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Understanding the general biology, biodiversity, ecology, and evolutionary history of organisms necessitates correct identification. Found worldwide in fresh, brackish, and some marine waters, rotifers can be difficult to identify due to their small size, complex characteristics, and dearth of keys to their identification. Moreover, many species lack a hard body wall (i.e., illoricate species), thus they are nearly impossible to identify when preserved. As a result detailed study of many illoricate rotifers is wanting. This is especially acute for the sessile rotifers where quality illustrations, either as line art or light or scanning electron photomicrographs, of adults and trophi is deficient. This leads to a serious impediment in providing a comprehensive accounting for some species. Lacinularia and Sinantherina (Monogononta; Gnesiotrocha; Flosculariidae) are two sessile genera in which the literature provides inadequate treatment. In this contribution we (1) provide simple, dichotomous keys for the identification of all valid species of both genera and (2) present collated information on their morphology thereby detailing where additional research is needed. Both keys focus on easily observable characters of adult female morphology, including features of their coronae, antennae, colony formation behaviors, and presence/absence of eyespots in the adults. We hope that our effort promotes additional research on these two genera, including better documentation of their trophi and general body morphology.   

Abstract Genome size is an important correlate of many biological features including body size, metabolic rate, and developmental rate, and can vary due to a variety of mechanisms, including incorporation of repetitive elements, duplication events, or reduction due to selective constraints. Our ability to understand the causes of genome size variation are hampered by limited sampling of many non-model taxa, including monogonont rotifers. Here we used high throughput Nanopore sequencing and flow cytometry to estimate genome sizes of nine species of monogonont rotifers representing seven families, including three representatives of Superorder Gnesiotrocha. We annotated the genomes and classified the repetitive elements. We also compared genome size with two biological features: body size and metabolic rate. Body sizes were obtained from the literature and our estimates. Oxygen consumption was used as a proxy for metabolic rate and was determined using a respirometer. We obtained similar genome size estimates from genome assemblies and flow cytometry, which were positively correlated with body size and size-specific respiration rate. Importantly, we determined that genome size variation is not due to increased numbers of repetitive elements or large regions of duplication. Instead, we observed higher numbers of predicted proteins as genome size increased, but currently many have no known function. Our results substantially expand the taxonomic scope of available genomes for Rotifera and provide opportunities for addressing genetic mechanisms underlying evolutionary and ecological processes in the phylum. 

Abstract Rotifers possess complex morphologies despite their microscopic size and simple appearance. Part of this complexity is hidden in the structure of their organs, which may be cellular or syncytial. Surprisingly, organs that are cellular in one taxon can be syncytial in another. Pedal glands are widespread across Rotifera and function in substrate attachment and/or egg brooding. These glands are normally absent inAsplanchna, which lack feet and toes that function as outlets for pedal glandular secretions in other rotifers. Here, we describe the ultrastructure of a pedal gland that is singular and syncytial inAsplanchnaaff.herricki, but is normally paired and cellular in all other rotifers.Asplanchnaaff.herrickihas a single large pedal gland that is active and secretory; it has a bipartite, binucleate, syncytial body and a cytosol filled with rough endoplasmic reticulum, Golgi, and several types of secretory vesicles. The most abundant vesicle type is large and contains a spherical electron‐dense secretion that appears to be produced through homotypic fusion of condensing vesicles produced by the Golgi. The vesicles appear to undergo a phase transition from condensed to decondensed along their pathway toward the gland lumen. Decondensation changes the contents to a mucin‐like matrix that is eventually exocytosed in a “kiss‐and‐run” fashion with the plasma membrane of the gland lumen. Exocytosed mucus enters the gland lumen and exits through an epithelial duct that is an extension of the syncytial integument. This results in mucus that extends from the rotifer as a long string as the animal swims through the water. The function of this mucus is unknown, but we speculate it may function in temporary attachment, prey capture, or floatation. 

Genus Pompholyx Gosse, 1851 (Rotifera; Monogononta; Testudinellidae) comprises three species described from freshwater plankton around the globe. Here we describe a new species of Pompholyx collected from a freshwater pond in Massachusetts, USA. The new species resembles its congeners with respect to the following characters: paired eyespots; a dorsally arched lorica with a dorsal occipital convexity behind the corona; lateral flared and rounded lorica surfaces; a ventral surface bearing an occipital concavity posterior of the mouth; a unique egg-gland system; and the absence of a foot. However, P. faciemlarva sp. n. differs from its congeners in possessing a transverse furrow on both the dorsal and ventral surfaces of the lorica. While the trophi of P. faciemlarva sp. n. generally resemble those of other species of Testudinellidae, they do have a symmetrical pattern of unci teeth (17/17) that differs from Pompholyx sulcata (17–20/18–21, right/left), the only other species in the genus with well-described trophi. The description of this new species enhances the floristic richness of freshwater in North America. 

Correct identification of species is necessary if we are to understand their biology, ecology, and evolutionary history, as well as to catalog their global biodiversity. This is acutely critical for many micrometazoans like rotifers, which are often difficult to identify because of their small size and complicated morphologies. Rotifers are ubiquitous micrometazoans that are found worldwide in fresh, brackish, and some marine waters. However, their study is hindered by a lack of both taxonomic expertise and concomitantly adequate guides to the identification of some taxa. These deficiencies are particularly true for the sessile species. To help alleviate these impediments, we assembled information from the literature on easily recognizable characters of all nine valid species in one notable genus: Floscularia (Monogononta; Gnesiotrocha; Flosculariidae). Using that information we developed a simple, dichotomous key to enable workers to identify species in this genus. Our key emphasizes easily observable characters of adult female morphology, including features of their tubes, anterior ends, trophi, and colony formation abilities, thereby allowing for relatively quick identification.  

ABSTRACT Many planktonic rotifers carry their oviposited eggs until hatching. In some species, the eggs are attached to the mother via secretions from her style gland, which forms a thread that extends from her cloaca. In species ofPompholyx, the mother possesses the rare ability to change the tension on the secreted thread, which alters the proximity of the egg with respect to her body. In this study, we used behavioral observations, confocal microscopy, and transmission electron microscopy to study the functional morphology of the stalk gland, which secretes a similar thread to the style gland. Our observations reveal that six longitudinal muscles insert on a stalk‐gland complex, which is a combination of a two‐headed gland and an epithelial duct that connects to the posterior cloaca. The gland secretes a single, long, electron‐dense thread that traverses the duct and attaches to the egg surface through the cloaca. Three retractor muscles insert on the stalk gland and function to pull the entire complex anteriorly, thereby increasing tension on the thread and moving the egg close to the mother's body. A set of three (two pairs and a single dorsal) protractor muscles antagonize these actions, and their contraction pulls the gland complex close to the cloaca, thereby releasing tension on the thread and allowing the egg to distance itself from the mother. The stalk gland complex does not appear to be homologous to the style glands of other rotifers, but we hypothesize that it functions as a form of maternal protection as is the case with style glands. 

Diapausing embryos of invertebrates represent investments in future populations. Thus, these embryos must be capable of withstanding a variety of environmental assaults. Consequently, their eggshells should be adapted to resist injuries from predators, sediments, or excessive shrinkage if desiccated. To date, there have been no direct nanomechanical measurements of the eggshells of most diapausing invertebrates. Here, we used three approaches to understand how eggshells of two rotifers, a freshwater species (Brachionus calyciflorus) and a brackish water species (B. plicatilis), tolerate harsh conditions: (1) atomic force microscopy to measure elasticity and hardness; (2) transmission electron microscopy to study ultrastructure; (3) scanning electron microscopy to examine surface features. We compare these values to measurements of brine shrimp (Artemia salina) cysts and mosquito (Aedes aegypti) overwintering eggs. Our results revealed that rotifer eggshells are structurally similar and have comparable nanomechanical values. While rotifer eggshells had lower Young’s moduli (ca. 13–16 MPa) and hardness values (1.84–1.85x10-2 GPa) than eggshells of Artemia and Aedes, eggshells of all species were relatively elastic and not particularly resistant to deformation. Pliancy of shells that form egg banks (i.e., Artemia, Brachionus) may be an adaptation to resist cracking under the physical forces of buried sediments. Though there are no obvious relationship between eggshell thickness, ultrastructure, ornamentation, or nanomechanical values in rotifer eggshells, we hypothesize that eggshell chemistry may play an important role in determining elasticity and hardness. Future studies should consider an integrative approach to understand importance of eggshell structure, chemistry, and mechanics in protecting diapausing embryos.