Segmented Worms Chapter 17 Annelids and Allied Taxa Phylum Annelida Clade Pleistoannelida Errantia Sedentaria Phylum Sipuncula Annelids and Allied Taxa Members of Phylum Sipuncula are benthic marine animals with unsegmented bodies. Molecular sequence data place echiurans within phylum Annelida. Sipunculans - Sister taxon to Annelida. Phylum Annelida Annelids are protostome coelomates in superphylum Lophotrochozoa. Spiral, determinate cleavage. Nervous system more centralized & circulatory system more complex than in previous phyla. Phylum Annelida Annelids are segmented worms. They have bodies composed of a series of fused rings. Earthworms, leeches, clam worms. Phylum Annelida The evolutionary innovation shown by annelids is segmentation (metamerism). Segmentation evolved separately in annelids, arthropods, and chordates. The body is divided into a series of segments, each having similar components of all major organ systems. Built in fail-safe. Allows for specialization. Phylum Annelida Many annelids have chitinous bristles called setae. Help in locomotion Anchor worm in place Deter predators Phylum Annelida Annelids can be found worldwide in marine, freshwater, and terrestrial habitats. Phylum Annelida – Body Plan Prostomium – anterior part followed by segmented body. Pygidium – terminal portion. Phylum Annelida – Body Plan Peritonia (layers of mesodermal epithelium) of adjacent segments meet to form septa. Fluid-filled coelom acts as a hydrostatic skeleton. Phylogeny Traditionally, annelids are divided among 3 classes: Class Polychaeta Class Oligochaeta Class Hirudinida Polychaeta is a paraphyletic class because ancestors of the clitellates arose from within it. Oligochaeta and Hirudinida form a monophyletic group called Clitellata. Characterized by reproductive structure called a clitellum. Class Oligochaeta is a paraphyletic group because ancestors of leeches arose from within it. Clade Pleistoannelida New Classification: Clade Errantia Clade Sedentaria Errantia Errant polychaetes have some features other annelids do not: A well developed head. Paired appendages, parapodia, that function as gills and aid in locomotion. No clitellum. Many setae Errantia Errant forms include pelagic and benthic types and are often predators or scavengers. Reproduction Gonads are temporary structures in polychaetes. Sexes usually separate. Fertilization is external. Early larva is a trochophore. Circulation and Respiration Most have parapodia and gills for gaseous exchange. Others use the body surface. Circulation varies. In Nereis a dorsal vessel carries blood forward and a ventral vessel carries blood posteriorly. Blood flows across between these major vessels in networks around the parapodia and intestine. In some, septa are incomplete and coelomic fluid serves circulatory function. Many polychaetes have respiratory pigments Hemoglobin, chlorocruorin or hemerythrin. Excretion Excretory organs vary, from protonephridia to metanephridia, and mixed forms. One pair per metamere. Inner end (nephrostome) opens into the coelomic cavity. Coelomic fluid enters the nephrostome. Selective resorption occurs along the nephridial duct. Nervous System and Sense Organs Double ventral nerve cord runs length of the worm with ganglia in each metamere. Sense organs include: Eyes, nuchal organs and statocysts. Eyes vary from simple eyespots to well-developed image-resolving eyes similar to mollusc eyes. Nuchal organs are ciliated sensory pits that are probably chemoreceptive. Some burrowing and tube-building polychaetes use statocysts to orient their body. Representative Errant Polychaetes Clam Worms: Nereis Errant polychaetes Live in mucus-lined burrows near low tide level. Come out of hiding places at night to search for food. Prostomium bears a pair of palps sensitive to touch and taste, a pair of short sensory tentacles, and two small dorsal eyes sensitive to light. Peristomium has a ventral mouth, a pair of jaws, and four pairs of sensory tentacles. Representative Errant Polychaetes Scale worms Flattened bodies are covered with broad scales. Some are large, all are carnivores and some are commensals in burrows of other organisms. Representative Errant Polychaetes Fireworms Have hollow, brittle setae that contain poisonous secretions. Feed on cnidarians. Sedentaria Sedentaria now includes the sedentary polychaetes (tubeworms, siboglinids), echiurans, oligochaetes and leeches. Sedentaria Sedentary forms often have elaborate devices for feeding and respiration. Filter or deposit feeders. Representative Sedentary Polychaetes Tubeworms Tube-dwellers May line their burrows with mucus Use cilia or mucus to obtain food Representative Sedentary Polychaetes Fanworms or Featherduster worms Unfurl tentacular crowns to feed. Food moved from radioles to mouth by ciliary action. Representative Sedentary Polychaetes Parchment Worms Lives in a U-shaped tube. Modified segments pump water through tube. Clade Siboglinidae (Pogonophorans) Formerly members of phylum Pogonophora (beardworms). Discovered in 1900. 150 species described. Most are small, less than 1 mm in diameter. Giant beardworms that live in deepwater hydrothermal vents are 3 m long and 5 cm in diameter. Family Siboglinidae (Pogonophorans) Most live in mud on ocean floor at depths of 100 - 10,000m. Sessile animals that secrete and live in long chitinous tubes. Tubes have general upright orientation in bottom sediments. Tubes are generally three or four times the length of the animal. http://www.youtube.com/watch?v=2FFnrW_SUdM Family Siboglinidae (Pogonophorans) Long cylindrical body covered with cuticle. Divided into a short anterior forepart, a long slender trunk, and a small, segmented opisthosoma. Tentacles are hollow extensions of the coelom and bear minute pinnules. Family Siboglinidae (Pogonophorans) No mouth or digestive tract. Nutrients such as glucose and amino acids absorbed from seawater through pinnules and microvilli of tentacles. Family Siboglinidae (Pogonophorans) Most energy derived from a mutualistic relationship with chemoautrophic bacteria that oxidizes hydrogen sulfide. Trophosome, derived embryonically from midgut, houses the bacteria. Family Siboglinidae (Pogonophorans) Sexes are separate. Research suggests that cleavage is unequal and atypical. Appears to be spiral. Coelom formed by schizocoely. Embryo Worm-shaped and ciliated. Poor swimmer. Probably carried by water currents until it settles. Osedax – bone eating worms http://www.youtube.com/watch?v=URi8KccVkks Family Echiuridae Approximately 140 species of marine worms that burrow into mud or sand. Live in empty snail shells or sand-dollar tests, or rocky crevices. Found in all oceans. Length varies from a few millimeters to 40 or 50 cm. Family Echiuridae – Form and Function Sausage-shaped. Inextensible proboscis anterior to the mouth. Often called spoon worms”. Simple nervous system with a ventral nerve running length of the body. Ciliated groove on the proboscis allows them to gather detritus over the mud while lying buried. Muscular body wall is covered by a cuticle and epidermis which may be smooth or covered by papillae. Family Echiuridae Large coelom. Digestive tract long and coiled. Most have a closed circulatory system with colorless blood. Hemoglobin found in certain cells and in coelomic corpuscles. Respiration probably occurs in hindgut which is continually filled and emptied by cloacal irrigation. Family Echiuridae Reproduction Sexes are separate. Gonads produced by special regions in peritoneum in each sex. Fertilization usually external. Early cleavage and trochophore stages similar to annelids. Clade Clitellata Class Oligochaeta and Class Hirudinida Form reproductive structure called a clitellum. Ring of secretory cells found in a band around the body. Permanent in oligochaetes but visible only during reproductive season in leeches. Members are derived annelids that lack parapodia. Hermaphroditic (monoecious) animals that exhibit direct development. Young develop inside a cocoon secreted by the clitellum, and emerge as small worms. Oligochaeta Class Oligochaeta includes earthworms and many freshwater worms. They possess setae, but not as much as polychaetes. Oligochaeta Earthworms are the most familiar oligochaetes, found in moist, rich soil. They can burrow deep underground and remain dormant in a slime chamber during dry weather. Setae help prevent slipping while burrowing. Oligochaeta Darwin wrote about earthworms in The Formation of Vegetable Mould Through the Action of Worms. He noted the beneficial activities of worms, aeration, moving nutrients up from subsoil, adding nitrogenous products, breakdown of organic matter in dead leaves etc. An earthworm can ingest its own weight in soil every 24 hours. Oligochaeta - Reproduction Earthworms are hermaphroditic – male and female organs in the same animal. When mating, two worms are held together by mucus secreted by the clitellum. Oligochaeta - Reproduction After mating, a cocoon forms around the clitellum, as it passes forward it gathers both gametes, and fertilization occurs inside. Oligochaeta - Reproduction Development occurs inside the cocoon and young worms hatch out. Development is direct, no larval stage. Oligochaeta - Feeding Food is stored in a thin-walled crop. Muscular gizzard grinds food into small pieces. Digestion and absorption occur in intestine. Oligochaeta - Excretion Each segment, except the 1st three and terminal one, have a pair of metanephridia. A ciliated funnel, the nephrostome, draws in wastes and leads through the septum. These coil until the nephridial duct ends at a bladder that empties outside at nephridiopore. Wastes from both the coelom and the blood capillary beds are discharged. Aquatic oligochaetes excrete toxic ammonia. Oligochaeta - Circulation and Respiration Coelomic fluid and blood transport food, wastes, and respiratory gases. Blood circulates in a closed system with five main trunks running lengthwise in the body. Dorsal vessel contains valves and functions as a true heart. Pumps blood anteriorly into 5 pairs of aortic arches. Aortic arches ensure steady pressure in ventral vessel. Oligochaeta - Nervous System and Sense Organs Central nervous system and peripheral nerves. Pair of cerebral ganglia connect around the pharynx to the ganglia of the ventral nerve cord. Neurosecretory cells in brain and ganglia secrete neurohormones. Regulate reproduction, secondary sex characteristics, and regeneration. Lack eyes but have many photoreceptors in the epidermis. Free nerve endings in tegument are probably tactile structures. Oligochaeta - General Behavior Avoid bright light (negative phototaxis). Chemical stimuli are important in locating food. Limited learning ability - primarily trial-and-error learning. Hirudinida Class Hirudinida includes the leeches. Primarily freshwater, a few marine & terrestrial. More common in tropical climates. Hirudinida Many leeches live as carnivores on small invertebrates. Some are temporary parasites. Some are permanent parasites – they never leave their host. Hirudinida Leeches are hermaphroditic and have a clitellum (only appears during breeding season), like oligochaetes. Leeches do not have setae. They’ve developed suckers for attachment and a specialized gut for storing large amounts of blood. Hirudinida - Respiration and Excretion Some fish leeches have gills. All other leeches exchange gases across epidermis. 10 to 17 pairs of nephridia. Coelomocytes and other special cells may assist in excretion. Hirudinida - Nervous and Sensory Systems Two “brains” Anterior fused ganglia form a ring around the pharynx. Seven pairs of posterior fused ganglia. 21 pairs of segmental ganglia in between along a double nerve cord. Epidermis contains free sensory nerve endings and photoreceptor cells. Pigment-cup ocelli are present. Hirudinida - Circulation Coelom reduced by invasion of connective tissue. Forms system of coelomic sinuses and channels. Some have a typical oligochaete circulatory system. Coelomic system is auxiliary. Some lack blood vessels and coelomic sinuses serve as only vascular system. Class Hirudinida Leeches are highly sensitive to stimuli associated with the presence of prey. Those that feed on mammals are attracted by warmth. Phylum Sipuncula Approximately 250 species of benthic marine worms. Sedentary, living in burrows of mud or sand, snail shells, coral crevices, or among vegetation. More than ½ restricted to tropical zones. Some are tiny, slender worms, but most range from 3 to 10 cm in length. Some are known as “peanut worms” because when disturbed, they contract to a peanut shape. Phylum Sipuncula - Form and Function No segmentation or setae. Slender, retractable introvert or proboscis at anterior end. Walls of the trunk are muscular. Phylum Sipuncula - Nutrition Some appear to be detritivores and others suspension feeders. Some nutrition may come from dissolved organic matter in the surrounding water. From burrow or hiding place, they extend tentacles to explore and feed. Collected organic matter moved from mucus on tentacles to mouth by ciliary action. Large fluid-filled coelom. Digestive tract is U-shaped. Phylum Sipuncula - Respiration Lack a circulatory and respiratory system. Gas exchange appears to occur across the introvert and tentacles. Phylum Sipuncula - Nervous and Sensory Systems Bilobed cerebral ganglion behind tentacles. Ventral cord extends the length of body. Phylum Sipuncula - Reproduction Sexes are separate. Sex organs develop seasonally within the connective tissue covering the origins of the retractor muscles. Sex cells are released through the nephridia. Asexual reproduction occurs by transverse fission. Phylogeny Similarities in the early development of molluscs, annelids, and some primitive arthropods indicate that these three groups are probably closely related. Trochophore larva Spiral cleavage Schizocoelous coelom formation Evolutionary Significance of Metamerism No satisfactory explanation for origins of metamerism and coelom has gained acceptance. Coelom may have been advantageous as a hydrostatic skeleton. Coelomic fluid would have acted as a circulatory fluid and reduce need for flame cells everywhere. Coelom could store gametes for timed release. Would require nervous and endocrine control. Evolutionary Significance of Metamerism Unlikely that segmentation is homologous among annelids, arthropods, and chordates. Current evidence supports the hypothesis that segmentation arose independently multiple times. Evolutionary Significance of Metamerism Selective advantage of a segmented body for annelids appears to lie in the efficiency of burrowing. However, does not explain segmentation in arthropods given the rigidity of the exoskeleton. Phylogeny Molluscs and annelids share many developmental features so are presumed to be closely related. However, shared features are likely to be a retained ancestral feature for lophotrochozoan protostomes. Molecular analyses place sipunculids closely related to the annelids.