in complex marine habitats such as coral reefs and the deep sea, where environmental heterogeneity supports high speciation rates. For instance, Polynoidae exhibit peak richness in the North Pacific and Tropical Indo-Pacific regions, with 94 species each, while deep-sea environments like hydrothermal vents host specialized clades such as glycerids adapted to extreme conditions.^[28] Subordinal breakdowns further highlight uneven distribution: Nereidiformia and Phyllodociformia contribute disproportionately to overall diversity due to their inclusion of families like Syllidae and Nereididae, whereas holoplanktonic families remain less speciose but ecologically distinct.^[28] Recent trends in Phyllodocida taxonomy show a steady increase in species descriptions, with no signs of deceleration since the 19th century, driven by advances in molecular barcoding that uncover hidden diversity in cosmopolitan taxa. A 2021 comprehensive review emphasized the understudied status of incertae sedis lineages and deep-sea forms, urging integrated morphological and genetic approaches to resolve taxonomic gaps.^[28] Endemism rates are notably high in isolated ecosystems, including hydrothermal vent communities (e.g., glycerids and polynoids) and polar regions like Antarctica, where up to 70% of polychaete species may be endemic due to biogeographic barriers.^[28] Conservation concerns for Phyllodocida are limited, with few species formally assessed as threatened on global lists, reflecting both their ecological resilience and understudied status. However, emerging threats from ocean acidification pose risks to larval stages across many families, potentially disrupting calcification in tube-building forms and reducing settlement success in vulnerable early life phases.^[46]

List of Families

Phyllodocida encompasses 29 families distributed across four recognized suborders and a group of taxa incertae sedis, comprising over 4,800 valid species in total (as of 2025).^[2]^[1] Suborder Aphroditiformia includes six families: Acoetidae (scale worms), Aphroditidae, Eulepethidae, Iphionidae, Polynoidae, and Sigalionidae (including Pholoidae as a synonym). These families are characterized by the presence of elytra or scale-like dorsal structures in many members, aiding in protection and locomotion, with approximately 1,340 species collectively; Polynoidae alone accounts for around 870 species.^[47]^[1] Suborder Glyceriformia consists of four families: Glyceridae (bloodworms), Goniadidae, Lacydoniidae, and Paralacydoniidae. Members are typically infaunal burrowers with an elongated, muscular eversible proboscis armed with jaws for predation, totaling around 180 species.^[48]^[1] Suborder Nereidiformia features eight primary families: Antonbruuniidae, Chrysopetalidae, Hesionidae, Microphthalmidae, Nereididae (ragworms), Pilargidae (including Kynephorinae), Syllidae (small predators), and Calamyzidae (formerly Nautiliniellidae). Key traits include a protrusible pharynx and diverse feeding strategies, with this suborder representing the largest diversity at about 2,400 species; Syllidae contributes roughly 1,100 species.^[49]^[1] Suborder Phyllodociformia contains three families: Alciopidae, Lopadorrhynchidae, and Phyllodocidae. These are often pelagic or epibenthic forms with a well-developed proboscis, encompassing approximately 530 species.^[50]^[1] Incertae sedis includes eight families with unresolved phylogenetic positions: Ichthyotomidae, Iospilidae, Nephtyidae, Pontodoridae, Sphaerodoridae, Tomopteridae (planktonic forms lacking chaetae and featuring transparent bodies), Typhloscolecidae, and Yndolaciidae. Notable traits include adaptations for holoplanktonic life in some, such as Tomopteridae, with around 360 species; Sphaerodoridae has 131 species marked by rows of epithelial tubercles.^[51]^[1] This classification reflects current taxonomic consensus, incorporating recent additions like Yndolaciidae from Arctic studies.^[1]

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Explorations on the ecological role of toxin secretion and delivery in ...
May 16, 2018 · Here we show that an inconspicuous phyllodocid uses toxins in its uncanny feeding strategy. The worm, a jawless active predator characterised by ...<|control11|><|separator|>
[31]
New research reveals swimming mechanics of the gossamer worm
Sep 28, 2021 · This ethereal worm is a graceful swimmer that “dances” through the midwater with the rhythmic paddling of its swimming legs. A new study ...
[32]
[PDF] Symbiotic Polychaetes: Review of known species - RERO DOC
Moreover, the effectiveness of the polychaete's camouflage is often heightened by their location on an appropriate site on the host surface. The segments of ...
[33]
Bioluminescence in Polynoid Scale Worms (Annelida: Polynoidae)
It is believed that Polynoidae bioluminescence is associated with a membrane enzyme known as “polynoidin,” which was isolated during the early 1980s from ...Missing: iridescent | Show results with:iridescent
[34]
An antipredation mechanism of the polychaete Phyllodoce mucosa ...
Aug 5, 2025 · The polychaete Phyllodoce mucosa exhibits an antipredation response via the extrusion ofa repulsive mucoid secretion. The mucus, secreted by ...
[35]
Reproductive Strategies and Developmental Patterns in Annelids
Aug 6, 2025 · The duct becomes ciliated and the most proximal cells are separated when the coelom extends by fluid accumulation between the lining cells.
[36]
Epitokous metamorphosis, reproductive swimming, and ... - ZooKeys
Jan 18, 2021 · Many nereidids show swarming behaviour (mass-swimming of sexually mature adults) to shed gametes freely into the water, accompanied by a common ...
[37]
[PDF] sexual reproductive modes in polychaetes: classification and diversity
or brood embryos within the female mantle cavity (morphologically, an external ... The polychaete worms. Definitions and keys to the orders, families and ...
[38]
Sperm ultrastructure of three Syllinae (Annelida, Phyllodocida ...
The noticeable taxonomic diversity of syllids (about 700 listed species) is also mirrored in the array of reproductive strategies as well as in sperm ...<|control11|><|separator|>
[39]
Wide-spread dispersal in a deep-sea brooding polychaete: the role ...
Jan 18, 2024 · The worms brood their young attached to the body segments inside the parental tubes assuming no free-swimming larval stages.
[40]
The normal development of Platynereis dumerilii (Nereididae ...
Dec 30, 2010 · Polychaete larval development comprises traditionally three major stages: the trochophore, the metatrochophore and the nectochaete. The ...Missing: eriochead | Show results with:eriochead
[41]
(PDF) Polychaetes have evolved feeding larvae numerous times
Aug 9, 2025 · 'Trochophore' is commonly used to designate larvae with opposed-band feeding and a particular set of ciliary bands. The trochophore has been ...Missing: lifespan | Show results with:lifespan
[42]
Polychaete - an overview | ScienceDirect Topics
The circulatory system is closed, and a heart-like organ is absent. In Potamodrilus, the female gonads are situated in segment five and male gonads in ...
[43]
Size and age structure of the scaleworms Lepidonotus squamatus ...
Aug 5, 2025 · The maximum life span of this species is not more than five years. The number of growth lines on the jaws of H. imbricata varies from 0 to 3.
[44]
https://www.researchgate.net/publication/282694801_Size_and_age_structure_of_the_scaleworms_Lepidonotus_squamatus_and_Harmothoe_imbricata_Polychaeta_Polynoidae_in_the_White_Sea
[45]
Ocean Acidification Increases Copper Toxicity to the Early Life ...
Jul 17, 2014 · Ocean Acidification Increases Copper Toxicity to the Early Life History Stages of the Polychaete Arenicola marina in Artificial Seawater. Click ...Missing: conservation | Show results with:conservation
[46]
WoRMS - World Register of Marine Species - Aphroditiformia
### Families under Suborder Aphroditiformia
[47]
WoRMS - World Register of Marine Species - Glyceriformia
### Summary of Families under Suborder Glyceriformia
[48]
WoRMS - World Register of Marine Species - Nereidiformia
### Families under Suborder Nereidiformia
[49]
https://www.marinespecies.org/aphia.php?p=taxdetails&id=928
[50]
WoRMS - World Register of Marine Species - Phyllodocida incertae sedis
### Summary of Families under Phyllodocida incertae sedis