Spatiotemporal variation in life history traits of three small fishes in streams of south-eastern Brazil

2015 ◽  
Vol 22 (2) ◽  
pp. 143-151 ◽  
Author(s):  
L. S. Lourenço ◽  
U. P. Souza ◽  
I. M. Fernandes ◽  
M. Petrere
2020 ◽  
Vol 77 (10) ◽  
pp. 1688-1699
Author(s):  
Nan Zheng ◽  
Matthew Robertson ◽  
Noel Cadigan ◽  
Fan Zhang ◽  
Joanne Morgan ◽  
...  

Fisheries management usually does not explicitly account for spatial variation in life history traits within populations. However, for some stocks this spatial variation may be substantial. We develop a spatiotemporal generalized linear model and fit the model to a long time series of maturation data for American plaice (Hippoglossoides platessoides) on the Grand Bank off Newfoundland and Labrador. The spatiotemporal correlation structure improves estimation of small-scale spatiotemporal variation in maturity across locations and times with limited or few samples. We test how American plaice maturity varies at three different spatial resolutions. We find improvements in model fit when decreasing spatial scales for higher spatial resolution due to high levels of spatial heterogeneity in American plaice maturity at age and size. Modeling variation in life history traits at the appropriate spatial and temporal scales is necessary for understanding population dynamics and developing appropriate fisheries management strategies.


2014 ◽  
Vol 65 (11) ◽  
pp. 943 ◽  
Author(s):  
Fabian I. Trinnie ◽  
Terence I. Walker ◽  
Paul L. Jones ◽  
Laurie J. Laurenson

Whether spatial variation occurs in the life-history traits of chondrichthyan species is important to fisheries modelling and assessments. A study on the reproductive parameters of Urolophus paucimaculatus from four separate regions across south-eastern Australia found regional differences in maximum total length (TL), size-at-maturity, size-at-maternity and litter sizes. Inshore embayments (Port Phillip Bay (PPB) and Corner Inlet (CI)) appear to allow for larger TLs (females and males) than do offshore areas (Lakes Entrance (LE) and Western Bass Strait (WBS)). Size-at-maturity and size-at-maternity decreased across longitude from west (PPB) to east (LE) and seasonality of parturition and ovulation occurred earlier in PPB (August–October) than in LE (September–December). Maximum litter size correlated with maximum TL (six in PPB, five in each of CI and LE, and four in WBS). There was uncertainty in classifying females for maternal condition because the reproductive cycle appears to range from a continuous annual cycle to a non-continuous biennial cycle. Much of the uncertainty arises from the ambiguity of observation of non-pregnant mature females, which have either aborted through capture and handling, or are in a ‘resting year’ between pregnancies. Most likely, the majority are reproducing annually with an unknown proportion of females non-continuous and resting between pregnancies.


1996 ◽  
Vol 47 (2) ◽  
pp. 365 ◽  
Author(s):  
F Juanes ◽  
JA Hare ◽  
AG Miskiewicz

Pomatomus saltatrix (Pisces:Pomatomidae) is a highly migratory, continental-shelf species with a worldwide subtropical distribution including the eastern coast of North America, the Gulf of Mexico, Mediterranean Sea, Black Sea, north-western Africa, the eastern coast of South America, the south-eastern coast of South Africa, and the south-eastern and south-westem coasts of Australia. This paper summarizes available life history information from the different regions where P. saltatrix occurs, with a focus on the early life history. The basic physical oceanography of these regions is also reviewed to elucidate patterns in larval transport. Comparison of these populations suggests that there are commonalties: adults migrate to spawning grounds; eggs and larvae are typically advected along-shore to juvenile nursery habitats; juveniles recruit to inshore habitats at a similar size, and there they grow rapidly and are mainly piscivorous, feeding primarily on atherinids and engraulids. There are also a number of life history traits that are quite variable among populations: the number of annual reproductive peaks, the number of juvenile cohorts, adult growth patterns and reproductive parameters. Comparison of these life history patterns leads to several non-exclusive hypotheses as to the adaptive significance of variations in life history traits. The goal is to identify areas where more research is needed to assess the degree to which populations of a global species are adapted to their local environment.


Zootaxa ◽  
2006 ◽  
Vol 1105 (1) ◽  
pp. 49 ◽  
Author(s):  
FRANCO ANDREONE ◽  
RONALD A. NUSSBAUM

We revise two stream frogs, Mantidactylus microtis and M. microtympanum, providing data on its known distribution and life history traits, based upon observations in nature. For M. microtis we show for the first time photographs of the live individuals, while for M. microtympanum we also describe its putative tadpoles. The transfer of microtis from Boophis to Mantidactylus is formally justified by morphological and ecological traits, e.g., the lack of nuptial pads, the torrenticolous life style and the low number of eggs. Mantidactylus microtis shares some characters with M. microtympanum: distribution (both live in south-eastern Madagascar), natural history (both are stream frogs), morphology (wide digital expansions, lack of femoral glands, presence of a mostly unforked omosternum, cryptic dorsal colouration, small tympanum, and presence of a derived cloacal structure). Mantidactylus microtympanum differs from the species of the subgenus Mantidactylus (M. grandidieri and M. guttulatus), to which it was so far ascribed, for the lack (vs. presence) of femoral glands, and presence of expanded (vs. moderately expanded) fingertips. Whether M. microtis and M. microtympanum are phylogenetically related, or their overall similarity is due to convergence, is discussed.


2020 ◽  
Vol 650 ◽  
pp. 7-18 ◽  
Author(s):  
HW Fennie ◽  
S Sponaugle ◽  
EA Daly ◽  
RD Brodeur

Predation is a major source of mortality in the early life stages of fishes and a driving force in shaping fish populations. Theoretical, modeling, and laboratory studies have generated hypotheses that larval fish size, age, growth rate, and development rate affect their susceptibility to predation. Empirical data on predator selection in the wild are challenging to obtain, and most selective mortality studies must repeatedly sample populations of survivors to indirectly examine survivorship. While valuable on a population scale, these approaches can obscure selection by particular predators. In May 2018, along the coast of Washington, USA, we simultaneously collected juvenile quillback rockfish Sebastes maliger from both the environment and the stomachs of juvenile coho salmon Oncorhynchus kisutch. We used otolith microstructure analysis to examine whether juvenile coho salmon were age-, size-, and/or growth-selective predators of juvenile quillback rockfish. Our results indicate that juvenile rockfish consumed by salmon were significantly smaller, slower growing at capture, and younger than surviving (unconsumed) juvenile rockfish, providing direct evidence that juvenile coho salmon are selective predators on juvenile quillback rockfish. These differences in early life history traits between consumed and surviving rockfish are related to timing of parturition and the environmental conditions larval rockfish experienced, suggesting that maternal effects may substantially influence survival at this stage. Our results demonstrate that variability in timing of parturition and sea surface temperature leads to tradeoffs in early life history traits between growth in the larval stage and survival when encountering predators in the pelagic juvenile stage.


2020 ◽  
Vol 27 (4) ◽  
pp. 195-200
Author(s):  
Ufuk Bülbül ◽  
Halime Koç ◽  
Yasemin Odabaş ◽  
Ali İhsan Eroğlu ◽  
Muammer Kurnaz ◽  
...  

Age structure of the eastern spadefoot toad, Pelobates syriacus from the Kızılırmak Delta (Turkey) were assessed using phalangeal skeletochronology. Snout-vent length (SVL) ranged from 42.05 to 86.63 mm in males and 34.03 to 53.27 mm in females. Age of adults ranged from 2 to 8 years in males and 3 to 5 years in females. For both sexes, SVL was significantly correlated with age. Males and females of the toads reached maturity at 2 years of age.


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