Ocean biogeochemistry plays a crucial role in sustaining the marine ecosystem and global carbon cycle. To investigate the oceanic biogeochemical responses to iron parameters in the tropical Pacific, we conducted sensitivity experiments using the Nucleus for European Modelling of the Ocean–Tracers of Ocean Phytoplankton with Allometric Zooplankton (NEMO-TOPAZ) model. Compared to observations, the NEMO-TOPAZ model overestimated the concentrations of chlorophyll and dissolved iron (DFe). The sensitivity tests showed that with increasing (+50%) iron scavenging rates, chlorophyll concentrations in the tropical Pacific were reduced by approximately 16%. The bias in DFe also decreased by approximately 7%; however, the sea surface temperature was not affected. As such, these results can facilitate the development of the model tuning strategy to improve ocean biogeochemical performance using the NEMOTOPAZ model.

본 실험은 광 환경이 자생 Veronica속 4종 구와꼬리풀, 봉래꼬리풀, 부산꼬리풀, 큰구와꼬리풀의 생장 및 개화에 미치는 영향을 구명하기 위해 실시하였다. 이중 봉래꼬리풀은 희귀 및 특산식물로 지정되어 있는 우리나라의 자생식물이며 부산꼬리풀은 우리나라에서도 부산지역에서만 자생하는 특산식물이자 자료부족종으로 분류된다. 실험은 2018년 3월 30일부 터 2018년 8월 17일까지 수행되었으며 Veronica속 4종을 0, 40, 60, 90% 차광환경에서 재배하였다. 구와꼬리풀을 0~60% 차광환경에서 재배시 90% 차광환경에서 재배한 개체보다 지상부의 생체중이 무겁고 엽수 및 가지수가 많아 생장이 유의하게 좋았다. 큰구와꼬리풀의 줄기 두께는 90% 차광환경에서 재배시 유의하게 얇아져 생장이 불량하였다. 구와꼬리풀과 큰구와꼬리풀은 0~60% 환경에서 재배시 모든 개체가 개화하였으며 90% 차광환경에서 재배한 개체보다 개화소요일수가 짧 아졌다. 봉래꼬리풀은 0~40% 차광환경에서 재배시 60~90% 차광환경에서 재배한 개체보다 지상부 및 건물증이 유의하게 증가하여 생육이 좋았으며, 관상가치 측면에서 가장 높은 점수를 받았다. 부산꼬리풀의 관상가치는 0, 40, 60, 90% 차광환경에서 재배시 각각 4.0, 3.0, 2.2, 1.0점으로 조사되어 동일한 Veronica속이라도 종에 따라서 광 민감도가 다양한 것을 확인하였다.

Persistent left cranial vena cava (PLCVC) is a remnant vessel connected with the coronary sinus and draining into the right atrium. A 3-month-old intact male Bichon Frise was evaluated for the presence of a mechanical murmur auscultation in the local animal hospital. No significant clinical signs were present on physical examination except mechanical murmur. Patent ductus arteriosus (PDA) was diagnosed in the imaging procedure. During the left thoracotomy, PLCVC was found. The vascular malformation made the surgical process difficult by hiding PDA from the left thoracotomy surgical view. PLCVC and the vagus nerve was carefully dissected and lifted to secure a clear surgical view of PDA. The ductus arteriosus was ligated. Computed tomography angiography (CTA) was performed postoperatively. On CTA, left brachiocephalic vein retaining connection with the coronary sinus draining into the right atrium was observed. CTA is highly recommended for dogs with PDA to provide better postoperative results.

본 실험은 저온처리 기간과 일장이 자생 돌마타리의 휴면타파와 생장 및 개화에 미치는 영향을 구명하기 위해 실시되었다. 노지에서 재배중인 돌마타리의 생물계절현상 반응(phenology) 을 3월부터 10월까지 조사하였다. 또한 저온처리 기간이 돌마타리 휴면타파 및 개화에 미치는 영향을 알아보기 위해 4°C 저온에 0, 3, 6, 9, 12주간 처리한 후 장일환경(16h), 25°C 온도조건에서 재배하면서 생육특성을 관찰하였다. 일장이 돌마타리의 생육 및 개화에 미치는 영향을 알아보기 위해 자연저온 처리된 돌마타리를 단일(9h), 중일(12h), 장일조건(16h)에서 재배하여 생육 특성을 관찰하였다. 야외에서 재배중인 돌마타리는 늦여름인 8월부터 9월까지 개화하는 특성을 보였다. 저온처리 기간에 따른 실험결과 9, 12주 저온처리를 받은 식물이 3, 6주간 저온처리 한 식물에 비해 개화소요일수가 유의하게 단축되었다. 돌마타리는 4°C 온도에서 9주 이상 처리시 33%의 개화율을 보이는 것으로 조사되었다. 일장에 따른 실험결과, 장일환경에서 재배된 돌마타리의 초장은 50.1cm였으나 단일 및 중일환경에서 재배된 식물의 초장은 각각 16.7, 16.1cm로 조사되었다. 돌마타리는 장일환경에서 16주간 재배 시 100% 개화하였으나 단일 및 중일 환경에서 재배 시 전혀 개화하지 않았다. 결론적으로 돌마타리 는 휴면타파 및 개화를 위해 저온을 필수적으로 요구하며 장일 환경조건에서만 개화하는 질적장일식물임을 확인하였다.

The Gwangneung arboretum, affiliated to the Korea Forest Research Institute, was established in 1987 and it became the Korea National Arboretum (KNA) in May 24, 1999. The entomological collection of KNA currently holds a total of 510,365 specimens of 6,849 species including more than 330 type specimens of Lepidoptera, Hemiptera, Hymenoptera, and Coleoptera are deposited. As the results of recent systematic studies by KNA entomologists, 67 new species were described, and 108 species were newly recorded from Korea and other countries. Not only we have conducted taxonomic studies but also have broaden our research boundary to natural enemy surveys for pine wilt disease vectors, plant and insect interaction, and exotic insect species monitoring. In this presentation, we would like to briefly introduce current entomological researches of KNA in the hope of future collaborations with other entomologists.

수노랑나비(Chitoria ulupi (Doherty, 1889))는 한반도 전역에 국지적으로 분포하는 종으로, 국외의 경우 인도, 미얀마, 라오스, 중국, 대만 등에 서식하는 것으로 알려져 있다. 이 종에 대한 생활사는 김과 서(2012)에 의해 확인된 유생기와 번데기의 형태 등이 일부 보고 된 것 이외에는 알려진 바가 없다. 본 연구에서는 한국산 수노랑나비의 생태적 습성(성충 산란행동, 점유행동, 짝짓기, 먹이습성 등)과 미성숙단계 (알, 유충, 번데기)의 형태적 특징 등 생활사 전반에 대하여 보고 하고자 한다.

Photosynthetic characteristics and growth responses of Phalaenopsis Queen Beer ‘Mantefon’ orchid were determined in plants exposed to variable carbon dioxide (CO2) concentrations at 2-, 24-, and 36-weeks age (i.e., corresponding to juvenile, young, and mature vegetative growth stages, respectively). Plants were grown at 400 (control), 800, or 1,600 μmol･mol-1 CO2 for 6 hours during the nighttime for 32 weeks. Phalaenopsis ‘Mantefon’ in 2- and 24-week-old plants grown at 1,600 μmol･mol-1 CO2 had increased leaf number and net CO2 uptake compared with the plants grown at 400 μmol･mol-1 CO2. In 36-week-old of Phalaenopsis ‘Mantefon’, leaf number was significantly greater in plant grown at 800 and 1,600 μmol･mol-1 conditions compared with plants grown at 400 μmol･mol-1 CO2. Leaves that emerged after the start of the CO2 treatment were initially longer in the plants grown at 1,600 μmol･mol-1 CO2 than at 400 μmol·mol-1 C O2, but the final leaf length was shortest in the plants grown at 1,600 μmol･mol-1 CO2 condition. Plants showed crassulancean acid metabolism characteristic of nighttime CO2 uptake regardless plant growth stages. We found that growers may be able to promote leaf growth with increasing leaf number and reducing time to leaf initiation in the 36-week-old (i.e., mature stage) plants with 800 – 1,600 μmol·mol-1 CO2 and 2- and 24-week-old (i.e., juvenile and young stages) plants with 1,600 μmol·mol-1 C O2 for Phalaenopsis ‘Mantefon’.

The purpose of this paper was to investigate the comparison of balance and muscle strength between dominant and non-dominant legs in adults. Thirty adults in their 20s participated in this study. The dominant and non-dominant legs were selected based on the dominant hands of the target. The subject's muscle strength of legs was measured with Nicholas MMT, and the balance was measured with BIO-Rescue. We compared the dominant and non-dominant legs based on the results. The result, indicated no statistical difference on balance and muscle strength between dominant and non-dominant legs(p>.05). The results of this study will be helpful in setting the effective treatment direction and treatment level, and in controlling posture, balance and motor function.

To date, there are no protocols optimized to the effective separation of spermatogonial stem cells (SSCs) from testicular cells derived from mouse testes, thus hindering studies based on mouse SSCs. In this study, we aimed to determine the most efficient purification method for the isolation of SSCs from mouse testes among previously described techniques. Isolation of SSCs from testicular cells derived from mouse testes was conducted using four different techniques: differential plating (DP), magnetic-activated cell sorting (MACS) post-DP, MACS, and positive and negative selection double MACS. DP was performed for 1, 2, 4, 8, or 16 h, and MACS was performed using EpCAM (MACSEpCAM), Thy1 (MACSThy1), or GFR α1 (MACSGFRα1) antibodies. The purification efficiency of each method was analyzed by measuring the percentage of cells that stained positively for alkaline phosphatase. DP for 8 h, MACSThy1 post-DP for 8 h, MACSGFRα1, positive selection double MACSGFRα1/EpCAM, and negative selection double MACSGFRα1/α-SMA were identified as the optimal protocols for isolation of SSCs from mouse testicular cells. Comparison of the purification efficiencies of the optimized isolation protocols showed that, numerically, the highest purification efficiency was obtained using MACSGFRα1. Overall, our results indicate that MACSGFRα1 is an appropriate purification technique for the isolation of SSCs from mouse testicular cells.

Microenvironments surrounded with various extracellular matrix (ECM) components can decide specifically the fate of spermatogonial stem cells (SSCs) and integrin heterodimers recognizing directly ECM proteins play an important role in transporting ECM-derived signals into cytoplasm, resulting in inducing a variety of biological functions such as cell attachment, self-renewal and differentiation. However, to date, studies on type of integrin heterodimers expressed functionally on the undifferentiated SSCs derived from mouse with hybrid strain remain unclear. Therefore, we tried to investigate systematically what kind of integrin heterodimers are expressed transcriptionally, translationally and functionally in the SSCs derived from testis of hybrid (B6CBAF1) mouse. For these, magnetic activated cell sorting (MACS) using Thy1 antibody was used for isolating SSCs from testis, and real-time PCR or fluorescence immunoassay was conducted for measuring transcriptional or translational level of integrin α and β subunits in the isolated SSCs. Subsequently, antibody inhibition assay was conducted for confirming functionality of presumed integrin heterodimers. As the results, transcriptional levels of genes encoding total 25 integrin subunits were quantified, 7 integrin α (α4, α6, α7, α9, αV, αL and αE) and 2 integrin β (β1 and β5) subunit genes showed significantly increased transcriptional up-regulation, compared to the other integrin subunit genes. In contrast, integrin α3, α5, α10 and α11, and integrin β2, β3, β4 and β7 were weakly transcribed. When translational levels of the integrin α subunits showing high transcription level (α4, α6, α7, α9, αV, αL and αE) were measured, significantly strong translational up-regulation of integrin α6, α7, α9, αV and αL subunit genes were detected, whereas integrin α4 and αE subunit genes were weakly. In case of integrin β subunit, β1 evaluated more expression than β5. Based on these results, we speculated that the undifferentiated SSCs derived from B6CBAF1 mouse might express integrin α4β 1, α6β1, α7β1, α9β1, αVβ1 or αVβ5 on plasma membrane. Subsequently, the hybrid strain SSCs showed significantly increased adhesion to fibronectin, laminin, tenascine-C and vitronectin and functional blocking of integrin α4β1, α6β1, α9β1, and αVβ1 or αVβ5 in SSCs significantly inhibited attachment to fibronectin, laminin, tenascin-C and vitronectin, respectively. Accordingly, we could identify that the hybrid (B6CBAF1) mouse-derived SSCs had integrin α4β1, α6β1, α9β1, αVβ1 or αVβ5 on plasma membrane. Moreover, this information will greatly contribute to constructing non-cellular niche supporting self-renewal of SSCs in the future.