Brood Size, Hatching Order and Hatching Date: Effects on Four Life-History Stages from Hatching to Recruitment in Western Gulls

10.2307/5547 ◽  
1994 ◽  
Vol 63 (2) ◽  
pp. 283 ◽  
Author(s):  
Larry Spear ◽  
Nadav Nur
Keyword(s):  
Life History ◽  
Brood Size ◽  
Hatching Date ◽  
Life History Stages ◽  
Hatching Order

The Influence of Hatching Date on Different Life-History Stages of Great Skuas Catharacta skua

1998 ◽  
Vol 29 (3) ◽  
pp. 299 ◽  
Author(s):  
Paulo Catry ◽  
Norman Ratcliffe ◽  
Robert W. Furness
Keyword(s):  
Life History ◽  
Hatching Date ◽  
Life History Stages

Weather conditions, brood size and hatching order affect Common SwiftApus apusnestlings’ survival and growth

Bird Study ◽  
2014 ◽  
Vol 62 (1) ◽  
pp. 64-77 ◽  
Author(s):  
Beatrice Sicurella ◽  
Mario Caffi ◽  
Manuela Caprioli ◽  
Diego Rubolini ◽  
Nicola Saino ◽  
...  
Keyword(s):  
Brood Size ◽  
Weather Conditions ◽  
Hatching Order ◽  
Survival And Growth

scholarly journals The movement ecology of seagrasses

2014 ◽  
Vol 281 (1795) ◽  
pp. 20140878 ◽  
Author(s):  
Kathryn McMahon ◽  
Kor-jent van Dijk ◽  
Leonardo Ruiz-Montoya ◽  
Gary A. Kendrick ◽  
Siegfried L. Krauss ◽  
...  
Keyword(s):  
Life History ◽  
Clonal Growth ◽  
Movement Ecology ◽  
Future Research ◽  
The Novel ◽  
Long Distance ◽  
Spatial And Temporal Scales ◽  
Life History Stages ◽  
Research Areas ◽  
Time Movement

A movement ecology framework is applied to enhance our understanding of the causes, mechanisms and consequences of movement in seagrasses: marine, clonal, flowering plants. Four life-history stages of seagrasses can move: pollen, sexual propagules, vegetative fragments and the spread of individuals through clonal growth. Movement occurs on the water surface, in the water column, on or in the sediment, via animal vectors and through spreading clones. A capacity for long-distance dispersal and demographic connectivity over multiple timeframes is the novel feature of the movement ecology of seagrasses with significant evolutionary and ecological consequences. The space–time movement footprint of different life-history stages varies. For example, the distance moved by reproductive propagules and vegetative expansion via clonal growth is similar, but the timescales range exponentially, from hours to months or centuries to millennia, respectively. Consequently, environmental factors and key traits that interact to influence movement also operate on vastly different spatial and temporal scales. Six key future research areas have been identified.

Population dynamics of Stenothoe valida Dana, 1852 (Amphipoda, Stenothoidae) at Cheongsapo beach of Busan, Republic of Korea

Crustaceana ◽  
2021 ◽  
Vol 94 (4) ◽  
pp. 413-429
Author(s):  
Ye Ji Lee ◽  
Won Gyu Park
Keyword(s):  
Population Dynamics ◽  
Life History ◽  
Sex Ratio ◽  
Brood Size ◽  
Ovigerous Female ◽  
Seasonal Pattern ◽  
Recruitment Rate ◽  
Republic Of Korea ◽  
Female Size ◽  
History Of

Abstract The population dynamics of Stenothoe valida Dana, 1852 were studied at Cheongsapo beach of Busan, Republic of Korea, from March 2019 to March 2020. Sampling was conducted once a month at low tide during spring tides. Specimens were grouped by the cephalic length at 0.025 mm intervals, and classified into four categories: females, ovigerous females, males and juveniles. The sex ratio, defined as females : total males + females, exceeded 0.5 during most of the study period. Brood size was significantly coupled with ovigerous female size. Two to four cohorts appeared at each study period. New cohorts occurred at almost every sampling except in the samples Jun-2, and Nov-2. Life span was estimated at 1-2 months. The juvenile ratio, the ratio of ovigerous females, and the recruitment rate estimated by FiSAT were commonly high in summer and winter. The life history of S. valida was not coupled with water temperature, but had a strong seasonal pattern.

scholarly journals Sublethal Effects of Crude Oil and Chemical Dispersants on Multiple Life History Stages of the Eastern Oyster, Crassostrea virginica

2020 ◽  
Vol 8 (10) ◽  
pp. 808
Author(s):  
Sara M. Garcia ◽  
Kevin T. Du Clos ◽  
Olivia H. Hawkins ◽  
Brad J. Gemmell
Keyword(s):  
Life History ◽  
Crude Oil ◽  
Crassostrea Virginica ◽  
Sublethal Effects ◽  
Oil Pollution ◽  
Eastern Oyster ◽  
Clearance Rates ◽  
Important Species ◽  
Life History Stages ◽  
Oil Exposure

The eastern oyster Crassostrea virginica is an ecologically and economically important species that is vulnerable to oil pollution. We assessed sublethal effects of soluble fractions of crude oil alone (WAF) and crude oil in combination with Corexit 9500 dispersant (CEWAF) on oysters at three life history stages. Veliger swimming, pediveliger settlement, and adult clearance rates were quantified after 24 h exposures to the contaminants. Veliger swimming speeds were not significantly impacted by 24 h exposures to WAF or CEWAF. A larger proportion of veligers were inactive following WAF and CEWAF exposure as compared to the control, but the effect was greater for pediveligers, and pediveliger settlement in the highest concentration CEWAF treatment decreased by 50% compared to controls. Thus, pediveligers may be particularly vulnerable to oil exposure. In the adults, we found significant clearance rates reductions that persisted 33 days after acute exposure to CEWAF. Knowledge of sublethal effects of oil and dispersant at multiple life history stages aids understanding of how this important species will respond to an oil spill.

The costs of reproduction in tree swallows (Tachycineta bicolor)

1991 ◽  
Vol 69 (10) ◽  
pp. 2540-2547 ◽  
Author(s):  
Nathaniel T. Wheelwright ◽  
Joanna Leary ◽  
Caragh Fitzgerald
Keyword(s):  
Life History ◽  
Clutch Size ◽  
Brood Size ◽  
Life History Theory ◽  
Tachycineta Bicolor ◽  
Laying Date ◽  
Tree Swallows ◽  
Costs Of Reproduction ◽  
Return Rates ◽  
Trade Offs

We investigated the effect of brood size on nestling growth and survival, parental survival, and future fecundity in tree swallows (Tachycineta bicolor) over a 4-year period (1987–1990) in an effort to understand whether reproductive trade-offs limit clutch size in birds. In addition to examining naturally varying brood sizes in a population on Kent Island, New Brunswick, Canada, we experimentally modified brood sizes, increasing or decreasing the reproductive burdens of females by two offspring. Unlike previous studies, broods of the same females were enlarged or reduced in up to 3 successive years in a search for evidence of cumulative costs of reproduction that might go undetected by a single brood manipulation. Neither observation nor experiment supported the existence of a trade-off between offspring quality and quantity, in contrast with the predictions of life-history theory. Nestling wing length, mass, and tarsus length were unrelated to brood size. Although differences between means were in the direction predicted, few differences were statistically significant, despite large sample sizes. Nestlings from small broods were no more likely to return as breeding adults than nestlings from large broods, but return rates of both groups were very low. Parental return rates were also independent of brood size, and there was no evidence of a negative effect of brood size on future fecundity (laying date, clutch size). Reproductive success, nestling size, and survival did not differ between treatments for females whose broods were manipulated in successive years. Within the range of brood sizes observed in this study, the life-history costs of feeding one or two additional nestlings in tree swallows appear to be slight and cannot explain observed clutch sizes. Costs not measured in this study, such as the production of eggs or postfledging parental care, may be more important in limiting clutch size in birds.

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