Life history and status of shortnose sturgeon (Acipenser brevirostrum) in the Potomac River

We collected the first life history information on shortnose sturgeon ( Acipenser brevirostrum ) in any of the rivers to Chesapeake Bay, the geographic center of the species range. In the Potomac River, two telemetry-tagged adult females used 124 km of river: a saltwater/freshwater reach at river km (rkm) 63−141 was the foraging−wintering concentration area, and one female migrated to spawn at rkm 187 in Washington, DC. The spawning migration explained the life history context of an adult captured 122 years ago in Washington, DC, supporting the idea that a natal population once lived in the river. Repeated homing migrations to foraging and wintering areas suggested the adults were residents, not transient coastal migrants. All habitats that adults need to complete life history are present in the river. The Potomac River shortnose sturgeon offers a rare opportunity to learn about the natural rebuilding of a sturgeon population.     

Sex differentiation and aspects of gametogenesis in shortnose sturgeon Acipenser brevirostrum Lesueur

Shortnose sturgeon Acipenser brevirostrum gonad samples were collected from industry-reared fish and wild broodstock at various developmental stages to elucidate patterns of gonadal differentiation and maturation. Genital ridges, containing germ cells, were present in 26 day-old fish and distinct gonads were present by day 54. Sturgeon gonads are known to consist of two tissue types (adipose and gametogenic) and both were present at 72 day. Anatomical differentiation of gonads occurred by 6 months and was advanced by 15 months. Ovaries had distinct lamellae while testes remained non-lamellate. Gonial proliferation had occurred by 15 months, but the cells were not identifiable as spermatogonia or oogonia. Small white 'pinhead' oocytes were macroscopically visible in ovaries as early as 36 months. At 43 months ovaries were clearly organized, with some areas containing only immature oocytes and other containing oocytes apparently developing as cohorts. Individual fish showed considerable variation: the level of development remained unchanged at 84 months in some females, while others showed clear progression towards sexual maturation at 48 months. Sperm cells were present in males as early as 52 months. Advanced development of ovarian follicles was observed only in biopsies of re-conditioned broodstock of wild origin. In the year before spawning, the most advanced oocytes became pigmented, the chorion thickened, the nucleus (germinal vesicle) migrated towards the micropyle complex at the animal pole, and ovulation occurred in May under appropriate environmental conditions.     

Behaviour and performance of juvenile shortnose sturgeon Acipenser brevirostrum at different water velocities

Critical swimming speeds (mean ± s . e .) for juvenile shortnose sturgeon Acipenser brevirostrum were 34·4 cm s⁻¹± 1·7 (2·18 ± 0·09 body lengths, BL s⁻¹). Swimming challenges at 10, 20 and 30 cm s⁻¹ revealed that juvenile A. brevirostrum are relatively poor swimmers, and that the fish did not significantly modify their swimming behaviour, although they spent more time substratum skimming ( i.e. contact with flume floor) at 30 cm s⁻¹ relative to 10 cm s⁻¹. When present, these behavioural responses are probably related to morphological features, such as flattened rostrum, large pectoral fins, flattened body shape and heterocercal tail, and may be important to reduce the costs of swimming.     

Repeat UCrit and endurance swimming in juvenile shortnose sturgeon (Acipenser brevirostrum)

Previous results show that juvenile shortnose sturgeon are steady swimmers and, compared with salmonids, generally have low critical swimming (UCrit) and endurance swimming capacities. Most studies on swimming capacities of sturgeon, and other fishes, include those where fish have only been swum once and the metrics of swimming performance are assessed (e.g., time swum, speed achieved). Under natural conditions, there are ample instances where fish undergo multiple swimming cycles when traversing fish ways, culverts and other sources of fast water flow. While some evidence exists for salmonids, the effects of repeat swimming are not well known for sturgeon. The current study consisted of two experiments. The first examined the UCrit of juvenile shortnose sturgeon following three consecutive swimming trials with a 30 min recovery period between subsequent tests. The second examined the endurance swimming capacities of juvenile shortnose sturgeon following three consecutive swimming trials with a 60 min recovery period between subsequent tests. Our findings indicate that (i) UCrit was consistent (~2 body lengths/s) among swimming trials; (ii) significant individual variation exists between individuals in the endurance swimming trials; and (iii) consistent results exist for individuals across swimming trials in both the UCrit and the endurance swimming tests. These results suggest that juvenile shortnose sturgeon have a high recovery capacity, and their behaviour and morphology likely reflect aspects of their swimming capacities.     

Hematology and plasma chemistry of wild shortnose sturgeon Acipenser brevirostrum from Delaware River,USA

The effects of gender, maturity, intersex condition and annual and seasonal variability were studied on hematology and plasma chemistry of wild shortnose sturgeon Acipenser brevirostrum from the Delaware River. A total of 68 fish were captured by gill net and examined in May‐June, and 61 additional fish were captured and examined in November during 2006–2011. Total leukocyte counts (WBC), leukogram, PCV and the plasmatic concentrations of 13 biochemical analytes were measured from these fish using standard clinical methods. Season and gender had no effect on hematologic indices, but PCV was inversely related to maturity of fish (robust intervals: 27–40% in immature fish, 21–36% in mature fish). Significant annual variation was detected in eosinophil (annual range in robust interval: 0–1176 lower limit, 670–7882 upper limit) and monocyte (0–210 lower limit, 560–1980 upper limit) counts (cells μl^?1). The lower limit of the robust interval varied annually by as much as 6% for sodium and 12% for chloride, while the upper limit of the robust interval varied annually by as much as 8% for sodium and 15% for chloride. Seasonal differences in mean sodium and chloride (6–7% higher in autumn) and proteins (5–13% higher in autumn) may reflect environmentally induced changes in osmoregulation, while aspartate aminotransferase was 38–55% higher in the spring. In females, calcium and total protein were highest in mature fish (robust intervals: 10.5–22.1 mg dl^?1 Ca²⁺, 4.1–6.9 g dl^?1 TP) compared to immature (7.3–16.9 mg dl^?1 Ca²⁺, 2.8–5.2 g dl^?1 TP) and developing fish (7.8–18.9 mg dl^?1 Ca²⁺, 3.2–5.6 g dl^?1 TP), indicating changes associated with vitellogenesis. Glucose was significantly higher in females (robust interval: 23–167 mg dl^?1) than males (35–138 mg dl^?1), possibly indicating gender‐based differences in energetic requirements. Intersex condition was associated with lowered glucose, potassium and creatinine phosphokinase. Reference intervals reported here are useful for evaluating the health and physiological condition of shortnose sturgeon.     

Population genetics of shortnose sturgeon Acipenser brevirostrum based on mitochondrial DNA control region sequences

Shortnose sturgeon is an anadromous North American acipenserid that since 1973 has been designated as federally endangered in US waters. Historically, shortnose sturgeon occurred in as many as 19 rivers from the St. John River, NB, to the St. Johns River, FL, and these populations ranged in census size from 10(1) to 10(4), but little is known of their population structure or levels of gene flow. We used the polymerase chain reaction (PCR) and direct sequence analysis of a 440 bp portion of the mitochondrial DNA (mtDNA) control region to address these issues and to compare haplotype diversity with population size. Twenty-nine mtDNA nucleotide-substitution haplotypes were revealed among 275 specimens from 11 rivers and estuaries. Additionally, mtDNA length variation (6 haplotypes) and heteroplasmy (2-5 haplotypes for some individuals) were found. Significant genetic differentiation (P < 0.05) of mtDNA nucleotide-substitution haplotypes and length-variant haplotypes was observed among populations from all rivers and estuaries surveyed with the exception of the Delaware River and Chesapeake Bay collections. Significant haplotype differentiation was even observed between samples from two rivers (Kennebec and Androscoggin) within the Kennebec River drainage. The absence of haplotype frequency differences between samples from the Delaware River and Chesapeake Bay reflects a probable current absence of spawning within the Chesapeake Bay system and immigration of fish from the adjoining Delaware River. Haplotypic diversity indices ranged between 0.817 and 0.641; no relationship (P > 0.05) was found between haplotype diversity and census size. Gene flow estimates among populations were often low (< 2.0), but were generally higher at the latitudinal extremes of their distribution. A moderate level of haplotype diversity and a high percentage (37.9%) of haplotypes unique to the northern, once-glaciated region suggests that northern populations survived the Pleistocene in a northern refugium. Analysis of molecular variance best supported a five-region hierarchical grouping of populations, but our results indicate that in almost all cases populations of shortnose sturgeon should be managed as separate units.     

The influence of flume length and group size on swimming performance in shortnose sturgeon Acipenser brevirostrum

The main objectives of this study were to determine optimal methodologies to assess the general swimming performance of juvenile shortnose sturgeon Acipenser brevirostrum. Swimming densities (group v. individual swimming) and flume length (2 v. 1 m) were altered to verify if any of those variables affected performance (i.e. time to fatigue) during critical swimming (U(crit)) and endurance tests. Results for both U(crit) and endurance swimming were not significantly different between fish swum in groups of five or fish swum individually. The U(crit) values, however, were c. 22% higher for fish swum in a longer flume. Although swimming fish in groups did not improve swimming performance, group swimming lowered the variance of the data. Results also reveal that juvenile A. brevirostrum may not possess an ability to swim at high speeds (i.e. burst phase) for long periods.     

Karyotype of North American shortnose sturgeon Acipenser brevirostrum with the highest chromosome number in the Acipenseriformes

The shortnose sturgeon Acipenser brevirostrum was revealed to have a larger number of chromosomes than previously reported for other sturgeon species. Its chromosome number ranged from 362 to 372 (of ten specimens examined), showing intraindividual variation. The karyotype of metaphase with the highest chromosome number (372) consisted of 89 pairs of macrochromosomes and 97 pairs of microchromosomes (fundamental number; NF=550). Although the microchromosomes were relatively shorter than the macrochromosomes, most of them had discernible arms and centromeres. Silver-stained nucleolar organizer regions (Ag-NORs) were localized on the telomeric regions of 5 pairs of chromosomes (Ag-NORs=10): 4 were made up of small meta/submetacentrics and 1 of acrocentrics. Polyploidy of A. brevirostrum should be hexaploid based on the karyotype, numerous chromosomes, Ag-NORs, and previously reported large genome size (ca. 13pg DNA/cell).Supplementary material to this paper is available in electronic format at http://dx.doi.org/10.1007/s10228-004-0257-z     

The effect of substratum type on aspects of swimming performance and behaviour in shortnose sturgeon Acipenser brevirostrum

The swimming performance and associated swimming behaviour (i.e. substratum‐skimming, station‐holding and free swimming) were assessed in shortnose sturgeon Acipenser brevirostrum during critical swimming and endurance swimming tests over a rough and a smooth substratum. It was hypothesized that the addition of a rough substratum in the swimming flume may provide a surface for the A. brevirostrum to grip and offer an energetic advantage. Substratum type did not affect the critical swimming performance, but A. brevirostrum consistently performed more bottom behaviours (i.e. substratum‐skimming and station‐holding) while on a smooth substratum. Acipenser brevirostrum had little contact with the rough substratum until the velocity was >1 body length s^?1. Endurance swimming time was significantly lower for A. brevirostrum over the rough bottom at the highest velocity (30 cm s^?1) which may be attributed to the observed increase in free swimming and decrease in bottom behaviours. During endurance swimming, the rough substratum was mainly used at intermediate velocities, suggesting that there may be a stability cost associated with being in contact with the rough substratum at certain velocities.     

Reproductive demographics,intersex, and altered hormone levels in shortnose sturgeon,Acipenser brevirostrum,from Delaware River,USA

Non‐lethal sampling techniques were used to document the reproductive structure of the shortnose sturgeon (Acipenser brevirostrum) population at a fish aggregation site (near Bordentown, New Jersey) in the Delaware River. A total of 68 fish were captured using gill nets (100 × 1.8 m, 12.7 or 15.2 cm mesh) and examined laparoscopically in May–June, and 61 additional fish captured and examined in November during 2006–2011. Six stages of reproductive development were identified in females and five stages were identified in males, encompassing differentiation through maturity in both sexes. Fish captured in the spring were predominantly immature with a higher proportion of females (1 : 1.2 M : F sex ratio), while mature males predominated in the autumn (5.7 : 1 M : F), indicating that the Bordentown area serves as an overwintering/pre‐spawn aggregation site. Three distinct forms of intersex were noted in gonads of 11.6% of fish examined: ovo‐testis, consisting of scattered spermatic cysts in predominantly immature ovary (3.9%); testis‐ova, consisting of ovarian lamellae projecting from a predominantly immature testes (4.7%); and zonal distribution, consisting of multiple, nearly‐homogenous pockets of either testicular or ovarian tissues along the gonad (3%). The hormone profile in fish with ovo‐testis was similar to that of immature males, while the hormone profile in fish with testis‐ova was similar to that of immature females. The relatively high prevalence of intersex raises concerns regarding potential reproductive effects and long‐term impacts on shortnose sturgeon in the Delaware River.     

First documented occurrences of the shortnose sturgeon (Acipenser brevirostrum,Lesueur, 1818) in the Saco River,Maine, USA

During sampling efforts to study the more abundant Atlantic sturgeon, Acipenser oxyrinchus oxyrinchus, between May of 2009 and November of 2011, four shortnose sturgeon were captured in gill nets near the mouth of the Saco River, Maine. Two of these individuals were tagged with acoustic transmitters to monitor their movement within the Saco River. Additionally, six shortnose sturgeon that had been tagged with acoustic transmitters in the Merrimack River, Massachusetts were detected on the acoustic array deployed within the Saco River and its estuary over this time period. These incidences represent the first verified documentation of shortnose sturgeon within this estuary.     

Ontogenetic behavior of Siberian sturgeon, Acipenser baerii: A synthesis between laboratory tests and field data

We have reviewed field data and studies on the behavior and development of Siberian sturgeon at early-life intervals and related them to different ecologically relevant environmental factors that may play a role in the distribution, recruitment, and survival of young fish. Four behavioral phases (swimming-up, rheotactism, shoaling, and foraging) are observed from hatching to the juvenile phase. Each behavior is associated with an early-life interval and might allow fish to occupy different river habitats, directly influencing their distribution, survival, and recruitment. River current intensity, substrate typology, food resources, and predation pressure seem to be the most important factors affecting the distribution of Siberian sturgeon free embryos and larvae, while juveniles and adult fish disperse and migrate according to food abundance and reproduction. Mechanisms involved in regulating downstream migration during Siberian sturgeon early life stages are different than those observed in anadromous sturgeon species. In all large Siberian rivers, with the exception of the Lake Baikal, the Siberian sturgeon is represented by population continuums, and in many cases the foraging range also includes the spawning areas. Ontogenetic changes in Siberian sturgeon behavior could be interpreted as a species-specific mechanism to maintain the population continuums described in this species without significant mixture of local populations within the river.     

Genetic issues in aquatic species management: the shortnose sturgeon (Acipenser brevirostrum) in the southeastern United States

Anadromous species occupy multiple freshwater,estuarine, and marine habitats, which posesspecial challenges in wildlife management. Inparticular, the level of immigration betweendrainages can be a critical factor in thedefinition of management units and the designof population-specific stocking programs. Thesemi-anadromous shortnose sturgeon (Acipenser brevirostrum) is listed as anendangered species under the Endangered SpeciesAct in the United States. To assess populationstructure in this species as a guide toeffective management, tissue samples werecollected from adult specimens (N = 198) fromfive river systems in the southeastern U.S.,and augmented with a sample from New Brunswick,Canada (N = 13), the extreme northern end ofthe species' range. Comparisons of mtDNAcontrol region sequences reveal a shallow genegenealogy and modest, but significant,population structuring (_st = 4.3%or _st = 17.7% when Canadian samplesare included). Populations inhabiting riversystems in the southeastern U.S. are closelyrelated, a pattern consistent with more recentdivergences along evolutionary timeframes. Haplotype diversity is moderate to high in mostdrainages (h = 0.383–1.000), exceptfor the Savannah and Edisto rivers, indicatingthat historical levels of mtDNA diversity mightbe largely intact outside of these drainages. Low mtDNA diversity in the Savannah andneighboring Edisto drainages might stem from anexperimental stocking effort during 1984–1992 that depressed overall genetic diversityin the Savannah and established or augmentedthe Edisto River population with a relativelylimited number of matrilines.     

Biology and life history of Dabry's sturgeon, Acipenser dabryanus, in the Yangtze River

Dabry's sturgeon, Acipenser dabryanus, is a relatively small (130 cm, 16 kg) and now rare sturgeon restricted to the Yangtze River Basin. It behaves as a resident freshwater fish, does not undertake long distance migrations (except for spawning), and lives in a variety of habitats. It historically spawned in the upper Yangtze River, but the spawning sites are unknown. Acipenser dabryanus reaches maturity earlier than do other Chinese sturgeons, which gives the species aquaculture potential, and artificial spawning has been carried out. However, the native population in the Yangtze has sharply declined in the last two decades due to overfishing, pollution and habitat alteration and destruction, especially since the construction of the Gezhouba Dam, which was built in 1981 across the Yangtze River at Yichang, Hubei Province. Since 1981, Dabry's sturgeon rarely occurs below the Gezhouba Dam because downstream movements are blocked. Clearly, conservation of Dabry's sturgeon must be emphasized. Conservation methods may include protecting habitats, controlling capture and stock replenishment.     

Oxygen consumption and haematology of juvenile shortnose sturgeon Acipenser brevirostrum during an acute 24 h saltwater challenge

This study focused on the acute physiological responses to saltwater exposure in juvenile shortnose sturgeon Acipenser brevirostrum. In two separate laboratory experiments, 2 year‐old A. brevirostrum were exposed to either full (32) or half‐strength (16) seawater for up to 24 h. First, oxygen consumption rates were used to estimate the metabolic costs over 24 h. Secondly, blood and muscle samples were analysed at 6, 12 and 24 h for water loss, various measures of osmoregulatory status (plasma osmolality and ions) and other standard haematological variables. Juveniles exposed to full‐strength seawater showed significant decreases in oxygen consumption rates during the 24 h exposure. Furthermore, seawater‐exposed fish had significantly increased plasma osmolality, ions (Na⁺ and Cl^?) and a 17% decrease in total wet mass over the 24 h exposure period. To a lesser extent, increases in osmolality, ions and mass loss were observed in fish exposed to half‐strength seawater but no changes to oxygen consumption. Cortisol was also significantly increased in fish exposed to full‐strength seawater. While plasma protein was elevated following 24 h in full‐strength seawater, haemoglobin, haematocrit and plasma glucose levels did not change with increased salinity. These results imply an inability of juvenile A. brevirostrum to regulate water and ions in full‐strength seawater within 24 h. Nonetheless, no mortality occurred in any exposure, suggesting that juvenile A. brevirostrum can tolerate short periods in saline environments.     

Ontogenetic Behavior and Migration of Chinese Sturgeon, Acipenser sinensis

The Chinese sturgeon, Acipenser sinensis, is an anadromous protected species that presently only spawns in the Yangtze River. Using laboratory experiments, we examined the behavioral preference of young Chinese sturgeon to physical habitat (water depth, illumination intensity, substrate color, and cover) and monitored their downstream migration. Hatchling free embryos were photopositive, preferred open habitat, and immediately upon hatching, swam far above the bottom using swim-up and drift. Downstream migration peaked on days 0–1, decreased about 50% or more during days 2–7, and ceased by day 8. Days 0–1 migrants were active both day and night, but days 2–7 migrants were most active during the day. After ceasing migration, days 8–11 embryos were photonegative, preferred dark substrate and sought cover. Free embryos developed into larvae and began feeding on day 12, when another shift in behavior occurred–larvae returned to photopositive behavior and preferred white substrate. The selective factor favoring migration of free embryos upon hatching and swimming far above the bottom may be avoidance of benthic predatory fishes. Free embryos, which must rely on yolk energy for activity and growth, only used 19 cumulative temperature degree-days for peak migration compared to 234 degree-days for growth to first feeding larvae, a 1:12 ratio of cumulative temperature units. This ratio suggests that sturgeon species with large migratory embryos, like Chinese sturgeon, which require a high level of energy to swim during migration, may migrate only a short time to conserve most yolk energy for growth.     

The status and distribution of lake sturgeon, Acipenser fulvescens, in the Canadian provinces of Manitoba, Ontario and Quebec: a genetic perspective

Genetic analysis of mitochondrial DNA sequence variation indicates that most of a sample of 396 lake sturgeon, Acipenser fulvescens, from the northern part of their range belonged to either one of two haplotypes. The vast majority of fish from the Great Lakes/St. Lawrence and Mississippi drainages were of a single haplotype while those from the Hudson/James Bay were composed of both haplotypes. This haplotypic distribution suggests that fish from one refugium (possibly Missourian) recolonized the Hudson-James Bay drainage while those from a second (possibly Mississippian) recolonized the Laurentian Great Lakes and St. Lawrence River. Lake sturgeon still inhabit much of their native postglacial distribution in Manitoba, Ontario and Quebec. However, the stresses of commercial overexploitation and habitat alteration, usually through hydroelectric dam construction and operation, have either singly or in tandem brought about the reduction, if not extirpation, of some populations within the range. The largest zone of extirpation and population reduction has occurred in the Lake Winnipeg drainage area, which covers more than one-third of Manitoba. Other areas where populations have been reduced to remnant levels, if not extirpated, include the lower Laurentian Great Lakes of Lake Ontario and Lake Erie. In northern Ontario, lake sturgeon populations whose riverine habitats have been fragmented by two or more dams are substantially reduced from their former levels. In Quebec, more attention has been paid to limiting the exploitive stresses on lake sturgeon populations. Combination of the genetic and status data suggests that both northern and southern populations of lake sturgeon (possibly from two glacial refugia) have been impacted severely from anthropogenic influences.     

The fishery,biology, and management of Atlantic sturgeon,Acipenser oxyrhynchus,in North America

Synopsis The Atlantic sturgeon supported major fisheries along the entire Atlantic coast of North America. These fisheries peaked about 1890 and then suffered almost total collapse by 1905. The Atlantic sturgeon is anadromous and highly susceptible to capture during spawning migrations. Further, this species biological characteristics makes it very vulnerable to man-induced changes in natural habitat and slow to recover. Atlantic sturgeon mature at an advanced age (7–27 year for females, depending on latitude), exhibit a long interspawning period (2–5 year), and require suitable riverine, estuarine, and coastal environments for successful completion of their life cycle. Today, only remnant stocks exist in areas of former abundance. Management regulations vary considerably from state to state and range from full protection to no protection. Biological data are needed to: identify and characterize specific spawning and nursery areas; delineate migratory patterns and recruitment to various stocks; establish stock abundance; and, assess effects of various management strategies. In order to protect remaining stocks, the imposition of a total harvesting moratorium is recommended.