Structure of Adnate Colony Portions in Crisiidae (Bryozoa Cyclostomata)

The “rhizoidsrdquo; surrounding the base of the erect “colony” emanating from the ancestrula in the Crisiidae, especially the simple species Crisidia cornuta (L.), are a regular adnate system of autozooids. Each autozooid is composed of a proximal adnate part and a distal peristome (in some species kenozooids are possibly intercalated). The autozooid peristomes support erect branches identical in budding and structure with the branch emanating from the erect peristome of the ancestrula. Thus, the complete crisiid colony consists of an adnate system of ancestrula and autozooids, which form erect branches from their peristomes. The adnate zooid system is comparable in autozooid morphology and budding pattern with simple uniserial stomatoporids. The tentative hypothesis is proposed that the crisiid group has developed from primitive stomatoporids; the adnate zooid system of the stomatoporids apparently evolved peristomial budding to produce the erect colony branches characteristic of crisiids.     

Functional differentiation in bryozoan colonies: a proteomic analysis

Bryozoans are typical modular organisms. They consist of repetitive structural units, the zooids. Bryozoan colonies grow by zooidal budding, with the distribution pattern of the budding loci underlying the diversity of colony forms. Budding is usually restricted to the colony periphery, where a “growing edge” or local terminal growth zones are formed. Non-budding parts of the colony can be functionally subdivided, too. In many species colonies consist of regular, often repetitive zones of feeding and non-feeding modules, associated with a periodical degeneration and regeneration of the polypide retractile tentacle crown with a gut and the accompanying musculature. The mechanisms of functional differentiation in bryozoan colonies are unknown. Presumably, budding and/or polypide recycling are induced or inhibited by certain determinants of functional specialization in different colony parts. An effective tool of their identification is the comparison of proteomes in functionally different zones. Here we report the results of proteomic analysis of three bryozoan species from the White Sea with a different colony form: Flustrellidra hispida, Terminoflustra membranaceotruncata and Securiflustra securifrons. Using differential two-dimensional electrophoresis (2D-DIGE), we compared proteomes of the growing edge, the zone with polypides and the zone without polypides. We assessed the general level of differences between the zones and revealed proteins whose relative abundance changed gradually along the proximal-distal colony axis. These proteins might be involved in the determination of the functional differentiation of the colony.     

Colony Structure in Flustra foliacea (Linnaeus) (Bryozoa,Chéilostomata)

Encrusting forms presumably represent the original mode of growth in the bryozoans. They usually exhibit a relatively low degree of colony integration. The numerous different erect colony types, certainly independently derived from this stage, show a higher degree of integration. Eventually forms arise with a strict pattern only little influenced by the environment. The Flustra foliacea colony holds an intermediate position in this respect. It forms an initial crust on a foreign substratum such as rock. The crust forms marginal lobes. The lobes collide two and two. The two components of each collision then rise back to back, owing to lack of space, into bilaminar fronds. The two zooid layers composing these erect branches and mutually encrusting the “auto-substratum” of their respective basal walls, grow much more rapidly than the initial crust on the “heterosubstratum” of the rock to finally comprise more than 95 % of the colony volume. The different rate of growth on “auto-” and “heterosubstratum” respectively is interpreted as indicating a preference for the “autosubstratum” and as the main force in the formation of erect branches. The Fl. foliacea case indicates one of the pathways from encrusting to erect colonies in the bryozoans. It is probably valid for at least some of the erect bilaminar colonies appearing in different parts of the bryozoan system.     

Flow and polypide distribution in the cheilostome bryozoan Bugula and their inference in Archimedes

Cilia-generated flow in the absence of ambient current is directed from frontal to reverse sides of branches in Bugula turrita, B. turbinata, B. neritina , and B. stolonifera , whether axes of feeding lophophores are perpendicular to the basal plane of branches or are tilted toward distal ends of branches. Ambient current less than 5 cm per second interacts with cilia-generated flow, but ambient flow of 15 cm per second destroys self-generated colonial flow and severely hampers feeding. Polypides are located in the more distal, younger portions of colonies, in species with and without polypide recycling, whereas zooids in the more proximal, older portions are senesced. Presence of feeding polypides in distal but not in proximal portions of the larger spiralled colonies of B. turrita and B. turbinata results in downward, slightly radially directed flow through the colony. The colonial flow passes directly from one whorl to the next-proximal so that water exits from low around the colony perimeter, and a proximally expanding conical stagnant zone occupies the interior of the colony. A substantial percentage of zooecia in distal whorls of well-preserved Archimedes is filled by sediment and inferred to have been occupied by actively feeding polypides. whereas spar-filled zooecia capped by terminal diaphragms were apparently senesced during the latter part of a colony's existence. The capped zooecia constitute an increasing percentage of the total in more proximal whorls. Generally similar colony form and inferred similarity in distribution of current-generating polypides in spiralled colonies of Bugula and in Archimedes suggest that colony-generated flow in Archimedes was similar to that in Bugula , passing downward and then outward, and only through the distal whorls of the colonies.     

A proposed reclassification of Bryum,Anomobryum and Brachymenium (Musci,Bryaceae)

Abstract

The traditional generic classification in the Bryoideae (Bryaceae) is based primarily on details of the sporophyte, particularly peristome reduction and capsule inclination. Recent research, however, has suggested that closely related species in Anomobryum can have very distinct capsules, varying from complete peristomes and inclined capsules to reduced peristomes and erect capsules. The suggestion is made here that sporophyte features, especially those related to peristome features, may obscure phylogenetic relationships. A revised classification is proposed, based on analyses of 100 species of Bryum, Anomobryum, and Brachymenium and sixteen sporophytic and gametophytic characters. The revised classification groups species with similar gametophores but is supported by at least some sporophytic characters. Analysis of variance and principal components analysis indicate that both the traditional and revised classification provide effective summaries of the variation within the 100 species examined. The new classification consists of three informal groups of species which can be recognized at generic rank. One comprises Bryum species, including those with reduced peristomes and inclined capsules. A second comprises all species of Anomobryum, as well as species of Bryum and Brachymenium with similar gametophores. The third group consists of the rosulate species of Bryum and Brachymenium. Phylogenetically, the second group may be more closely related to Pohlia than to the species in the first and third groups. The third group appears to be most closely related to Rhodobryum and Plagiomnium. Suggested names are provided for groups one and three, while the name Bryum is retained for group two. No nomenclatural changes are made, however, until more research is done.     

Hoeverella krauseae gen. et sp. nov., an unusual uniserial cheilostome bryozoan from the campanian of hannover

Hoeverellakrauseae gen. et sp. nov. is a peculiar runner-like anascan cheilostome bryozoan known from a single well-preserved specimen encrusting a belemnite guard. The colony comprises about 60 zooids, each of fusiform/pyriform shape and having a small “opesia” within which is situated an enigmatic ring structure. Several interpretations are possible for the ring structure: “regeneration”, closure plate, foreign organism inhabiting the zooecium, or socket of articulation for an erect branch or anAetea- like erect distal tube. Unusually for a runner-like bryozoan only one branch ramification occurs in the entire colony. The systematic position ofHoeverella is uncertain; however, it may be related to the electrid genusHerpetopora.     

HYBRIDIZATION AND CRYPTIC SPECIES IN DICAMPTODON (CAUDATA: DICAMPTODONTIDAE)

The salamander genus Dicamptodon consists of at least four genetically divergent groups of populations with 10–19 fixed allelic differences (out of 31 loci scored) between populations in alternative groups. One of these groups corresponds to D. copei; the other three until now usually have been considered to belong to the single morphologically homogeneous species D. ensatus. Two instances of geographic contact between genetic units occur in the genus, one between D. copei and “D. ensatus” in northern Oregon and the other between two highly divergent types of “D. ensatus” in coastal northern Calfornia. In the former case no hybridization occurs, while in the latter a narrow hybrid zone has been observed. There appears to be selection against hybrids within this hybrid zone, and introgression beyond the zone is apparently nonexistent. The population groups therefore appear to be genetically independent units, and Dicamptodon is best considered to consist of four species: D. copei, D. ensatus, D. tenebrosus, and D. aterrimus.     

Multizooidal Budding in Parasmittina trispinosa (Johnston) (Bryozoa,Cheilostomata)

Two principally different wall types occur in the bryozoan colony: Exterior walls delimiting the super-individual, the colony, against its surroundings and interior walls dividing the body cavity of the colony thus defined into units which develop into sub-individuals, the zooids. In the gymnolaemate bryozoans generally, whether uniserial or multiserial, the longitudinal zooid walls are exterior, the transverse (proximal and distal) zooid walls interior ones. The radiating zooid rows grow apically to form “tubes” each surrounded by exterior walls but subdivided by interior (transverse) walls. The stenolaemate bryozoans show a contrasting mode of growth in which the colony swells in the distal direction to form one confluent cavity surrounded by an exterior wall but internally subdivided into zooids by interior walls. In the otherwise typical gymnolaemate Parasmittina trispinosa the growing edge is composed of a series of “giant buds” each surrounded by exterior walls on its lateral, frontal, basal and distal sides and forming an undifferentiated chamber usually 2–3 times as broad and 3 or more times as long as the final zooid. Its lumen is subdivided by interior walls into zooids 2–3, occasionally 4, in breadth. This type of zooid formation is therefore similar to the “common bud” or, better-named, “multizooidal budding” characteristic of the stenoleamates but has certainly evolved independently as a special modification of the usual gymnolaemate budding.     

ARCHITECTURE AND CROWN GEOMETRY IN TABEBUIA ROSEA (BIGNONIACEAE)

In the tropical tree Tabebuia rosea, seedlings form an erect unbranched stem with rhythmic growth. Three distinct and predictable geometrical stages are then recognized in crown development. Sympodial branching begins with the arrest of the terminal bud of the trunk and symmetric outgrowth of a pair of subtending lateral buds. During an intermediate phase, branching becomes asymmetric at about Order 5. At each sympodial bifurcation there is differentiation between vigorous, relatively straight main branches (leaders) and less vigorous laterals forming regular pseudomonopodial branch complexes, which collectively constitute the cup-shaped crown. Finally, dormant lateral buds in the lowest bifurcation of the trunk are released and reiterate the original crown form. Ultimately an erect, apparently monopodial tree is formed by a set of superimposed cup-shaped crowns. Crown development of Tabebuia is unique because it involves predictable ontogenic changes in branching patterns. Crowns of open-grown Tabebuia consist of relatively few, wide branch tiers, crowns of forest grown trees are tall and narrow. Analysis of the adaptive geometry of wide vs. narrow crowns through computer simulation illustrates the precise cost of mechanical support for terminal leaf rosettes at successive developmental phases and suggests that tall, erect, narrow, and multi-tiered crowns are more efficient than wide open crowns.     

MORPHOLOGY AND MOLECULAR PHYLOGENY OF AUREOPHYCUS ALEUTICUS GEN. ET SP. NOV. (LAMINARIALES,PHAEOPHYCEAE) FROM THE ALEUTIAN ISLANDS1

A previously unknown species of kelp was collected on Kagamil Island, Aleutian Islands. The species can be easily distinguished from any known laminarialean alga: the erect sporophytic thallus is composed of a thin lanceolate blade attaining ～2 m in height and ～0.50 m in width, without midrib, and the edge of the blade at the transition zone is thickened to form a V‐shape; the stipe is solid and flattened, slightly translucent, attaining ～1 m in length; the holdfast is semidiscoidal and up to 0.15 m in diameter. Anatomically, the blade has the typical trumpet‐shaped hyphae characteristic of the Chordaceae and derived foliose laminarialean species (i.e., Alariaceae/Laminariaceae/Lessoniaceae). No hair pits or mucilaginous structures were observed on the blade or stipe. No fertile sporophytes were collected, but abundant juvenile sporophytes were observed in the field. In the molecular phylogenetic analyses using chloroplast rbcL gene, nuclear ITS1‐5.8S‐ITS2 rDNA, and mitochondria nad6 DNA sequences, the new species (Aureophycus aleuticus gen. et sp. nov.) showed a closer relationship with Alariaceae of conventional taxonomy, or the “Group 1” clade of Lane et al. (2006) including Alaria and related taxa than with other groups, although the species was not clearly included in the group. Aureophycus may be a key species in elucidating the evolution of the Alariaceae within the Laminariales. Because of the lack of information on reproductive organs and insufficient resolution of the molecular analyses, we refrain from assigning the new species to a family, but we place the new species in a new genus in the Laminariales.     

ECOLOGICAL GENETICS OF A MOSAIC HYBRID ZONE: MITOCHONDRIAL,NUCLEAR, AND REPRODUCTIVE DIFFERENTIATION OF CRICKETS BY SOIL TYPE

We investigated the effects that habitat variation has on the structure and dynamics of a hybrid zone between two closely related crickets in Connecticut. A collecting protocol was developed in which crickets were sampled from characteristic habitats on either side of the hybrid zone and from two distinct habitat types within the zone. Presumptive pure Gryllus pennsylvanicus were sampled from fields in northwestern Connecticut and represent “inland” populations. “Pure” Gryllus firmus were sampled from beaches along the coast and represent the “coastal” populations. Crickets from within the hybrid zone were sampled from two different soil types: the “loam” populations from loamy soils and the “sand” populations from sandy soils. Moreover, an attempt was made to identify closely adjacent sand and loam localities to determine the scale of habitat variation and its possible effects on hybrid-zone structure. In general, there was little variation in morphological traits or in allozyme and mtDNA genotype frequencies among localities from within each of the four habitat types. Between each of the closely situated sand and loam localities within the hybrid zone, however, there were very significant differences in each of these sets of markers. In addition, crickets from hybrid-zone populations were tested for reproductive isolation. The asymmetric outcome of hybrid crosses that exists across the zone (Harrison, 1983) also exists on a finer ecological scale within the zone. Thus, this hybrid zone is a mosaic of strikingly differentiated populations. The dynamics of hybrid zones with mosaic structures are discussed in contrast to the traditional clinal models. The data are also discussed in light of the semipermeable nature of species boundaries. The extent to which a species boundary is permeable varies not only from one genetic marker to the next, but also with the ecological and geographic context of species interaction.     

Verosphacela silvae sp. nov. (Onslowiaceae, Phaeophyceae) from the Mediterranean Sea

We describe Verosphacela silvae sp. nov., from the Mediterranean Sea. It consists of horizontal filaments living on the lower face of the red alga Peyssonnelia rubra (Greville) J. Agardh, from which erect filaments up to 1.5 mm high rise and grow upright after passing through the thallus of the supporting species. There are both horizontal and erect filaments growing by apical cells. In the subapical cells, 1–2 longitudinal divisions occur (more frequently in the erect filaments) but no secondary transverse divisions occur. Erect filaments bear lateral propagules on a stalk of one to three (rarely more) cells. Propagules, with neither apical cells nor arms, consist of seven cells. Zoidangia are borne at the apex of erect laterals. The new species differs from V. ebrachia Henry mainly in habit, propagules and zoidangia. In addition, distinct from V. ebrachia, filaments of V. silvae never penetrate between the cuticle and the cell wall of the supporting alga. Moreover, propagules of V. silvae consist of seven cells, whereas those of V. ebrachia consist of 9–13 cells, and zoidangia are terminal on laterals in V. silvae, whereas in V. ebrachia they are sessile on both axes and laterals.     

Geminivirus transmission and biological characterisation of Bemisia tabaci (Gennadius) biotypes from different geographic regions

Eighteen populations of Bemisia tabaci, collected from different geographic locations (North & Central America, the Caribbean, Africa, the Middle East, Asia and Europe), were studied to identify and compare biological and genetic characteristics that can be used to differentiate biotypes. The morphology of the fourth instar/pupal stage and compound eye structures of adults were investigated using scanning electron microscopy and found to be typical of the species among all biotypes and populations studied. Setae and spines of B. tabaci larval scales from the same colony were highly variable depending on the host plant species or leaf surface characteristics. The location and the morphology of caudal setae, characteristic of all B. tabaci studied to date, were present in all colonies. However, differences in adult body lengths and in the ability to induce phy to toxic disorders in certain plant species were found between biotypes or populations. The recently identified “B” biotype, characterised by a diagnostic esterase banding pattern and by its ability to induce phytotoxic responses in squash, honeysuckle and nightshade was readily distinguished from non-“B” biotype populations. None of the non-“B” biotypes studied, were found to induce phytotoxic responses. Nine populations examined showed typical “B” biotype characteristics, regardless of country of origin. All tested populations, determined as “B” or “B”-like biotypes successfully mated with other “B” biotype colonies from different geographic areas. Non-“B” biotype colonies did not interbreed with other biotypes. The B. tabaci populations were tested for their ability to transmit 15 whitefly-transmitted geminiviruses (WTGs) from different geographic areas with a wide range of symptom types. All WTGs were transmitted by the “B” biotype colonies and by most non-“B” biotype colonies, with the exception of three viruses found in ornamental plants which were non-transmissible by any colony. Some non-“B” biotypes would not transmit certain geminiviruses and some geminiviruses were more efficiently transmitted than were others.     

Phylogenetic inference and peristome evolution in haplolepideous mosses,focusing on Pseudoditrichaceae and Ditrichaceae s. l.

Pseudoditrichum mirabile, the only species of Pseudoditrichaceae, has been known for a long time from a single collection from the Canadian Arctic. Its systematic position remained enigmatic due to similarity in gametophyte structure with Ditrichaceae, a family that has simple peristomes, whereas the peristome in Pseudoditrichum is double. Due to this difference, Pseudoditrichum was classified in either Funariales or Bryales. A recent discovery of this species in the Anabar Plateau in northern Siberia has allowed its phylogenetic position to be tested based on plastid rps4 and rbcL and mitochondrial nad5 sequences. The results of this research reject the earlier hypotheses. Instead, the molecular analysis resolves Pseudoditrichum in a clade with Chrysoblastella chilensis (formerly Ditrichaceae) in the haplolepideous lineage. The peristome of Pseudoditrichum is of a previously unknown type with a fully developed exostome and hyaline endostome elements opposite the exostome teeth, based not on the 4:2:4 peristomial formula, but on 4:2:3. Double peristomes of the same type, albeit rather strongly reduced, occur in Catoscopium, Chrysoblastella, Distichium and Ditrichum flexicaule. The polyphyly of Ditrichaceae is confirmed by molecular phylogenetic analysis, and Ditrichum flexicaule and D. gracile are segregated into the new genus Flexitrichum and family Flexitrichaceae. An independent status of the recently resurrected family Distichiaceae is supported, and segregation of Chrysoblastella and Saelania into new monospecific families is proposed.     

Schischcatella (Fenestrata,Bryozoa) from the Devonian of the Rhenish Massif,Germany

Abstract: The Devonian fenestrate bryozoan, Schischcatella Waschurova, 1964 , possessed colonies in the form of low, erect bifoliate fronds that grew from an encrusting sheet‐like base with autozooecia arranged in biserial, bifurcating rows. This growth habit is unique in fenestrates, which normally had unilaminate arborescent colonies. Originally, Schischcatella was described from the Lower Devonian of Tajikistan. This article describes a new species, S. heinorum sp. nov., from the Middle Devonian of the Eifel (western Rhenish Massif, Germany) with additional material from the Lower Devonian of the Kellerwald (eastern Rhenish Massif, Germany). External and internal morphologies of this bryozoan have been studied using abundant material. The growth habit of Schischcatella suggests a completely different pattern of feeding currents than that in the normal fenestrate colony. The outflow of the filtered water occurred only on edges of colonies between rami. In the absence of chimneys (areas of vertical water expelling), such a functional morphology may have restricted extension of the colony in a distal direction. The evolution of Schischcatella is apparently an example of paedomorphosis, the genus evolved from an unknown semicosciniid species by the early ontogenetic interruption of colony development and further changes in the mode of growth.     

Friend or foe? Differential aggression towards neighbors and strangers in the ant Liometopum microcephalum (Hymenoptera: Formicidae)

Intra- and interspecific aggression is quite common in ants, from occasional conflicts to large-scale territorial disputes. The “nasty neighbor” phenomenon describes the differential aggressive treatment of neighbors versus foreign intruders. Due to the fact that workers of a given colony meet rival neighbors more often at food resources, they treat them as threats to their colony. The reverse can also happen: the “dear enemy” effect arises when an already known rival is treated less aggressively due to accommodation, than an unknown distant one. In the current study, we analyzed the effect of distance on the aggressiveness of Liometopum microcephalum, a territorial arboricolous ant, towards non-nestmates in two large populations. Our results show that aggression did not increase with distance, but it was higher among neighbors than among workers coming from distant nests. The results of the study are consistent with the nasty neighbor scenario, and do not support the hypothesis that the studied populations would be polydomous systems of interconnected nests.     

Cngsc, a homologue of goosecoid, participates in the patterning of the head, and is expressed in the organizer region of Hydra.

We have isolated Cngsc, a hydra homologue of goosecoid gene. The homeodomain of Cngsc is identical to the vertebrate (65-72%) and Drosophila (70%) orthologues. When injected into the ventral side of an early Xenopus embryo, Cngsc induces a partial secondary axis. During head formation, Cngsc expression appears prior to, and directly above, the zone where the tentacles will emerge, but is not observed nearby when the single apical tentacle is formed. This observation indicates that the expression of the gene is not necessary for the formation of a tentacle per se. Rather, it may be involved in defining the border between the hypostome and the tentacle zone. When Cngsc(+) tip of an early bud is grafted into the body column, it induces a secondary axis, while the adjacent Cngsc(-) region has much weaker inductive capacities. Thus, Cngsc is expressed in a tissue that acts as an organizer. Cngsc is also expressed in the sensory neurons of the tip of the hypostome and in the epithelial endodermal cells of the upper part of the body column. The plausible roles of Cngsc in organizer function, head formation and anterior neuron differentiation are similar to roles goosecoid plays in vertebrates and Drosophila. It suggests widespread evolutionary conservation of the function of the gene.     

Ontogeny of the fused tentacles in three species of ommastrephid squids (Cephalopoda, Ommastrephidae)

Abstract. The tentacles of ommastrephid squids fuse during embryonic development and remain fused as they grow through hatching, but eventually separate to become two fully functional adult tentacles. The external anatomy of individuals at several post‐hatching ontogenetic stages of three species of ommastrephid squids (Ommastrephes bartramii, Sthenoteuthis oualaniensis, and Hyaloteuthis pelagica) was examined using scanning electron microscopy and morphometrics. The fusion of the transverse muscle mass of the tentacles was examined using light microscopy. Five ontogenetic stages of tentacle separation were defined based on landmark features such as the extent of the fusion and the presence of suckers or sucker buds at the distal tip. The total tentacle length and fused tentacle length reached a maximum when the dorsal mantle length (ML) equaled 3–4 mm (H. pelagica) or 4–6 mm (O. bartramii, S. oualaniensis), and then decreased with increasing ML. The average split length (measured from the base of the tentacles to the point of tentacle fusion) increased gradually with increasing ML, and the separate tentacle diameter was roughly half the diameter of the fused portion at all sizes. In all three species, separation of the fused tentacles began earlier in development (2–3‐mm ML) and was more advanced at smaller sizes than previously reported. The sizes presented here are conservative because excess epithelium at the location of the split may disguise the actual site of separation. Post‐separation tentacles were much shorter than the arms, and the carpal region appeared torn in 2 of the 4 specimens of S. oualaniensis examined. Finally, none of the original distal tip suckers were retained on the post‐separation tentacles of S. oualaniensis. These observations are consistent with the hypothesis that the tentacles separate gradually then rupture at the “wrist” (presumptive carpus), and argue against the possibility of prey capture by the fused tentacles.     

An IQGAP-related gene is activated during tentacle formation in the simple metazoan Hydra

Differentiation of body column epithelial cells into tentacle epithelial cells in Hydra is accompanied by changes in both cell shape and cell-cell contact. The molecular mechanism by which epithelial cells acquire tentacle cell characteristics is unknown. Here we report that expression of a Hydra homologue of the mammalian IQGAP1 protein is strongly upregulated during tentacle formation. Like mammalian IQGAP, Hydra IQGAP1 contains an N-terminal calponin-homology domain, IQ repeats and a conserved C terminus. In adult polyps a high level of Hydra IQGAP1 mRNA is detected at the basis of tentacles. Consistent with a role in tentacle formation, IQGAP1 expression is activated during head regeneration and budding at a time when tentacles are emerging. The observations support the previous hypothesis that IQGAP proteins are involved in cytoskeletal as well as cell-cell contact rearrangements. Received: 25 January 2000 / Accepted: 2 May 2000     

Unexpected hybridization reveals the utility of genetics in native plant restoration

Native plant materials (NPMs) are increasingly utilized during the restoration of disturbed plant communities. Here, we analyze next‐generation genetic sequencing data for Hilaria jamesii, a dominant graminoid across drylands of the southwestern United States, and document that the species' only commercially‐available NPM, “Viva,” is a hybrid between H. jamesii and its sister species, Hilaria mutica. In fact, hybrids between these species are common where they geographically overlap. Furthermore, we show that the “Viva” hybrid has successfully been moved beyond the hybrid zone and into the core range of H. jamesii. The potential ramifications of introducing novel genetic material into H. jamesii are discussed, as well as the utility of genetic analyses to protect species' natural patterns of genetic diversity and help managers make informed decisions regarding the development and deployment of NPMs.