Photoperiod and temperature regulation of the life history of Porphyra columbina (Rhodophyta, Bangiales) from central Chile

1986 ◽  
Vol 64 (9) ◽  
pp. 1867-1872 ◽  
Author(s):  
M. Avila ◽  
B. Santelices ◽  
J. McLachlan

The effects of temperature (10, 15, 20 °C) and photoperiod (8:16, 12:12, 16:8 (hours of light: hours of dark)) on the growth and reproduction of different stages in the life history of Porphyra columbina Montagne were assessed. The conchocelis phase had higher growth rates at 12 h light:12 h dark, 45 μmol m−2 s−1, and 15 °C. Under all the temperatures and photoperiods tested, the conchocelis phase could propagate either by monospores or vegetative fragmentation. Conchosporangia were formed only at 10 °C and 8 h light:16 h dark or at 15 °C and either 8 h light:16 h dark or 12 h light:12 h dark. Long photoperiods inhibited conchosporangia formation at all temperatures tested with the exception of 20 °C and 16 h light:8 h dark, where sporangia was formed once. Conchospores were released when the temperature was decreased (15 to 10 °C) maintaining the photoperiod. Conchospore germination occurred under the three photoperiods and temperatures tested. Growth of juvenile fronds was maximum at 15 °C and either 12 h light:12 h dark or 16 h light:8 h dark. Fronds formed carpospores and spermatia at 15 °C and 16 h light:8 h dark only. With optimum conditions the life history was completed in 60 days. Spermatia had three chromosomes (n = 3).

1986 ◽  
Vol 64 (7) ◽  
pp. 1499-1506 ◽  
Author(s):  
Carla D'Antonio

Components of the growth and life history of the red alga Rhodomela larix (Turner) C. Agardh were studied during an 18-month period at a high intertidal and a low intertidal site on the central Oregon coast. Growth was measured by following (i) individually marked upright axes, (ii) clumps of axes thought to represent individual plants, and (iii) large patches of R. larix. Variation in size and growth was common among axes, and portions of some axes were clearly perennial. Plants grew most rapidly in the spring and summer (up to 1.2 mm/day) with a large amount of variation occurring between and within zones and among seasons. Overall, plants at the higher site were shorter and had fewer branches during most of the year than plants at the lower site. Gametophytes were more common in the higher site, while tetrasporophytes predominated at both sites. Reproductive axes were present throughout the observation period, although little recruitment of sexual propagules was seen, implying that populations may be maintained by vegetative perennation of individual plants.


1977 ◽  
Vol 55 (1) ◽  
pp. 161-168 ◽  
Author(s):  
Graham R. Daborn

The life history of B. mackini was studied in a large argillotrophic lake during 1970–1972. Hatching began immediately after spring thaw and was terminated by rising salinity 10 days to 2 weeks later. Growth rates reached maxima of 1 mm/day at 4 weeks of age and then declined as mean size approached 22–23 mm at 7–8 weeks. Clutch sizes varied as a function of female length. Maximum biomass of 580 mg dry weight/m2 (2700 cal/m2) was reached in late May, of which 3.9% per day was consumed by B. gigas. Source of the energy is presumed to be a bacteria – organic matter complex associated with suspended particles. Life cycle details are compared with other fairy shrimp species and the role of B. mackini in the community is discussed.


Parasitology ◽  
1926 ◽  
Vol 18 (2) ◽  
pp. 144-147 ◽  
Author(s):  
C. L. Walton ◽  
W. Norman Jones

1. Egg masses of Limnaea truncatula collected in March 1925 were isolated and hatched in the Laboratory. The average number of ova per mass (for 20) proved to be 9·75.2. The hatching period lasted 12 to 26 days, with an average of 20–21 days (for the Spring generation).3. On hatching, young snails were isolated, reared, and again oviposited during the first week of July. Ova from these snails again hatched during the first week of August.4. It is thus shown that L. truncatula is self fertile; that oviposition can commence at a shell altitude of 4 to 4·5 mm.5. Further data on growth-rates were obtained, showing that two (and probably three) generations occur between March and October.


BioControl ◽  
2019 ◽  
Vol 64 (6) ◽  
pp. 633-643
Author(s):  
Cecilia Falla ◽  
Adriana Najar-Rodriguez ◽  
Maria Minor ◽  
Kerry Harrington ◽  
Quentin Paynter ◽  
...  

2020 ◽  
Author(s):  
Chuliang Song ◽  
Lawrence H. Uricchio ◽  
Erin A. Mordecai ◽  
Serguei Saavedra

AbstractCompetitive exclusion can be classified as deterministic or as historically contingent. While competitive exclusion is the norm in nature, it has remained unclear when multispecies communities should be dominated by deterministic or contingent exclusion. Here, we provide a general theoretical approach to explain both the emergence and sources of competitive exclusion in multispecies communities. We illustrate our approach on an empirical competition system between annual and perennial plant species. First, we find that the life-history of perennial species increases the probability of observing contingent exclusion by increasing their effective intrinsic growth rates. Second, we find a shift from contingent exclusion to dominance with increasing numbers of competing species. Third, we find that the probability of observing contingent exclusion increases with weaker intraspecific competition, and not by the level of hierarchical competition. Our work provides a framework to increase our understanding about the predictability of species survival in multispecies communities.


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