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1

Caddy, J. F. "Modelling Stock–Recruitment Processes in Crustacea: Some Practical and Theoretical Perspectives." Canadian Journal of Fisheries and Aquatic Sciences 43, no. 11 (November 1, 1986): 2330–44. http://dx.doi.org/10.1139/f86-285.

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Several approaches toward development of stock and recruitment models for exploited crustacean populations are reviewed. Such approaches include modifications of classical stock–recruitment models, or ones more directly related to crustacean biology. The latter are believed to offer the most promise for practical application. Standard yield per recruit models using continuous growth functions have been applied to crustacean stocks, but moult increment – frequency versions of yield per recruit calculations better reflect the discrete growth in crustaceans and changes in growth on maturity. They can be extrapolated easily to calculate fecundity per recruit and assess the impact of exploitation on spawning potential. Simple, semiquantitative approaches, such as life history tables, promote investigation of hypotheses of growth, mortality, maturity/fecundity, and harvesting strategy on management, but like yield per recruit models, cannot easily take into account density-dependent recruitment. We may look forward to the development of models that take into account the nature of crustacean life histories, reflecting the need for cross-scheduling of growth and reproduction in environmentally limiting conditions. Modelling life history processes in biological time units related to moult cycle duration, and cross-converting to real time for consideration of the fisheries component, should offer a notable simplification of the modelling process. The existence of several "choices" for an individual crustacean at different points in the moulting/reproduction cycles makes cohort models cumbersome and seems to require the adoption of a stochastic approach, for instance Markov-related processes, which better take into account complexities of biology and fishery-related processes. For many crustaceans, recruitment is believed to be subject to a "bottleneck" somewhere subsequent to the early larval stages, and identification of the species niche for postlarval stages could be of great practical importance for management and stock enhancement. The concept of the fractal surface as a postlarval and juvenile habitat is suggested as a promising approach, and an expression for natural mortality at size is derived for obligate crevice dwellers on a fractal surface. In relatively few circumstances for Crustacea have density-dependent factors been demonstrated in the field as affecting spawning success and the survival to recruitment of postlarval and juvenile stages. Recruit survival appears to be dominated by environmental conditions that vary significantly; seasonal timing of larval release depending on environmental change from year to year. Short-cutting the investigation of precise impacts of stock density, fishing effort, and environment on recruitment can be achieved using production models, delayed recruitment models, models with autoregressive terms, or production models using mortality rates, where effort definition is difficult and catchability a function of behaviour and environnment. The overriding influence of environment on recruitment success is illustrated for both short- and long-lived species in the tropics and northern latitudes, and this is especially true for high unit value Crustacea resources whose heavily exploited fisheries generally operate at low spawning stock sizes. Fluctuating predator density, or other multispecies interactions, affect recruitment and available number of niches, and modelling of trophic relationships has promise. The range of possible models corresponds to various degrees of refinement of the data base, and the importance of biotic, abiotic, and geographical factors in controlling crustacean recruitment is stressed. Also of fundamental importance are the economics of exploitation of species with a high and elastic demand, which results in high actual and latent levels of effort, fisheries heavily dependent on incoming year-classes, and serious problems in maintaining exploitation rates at reasonable levels.
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2

Takahashi, Tomohiro, and Seiji Goshima. "The growth, reproduction and body color pattern of Cleantiella isopus (Isopoda: Valvifera) in Hakodate Bay, Japan." Crustacean Research 41 (2012): 1–10. http://dx.doi.org/10.18353/crustacea.41.0_1.

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3

Wada, Satoshi, Takashi Oba, Kazuyoshi Nakata, and Atsushi Ito. "Temporal allocation pattern between reproduction and growth within a breeding season of the hermit crab Pagurus nigrivittatus." Crustacean Research 37 (2008): 67–73. http://dx.doi.org/10.18353/crustacea.37.0_67.

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4

Gao, Tianxiang, Shinji Tsuchida, and Seiichi Watanabe. "Growth and reproduction of Rhynchoplax coralicola Rathbun (Brachyura: Hymenosomatidae)." Crustacean Research 23 (1994): 108–16. http://dx.doi.org/10.18353/crustacea.23.0_108.

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5

El Haj, A. J., and N. M. Whiteley. "Molecular Regulation of Muscle Growth in Crustacea." Journal of the Marine Biological Association of the United Kingdom 77, no. 1 (February 1997): 95–106. http://dx.doi.org/10.1017/s0025315400033804.

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Tissue growth in Crustacea occurs at specific stages of the moult cycle and is influenced by a number of physical, hormonal and environmental factors. In order to understand the mechanisms responsible for controlling intermittent muscle growth in Crustacea, the effects of various factors on rates of protein synthesis and gene expression for the myofibrillar proteins, have been examined. These studies include the effects of mechanical stretch on muscle fibres; the influence of the moulting hormones, ecdysteroids; and the effect of temperature which is an important environmental variable. Sarcomeric proteins have been cloned and used to measure mRNA levels of actin, myosin HC and tropomyosin in various muscles over the moult cycle. Results from these studies demonstrate that both transcriptional and translational regulation occurs in response to hormonal and mechanical stimulation. Temperature has a direct effect on rates of protein synthesis and transcription in intermoult muscles but overall protein turnover may remain unchanged due to a concomitant increase in protein degradation rates.
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6

Kawai, Tadashi, Tatsuo Hamano, and Shuhei Matsuura. "Molting and growth of the Japanese crayfish Cambaroides japonicus reared in the laboratory." Crustacean Research 24 (1995): 65–68. http://dx.doi.org/10.18353/crustacea.24.0_65.

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7

Otani, Takuya, Takao Yamaguchi, and Tohru Takahashi. "Population structure, growth and reproduction of the fiddler crab, Uca arcuata (De Haan)." Crustacean Research 26 (1997): 109–24. http://dx.doi.org/10.18353/crustacea.26.0_109.

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8

Fuseya, Reiko, and Seiichi Watanabe. "Growth and reproduction of the spider crab, Pugettia quadridens quadridens (De Haan) (Brachyura: Majidae)." Crustacean Research 22 (1993): 75–81. http://dx.doi.org/10.18353/crustacea.22.0_75.

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9

Pentecost, A. "Growth and Calcification of the Cyanobacterium Homoeothrix crustacea." Microbiology 134, no. 10 (October 1, 1988): 2665–71. http://dx.doi.org/10.1099/00221287-134-10-2665.

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10

GREEN, J. "GROWTH, SIZE AND REPRODUCTION IN DAPHNIA (CRUSTACEA: CLADOCERA)*." Proceedings of the Zoological Society of London 126, no. 2 (August 20, 2009): 173–204. http://dx.doi.org/10.1111/j.1096-3642.1956.tb00432.x.

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11

Yamada, Hideaki, and Yoh Yamashita. "Effects of temperature on intermolt period, growth rate and reproduction rate in Acanthomysis mitsukurii (Crustacea: Mysidacea)." Crustacean Research 29 (2000): 160–69. http://dx.doi.org/10.18353/crustacea.29.0_160.

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12

Kobayashi, Satoshi, and Shuhei Matsuura. "Relative growth of chela of the Japanese mitten crab Eriocheir japonica (De Haan) during the juvenile stages." Crustacean Research 25 (1996): 1–6. http://dx.doi.org/10.18353/crustacea.25.0_1.

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13

Takeshima, Satoshi, Shigeki Dan, Yuming Sui, Masaki Oshiro, and Katsuyuki Hamasaki. "Relative growth of pereiopods of the megalopa and early juveniles of Portunus trituberculatus (Miers, 1876) (Brachyura: Portunidae)." Crustacean Research 47 (December 5, 2018): 125–36. http://dx.doi.org/10.18353/crustacea.47.0_125.

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14

Doi, Wataru, Shunsuke Kato, Daiki Itoh, Akira Mizutani, and Hiroyoshi Kohno. "Distribution, size structure, and relative growth of Epigrapsus politus (Brachyura: Gecarcinidae) in a subtropical bay in Japan." Crustacean Research 48 (December 4, 2019): 145–57. http://dx.doi.org/10.18353/crustacea.48.0_145.

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15

Holdich, D. M. "Reproduction, growth and bionomics of Dynamene bidentata (Crustacea: Isopoda)." Journal of Zoology 156, no. 2 (August 20, 2009): 137–53. http://dx.doi.org/10.1111/j.1469-7998.1968.tb05925.x.

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16

Lowder, Kaitlyn B., Michael C. Allen, James M. D. Day, Dimitri D. Deheyn, and Jennifer R. A. Taylor. "Assessment of ocean acidification and warming on the growth, calcification, and biophotonics of a California grass shrimp." ICES Journal of Marine Science 74, no. 4 (January 18, 2017): 1150–58. http://dx.doi.org/10.1093/icesjms/fsw246.

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Cryptic colouration in crustaceans, important for both camouflage and visual communication, is achieved through physiological and morphological mechanisms that are sensitive to changes in environmental conditions. Consequently, ocean warming and ocean acidification can affect crustaceans’ biophotonic appearance and exoskeleton composition in ways that might disrupt colouration and transparency. In the present study, we measured growth, mineralization, transparency, and spectral reflectance (colouration) of the caridean grass shrimp Hippolyte californiensis in response to pH and temperature stressors. Shrimp were exposed to ambient pH and temperature (pH 8.0, 17 °C), decreased pH (pH 7.5, 17 °C), and decreased pH/increased temperature (pH 7.5, 19 °C) conditions for 7 weeks. There were no differences in either Mg or Ca content in the exoskeleton across treatments nor in the transparency and spectral reflectance. There was a small but significant increase in percent growth in the carapace length of shrimp exposed to decreased pH/increased temperature. Overall, these findings suggest that growth, calcification, and colour of H. californiensis are unaffected by decreases of 0.5 pH units. This tolerance might stem from adaptation to the highly variable pH environment that these grass shrimp inhabit, highlighting the multifarious responses to ocean acidification, within the Crustacea.
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17

Hamasaki, Katsuyuki, Sota Nishimoto, Masakazu Okada, Asahi Kimura, Kosei Otsubo, and Shigeki Dan. "Dietary effects of phytoplankton and zooplankton on larval survival, duration and growth of four Caridina species (Decapoda: Caridea: Atyidae) under laboratory conditions." Crustacean Research 49 (November 11, 2020): 225–37. http://dx.doi.org/10.18353/crustacea.49.0_225.

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18

Darling, Marilyn S., and Karl M. Wilbur. "A Method for Measuring Growth in Living Barnacles (Crustacea: Cirripedia)." Journal of the Marine Biological Association of the United Kingdom 73, no. 3 (August 1993): 723–26. http://dx.doi.org/10.1017/s0025315400033257.

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A buoyant-weight method is described for the non-destructive estimation of fresh weight, total dry weight, shell weight and dry weight of organic matter in living barnacles Balanus amphitrite amphitrite Darwin. The method involves developing regression equations relating weight in air of these parameters to the buoyant weight of living barnacles in sea water. Buoyant weights of barnacles can then be used with the regression equations to obtain the weight in air of these consitituents, making possible the measurement of rates of shell growth and growth in dry weight without disturbance to the living animal. The method has been developed for the analysis of groups of juvenile barnacles cultured on coverslips, ranging in total dry weight from 1 to 60 mg, and for single mature individuals from 75 to 800 mg total dry weight. The buoyant-weight method has been used to measure shell growth of 2–3 mg d-1 in barnacles of 48 mg mean initial total dry weight cultured at 28°C.
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19

Siegel, V. "Age and growth of Antarctic Euphausiacea (Crustacea) under natural conditions." Marine Biology 96, no. 4 (December 1987): 483–95. http://dx.doi.org/10.1007/bf00397966.

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20

COLLINS, PABLO, and ANA PETRIELLA. "Growth pattern of isolated prawns ofMacrobrachium borellii(Crustacea, Decapoda, Palaemonidae)." Invertebrate Reproduction & Development 36, no. 1-3 (September 1999): 87–91. http://dx.doi.org/10.1080/07924259.1999.9652682.

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21

Seaman, M. T., D. J. Kok, B. J. von Schlichting, and A. J. Kruger. "Natural growth and reproduction in Triops granarius (Lucas) (Crustacea: Notostraca)." Hydrobiologia 212, no. 1 (April 1991): 87–94. http://dx.doi.org/10.1007/bf00025991.

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22

Mauchline, J. "Growth and production of Euphausiacea (Crustacea) in the Rockall Trough." Marine Biology 90, no. 1 (December 1985): 19–26. http://dx.doi.org/10.1007/bf00428210.

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23

Procheş, Şerban, and David J. Marshall. "Epiphytic algal cover and sediment deposition as determinants of arthropod distribution and abundance on mangrove pneumatophores." Journal of the Marine Biological Association of the United Kingdom 82, no. 6 (November 21, 2002): 937–42. http://dx.doi.org/10.1017/s0025315402006422.

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We report here an investigation on intertidal mangrove pneumatophores, examining the relationships between arthropod abundance (for ten taxa, mostly belonging to the meiofaunal size-class), algal biomass and sediment cover. There was a strong correlation between the mass of sediment and the mass of macroalgae, supporting the assumption that pneumatophore sediment cover depends on algal growth. These two components of pneumatophore cover were negatively related to elevation, an effect probably relating to desiccation-limited algal growth towards the pneumatophore tips. Total arthropod abundance and that of some taxa (particularly, Uropodidae (Acari), Metidae (Crustacea), Ceratopogonidae (Insecta) and Empidoidea (Insecta)), was negatively correlated with elevation and positively correlated with sediment and algal cover, suggesting a good relationship between abundance and habitat availability. Other arthropod taxa (particularly, Halacaridae (Acari)) however, showed the opposite pattern of relationships. When the pneumatophore cover was physically removed, in an experiment to assess assemblage recovery rates, some arthropod taxa (Halacaridae (Acari), Harpacticoidea (Crustacea) and Ceratopogonidae (Insecta)) had completely recovered by 25 weeks, while others (Tanaididae (Crustacea) and Empidoidea (Insecta)) only partially recovered.
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24

Mitchell, S. A. "The growth rate and growth efficiency of Streptocephalus macrourus (Crustacea, Anostraca) cultured on microalgae." Hydrobiologia 212, no. 1 (April 1991): 1–10. http://dx.doi.org/10.1007/bf00025980.

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25

Carmona-Suárez, Carlos A. "Reproductive biology and relative growth in the spider crab Maja crispata (Crustacea: Brachyura: Majidae)." Scientia Marina 67, no. 1 (March 30, 2003): 75–80. http://dx.doi.org/10.3989/scimar.2003.67n175.

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26

Paterson, Michael J., Cheryl L. Podemski, Wilhelmina J. Findlay, David L. Findlay, and Alex G. Salki. "The response of zooplankton in a whole-lake experiment on the effects of a cage aquaculture operation for rainbow trout (Oncorhynchus mykiss)." Canadian Journal of Fisheries and Aquatic Sciences 67, no. 11 (November 2010): 1852–61. http://dx.doi.org/10.1139/f10-106.

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There is hope that increased development of aquaculture will help meet future global needs for protein. The growth of the freshwater aquaculture industry in Canada, however, has been hampered by insufficient information on environmental impacts. We examined the effects of an experimental cage aquaculture operation for rainbow trout ( Oncorhynchus mykiss ) on planktonic Crustacea and rotifers using 6 years of precage and 7 years of postcage data. Following the initiation of aquaculture, total crustacean and rotifer biomass, egg production, and depth distributions did not change significantly when compared with data from three nearby unimpacted lakes. We found statistically detectable increases in densities of Bosmina cf. longirostris and Diacyclops thomasi and an overall change in crustacean zooplankton community structure using correspondence analysis. The response of zooplankton was less than we expected because comparatively large changes were observed in phytoplankton biomass, hypolimnetic O2, and densities of invertebrate ( Mysis diluviana ) and fish predators. Our study emphasizes the need to monitor multiple variables when assessing the ecosystem impacts of potential stressors such as aquaculture.
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27

Jacinto, David, Nélia Penteado, Diana Pereira, Alina Sousa, and Teresa Cruz. "Growth rate variation of the stalked barnacle Pollicipes pollicipes (Crustacea: Cirripedia) using calcein as a chemical marker." Scientia Marina 79, no. 1 (March 2, 2015): 117–23. http://dx.doi.org/10.3989/scimar.04135.08b.

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28

Keskinen, Essi, Yasuharu Takaku, V. Benno Meyer-Rochow, and Takahiko Hariyama. "Postembryonic Eye Growth in the Seashore Isopod Ligia exotica (Crustacea, Isopoda)." Biological Bulletin 202, no. 3 (June 2002): 223–31. http://dx.doi.org/10.2307/1543472.

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29

Zhao, Wen, Zhixin You, Jie Wei, and Shan Wang. "Compensatory population growth in Daphniopsis tibetana Sars (Crustacea: Cladocera) following starvation." Limnology 18, no. 2 (August 26, 2016): 167–74. http://dx.doi.org/10.1007/s10201-016-0499-2.

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30

Takeuchi, I., and R. Hirano. "Growth and reproduction ofCaprella danilevskii (Crustacea: Amphipoda) reared in the laboratory." Marine Biology 110, no. 3 (October 1991): 391–97. http://dx.doi.org/10.1007/bf01344358.

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31

Sakunwattana, Taksaorn, Phattarunda Jaree, Vichien Rimphanitchayakit, Anchalee Tassanakajon, and Sirinit Tharntada. "Antibacterial and antiproteinase activities of a double whey acidic protein domain-containing protein from Penaeus vannamei Boone, 1931 (Decapoda, Penaeidae)." Crustaceana 93, no. 1 (February 6, 2020): 51–69. http://dx.doi.org/10.1163/15685403-00003962.

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Abstract Double whey acidic protein domain-containing proteins (DWDs) or secretory leukocyte protease inhibitor (SLPI)-like proteins, have been identified in many species of Crustacea. The PvDWD1 from Penaeus vannamei was the first SLPI-like protein identified in a crustacean. Herein, we report that the expression of PvDWD1 was up-regulated at 6 h after acute hepatopancreatic necrosis disease (AHPND)-causing Vibrio parahaemolyticus (VPAHPND) challenge. Similarly, after a different stress other than bacterial infection, the chronic non-lethal heat shock (NLHS) induction, the expression of the PvDWD1 gene was increased at 6 and 24 h after chronic NLHS treatment. The recombinant PvDWD1 (rPvDWD1) protein was over-expressed and tested for its deleterious activity against the bacteria. The rPvDWD1 protein exhibited growth inhibitory activity against Bacillus megaterium and VPAHPND. Moreover, the rPvDWD1 protein possessed an antiproteinase activity against the secreted proteinases from Bacillus subtilis and VPAHPND. The PvDWD1 perhaps functions in shrimp immunity through antimicrobial and antiproteinase properties.
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32

Keunecke, Karina A., Fernando D'Incao, and Duane B. Fonseca. "Growth and mortality of Hepatus pudibundus (Crustacea: Calappidae) in south-western Brazil." Journal of the Marine Biological Association of the United Kingdom 87, no. 4 (July 30, 2007): 885–91. http://dx.doi.org/10.1017/s0025315407056718.

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The predatory action of the pink shrimp (Farfantepenaeus brasiliensis and Farfantepenaeus paulensis) trawling fishery in south-western Brazil affects populations of some benthic species and Hepatus pudibundus is an abundant by-catch in this fishery. Individual growth and mortality of H. pudibundus were studied by taking monthly samples for a year from the by-catch of the pink shrimp fishery in the Ubatuba region. The von Bertalanffy growth model described growth of H. pudibundus (K=2.73 y-1, CW∞=82.97 mm; K=2.62 y-1, CW∞=66.72 mm, for males and females respectively). Modal progression of the monthly average sizes was related to increasing values of relative condition index. The instantaneous coefficients of total, natural, and fishing mortality were: males, Z=7.62 y-1; M=1.80 y-1; F=5.83 y-1; females, Z=7.36 y-1; M=1.80 y-1; F=5.56 y-1. Length composition and mortality analysis suggest that H. pudibundus in the Ubatuba region might be overfished.
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33

Blomsterberg, Mikkel, Henrik Glenner, and Jens T. Høeg. "Growth and molting in epizoic pedunculate barnacles genusOctolasmis(Crustacea: Thecostraca: Cirripedia: Thoracica)." Journal of Morphology 260, no. 2 (March 31, 2004): 154–64. http://dx.doi.org/10.1002/jmor.10132.

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34

Gerasimov, Yuri Leonidovich, and Anna Vsevolodovna Shabanova. "The Crustcea and Rotifera in the pond near «Piramida» shopping mall (Samara) in 2013." Samara Journal of Science 5, no. 1 (March 1, 2016): 18–23. http://dx.doi.org/10.17816/snv20161103.

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The composition and population sizez of the Crustacea and Rorifera species were studied in an urban pond after its melioration. 30 Rotifera species (52 species before melioration) and 20 Crustacea species (33 species before melioration) were found in 2013. Brachionidae, Synchaetidae и Asplanchnidae remain dominant in the Rotifera community. Cyclopoidae were dominant in the Crustacea community (Daphniidae dominated before melioration). The quantity of Bosminidae и Chydoridae considerably increased. On the whole the quantity of animal plankton decreased by 15% in 2013. In 2010 rises of the quantity were observed twice, in June and in August; in 2013 there was only one rise of the quantity of the plankton in July. The number of female individuals with eggs increased. The pond refers to the -mesosaprobic zone, the level of contamination in terms of saprobity indicators decreased. The Shannon index of species diversity was calculated. Removal of macrophytes caused decrease of littoral species and growth of plankton invertebrates. The hydrochemical analysis revealed the excess of the maximum permissible concentration of BOC5, АSАS, Cu, Fe and Zn
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35

Shinozaki-Mendes, R. A., and R. Lessa. "Ontogenetic trajectories in Callinectes danae (Crustacea: Brachyura): sex and age polymorphism." Journal of the Marine Biological Association of the United Kingdom 99, no. 1 (October 30, 2017): 111–18. http://dx.doi.org/10.1017/s0025315417001758.

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We analysed the morphological variations through geometric morphometric approaches of the dorsal and ventral views of growing male and female Callinectes danae Smith 1869, based on the hypothesis that swimming crabs present polymorphism during growth. Our research identified six instars for females, seven instars for males and one instar for unsexed individuals (young). The sixth instar of females and the seventh instar of males were composed of adults. We identified 20 landmarks from the dorsal view, and 16 landmarks from the ventral view. Based on canonical analysis and Procrustes distance, we observed the formation of clearly separated instars (both views), indicating a significant change during ontogeny, not only in the pubertal moult. The most prevalent changes occurred in the abdomen, with males thinning and females broadening the abdomen during growth. In the dorsal view, we observed a displacement of anterolateral spines to the posterior region throughout the growth period and that the anterolateral and frontal teeth of juveniles were more ornate than those of adults. The ontogenetic trajectories for males and females have similar origins and follow different directions over the instars, with maximum distance after the pubertal moult (P < 0.05).
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36

Montemayor-L, G. "Growth Pattern Of Three Euphasiid Species (Crustacea: Euphausiacea) Off Ensenada, Baja California, Mexico." Ciencias Marinas 13, no. 1 (February 1, 1987): 52–60. http://dx.doi.org/10.7773/cm.v13i1.525.

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37

Pasternak, A., V. Mikheev, and ET Valtonen. "Growth and development of Argulus coregoni (Crustacea: Branchiura) on salmonid and cyprinid hosts." Diseases of Aquatic Organisms 58 (2004): 203–7. http://dx.doi.org/10.3354/dao058203.

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38

Fockedey, Nancy, Jan Mees, Marnix Vangheluwe, Tim Verslycke, Colin R. Janssen, and Magda Vincx. "Temperature and salinity effects on post-marsupial growth of Neomysis integer (Crustacea: Mysidacea)." Journal of Experimental Marine Biology and Ecology 326, no. 1 (December 2005): 27–47. http://dx.doi.org/10.1016/j.jembe.2005.05.005.

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39

Takeuchi, Ichiro, and Reijiro Hirano. "Growth and reproduction of the epifaunal amphipod Caprella okadai Arimoto (Crustacea: Amphipoda: caprellidea)." Journal of Experimental Marine Biology and Ecology 161, no. 2 (October 1992): 201–12. http://dx.doi.org/10.1016/0022-0981(92)90097-t.

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40

Tararam, Airton Santo, Hilda de Souza Lima Mesquita, Yoko Wakabara, and Clóvis A. Peres. "Food ingestion and assimilation by Hyale media (Dana, 1853) (Crustacea - Amphipoda)." Boletim do Instituto Oceanográfico 38, no. 1 (1990): 11–21. http://dx.doi.org/10.1590/s0373-55241990000100003.

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The feeding of Hyale media was analysed under laboratory conditions in winter and summer temperatures. The results showed that assimilation rates increased following food ingestion rates and decreased when egestion rates increased. In winter temperatures no significant differences were found in the assimilation rates among developmental stages and sexes. In summer temperatures assimilation rates for ovigerous and non-ovigerous females were higher than those found for adult and young males. Although not statistically analysed, mean assimilation efficiencies were highest among ovigerous females and adult males, in summer. The quantitative and qualitative variations found in the assimilation efficiency and rates were explained by the differential effect of temperature on the specific growth rate and in the physiological conditions of each growth stage concerned.
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41

Iguchi, N. "Effects of temperature on metabolism, growth and growth efficiency of Thysanoessa longipes (Crustacea: Euphausiacea) in the Japan Sea." Journal of Plankton Research 27, no. 1 (September 30, 2004): 1–10. http://dx.doi.org/10.1093/plankt/fbh146.

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42

Rainer, SF, and P. Unsworth. "Ecology and production of Nebalia sp. (Crustacea : Leptostraca) in a shallow-water seagrass community." Marine and Freshwater Research 42, no. 1 (1991): 53. http://dx.doi.org/10.1071/mf9910053.

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Nebalia sp. is an abundant epifaunal crustacean in seagrass meadows at Seven Mile Beach, Western Australia, in water temperatures of 16-27�C. Its maximum length is 6.0-6.4 mm; females generally reach maturity when 4 mm long and males when 5 mm long. They breed throughout the year, and juveniles comprised 94% of animals sampled (n = 880). Males comprised only 11% of mature animals in field samples, compared with 40% in field chambers and 67% in the stomachs of nocturnal fish predators. Abundance during the year reflected changes in growth rate (0.050-0.088 mm day-1), mortality rate (0.020-0.069 day-1) and life span (49-102 days). The annual production of Nebalia sp. in seagrass meadows was estimated at 5.8 g ash-free dry weight (AFDW) m-2, with a corresponding P :B (production:biomass) ratio of 22.5. Predation is probably the main source of mortality at times of high density of Nebalia sp., and at least three significant fish predators on Nebalia sp. were found. Together with Nebalia sp., small crustaceans with high P:B ratios may have a significant role in secondary production in the seagrass beds at Seven Mile Beach.
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43

Fonseca, Duane B., and Fernando D'Incao. "Growth and reproductive parameters of Kalliapseudes schubartii in the estuarine region of the Lagoa dos Patos (southern Brazil)." Journal of the Marine Biological Association of the United Kingdom 83, no. 5 (September 19, 2003): 931–35. http://dx.doi.org/10.1017/s0025315403008087h.

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Kalliapseudes schubartii (Crustacea: Tanaidacea) is a tube dwelling invertebrate living in estuarine soft bottoms with distribution along the south-east and southern Brazilian and Uruguayan coasts. Individual growth, and reproduction were examined by taking samples for a year in the estuarine region of the Lagoa dos Patos (southern Brazil). The von Bertalanffy model described growth of K. schubartii (K=4.54 y−1, L∞=13.22 mm). Reproductive activity was observed in spring and summer. No relationship was observed between total length of females and brood size. Eggs, embryos, and mancas were often observed in a marsupium. Relative growth analysis showed two levels of allometry in the growth of chelipeds of males.
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44

TIPPELT, LISA, and MARTIN SCHWENTNER. "Taxonomic assessment of Australian Eocyzicus species (Crustacea: Branchiopoda: Spinicaudata)." Zootaxa 4410, no. 3 (April 18, 2018): 401. http://dx.doi.org/10.11646/zootaxa.4410.3.1.

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Herein we describe nine species of Eocyzicus from Australia and re-describe the morphological variability of Eocyzicus parooensis Richter & Timms, 2005 and Eocyzicus argillaquus Timms & Richter, 2009. All species were previously delimited by molecular phylogenetic analyses and the species descriptions are based on the same individuals. Characters were scored with the aid of the taxonomic software DELTA. The morphological analyses largely corroborated the previously delimited species despite high levels of intraspecific variability that overlapped with interspecific variation in many instances. Morphological species delimitation was generally supported by principal component and canonical variate analyses. Characters best suited for morphological species identification were the numbers of growth lines on the carapace, the number of telsonic spines and the number of setae on the furca.
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45

Johansen, Per-Otto. "Contribution to the knowledge of growth and postmarsupial development of Natatolana borealis (Crustacea: Isopoda)." Journal of the Marine Biological Association of the United Kingdom 80, no. 4 (August 2000): 623–32. http://dx.doi.org/10.1017/s0025315400002447.

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Postmarsupial development and growth of Natatolana borealis were studied from Skogsvåg and Raknesvåg on the western coast of Norway. Growth was determined from size and instar stage distributions. Growth was also examined in laboratory kept isopods that were collected from Skogsvåg. The postmarsupial instar stages were identified using the number of articles and the position of setae on the flagellum of the first antenna and other morphological features. The mean size of isopods in instar stages 1—3 did not show any significant seasonal variation in Raknesvåg. The estimated growth and mortality rates of males and females were not significantly different. Nine and 11 postmarsupial instar stages were found in material from Skogsvåg and Raknesvåg, respectively. The life span from instar stage 1 to 9 of male and female N. borealis from western Norway was estimated to be 3—4 y. Mortality rate increased significantly from instar stage 9 to 10 of both sexes. Isopods that attained instar stage 10 and instar stage 11 in Raknesvåg, may have lived 4—5 y. The mean size of instar stages 8 and 9 and the size-to-weight relationships were significantly higher in material from Raknesvåg relative to that from Skogsvåg and may have been caused by differences in food access and predation pressure at the two study sites. Specimens sampled from the Bay of Monaco attained smaller adult size than the isopods from the Norwegian population.
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46

Robinson, M., and O. Tully. "Dynamics of a subtidal population of the porcellanid crab Pisidia longicornis (Decapoda: Crustacea)." Journal of the Marine Biological Association of the United Kingdom 80, no. 1 (February 2000): 75–83. http://dx.doi.org/10.1017/s0025315499001587.

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A subtidal population of the anomuran crab, Pisidia longicornis was sampled quantitatively throughout 1997. Divers, using SCUBA equipment, conducted suction sampling each month, with concentrated effort directed towards the settlement season. Pisidia occurred in very high densities, constituting the major component of decapod community abundance. Gravid females were detected between March and September. Newly settled megalopae were present in benthic samples from June until late September. Six distinct settlement events were detected during this period, with pulses coinciding with low spring tides. Body size at settlement decreased as temperature during larval development increased. The rapid growth of each distinct settlement group was followed over time through each subsequent crab stage up to maximum adult size. Growth was suspended between December and April. Survival within each distinct settlement group was density-independent during the first summer's growth. Mortality increased between June and July settlement events, with the rate of decline remaining a linear function.
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47

Khan, R. A., and E. M. Lee. "Influence of Lernaeocera branchialis (Crustacea: Copepoda) on Growth Rate of Atlantic COD, Gadus morhua." Journal of Parasitology 75, no. 3 (June 1989): 449. http://dx.doi.org/10.2307/3282604.

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48

Martens, Koen. "Effects of Temperature and Salinity on Postembryonic Growth in Mytilocypris Henricae (Chapman) (Crustacea, Ostracoda)." Journal of Crustacean Biology 5, no. 2 (April 1, 1985): 258–72. http://dx.doi.org/10.2307/1547873.

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49

Molyneaux, Douglas B., and Thomas C. Shirley. "Molting and growth of eyestalk-ablated juvenile red king crabs, paralithodes camtschatica (crustacea: lithodidae)." Comparative Biochemistry and Physiology Part A: Physiology 91, no. 2 (January 1988): 245–51. http://dx.doi.org/10.1016/0300-9629(88)90412-4.

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50

Cook, Elizabeth J., Kate J. Willis, and M. Lozano-Fernandez. "Survivorship, growth and reproduction of the non-native Caprella mutica Schurin, 1935 (Crustacea: Amphipoda)." Hydrobiologia 590, no. 1 (October 2007): 55–64. http://dx.doi.org/10.1007/s10750-007-0757-8.

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