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Is the GDH/RNH4+ ratio in the mesozooplankton constant through different oceanic systems?

Fernández-Urruzola, Igor

Abstract

Nitrogen (N) is essential for life, but its availability is frequently limited in ocean ecosystems. Among all the compounds which influence the N pool, ammonium (NH4+) represents the major source of N for autotrophs. This NH4+ is provided by bacterial remineralization and heterotrophic grazers, with the mesozooplankton responsible for 12% to 33% of the total NH4+ recycled. Quantifying the excretion physiology of zooplankton is then, necessary to understand the basis of an aquatic ecosystem?s productivity. The measurement of glutamate dehydrogenase (GDH) activity has been widely used to assess the NH4+ excretion rates in planktonic communities. However, its relationship with the physiology varies with temperature and the nutritional status of the organisms, among other variables. Here we compare the GDH/RNH4+ ratio between oceanic regions with different trophic conditions. Strengthening our knowledge of the relationship between GDH activities and the NH4+ excretion rates will lead to more meaningful interpretations of the mesoscale variations in planktonic NH4+ excretion.

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ZOOPLANKTON METABOLISM: ENZYMATIC AND PHISIOLOGICAL RATES I Institute of Oceanography and Global Change, Biological Oceanography Group, University of Las Palmas de Gran Canaria, Canary Islands, Spain. E-mail address: [email protected]c.es (I) Nitrogen availability is frequently limited in ocean ecosystems. (II) Phytoplankton can use inorganic fixed-nitrogen compounds (NH4+, NO3-, NO2-), as well as some organic compounds (urea, free amino acids). (III) Other pathways of N cycling (Denitrification, Anammox and DNRA) can occur in OMZ and sediments. (Dugdale and Goering, 1967; Zehr and Ward, 2002; Brandes et al., 2007; Francis et al., 2007; Yool et al., 2007). Zehr and Kudela (2011) INTRODUCTION Classical tenets of Nitrogen Cycle (I) NH4+ is an intermeditate product in decomposition of organic matter, which constitutes the most reduced form of N. (II) NH4+ sustains a global average of 80 % of the authotroph’s requeriments (Harrison, 1992), with the mesozooplankton responsible for 12 – 23 % (Hernández-León, 2008). Zehr and Kudela (2011) INTRODUCTION Importance of NH4+ in marine systems RECYCLYING EFFICIENCY Nutritional History (Miller and Roman, 2008; Saba et al., 2009) Temperature (Ikeda, 1985) Trophic Interactions (Glibert, 1998) WATER BOTTLE–INCUBATIONS ENZYMATIC ASSAYS (GDH) Direct measurement. High data acquisition rate. Low data acquisition rate. Measurement of potential NH4+ excretion. Complicated by organism manipulation, Variability in the GDH/RNH4+ ratio. overcrowding and starvation. (Mulling et al., 1975; Ikeda and Skjoldal, 1980; Bidigare, 1983) (Bidigare and King, 1981) INTRODUCTION How to determine NH4+ excretion in zooplankton? Vmax (I) GDH is found in high levels in planktonic crustaceans (Regnault, 1987). Its role in amino acids catabolism agues for its control over a great proportion of NH4+ excretion. Modified from Yuen and Chiew (2010) INTRODUCTION Biochemistry of NH4+ in marine zooplankton (II) Good correlation with NH4+ excretion in several marine zooplankters. INTRODUCTION Biochemistry of NH4+ in marine zooplankton Park et al. (1986) Table I. Correlation coefficients between GDH and RNH4+ calculated in different works. Some factors could affect the relationship between GDH activity and NH4+ excretion!! – Physiology and biochemistry should share scaling exponent (Berges et al., 1993). – Changes in nutritional state lead to increase the variability (Park, 1986; Hernández-León and Torres, 1997; Fernández-Urruzola et al., 2011). Y = a · Wb (Kleiber, 1961) INTRODUCTION Variability in the GDH to NH4+ excretion ratio MATERIAL AND METHODS Location and Sampling MALASPINA 2010: leg 7 June 2011 CAMVALEX I April 2011 SUCCESSION September 2011 MALASPINA 2010: legs 3 - 4 February 2011 MATERIAL AND METHODS Experimental design 150 m sampling SIZE FRACTIONATION Data analysis Laboratory work at institute PHYSIOLOGYCAL ANALYSES ON BOARD (Holmes et al., 1999) Storage in criovials at -80 oC 100 – 500 µm 500 – 1000 µm > 1000 µm GDH Activity (Bidigare and King, 1981) Intracelullar Substrates (Glutamate and NAD+) Protein mass (Lowry, 1951) - Rapid fall of nitrogen release after depletion of the food source (Mayzaud, 1976; Ikeda and Skjodal, 1980). - GDH does not vary significantly with environmental changes, proving its constitutive nature. RESULTS AND DISCUSSION GDH activity to NH4+ excretion relationship RESULTS AND DISCUSSION Intracellular substrate levels as a key factor RNH4+ NAD+ NADP+ Aguiar-González et al. (2012) Roy and Packard (1998) found a decrease in intracellular substrates concentrations with food source limitation. As a concequence, the actual enzimatic rates would also decrease. Time (h) Substrate (µmols) FOOD LIMITATION An enzyme kinetic-based model should predict the in vivo RNH4+ on natural samples of zooplankton from different productivity areas. RESULTS AND DISCUSSION Future work Packard and Gómez (2008) (I) GDH/RNH4+ is not constant in all the marine ecosystems sampled so far. However, the ratios argue that the zooplankton communities are in a healthy physiological state. (II) Starvation causes NH4+ excretion and GDH activity to diverge more than does biomass. (III) Intracellular substrate levels should explain the variability between the physiological and enzimatic rates. As a result, a kinetic-based model would predict in vivo NH4+ excretion rates better than other theories based in biomass, such as the MTE. SUMMARY This research is framed in the EXZOME project (CTM 2008 – 01616/MAR), which is funded by the extinct Spanish Science and Education Ministry. I. Fernandez-Urruzola receives finantial support from the Formation and Perfection of the Researcher Personal Program from the Basque Government. I also thank to MALASPINA 2010 (CSD-20080077) and SUCCESSION projects for inviting me to participate in their cruises. AWKNOLEDGEMENTS ZOOPLANKTON METABOLISM: ENZYMATIC AND PHISIOLOGICAL RATES I Institute of Oceanography and Global Change, Biological Oceanography Group, University of Las Palmas de Gran Canaria, Canary Islands, Spain. E-mail address: [email protected]c.es