Life histories of large,grazing copepods in a subarctic ocean gyre: Neocalanus plumchrus,Neocalanus cristatus, and Eucalanus bungii in the Northeast Pacific

Life histories for the dominant, larger copepods of the subartic Pacific have been constructed by sampling from weatherships patrolling Ocean Station P (50°N, 145°W) during 1980 and 1981. Neocalanus plumchrus reproduced at depths below 250 m from July through February. Copepodite stages were present in surface layers from October through August with a large peak in numbers and biomass in spring. Fifth copepodites prepared for diapuse in 38 days during spring and descended to depths below 250 m. They commenced immediately to mature, and the females reproduced without renewed feeding. This schedule contrasts with that of the population in the Strait of Georgia, which remains in diapause from July to January and matures exclusively in January and February. There appears to be a difference between the coastal and oceanic habitats in preparing the diapausing individuals for maturation.Maturation of the diapausing stock of N. plumchrus maintained constant adult populations, averaging 714 males m^?2 from June through October and 1,434 females m^?2 from August through January. This constancy, together with the exponential pattern of decline in the diapause stock from September through February, suggests that density of adults may regulate maturation of fifth copepodites. Offspring of individuals delaying maturation and, thus, reproduction would benefit from the resulting moderation of intraspecific competition, probably that among copepodites.Reproduction of Neocalanus cristatus also occurred below 250 m, and, while spawning was continuous through the year, there was a substantial peak in November. That resulted in a peak of abundance for early copepodite stages in mid-winter, and a peak for the fifth copepodite stage in June. Stocking of the population of fifth copepodites in diapause below 250 m occurred from July through October. Some fifth copepodites were present in surface layers through the entire summer, and some younger copepodites persisted through the summer in progressively declining abundance just below the mixed layer. In autumn 1980 resurgence of early copepodite populations was rapid, occurring during the course of a prolonged October storm. The storm may have improved the habitat either by cooling the mixed layer or by resupplying nutrients to the euphotic zone.Eucalanus bungii reproduced in the mixed layer in early May and in early July. The first event was a spawning by females that had previously spawned in 1979 and then had returned to diapause. The second, heavier spawning (more females, more eggs per female) was by newly matured females from stocks that had overwintered as fifth copepodites. Nauplii peaked sharply in abundance on 19 July, one week after the peak in spawning. First and second copepodites peaked on 1 August, and all had advanced to the third copepodite stage by September. The diapause stock was established by September, principally between 250 and 500 m, and consisted of copepodite stages from third to sixth. Duration of the E. bungii life cycle appears to be typically two years. New nauplii develop as far as the third or fourth copepodite stage during their first summer, then enter diapause. The second summer they advance to the fifth copepodite stage and reenter diapause. Fifth copepodites mature in their third summer at two years of age. The males remain at depth and mate without subsequent feeding. Females migrate at night to the mixed layer where spawning occurs. About 20% of females that had already spawned in 1980 reentered diapause. They would reproduce again in their fourth summer at three years of age. All aspects of the life cycle suggest low mortality rates for copepodite stages, particularly at depth in the habitat occupied during diapuse. There can be no premium on rapid reproduction for E. bungii in the subartic Pacific, and there must even be benefit from spreading reproduction between years. This iteroparity may amount to a “bet-hedging” tactic, the young from a given mother having more than one chance to find sustaining conditions. It also produces gene flow between the year classes of the biennial life cycle.     

A merine seismic refraction study of the Santa Barbara Channel,California

Seismic data from a 186 km-long refraction profile in the Santa Barbara Channel have been interpreted using several velocity inversion techniques. Data were obtained during two cruises in 1978 and 1979. Seismic arrivals from fifty explosions of between 1 and 300 lbs. of TNT were recorded by two ocean bottom seismometers, four permanent ocean bottom stations (University of Southern California), and much of the United States Geological Survey/California Institute of Technology southern California seismic network. Travel-time inversion gives a V _p of 6.3 km sec^-1 at 7.2 km depth above 7.2 km sec^-1 at 14.4 km depth at the western end of the channel. At the eastern end, solutions suggest three sediment refractors overlying V _p of 6.4 km sec^-1 at 7.3 km depth, above 7.0 km sec^-1 at 11.6 km depth, above mantle arrivals with V _p of 8.3 km sec^-1 at 21.8 km depth. The velocity structure determined by these methods suggests that the channel has a sedimentary fill of from 4 to 7 km and a layer of mafic plus ultramafic rock 14 to 17 km thick. The greatest thicknesses of sediments are restricted to east of Point Conception. The velocity data also suggest that the Franciscan formation may not be present beneath the channel. Rather, the crust here may represent a thickened portion of the Coast Range ophiolite.     

Monitoring Measurements from the Jason-1 Microwave Radiometer and Independent Validation with GPS

The Jason-1 Microwave Radiometer (JMR) provides measurements of the wet troposphere content to correct the altimetric range measurement for the associated path delay. Various techniques are used to monitor the JMR wet troposphere path delays, with measurements of zenith troposphere content from terrestrial GPS sites used as an independent verification technique. Results indicate that an unexpected offset of approximately +4.1 ± 1.2 mm (drier) emerged in the JMR measurements of wet path delay between cycles 28-32 of the Jason-1 mission, and that the measurements may be drifting at a rate of approximately -0.5 mm/year. These anomalies are shown to be caused by a -0.7 K offset in 23.8 GHz brightness temperatures between cycles 28-32, and a 0.16 ± 0.04 and -0.45 ± 0.08 K/year drift in the 18.7 and 34.0 GHz brightness temperatures, respectively. Intercomparison of the 3-Hz JMR brightness temperature measurements show that they have been drifting with respect to each other, and that a dependence on yaw-steering regime is present in these measurements. An offset of 0.5 m/s between cycles 28-32 and a drift of approximately 0.5 m/s/year in the JMR wind speed measurements is also associated with these anomalies in the 1-Hz brightness temperatures. These errors in JMR wind speeds presently have a negligible impact on the retrieved JMR path delays.     

Stable isotope analysis of Pacific salmon: insight into trophic status and oceanographic conditions over the last 30 years

Food web interactions and the response of Pacific salmon to physical processes in the North Pacific Ocean over interannual and interdecadal timescales are explored using naturally occurring stable isotope ratios of carbon (¹³C/¹²C) and nitrogen (¹⁵N/¹⁴N). Stable isotope analyses of five species of sexually mature North Pacific salmon from Alaska (Oncorhynchus spp.) cluster into three groups: chinook salmon (O. tshawytscha) have the highest values, followed by coho (O. kisutch), with chum (O. keta), sockeye (O. nerka), and pink (O. gorbuscha) together having the lowest values. Although detailed isotopic data on salmon prey are lacking, there are limited data on relevant prey items from areas in which they are found in high abundance. These data suggest that the characteristics of the sockeye, pink and chum we have analyzed are compatible with their diets including open ocean squid and zooplankton, which are in general agreement with stomach content analyses. Isotope relationships between muscle and scale show consistent relationships for both δ¹³C (R²=0.98) and δ¹⁵N (R²=0.90). Thus, scales, which have been routinely archived for many systems, can be used for retrospective analyses. Archived sockeye salmon scales spanning 1966–1999 from Red Lake, Kodiak Island, Alaska were analyzed for their stable isotope ratios of carbon and nitrogen. The δ¹⁵N record displays a decreasing trend of ˜3‰ from 1969–1982 and an increasing trend of ˜3‰ from 1982–1992, while the variations in δ¹³C are relatively minor. These trends may result from factors such as shifts in trophic level of feeding and/or feeding location, or may originate at the base of the food web via changes in processes such as nutrient cycling or primary productivity. Detailed studies on prey isotopic variability and its controls are needed to distinguish between these factors, and thus to improve the use of stable isotope analysis as a tool to learn more about present and past ecosystem change in the North Pacific and its relation to climatic change.     

The threshold feeding response of microzooplankton within Pacific high-nitrate low-chlorophyll ecosystem models under steady and variable iron input

The equatorial Pacific is an HNLC (High-Nitrate Low-Chlorophyll) region. Modeling and in-situ process studies have confirmed the importance of microzooplankton grazing in this ecosystem. Unfortunately, both the parameters and functions representing microzooplankton grazing within current ecosystem models are poorly constrained. We used a simple 4-component food web model to test the assumption that a lower grazing threshold, which is common in many models, is necessary to achieve the HNLC condition. Without the grazing threshold, the model did not reproduce the HNLC condition. However, by raising the half-saturation constant within the microzooplankton functional response with no threshold, it was possible to reproduce the critical dynamics of the HNLC condition under both steady and moderate seasonal variability in nutrient input. It was also possible to reproduce the HNLC system using a sigmoidal functional response for the microzooplankton, with results somewhere between the other two forms of the model, although this version had the highest sensitivity to changes in its parameters. The three models predicted similar phytoplankton biomass and primary productivity under steady nutrient input, but diverge in these metrics as the amplitude of nutrient input variability increases. These three functional responses also imply certain important differences in the microzooplankton community. Whereas the threshold model had the least sensitivity to parameter choice, the high half-saturation constant, no-threshold model may actually be a better approximation when modeling a community of grazers. Ecosystem models that predict carbon production and export in HNLC regions can be very sensitive to assumptions concerning microzooplankton grazing; future studies need to concentrate on the functional responses of microzooplankton before these models can be used for predicting fluxes in times or regions where forcing is beyond that used to constrain the original model.