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Spring Tides (spring + tide)
Selected AbstractsRecruitment of Anguilla spp. glass eels in the Waikato River, New Zealand.JOURNAL OF FISH BIOLOGY, Issue 9 2009Evidence of declining migrations? The timing of Anguilla spp. glass eel recruitment into the Waikato River, North Island, New Zealand, was studied over a 2 year period (2004,2005). While glass eels of both the shortfin eel Anguilla australis and the endemic longfin eel Anguilla dieffenbachii were caught, the former comprised >97% of the species composition. There was a positive correlation of glass eel migrations with spring tides, with peak migration periods typically occurring within a few hours of the peak of high tide, and between 2 and 4 days after the day of spring tide. Both water temperature and discharge had significant inverse relationships with glass eel catches, with temperature explaining >30% of the variance in catch periodicity. Comparison of catch data 30 years apart showed that main migration periods appear to occur several weeks earlier today than previously. Reduced catch per unit effort and duration of runs from recent years' sampling (compared with the 1970s) indicate that a reduction in recruitment may also have occurred during this period, something recorded in other temperate species of Anguilla. [source] HABITAT DIFFERENCES IN THE TIMING OF REPRODUCTION OF THE INVASIVE ALGA SARGASSUM MUTICUM (PHAEOPHYTA, SARGASSACEAE) OVER TIDAL AND LUNAR CYCLES,JOURNAL OF PHYCOLOGY, Issue 1 2009Carla Monteiro Sargassum muticum (Yendo) Fensholt is an invasive species that is firmly established on intertidal and subtidal rocky shores of Europe and the Pacific coast of North America. Local success and spread of S. muticum is thought to rely on its reproductive potential that seems dependent on exogenous factors like tidal and lunar cycles. This study is the first to compare the reproductive patterns (periodicity of egg expulsion and embryo settlement) of this invader in two different habitats: the middle and low intertidal. The combination of monthly, daily, and tidal samples at triplicate sites within each habitat showed a semilunar periodicity of egg expulsion and embryo settlement coincident with increasing tidal amplitude just before full and new moons. In both habitats, duration of each egg expulsion event was ,1 week, and embryo settlement occurred during the first daily low tide and with the incoming high tide during spring tides. However, both expulsion and settlement started 1,2 d earlier, expulsion saturation was faster, and settlement was higher in the mid- compared to the low intertidal. Our results suggest that the exact timing of gamete expulsion and embryo release of S. muticum responds to local factors, including tidal cues, which result in differences between mid- and low-intertidal habitats. [source] ARE SPERM LIMITING IN THE SEA?JOURNAL OF PHYCOLOGY, Issue 2000M. L. Berndt The reproductive success of marine species with external fertilization depends on environmental conditions during gamete release. There is special interest presently in whether water motion causes sperm limitation under natural conditions. We investigated gamete release of Fucus vesiculosus from an exposed shore to ascertain: 1) when gametes are released during the tidal cycle, 2) when fertilization occurs, and 3) what the natural sperm:egg ratios are. Water samples were collected and concentrated over five minutes every half hour off Pemaquid Point, ME from three replicate sites within each of two locations using a pump-filter device. Immunofluorescence microscopy revealed that gamete release occurred only on the two calmest spring tides. Sperm became present in the water column at the same time as oogonia (30 min,1 h prior to high tide [HT]) and reached peak concentration at exactly HT. The sperm:egg ratio was 76:1 on 8 Oct 1999 and 21:1 on 8 Nov 1999 at exactly 30 min prior to HT and dropped sharply after HT. Gametes continued to be collected for several hours after HT but analysis of pronuclear position in aceto-iron-hematoxylin stained eggs revealed that all fertilization occurred at approximately HT. We modelled the total number of days when reproduction was possible using these results and wind and wave data from the National Data Buoy Center. Our research provides evidence that gamete release by F. vesiculosus occurs at slack HT on calm days and that sperm are not a limiting factor in fertilization for this species. [source] Adaptation of reef and mangrove sponges to stress: evidence for ecological speciation exemplified by Chondrilla caribensis new species (Demospongiae, Chondrosida)MARINE ECOLOGY, Issue 2007Klaus Rützler Abstract Sponges (Porifera) in mangroves have adapted to a wide range of environmental parameters except for extended periods of exposure to freshwater or air. Many marine mangrove islands are located in the shallow backwaters of coral reefs in Belize and elsewhere in the Caribbean and have a mean tidal range of only 15 cm. They are densely populated by sponges, mostly attached to subtidal red-mangrove stilt roots and peat banks lining tidal channels. Some species are endemic to mangroves, others are immigrants from nearby reefs. Mangrove endemics endure environmental hardships, such as occasional exposure to air during spring tides, temperature and salinity extremes, fine sediments, even burial in detritus. Reef immigrants into mangroves enjoy protection from spongivores that do not stray into the swamp but they eventually succumb to environmental stress. There is evidence exemplified by the common demosponge Chondrilla aff. nucula, that sponges flourishing in both mangrove and reef habitats may develop separate ecologically specialized and reproductively isolated populations. Such processes can lead to genetic modifications and thus serve as mechanisms for ecological speciation. Because Chondrilla nucula Schmidt was first described from the Mediterranean Sea, it was long suspected that the western Atlantic population may be a separate species. New morphological and molecular evidence prompt us to describe it under a new name, Chondrilla caribensis, with two ecological forms, forma caribensis from mangroves and lagoons, and forma hermatypica from open reefs. [source] | ||||||||||