The phytogeography ofCladophora (Chlorophyceae) in the northern Atlantic Ocean,in comparison to that of other benthic algal species

About 43Cladophora species inhabit the coasts of the northern Atlantic Ocean. These can be subdivided into seven distribution groups: (a) the tropical western Atlantic group (16 species); (b) the warm temperate Mediterranean-Atlantic group (9 species); (c) the warm temperate North American group (1 species); (d) the Arctic group (1 species); (e) the amphiatlantic tropical to warm temperature group (7 species); (f) the amphiatlantic tropical to temperate group (4 species), and (g) the amphiatlantic temperate group (5 species). These groups agree with general phytogeographic patterns. Thus, the high numbers of species restricted to the tropical western Atlantic region and the warm temperate Mediteranean-Atlantic region are in agreement with the richness and high degree of endemism of these regions. The fact that all species occurring in northeast America also occur in Europe agrees with the high floristic similarity of the boreal areas in America and Europe. The sediment coasts of the Carolinas are an efficient barrier to the south-north dispersal of benthic algae. The temperature bound phytogeographic limits are set in most cases by the species ability to survive adverse temperatures; for “northern” species to survive a high summer temperature in the south, and for “southern” species to survive a low winter temperature in the north. The limits in the Arctic region are all set by the species ability for sufficient growth and reproduction in summer. Conversely, only few northern species have a southern limit which is set by a winter temperature that is not too high for sufficient growth and reproduction. Most species of this group are winter-annuals at their southern limit, and summer-annuals at their northern limit. A comparatively small number of species with a tropical-to-warm temperate distribution have a northern limit at temperate latitudes which is set by a sufficiently high summer temperature for growth and reproduction. A high proportion of this group are lagoonal or quiet water species, which profit by higher summer temperatures in sheltered waters.C. vagabunda is an example.C. rupestris andC. sericea have an amphiboreal distribution and also occur in the southern temperate belt. They probably used a Pleistocene temperature drop to disperse, through the Atlantic along the African coast, from one hemisphere to the other. In the Pacific temperatures were not sufficiently low for this dispersal; and hence these two species reached the Pacific probably by way of the Bering Strait.     

The distribution of benthic marine algae in relation to the temperature regulation of their life histories

Mainly on the basis of the distribution patterns of 42 species of the recently revised genus Cladopkora (Chlorophyceae) in the north Atlantic Ocean, it appeared possible to distinguish 10 phytogeographic distribution groups of wide applicability. Experimentally determined critical temperatures limiting essential events in the life histories of 17 benthic algal species were used to infer possible phytogeographic boundaries; these appeared to fit closely the phytogeographic boundaries derived from field-distribution data. For a temperate species, at least six different boundaries can be postulated and should be checked in the northern hemisphere: (1) the ‘northern lethal boundary’ (corresponding to the lowest winter temperature which a species can survive); (2) the ‘northern growth boundary’ (corresponding to the lowest summer temperature which, over a period of several months, permits sufficient growth); (3) the ‘northern reproductive boundary’ (corresponding to the lowest summer temperature permitting reproduction over a period of several months); (4–6) the corresponding southern boundaries. Photoperiodic responses may influence the temperature responses. Many phytogeographic boundaries appear to be of a composite nature. For instance, the southern boundary of Laminaria digitata follows the European 10°C February isotherm (which corresponds to the highest winter temperature permitting fertility in the female gametophyte, i.e. to the ‘southern reproductive boundary’), and the American 19°C summer isotherm (corresponding to the ‘southern lethal boundary’). Thus, experimental evidence supports the validity of eight of the following 10 distribution groups (for distribution groups 2 and 6, such evidence could not be found): (1) the amphiatlantic tropical-to-warm temperate group, with a north-eastern extension (examples: Gracilaria foliifera and Centroceras clavulalum); (2) the amphiatlantic tropical-to-warm temperate group, with a north-western extension (example: Hypnea musciformis); (3) the amphiatlantic tropical-to-temperate group (example: Sphacelaria rigidula =furcigera); (4) the amphiatlantic temperate group: the Cladophora rupestris type (examples: Callithamnion hookeri, Dumontia contorta; Laminaria saccharina is transitional to type 10, I., digitata to types 5 and 10); (5) the amphiatlantic temperate group: the Cl. albida type (examples: Scytosiphon lomentaria, Petalonia fascia); (6) the tropical western Atlantic group; (7) the north-east American tropical-to-temperate group (example: Gracilaria tikvahiae); (8) the north-east American temperate group and the corresponding Japanese temperate group (examples: Campylaephora hypneoides and Sargassum muticum); (9) the warm-temperate Mediterranean-Atlantic group, and the corresponding warm-temperate Californian group (examples: Saccorhiza polyschides, Laminaria hyperborea, I., ockroleuca, Macrocystis pyrifera, Hedophyllum sessile); (10) the Arctic group (examples: Saccorhiza dermatodea and Sphacelaria arctica). Distribution groups 6, 9 and 10 have comparatively narrow temperature ranges with a span of 18 22°C between their lethal boundaries and of 5 12°C between their reproductive or growth boundaries. These narrow temperature ranges limit the species in these groups to the tropics; the temperate coasts on the eastern sides of the north Pacific and north Atlantic Oceans and in the southern hemisphere; and to the Arctic, respectively. The narrow temperature ranges of group 9 make the species in this group unfit for life on the western temperate coasts of the north Pacific and north Atlantic Oceans, where algae must cope with annual temperature fluctuations of more than 20°C. Conversely, algae in group 8 (containing the numerous Japanese endemic species) are characterized by wide temperature spans (e.g. 29°C between ‘lethal boundaries’, 12–19°C between ‘growth and/or reproductive boundaries’) and must be potentially capable of occupying wide latitudinal belts on temperate coasts along the east sides of the north Pacific and north Atlantic Oceans. Algae ‘escaped’ from Japan, such as Sargassum muticum, conform to this picture. Apparently Japanese algae do not have the capacity for long distance dispersal. The corresponding east American coasts (30–45 N) harbour very few endemic species, probably as a result of the adverse nature of these sediment coasts for benthic macroalgae and their functioning as a barrier to latitudinal displacements of the flora during glaciations. The remaining distribution groups (1,2,3,4,5,7) are characterized by wide temperature spans and wide distributions, often in both the Atlantic and Pacific Oceans and in both hemispheres. Six temperate species (in distribution groups 4, 5 and 9) with an amphiaequatorial distribution have similar winter-temperature maxima permitting reproduction and corresponding with winter isotherms of 15–17°C; their upper lethal temperatures are more dissimilar and correspond with summer isotherms of 20–30°C. Their amphiaequatorial distribution can be explained by assuming glacial temperature drops along east Pacific and east Atlantic equatorial coasts in narrow belts of intensified upwelling during the presumably intensified glacial circulation of the ocean gyres.     

A COMPARATIVE STUDY OF TEMPERATURE RESPONSES OF CARIBBEAN SEAWEEDS FROM DIFFERENT BIOGEOGRAPHIC GROUPS1

Temperature tolerances were determined for Caribbean isolates (total 31) of seaureds belonging to three distributional groups: 1) species confined to the tropical western Atlantic (Botryocladia spinulifera, Chamaedoris peniculum, Cladophoropsis sundanensis, Dictyopteris justii, Dictyurus occidentalis, Haloplegma duperreyi, and Heterosiphonia gibbesii); 2) amphi-Atlantic species with a (sub)tropical distribution that have their northern boundary in the eastern Atlantic at the tropical Cape Verde Islands (Bryothamnion triquetrum and Ceramium nitens) or the subtropical Canary Islands (Ceratodictyon intricatum, Coelothrix irregularis, Dictyopteris delicatula, Ernodesmis verticillata, and Lophocladia trichoclados; and 3) species with an am-phi-Atlantic tropical to warm-temperate distribution also occurring in the Mediterranean (Cladophoropsis membranacea, Digenea simplex, Microdictyon boergesenii, and Wurdemannia miniata). For some isolates, growth response curves and temperature requirements for reproduction were also determined. Growth occurred in the range (18)20–30° C with optimum growth rates at 25°–30°C, irrespective of distribution group. Reproduction generally occurred at (20)25°–30° C although there were some exceptions. Species were extremely stenothermal, with those restricted to the western Atlantic surviving a total range of only 10/13° C (between 18/20° and 30/33° C). Tolerance to high temperatures was correlated with vertical position in the iniertidal/subtidal zone rather than biogeography grouping. Species restricted to the subtidal were the least tolerant, with permanent survival at 30° C but not at 33°C. Tolerance to low temperatures was not different in subtidal and intertidal species but was significantly better in am phi-Atlantic than in western Atlantic species. In the former group, damage occurred at 15°–18° C but in the latter group at 18°-20° C. We propose that these differences in low-temperature tolerances in Caribbean populations of species from different distribution groups reflect adaptations to glacial cold-stress in the tropical eastern Atlantic and subsequent trans-Atlantic dispersal.     

Temperature responses of tropical to warm temperateCladophora species in relation to their distribution in the North Atlantic Ocean

The relationship between distribution boundaries and temperature responses of some North AtlanticCladophora species (Chlorophyta) was experimentally examined under various regimes of temperature, light and daylength. Experimentally determined critical temperature intervals, in which survival, growth or reproduction was limited, were compared with annual temperature regimes (monthly means and extremes) at sites inside and outside distribution boundaries. The species tested belonged to two phytogeographic groups: (1) the tropical West Atlantic group (C. submarina: isolate from Curaçao) and (2) the amphiatlantic tropical to warm temperate group (C. prolifera: isolate from Corsica;C. coelothrix: isolates from Brittany and Curaçao; andC. laetevirens: isolates from deep and shallow water in Corsica and from Brittany). In accordance with distribution from tropical to warm temperate regions, each of the species grew well between 20–30°C and reproduction and growth were limited at and below 15°C. The upper survival limit in long days was <35°C in all species but high or maximum growth rates occurred at 30°C.C. prolifera, restricted to the tropical margins, had the most limited survival at 35°C. Experimental evidence suggests thatC. submarina is restricted to the Caribbean and excluded from the more northerly American mainland and Gulf of Mexico coasts by sporadic low winter temperatures in the nearshore waters, when cold northerly weather penetrates far south every few years. Experimental evidence suggests thatC. prolifera, C. coelothrix andC. laetevirens are restricted to their northern European boundaries by summer temperatures too low for sufficient growth and/or reproduction. Their progressively more northerly located boundaries were accounted for by differences in growth rates over the critical 10–15°C interval.C. prolifera andC. coelothrix are excluded or restricted in distribution on North Sea coasts by lethal winter temperatures, again differences in cold tolerance accounting for differences in their distribution patterns. On the American coast, species were probably restricted by lethal winter temperatures in the nearshore and, in some cases, by the absence of suitable hard substrates in the more equable offshore waters. Isolates from two points along the European coast (Brittany, Corsica) ofC. laetevirens showed no marked differences in their temperature tolerance but the Caribbean and European isolates ofC. coelothrix differed markedly in their tolerance to low temperatures, the lethal limit of the Caribbean isolate lying more than 5°C higher (at ca 5°C).     

Temperature,light, and photoperiod responses of some Northeast American and West European endemic rhodophytes in relation to their geographic distribution

The relationship between distributional boundaries and temperature responses of some Northeast American and West European endemic and amphiatlantic rhodophytes was experimentally determined under varying regimes of temperature, light, and daylength. Potentially critical temperatures, derived from open ocean surface summer and winter isotherms, were inferred from distributional data for each of these algae. On the basis of the distributional data the algae fall within the limits of three phytogeographic groups: (1) the Northeast American tropical-to-temperate group; (2) the warm-temperate Mediterranean Atlantic group; and (3) the amphiatlantic tropical-to-warm temperate group. Experimental evidence suggests that the species belonging to the northeast American tropical-to-temperate group(Grinnellia americana, Lomentaria baileyana, andAgardhiella subulata) have their northern boundaries determined by a minimum summer temperature high enough for sufficient growth and/or reproduction. The possible restriction of 2 species (G. americana andL. baileyana) to the tropical margins may be caused by summer lethal temperatures (between 30 and 35 °C) or because the gradual disintegration of the upright thalli at high temperatures (>30 °C) promotes an ephemeral existence of these algae towards their southern boundaries. Each of the species have a rapid growth and reproductive potential between 15–30 °C with a broad optimum between 20–30 °C. The lower limit of survival of each species was at least 0 °C (tested in short days only). Growth and reproduction data imply that the restrictive distribution of these algae to the Americas may be due to the fact that for adequate growth and/or reproduction water temperatures must exceed 20 °C. At temperatures 15 °C reproduction and growth are limited, and the amphiatlantic distribution through Iceland would not be permitted. On the basis of experimental evidence, the species belonging to the warm-temperate Mediterranean Atlantic group(Halurus equisetifolius), Callophyllis laciniata, andHypoglossum woodwardii), have their northern boundaries determined by winter lethal temperatures. Growth ofH. equisetifolius proceeded from 10–25 °C, that ofC. laciniata andH. woodwardii from 5–25 °C, in each case with a narrow range for optimal growth at ca. 15 °C. Tetrasporelings ofH. woodwardii showed limited survival at 0 °C for up to 4 d. For all members of the group tetrasporangia occurred from 10–20 °C. The southern boundary ofH. equisetifolius andC. laciniata is a summer lethal temperature whereas that ofH. woodwardii possibly is a winter growth and reproduction limit. Since each member of this group has a rather narrow growth and survival potential at temperatures <5 °C and >20 °C, their occurrence in northeast America is unlikely. The (irregular) distribution ofSolieria tenera (amphiatlantic tropical-to-warm temperate) cannot be entirely explained by the experimental data (possibly as a result of taxonomic uncertainties).Paper presented at the Seaweed Biogeography Workshop of the International Working Group on Seaweed Biogeography, held from 3–7 April, 1984 at the Department of Marine Biology, University of Groningen (The Netherlands). Convenor: C. van den Hoek.     

Thermal tolerance in widespread and tropical Drosophila species: does phenotypic plasticity increase with latitude?

The distribution of insects can often be related to variation in their response to thermal extremes, which in turn may reflect differences in plastic responses or innate variation in resistance. Species with widespread distributions are expected to have evolved higher levels of plasticity than those from restricted tropical areas. This study compares adult thermal limits across five widespread species and five restricted tropical species of Drosophila from eastern Australia and investigates how these limits are affected by developmental acclimation and hardening after controlling for environmental variation and phylogeny. Irrespective of acclimation, cold resistance was higher in the widespread species. Developmental cold acclimation simulating temperate conditions extended cold limits by 2°-4°C, whereas developmental heat acclimation under simulated tropical conditions increased upper thermal limits by <1°C. The response to adult heat-hardening was weak, whereas widespread species tended to have a larger cold-hardening response that increased cold tolerance by 2°-5°C. These patterns persisted after phylogenetic correction and when flies were reared under high and low constant temperatures. The results do not support the hypothesis that widely distributed species have larger phenotypic plasticity for thermal tolerance limits, and Drosophila species distributions are therefore more closely linked to differences in innate thermal tolerance limits.     

Simultaneous and sympatric occurrence of early juveniles of Acanthopagruslatus and A.schlegelii (Sparidae) in the estuary of northern Vietnam

Limnology - Acanthopagruslatus and A.schlegelii (Sparidae) are closely related species distributed in northern tropical to temperate coastal waters of eastern Asia. Early life histories of the two...     

Thermal tolerance ranges and climate variability: A comparison between bivalves from differing climates

The climate variability hypothesis proposes that in variable temperate climates poikilothermic animals have wide thermal tolerance windows, whereas in constant tropical climates they have small thermal tolerance windows. In this study we quantified and compared the upper and lower lethal thermal tolerance limits of numerous bivalve species from a tropical (Roebuck Bay, north western Australia) and a temperate (Wadden Sea, north western Europe) tidal flat. Species from tropical Roebuck Bay had higher upper and lower lethal thermal limits than species from the temperate Wadden Sea, and Wadden Sea species showed an ability to survive freezing temperatures. The increased freezing resistance of the Wadden Sea species resulted in thermal tolerance windows that were on average 7 °C greater than the Roebuck Bay species. Furthermore, at a local-scale, the upper lethal thermal limits of the Wadden Sea species were positively related to submersion time and thus to encountered temperature variation, but this was not the case for the Roebuck Bay species. A review of previous studies, at a global scale, showed that upper lethal thermal limits of tropical species are closer to maximum habitat temperatures than the upper lethal thermal limits of temperate species, suggesting that temperate species are better adapted to temperature variation. In this study, we show for the first time, at both local and global scales, that the lethal thermal limits of bivalves support the climate variability effect in the marine environment.     

Seasonality of peak metabolic rate in non‐migrant tropical birds

Birds that are year‐round residents of temperate and tropical regions have divergent life histories. Tropical birds have a slower ‘pace of life’, one characteristic of which includes lower peak metabolic rate and daily activity levels. Temperate resident birds are faced with seasonal variation in thermogenic demand. This challenge is met with seasonally increased peak metabolic rate during winter. These thermogenic demands are much lower in birds that are year‐round tropical residents. By measuring peak (summit) metabolic rate in tropical and temperate resident bird species during summer and winter, we asked whether tropical birds exhibit seasonality in peak metabolic rate, and if the direction of seasonality differs between tropical and temperate species. We measured summit metabolism in seven tropical and one temperate species during the winter and during the summer breeding season to test the hypothesis that summit metabolism of tropical residents would change seasonally. We consider whether metabolic seasonality is associated with breeding season for tropical species. We found that summit metabolism was significantly greater during the summer for most tropical residents, while the temperate resident matched several previous reports with higher summit metabolism in winter. We conclude that metabolic seasonality occurs in tropical residents and differs from temperate residents, suggesting that breeding during the summer may be driving relatively higher metabolism as compared to winter thermogenesis in temperate birds.     

Life history strategies of cladocerans: comparisons of tropical and temperate taxa

We review recent works on different life history variables of cladoceran taxa in tropical and temperate freshwater bodies, comparing the strategies that cladocerans have evolved to adapt to contrasting environmental conditions in the two geographical regions. These life-history parameters relate to age and size at maturity, survival, fecundity, life-expectancy at birth, lifespan, gross, and net reproductive rates, generation time, the rate of population increase, peak population density and day of peak abundance. We also discuss the role of photoperiod and temperature on some of these life history parameters. We found a general paucity of experimental work and field data in tropics on cladocerans. There is very limited information on the few Daphnia species found in the tropics. The misconception of low species diversity of cladocerans in the tropics arose due to several reasons including lack of extensive and intensive field collections. Higher water temperatures apparently promote permanent infestation of tropical waters with toxic cyanobacteria, which reduce the zooplankton diversity. In addition to higher temperatures in the tropics, the year-round high predation pressure of planktivorous fish probably causes the tropical species, particularly in pelagic habitats, to reach maturity earlier (< 3 days) than in temperate regions. Species of Daphnia in temperate regions are particularly adapted to living at food concentrations that are much lower and seasonably more variable than those for tropical genera such as Diaphanosoma. This is further corroborated by the more than an order of magnitude higher threshold food concentration (TFC) for tropical Cladocera than for their temperate counterparts. Fecundity patterns differ between tropical and temperate cladoceran taxa: cultured under optimal temperature regimes, tropical taxa have fewer eggs than temperate species of a comparable body size. Predation pressure may act differently depending on the size of the cladoceran neonates and thus on their population size structure. Global warming and climate changes seem to affect the behaviour (migration), distribution, and abundance of cladocerans. Apparently, in direct response to these changes, the possibility of encountering the tropical cladocerans in the northern, temperate hemisphere (bioinvasions) is on the rise.     

Life in 3-D: life history strategies in tunas, mackerels and bonitos

The scombrids (tunas, bonitos, Spanish mackerels and mackerels) sustain some of the most important fisheries in the world and their sustainable management depends on better understanding of their life history strategies. Here, we first assemble life history information on maximum size, growth, longevity, maturity, fecundity and spawning duration and interval for all scombrid species. Second we characterize their life history patterns and trait co-variation and evaluate how many principal axes of trait variation underlie scombrid life history strategies. Most of their life history variation can be explained along three axes or dimensions: size, speed, and reproductive schedule. Body size governs the first axis ranking species along a small-large continuum. The second axis was mostly influenced by time-related traits, such as longevity, growth rates, spawning duration, time between spawning events, ranking species along a slow-fast continuum of life histories. Scombrid species with the slowest life histories such as Atlantic bluefin tuna Thunnus thynnus and Atlantic mackerel Scomber scombrus tend to inhabit more temperate waters while species with faster life histories such as yellowfin tuna Thunnus albacares and short mackerel Rastrelliger brachysoma are typically found in more tropical waters. The third axis comprises the negative relationship between number of eggs produced at length of maturity and rate in gain of fecundity with size describing the schedule of reproductive allocation which reflects a fundamental trade-off between reproduction and growth. Finally, in addition we show that the life history strategies of scombrids conform more closely to the Periodic and Opportunistic strategists within the triangular model of fish life histories.     

Stomatal sensitivity to vapour pressure deficit of temperate and tropical evergreen rainforest trees of Australia

Although rainforests of eastern Australia grow in regions of high precipitation, there is a shift from a summer dry season in the temperate south to a winter dry season in the tropical north. Therefore, rainforest trees of eastern Australia provide an opportunity to investigate stomatal sensitivity of mesic trees to vapour pressure deficit (VPD) along a gradient in seasonality of precipitation. Eight rainforest canopy tree species were selected to cover the latitudinal range of rainforests in eastern Australia. Seedlings of these species were grown for a year in glasshouses under ambient conditions or at low VPD and water vapour exchange of leaves was measured during summer. Tropical species, which experience summer-dominant precipitation, showed higher stomatal sensitivities to VPD than temperate species, which experience winter-dominant precipitation. Growing plants under a low VPD increased stomatal sensitivity to increasing VPD in most species. The high stomatal sensitivity to VPD of the tropical species is consistent with the infrequent water stress experienced during their growing season and suggests a high susceptibility to water deficits. In contrast, temperate species may use other mechanisms to maintain photosynthesis under the relatively drier conditions of the temperate growing season.     

Patterns of diversity of the north-eastern Atlantic blenniid fish fauna (Pisces: Blenniidae)

This paper presents an analysis of the distributional patterns of blenniids (Pisces: Blenniidae) in the north‐eastern Atlantic. Two peaks of species diversity were found, both in terms of number of species and number of endemics: one in the tropical African coast and another in the Mediterranean Sea. A cluster analysis of similarity values (Jaccard coefficient) among the eastern Atlantic zoogeographical areas, revealed the following groups: a north temperate group, a tropical group formed by the tropical African coast and Mauritania, another group formed by the islands of Cape Verde, a south temperate group (South Africa), and a southern Atlantic group formed by the islands of Ascension and St Helena. Within the north temperate group, the subgroups with higher similarities were: Azores and Madeira, Canary Islands and Morocco, and the Mediterranean and the Atlantic coast of the Iberian Peninsula. Based on affinity indices, the probable directions of faunal flows were inferred. The tropical coast of Africa and the Mediterranean emerged from this analysis as probable speciation centres of the north‐eastern Atlantic blenniid fauna. The Mediterranean may have also acted as a refuge during glacial periods.     

Geographical and experimental assessment of the distribution ofGracilaria species (Rhodophyta: Gigartinales) in relation to temperature

Tolerance and growth at temperatures from 0° to 36°C were investigated using 15 species and strains ofGracilaria Grev. isolated from tropical and temperate coasts of the Atlantic and eastern Pacific Oceans. All survived a minimum of 15°C and, with two exceptions, a maximum of 28°C. Only two species tolerated 34°C and none 36°C which was rapidly lethal. Isolates intolerant of temperatures less than 15°C were generally species known only from tropical waters, whereas species isolated from temperate waters tended to be eurythermal, and most seemed not to be restricted to cooler waters. Maximum growth of warm-water isolates tended to occur over a broad range of warmer temperatures, 20°C and higher, and usually extended to the upper limits of thermal tolerance. Isolates from temperate waters showed maximum growth at 20° or 15°C, and there was no appreciable growth of any of the isolates below 10°C. These experimental results are in accord with known distributional patterns ofGracilaria. There is a correlation between temperature and number of species, with most species reported from warm-water areas where the mean water temperature is 25°C or more. Where the 3-month mean minimum temperature is less than 20°C, there is a rapid decline in number of species. In the eastern Atlantic, the relationship is less obvious as few species have been reported from the warm-water region. This is quite likely the result of other environmental factors.NRCC No. 23817Paper presented at the Seaweed Biogeography Workshop of the International Working Group on Seaweed Biogeography, held from 3–7 April 1984 at the Department of Marine Biology, Rijksuniversiteit Groningen (The Netherlands). Convenor: C. van den Hoek.     

Photosynthetic responses to vapour pressure deficit in temperate and tropical evergreen rainforest trees of Australia

Rainforests occur in high precipitation areas of eastern Australia, along a gradient in seasonality of precipitation, ranging from a summer dry season in the temperate south to a winter dry season in the tropical north. The response of net photosynthesis to increasing vapour pressure deficit (VPD) was measured in a range of Australian rainforest trees from different latitudes to investigate possible differences in their response to atmospheric drought. Plants were grown in glasshouses under ambient or low VPD to determine the effect of growth VPD on the photosynthetic response. Temperate species, which experience low summer precipitation, were found to maintain maximum net photosynthesis over the measurement range of VPD (0.5–1.9 kPa). In contrast, the tropical species from climates with high summer precipitation showed large reductions in net photosynthesis with increasing VPD. Temperate species showed higher intrinsic water-use efficiencies under low VPD than the tropical species, whereas their efficiencies were similar under high VPD. Growing plants under a low VPD had little effect on either the photosynthetic response to VPD or the intrinsic water-use efficiency of the species. These different responses of gas exchange to VPD shown by the tropical and temperate rainforest species may reflect different strategies to maximise productivity in their respective climates.     

Tropical and temperate freshwater amphidromy: a comparison between life history characteristics of Sicydiinae,ayu, sculpins and galaxiids

Amphidromy is a distinctive form of diadromy, but differences in the life histories of tropical and temperate amphidromous fishes suggest that there are two types of freshwater amphidromy. The life histories of Sicydiinae gobies, ayu (Plecoglossus altivelis), Japanese sculpins (Cottus) and galaxiids (Galaxiidae), suggest that the Sicydiinae are representatives of tropical freshwater amphidromy, whereas ayu, sculpins and galaxiids are representatives of temperate freshwater amphidromy. The Sicydiine larval stage may be required to occur in the ocean for all species, but ayu, sculpins and galaxiids have landlocked or fluvial forms with larvae that do not need to enter the ocean for larval feeding and growth. This suggests that Sicydiine larvae have a high oceanic dependency whereas ayu, sculpins and galaxiid larvae have a low oceanic dependency. Freshwater amphidromous fish in tropical and temperate zones appear to have developed two different strategies in the evolution of their life histories. It is likely that the evolutionary direction of the larval stage of tropical amphidromy is to remain in the sea and that of temperate amphidromy is towards having the ability to remain in freshwater if needed. Tropical and temperate amphidromy appear to be biologically informative categories and evaluations of this hypothesis will facilitate better understanding of the various forms of amphidromy in the future.     

Thermal tolerance of tropical and temperate alpine plants suggests that ‘mountain passes are not higher in the tropics’

Aim

Tolerance of species to extreme temperatures largely determines their distribution and vulnerability to climate change. We examined thermal tolerance in tropical and temperate alpine plants, testing the hypotheses that: (a) temperate plants are resistant to more extreme temperatures and have an overall wider thermal tolerance breadth (TTB); (b) TTB in temperate plants is wider than TTB in tropical plants during the entire growing season; (c) resistance to frost and heat varies during the season in temperate plants but not in tropical plants; (d) TTB of a species predicts its latitudinal range.

Location

Tropical (Ecuador, Bolivia) and temperate (USA, Austria) mountains.

Time period

Four periods of the growing season (2014, 2016–2019).

Major taxa

Ninety-six vascular plant species.

Methods

We employed the electrolyte leakage method to estimate the temperature resistance, that is, the temperature at which 50% tissue injury (Lt50) occurs in leaves. We used phylogenetic linear mixed-effect models in a Bayesian framework to test for differences between the plant groups.

Results

Temperate and tropical plants do not differ in their temperature resistance. The four hypotheses are rejected since: (a) temperate plants do not have significantly wider overall TTB compared to tropical plants, (b) TTB of temperate plants is wider than TTB of tropical plants only at the end of the temperate summer, (c) seasonal acclimation is observed in both plant groups, (d) the latitudinal range of the plants is not related to TTB.

Main conclusions

The lack of TTB differences between temperate and tropical alpine plants is consistent with trends observed in ectothermic animals, which suggests a general latitudinal pattern in high-elevation poikilotherm organisms. Limited acclimation capacity to cope with long freezing exposures restricts the occurrence of tropical alpine species to thermally aseasonal environments making them particularly vulnerable to climate change.     

The biology and life history of arctic populations of the littoral mite Ameronothrus lineatus (Acari, Oribatida)

The present study attempts to elucidate possible microevolutionary adaptations of life-history traits of high-latitude populations of the holarctic, littoral oribatid mite Ameronothrus lineatus by comparing arctic and temperate populations. Additionally, the paper provides an overview of the limited research on general ecology and population biology of arctic populations. In the Arctic the larviparous A. lineatus has a 5-year life cycle (larva-to-larva), and adults survive a further 2–3 years. High survival to maturity is consistent with a low lifetime reproductive output of ca. 20 larvae. The life history can be regarded as an extreme version of the typical oribatid life history. However, several life-history features suggest specific adaptations of arctic populations. In particular, the pre-moult resting stage is synchronized with the warmest part of the arctic summer, which shortens this vulnerable part of development. High reproductive investment by females at relatively low temperatures may represent a physiological adaptation to the cool arctic summer. Finally, prolonged cold exposure positively affects reproduction and survival the following summer, suggesting adaptation of the species to the highly seasonal arctic environment. On the other hand, the ability of all life-cycle stages to overwinter, and a flexible life history with the species being able to take advantage of favourable climatic conditions to accelerate development and larviposition, seem to be ancestral features. Thus, the success of A. lineatus in arctic habitats is probably attributable to a combination of derived and ancestral life-history traits. Studies of conspecific temperate populations are required to elucidate further local adaptations of arctic populations.     

TEMPERATURE RESPONSES AND EVOLUTION OF THERMAL TRAITS IN CLADOPHOROPSIS MEMBRANACEA (SIPHONOCLADALES,CHLOROPHYTA)1

Temperature tolerances and relative growth rates were determined for different isolates of the tropical to warm temperate seaweed species Cladophoropsis membranacea (C. Agardh) Boergesen (Siphonodadales, Chlorophyta) and some related taxa. Most isolates of C membranacea survived undamaged at 18° C for at least 8 weeks. Lower temperatures (5°–15°C) were tolerated for shorter periods of time but caused damage to cells. All isolates survived temperatures up to 34° C, whereas isolates from the eastern Mediterranean and Red Sea survived higher temperatures up to 36°C. Growth occurred between 18° and 32° C, but an isolate from the Red Sea had an extended growth range, reaching its maximum at 35°C. Struvea anastomosans (Harvey) Piccone & Grunow, Cladophoropsis sundanensis Reinbold, and an isolate of C. membranacea from Hawaii were slightly less cold- tolerant, with damage occurring at 18°C. Upper survival temperatures were between 32° and 36° C in these taxa. Temperature response data were mapped onto a phylogenetic tree. Tolerance for low temperatures appears to be a derived character state that supports the hypothesis that C. membranacea originated from a strictly tropical ancestor. Isolates from the Canary Islands, which is near the northern limit of distribution, are ill adapted to local temperature regimes. Isolates from the eastern Mediterranean and Red Sea show some adaptation to local temperature stress. They are isolated from those in the eastern Atlantic by a thermal barrier at the entrance of the Mediterranean.