Frontal filament morphogenesis in the salmon louse Lepeophtheirus salmonis.

The objective of the present study was to understand how and when the frontal filament (FF) in the salmon louse Lepeophtheirus salmonis is produced by examining the sequence of morphological changes leading to FF production in the copepodid and early chalimus stages. Atlantic salmon (Salmo salar) were heavily infested with newly molted copepodids. Sea lice were sampled prior to infestation and at 1, 2, 3, 4, 5, 6, 7, 8, and 9 days postinfestation. FF morphogenesis from newly molted copepodid to chalimus II, i.e., through 2 molts, was studied using high-resolution light microscopy of serial transverse and sagittal resin sections. Three groups of cells, identified as A, B, and C, are thought to be involved in the production of the secretions (S1 and S2) that form the filament material. The amount and shape of S1 and S2 and their association with B- and C-group cells, respectively, changed with the molt cycle. The following scenario for FF development is proposed: the first secretion to form after the molt for both copepodid and chalimus stages is S1, and it is formed by B-group cells and becomes the basal plate of the external FE C-group cells produce S2 during mid-intermolt to premolt stage. The S2 becomes the stem of the external FE In premolt larvae, S1 and S2 were contained within a cuticle-lined invagination that had a form similar to that of the extruded filament. The axial duct present in both copepodid and chalimus originates from the A-group cells and probably carries a secretion used to attach the filament to the host. This study provides strong evidence that L. salmonis produces a new filament with each molt, creating the possibility of using a sea lice control method based on interference with filament production more feasible.     

Taxonomic studies on brackish copepods in Korean waters--II. Ontogeny and phylogeny of appendages in copepodid stages of Tortanus derjugini Smirnov, 1935 (Copepoda, Calanoida)

The development of all copepodid stages of a brackish calanoidcopepod Tortanus (Eutortanus) derjugini from western Korea isinvestigated. Homologies of segmentation and setation in adultcharacters are traced through all copepodid stages. The fourthand fifth pedigers are secondarily fused at the moult to theadult. Antennulary setation shows sexual dimorphism first atstage IV. The exopod of leg 1 is divided into two segments withoutaddition of any element at the moult to stage II, while an innerseta on the first segment is newly added at the moult to stageIII. This pattern differs from the basic pattern proposed forother copepods, in which the division of the exopod is precededby the formation of an element or both occur at the same time.In the fifth leg of the male some elements are suppressed duringthe final moult into the adult. The ontogenetic analyses indicatethat adult characters of some subgenera of Tortanus are expressedby their suppressions at the developmental phases. Suppressionof elements is important for the evolution of Tortanus.     

The occurrence of Lepeophtheirus salmonis and Caligus clemensi (Copepoda: Caligidae) on three-spine stickleback Gasterosteus aculeatus in coastal British Columbia

Infections with sea lice species belonging to Lepeophtheirus and Caligus are reported from examinations of 1,309 three-spine sticklebacks collected in coastal British Columbia. Over 97% of the 19,960 Lepeophtheirus specimens and nearly 96% of the 2,340 Caligus specimens were in the copepodid and chalimus developmental stages. The parasites were identified as Lepeophtheirus salmonis and Caligus clemensi based on morphology of adult stages. Between 1,763 and 1,766 base pairs (bp) of 18S rDNA from adult specimens collected from sticklebacks and salmon differed from the GenBank L. salmonis reference sequence by a single bp and were distinct from those of 2 other Lepeophtheirus species. A 530-bp region of 18S rDNA from chalimus stages of Lepeophtheirus obtained from sticklebacks and salmon was identical to that of the L. salmonis reference sequence. The three-spine stickleback is a new host record for L. salmonis. The prevalence of L. salmonis was 83.6% and that of C. clemensi was 42.8%. The intensities of these infections were 18.3 and 4.2, respectively. There was no significant relationship between sea lice abundance and stickleback condition factor. Significant spatial and temporal variations both in abundance of sea lice and surface seawater salinities were measured. The abundance of both sea lice species was lowest in zones in which surface seawater salinity was also lowest. Sticklebacks appear to serve as temporary hosts, suggesting a role of this host in the epizootiology of L. salmonis. The stickleback may be a useful sentinel species with which to monitor spatial and temporal changes in the abundance of L. salmonis and C. clemensi.     

Late postnaupliar development of Monstrilla sp. (Copepoda: Monstrilloida), a protelean endoparasite of benthic polychaetes

Polychaete specimens from Hawaii were infected by the copepod Monstrilla. The development of these protelean parasites has remained unstudied for more than a century. Three postnaupliar endoparasitic stages were obtained: copepodids CIII, CIV, and CV, the latter stage found previous to and during emergence. Copepodid development, including the body and appendages (antennules, legs 1–4, caudal rami), is described and analyzed. The feeding tubes and the exiting from the host are also described. In light of the recently proposed inclusion of monstrilloids among caligiform copepods, it was found that monstrilloid copepodid development diverges from caligiforms and other copepod groups in: (1) the segmentation of the urosome at CIII, (2) the early formation of a genital complex, (3) early completion of swimming legs setation, at CIII; (4) delayed segmentation of rami of leg 3 at CIII (vs. the usual two-segmented pattern), (5) loss of one exopodal seta of leg 1 at CIV, (6) full development of leg 1 endopod vs. usually vestigial condition in caligiforms; (7) earlier segmentation of leg 4 rami, and (8) stable interstage (CIII–CV) setation pattern of legs 3 and 4. Overall, monstrilloid development appears to have unique characters and their phylogenetic relations deserve further study.     

The life-cycle of Ergasilus briani Markewitsch, 1993 (Copepoda: Poecilostomatoida)

The life cycle of Ergasilus briani is shown to consist of six nauplius stages, five copepodid stages and the adults. Only the adult female is parasitic. The free-living stages are described in detail. The presence of three aesthetascs on the antennules of all copepodid stages and the adult is noted for the first time. Unusual aspects of E. briani development include: the antennule is sexually dimorphic from copepodid IV onwards, the dimorphism being expressed in the numbers of setae present on the more proximal segments, and the first appearance of the male maxilliped is at the copepodid II stage. The endopodal setation of the male maxilliped is the maximum known within the Poecilostomatoida. The striking pigmentation of the developmental stages of ergasilids is noted and discussed.     

Development of functional adaptation to clasping behaviour in harpacticoid copepods (Copepoda,Harpacticoida)

The copepodite antennule development of several harpacticoid families is studied and male antennule development of 5 species is schematically illustrated. The origin of newly formed segments can be determined by seta numbers of segments, relative segment length, furrows indicating previous articulations and by the position of the segment which bears the proximal aesthetasc. At least in some species sexual dimorphism of antennules is present from C II onwards. Females practically reach the adult antennular state at C V whereas males undergo drastic changes from C V to C VI with proximal addition of segments, and often with distal fusions and formation of a unique armature due to functional adaptations in clasping behaviour. No correlation has been found between clasping mode, male antennule type and taxonomic level. In closely related species of the same genus both chirocer and subchirocer antennules are found. The postnaupliar development of the chirocer type can proceed along different ways. Consequently it is suggested that at least chirocer antennules have originated several times independently during harpacticoid evolution.     

Effects of sea lice (Lepeophtheirus salmonis Kröyer, 1837) infestation on macrophage functions in Atlantic salmon (Salmo salar L.)

Experiments were conducted to determine the effects of sea lice, Lepeophtheirus salmonis, on non-specific defence mechanisms in Atlantic salmon, Salmo salar, by experimentally infesting hatchery-reared 1 and 2 year old post-smolts, S1 and S2, with laboratory grown infective copepodids at moderate to high infection intensities ranging from 15-285 lice per fish. The effects of sea lice-induced stress were investigated by measuring the blood levels of cortisol and glucose as indicators of primary and secondary stress responses, and by changes in macrophage respiratory burst activity and phagocytosis as indicators of tertiary stress responses as well as non-specific defence mechanisms. Fish were sampled prior to sea lice infestation at day 0 and at days 3, 7, 14 and 21 post-infestation. Sea lice were at copepodid stage at day 3, at chalimus stages at days 7 and 14, and at pre-adult stage at day 21. Blood levels of cortisol and glucose were found to be significantly increased at day 21 in fish-infested with the highest levels. Macrophage respiratory burst and phagocytic activities were found to be significantly decreased only at day 21. These results indicate that sea lice do not suppress host defence mechanisms during the earlier stages of infestation. They do have effects on the development of chronic stress and on the host non-specific defence mechanisms soon after the lice reach the pre-adult stage.     

Nervous system development in the fairy shrimp Branchinella sp. (Crustacea: Branchiopoda: Anostraca): Insights into the development and evolution of the branchiopod brain and its sensory organs

Using immunohistochemical labeling against acetylated a‐tubulin and serotonin in combination with confocal laser scanning microscopy and 3D‐reconstruction, we investigated the temporary freshwater pond inhabitant Branchinella sp. (Crustacea: Branchiopoda: Anostraca) for the first time to provide detailed data on the development of the anostracan nervous system. Protocerebral sense organs such as the nauplius eye and frontal filament organs are present as early as the hatching stage L0. In the postnaupliar region, two terminal pioneer neurons grow from posterior to anterior to connect the mandibular neuromeres. The first protocerebral neuropil to emerge is not part of the central complex but represents the median neuropil, and begins to develop from L0+ onwards. In stage L3, the first evidence of developing compound eyes is visible. This is followed by the formation of the visual neuropils and the neuropils of the central complex in the protocerebrum. From the deutocerebral lobes, the projecting neuron tract proceeds to both sides of the lateral protocerebrum, forming a chiasma just behind the central body. In the postnaupliar region, the peripheral nervous system, commissures and connectives develop along an anterior–posterior gradient after the fasciculation of the terminal pioneer neurons with the mandibular neuromere. The peripheral nervous system in the thoracic segments consists of two longitudinal neurite bundles on each side which connect the intersegmental nerves, together with the ventral nervous system forming an orthogon‐like network. Here, we discuss, among other things, the evidence of a fourth nauplius eye nerve and decussating projecting neuron tract found in Branchinella sp., and provide arguments to support our view that the crustacean frontal filament (organ) and onychophoran primary antenna are homologous. J. Morphol. 277:1423–1446, 2016. © 2016 Wiley Periodicals, Inc.     

The formation of the nervous system during larval development in Triops cancriformis (Bosc) (crustacea,Branchiopoda): An immunohistochemical survey

We provide data of the development of thenervous system during the first five larval stages of Triops cancriformis. We use immunohistochemical labeling (against acetylated α‐tubulin, serotonin, histamine, and FMRFamide), confocal laser scanning microscopy analysis, and 3D‐reconstruction. The development of the nervous system corresponds with the general anamorphic development in T. cancriformis. In larval stage I (L I), all brain parts (proto‐, deuto‐, and tritocerebrum), the circumoral connectives, and the mandibular neuromere are already present. Also, the frontal filaments and the developing nauplius eye are already present. However, until stage L III, the nauplius eye only consists of three cups. Throughout larval development, the protocerebral network differentiates into distinct subdivisions. In the postnaupliar region, additional neuromeres and their commissures emerge in an anteroposterior gradient. The larval nervous system in L V consists of a differentiated protocerebrum including a central body, a nauplius eye comprising four cups, a circumoral nerve ring, mandibular‐ and postnaupliar neuromeres up to the seventh thoracic segment, each featuring an anterior and a posterior commissure, and two parallel connectives. The presence of a protocerebral bridge is questionable. The distribution of neurotransmitters in L I is restricted to the naupliar nervous system. Over the course of the five stages of development, neurotransmitter distribution also follows an anteroposterior gradient. Each neuromere is equipped with two ganglia innervating the locomotional appendages and possesses a specific neurotransmitter distribution pattern. We suggest a correlation between neurotransmitter expression and locomotion. J. Morphol., 2010. © 2010 Wiley‐Liss, Inc.     

Effect of procercoids of Triaenophorus nodulosus on the biology of their 1st imtermediate hosts Cyclops strenuus]

The effect of procercoids of T. nodulosus on the periods of metamorphosis, fecundity, survival and the capacity to infect C. strenuus at all copepodid stages (I-V) was studied experimentally. It has been first shown that early copepodid stages (I-III) can be easily infected and serve as first intermediate hosts of T. nodulosus. Under the effect of the parasite the metamorphosis periods of the I and 2-nd copepodid stages increase considerably even at the low infection intensity while at the IV and V copepodid stages--only at the high infection intensity. If the infection takes place at the IV copepodid stage the female fecundity decreases even at a high infection intensity. The life span of infected and noninfected cyclops coincides. At early developmental stages the relations in the system "T. nodulosus-C. strenuus" manifest themselves in different ways and result in the breach of the important biological function of the host.     

First descriptions of copepodid stages, sexual dimorphism and intraspecific variability of Mesocletodes Sars, 1909 (Copepoda, Harpacticoida, Argestidae), including the description of a new species with broad abyssal distribution

Mesocletodes Sars, 1909a encompasses 37 species to date. Initial evidence on intraspecific variability and sexual dimorphism has been verified for 77 specimens of Mesocletodes elmari sp. n. from various deep-sea regions, and ontogenetic development has been traced for the first time. Apomorphies are a strong spinule-like pinna on the mx seta that is fused to the basis, P2-P4 exp3 proximal outer seta lost, P1-P4 enp2 extremely elongated, furcal rami elongated, female body of prickly appearance, female P2-P4 enp2 proximal inner seta lost. Intraspecific variability involves spinulation, ornamentation and size of the body and setation and spinulation of pereiopods. Sexually dimorphic modifications of adult females include prickly appearance of the body, P1 enp exceeds exp in length, P1 coxa externally broadened, seta of basis arising from prominent protrusion, hyaline frills of body somites ornate. Sexual dimorphism in adult males is expressed in smaller body size, haplocer A1, 2 inner setae on P2-P4 enp2 and on P5 exp, P5 basendopodal lobe with 2 setae. Some modifications allow sexing of copepodid stages. The female A1 is fully developed in CV, the male A1 undergoes extensive modifications at the last molt. P1-P4 are fully developed in CV. Mesocletodes faroerensis and Mesocletodes thielei lack apomorphies of Mesocletodes and are excluded.     

Motion behavior of nauplii and early copepodid stages of marine planktonic copepods

The goal of this study was to quantify periods of activity andvelocities of late naupliar and early copepodid stages of planktoniccopepods occurring regularly on the southeastern continentalshelf of the USA. We obtained quantitative information on eightspecies, including adult females of Oithona plumifera. All studieswere conducted at food concentrations near or above satiationlevels. Activities ranged from 0.85% (adult females of O.plumifera)to 100% of time (nauplii and copepodids of various calanoidspecies). Motion velocities (excluding escape motion) coveredmore than one order of magnitude: from 0.39 mm s^–1 fornauplii of Temora stylifera to 5.24 mm s^–1 for naupliiof Oncaea mediterranea. Ranges of activities of species rangefrom occasional for early juveniles to adult females of O.plumiferato 100% for the same range of T.stylifera, the latter creatinga feeding current from N III onwards, the former not at all.Of notable interest is Centropages velificatus which moves intermittentlyas a late nauplius, continuously as an early copepodid and intermittentlyas an adult. All observed calanoid late nauplii and copepodidsmove in three dimensions, excluding copepodids of the shelfbreak/oceanicParacalanus aculeatus. The results indicate not only significantdifferences in motion behavior between cyclopoids and calanoids,but also between calanoid species. Yet, some calanoid speciesshow little ontogenetic changes at all.     

Spatial distribution patterns of trees at different life stages in a warm temperate forest

We have investigated tree distributions in relation to topography between different tree life history stages, from the seed-dispersal stage to the adult stage in a warm temperate evergreen broadleaved forest on Yakushima Island, Japan, to clarify the critical stages in determining adult tree distributions. We conducted a census of all living trees > or =30 cm tall and collected seed falls over three years using 25 seed traps in a 50 m x 50 m quadrat. Four life stages were defined: stage 1, dispersed seed; stage 2, individuals taller than 30 cm and diameter at breast height (DBH) < 1 cm; stage 3, trunks 1 cm < or = DBH < 10 cm; stage 4, trunks with DBH > or = 10 cm. We classified 17 common tree species into three groups; group A was distributed mainly on the upper slope, group B on the lower slope, and group C on both. Most of group A and B trees at stages 2-4 showed an aggregated distribution along the topographical gradient. The densities at stage 1 showed weaker aggregations according to slope. Topography-specific tree distribution was probably determined at the regeneration stage, and later survival was less effective as a mechanism of vegetation differentiation.     

Cell lineage,axis formation,and the origin of germ layers in the amphipod crustacean Orchestia cavimana

Embryos of the amphipod crustacean Orchestia cavimana are examined during cleavage, gastrulation, and segmentation by using in vivo labelling. Single blastomeres of the 8- and 16-cell stages were labelled with DiI to trace cell lineages. Early cleavage follows a distinct pattern and the a/p and d/v body axes are already determined at the 4- and 8-cell stages, respectively. In these stages, the germinal rudiment and the naupliar mesoderm can be traced back to a single blastomere each. In addition, the ectoderm and the postnaupliar mesoderm are separated into right and left components. At the16-cell stage, naupliar ectoderm is divided from the postnaupliar ectoderm, and extraembryonic lineages are separated from postnaupliar mesoderm and endoderm. From our investigation, it is evident that the cleavage pattern and cell lineage of Orchestia cavimana are not of the spiral type. Furthermore, the results of the labelling show many differences to cleavage patterns and cell lineages in other crustaceans, in particular, other Malacostraca. The cleavage and cell lineage patterns of the amphipod Orchestia are certainly derived within Malacostraca, whose ancestral cleavage mode was most likely of the superficial type. On the other hand, Orchestia exhibits a stereotyped cell division pattern during formation and differentiation of the germ band that is typical for malacostracans. Hence, a derived (apomorphic) early cleavage pattern is the ontogenetic basis for an evolutionarily older cell division pattern of advanced developmental stages. O. cavimana offers the possibility to trace the lineages and the fates of cells from early developmental stages up to the formation of segmental structures, including neurogenesis at a level of resolution that is not matched by any other arthropod system.     

Morphology and distribution of antennal sensilla of the tarnished plant bug,Lygus lineolaris (Palisot de beauvois) (Hemiptera: Miridae)

Sensilla on the antennae of adult and last-instar nymphs of the tarnished plant bug, Lygus lineolaris (Hemiptera: Miridae), were examined with light, scanning and transmission electron microscopy. Six different types were identified in adult females and males and 5 types in last-instar nymphs: types 1 and 4 are sensilla trichodea, 2 and 3 are sensilla chaetica, and 5 and 6 are sensilla basiconica. Type 1 are located at distal region of terminal segment and type 2 are located at distal regions of proximal 3 segments in both adults and nymphs. Type 3 is present on all segments, more numerous on scape and pedicel and less abundant on distal third and fourth segments in both adult and nymphal stages. Types 4 and 6 are absent on the scape and present on the distal 3 antennal segments in adults, but they are present only on the distal-most antennal segment in nymphs. Type 5 sensilla are present only on second antennal segments in adults and are absent in nymphs. Sexual dimorphism is observed in total numbers: there are significantly more type(s) 3, 4, 5 and 6 sensilla in adult males than adult females. Types 1, 4 and 5 are multiporous with thin cuticle, branched dendrites and pore tubules which suggests an olfactory function. These sensilla have 3, 3 and 2 neurons, respectively. The type 6 sensillum has an apical pore and pores in the cuticular wall, and is innervated by 5 nerve cells with unbranched dendrites. Sensillar types 2 and 3 have thick cuticle, a single apical pore and nerve cells with unbranched dendrites. Type 2 has 1 neuron and type 3 has 2 chambers and 2 nerve cells.     

The scaling and structure of aquatic animal wakes

Animal generated water movements are visualized and quantifiedusing two-dimensional particle image velocimetry (PIV). Theresulting vector flow fields allow for the study of the distributionof velocity, vorticity and vortices. Structural and temporalaspects of animal-induced flows covering a range of Reynolds(Re) numbers between less than 1 to more than 10⁴ are presented. Maps of flow induced by continuous foraging and intermittentescape responses of tethered nauplius and copepodid stages ofthe marine copepod Temora longicornis offer insight in viscosity-dominatedflow regimes. Fast escape responses of the equally sized largestnauplius stage and the smallest copepodid stage are compared.The nauplius moves by generating a viscous flow pattern withhigh velocities and vorticity; the copepodid moves by usinginertial effects to produce a vortex ring with a rearward jetthrough the center. Larvae and small adult fish (zebra danio) use a burst-and-coast-swimmingmode at Re numbers up to 6,000, shedding a vortex ring withthe associated jet at the tail during the burst phase. Flowpatterns during the coasting phase differ between the smalllarvae and larger adults due to the changes in importance ofviscosity. A 12 cm long mullet swimming in a continuous mode generatesa chain of vortex rings with a backward undulating jet throughthe centers of the rings at Re numbers of 4 x 10⁴ in inertia-dominatedregimes. Our empirical results provide realistic insight in the scaleeffects determining the morphology of the interactions betweenanimals and water.     

Ontogenetic niches of a planktonic copepod in Lake Biwa studied on a fine temporal scale

Eodiaptomus japonicus was collected in the north basin of Lake Biwa, Japan, on six dates from 11 to 25 June 1987. Temporal changes in its vertical distribution and reproduction indices were small, but those in its abundance were large. Mortality was high in the naupliar stage I and from copepodid stage III to adult stage. The latter fact and low proportion of females in adulthood suggest heavy predation by fishes which prefer larger prey.Eodiaptomus japonicus showed ontogenetic vertical migration within the epilimnion. The direction of the migration was upward in the early naupliar stages and downward in the late naupliar and early copepodid stages. Both migrations resulted in raising mortality in the corresponding or succeeding stages, probably expressing the behavioral constraints ofE. japonicus.     

MORPHOGENESIS OF THE RETINAL RODS : AN ELECTRON MICROSCOPE STUDY

The morphogenesis of the retinal rods has been studied with the electron microscope in white mice from birth up to the 16th day of age. Observations have been mainly concentrated on specimens of the 8th and 12th days and on the differentiation of the inner and outer segments of the retinal rods. In the morphogenesis of the outer segment three main stages have been considered. The first stage consists in the development of a primitive cilium projecting from a bulge of protoplasm which constitutes the primordium of the inner segment. A basal body, nine pairs of peripheral filaments, a surface membrane, and a matrix filled with a fine vesicular material have been recognized as components of the primitive cilium. The vesicles are called "morphogenetic material" because it is believed that they represent the macromolecular primordium of the rod sacs of the future outer segment. The second stage corresponds to the great enlargment of the apical region of the primitive cilium due to the rapid building up of the lamellar material of the rod sacs. The primitive rod sacs appear to be connected with the ciliary filaments. The basal portion of the primitive cilium remains undifferentiated and constitutes the connecting cilium of the adult rod (1). The third stage consists in the remodelling and reorientation of the rod sacs into their permanent transverse disposition. This process starts in the middle portion of the outer segments and proceeds towards both extremities which can be considered as zones of growth of the outer segment. The inner segment is at the beginning a bulge of protoplasm containing unoriented mitochondria, a basal body, a small Golgi zone, and numerous dense particles. Then this region becomes elongated and the different components assume the stratified disposition found in the adult (1). The demonstration that the entire outer segment of the rod cell is the result of the differentiation of a primitive cilium is discussed in view of the conflicting interpretations found in the literature. The possible macromolecular mechanisms that may be involved in the submicroscopic morphogenesis of the rod sacs are discussed and the possible role of the morphogenetic material is considered. The results described in this paper confirm and extend the interpretation of the submicroscopic morphology of the adult rod cell as presented in a previous paper (1).     

Testing the phylogenetic position of Cambrian pancrustacean larval fossils by coding ontogenetic stages

The study of ontogeny as an integral part of understanding the pattern of evolution dates back over 200 years, but only recently have ontogenetic data been explicitly incorporated into phylogenetic analyses. Pancrustaceans undergo radical ontogenetic changes. The spectacular upper Cambrian “Orsten” fauna preserves phosphatized fossil larvae, including putative crown‐group pancrustaceans with amazingly complete developmental sequences. The putative presence and nature of adult stages remains a source of debate, causing spurious placements in a traditional morphological analysis. We introduce a new coding method where each semaphoront (discrete larval or adult stage) is considered an operational taxonomic unit. This avoids a priori assumptions of heterochrony. Characters and their states are defined to identify changes in morphology throughout ontogeny. Phylogenetic analyses of semaphoronts produced possible relationships of each Orsten fossil to the crown‐group clade expected from morphology shared with extant larvae. Bredocaris is a member of the stem lineage of Thecostraca or (Thecostraca + Copepoda), and Yicaris and Rehbachiella are probably members of the stem lineage of Cephalocarida. These placements rely directly on comparisons between extant and fossil larval character states. The position of Phosphatocopina remains unresolved. This method may have broader applications to other phylogenetic problems which may rely on ontogenetically variable homology statements.